scholarly article | Q13442814 |
P50 | author | Sydney Brenner | Q234463 |
P2093 | author name string | Brenner S | |
S Brenner | |||
P2860 | cites work | The DNA of Caenorhabditis elegans | Q33989680 |
Tetramisole (R 8299), a new, potent broad spectrum anthelmintic | Q44842551 | ||
Genetic maping of the free-living nematode Caenorhabditis elegans Maupas 1900, var. Bergerac. I. Study of two dwarf mutants | Q70589477 | ||
P433 | issue | 1 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Caenorhabditis elegans | Q91703 |
Homeobox protein unc-39 CELE_F56A12.1 | Q29793188 | ||
Calcium-dependent secretion activator CELE_ZK897.1 | Q29796376 | ||
Rab-3-interacting molecule unc-10 CELE_T10A3.1 | Q29796519 | ||
Acetylcholine receptor subunit beta-type unc-29 CELE_T08G11.5 | Q29798156 | ||
Adapter protein unc-53 CELE_F45E10.1 | Q29805183 | ||
Acetylcholine receptor subunit alpha-type unc-38 CELE_F21F3.5 | Q29806938 | ||
JNK-interacting protein CELE_ZK1098.10 | Q29808330 | ||
P1104 | number of pages | 24 | |
P304 | page(s) | 71-94 | |
P577 | publication date | 1974-05-01 | |
P1433 | published in | Genetics | Q3100575 |
P1476 | title | THE GENETICS OF <i>CAENORHABDITIS ELEGANS</i> | |
The genetics of Caenorhabditis elegans | |||
P478 | volume | 77 |
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Q90435755 | A metabolic switch regulates the transition between growth and diapause in C. elegans |
Q34134592 | A metabolomic strategy defines the regulation of lipid content and global metabolism by Δ9 desaturases in Caenorhabditis elegans |
Q41383148 | A method for measuring fatty acid oxidation in C. elegans |
Q27315894 | A method to rapidly create protein aggregates in living cells. |
Q37104707 | A microRNA program in the C. elegans hypodermis couples to intestinal mTORC2/PQM-1 signaling to modulate fat transport |
Q92369250 | A microRNA switch controls dietary restriction-induced longevity through Wnt signaling |
Q36713994 | A microcosm of the biomedical research experience for upper-level undergraduates |
Q27335412 | A microfluidic device and automatic counting system for the study of C. elegans reproductive aging |
Q38654794 | A microfluidic device for automated, high-speed microinjection of Caenorhabditis elegans |
Q30541240 | A microfluidic phenotype analysis system reveals function of sensory and dopaminergic neuron signaling in C. elegans electrotactic swimming behavior |
Q57290989 | A microfluidic platform for lifelong high-resolution and high throughput imaging of subtle aging phenotypes in C. elegans |
Q41207206 | A mir-231-Regulated Protection Mechanism against the Toxicity of Graphene Oxide in Nematode Caenorhabditis elegans |
Q30478191 | A missense mutation in Caenorhabditis elegans prohibitin 2 confers an atypical multidrug resistance |
Q43217923 | A model of elegance |
Q35595457 | A model of stem cell population dynamics: in silico analysis and in vivo validation |
Q35098053 | A modular system of DNA enhancer elements mediates tissue-specific activation of transcription by high dietary zinc in C. elegans |
Q36217172 | A molecular mechanism for the requirement of PAT-4 (integrin-linked kinase (ILK)) for the localization of UNC-112 (Kindlin) to integrin adhesion sites |
Q42050028 | A molecular readout of long-term olfactory adaptation in C. elegans |
Q35346021 | A molecular switch that governs mitochondrial fusion and fission mediated by the BCL2-like protein CED-9 of Caenorhabditis elegans |
Q30844489 | A multi-animal tracker for studying complex behaviors |
Q27335780 | A multi-channel device for high-density target-selective stimulation and long-term monitoring of cells and subcellular features in C. elegans |
Q99716350 | A multi-layered and dynamic apical extracellular matrix shapes the vulva lumen in Caenorhabditis elegans |
Q52363982 | A multi-omic analysis reveals the role of fumarate in regulating the virulence of enterohemorrhagic Escherichia coli. |
Q37365584 | A multi-protein receptor-ligand complex underlies combinatorial dendrite guidance choices in C. elegans. |
Q41548236 | A multi-trap microfluidic chip enabling longitudinal studies of nerve regeneration in Caenorhabditis elegans |
Q64237719 | A multicellular rosette-mediated collective dendrite extension |
Q58320918 | A multispectral optical illumination system with precise spatiotemporal control for the manipulation of optogenetic reagents |
Q28291095 | A murine neural-specific homolog corrects cholinergic defects in Caenorhabditis elegans unc-18 mutants |
Q91627582 | A muscle-epidermis-glia signaling axis sustains synaptic specificity during allometric growth in Caenorhabditis elegans |
Q59090188 | A mutation in Caenorhabditis elegans that increases recombination frequency more than threefold |
Q24532227 | A mutation in the age-1 gene in Caenorhabditis elegans lengthens life and reduces hermaphrodite fertility |
Q34012982 | A mutation of cdc-25.1 causes defects in germ cells but not in somatic tissues in C. elegans |
Q33700093 | A native chromatin purification system for epigenomic profiling in Caenorhabditis elegans |
Q30838501 | A natural product inhibits the initiation of α-synuclein aggregation and suppresses its toxicity |
Q59055953 | A natural variant and engineered mutation in a GPCR promote DEET resistance in C. elegans |
Q37122713 | A negative-feedback loop between the detoxification/antioxidant response factor SKN-1 and its repressor WDR-23 matches organism needs with environmental conditions |
Q86803688 | A nematicidal toxin fromPleurotus ostreatus NRRL 3526 |
Q37189132 | A neomorphic syntaxin mutation blocks volatile-anesthetic action in Caenorhabditis elegans |
Q30820116 | A network approach to discerning the identities of C. elegans in a free moving population. |
Q27306247 | A network of HSPG core proteins and HS modifying enzymes regulates netrin-dependent guidance of D-type motor neurons in Caenorhabditis elegans |
Q35991850 | A network of PUF proteins and Ras signaling promote mRNA repression and oogenesis in C. elegans |
Q41952394 | A network of stimulatory and inhibitory Galpha-subunits regulates olfaction in Caenorhabditis elegans |
Q30498840 | A neurodegenerative disease mutation that accelerates the clearance of apoptotic cells |
Q27324458 | A neuromedin U receptor acts with the sensory system to modulate food type-dependent effects on C. elegans lifespan |
Q44540366 | A neuron-specific antigen in C. elegans allows visualization of the entire nervous system |
Q54976796 | A neuronal MAP kinase constrains growth of a C. elegans sensory dendrite throughout the life of the organism. |
Q33520198 | A neuronal acetylcholine receptor regulates the balance of muscle excitation and inhibition in Caenorhabditis elegans |
Q37013595 | A neuronal signaling pathway of CaMKII and Gqα regulates experience-dependent transcription of tph-1. |
Q36304420 | A new Caenorhabditis elegans model of human huntingtin 513 aggregation and toxicity in body wall muscles |
Q42233288 | A new group-training procedure for habituation demonstrates that presynaptic glutamate release contributes to long-term memory in Caenorhabditis elegans |
Q32058603 | A new marker for mosaic analysis in Caenorhabditis elegans indicates a fusion between hyp6 and hyp7, two major components of the hypodermis |
Q35250410 | A new methodology for evaluation of nematode viability |
Q27319371 | A new role for the GARP complex in microRNA-mediated gene regulation |
Q33878175 | A non-canonical site reveals the cooperative mechanisms of microRNA-mediated silencing |
Q34999266 | A non-cell-autonomous role for Ras signaling in C. elegans neuroblast delamination |
Q27319860 | A novel 3-hydroxysteroid dehydrogenase that regulates reproductive development and longevity |
Q30362915 | A novel BK channel-targeted peptide suppresses sound evoked activity in the mouse inferior colliculus. |
Q30573844 | A novel CaM kinase II pathway controls the location of neuropeptide release from Caenorhabditis elegans motor neurons |
Q24300077 | A novel GDP-D-glucose phosphorylase involved in quality control of the nucleoside diphosphate sugar pool in Caenorhabditis elegans and mammals |
Q27934502 | A novel Golgi membrane protein is a partner of the ARF exchange factors Gea1p and Gea2p. |
Q36424229 | A novel and conserved protein AHO-3 is required for thermotactic plasticity associated with feeding states in Caenorhabditis elegans |
Q35634528 | A novel candidate cis-regulatory motif pair in the promoters of germline and oogenesis genes in C. elegans |
Q33954502 | A novel dominant transformer allele of the sex-determining gene her-1 of Caenorhabditis elegans |
Q24676337 | A novel family of C. elegans snRNPs contains proteins associated with trans-splicing |
Q30651037 | A novel function for the Caenorhabditis elegans torsin OOC-5 in nucleoporin localization and nuclear import |
Q37518117 | A novel function for the MAP kinase SMA-5 in intestinal tube stability. |
Q33330189 | A novel function for the presenilin family member spe-4: inhibition of spermatid activation in Caenorhabditis elegans |
Q94554291 | A novel functional cross-interaction between opioid and pheromone signaling may be involved in stress avoidance in Caenorhabditis elegans |
Q34611353 | A novel gain-of-function mutant of the cyclic GMP-dependent protein kinase egl-4 affects multiple physiological processes in Caenorhabditis elegans |
Q30497598 | A novel heme-responsive element mediates transcriptional regulation in Caenorhabditis elegans |
Q28476171 | A novel high throughput assay for anthelmintic drug screening and resistance diagnosis by real-time monitoring of parasite motility |
Q42089588 | A novel interaction between aging and ER overload in a protein conformational dementia |
Q37561658 | A novel mechanism underlies caspase-dependent conversion of the dicer ribonuclease into a deoxyribonuclease during apoptosis |
Q27332814 | A novel molecular solution for ultraviolet light detection in Caenorhabditis elegans |
Q28510855 | A novel mouse model for inhibition of DOHH-mediated hypusine modification reveals a crucial function in embryonic development, proliferation and oncogenic transformation |
Q27325410 | A novel mutation in β integrin reveals an integrin-mediated interaction between the extracellular matrix and cki-1/p27KIP1 |
Q35050899 | A novel nondevelopmental role of the sax-7/L1CAM cell adhesion molecule in synaptic regulation in Caenorhabditis elegans |
Q56888673 | A novel peptide restricts ethanol modulation of the BK channel and |
Q36678015 | A novel protein phosphatase is a binding partner for the protein kinase domains of UNC-89 (Obscurin) in Caenorhabditis elegans |
Q89175180 | A novel requirement for ubiquitin-conjugating enzyme UBC-13 in retrograde recycling of MIG-14/Wntless and Wnt signaling |
Q27346610 | A novel role for the zinc-finger transcription factor EGL-46 in the differentiation of gas-sensing neurons in Caenorhabditis elegans |
Q36841493 | A novel serine protease, Sep1, from Bacillus firmus DS-1 has nematicidal activity and degrades multiple intestinal-associated nematode proteins |
Q36878583 | A novel strategy for cell-autonomous gene knockdown in Caenorhabditis elegans defines a cell-specific function for the G-protein subunit GOA-1. |
Q27345161 | A novel zf-MYND protein, CHB-3, mediates guanylyl cyclase localization to sensory cilia and controls body size of Caenorhabditis elegans |
Q57150050 | A novelstreptomyces species for controlling plant-parasitic nematodes |
Q24337473 | A nuclear role for the respiratory enzyme CLK-1 in regulating mitochondrial stress responses and longevity |
Q67230494 | A pH-correctable, DNA-based fluorescent reporter for organellar calcium |
Q42734778 | A pair of RNA-binding proteins controls networks of splicing events contributing to specialization of neural cell types |
Q39859490 | A pathoadaptive deletion in an enteroaggregative Escherichia coli outbreak strain enhances virulence in a Caenorhabditis elegans model. |
Q37301953 | A pathogenesis assay using Saccharomyces cerevisiae and Caenorhabditis elegans reveals novel roles for yeast AP-1, Yap1, and host dual oxidase BLI-3 in fungal pathogenesis |
Q47341154 | A pathway for low zinc homeostasis that is conserved in animals and acts in parallel to the pathway for high zinc homeostasis |
Q30436503 | A pathway for phagosome maturation during engulfment of apoptotic cells |
Q42519582 | A pathway for unicellular tube extension depending on the lymphatic vessel determinant Prox1 and on osmoregulation |
Q59659395 | A persistent mitochondrial deletion reduces fitness and sperm performance in heteroplasmic populations of C. elegans |
Q37688644 | A perspective on optical developments in microfluidic platforms for Caenorhabditis elegans research |
Q34711569 | A pheromone-induced developmental switch in Caenorhabditis elegans: Temperature-sensitive mutants reveal a wild-type temperature-dependent process |
Q37541319 | A phorbol ester/diacylglycerol-binding protein encoded by the unc-13 gene of Caenorhabditis elegans. |
Q43068649 | A photoconvertible reporter of the ubiquitin-proteasome system in vivo |
Q35573955 | A phylogeny of caenorhabditis reveals frequent loss of introns during nematode evolution |
Q36557055 | A point mutation in the extracellular domain activates LET-23, the Caenorhabditis elegans epidermal growth factor receptor homolog. |
Q37461018 | A possible role for FRM-1, a C. elegans FERM family protein, in embryonic development |
Q41977207 | A post-docking role for active zone protein Rim. |
Q33264396 | A posterior centre establishes and maintains polarity of the Caenorhabditis elegans embryo by a Wnt-dependent relay mechanism |
Q37514492 | A pre- and co-knockdown of RNAseT enzyme, Eri-1, enhances the efficiency of RNAi induced gene silencing in Caenorhabditis elegans |
Q33714088 | A programmable microvalve-based microfluidic array for characterization of neurotoxin-induced responses of individual C. elegans |
Q47191264 | A programmable platform for sub-second multichemical dynamic stimulation and neuronal functional imaging in C. elegans |
Q58758120 | A protein-protein interaction underlies the molecular basis for substrate recognition by an adenosine-to-inosine RNA-editing enzyme |
Q34198686 | A proteomic view of Caenorhabditis elegans caused by short-term hypoxic stress |
Q35202076 | A protocol to infect Caenorhabditis elegans with Salmonella typhimurium |
Q35156707 | A quality control mechanism coordinates meiotic prophase events to promote crossover assurance |
Q34137535 | A quantitative targeted proteomics approach to validate predicted microRNA targets in C. elegans |
Q90091454 | A quiescent state following mild sensory arousal in Caenorhabditis elegans is potentiated by stress |
Q50469080 | A rapid colorimetric assay for the quantitation of the viability of free-living larvae of nematodes in vitro. |
Q35412260 | A rapid protocol for integrating extrachromosomal arrays with high transmission rate into the C. elegans genome |
Q99564822 | A rationally designed bicyclic peptide remodels Aβ42 aggregation in vitro and reduces its toxicity in a worm model of Alzheimer's disease |
Q33784965 | A recent global selective sweep on the age-1 phosphatidylinositol 3-OH kinase regulator of the insulin-like signaling pathway within Caenorhabditis remanei. |
Q37018894 | A redox-sensitive peroxiredoxin that is important for longevity has tissue- and stress-specific roles in stress resistance |
Q40557212 | A related moderately repetitive DNA family in the nematodes Ascaris lumbricoides and Panagrellus silusiae |
Q35054174 | A ribonuclease coordinates siRNA amplification and mRNA cleavage during RNAi |
Q50421780 | A robotic multidimensional directed evolution approach applied to fluorescent voltage reporters. |
Q35545435 | A role for Ras in inhibiting circular foraging behavior as revealed by a new method for time and cell-specific RNAi |
Q28483291 | A role for SKN-1/Nrf in pathogen resistance and immunosenescence in Caenorhabditis elegans |
Q27314537 | A role for autophagy in the extension of lifespan by dietary restriction in C. elegans |
Q37410416 | A role for dynein in the inhibition of germ cell proliferative fate |
Q35038989 | A role for peroxidasin PXN-1 in aspects of C. elegans development |
Q47069429 | A role for post-transcriptional control of endoplasmic reticulum dynamics and function in C. elegans germline stem cell maintenance |
Q39432819 | A role for separase in the regulation of RAB-11-positive vesicles at the cleavage furrow and midbody |
Q37612782 | A role for septin 2 in Drp1-mediated mitochondrial fission |
Q34628996 | A role for the Parkinson's disease protein DJ-1 as a chaperone and antioxidant in the anhydrobiotic nematode Panagrolaimus superbus |
Q29618304 | A role for the RNase III enzyme DCR-1 in RNA interference and germ line development in Caenorhabditis elegans |
Q34198556 | A role for the centrosome and PAR-3 in the hand-off of MTOC function during epithelial polarization |
Q21144893 | A role for the malignant brain tumour (MBT) domain protein LIN-61 in DNA double-strand break repair by homologous recombination |
Q35874945 | A role for α-adducin (ADD-1) in nematode and human memory |
Q37695064 | A role of the LIN-12/Notch signaling pathway in diversifying the non-striated egg-laying muscles in C. elegans |
Q33963024 | A screen for genetic loci required for body-wall muscle development during embryogenesis in Caenorhabditis elegans. |
Q33969917 | A screen for genetic loci required for hypodermal cell and glial-like cell development during Caenorhabditis elegans embryogenesis |
Q36352289 | A screen for protective drugs against delayed hypoxic injury |
Q43268892 | A secreted complement-control-related protein ensures acetylcholine receptor clustering. |
Q36272987 | A selection for myosin heavy chain mutants in the nematode Caenorhabditis elegans |
Q35238305 | A semi-dominant mutation in the general splicing factor SF3a66 causes anterior-posterior axis reversal in one-cell stage C. elegans embryos |
Q55490970 | A sensory-motor neuron type mediates proprioceptive coordination of steering in C. elegans via two TRPC channels. |
Q27311395 | A sexually conditioned switch of chemosensory behavior in C. elegans |
Q35367042 | A shift of the TOR adaptor from Rictor towards Raptor by semaphorin in C. elegans |
Q27320732 | A shift to organismal stress resistance in programmed cell death mutants |
Q90208736 | A short motif in the N-terminal region of α-synuclein is critical for both aggregation and function |
Q41924301 | A simple and rapid method for combining fluorescent in situ RNA hybridization (FISH) and immunofluorescence in the C. elegans germline |
Q48208354 | A simple answer to complex questions: Caenorhabditis elegans as an experimental model for examining the DNA damage response and disease genes. |
Q47417533 | A simple culture system for long-term imaging of individual C. elegans |
Q34529966 | A simplified counter-selection recombineering protocol for creating fluorescent protein reporter constructs directly from C. elegans fosmid genomic clones |
Q33565326 | A single amino acid change converts the sugar sensor SGLT3 into a sugar transporter |
Q34587200 | A single immunoglobulin-domain protein required for clustering acetylcholine receptors in C. elegans |
Q33752587 | A single unpaired and transcriptionally silenced X chromosome locally precludes checkpoint signaling in the Caenorhabditis elegans germ line |
Q34990666 | A small conductance calcium-activated K+ channel in C. elegans, KCNL-2, plays a role in the regulation of the rate of egg-laying |
Q33570139 | A small heat shock protein enables Escherichia coli to grow at a lethal temperature of 50°C conceivably by maintaining cell envelope integrity. |
Q42423561 | A small nucleolar RNA functions in rRNA processing in Caenorhabditis elegans |
Q34592800 | A snapshot of the physical and functional wiring of the Eps15 homology domain network in the nematode. |
Q34985669 | A soma-to-germline transformation in long-lived Caenorhabditis elegans mutants |
Q42588671 | A spatial and temporal map of C. elegans gene expression |
Q42593287 | A specific set of exon junction complex subunits is required for the nuclear retention of unspliced RNAs in Caenorhabditis elegans |
Q35598454 | A specific subset of transient receptor potential vanilloid-type channel subunits in Caenorhabditis elegans endocrine cells function as mixed heteromers to promote neurotransmitter release |
Q30856481 | A spindle checkpoint functions during mitosis in the early Caenorhabditis elegans embryo |
Q36844155 | A starvation-induced noncoding RNA modulates expression of Dicer-regulated genes |
Q28281375 | A steroid receptor-microRNA switch regulates life span in response to signals from the gonad |
Q36703704 | A stochastic neuronal model predicts random search behaviors at multiple spatial scales in C. elegans. |
Q34608418 | A stomatin and a degenerin interact to control anesthetic sensitivity in Caenorhabditis elegans |
Q35976800 | A streamlined tethered chromosome conformation capture protocol. |
Q34684624 | A stress-sensitive reporter predicts longevity in isogenic populations of Caenorhabditis elegans |
Q83229390 | A structural mechanism for phosphorylation-dependent inactivation of the AP2 complex |
Q48523396 | A study of Caenorhabditis elegans DAF-2 mutants by metabolomics and differential correlation networks. |
Q31002019 | A survey of new temperature-sensitive, embryonic-lethal mutations in C. elegans: 24 alleles of thirteen genes |
Q34889521 | A synaptic DEG/ENaC ion channel mediates learning in C. elegans by facilitating dopamine signalling |
Q52722118 | A synthetic icosahedral DNA-based host-cargo complex for functional in vivo imaging. |
Q34318514 | A systematic analysis of protein palmitoylation in Caenorhabditis elegans |
Q34731338 | A systems biological view of intracellular pathogens |
Q37622444 | A tachykinin-like neuroendocrine signalling axis couples central serotonin action and nutrient sensing with peripheral lipid metabolism |
Q28542766 | A target repurposing approach identifies N-myristoyltransferase as a new candidate drug target in filarial nematodes |
Q34615840 | A targeted RNAi screen for genes involved in chromosome morphogenesis and nuclear organization in the Caenorhabditis elegans germline |
Q33574854 | A team of heterochromatin factors collaborates with small RNA pathways to combat repetitive elements and germline stress |
Q93022917 | A tensile trilayered cytoskeletal endotube drives capillary-like lumenogenesis |
Q47069215 | A tension-induced mechanotransduction pathway promotes epithelial morphogenesis. |
Q83225148 | A terminal selector prevents a Hox transcriptional switch to safeguard motor neuron identity throughout life |
Q61806359 | A tetracycline-dependent ribozyme switch allows conditional induction of gene expression in Caenorhabditis elegans |
Q27311422 | A tissue-specific approach to the analysis of metabolic changes in Caenorhabditis elegans |
Q58612849 | A tissue-specific enhancer of the C. elegans nhr-67/tailless gene drives coordinated expression in uterine stem cells and the differentiated anchor cell |
Q30796512 | A tissue-specific protein purification approach in Caenorhabditis elegans identifies novel interaction partners of DLG-1/Discs large. |
Q33552858 | A toolkit for rapid gene mapping in the nematode Caenorhabditis briggsae |
Q27349187 | A transcription elongation factor that links signals from the reproductive system to lifespan extension in Caenorhabditis elegans |
Q52649100 | A transcription factor collective defines the HSN serotonergic neuron regulatory landscape. |
Q35588119 | A transcriptional program promotes remodeling of GABAergic synapses in Caenorhabditis elegans |
Q39896857 | A transcriptional regulatory cascade that controls left/right asymmetry in chemosensory neurons of C. elegans |
Q36466883 | A transgenerational role of the germline nuclear RNAi pathway in repressing heat stress-induced transcriptional activation in C. elegans |
Q44130592 | A transgenic approach to live imaging of heparan sulfate modification patterns |
Q28769077 | A transmembrane guanylyl cyclase (DAF-11) and Hsp90 (DAF-21) regulate a common set of chemosensory behaviors in caenorhabditis elegans |
Q35761575 | A transposon-related palindromic repetitive sequence fromC. elegans |
Q27437606 | A two-gene balance regulates Salmonella typhimurium tolerance in the nematode Caenorhabditis elegans |
Q83230497 | A two-step mechanism for the inactivation of microtubule organizing center function at the centrosome |
Q33552180 | A two-tiered compensatory response to loss of DNA repair modulates aging and stress response pathways |
Q33795335 | A type IV pilin, PilA, Contributes To Adherence of Burkholderia pseudomallei and virulence in vivo. |
Q30492719 | A tyramine-gated chloride channel coordinates distinct motor programs of a Caenorhabditis elegans escape response |
Q34131485 | A ubiquitin E2 variant protein acts in axon termination and synaptogenesis in Caenorhabditis elegans |
Q40625715 | A uniform genetic nomenclature for the nematode Caenorhabditis elegans |
Q34280094 | A unique regulator contributes to quorum sensing and virulence in Burkholderia cenocepacia |
Q24796436 | A universal method for automated gene mapping |
Q40404565 | A variant Tc4 transposable element in the nematode C. elegans could encode a novel protein |
Q41786814 | A visible allele of the muscle gene sup-10X of C. elegans |
Q89802253 | A wake-active locomotion circuit depolarizes a sleep-active neuron to switch on sleep |
Q46925573 | A wax ester promotes collective host finding in the nematode Pristionchus pacificus. |
Q28596381 | A widely employed germ cell marker is an ancient disordered protein with reproductive functions in diverse eukaryotes |
Q27321899 | A wild C. elegans strain has enhanced epithelial immunity to a natural microsporidian parasite |
Q37343724 | A yeast two-hybrid screen for SYP-3 interactors identifies SYP-4, a component required for synaptonemal complex assembly and chiasma formation in Caenorhabditis elegans meiosis |
Q60956829 | A-to-I RNA Editing Affects lncRNAs Expression after Heat Shock |
Q42317731 | A-to-I RNA editing promotes developmental stage-specific gene and lncRNA expression |
Q52273141 | ACaenorhabditis elegans dauer-inducing pheromone and an antagonistic component of the food supply. |
Q41953509 | ADBP-1 regulates an ADAR RNA-editing enzyme to antagonize RNA-interference-mediated gene silencing in Caenorhabditis elegans |
Q30575182 | ADF/cofilin promotes invadopodial membrane recycling during cell invasion in vivo |
Q37383656 | ADM-1, a protein with metalloprotease- and disintegrin-like domains, is expressed in syncytial organs, sperm, and sheath cells of sensory organs in Caenorhabditis elegans |
Q24684472 | AFF-1, a FOS-1-regulated fusogen, mediates fusion of the anchor cell in C. elegans |
Q35180330 | AGS-3 alters Caenorhabditis elegans behavior after food deprivation via RIC-8 activation of the neural G protein G αo. |
Q55076223 | AIM interneurons mediate feeding suppression through the TYRA-2 receptor in C. elegans. |
Q45327685 | AIP limits neurotransmitter release by inhibiting calcium bursts from the ryanodine receptor |
Q37252719 | AIP-1 ameliorates beta-amyloid peptide toxicity in a Caenorhabditis elegans Alzheimer's disease model |
Q36255964 | AIR-2: An Aurora/Ipl1-related protein kinase associated with chromosomes and midbody microtubules is required for polar body extrusion and cytokinesis in Caenorhabditis elegans embryos |
Q41626298 | ALG-5 is a miRNA-associated Argonaute required for proper developmental timing in the Caenorhabditis elegans germline |
Q35670673 | AMP-Activated Kinase Regulates Lipid Droplet Localization and Stability of Adipose Triglyceride Lipase in C. elegans Dauer Larvae |
Q35908579 | AMP-Activated Protein Kinase Regulates Oxidative Metabolism in Caenorhabditis elegans through the NHR-49 and MDT-15 Transcriptional Regulators |
Q36608838 | AMPK activation protects from neuronal dysfunction and vulnerability across nematode, cellular and mouse models of Huntington's disease. |
Q41124214 | AMPK acts as a molecular trigger to coordinate glutamatergic signals and adaptive behaviours during acute starvation. |
Q41677861 | AMPK blocks starvation-inducible transgenerational defects in Caenorhabditis elegans |
Q92541143 | AMPK regulates germline stem cell quiescence and integrity through an endogenous small RNA pathway |
Q37532226 | ANK repeat-domain of SHN-1 Is indispensable for in vivo SHN-1 function in C. elegans |
Q47129524 | APC/CFZR-1 Controls SAS-5 Levels To Regulate Centrosome Duplication in Caenorhabditis elegans. |
Q33894454 | APH-1 is a multipass membrane protein essential for the Notch signaling pathway in Caenorhabditis elegans embryos |
Q35629330 | APL-1, a Caenorhabditis elegans protein related to the human beta-amyloid precursor protein, is essential for viability |
Q36028971 | APL-1, the Alzheimer's Amyloid precursor protein in Caenorhabditis elegans, modulates multiple metabolic pathways throughout development |
Q33873626 | APX-1 can substitute for its homolog LAG-2 to direct cell interactions throughout Caenorhabditis elegans development |
Q36536624 | APY-1, a novel Caenorhabditis elegans apyrase involved in unfolded protein response signalling and stress responses. |
Q90726570 | ASICs Mediate Food Responses in an Enteric Serotonergic Neuron that Controls Foraging Behaviors |
Q27317086 | ASM-3 acid sphingomyelinase functions as a positive regulator of the DAF-2/AGE-1 signaling pathway and serves as a novel anti-aging target |
Q64101644 | ATG-18 and EPG-6 are Both Required for Autophagy but Differentially Contribute to Lifespan Control in |
Q38216205 | ATG13: just a companion, or an executor of the autophagic program? |
Q91934367 | ATGL-1 mediates the effect of dietary restriction and the insulin/IGF-1 signaling pathway on longevity in C. elegans |
Q64387176 | ATM and ATR Influence Meiotic Crossover Formation Through Antagonistic and Overlapping Functions in |
Q41333498 | ATP depletion is the major cause of MPP+ induced dopamine neuronal death and worm lethality in alpha-synuclein transgenic C. elegans |
Q24316943 | ATP-2 interacts with the PLAT domain of LOV-1 and is involved in Caenorhabditis elegans polycystin signaling |
Q34886289 | ATP-binding cassette transporters are required for efficient RNA interference in Caenorhabditis elegans |
Q59792585 | ATP-dependent membrane remodeling links EHD1 functions to endocytic recycling |
Q27307794 | ATX-2, the C. elegans Ortholog of Human Ataxin-2, Regulates Centrosome Size and Microtubule Dynamics |
Q30010000 | Abelson interactor-1 (ABI-1) interacts with MRL adaptor protein MIG-10 and is required in guided cell migrations and process outgrowth in C. elegans |
Q36648685 | Aberrant Activation of p38 MAP Kinase-Dependent Innate Immune Responses Is Toxic to Caenorhabditis elegans. |
Q27309058 | Aberrant fat metabolism in Caenorhabditis elegans mutants with defects in the defecation motor program |
Q28512722 | Aberrant morphology and residual transmitter release at the Munc13-deficient mouse neuromuscular synapse |
Q33436384 | Abl kinase inhibits the engulfment of apoptotic [corrected] cells in Caenorhabditis elegans |
Q89454784 | Ablation of N-acetylglucosaminyltransferases in Caenorhabditis induces expression of unusual intersected and bisected N-glycans |
Q35998452 | Abnormal Osmotic Avoidance Behavior in C. elegans Is Associated with Increased Hypertonic Stress Resistance and Improved Proteostasis |
Q34632518 | Absence of effects of Sir2 overexpression on lifespan in C. elegans and Drosophila |
Q36100107 | Accelerating Gene Discovery by Phenotyping Whole-Genome Sequenced Multi-mutation Strains and Using the Sequence Kernel Association Test (SKAT) |
Q33669674 | Acidic intracellular pH shift during Caenorhabditis elegans larval development. |
Q57492550 | Acoustic Compressibility of Caenorhabditis elegans |
Q40650904 | Acquired Tolerance to Ivermectin and Moxidectin after Drug Selection Pressure in the Nematode Caenorhabditis elegans |
Q91640934 | Acrocomia aculeata (Jacq.) Lodd. ex Mart. Leaves Increase SIRT1 Levels and Improve Stress Resistance |
Q48399592 | Actin gene family of Caenorhabditis elegans |
Q37322303 | Actin-ADF/cofilin rod formation in Caenorhabditis elegans muscle requires a putative F-actin binding site of ADF/cofilin at the C-terminus |
Q30498168 | Action potentials drive body wall muscle contractions in Caenorhabditis elegans |
Q33259341 | Activated AKT/PKB signaling in C. elegans uncouples temporally distinct outputs of DAF-2/insulin-like signaling |
Q34229357 | Activated and inactivated immune responses in Caenorhabditis elegans against Photorhabdus luminescens TT01 |
Q45084931 | Activation of EGL-47, a Galpha(o)-coupled receptor, inhibits function of hermaphrodite-specific motor neurons to regulate Caenorhabditis elegans egg-laying behavior. |
Q88363436 | Activation of Gαq Signaling Enhances Memory Consolidation and Slows Cognitive Decline |
Q58707452 | Activation of RHO-1 in cholinergic motor neurons competes with dopamine signalling to control locomotion |
Q41789646 | Activation of SKN-1 by novel kinases in Caenorhabditis elegans |
Q35776646 | Activation of Wnt signaling bypasses the requirement for RTK/Ras signaling during C. elegans vulval induction |
Q39458782 | Activation of hypodermal differentiation in the Caenorhabditis elegans embryo by GATA transcription factors ELT-1 and ELT-3 |
Q33730434 | Activation of the endoplasmic reticulum unfolded protein response by lipid disequilibrium without disturbed proteostasis in vivo |
Q33375026 | Activation of the unfolded protein response is required for defenses against bacterial pore-forming toxin in vivo. |
Q64110388 | Active backlight for automating visual monitoring: An analysis of a lighting control technique for Caenorhabditis elegans cultured on standard Petri plates |
Q64065395 | Active propagation of dendritic electrical signals in C. elegans |
Q34727856 | Active torque generation by the actomyosin cell cortex drives left-right symmetry breaking |
Q34666406 | Active transcriptomic and proteomic reprogramming in the C. elegans nucleotide excision repair mutant xpa-1. |
Q27318730 | Active transport and diffusion barriers restrict Joubert Syndrome-associated ARL13B/ARL-13 to an Inv-like ciliary membrane subdomain |
Q38811816 | Activity of caffeic acid phenethyl ester in Caenorhabditis elegans |
Q42356879 | Activity of the C. elegans egg-laying behavior circuit is controlled by competing activation and feedback inhibition |
Q33952357 | Activity of the sex-determining gene tra-2 is modulated to allow spermatogenesis in the C. elegans hermaphrodite |
Q50091958 | Actomyosin contractility regulators stabilize the cytoplasmic bridge between the two primordial germ cells during Caenorhabditis elegans embryogenesis. |
Q30536896 | Actomyosin-based self-organization of cell internalization during C. elegans gastrulation |
Q90646006 | Acute Effects of Drugs on Caenorhabditis elegans Movement Reveal Complex Responses and Plasticity |
Q39355888 | Acute exposure to a Mn/Zn ethylene-bis-dithiocarbamate fungicide leads to mitochondrial dysfunction and increased reactive oxygen species production in Caenorhabditis elegans |
Q35638842 | Acyl-CoA Dehydrogenase Drives Heat Adaptation by Sequestering Fatty Acids |
Q37691717 | Adaptive capacity to bacterial diet modulates aging in C. elegans |
Q36510548 | Additional evidence for an eight-transmembrane-domain topology for Caenorhabditis elegans and human presenilins |
Q33961353 | Additional sequence complexity in the muscle gene, unc-22, and its encoded protein, twitchin, of Caenorhabditis elegans |
Q37247900 | Adenine nucleotide translocator cooperates with core cell death machinery to promote apoptosis in Caenorhabditis elegans. |
Q33967919 | Adjustments, extinction, and remains of selenocysteine incorporation machinery in the nematode lineage. |
Q51354843 | Adsorbable organic bromine compounds (AOBr) in aquatic samples: a nematode-based toxicogenomic assessment of the exposure hazard. |
Q38658521 | Adult stem cell lineage tracing and deep tissue imaging |
Q37689890 | Adverse Effects of Hydroalcoholic Extracts and the Major Components in the Stems of Impatiens balsamina L. on Caenorhabditis elegans |
Q37499376 | Adverse effects from clenbuterol and ractopamine on nematode Caenorhabditis elegans and the underlying mechanism |
Q36236213 | Aflatoxin B₁-Induced Developmental and DNA Damage in Caenorhabditis elegans |
Q28608621 | Agarose Microchambers for Long-term Calcium Imaging of Caenorhabditis elegans |
Q40877739 | Age dependent changes in the behavior of Caenorhabditis elegans on attraction to Escherichia coli |
Q92523995 | Age- and stress-associated C. elegans granulins impair lysosomal function and induce a compensatory HLH-30/TFEB transcriptional response |
Q36255367 | Age-Dependent Neuroendocrine Signaling from Sensory Neurons Modulates the Effect of Dietary Restriction on Longevity of Caenorhabditis elegans |
Q36507786 | Age-Related Phasic Patterns of Mitochondrial Maintenance in Adult Caenorhabditis elegans Neurons |
Q70293860 | Age-correlated changes in the DNA template in the nematode Caenorhabditis elegans |
Q37671517 | Age-dependent changes in mitochondrial morphology and volume are not predictors of lifespan |
Q28572651 | Age-dependent deterioration of nuclear pore complexes causes a loss of nuclear integrity in postmitotic cells |
Q24537685 | Age-related changes of nuclear architecture in Caenorhabditis elegans |
Q30577999 | Age-related degeneration of the egg-laying system promotes matricidal hatching in Caenorhabditis elegans |
Q37298883 | Age-related micro-RNA abundance in individual C. elegans |
Q48230373 | Ageing and hypoxia cause protein aggregation in mitochondria |
Q39656906 | Aging and SKN-1-dependent Loss of 20S Proteasome Adaptation to Oxidative Stress in C. elegans. |
Q34627916 | Aging can be genetically dissected into component processes using long-lived lines of Caenorhabditis elegans |
Q36728110 | Alcaligenes faecalis ZD02, a Novel Nematicidal Bacterium with an Extracellular Serine Protease Virulence Factor |
Q35135023 | Alcohol disinhibition of behaviors in C. elegans |
Q42024884 | All the microbiology nematodes can teach us. |
Q34082199 | Allele-specific suppressors of lin-1(R175Opal) identify functions of MOC-3 and DPH-3 in tRNA modification complexes in Caenorhabditis elegans |
Q35863035 | Allelic ratios and the mutational landscape reveal biologically significant heterozygous SNVs |
Q27334318 | Allyl isothiocyanate that induces GST and UGT expression confers oxidative stress resistance on C. elegans, as demonstrated by nematode biosensor |
Q36325218 | Alpha spectrin is essential for morphogenesis and body wall muscle formation in Caenorhabditis elegans |
Q27934988 | Alpha-synuclein is part of a diverse and highly conserved interaction network that includes PARK9 and manganese toxicity |
Q36294632 | Alteration of Caenorhabditis elegans gene expression by targeted transformation |
Q36659504 | Alterations in cell lineage following laser ablation of cells in the somatic gonad of Caenorhabditis elegans |
Q37079604 | Altered Function of the DnaJ Family Cochaperone DNJ-17 Modulates Locomotor Circuit Activity in a Caenorhabditis elegans Seizure Model |
Q40967033 | Altered Sensory Code Drives Juvenile-to-Adult Behavioral Maturation in Caenorhabditis elegans. |
Q35013461 | Altered bacterial metabolism, not coenzyme Q content, is responsible for the lifespan extension in Caenorhabditis elegans fed an Escherichia coli diet lacking coenzyme Q. |
Q54403950 | Altered establishment of cell lineages in theCaenorhabditis elegans embryo after suppression of the first cleavage supports a concentration-dependent decision mechanism. |
Q36530672 | Altered expression of an L1-specific, O-linked cuticle surface glycoprotein in mutants of the nematode Caenorhabditis elegans |
Q24652699 | Alternative induction of meiotic recombination from single-base lesions of DNA deaminases |
Q35201720 | Alternative olfactory neuron fates are specified by the LIM homeobox gene lim-4. |
Q40625066 | Alternative splicing of N- and C-termini of a C. elegans ClC channel alters gating and sensitivity to external Cl- and H+. |
Q98192779 | Alternative splicing of coq-2 controls the level of rhodoquinone in animals |
Q33611000 | Alternative trans-splicing of Caenorhabditis elegans sma-9/schnurri generates a short transcript that provides tissue-specific function in BMP signaling |
Q42918980 | Alternatively spliced isoforms encoded by cadherin genes from C. elegansgenome |
Q52644082 | Alzheimer's Disease and Sleep-Wake Disturbances: Amyloid, Astrocytes, and Animal Models. |
Q38139529 | Alzheimer's disease drug discovery: in vivo screening using Caenorhabditis elegans as a model for β-amyloid peptide-induced toxicity |
Q36402065 | Amelioration of metal-induced toxicity in Caenorhabditis elegans: utility of chelating agents in the bioremediation of metals |
Q35830248 | Ammonia excretion in Caenorhabditis elegans: mechanism and evidence of ammonia transport of the Rhesus protein CeRhr-1. |
Q28472969 | Ammonium-acetate is sensed by gustatory and olfactory neurons in Caenorhabditis elegans |
Q37048354 | Amphetamine activates an amine-gated chloride channel to generate behavioral effects in Caenorhabditis elegans |
Q37359550 | Amplification of siRNA in Caenorhabditis elegans generates a transgenerational sequence-targeted histone H3 lysine 9 methylation footprint |
Q28649959 | Amyloid domains in the cell nucleus controlled by nucleoskeletal protein lamin B1 reveal a new pathway of mercury neurotoxicity |
Q27312214 | An AGEF-1/Arf GTPase/AP-1 ensemble antagonizes LET-23 EGFR basolateral localization and signaling during C. elegans vulva induction |
Q27313222 | An ALS-linked mutant SOD1 produces a locomotor defect associated with aggregation and synaptic dysfunction when expressed in neurons of Caenorhabditis elegans |
Q41834228 | An AMPK-FOXO pathway mediates longevity induced by a novel method of dietary restriction in C. elegans |
Q37099127 | An Abundant Class of Non-coding DNA Can Prevent Stochastic Gene Silencing in the C. elegans Germline. |
Q36971366 | An Afg2/Spaf-related Cdc48-like AAA ATPase regulates the stability and activity of the C. elegans Aurora B kinase AIR-2 |
Q38725828 | An Ancient, Unified Mechanism for Metformin Growth Inhibition in C. elegans and Cancer |
Q47232485 | An Antimicrobial Peptide and Its Neuronal Receptor Regulate Dendrite Degeneration in Aging and Infection. |
Q42290860 | An Aversive Response to Osmotic Upshift in Caenorhabditis elegans |
Q37334917 | An ER-resident membrane protein complex regulates nicotinic acetylcholine receptor subunit composition at the synapse |
Q58728265 | An Efficient Genome Editing Strategy To Generate Putative Null Mutants in Using CRISPR/Cas9 |
Q47293175 | An Elongin-Cullin-SOCS Box Complex Regulates Stress-Induced Serotonergic Neuromodulation. |
Q35963706 | An Eph receptor sperm-sensing control mechanism for oocyte meiotic maturation in Caenorhabditis elegans |
Q40056909 | An Evolutionarily Conserved Pathway Essential for Orsay Virus Infection of Caenorhabditis elegans |
Q47231364 | An Expanded Role for the RFX Transcription Factor DAF-19, with Dual Functions in Ciliated and Non-ciliated Neurons |
Q30489873 | An Eye on Age-Related Macular Degeneration: The Role of MicroRNAs in Disease Pathology. |
Q47069492 | An FGF receptor signaling pathway is required for the normal cell migrations of the sex myoblasts in C. elegans hermaphrodites |
Q37349779 | An H4K16 histone acetyltransferase mediates decondensation of the X chromosome in C. elegans males |
Q35193313 | An HMG1-like protein facilitates Wnt signaling in Caenorhabditis elegans |
Q39096917 | An Inquiry-Based Approach to Study the Synapse: Student-Driven Experiments Using C. elegans |
Q46018404 | An Intracellular Pathogen Response Pathway Promotes Proteostasis in C. elegans. |
Q47558391 | An Investigation of the Potential Antifungal Properties of CNC-2 in Caenorhabditis elegans |
Q37594264 | An NAD(+) biosynthetic pathway enzyme functions cell non-autonomously in C. elegans development |
Q89291583 | An RNA-Binding Multimer Specifies Nematode Sperm Fate |
Q35071050 | An RNAi-based dimorphic genetic screen identified the double bromodomain protein BET-1 as a sumo-dependent attenuator of RAS-mediated signalling |
Q34713924 | An RNAi-based suppressor screen identifies interactors of the Myt1 ortholog of Caenorhabditis elegans |
Q37107003 | An Sp1 transcription factor coordinates caspase-dependent and -independent apoptotic pathways |
Q68724124 | An X-autosome fusion chromosome of Caenorhabditis elegans |
Q33994977 | An acetylcholinesterase-deficient mutant of the nematode Caenorhabditis elegans |
Q35856949 | An activating mutation in sos-1 identifies its Dbl domain as a critical inhibitor of the epidermal growth factor receptor pathway during Caenorhabditis elegans vulval development |
Q27346623 | An alpha-catulin homologue controls neuromuscular function through localization of the dystrophin complex and BK channels in Caenorhabditis elegans |
Q89873119 | An alternatively spliced, non-signaling insulin receptor modulates insulin sensitivity via insulin peptide sequestration in C. elegans |
Q61446520 | An ancient role for collier/Olf/Ebf (COE)-type transcription factors in axial motor neuron development |
Q36235722 | An ankyrin-related gene (unc-44) is necessary for proper axonal guidance in Caenorhabditis elegans |
Q41854059 | An anoxia-starvation model for ischemia/reperfusion in C. elegans |
Q36593553 | An anticancer drug suppresses the primary nucleation reaction that initiates the production of the toxic Aβ42 aggregates linked with Alzheimer's disease |
Q46252468 | An asymmetric attraction model for the diversity and robustness of cell arrangement in nematodes. |
Q34714921 | An asymmetric chromosome pair undergoes synaptic adjustment and crossover redistribution during Caenorhabditis elegans meiosis: implications for sex chromosome evolution |
Q47239050 | An atlas of Caenorhabditis elegans chemoreceptor expression |
Q38637521 | An automated compound screening for anti-aging effects on the function of C. elegans sensory neurons |
Q50421789 | An automated method for the analysis of food intake behaviour in Caenorhabditis elegans. |
Q38402249 | An automated microfluidic system for screening Caenorhabditis elegans behaviors using electrotaxis |
Q24793351 | An automated system for measuring parameters of nematode sinusoidal movement |
Q61198343 | An autonomous DNA nanomachine maps spatiotemporal pH changes in a multicellular living organism |
Q37387856 | An eIF4E-binding protein regulates katanin protein levels in C. elegans embryos |
Q41860377 | An elt-3/elt-5/elt-6 GATA transcription circuit guides aging in C. elegans |
Q27333115 | An engineering approach to extending lifespan in C. elegans |
Q41548039 | An enhanced C. elegans based platform for toxicity assessment. |
Q33710158 | An essential role for XBP-1 in host protection against immune activation in C. elegans |
Q41074972 | An essential ubiquitin-conjugating enzyme with tissue and developmental specificity in th nematode Caenorhabditis elegans. |
Q37473134 | An evolutionarily conserved presynaptic protein is required for isoflurane sensitivity in Caenorhabditis elegans |
Q27346568 | An evolutionarily conserved switch in response to GABA affects development and behavior of the locomotor circuit of Caenorhabditis elegans |
Q92003516 | An excreted small molecule promotes C. elegans reproductive development and aging |
Q36451998 | An exon that prevents transport of a mature mRNA. |
Q35720447 | An explicit test of the phospholipid saturation hypothesis of acquired cold tolerance in Caenorhabditis elegans |
Q42093553 | An expression screen for RhoGEF genes involved in C. elegans gonadogenesis |
Q41962677 | An extracellular adhesion molecule complex patterns dendritic branching and morphogenesis. |
Q36862533 | An extrasynaptic GABAergic signal modulates a pattern of forward movement in Caenorhabditis elegans |
Q27320765 | An image-free opto-mechanical system for creating virtual environments and imaging neuronal activity in freely moving Caenorhabditis elegans |
Q24793344 | An imaging system for standardized quantitative analysis of C. elegans behavior |
Q71334987 | An immunohistochemical study of the 32-kDa galectin (beta-galactoside-binding lectin) in the nematode Caenorhabditis elegans |
Q34407919 | An in vivo C. elegans model system for screening EGFR-inhibiting anti-cancer drugs |
Q27315937 | An in vivo EGF receptor localization screen in C. elegans Identifies the Ezrin homolog ERM-1 as a temporal regulator of signaling |
Q47101276 | An in vivo genetic screen for genes involved in spliced leader trans-splicing indicates a crucial role for continuous de novo spliced leader RNP assembly |
Q92622793 | An inexpensive programmable optogenetic platform for controlled neuronal activation regimens in C. elegans |
Q34602710 | An insulin-like signaling pathway affects both longevity and reproduction in Caenorhabditis elegans. |
Q30524858 | An integrated fiber-optic microfluidic device for detection of muscular force generation of microscopic nematodes |
Q35107064 | An integrated platform enabling optogenetic illumination of Caenorhabditis elegans neurons and muscular force measurement in microstructured environments |
Q41853152 | An integrated serotonin and octopamine neuronal circuit directs the release of an endocrine signal to control C. elegans body fat. |
Q27312196 | An integrated strategy to study muscle development and myofilament structure in Caenorhabditis elegans |
Q35049148 | An internal deletion mutant of a myosin heavy chain in Caenorhabditis elegans |
Q40959295 | An intersectional gene regulatory strategy defines subclass diversity of C. elegans motor neurons. |
Q24294713 | An intracellular serpin regulates necrosis by inhibiting the induction and sequelae of lysosomal injury |
Q42142729 | An introduction to worm lab: from culturing worms to mutagenesis. |
Q36321136 | An ion channel of the degenerin/epithelial sodium channel superfamily controls the defecation rhythm in Caenorhabditis elegans |
Q28362206 | An isoform of eIF4E is a component of germ granules and is required for spermatogenesis in C. elegans |
Q30588525 | An open-source analytical platform for analysis of C. elegans swimming-induced paralysis |
Q47298913 | An optogenetic arrhythmia model to study catecholaminergic polymorphic ventricular tachycardia mutations |
Q30539096 | An organelle gatekeeper function for Caenorhabditis elegans UNC-16 (JIP3) at the axon initial segment |
Q40071721 | An oxytocin-dependent social interaction between larvae and adult C. elegans. |
Q28487176 | An ultra high-throughput, whole-animal screen for small molecule modulators of a specific genetic pathway in Caenorhabditis elegans |
Q34365145 | An uncapped RNA suggests a model for Caenorhabditis elegans polycistronic pre-mRNA processing |
Q33373524 | An unexpectedly high degree of specialization and a widespread involvement in sterol metabolism among the C. elegans putative aminophospholipid translocases |
Q30529364 | Analysis of C. elegans NR2E nuclear receptors defines three conserved clades and ligand-independent functions |
Q37472984 | Analysis of C. elegans muscle transcriptome using trans-splicing-based RNA tagging (SRT). |
Q30536514 | Analysis of Ca2+ signaling motifs that regulate proton signaling through the Na+/H+ exchanger NHX-7 during a rhythmic behavior in Caenorhabditis elegans |
Q42126012 | Analysis of Drosophila paramyosin: identification of a novel isoform which is restricted to a subset of adult muscles |
Q64263299 | Analysis of Mutants Suggests Kamin Blocking in C. elegans is Due to Interference with Memory Recall Rather than Storage |
Q30540659 | Analysis of NPR-1 reveals a circuit mechanism for behavioral quiescence in C. elegans |
Q37485618 | Analysis of a lin-42/period Null Allele Implicates All Three Isoforms in Regulation of Caenorhabditis elegans Molting and Developmental Timing |
Q33954666 | Analysis of a mutator activity necessary for germline transposition and excision of Tc1 transposable elements in Caenorhabditis elegans. |
Q37614633 | Analysis of a transposable element in Caenorhabditis elegans |
Q30581890 | Analysis of centriole elimination during C. elegans oogenesis |
Q34846048 | Analysis of conserved residues in the betapat-3 cytoplasmic tail reveals important functions of integrin in multiple tissues. |
Q34989396 | Analysis of genetic code ambiguity arising from nematode-specific misacylated tRNAs |
Q33214158 | Analysis of long-lived C. elegans daf-2 mutants using serial analysis of gene expression |
Q33895337 | Analysis of multiple ethyl methanesulfonate-mutagenized Caenorhabditis elegans strains by whole-genome sequencing |
Q33961974 | Analysis of mutations in the sqt-1 and rol-6 collagen genes of Caenorhabditis elegans |
Q30480641 | Analysis of nematode mechanics by piezoresistive displacement clamp |
Q34602420 | Analysis of osm-6, a gene that affects sensory cilium structure and sensory neuron function in Caenorhabditis elegans |
Q24550910 | Analysis of smu-1, a gene that regulates the alternative splicing of unc-52 pre-mRNA in Caenorhabditis elegans |
Q37742134 | Analysis of the NK2 homeobox gene ceh-24 reveals sublateral motor neuron control of left-right turning during sleep |
Q34514250 | Analysis of the Na+/Ca2+ exchanger gene family within the phylum Nematoda |
Q92282289 | Analysis of the Pseudomonas aeruginosa Aminoglycoside Differential Resistomes Allows Defining Genes Simultaneously Involved in Intrinsic Antibiotic Resistance and Virulence |
Q36643765 | Analysis of the VPE sequences in the Caenorhabditis elegans vit-2 promoter with extrachromosomal tandem array-containing transgenic strains |
Q37321090 | Analysis of the constancy of DNA sequences during development and evolution of the nematode Caenorhabditis elegans |
Q33964447 | Analysis of the multiple roles of gld-1 in germline development: interactions with the sex determination cascade and the glp-1 signaling pathway |
Q37283534 | Analyzing observed or hidden heterogeneity on survival and mortality in an isogenic C. elegans cohort |
Q38662569 | Analyzing the locomotory gaitprint of Caenorhabditis elegans on the basis of empirical mode decomposition |
Q36544676 | Anatomy, physiology and pharmacology of Caenorhabditis elegans pharynx: a model to define gene function in a simple neural system |
Q36150010 | Anchoring of Heterochromatin to the Nuclear Lamina Reinforces Dosage Compensation-Mediated Gene Repression. |
Q35558916 | Ancient and novel small RNA pathways compensate for the loss of piRNAs in multiple independent nematode lineages |
Q27309126 | Angiotensin Converting Enzyme (ACE) Inhibitor Extends Caenorhabditis elegans Life Span |
Q35154658 | Anhydrobiosis and freezing-tolerance: adaptations that facilitate the establishment of Panagrolaimus nematodes in polar habitats |
Q35589962 | Animal models in the drug discovery pipeline for Alzheimer's disease |
Q24542489 | Animal virus replication and RNAi-mediated antiviral silencing in Caenorhabditis elegans |
Q33695859 | Anisotropies in cortical tension reveal the physical basis of polarizing cortical flows |
Q35201877 | Antagonism between G(o)alpha and G(q)alpha in Caenorhabditis elegans: the RGS protein EAT-16 is necessary for G(o)alpha signaling and regulates G(q)alpha activity |
Q50547684 | Antagonistic Behaviors of NMY-1 and NMY-2 Maintain Ring Channels in the C. elegans Gonad. |
Q38683328 | Antagonistic Serotonergic and Octopaminergic Neural Circuits Mediate Food-Dependent Locomotory Behavior in Caenorhabditis elegans |
Q33807573 | Antagonistic Smad transcription factors control the dauer/non-dauer switch in C. elegans |
Q98506392 | Antagonistic control of C. elegans germline stem cell proliferation and differentiation by PUF proteins FBF-1 and FBF-2 |
Q61818408 | Antagonistic paralogs control a switch between growth and pathogen resistance in C. elegans |
Q47241343 | Antagonistic regulation of trafficking to Caenorhabditis elegans sensory cilia by a Retinal Degeneration 3 homolog and retromer |
Q51200222 | Antagonistically pleiotropic allele increases lifespan and late-life reproduction at the cost of early-life reproduction and individual fitness. |
Q36833634 | Anterior PAR proteins function during cytokinesis and maintain DYN-1 at the cleavage furrow in Caenorhabditis elegans |
Q92916388 | Anterior-enriched filopodia create the appearance of asymmetric membrane microdomains in polarizing C. elegans zygotes |
Q43121482 | Anthelmintic activity of KSI-4088 against Caenorhabditis elegans |
Q21092703 | Anthranilate fluorescence marks a calcium-propagated necrotic wave that promotes organismal death in C. elegans |
Q38704367 | Anti-Onchocerca and Anti-Caenorhabditis Activity of a Hydro-Alcoholic Extract from the Fruits of Acacia nilotica and Some Proanthocyanidin Derivatives |
Q37029621 | Anti-aging effects of deuterium depletion on Mn-induced toxicity in a C. elegans model |
Q64916053 | Anti-aging effects of long-term space missions, estimated by heart rate variability. |
Q41575658 | Anti-aging treatments slow propagation of synucleinopathy by restoring lysosomal function. |
Q38456671 | Anti-amyloid compounds protect from silica nanoparticle-induced neurotoxicity in the nematode C. elegans |
Q92220099 | Antiaging, Stress Resistance, and Neuroprotective Efficacies of Cleistocalyx nervosum var. paniala Fruit Extracts Using Caenorhabditis elegans Model |
Q21143894 | Antidepressants of the serotonin-antagonist type increase body fat and decrease lifespan of adult Caenorhabditis elegans |
Q28469125 | Antifungal chemical compounds identified using a C. elegans pathogenicity assay |
Q46267394 | Antimicrobial, Anthelmintic, and Antiviral Activity of Plants Traditionally Used for Treating Infectious Disease in the Similipal Biosphere Reserve, Odisha, India |
Q34307513 | Antinematode activity of Violacein and the role of the insulin/IGF-1 pathway in controlling violacein sensitivity in Caenorhabditis elegans |
Q42225850 | Antioxidant capacity of "Mexican arnica" Heterotheca inuloides Cass natural products and some derivatives: their anti-inflammatory evaluation and effect on C. elegans life span |
Q37661301 | Antioxidant response is a protective mechanism against nutrient deprivation in C. elegans |
Q36044909 | Antioxidative Activities of Both Oleic Acid and Camellia tenuifolia Seed Oil Are Regulated by the Transcription Factor DAF-16/FOXO in Caenorhabditis elegans |
Q42185376 | Antipsychotic drugs activate the C. elegans akt pathway via the DAF-2 insulin/IGF-1 receptor |
Q37011467 | Antipsychotic drugs alter neuronal development including ALM neuroblast migration and PLM axonal outgrowth in Caenorhabditis elegans |
Q40923623 | Antipsychotic drugs disrupt normal development in Caenorhabditis elegans via additional mechanisms besides dopamine and serotonin receptors |
Q40508050 | Antiviral RNA Interference against Orsay Virus Is neither Systemic nor Transgenerational in Caenorhabditis elegans |
Q64236013 | ApoE-associated modulation of neuroprotection from Aβ-mediated neurodegeneration in transgenic |
Q26825381 | Apoptosis in C. elegans: lessons for cancer and immunity |
Q33389871 | Apoptosis maintains oocyte quality in aging Caenorhabditis elegans females |
Q27309277 | Apparatus for investigating the reactions of soft-bodied invertebrates to controlled humidity gradients |
Q33619474 | Appetitive Olfactory Learning and Long-Term Associative Memory in Caenorhabditis elegans |
Q49827180 | Application of RNAi and Heat-shock-induced Transcription Factor Expression to Reprogram Germ Cells to Neurons in C. elegans. |
Q40240144 | Application of a C. elegans dopamine neuron degeneration assay for the validation of potential Parkinson's disease genes. |
Q28476134 | Application of a mathematical model to describe the effects of chlorpyrifos on Caenorhabditis elegans development |
Q42595215 | Application of physiologically based modelling and transcriptomics to probe the systems toxicology of aldicarb for Caenorhabditis elegans (Maupas 1900). |
Q57810558 | Applications of Invertebrate Animal Models to Dimorphic Fungal Infections |
Q38432233 | Applications of cold temperature stress to age fractionate Caenorhabditis elegans: a simple inexpensive technique |
Q33790814 | Applying gene regulatory network logic to the evolution of social behavior. |
Q40897301 | Aquaporins-2 and -4 regulate glycogen metabolism and survival during hyposmotic-anoxic stress in Caenorhabditis elegans |
Q34613984 | Arabidopsis genes essential for seedling viability: isolation of insertional mutants and molecular cloning. |
Q33734647 | Argonautes ALG-3 and ALG-4 are required for spermatogenesis-specific 26G-RNAs and thermotolerant sperm in Caenorhabditis elegans |
Q34393505 | Argonautes promote male fertility and provide a paternal memory of germline gene expression in C. elegans |
Q30539854 | Arl8/ARL-8 functions in apoptotic cell removal by mediating phagolysosome formation in Caenorhabditis elegans |
Q33940408 | Arp2/3 promotes junction formation and maintenance in the Caenorhabditis elegans intestine by regulating membrane association of apical proteins |
Q33832471 | Arrestin and the multi-PDZ domain-containing protein MPZ-1 interact with phosphatase and tensin homolog (PTEN) and regulate Caenorhabditis elegans longevity |
Q41840764 | Arrhythmogenic effects of mutated L-type Ca 2+-channels on an optogenetically paced muscular pump in Caenorhabditis elegans |
Q30488078 | Artificial dirt: microfluidic substrates for nematode neurobiology and behavior |
Q35015054 | Assaying environmental nickel toxicity using model nematodes |
Q41299732 | Assays for direct and indirect effects of C. elegans endo-siRNAs |
Q36233664 | Assembly of body wall muscle and muscle cell attachment structures in Caenorhabditis elegans |
Q36744905 | Assembly of the Synaptonemal Complex Is a Highly Temperature-Sensitive Process That Is Supported by PGL-1 During Caenorhabditis elegans Meiosis |
Q64243667 | Assessing effects of germline exposure to environmental toxicants by high-throughput screening in C. elegans |
Q35090086 | Assessing the pathogenic potential of human Nephronophthisis disease-associated NPHP-4 missense mutations in C. elegans |
Q33963852 | Assessing the viability of mutant and manipulated sperm by artificial insemination of Caenorhabditis elegans |
Q91866554 | Assessment and Maintenance of Unigametic Germline Inheritance for C. elegans |
Q33953569 | Assessment of X chromosome dosage compensation in Caenorhabditis elegans by phenotypic analysis of lin-14. |
Q37057209 | Assessment of normal and mutant human presenilin function in Caenorhabditis elegans |
Q55101868 | Assessment of the behaviour and survival of nematodes under low oxygen concentrations. |
Q42997678 | Association of several small heat-shock proteins with reproductive tissues in the nematode Caenorhabditis elegans |
Q47231153 | Asymmetric Flows in the Intercellular Membrane during Cytokinesis |
Q36291344 | Asymmetric Wnt Pathway Signaling Facilitates Stem Cell-Like Divisions via the Nonreceptor Tyrosine Kinase FRK-1 in Caenorhabditis elegans |
Q37124367 | Asymmetric enrichment of PIE-1 in the Caenorhabditis elegans zygote mediated by binary counterdiffusion |
Q35765873 | Asymmetric localizations of LIN-17/Fz and MIG-5/Dsh are involved in the asymmetric B cell division in C. elegans |
Q34242931 | Asymmetric neuroblast divisions producing apoptotic cells require the cytohesin GRP-1 in Caenorhabditis elegans |
Q27302973 | Asymmetry of early endosome distribution in C. elegans embryos |
Q33905116 | Asynchronous Cholinergic Drive Correlates with Excitation-Inhibition Imbalance via a Neuronal Ca2+ Sensor Protein |
Q36410016 | Atypical antidepressants extend lifespan of Caenorhabditis elegans by activation of a non-cell-autonomous stress response |
Q64100003 | Aurora A depletion reveals centrosome-independent polarization mechanism in |
Q36703597 | Aurora-A mediated histone H3 phosphorylation of threonine 118 controls condensin I and cohesin occupancy in mitosis. |
Q33521213 | AutoEPG: software for the analysis of electrical activity in the microcircuit underpinning feeding behaviour of Caenorhabditis elegans |
Q39036054 | Automated Analysis of C. elegans Swim Behavior Using CeleST Software |
Q52625597 | Automated C. elegans embryo alignments reveal brain neuropil position invariance despite lax cell body placement. |
Q41554058 | Automated and controlled mechanical stimulation and functional imaging in vivo in C. elegans |
Q57182059 | Automated classification of synaptic vesicles in electron tomograms of C. elegans using machine learning |
Q55510520 | Automated detection and manipulation of sleep in C. elegans reveals depolarization of a sleep-active neuron during mechanical stimulation-induced sleep deprivation. |
Q53829215 | Automated fluid delivery from multiwell plates to microfluidic devices for high-throughput experiments and microscopy. |
Q93362478 | Automated high-content phenotyping from the first larval stage till the onset of adulthood of the nematode Caenorhabditis elegans |
Q37218848 | Automated screening for mutants affecting dopaminergic-neuron specification in C. elegans |
Q41765566 | Autonomous and non-autonomous roles of DNase II during cell death in C. elegans embryos |
Q36016590 | Autonomous and nonautonomous regulation of Wnt-mediated neuronal polarity by the C. elegans Ror kinase CAM-1 |
Q30530756 | Autonomous screening of C. elegans identifies genes implicated in synaptogenesis |
Q35316092 | Autophagy and lipid metabolism coordinately modulate life span in germline-less C. elegans |
Q27311265 | Autophagy and modular restructuring of metabolism control germline tumor differentiation and proliferation in C. elegans |
Q90458564 | Autophagy compensates for defects in mitochondrial dynamics |
Q36052209 | Autophagy genes unc-51 and bec-1 are required for normal cell size in Caenorhabditis elegans |
Q88515082 | Autophagy in C. elegans development |
Q64947657 | Autophagy of germ-granule components, PGL-1 and PGL-3, contributes to DNA damage-induced germ cell apoptosis in C. elegans. |
Q34119935 | Autophagy protects C. elegans against necrosis during Pseudomonas aeruginosa infection |
Q36897647 | Autophagy protects against hypoxic injury in C. elegans |
Q56529889 | Autophagy-dependent ribosomal RNA degradation is essential for maintaining nucleotide homeostasis during development |
Q36810995 | Autophagy-mediated longevity is modulated by lipoprotein biogenesis |
Q34572568 | Autosomal genes of autosomal/X-linked duplicated gene pairs and germ-line proliferation in Caenorhabditis elegans. |
Q64936818 | Auxin-Mediated Sterility Induction System for Longevity and Mating Studies in Caenorhabditis elegans. |
Q36412425 | Avermectin B1a, a paralyzing anthelmintic that affects interneurons and inhibitory motoneurons in Ascaris |
Q27308650 | Aversive Behavior in the Nematode C. elegans Is Modulated by cGMP and a Neuronal Gap Junction Network |
Q35278734 | Aversive olfactory learning and associative long-term memory in Caenorhabditis elegans |
Q27310148 | Axon Regeneration Is Regulated by Ets-C/EBP Transcription Complexes Generated by Activation of the cAMP/Ca2+ Signaling Pathways |
Q34029714 | Axon regeneration pathways identified by systematic genetic screening in C. elegans |
Q35542080 | Axon response to guidance cues is stimulated by acetylcholine in Caenorhabditis elegans |
Q90520281 | Axonal Mitochondria Modulate Neuropeptide Secretion Through the Hypoxic Stress Response in Caenorhabditis elegans |
Q33849953 | Axonal regeneration proceeds through specific axonal fusion in transected C. elegans neurons |
Q36528830 | Axotomy-induced HIF-serotonin signalling axis promotes axon regeneration in C. elegans |
Q89857184 | A spontaneous complex structural variant in rcan-1 increases exploratory behavior and laboratory fitness of Caenorhabditis elegans |
Q35110827 | Açaí (Euterpe oleracea Mart.) modulates oxidative stress resistance in Caenorhabditis elegans by direct and indirect mechanisms |
Q41975309 | B-LINK: a hemicentin, plakin, and integrin-dependent adhesion system that links tissues by connecting adjacent basement membranes |
Q37669237 | BAF-1 mobility is regulated by environmental stresses |
Q42266336 | BINDING SITE ANALYSIS OF THE CAENORHABDITIS ELEGANS NR4A NUCLEAR RECEPTOR NHR-6 DURING DEVELOPMENT. |
Q34982547 | BIR-1, a Caenorhabditis elegans homologue of Survivin, regulates transcription and development |
Q33811705 | BLMP-1/Blimp-1 regulates the spatiotemporal cell migration pattern in C. elegans |
Q57055372 | BMP Signaling Determines Body Size via Transcriptional Regulation of Collagen Genes in |
Q37599821 | BMP signaling requires retromer-dependent recycling of the type I receptor |
Q48190542 | BRAP-2 promotes DNA damage induced germline apoptosis in C. elegans through the regulation of SKN-1 and AKT-1. |
Q42094418 | BRC-1 acts in the inter-sister pathway of meiotic double-strand break repair. |
Q34610254 | Bacillus thuringiensis (Bt) toxin susceptibility and isolation of resistance mutants in the nematode Caenorhabditis elegans |
Q35900236 | Bacillus thuringiensis Crystal Protein Cry6Aa Triggers Caenorhabditis elegans Necrosis Pathway Mediated by Aspartic Protease (ASP-1). |
Q24554220 | Bacillus thuringiensis crystal proteins that target nematodes |
Q90076309 | Bacteria increase host micronutrient availability: mechanisms revealed by studies in C. elegans |
Q28708978 | Bacteria, yeast, worms, and flies: exploiting simple model organisms to investigate human mitochondrial diseases |
Q61478594 | Bacterial Feeders, the Nematode Caenorhabditis elegans and the Flagellate Cercomonas longicauda, have different Effects on Outcome of Competition among the Pseudomonas Biocontrol Strains CHA0 and DSS73 |
Q46379110 | Bacterial Metabolism Affects the C. elegans Response to Cancer Chemotherapeutics. |
Q90680936 | Bacterial Metabolites Produced Under Iron Limitation Kill Pinewood Nematode and Attract Caenorhabditis elegans |
Q33942460 | Bacterial attraction and quorum sensing inhibition in Caenorhabditis elegans exudates. |
Q28539137 | Bacterial fatty acids enhance recovery from the dauer larva in Caenorhabditis elegans |
Q90623130 | Bacterially produced metabolites protect C. elegans neurons from degeneration |
Q38954663 | Bacterium-induced internal egg hatching frequency is predictive of life span in Caenorhabditis elegans populations |
Q37631463 | Baculovirus p35 prevents developmentally programmed cell death and rescues a ced-9 mutant in the nematode Caenorhabditis elegans |
Q27314433 | Balanced trade-offs between alternative strategies shape the response of C. elegans reproduction to chronic heat stress |
Q30832225 | Balancing selection shapes density-dependent foraging behaviour |
Q30480524 | Barrier to autointegration factor blocks premature cell fusion and maintains adult muscle integrity in C. elegans |
Q33927411 | Barrier-to-autointegration factor is required to segregate and enclose chromosomes within the nuclear envelope and assemble the nuclear lamina |
Q33900050 | Basement membrane sliding and targeted adhesion remodels tissue boundaries during uterine-vulval attachment in Caenorhabditis elegans |
Q34308202 | Basic Caenorhabditis elegans methods: synchronization and observation |
Q27310291 | Basolateral Endocytic Recycling Requires RAB-10 and AMPH-1 Mediated Recruitment of RAB-5 GAP TBC-2 to Endosomes |
Q44727445 | Batrachochytrium dendrobatidis can infect and cause mortality in the nematode Caenorhabditis elegans |
Q49416945 | Behavioral Assays to Study Oxygen and Carbon Dioxide Sensing in Caenorhabditis elegans. |
Q50978499 | Behavioral Deficits Following Withdrawal from Chronic Ethanol Are Influenced by SLO Channel Function in Caenorhabditis elegans. |
Q58725753 | Behavioral Mechanisms That Depend on Dopamine and Serotonin in Interact With the Antipsychotics Risperidone and Aripiprazole |
Q37218474 | Behavioral adaptation in C. elegans produced by antipsychotic drugs requires serotonin and is associated with calcium signaling and calcineurin inhibition |
Q27347575 | Behavioral and immune responses to infection require Gαq- RhoA signaling in C. elegans |
Q34999318 | Behavioral and metabolic effects of the atypical antipsychotic ziprasidone on the nematode Caenorhabditis elegans |
Q47069077 | Behavioral choice between conflicting alternatives is regulated by a receptor guanylyl cyclase, GCY-28, and a receptor tyrosine kinase, SCD-2, in AIA interneurons of Caenorhabditis elegans. |
Q36042389 | Behavioral decay in aging male C. elegans correlates with increased cell excitability |
Q34594984 | Behavioral deficits during early stages of aging in Caenorhabditis elegans result from locomotory deficits possibly linked to muscle frailty |
Q24545389 | Behavioral degradation under mutation accumulation in Caenorhabditis elegans |
Q37185893 | Behavioral impact of neurotransmitter-activated G-protein-coupled receptors: muscarinic and GABAB receptors regulate Caenorhabditis elegans locomotion |
Q30541212 | Behavioral response of Caenorhabditis elegans to localized thermal stimuli |
Q28475427 | Behavioural and genetic evidence for C. elegans' ability to detect volatile chemicals associated with explosives |
Q35823284 | Bending amplitude - a new quantitative assay of C. elegans locomotion: identification of phenotypes for mutants in genes encoding muscle focal adhesion components |
Q34990127 | Beneficial effects of wheat gluten hydrolysate to extend lifespan and induce stress resistance in nematode Caenorhabditis elegans |
Q30482093 | Beta-catenin asymmetry is regulated by PLA1 and retrograde traffic in C. elegans stem cell divisions |
Q90676230 | Betaine reduces β-amyloid-induced paralysis through activation of cystathionine-β-synthase in an Alzheimer model of Caenorhabditis elegans |
Q36984702 | Beyond autophagy: New roles for ULK1 in immune signaling and interferon responses |
Q29147524 | Biallelic Variants in UBA5 Reveal that Disruption of the UFM1 Cascade Can Result in Early-Onset Encephalopathy |
Q37715828 | Bicarbonate modulates oxidative and functional damage in ischemia-reperfusion. |
Q34979896 | Bidirectional regulation of thermotaxis by glutamate transmissions in Caenorhabditis elegans |
Q36985290 | Bidirectional temperature-sensing by a single thermosensory neuron in C. elegans |
Q30432881 | Bidirectional thermotaxis in Caenorhabditis elegans is mediated by distinct sensorimotor strategies driven by the AFD thermosensory neurons |
Q37713202 | Bifid Shape Is Intrinsic to Bifidobacterium adolescentis |
Q90341020 | Binucleate germ cells in Caenorhabditis elegans are removed by physiological apoptosis |
Q33743307 | Bio-electrospraying the nematode Caenorhabditis elegans: studying whole-genome transcriptional responses and key life cycle parameters. |
Q41044997 | Bioassay-Guided Fractionation of a Leaf Extract from Combretum mucronatum with Anthelmintic Activity: Oligomeric Procyanidins as the Active Principle. |
Q35673187 | Biochemical and cell biological analysis of actin in the nematode Caenorhabditis elegans |
Q41638244 | Biochemical characterization of the cuticle collagen of the nematode Caenorhabditis elegans |
Q64892399 | Bioenergetic Health Assessment of a Single Caenorhabditis elegans from Postembryonic Development to Aging Stages via Monitoring Changes in the Oxygen Consumption Rate within a Microfluidic Device. |
Q28476706 | Biofilm development on Caenorhabditis elegans by Yersinia is facilitated by quorum sensing-dependent repression of type III secretion |
Q43116191 | Bioinformatic and biochemical studies point to AAGR-1 as the ortholog of human acid alpha-glucosidase in Caenorhabditis elegans |
Q72114051 | Biological responses in Caenorhabditis elegans to high magnetic fields |
Q72524864 | Biological responsiveness to the phorbol esters and specific binding of [3H]phorbol 12,13-dibutyrate in the nematodeCaenorhabditis elegans, a manipulable genetic system |
Q33814822 | Biologically constrained optimization based cell membrane segmentation in C. elegans embryos |
Q36076855 | Biomechanical profiling of Caenorhabditis elegans motility |
Q36438453 | Biosafety Test for Plant Growth-Promoting Bacteria: Proposed Environmental and Human Safety Index (EHSI) Protocol |
Q91598399 | Biosafety assessment of water samples from Wanzhou watershed of Yangtze Three Gorges Reservior in the quiet season in Caenorhabditis elegans |
Q35639921 | Bisecting Galactose as a Feature of N-Glycans of Wild-type and Mutant Caenorhabditis elegans |
Q28384992 | Bisphenol A impairs the double-strand break repair machinery in the germline and causes chromosome abnormalities |
Q34601375 | Bizarre tRNAs inferred from DNA sequences of mitochondrial genomes of nematode worms |
Q42613662 | Block of an ether-a-go-go-like K(+) channel by imipramine rescues egl-2 excitation defects in Caenorhabditis elegans |
Q48375647 | Blocking memory reconsolidation reverses memory-associated changes in glutamate receptor expression. |
Q41943957 | Blueberry polyphenols increase lifespan and thermotolerance in Caenorhabditis elegans |
Q36895324 | Body size change in various nematodes depending on bacterial food, sex and growth temperature |
Q37610826 | Border patrol: insights into the unique role of perlecan/heparan sulfate proteoglycan 2 at cell and tissue borders |
Q35905496 | Both Chromosome Decondensation and Condensation Are Dependent on DNA Replication in C. elegans Embryos. |
Q50046696 | Both live and dead Enterococci activate Caenorhabditis elegans host defense via immune and stress pathways. |
Q27324230 | Both the caspase CSP-1 and a caspase-independent pathway promote programmed cell death in parallel to the canonical pathway for apoptosis in Caenorhabditis elegans |
Q64101973 | Bottom-Up Approaches to Synthetic Cooperation in Microbial Communities |
Q41443201 | Boundary cells restrict dystroglycan trafficking to control basement membrane sliding during tissue remodeling |
Q36492575 | Brain selective transgene expression in zebrafish using an NRSE derived motif. |
Q27342729 | Branched-chain amino acid catabolism is a conserved regulator of physiological ageing |
Q90267751 | Bright split red fluorescent proteins for the visualization of endogenous proteins and synapses |
Q89869645 | Broadly conserved roles of TMEM131 family proteins in intracellular collagen assembly and secretory cargo trafficking |
Q42005058 | Burkholderia pseudomallei kills Caenorhabditis elegans through virulence mechanisms distinct from intestinal lumen colonization |
Q30524103 | Bypassing the Greatwall-Endosulfine pathway: plasticity of a pivotal cell-cycle regulatory module in Drosophila melanogaster and Caenorhabditis elegans |
Q34629047 | C. elegans ADAMTS ADT-2 regulates body size by modulating TGFβ signaling and cuticle collagen organization |
Q54266223 | C. elegans ADARs antagonize silencing of cellular dsRNAs by the antiviral RNAi pathway. |
Q36425522 | C. elegans AMPKs promote survival and arrest germline development during nutrient stress |
Q37258634 | C. elegans AP-2 and retromer control Wnt signaling by regulating mig-14/Wntless |
Q27336284 | C. elegans ATAD-3 is essential for mitochondrial activity and development |
Q30583153 | C. elegans Anillin proteins regulate intercellular bridge stability and germline syncytial organization |
Q33820814 | C. elegans BED domain transcription factor BED-3 controls lineage-specific cell proliferation during organogenesis |
Q38356322 | C. elegans CARMIL negatively regulates UNC-73/Trio function during neuronal development |
Q35106336 | C. elegans CEP-1/p53 and BEC-1 are involved in DNA repair |
Q27317562 | C. elegans Demonstrates Distinct Behaviors within a Fixed and Uniform Electric Field |
Q34542968 | C. elegans Dicer interacts with the P-granule component GLH-1 and both regulate germline RNPs |
Q27303527 | C. elegans EIF-3.K promotes programmed cell death through CED-3 caspase |
Q35779330 | C. elegans EOR-1/PLZF and EOR-2 positively regulate Ras and Wnt signaling and function redundantly with LIN-25 and the SUR-2 Mediator component |
Q58735758 | C. elegans Eats Its Own Intestine to Make Yolk Leading to Multiple Senescent Pathologies |
Q39119017 | C. elegans FOG-3/Tob can either promote or inhibit germline proliferation, depending on gene dosage and genetic context |
Q42846523 | C. elegans G protein regulator RGS-3 controls sensitivity to sensory stimuli |
Q35004999 | C. elegans GLA-3 is a novel component of the MAP kinase MPK-1 signaling pathway required for germ cell survival |
Q41666488 | C. elegans GLP-1/Notch activates transcription in a probability gradient across the germline stem cell pool |
Q24649055 | C. elegans La-related protein, LARP-1, localizes to germline P bodies and attenuates Ras-MAPK signaling during oogenesis |
Q35039941 | C. elegans NIMA-related kinases NEKL-2 and NEKL-3 are required for the completion of molting |
Q36165731 | C. elegans PAT-9 is a nuclear zinc finger protein critical for the assembly of muscle attachments |
Q37189050 | C. elegans RNA-binding proteins PUF-8 and MEX-3 function redundantly to promote germline stem cell mitosis |
Q27331617 | C. elegans SIRT6/7 homolog SIR-2.4 promotes DAF-16 relocalization and function during stress |
Q41006645 | C. elegans SMA-10 regulates BMP receptor trafficking |
Q33701707 | C. elegans SWAN-1 Binds to EGL-9 and regulates HIF-1-mediated resistance to the bacterial pathogen Pseudomonas aeruginosa PAO1. |
Q92169924 | C. elegans Tensin Promotes Axon Regeneration by Linking the Met-like SVH-2 and Integrin Signaling Pathways |
Q27308714 | C. elegans VANG-1 modulates life span via insulin/IGF-1-like signaling |
Q58090914 | C. elegans ZHP-4 is required at multiple distinct steps in the formation of crossovers and their transition to segregation competent chiasmata |
Q33294705 | C. elegans agrin is expressed in pharynx, IL1 neurons and distal tip cells and does not genetically interact with genes involved in synaptogenesis or muscle function |
Q36909674 | C. elegans and H. sapiens mRNAs with edited 3' UTRs are present on polysomes |
Q94453416 | C. elegans and Neurodegeneration In Caenorhabditis Elegans: Anatomy, Life Cycles and Biological Functions |
Q46591244 | C. elegans and mutants with chronic nicotine exposure as a novel model of cancer phenotype |
Q27317135 | C. elegans are protected from lethal hypoxia by an embryonic diapause |
Q36967334 | C. elegans as a model organism for in vivo screening in cancer: effects of human c-Met in lung cancer affect C. elegans vulva phenotypes |
Q41618319 | C. elegans avoids toxin-producing Streptomyces using a seven transmembrane domain chemosensory receptor |
Q34460280 | C. elegans bicd-1, homolog of the Drosophila dynein accessory factor Bicaudal D, regulates the branching of PVD sensory neuron dendrites |
Q30851817 | C. elegans chromosomes connect to centrosomes by anchoring into the spindle network |
Q27316918 | C. elegans ciliated sensory neurons release extracellular vesicles that function in animal communication |
Q64252642 | C. elegans collectively forms dynamical networks |
Q36426425 | C. elegans dystroglycan coordinates responsiveness of follower axons to dorsal/ventral and anterior/posterior guidance cues |
Q38170221 | C. elegans epigenetic regulation in development and aging |
Q33252629 | C. elegans feeding defective mutants have shorter body lengths and increased autophagy |
Q42142573 | C. elegans fmi-1/flamingo and Wnt pathway components interact genetically to control the anteroposterior neurite growth of the VD GABAergic neurons |
Q27346787 | C. elegans germ cells show temperature and age-dependent expression of Cer1, a Gypsy/Ty3-related retrotransposon |
Q28756805 | C. elegans germ cells switch between distinct modes of double-strand break repair during meiotic prophase progression |
Q33644482 | C. elegans germline-deficient mutants respond to pathogen infection using shared and distinct mechanisms |
Q27027125 | C. elegans in high-throughput drug discovery |
Q100443908 | C. elegans methionine/S-adenosylmethionine cycle activity is sensed and adjusted by a nuclear hormone receptor |
Q39453147 | C. elegans midbodies are released, phagocytosed and undergo LC3-dependent degradation independent of macroautophagy |
Q37171999 | C. elegans mig-6 encodes papilin isoforms that affect distinct aspects of DTC migration, and interacts genetically with mig-17 and collagen IV |
Q36787597 | C. elegans miro-1 Mutation Reduces the Amount of Mitochondria and Extends Life Span |
Q35007982 | C. elegans mitotic cyclins have distinct as well as overlapping functions in chromosome segregation |
Q41764579 | C. elegans neurons jettison protein aggregates and mitochondria under neurotoxic stress |
Q27313772 | C. elegans nucleostemin is required for larval growth and germline stem cell division |
Q36136040 | C. elegans piRNAs mediate the genome-wide surveillance of germline transcripts |
Q35394680 | C. elegans positive butanone learning, short-term, and long-term associative memory assays. |
Q34603005 | C. elegans positive olfactory associative memory is a molecularly conserved behavioral paradigm |
Q27304475 | C. elegans rrf-1 mutations maintain RNAi efficiency in the soma in addition to the germline |
Q37346733 | C. elegans sensing of and entrainment along obstacles require different neurons at different body locations |
Q24803406 | C. elegans serine-threonine kinase KIN-29 modulates TGFbeta signaling and regulates body size formation |
Q33585874 | C. elegans ten-1 is synthetic lethal with mutations in cytoskeleton regulators, and enhances many axon guidance defective mutants |
Q36470009 | C. elegans tracking and behavioral measurement |
Q34154831 | C. elegans twist gene expression in differentiated cell types is controlled by autoregulation through intron elements |
Q33952266 | C. elegans unc-105 mutations affect muscle and are suppressed by other mutations that affect muscle |
Q34350141 | C. elegans whole-genome sequencing reveals mutational signatures related to carcinogens and DNA repair deficiency |
Q36618049 | C. elegans Body Cavity Neurons Are Homeostatic Sensors that Integrate Fluctuations in Oxygen Availability and Internal Nutrient Reserves |
Q93274049 | C. elegans Heterochromatin Factor SET-32 Plays an Essential Role in Transgenerational Establishment of Nuclear RNAi-Mediated Epigenetic Silencing |
Q54960382 | C. elegans MRP-5 Exports Vitamin B12 from Mother to Offspring to Support Embryonic Development. |
Q42774327 | C. elegans Stress-Induced Sleep Emerges from the Collective Action of Multiple Neuropeptides |
Q47069074 | C. elegans Punctin specifies cholinergic versus GABAergic identity of postsynaptic domains. |
Q36923156 | C13C4.5/Spinster, an evolutionarily conserved protein that regulates fertility in C. elegans through a lysosome-mediated lipid metabolism process |
Q33787866 | CACN-1/Cactin interacts genetically with MIG-2 GTPase signaling to control distal tip cell migration in C. elegans |
Q27320065 | CACN-1/Cactin plays a role in Wnt signaling in C. elegans |
Q36952338 | CAMKII and calcineurin regulate the lifespan of Caenorhabditis elegans through the FOXO transcription factor DAF-16. |
Q36446568 | CAPS and syntaxin dock dense core vesicles to the plasma membrane in neurons |
Q41536357 | CAPS-1 requires its C2, PH, MHD1 and DCV domains for dense core vesicle exocytosis in mammalian CNS neurons |
Q28768631 | CAR-1, a protein that localizes with the mRNA decapping component DCAP-1, is required for cytokinesis and ER organization in Caenorhabditis elegans embryos |
Q36350840 | CAS-1, a C. elegans cyclase-associated protein, is required for sarcomeric actin assembly in striated muscle |
Q24647480 | CASY-1, an ortholog of calsyntenins/alcadeins, is essential for learning in Caenorhabditis elegans |
Q35018773 | CATP-6, a C. elegans ortholog of ATP13A2 PARK9, positively regulates GEM-1, an SLC16A transporter |
Q57462383 | CBD-1 organizes two independent complexes required for eggshell vitelline layer formation and egg activation in C. elegans |
Q35809678 | CCDC-55 is required for larval development and distal tip cell migration in Caenorhabditis elegans |
Q36838452 | CDC-25.2, a C. elegans ortholog of cdc25, is essential for the progression of intestinal divisions |
Q36197468 | CDC-42 Orients Cell Migration during Epithelial Intercalation in the Caenorhabditis elegans Epidermis |
Q36192735 | CDC-48/p97 coordinates CDT-1 degradation with GINS chromatin dissociation to ensure faithful DNA replication |
Q27315832 | CDK-1 and two B-type cyclins promote PAR-6 stabilization during polarization of the early C. elegans embryo |
Q35550786 | CDK-1 inhibits meiotic spindle shortening and dynein-dependent spindle rotation in C. elegans |
Q35780509 | CDK-9/cyclin T (P-TEFb) is required in two postinitiation pathways for transcription in the C. elegans embryo |
Q27333071 | CED-10/Rac1 regulates endocytic recycling through the RAB-5 GAP TBC-2 |
Q37011419 | CEH-20/Pbx and UNC-62/Meis function upstream of rnt-1/Runx to regulate asymmetric divisions of the C. elegans stem-like seam cells |
Q58179880 | CFL-1, a novel F-box protein with leucine-rich repeat may interact with UNC-10 for the regulation of defecation and daumone response in Caenorhabditis elegans |
Q30492822 | CGEF-1 and CHIN-1 regulate CDC-42 activity during asymmetric division in the Caenorhabditis elegans embryo |
Q88764250 | CHCA-1 is a copper-regulated CTR1 homolog required for normal development, copper accumulation, and copper-sensing behavior in Caenorhabditis elegans |
Q35857063 | CIF-1, a shared subunit of the COP9/signalosome and eukaryotic initiation factor 3 complexes, regulates MEL-26 levels in the Caenorhabditis elegans embryo |
Q36692554 | CLASPs function redundantly to regulate astral microtubules in the C. elegans embryo |
Q37101261 | CLEC-38, a transmembrane protein with C-type lectin-like domains, negatively regulates UNC-40-mediated axon outgrowth and promotes presynaptic development in Caenorhabditis elegans |
Q37041556 | CLHM-1 is a functionally conserved and conditionally toxic Ca2+-permeable ion channel in Caenorhabditis elegans |
Q27324477 | COM-1 promotes homologous recombination during Caenorhabditis elegans meiosis by antagonizing Ku-mediated non-homologous end joining |
Q35453239 | COMP-1 promotes competitive advantage of nematode sperm. |
Q49550787 | CONSERVED AND EXAPTED FUNCTIONS OF NUCLEAR RECEPTORS IN ANIMAL DEVELOPMENT. |
Q35205253 | CPEB proteins control two key steps in spermatogenesis in C. elegans |
Q36643001 | CPNA-1, a copine domain protein, is located at integrin adhesion sites and is required for myofilament stability in Caenorhabditis elegans |
Q33340985 | CRA-1 uncovers a double-strand break-dependent pathway promoting the assembly of central region proteins on chromosome axes during C. elegans meiosis |
Q40184094 | CRAC channel activity in C. elegans is mediated by Orai1 and STIM1 homologues and is essential for ovulation and fertility |
Q58579144 | CRELD1 is an evolutionarily-conserved maturational enhancer of ionotropic acetylcholine receptors |
Q42068694 | CRIP homologues maintain apical cytoskeleton to regulate tubule size in C. elegans |
Q58555035 | CRISPR-Cas9 human gene replacement and phenomic characterization in to understand the functional conservation of human genes and decipher variants of uncertain significance |
Q41257651 | CRISPR-mediated genetic interaction profiling identifies RNA binding proteins controlling metazoan fitness |
Q64388852 | CRISPR/Cas9 Methodology for the Generation of Knockout Deletions in Caenorhabditis elegans |
Q27324070 | CRL2(LRR-1) E3-ligase regulates proliferation and progression through meiosis in the Caenorhabditis elegans germline |
Q35160522 | CRN-1, a Caenorhabditis elegans FEN-1 homologue, cooperates with CPS-6/EndoG to promote apoptotic DNA degradation |
Q37285693 | CSN-5, a component of the COP9 signalosome complex, regulates the levels of UNC-96 and UNC-98, two components of M-lines in Caenorhabditis elegans muscle |
Q36296247 | CSR-1 RNAi pathway positively regulates histone expression in C. elegans |
Q35635081 | CSR-1 and P granules suppress sperm-specific transcription in the C. elegans germline. |
Q38736268 | CUL-2LRR-1 and UBXN-3 drive replisome disassembly during DNA replication termination and mitosis |
Q33428565 | CUTI-1: A novel tetraspan protein involved in C. elegans CUTicle formation and epithelial integrity |
Q33632440 | CYK-4 regulates Rac, but not Rho, during cytokinesis |
Q39269905 | Ca2+ permeability and Na+ conductance in cellular toxicity caused by hyperactive DEG/ENaC channels |
Q36256349 | Ca2+-dependent muscle dysfunction caused by mutation of the Caenorhabditis elegans troponin T-1 gene |
Q100496368 | Cadherin preserves cohesion across involuting tissues during C. elegans neurulation |
Q66959548 | Cadmium toxicity in the free-living nematode, Caenorhabditis elegans |
Q35026072 | Caenorhabditis Elegans Mutants Predict Regulation of Fatty Acids and Endocannabinoids by the CYP-35A Gene Family |
Q90411124 | Caenorhabditis Sieve: A Low-tech Instrument and Methodology for Sorting Small Multicellular Organisms |
Q35767461 | Caenorhabditis elegans ALG-1 antimorphic mutations uncover functions for Argonaute in microRNA guide strand selection and passenger strand disposal. |
Q41501549 | Caenorhabditis elegans ATPase inhibitor factor 1 (IF1) MAI-2 preserves the mitochondrial membrane potential (Δψm) and is important to induce germ cell apoptosis. |
Q27305915 | Caenorhabditis elegans Aurora A kinase is required for the formation of spindle microtubules in female meiosis |
Q47158462 | Caenorhabditis elegans BUB-3 and SAN-1/MAD3 Spindle Assembly Checkpoint Components Are Required for Genome Stability in Response to Treatment with Ionizing Radiation |
Q41445381 | Caenorhabditis elegans CES-1 Snail Represses pig-1 MELK Expression To Control Asymmetric Cell Division |
Q33920043 | Caenorhabditis elegans CNK-1 promotes Raf activation but is not essential for Ras/Raf signaling |
Q64212158 | Caenorhabditis elegans DLC-1 associates with ribonucleoprotein complexes to promote mRNA regulation |
Q34012568 | Caenorhabditis elegans DNA mismatch repair gene msh-2 is required for microsatellite stability and maintenance of genome integrity |
Q28504598 | Caenorhabditis elegans DYF-2, an orthologue of human WDR19, is a component of the intraflagellar transport machinery in sensory cilia |
Q35609813 | Caenorhabditis elegans EFA-6 limits microtubule growth at the cell cortex |
Q36139047 | Caenorhabditis elegans EVL-14/PDS-5 and SCC-3 Are Essential for Sister Chromatid Cohesion in Meiosis and Mitosis |
Q34619232 | Caenorhabditis elegans Galphaq regulates egg-laying behavior via a PLCbeta-independent and serotonin-dependent signaling pathway and likely functions both in the nervous system and in muscle |
Q21145855 | Caenorhabditis elegans HCF-1 functions in longevity maintenance as a DAF-16 regulator |
Q47102811 | Caenorhabditis elegans HIF-1 Is Broadly Required for Survival in Hydrogen Sulfide |
Q27348561 | Caenorhabditis elegans HIM-18/SLX-4 interacts with SLX-1 and XPF-1 and maintains genomic integrity in the germline by processing recombination intermediates |
Q35907679 | Caenorhabditis elegans Heterochromatin protein 1 (HPL-2) links developmental plasticity, longevity and lipid metabolism |
Q34613614 | Caenorhabditis elegans MES-3 is a target of GLD-1 and functions epigenetically in germline development. |
Q37629340 | Caenorhabditis elegans Male Copulation Circuitry Incorporates Sex-Shared Defecation Components To Promote Intromission and Sperm Transfer |
Q42045833 | Caenorhabditis elegans Muscleblind homolog mbl-1 functions in neurons to regulate synapse formation |
Q30503264 | Caenorhabditis elegans NPR-1-mediated behaviors are suppressed in the presence of mucoid bacteria |
Q34644668 | Caenorhabditis elegans OSR-1 regulates behavioral and physiological responses to hyperosmotic environments |
Q33552849 | Caenorhabditis elegans P5B-type ATPase CATP-5 operates in polyamine transport and is crucial for norspermidine-mediated suppression of RNA interference |
Q36643905 | Caenorhabditis elegans PIG-1/MELK acts in a conserved PAR-4/LKB1 polarity pathway to promote asymmetric neuroblast divisions |
Q34442081 | Caenorhabditis elegans RME-6 is a novel regulator of RAB-5 at the clathrin-coated pit |
Q34384139 | Caenorhabditis elegans RSD-2 and RSD-6 promote germ cell immortality by maintaining small interfering RNA populations |
Q27347461 | Caenorhabditis elegans SMA-10/LRIG is a conserved transmembrane protein that enhances bone morphogenetic protein signaling |
Q35950217 | Caenorhabditis elegans SMG-2 selectively marks mRNAs containing premature translation termination codons |
Q30502438 | Caenorhabditis elegans SNAP-29 is required for organellar integrity of the endomembrane system and general exocytosis in intestinal epithelial cells |
Q47696338 | Caenorhabditis elegans SORB-1 localizes to integrin adhesion sites and is required for organization of sarcomeres and mitochondria in myocytes |
Q35115057 | Caenorhabditis elegans SOS-1 is necessary for multiple RAS-mediated developmental signals |
Q33775151 | Caenorhabditis elegans SUR-5, a novel but conserved protein, negatively regulates LET-60 Ras activity during vulval induction |
Q37655705 | Caenorhabditis elegans SWI/SNF subunits control sequential developmental stages in the somatic gonad |
Q33853152 | Caenorhabditis elegans TRPV channels function in a modality-specific pathway to regulate response to aberrant sensory signaling |
Q44396227 | Caenorhabditis elegans UNC-103 ERG-like potassium channel regulates contractile behaviors of sex muscles in males before and during mating. |
Q47069069 | Caenorhabditis elegans VEM-1, a novel membrane protein, regulates the guidance of ventral nerve cord-associated axons. |
Q92957674 | Caenorhabditis elegans and its applicability to studies on restless legs syndrome |
Q28742056 | Caenorhabditis elegans aristaless/Arx gene alr-1 restricts variable gene expression |
Q90295649 | Caenorhabditis elegans as a model animal for investigating fungal pathogenesis |
Q38101676 | Caenorhabditis elegans as a model for intracellular pathogen infection |
Q34855656 | Caenorhabditis elegans as a model host for Staphylococcus aureus pathogenesis |
Q36443336 | Caenorhabditis elegans as a model in developmental toxicology |
Q26851244 | Caenorhabditis elegans as a model organism to study APP function |
Q37438482 | Caenorhabditis elegans as a model system for studying non-cell-autonomous mechanisms in protein-misfolding diseases |
Q38931076 | Caenorhabditis elegans as a platform to study the mechanism of action of synthetic antitumor lipids |
Q28385792 | Caenorhabditis elegans as an alternative in vivo model to determine oral uptake, nanotoxicity, and efficacy of melatonin-loaded lipid-core nanocapsules on paraquat damage |
Q37954135 | Caenorhabditis elegans as an experimental tool for the study of complex neurological diseases: Parkinson's disease, Alzheimer's disease and autism spectrum disorder |
Q28543596 | Caenorhabditis elegans bacterial pathogen resistant bus-4 mutants produce altered mucins |
Q34800776 | Caenorhabditis elegans body mechanics are regulated by body wall muscle tone |
Q42555122 | Caenorhabditis elegans caspase homolog CSP-2 inhibits CED-3 autoactivation and apoptosis in germ cells |
Q34337954 | Caenorhabditis elegans chaperonin CCT/TRiC is required for actin and tubulin biogenesis and microvillus formation in intestinal epithelial cells |
Q35002660 | Caenorhabditis elegans chromatin-associated proteins SET-2 and ASH-2 are differentially required for histone H3 Lys 4 methylation in embryos and adult germ cells |
Q21558513 | Caenorhabditis elegans cyclin B3 is required for multiple mitotic processes including alleviation of a spindle checkpoint-dependent block in anaphase chromosome segregation |
Q82639380 | Caenorhabditis elegans dpy-14: an essential collagen gene with unique expression profile and physiological roles in early development |
Q35685464 | Caenorhabditis elegans embryonic axial patterning requires two recently discovered posterior-group Hox genes |
Q37072668 | Caenorhabditis elegans employs innate and learned aversion in response to bacterial toxic metabolites tambjamine and violacein |
Q35150234 | Caenorhabditis elegans evolves a new architecture for the multi-aminoacyl-tRNA synthetase complex |
Q27305089 | Caenorhabditis elegans exhibit a coupling between the defecation motor program and directed locomotion |
Q33994703 | Caenorhabditis elegans fertilization-defective mutants with abnormal sperm |
Q33895371 | Caenorhabditis elegans fibroblast growth factor receptor signaling can occur independently of the multi-substrate adaptor FRS2. |
Q35885537 | Caenorhabditis elegans flamingo cadherin fmi-1 regulates GABAergic neuronal development |
Q37357908 | Caenorhabditis elegans functional orthologue of human protein h-mucolipin-1 is required for lysosome biogenesis |
Q34575957 | Caenorhabditis elegans galectins LEC-6 and LEC-10 interact with similar glycoconjugates in the intestine |
Q38567060 | Caenorhabditis elegans genes required for the engulfment of apoptotic corpses function in the cytotoxic cell deaths induced by mutations in lin-24 and lin-33 |
Q29036482 | Caenorhabditis elegans genes sma-2, sma-3, and sma-4 define a conserved family of transforming growth factor beta pathway components |
Q33463267 | Caenorhabditis elegans genomic response to soil bacteria predicts environment-specific genetic effects on life history traits |
Q36383142 | Caenorhabditis elegans glp-4 Encodes a Valyl Aminoacyl tRNA Synthetase |
Q37079542 | Caenorhabditis elegans histone deacetylase hda-1 is required for morphogenesis of the vulva and LIN-12/Notch-mediated specification of uterine cell fates |
Q27336177 | Caenorhabditis elegans histone methyltransferase MET-2 shields the male X chromosome from checkpoint machinery and mediates meiotic sex chromosome inactivation |
Q33257010 | Caenorhabditis elegans in the study of SMN-interacting proteins: a role for SMI-1, an orthologue of human Gemin2 and the identification of novel components of the SMN complex |
Q47960880 | Caenorhabditis elegans innexins regulate active zone differentiation |
Q30475856 | Caenorhabditis elegans inositol 5-phosphatase homolog negatively regulates inositol 1,4,5-triphosphate signaling in ovulation |
Q47069334 | Caenorhabditis elegans integrates the signals of butanone and food to enhance chemotaxis to butanone. |
Q36173833 | Caenorhabditis elegans intersectin: a synaptic protein regulating neurotransmission |
Q34661750 | Caenorhabditis elegans kettin, a large immunoglobulin-like repeat protein, binds to filamentous actin and provides mechanical stability to the contractile apparatuses in body wall muscle |
Q47069394 | Caenorhabditis elegans levamisole resistance genes lev-1, unc-29, and unc-38 encode functional nicotinic acetylcholine receptor subunits |
Q34609776 | Caenorhabditis elegans lin-13, a member of the LIN-35 Rb class of genes involved in vulval development, encodes a protein with zinc fingers and an LXCXE motif |
Q34610796 | Caenorhabditis elegans lin-25: a study of its role in multiple cell fate specification events involving Ras and the identification and characterization of evolutionarily conserved domains |
Q34614474 | Caenorhabditis elegans lin-45 raf is essential for larval viability, fertility and the induction of vulval cell fates |
Q27307942 | Caenorhabditis elegans maintains highly compartmentalized cellular distribution of metals and steep concentration gradients of manganese |
Q33920740 | Caenorhabditis elegans male sensory-motor neurons and dopaminergic support cells couple ejaculation and post-ejaculatory behaviors |
Q24657320 | Caenorhabditis elegans mboa-7, a member of the MBOAT family, is required for selective incorporation of polyunsaturated fatty acids into phosphatidylinositol |
Q35590108 | Caenorhabditis elegans microRNAs of the let-7 family act in innate immune response circuits and confer robust developmental timing against pathogen stress |
Q42030041 | Caenorhabditis elegans mom-4 is required for the activation of the p38 MAPK signaling pathway in the response to Pseudomonas aeruginosa infection |
Q28140164 | Caenorhabditis elegans msh-5 is required for both normal and radiation-induced meiotic crossing over but not for completion of meiosis |
Q36952009 | Caenorhabditis elegans mutant allele identification by whole-genome sequencing |
Q33955219 | Caenorhabditis elegans mutants defective in the functioning of the motor neurons responsible for egg laying |
Q33965279 | Caenorhabditis elegans mutants resistant to inhibitors of acetylcholinesterase |
Q27348836 | Caenorhabditis elegans myotubularin MTM-1 negatively regulates the engulfment of apoptotic cells |
Q42786093 | Caenorhabditis elegans neuron degeneration and mitochondrial suppression caused by selected environmental chemicals |
Q98507748 | Caenorhabditis elegans nuclear RNAi factor SET-32 deposits the transgenerational histone modification, H3K23me3 |
Q36665854 | Caenorhabditis elegans num-1 negatively regulates endocytic recycling |
Q30575897 | Caenorhabditis elegans oocyte meiotic spindle pole assembly requires microtubule severing and the calponin homology domain protein ASPM-1. |
Q43098295 | Caenorhabditis elegans oocytes detect meiotic errors in the absence of canonical end-on kinetochore attachments |
Q27305177 | Caenorhabditis elegans paraoxonase-like proteins control the functional expression of DEG/ENaC mechanosensory proteins |
Q34442206 | Caenorhabditis elegans period homolog lin-42 regulates the timing of heterochronic miRNA expression |
Q28750024 | Caenorhabditis elegans pheromones regulate multiple complex behaviors |
Q27305990 | Caenorhabditis elegans polo-like kinase PLK-1 is required for merging parental genomes into a single nucleus |
Q94524550 | Caenorhabditis elegans processes sensory information to choose between freeloading and self-defense strategies |
Q36173843 | Caenorhabditis elegans prom-1 is required for meiotic prophase progression and homologous chromosome pairing |
Q27312285 | Caenorhabditis elegans protein arginine methyltransferase PRMT-5 negatively regulates DNA damage-induced apoptosis |
Q41842418 | Caenorhabditis elegans pseudouridine synthase 1 activity in vivo: tRNA is a substrate, but not U2 small nuclear RNA |
Q34249121 | Caenorhabditis elegans recognizes a bacterial quorum-sensing signal molecule through the AWCON neuron. |
Q42523611 | Caenorhabditis elegans reporter fusion genes generated by seamless modification of large genomic DNA clones |
Q57255206 | Caenorhabditis elegans respond to high-glucose diets through a network of stress-responsive transcription factors |
Q37086624 | Caenorhabditis elegans responses to bacteria from its natural habitats |
Q36587943 | Caenorhabditis elegans reveals a FxNPxY-independent low-density lipoprotein receptor internalization mechanism mediated by epsin1. |
Q43871029 | Caenorhabditis elegans screen reveals role of PAR-5 in RAB-11-recycling endosome positioning and apicobasal cell polarity |
Q35409422 | Caenorhabditis elegans selects distinct crawling and swimming gaits via dopamine and serotonin |
Q34281276 | Caenorhabditis elegans spermatozoan locomotion: amoeboid movement with almost no actin |
Q35894654 | Caenorhabditis elegans susceptibility to gut Enterococcus faecalis infection is associated with fat metabolism and epithelial junction integrity |
Q36854957 | Caenorhabditis elegans teneurin, ten-1, is required for gonadal and pharyngeal basement membrane integrity and acts redundantly with integrin ina-1 and dystroglycan dgn-1 |
Q42807700 | Caenorhabditis elegans triple null mutant lacking UDP-N-acetyl-D-glucosamine:alpha-3-D-mannoside beta1,2-N-acetylglucosaminyltransferase I. |
Q42724593 | Caenorhabditis elegans wsp-1 regulation of synaptic function at the neuromuscular junction |
Q37979713 | Caenorhabditis elegans, a model organism for investigating immunity |
Q39775809 | Caenorhabditis elegans-applications to nematode genomics |
Q33736292 | Caenorhabditis elegans: A useful model for studying metabolic disorders in which oxidative stress is a contributing factor. |
Q52462059 | Caenorhabditis elegans: Occurrence and metabolism of ecdysteroids in adults and dauer larvae |
Q33658107 | Caenorhabditis elegans: a model to investigate oxidative stress and metal dyshomeostasis in Parkinson's disease |
Q90477581 | Caenorhabditis elegans: a model to understand host-microbe interactions |
Q36927018 | Caenorhabditis elegans: an emerging model in biomedical and environmental toxicology. |
Q30431794 | Caenorhabditis is a metazoan host for Legionella |
Q36012562 | Caenorhabditis microbiota: worm guts get populated |
Q36761278 | Caenorhabditis-in-drop array for monitoring C. elegans quiescent behavior. |
Q37269214 | Caenorhabditits elegans LRK-1 and PINK-1 act antagonistically in stress response and neurite outgrowth |
Q38541181 | Caffeine Induces the Stress Response and Up-Regulates Heat Shock Proteins in Caenorhabditis elegans |
Q41579045 | Caffeine induces high expression of cyp-35A family genes and inhibits the early larval development in Caenorhabditis elegans |
Q42197388 | Caffeine-induced food-avoidance behavior is mediated by neuroendocrine signals in Caenorhabditis elegans |
Q50910310 | Calcineurin Antagonizes AMPK to Regulate Lipolysis in Caenorhabditis elegans. |
Q33526851 | Calcineurin and protein kinase G regulate C. elegans behavioral quiescence during locomotion in liquid |
Q92100976 | Calcineurin tax-6 regulates male ray development and counteracts with kin-29 kinase in Caenorhabditis elegans |
Q30846950 | Calcineurin, a calcium/calmodulin-dependent protein phosphatase, is involved in movement, fertility, egg laying, and growth in Caenorhabditis elegans |
Q33719615 | Calcium dynamics regulating the timing of decision-making in C. elegans. |
Q43323174 | Calcium feedback mechanisms regulate oscillatory activity of a TRP-like Ca2+ conductance in C. elegans intestinal cells |
Q38065478 | Calcium signaling surrounding fertilization in the nematode Caenorhabditis elegans |
Q34610776 | Calcium/calmodulin-dependent protein kinase II regulates Caenorhabditis elegans locomotion in concert with a G(o)/G(q) signaling network. |
Q89408661 | Calnexin revealed as an ether-a-go-go chaperone by getting mutant worms up and going |
Q33954183 | Caloric restriction and the aging process: a critique |
Q27335029 | Calpains mediate integrin attachment complex maintenance of adult muscle in Caenorhabditis elegans |
Q39210284 | Calreticulin, a calcium-binding molecular chaperone, is required for stress response and fertility in Caenorhabditis elegans |
Q42042022 | Canalization of C. elegans Vulva Induction against Anatomical Variability |
Q37410095 | Candida albicans hyphal formation and virulence assessed using a Caenorhabditis elegans infection model |
Q27349803 | Candida albicans infection of Caenorhabditis elegans induces antifungal immune defenses |
Q41732875 | Cannabinoids Activate Monoaminergic Signaling to Modulate Key C. elegans Behaviors. |
Q92459158 | Cannabinoids Stimulate the TRP Channel-Dependent Release of Both Serotonin and Dopamine to Modulate Behavior in C. elegans |
Q36635707 | CapSeq and CIP-TAP identify Pol II start sites and reveal capped small RNAs as C. elegans piRNA precursors |
Q35868787 | Carqueja (Baccharis trimera) Protects against Oxidative Stress and β-Amyloid-Induced Toxicity in Caenorhabditis elegans |
Q36677241 | Cas9 Variants Expand the Target Repertoire in Caenorhabditis elegans |
Q34559547 | Casein kinase II and calcineurin modulate TRPP function and ciliary localization |
Q37612443 | Casein kinase II is required for proper cell division and acts as a negative regulator of centrosome duplication in Caenorhabditis elegans embryos |
Q58757966 | Caspase Is Required for Asymmetric Divisions That Generate Cells Programmed To Die |
Q34633364 | Caspase-activated phosphoinositide binding by CNT-1 promotes apoptosis by inhibiting the AKT pathway |
Q34384760 | Caspase-mediated activation of Caenorhabditis elegans CED-8 promotes apoptosis and phosphatidylserine externalization |
Q35610014 | Catalases Induction in High Virulence Pinewood Nematode Bursaphelenchus xylophilus under Hydrogen Peroxide-Induced Stress. |
Q42033777 | Catalpol Modulates Lifespan via DAF-16/FOXO and SKN-1/Nrf2 Activation in Caenorhabditis elegans |
Q35184459 | Cdk1 phosphorylates SPAT-1/Bora to trigger PLK-1 activation and drive mitotic entry in C. elegans embryos |
Q34116832 | Ce-Duox1/BLI-3 generated reactive oxygen species trigger protective SKN-1 activity via p38 MAPK signaling during infection in C. elegans |
Q24645333 | Ce-Duox1/BLI-3 generates reactive oxygen species as a protective innate immune mechanism in Caenorhabditis elegans |
Q35756670 | Ce-emerin and LEM-2: essential roles in Caenorhabditis elegans development, muscle function, and mitosis |
Q34596107 | CeRh1 (rhr-1) is a dominant Rhesus gene essential for embryonic development and hypodermal function in Caenorhabditis elegans |
Q34981283 | Celecoxib extends C. elegans lifespan via inhibition of insulin-like signaling but not cyclooxygenase-2 activity |
Q58582163 | Cell Cycle Analysis in the C. elegans Germline with the Thymidine Analog EdU |
Q92085462 | Cell Non-autonomous Function of daf-18/PTEN in the Somatic Gonad Coordinates Somatic Gonad and Germline Development in C. elegans Dauer Larvae |
Q34003205 | Cell architecture: surrounding muscle cells shape gland cell morphology in the Caenorhabditis elegans pharynx |
Q55406419 | Cell cycle accumulation of the proliferating cell nuclear antigen PCN-1 transitions from continuous in the adult germline to intermittent in the early embryo of C. elegans. |
Q41549003 | Cell cycle controls stress response and longevity in C. elegans |
Q36785967 | Cell cycle features of C. elegans germline stem/progenitor cells vary temporally and spatially. |
Q30483390 | Cell cycle progression requires the CDC-48UFD-1/NPL-4 complex for efficient DNA replication |
Q30480472 | Cell cycle regulators control centrosome elimination during oogenesis in Caenorhabditis elegans |
Q36325151 | Cell cycle- and swelling-induced activation of a Caenorhabditis elegans ClC channel is mediated by CeGLC-7alpha/beta phosphatases |
Q67291704 | Cell cycling and DNA replication in a mutant blocked in cell division in the nematode Caenorhabditis elegans |
Q34069175 | Cell division and targeted cell cycle arrest opens and stabilizes basement membrane gaps |
Q35810755 | Cell excitability necessary for male mating behavior in Caenorhabditis elegans is coordinated by interactions between big current and ether-a-go-go family K(+) channels |
Q24336986 | Cell fate-specific regulation of EGF receptor trafficking during Caenorhabditis elegans vulval development |
Q97557528 | Cell lineage-dependent chiral actomyosin flows drive cellular rearrangements in early C. elegans development |
Q33956855 | Cell lineages of the embryo of the nematode Caenorhabditis elegans |
Q37181890 | Cell size and fat content of dietary-restricted Caenorhabditis elegans are regulated by ATX-2, an mTOR repressor |
Q27308063 | Cell-Autonomous and Non-Cell-Autonomous Regulation of a Feeding State-Dependent Chemoreceptor Gene via MEF-2 and bHLH Transcription Factors |
Q36160486 | Cell-Type Specific Responses to DNA Replication Stress in Early C. elegans Embryos |
Q36408700 | Cell-cycle regulation of NOTCH signaling during C. elegans vulval development |
Q56532985 | Cell-intrinsic and -extrinsic mechanisms promote cell-type-specific cytokinetic diversity |
Q89560219 | Cell-lineage and developmental defects of temperature-sensitive embryonic arrest mutants of the nematodeCaenorhabditis elegans |
Q36570593 | Cell-specific microarray profiling experiments reveal a comprehensive picture of gene expression in the C. elegans nervous system |
Q27355204 | Cell-specific monitoring of protein synthesis in vivo |
Q47118911 | Cell-to-cell Transmission of Polyglutamine Aggregates in C. elegans |
Q27310046 | Cell-to-cell heterogeneity in cortical tension specifies curvature of contact surfaces in Caenorhabditis elegans embryos |
Q37391467 | Cell-to-cell spread of microsporidia causes Caenorhabditis elegans organs to form syncytia |
Q52372837 | Cell-type specific sequencing of microRNAs from complex animal tissues. |
Q35627884 | Cells change their sensitivity to an EGF morphogen gradient to control EGF-induced gene expression |
Q35001866 | Cellular analyses of the mitotic region in the Caenorhabditis elegans adult germ line |
Q35556817 | Cellular hallmarks reveal restricted aerobic metabolism at thermal limits |
Q37689126 | Centriolar SAS-7 acts upstream of SPD-2 to regulate centriole assembly and pericentriolar material formation. |
Q36205673 | Centripetal flow of pseudopodial surface components could propel the amoeboid movement of Caenorhabditis elegans spermatozoa |
Q30487010 | Centrosome attachment to the C. elegans male pronucleus is dependent on the surface area of the nuclear envelope |
Q36147639 | Centrosome movement in the early divisions of Caenorhabditis elegans: a cortical site determining centrosome position |
Q27334416 | Centrosome/Cell cycle uncoupling and elimination in the endoreduplicating intestinal cells of C. elegans |
Q40104391 | Cerium oxide nanoparticle aggregates affect stress response and function in Caenorhabditis elegans |
Q35596765 | Challenging muscle homeostasis uncovers novel chaperone interactions in Caenorhabditis elegans |
Q27308921 | Changes in cGMP levels affect the localization of EGL-4 in AWC in Caenorhabditis elegans |
Q97634549 | Changes in ferrous iron and glutathione promote ferroptosis and frailty in aging Caenorhabditis elegans |
Q35910043 | Changes in intestinal microflora of Caenorhabditis elegans following Bacillus nematocida B16 infection |
Q37439715 | Changes in translation rate modulate stress-induced damage of diverse proteins |
Q57453076 | Changes to social feeding behaviors are not sufficient for the fitness gains of the N2 reference strain |
Q92024438 | Chaperone biomarkers of lifespan and penetrance track the dosages of many other proteins |
Q40443426 | Chapter 14 Methods for the Study of Cell Death in the Nematode Caenorhabditis elegans |
Q37628059 | Characterization and function analysis of a novel gene, Hc-maoc-1, in the parasitic nematode Haemonochus contortus |
Q38485771 | Characterization and regulation of the trehalose synthesis pathway and its importance in the pathogenicity of Cryptococcus neoformans |
Q33959725 | Characterization of Caenorhabditis elegans lectin-binding mutants |
Q35906028 | Characterization of HAF-4- and HAF-9-localizing organelles as distinct organelles in Caenorhabditis elegans intestinal cells |
Q39859891 | Characterization of HCP-6, a C. elegans protein required to prevent chromosome twisting and merotelic attachment |
Q44180879 | Characterization of K(+) currents using an in situ patch clamp technique in body wall muscle cells from Caenorhabditis elegans |
Q34572522 | Characterization of Mos1-mediated mutagenesis in Caenorhabditis elegans: a method for the rapid identification of mutated genes |
Q34571855 | Characterization of N-acyl phosphatidylethanolamine-specific phospholipase-D isoforms in the nematode Caenorhabditis elegans |
Q67817522 | Characterization of a germ-line proliferation mutation in C. elegans |
Q42795198 | Characterization of a high-affinity membrane-associated ornithine decarboxylase from the free-living nematode Caenorhabditis elegans |
Q36262065 | Characterization of alpha1(IV) collagen mutations in Caenorhabditis elegans and the effects of alpha1 and alpha2(IV) mutations on type IV collagen distribution |
Q34217318 | Characterization of an Nmr homolog that modulates GATA factor-mediated nitrogen metabolite repression in Cryptococcus neoformans. |
Q36235730 | Characterization of beta pat-3 heterodimers, a family of essential integrin receptors in C. elegans |
Q24804185 | Characterization of gana-1, a Caenorhabditis elegans gene encoding a single ortholog of vertebrate alpha-galactosidase and alpha-N-acetylgalactosaminidase |
Q33908106 | Characterization of low molecular weight chemical fractions of dry bean (Phaseolus vulgaris) for bioactivity using Caenorhabditis elegans longevity and metabolite fingerprinting |
Q27309255 | Characterization of microsporidia-induced developmental arrest and a transmembrane leucine-rich repeat protein in Caenorhabditis elegans |
Q40044642 | Characterization of protein dynamics in asymmetric cell division by scanning fluorescence correlation spectroscopy |
Q34607844 | Characterization of seven genes affecting Caenorhabditis elegans hindgut development. |
Q34136079 | Characterization of the C. elegans erlin homologue |
Q37286820 | Characterization of the Caenorhabditis elegans Islet LIM-homeodomain ortholog, lim-7. |
Q42706641 | Characterization of the Dictyostelium homolog of chromatin binding protein DET1 suggests a conserved pathway regulating cell type specification and developmental plasticity |
Q34718544 | Characterization of the complete uric acid degradation pathway in the fungal pathogen Cryptococcus neoformans |
Q40309231 | Characterization of the crawling activity of Caenorhabditis elegans using a Hidden Markov model |
Q37366639 | Characterization of the effects of methylmercury on Caenorhabditis elegans |
Q48069748 | Characterization of the let-653 gene in Caenorhabditis elegans |
Q39765759 | Characterization of the mitochondria of the free-living nematode, caenorhabditis elegans |
Q33538327 | Characterization of the octamer, a cis-regulatory element that modulates excretory cell gene-expression in Caenorhabditis elegans |
Q30577086 | Characterizations of kinetic power and propulsion of the nematode Caenorhabditis elegans based on a micro-particle image velocimetry system |
Q43272697 | Characterizing the transcriptional regulation of let-721, a Caenorhabditis elegans homolog of human electron flavoprotein dehydrogenase |
Q34313471 | Charting the secretory pathway in a simple eukaryote |
Q36117302 | Checkpoint silencing during the DNA damage response in Caenorhabditis elegans embryos |
Q28831221 | Chemical activation of a food deprivation signal extends lifespan |
Q33540113 | Chemical enhancement of torsinA function in cell and animal models of torsion dystonia |
Q28469000 | Chemical genetics reveals an RGS/G-protein role in the action of a compound |
Q35125653 | Chemical genetics: tailoring tools for cell biology |
Q24792612 | Chemically defined medium and Caenorhabditis elegans |
Q34324294 | Chemosensation of bacterial secondary metabolites modulates neuroendocrine signaling and behavior of C. elegans |
Q28535013 | Chicoric acid is an antioxidant molecule that stimulates AMP kinase pathway in L6 myotubes and extends lifespan in Caenorhabditis elegans |
Q42411795 | Chiral forces organize left-right patterning in C. elegans by uncoupling midline and anteroposterior axis |
Q41492916 | Chloride intracellular channel proteins respond to heat stress in Caenorhabditis elegans. |
Q30530373 | Chloride intracellular channels modulate acute ethanol behaviors in Drosophila, Caenorhabditis elegans and mice. |
Q40124271 | Chlorophyll enhances oxidative stress tolerance in Caenorhabditis elegans and extends its lifespan |
Q91747631 | Choice between 1- and 2-furrow cytokinesis in Caenorhabditis elegans embryos with tripolar spindles |
Q37462522 | Cholesterol-responsive metabolic proteins are required for larval development in Caenorhabditis elegans |
Q24532166 | Choline acetyltransferase-deficient mutants of the nematode Caenorhabditis elegans |
Q36052286 | Choline transport and de novo choline synthesis support acetylcholine biosynthesis in Caenorhabditis elegans cholinergic neurons |
Q47888643 | Cholinergic Sensorimotor Integration Regulates Olfactory Steering. |
Q66990140 | Chromatin diminution and a chromosomal mechanism of sexual differentiation in Strongyloides papillosus |
Q33855919 | Chromatin silencing and the maintenance of a functional germline in Caenorhabditis elegans |
Q33956076 | Chromosome I duplications in Caenorhabditis elegans |
Q27337287 | Chromosome painting reveals asynaptic full alignment of homologs and HIM-8-dependent remodeling of X chromosome territories during Caenorhabditis elegans meiosis |
Q28191439 | Chromosome rearrangements in Caenorhabditis elegans |
Q89946693 | Chromosome-Level Assembly of the Caenorhabditis remanei Genome Reveals Conserved Patterns of Nematode Genome Organization |
Q64230608 | Chromosome-Wide Evolution and Sex Determination in the Three-Sexed Nematode |
Q30514475 | Chromosome-scale selective sweeps shape Caenorhabditis elegans genomic diversity |
Q37306058 | Chromosome-wide mechanisms to decouple gene expression from gene dose during sex-chromosome evolution. |
Q34549978 | Chronic exposure to perfluorooctane sulfonate induces behavior defects and neurotoxicity through oxidative damages, in vivo and in vitro |
Q48147960 | Cilia length and intraflagellar transport regulation by kinases PKG-1 and GCK-2 in C. elegans sensory neurons |
Q89891228 | Ciliary Rab28 and the BBSome negatively regulate extracellular vesicle shedding |
Q36111257 | Ciliogenesis in Caenorhabditis elegans requires genetic interactions between ciliary middle segment localized NPHP-2 (inversin) and transition zone-associated proteins |
Q34698580 | Ciliopathy proteins establish a bipartite signaling compartment in a C. elegans thermosensory neuron |
Q34313947 | Circadian regulation of olfaction and an evolutionarily conserved, nontranscriptional marker in Caenorhabditis elegans |
Q37474064 | Circadian rhythms identified in Caenorhabditis elegans by in vivo long-term monitoring of a bioluminescent reporter |
Q46467727 | Circadian stress tolerance in adult Caenorhabditis elegans |
Q36081107 | Circuit mechanisms encoding odors and driving aging-associated behavioral declines in Caenorhabditis elegans |
Q61447888 | Circular Estimate Method (CEM) - a Simple Method to Estimate Culture Densities in Liquid Medium |
Q35579771 | Cis- and trans-regulatory mechanisms of gene expression in the ASJ sensory neuron of Caenorhabditis elegans. |
Q30745681 | Cki-1 links cell division and cell fate acquisition in the C. elegans somatic gonad |
Q47163565 | Clarinet (CLA-1), a novel active zone protein required for synaptic vesicle clustering and release. |
Q52317053 | Classification and prediction of toxicity of chemicals using an automated phenotypic profiling of Caenorhabditis elegans. |
Q35944782 | Clathrin and AP-1 regulate apical polarity and lumen formation during C. elegans tubulogenesis |
Q27322704 | Clathrin and AP2 are required for phagocytic receptor-mediated apoptotic cell clearance in Caenorhabditis elegans |
Q70340483 | Cleavage of two yolk proteins from a precursor in Caenorhabditis elegans |
Q40491333 | Cloning and analysis of cDNA sequences coding for two 16 kllodalton heat shock proteins (hsps) inCaenorhabditis elegans:homology with the small hsps ofDrosophila |
Q40410016 | Cloning and characterization of the C. elegans histidyl-tRNA synthetase gene |
Q40109504 | Cloning of Contractile Protein Genes |
Q36189468 | Cloning of nematode tRNA genes and their expression in the frog oocyte |
Q34049435 | Clustered LAG-1 binding sites in lag-1/CSL are involved in regulating lag-1 expression during lin-12/Notch-dependent cell-fate specification |
Q36470497 | Clustering of genetically defined allele classes in the Caenorhabditis elegans DAF-2 insulin/IGF-1 receptor |
Q33847212 | Co-regulation of the DAF-16 target gene, cyp-35B1/dod-13, by HSF-1 in C. elegans dauer larvae and daf-2 insulin pathway mutants |
Q52450007 | Cochlioquinone A, a nematocidal agent which competes for specific [3H]ivermectin binding sites. |
Q38923380 | Cockayne syndrome: Clinical features, model systems and pathways |
Q57083282 | Codon adaptation–based control of protein expression in C. elegans |
Q30496117 | Coenzyme Q protects Caenorhabditis elegans GABA neurons from calcium-dependent degeneration |
Q42726025 | Coevolutionary interactions with parasites constrain the spread of self-fertilization into outcrossing host populations |
Q35222697 | Coexpressed D1- and D2-like dopamine receptors antagonistically modulate acetylcholine release in Caenorhabditis elegans |
Q38611746 | Coherent anti-Stokes Raman scattering (CARS) spectroscopy in Caenorhabditis elegans and Globodera pallida: Evidence for an ivermectin-activated decrease in lipid stores |
Q46421314 | Collaboration within the M1 aminopeptidase family promotes reproductive success in Caenorhabditis elegans |
Q27332129 | Colored polydimethylsiloxane micropillar arrays for high throughput measurements of forces applied by genetic model organisms. |
Q90391698 | Combinatorial Contact Cues Specify Cell Division Orientation by Directing Cortical Myosin Flows |
Q42206086 | Combinatorial RNA interference in Caenorhabditis elegans reveals that redundancy between gene duplicates can be maintained for more than 80 million years of evolution |
Q27690760 | Combinatorial chemistry in nematodes: modular assembly of primary metabolism-derived building blocks. |
Q27321712 | Combinatorial regulation of meiotic holliday junction resolution in C. elegans by HIM-6 (BLM) helicase, SLX-4, and the SLX-1, MUS-81 and XPF-1 nucleases |
Q33940136 | Combinatorial roles of heparan sulfate proteoglycans and heparan sulfates in Caenorhabditis elegans neural development. |
Q52621271 | Combined flow cytometry and high-throughput image analysis for the study of essential genes in Caenorhabditis elegans. |
Q33582514 | Combined informatic and expression screen identifies the novel DAF-16 target HLH-13 |
Q64988443 | Combining Zebrafish and CRISPR/Cas9: Toward a More Efficient Drug Discovery Pipeline. |
Q34753250 | Communication between oocytes and somatic cells regulates volatile pheromone production in Caenorhabditis elegans |
Q30416343 | Community-associated and healthcare-associated methicillin-resistant Staphylococcus aureus virulence toward Caenorhabditis elegans compared |
Q35689582 | Comparative Analysis of Stress Induced Gene Expression in Caenorhabditis elegans following Exposure to Environmental and Lab Reconstituted Complex Metal Mixture |
Q93387142 | Comparative Genome Analysis and Evaluation of Probiotic Characteristics of Lactobacillus plantarum Strain JDFM LP11 |
Q36744946 | Comparative Genomics of Serial Isolates of Cryptococcus neoformans Reveals Gene Associated With Carbon Utilization and Virulence. |
Q36283555 | Comparative Metabolomic Profiling Reveals That Dysregulated Glycolysis Stemming from Lack of Salvage NAD+ Biosynthesis Impairs Reproductive Development in Caenorhabditis elegans |
Q52109044 | Comparative and experimental embryogenesis of Plectidae (Nematoda). |
Q37573216 | Comparative assessment of fluorescent proteins for in vivo imaging in an animal model system |
Q33396644 | Comparative developmental expression profiling of two C. elegans isolates |
Q34883529 | Comparative functional characterization of the CSR-1 22G-RNA pathway in Caenorhabditis nematodes |
Q36515842 | Comparative genetics of sex determination: masculinizing mutations in Caenorhabditis briggsae |
Q37015880 | Comparative genomic analysis of upstream miRNA regulatory motifs in Caenorhabditis |
Q34621750 | Comparative genomics and functional study of lipid metabolic genes in Caenorhabditis elegans |
Q28650362 | Comparative genomics and transcriptomics analyses reveal divergent lifestyle features of nematode endoparasitic fungus Hirsutella minnesotensis |
Q38431937 | Comparative proteome analysis between C . briggsae embryos and larvae reveals a role of chromatin modification proteins in embryonic cell division. |
Q37143477 | Comparative studies of Munc18c and Munc18-1 reveal conserved and divergent mechanisms of Sec1/Munc18 proteins. |
Q60044695 | Comparative toxicogenomics of three insensitive munitions constituents 2,4-dinitroanisole, nitroguanidine and nitrotriazolone in the soil nematode Caenorhabditis elegans |
Q47671895 | Comparing Caenorhabditis elegans gentle and harsh touch response behavior using a multiplexed hydraulic microfluidic device |
Q40723863 | Comparing mutants, selective breeding, and transgenics in the dissection of aging processes of Caenorhabditis elegans |
Q111269205 | Comparison of lipidome profiles of Caenorhabditis elegans—results from an inter-laboratory ring trial |
Q45921125 | Comparison of motility, recovery, and methyl-thiazolyl-tetrazolium reduction assays for use in screening plant products for anthelmintic activity. |
Q41661219 | Comparison of proteomic and metabolomic profiles of mutants of the mitochondrial respiratory chain in Caenorhabditis elegans |
Q35832941 | Comparisons of Caenorhabditis Fucosyltransferase Mutants Reveal a Multiplicity of Isomeric N-Glycan Structures |
Q34184796 | Comparisons with Caenorhabditis (approximately 100 Mb) and Drosophila (approximately 175 Mb) using flow cytometry show genome size in Arabidopsis to be approximately 157 Mb and thus approximately 25% larger than the Arabidopsis genome initiative est |
Q30810825 | Compartmentalization of the endoplasmic reticulum in the early C. elegans embryos |
Q36087123 | Compartmentalized calcium dynamics in a C. elegans interneuron encode head movement |
Q34336650 | Competence for chemical reprogramming of sexual fate correlates with an intersexual molecular signature in Caenorhabditis elegans |
Q39291325 | Competition and resilience between founder and introduced bacteria in the Caenorhabditis elegans gut. |
Q33320351 | Complementary RNA amplification methods enhance microarray identification of transcripts expressed in the C. elegans nervous system |
Q33847856 | Complete killing of Caenorhabditis elegans by Burkholderia pseudomallei is dependent on prolonged direct association with the viable pathogen |
Q30542170 | Completion of cytokinesis in C. elegans requires a brefeldin A-sensitive membrane accumulation at the cleavage furrow apex |
Q41642422 | Complex Locomotion Behavior Changes Are Induced in Caenorhabditis elegans by the Lack of the Regulatory Leak K+ Channel TWK-7. |
Q35201304 | Complex coding of endogenous siRNA, transcriptional silencing and H3K9 methylation on native targets of germline nuclear RNAi in C. elegans |
Q42947462 | Complex cooperative functions of heparan sulfate proteoglycans shape nervous system development in Caenorhabditis elegans. |
Q36778085 | Complex network of Wnt signaling regulates neuronal migrations during Caenorhabditis elegans development |
Q36918612 | Complex patterns of alternative splicing mediate the spatial and temporal distribution of perlecan/UNC-52 in Caenorhabditis elegans |
Q34606072 | Complexity of developmental control: analysis of embryonic cell lineage specification in Caenorhabditis elegans using pes-1 as an early marker |
Q35162287 | Comprehensive assessment of germline chemical toxicity using the nematode Caenorhabditis elegans |
Q47135374 | Comprehensive functional genomics using Caenorhabditis elegans as a model organism |
Q49203409 | Comprehensive list of SUMO targets in Caenorhabditis elegans and its implication for evolutionary conservation of SUMO signaling. |
Q90151666 | Comprehensive phenotyping and transcriptome profiling to study nanotoxicity in C. elegans |
Q42837475 | Computational and molecular characterization of multiple isoforms of lfe-2 gene in nematode C. elegans |
Q34559077 | Computer assisted assembly of connectomes from electron micrographs: application to Caenorhabditis elegans |
Q30664217 | Computer-Assisted Transgenesis of Caenorhabditis elegans for Deep Phenotyping |
Q55002161 | Condensin I protects meiotic cohesin from WAPL-1 mediated removal. |
Q41839103 | Condensin and the spindle midzone prevent cytokinesis failure induced by chromatin bridges in C. elegans embryos |
Q37419745 | Condition-adapted stress and longevity gene regulation by Caenorhabditis elegans SKN-1/Nrf. |
Q30476857 | Conditional dominant mutations in the Caenorhabditis elegans gene act-2 identify cytoplasmic and muscle roles for a redundant actin isoform |
Q33820575 | Conditional gene expression and RNAi using MEC-8-dependent splicing in C. elegans |
Q34356248 | Conditioning protects C. elegans from lethal effects of enteropathogenic E. coli by activating genes that regulate lifespan and innate immunity |
Q52323065 | Conformational flexibility within the nascent polypeptide-associated complex enables its interactions with structurally diverse client proteins. |
Q34585640 | Connecting a connectome to behavior: an ensemble of neuroanatomical models of C. elegans klinotaxis |
Q47143344 | Connectomics, the Final Frontier |
Q45359638 | Consequences of a multi-generation exposure to uranium on Caenorhabditis elegans life parameters and sensitivity |
Q33579544 | Conservation of MAP kinase activity and MSP genes in parthenogenetic nematodes |
Q41058884 | Conservation of anatomically restricted glycosaminoglycan structures in divergent nematode species |
Q30649254 | Conservation of glp-1 regulation and function in nematodes |
Q50640299 | Conservation of large foci formation in arrested oocytes of Caenorhabditis nematodes. |
Q34250264 | Conservation of the C.elegans tra-2 3'UTR translational control |
Q46466764 | Conserved Ankyrin Repeat Proteins and Their NIMA Kinase Partners Regulate Extracellular Matrix Remodeling and Intracellular Trafficking in Caenorhabditis elegans |
Q27310130 | Conserved Genetic Interactions between Ciliopathy Complexes Cooperatively Support Ciliogenesis and Ciliary Signaling |
Q35330343 | Conserved RNA-binding proteins required for dendrite morphogenesis in Caenorhabditis elegans sensory neurons |
Q57294012 | Conserved SUN-KASH Interfaces Mediate LINC Complex-Dependent Nuclear Movement and Positioning |
Q30588363 | Conserved behavioral and genetic mechanisms in the pre-hatching molt of the nematode Pristionchus pacificus |
Q40784594 | Conserved function of Caenorhabditis elegans UNC-30 and mouse Pitx2 in controlling GABAergic neuron differentiation. |
Q33760559 | Conserved genes act as modifiers of invertebrate SMN loss of function defects |
Q35119773 | Conserved ion and amino acid transporters identified as phosphorylcholine-modified N-glycoproteins by metabolic labeling with propargylcholine in Caenorhabditis elegans cells |
Q37061838 | Conserved miRNAs are candidate post-transcriptional regulators of developmental arrest in free-living and parasitic nematodes |
Q27324552 | Conserved nutrient sensor O-GlcNAc transferase is integral to C. elegans pathogen-specific immunity |
Q33312863 | Conserved regulation of MAP kinase expression by PUF RNA-binding proteins |
Q33953637 | Conserved role of SIRT1 orthologs in fasting-dependent inhibition of the lipid/cholesterol regulator SREBP. |
Q27346722 | Conserved role of unc-79 in ethanol responses in lightweight mutant mice |
Q52162090 | Conserved roles of C. elegans and human MANFs in sulfatide binding and cytoprotection |
Q30420695 | Conserved single residue in the BK potassium channel required for activation by alcohol and intoxication in C. elegans |
Q90389873 | Constitutive XBP-1s-mediated activation of the endoplasmic reticulum unfolded protein response protects against pathological tau |
Q52231856 | Constructing balancer chromosomes for genetic screens in Drosophila hydei. |
Q36778723 | Context Specificity of Stress-activated Mitogen-activated Protein (MAP) Kinase Signaling: The Story as Told by Caenorhabditis elegans |
Q36406376 | Context-dependent modulation of Pol II CTD phosphatase SSUP-72 regulates alternative polyadenylation in neuronal development |
Q42770857 | Context-dependent regulation of feeding behaviour by the insulin receptor, DAF-2, in Caenorhabditis elegans |
Q46256502 | Contribution of riboflavin supply pathways to Vibrio cholerae in different environments |
Q33668945 | Contribution of the cyclic nucleotide gated channel subunit, CNG-3, to olfactory plasticity in Caenorhabditis elegans |
Q32175942 | Contribution of trans regulatory eQTL to cryptic genetic variation in C. elegans. |
Q36446208 | Contributions of mRNA abundance, ribosome loading, and post- or peri-translational effects to temporal repression of C. elegans heterochronic miRNA targets |
Q35855662 | Control of C. elegans hermaphrodite gonad size and shape by vab-3/Pax6-mediated regulation of integrin receptors |
Q28610712 | Control of Caenorhabditis elegans germ-line stem-cell cycling speed meets requirements of design to minimize mutation accumulation |
Q35417597 | Control of Cdc14 activity coordinates cell cycle and development in Caenorhabditis elegans |
Q37615366 | Control of Neuropeptide Expression by Parallel Activity-dependent Pathways in Caenorhabditis elegans |
Q27305280 | Control of Protein Activity and Cell Fate Specification via Light-Mediated Nuclear Translocation |
Q27333582 | Control of apoptosis by asymmetric cell division |
Q36742440 | Control of cell cycle timing during C. elegans embryogenesis |
Q33371683 | Control of feeding behavior in C. elegans by human G protein-coupled receptors permits screening for agonist-expressing bacteria |
Q31053233 | Control of intestinal bacterial proliferation in regulation of lifespan in Caenorhabditis elegans |
Q47278848 | Control of meiotic pairing and recombination by chromosomally tethered 26S proteasome. |
Q47267699 | Control of morphology and virulence by ADP-ribosylation factors (Arf) in Mucor circinelloides. |
Q34874075 | Control of neuronal subtype identity by the C. elegans ARID protein CFI-1. |
Q30480554 | Control of nuclear centration in the C. elegans zygote by receptor-independent Galpha signaling and myosin II. |
Q24318969 | Control of rapsyn stability by the CUL-3-containing E3 ligase complex |
Q36151090 | Control of sex-specific apoptosis in C. elegans by the BarH homeodomain protein CEH-30 and the transcriptional repressor UNC-37/Groucho |
Q35031288 | Control of stem cell self-renewal and differentiation by the heterochronic genes and the cellular asymmetry machinery in Caenorhabditis elegans |
Q28345580 | Control of vulval cell division number in the nematode Oscheius/Dolichorhabditis sp. CEW1 |
Q30587324 | Controlled sumoylation of the mevalonate pathway enzyme HMGS-1 regulates metabolism during aging |
Q42161032 | Controlling gene expression with the Q repressible binary expression system in Caenorhabditis elegans |
Q30597606 | Controlling interneuron activity in Caenorhabditis elegans to evoke chemotactic behaviour |
Q34570693 | Convergent, RIC-8-dependent Galpha signaling pathways in the Caenorhabditis elegans synaptic signaling network |
Q35145747 | Conversion of the LIN-1 ETS protein of Caenorhabditis elegans from a SUMOylated transcriptional repressor to a phosphorylated transcriptional activator |
Q36199571 | Cooperative target mRNA destabilization and translation inhibition by miR-58 microRNA family in C. elegans |
Q24309646 | Coordinate expression of NADPH-dependent flavin reductase, Fre-1, and Hint-related 7meGMP-directed hydrolase, DCS-1 |
Q84920074 | Coordinate regulation of gene expression in the C. elegans excretory cell by the POU domain protein CEH-6 |
Q27334219 | Coordinate regulation of lipid metabolism by novel nuclear receptor partnerships |
Q36215319 | Coordinated inhibition of C/EBP by Tribbles in multiple tissues is essential for Caenorhabditis elegans development |
Q41680627 | Coordinated transcriptional regulation of the unc-25 glutamic acid decarboxylase and the unc-47 GABA vesicular transporter by the Caenorhabditis elegans UNC-30 homeodomain protein |
Q39729704 | Coordinates, DNA content and heterogeneity of cell nuclei and segments of the Caenorhabditis elegans intestine |
Q48334050 | Coordination of Heparan Sulfate Proteoglycans with Wnt Signaling To Control Cellular Migrations and Positioning in Caenorhabditis elegans. |
Q36429840 | Coordination of Recombination with Meiotic Progression in the Caenorhabditis elegans Germline by KIN-18, a TAO Kinase That Regulates the Timing of MPK-1 Signaling |
Q30537956 | Coordination of behavioral hierarchies during environmental transitions in Caenorhabditis elegans |
Q27319972 | Coordination of cell proliferation and cell fate determination by CES-1 snail |
Q34472739 | Coordination of mitophagy and mitochondrial biogenesis during ageing in C. elegans |
Q33471793 | Coordination of opposing sex-specific and core muscle groups regulates male tail posture during Caenorhabditis elegans male mating behavior |
Q36212000 | Copper Oxide Nanoparticles Impact Several Toxicological Endpoints and Cause Neurodegeneration in Caenorhabditis elegans. |
Q84553429 | Copper reduces Aβ oligomeric species and ameliorates neuromuscular synaptic defects in a C. elegans model of inclusion body myositis |
Q33526497 | Copy number variation in the genomes of twelve natural isolates of Caenorhabditis elegans |
Q47403640 | Core Richness of N-Glycans of Caenorhabditis elegans: A Case Study on Chemical and Enzymatic Release. |
Q34867860 | Core promoter T-blocks correlate with gene expression levels in C. elegans |
Q41266806 | Correction for specimen movement and rotation errors for in-vivo Optical Projection Tomography |
Q36120991 | Correlation of the physical and genetic maps in the lin-12 region of Caenorhabditis elegans |
Q36428045 | Cortical PAR polarity proteins promote robust cytokinesis during asymmetric cell division. |
Q91951635 | Cortical anchoring of the microtubule cytoskeleton is essential for neuron polarity |
Q28270015 | Cortical and cytoplasmic flow polarity in early embryonic cells of Caenorhabditis elegans |
Q37426824 | Cortical flow aligns actin filaments to form a furrow. |
Q40996346 | Cortical granule exocytosis in C. elegans is regulated by cell cycle components including separase |
Q30540268 | Counterbalance between BAG and URX neurons via guanylate cyclases controls lifespan homeostasis in C. elegans |
Q33305345 | Counting mutagenized genomes and optimizing genetic screens in Caenorhabditis elegans |
Q50420511 | Coupling of Rigor Mortis and Intestinal Necrosis during C. elegans Organismal Death. |
Q43364726 | Critical residues of the Caenorhabditis elegans unc-2 voltage-gated calcium channel that affect behavioral and physiological properties. |
Q34011653 | Critical role of Caenorhabditis elegans homologs of Cds1 (Chk2)-related kinases in meiotic recombination |
Q64065610 | Cross Talk with the GAR-3 Receptor Contributes to Feeding Defects in Mutants |
Q36094079 | Cross-Genome Clustering of Human and C. elegans G-Protein Coupled Receptors |
Q33878802 | Crossing over during Caenorhabditis elegans meiosis requires a conserved MutS-based pathway that is partially dispensable in budding yeast |
Q90110548 | Crossover Position Drives Chromosome Remodeling for Accurate Meiotic Chromosome Segregation |
Q30421573 | Crossover distribution and frequency are regulated by him-5 in Caenorhabditis elegans |
Q37412741 | Crossover heterogeneity in the absence of hotspots in Caenorhabditis elegans |
Q36942440 | Crossovers trigger a remodeling of meiotic chromosome axis composition that is linked to two-step loss of sister chromatid cohesion |
Q35546391 | Cryoimmobilization and three‐dimensional visualization of C. elegans ultrastructure |
Q27652750 | Crystal Structure of CRN-4: Implications for Domain Function in Apoptotic DNA Degradation |
Q39036030 | Cultivation of Caenorhabditis elegans in Three Dimensions in the Laboratory |
Q92257617 | Curative Treatment of Candidiasis by the Live Biotherapeutic Microorganism Lactobacillus rhamnosus Lcr35® in the Invertebrate Model Caenorhabditis elegans: First Mechanistic Insights |
Q35579804 | Cuticle integrity and biogenic amine synthesis in Caenorhabditis elegans require the cofactor tetrahydrobiopterin (BH4). |
Q36205056 | Cuticle of Caenorhabditis elegans: its isolation and partial characterization |
Q33742202 | Cyanobacterial xenobiotics as evaluated by a Caenorhabditis elegans neurotoxicity screening test |
Q41715971 | Cyclin B3 and dynein heavy chain cooperate to increase fitness in the absence of mdf-1/MAD1 in Caenorhabditis elegans |
Q41285256 | Cyclin CYB-3 controls both S-phase and mitosis and is asymmetrically distributed in the early C. elegans embryo |
Q33283516 | Cyclin E and CDK2 repress the terminal differentiation of quiescent cells after asymmetric division in C. elegans |
Q27342769 | Cyclin E and Cdk2 control GLD-1, the mitosis/meiosis decision, and germline stem cells in Caenorhabditis elegans |
Q36083185 | Cyclin-dependent kinase 5 regulates the polarized trafficking of neuropeptide-containing dense-core vesicles in Caenorhabditis elegans motor neurons |
Q24548047 | Cystamine and cysteamine increase brain levels of BDNF in Huntington disease via HSJ1b and transglutaminase |
Q40127864 | Cysteine protease cathepsin B mediates radiation-induced bystander effects |
Q36895980 | Cytokinesis and midzone microtubule organization in Caenorhabditis elegans require the kinesin-like protein ZEN-4. |
Q36282224 | Cytokinesis is not controlled by calmodulin or myosin light chain kinase in the Caenorhabditis elegans early embryo |
Q33948186 | Cytoplasmic dynein light intermediate chain is required for discrete aspects of mitosis in Caenorhabditis elegans |
Q37693481 | Cytoplasmic-Nuclear Incompatibility Between Wild Isolates of Caenorhabditis nouraguensis |
Q46318333 | Cytoskeletal variations in an asymmetric cell division support diversity in nematode sperm size and sex ratios. |
Q41195529 | Cytotoxicity of hydrogen peroxide produced by Enterococcus faecium |
Q37706220 | D-Glucosamine supplementation extends life span of nematodes and of ageing mice |
Q28483848 | D1 dopamine receptor signaling is modulated by the R7 RGS protein EAT-16 and the R7 binding protein RSBP-1 in Caenoerhabditis elegans motor neurons |
Q90243921 | DAF-16 and SMK-1 Contribute to Innate Immunity During Adulthood in Caenorhabditis elegans |
Q27309247 | DAF-16 and TCER-1 Facilitate Adaptation to Germline Loss by Restoring Lipid Homeostasis and Repressing Reproductive Physiology in C. elegans |
Q36470586 | DAF-16-dependent suppression of immunity during reproduction in Caenorhabditis elegans |
Q42140945 | DAF-16/FOXO and EGL-27/GATA promote developmental growth in response to persistent somatic DNA damage |
Q92021484 | DAF-16/FOXO promotes taste avoidance learning independently of axonal insulin-like signaling |
Q47069573 | DAF-18/PTEN locally antagonizes insulin signalling to couple germline stem cell proliferation to oocyte needs in C. elegans. |
Q33615014 | DAF-18/PTEN signals through AAK-1/AMPK to inhibit MPK-1/MAPK in feedback control of germline stem cell proliferation |
Q58786850 | DAF-21/Hsp90 is required for C. elegans longevity by ensuring DAF-16/FOXO isoform A function |
Q57153658 | DARPins recognizing mTFP1 as novel reagents for and protein manipulations |
Q30458737 | DEPDC1/LET-99 participates in an evolutionarily conserved pathway for anti-tubulin drug-induced apoptosis |
Q36731916 | DEPS-1 promotes P-granule assembly and RNA interference in C. elegans germ cells |
Q30487217 | DEX-1 and DYF-7 establish sensory dendrite length by anchoring dendritic tips during cell migration |
Q27309504 | DLK-1/p38 MAP Kinase Signaling Controls Cilium Length by Regulating RAB-5 Mediated Endocytosis in Caenorhabditis elegans |
Q36490833 | DNA Damage Sensitivity Assays in Caenorhabditis elegans |
Q42767202 | DNA damage in germ cells induces an innate immune response that triggers systemic stress resistance |
Q37299465 | DNA damage leads to progressive replicative decline but extends the life span of long-lived mutant animals. |
Q34525913 | DNA double-strand break repair in Caenorhabditis elegans |
Q36483479 | DOG-1 is the Caenorhabditis elegans BRIP1/FANCJ homologue and functions in interstrand cross-link repair |
Q35829539 | DOP-2 D2-Like Receptor Regulates UNC-7 Innexins to Attenuate Recurrent Sensory Motor Neurons during C. elegans Copulation |
Q35757652 | DPL-1 DP, LIN-35 Rb and EFL-1 E2F act with the MCD-1 zinc-finger protein to promote programmed cell death in Caenorhabditis elegans |
Q41586331 | DPY-17 and MUA-3 Interact for Connective Tissue-Like Tissue Integrity in Caenorhabditis elegans: A Model for Marfan Syndrome |
Q33693747 | DRE-1/FBXO11-dependent degradation of BLMP-1/BLIMP-1 governs C. elegans developmental timing and maturation |
Q24300382 | DVC1 (C1orf124) is a DNA damage-targeting p97 adaptor that promotes ubiquitin-dependent responses to replication blocks |
Q36488992 | DYC-1, a protein functionally linked to dystrophin in Caenorhabditis elegans is associated with the dense body, where it interacts with the muscle LIM domain protein ZYX-1 |
Q28731030 | Daf-2 signaling modifies mutant SOD1 toxicity in C. elegans |
Q38938242 | Dataset of proteomics analysis of aging C. elegans exposed to Pseudomonas aeruginosa strain PA01. |
Q34610771 | Dauer formation induced by high temperatures in Caenorhabditis elegans |
Q30625412 | Dauer-independent insulin/IGF-1-signalling implicates collagen remodelling in longevity |
Q36351654 | Dauer-specific dendrite arborization in C. elegans is regulated by KPC-1/Furin |
Q27674590 | De novo GTP Biosynthesis Is Critical for Virulence of the Fungal Pathogen Cryptococcus neoformans |
Q42172880 | DeActs: genetically encoded tools for perturbing the actin cytoskeleton in single cells. |
Q37128615 | Deciphering and modulating G protein signalling in C. elegans using the DREADD technology |
Q38960929 | Decoding sORF translation - from small proteins to gene regulation |
Q37644161 | Decoupling the downstream effects of germline nuclear RNAi reveals that H3K9me3 is dispensable for heritable RNAi and the maintenance of endogenous siRNA-mediated transcriptional silencing in Caenorhabditis elegans |
Q40895978 | Decreased energy metabolism extends life span in Caenorhabditis elegans without reducing oxidative damage |
Q37142721 | Decreased function of survival motor neuron protein impairs endocytic pathways. |
Q33627433 | Decreased microRNA levels lead to deleterious increases in neuronal M2 muscarinic receptors in Spinal Muscular Atrophy models |
Q46633778 | Decreased sensory stimulation reduces behavioral responding, retards development, and alters neuronal connectivity in Caenorhabditis elegans. |
Q28596873 | Deep Proteome Analysis Identifies Age-Related Processes in C. elegans |
Q34125936 | Deep conservation of genes required for both Drosphila melanogaster and Caenorhabditis elegans sleep includes a role for dopaminergic signaling |
Q30829767 | Deep phenotyping unveils hidden traits and genetic relations in subtle mutants |
Q83225462 | Deep sampling of Hawaiian reveals high genetic diversity and admixture with global populations |
Q36297709 | Defective lipid metabolism associated with mutation in klf-2 and klf-3: important roles of essential dietary salts in fat storage |
Q90573595 | Defects in CISD-1, a mitochondrial iron-sulfur protein, lower glucose level and ATP production in Caenorhabditis elegans |
Q37417567 | Defects in synaptic vesicle docking in unc-18 mutants |
Q27312120 | Defects in tRNA modification associated with neurological and developmental dysfunctions in Caenorhabditis elegans elongator mutants |
Q27313906 | Defects in the C. elegans acyl-CoA synthase, acs-3, and nuclear hormone receptor, nhr-25, cause sensitivity to distinct, but overlapping stresses |
Q36451459 | Deficiency for the ubiquitin ligase UBE3B in a blepharophimosis-ptosis-intellectual-disability syndrome |
Q35763081 | Deficiency of cardiolipin synthase causes abnormal mitochondrial function and morphology in germ cells of Caenorhabditis elegans |
Q37154034 | Deficiency of α-glucosidase I alters glycoprotein glycosylation and lifespan in Caenorhabditis elegans. |
Q90231079 | Deficit in the epidermal barrier induces toxicity and translocation of PEG modified graphene oxide in nematodes |
Q38434355 | Defining Minimal Binding Regions in Regulator of Presynaptic Morphology 1 (RPM-1) Using Caenorhabditis elegans Neurons Reveals Differential Signaling Complexes |
Q41735227 | Defining heterochromatin in C. elegans through genome-wide analysis of the heterochromatin protein 1 homolog HPL-2. |
Q92377364 | Degron-tagged reporters probe membrane topology and enable the specific labelling of membrane-wrapped structures |
Q34519045 | Delayed accumulation of intestinal coliform bacteria enhances life span and stress resistance in Caenorhabditis elegans fed respiratory deficient E. coli |
Q37631165 | Delayed innocent bystander cell death following hypoxia in Caenorhabditis elegans |
Q36236128 | Delaying aging and the aging-associated decline in protein homeostasis by inhibition of tryptophan degradation. |
Q36667214 | Deletion of Phytochelatin Synthase Modulates the Metal Accumulation Pattern of Cadmium Exposed C. elegans |
Q27320578 | Deletion of microRNA-80 activates dietary restriction to extend C. elegans healthspan and lifespan |
Q41977041 | Deletion of smn-1, the Caenorhabditis elegans ortholog of the spinal muscular atrophy gene, results in locomotor dysfunction and reduced lifespan |
Q40261652 | Deletion of the ubiquitin ligase CHIP leads to the accumulation, but not the aggregation, of both endogenous phospho- and caspase-3-cleaved tau species. |
Q34926861 | Deletion of thioredoxin reductase and effects of selenite and selenate toxicity in Caenorhabditis elegans |
Q47117425 | Delivery of Native Proteins into C. elegans Using a Transduction Protocol Based on Lipid Vesicles |
Q42728547 | Dendritic tree extraction from noisy maximum intensity projection images in C. elegans |
Q34201832 | Dependence of the sperm/oocyte decision on the nucleosome remodeling factor complex was acquired during recent Caenorhabditis briggsae evolution |
Q34613790 | Depletion of a novel SET-domain protein enhances the sterility of mes-3 and mes-4 mutants of Caenorhabditis elegans |
Q27321332 | Depletion of the C. elegans NAC engages the unfolded protein response, resulting in increased chaperone expression and apoptosis |
Q36896039 | Depletion of the ER chaperone ENPL-1 sensitizes C. elegans to the anticancer drug cisplatin |
Q36130602 | Derlin-dependent retrograde transport from endosomes to the Golgi apparatus |
Q52568650 | Descending pathway facilitates undulatory wave propagation in Caenorhabditis elegans through gap junctions. |
Q36804808 | Description of International Caenorhabditis elegans Experiment first flight (ICE-FIRST). |
Q37142020 | Detecting heterozygosity in shotgun genome assemblies: Lessons from obligately outcrossing nematodes |
Q36974730 | Detection of Burkholderia pseudomallei toxin-mediated inhibition of protein synthesis using a Caenorhabditis elegans ugt-29 biosensor |
Q34813668 | Detection of deletions in the mitochondrial genome of Caenorhabditis elegans |
Q24811232 | Detection of nuclei in 4D Nomarski DIC microscope images of early Caenorhabditis elegans embryos using local image entropy and object tracking |
Q28302830 | Determination of cell division axes in the early embryogenesis of Caenorhabditis elegans |
Q37227647 | Determination of reliable reference genes for multi-generational gene expression analysis on C. elegans exposed to abused drug nicotine |
Q35974179 | Determining Physical Properties of the Cell Cortex |
Q42015526 | Determining the biomechanics of touch sensation in C. elegans |
Q33539805 | Detoxification of multiple heavy metals by a half-molecule ABC transporter, HMT-1, and coelomocytes of Caenorhabditis elegans |
Q27329642 | Deubiquitylation machinery is required for embryonic polarity in Caenorhabditis elegans |
Q46416251 | Development and evaluation of an in vivo assay in Caenorhabditis elegans for screening of compounds for their effect on cytochrome P450 expression |
Q43036378 | Development of Small Molecular Proteasome Inhibitors Using a Caenorhabditis elegans Screen. |
Q94563639 | Development of a low-cost, user-customizable, high-speed camera |
Q35865372 | Development of a transformation system for Hirsutella spp. and visualization of the mode of nematode infection by GFP-labeled H. minnesotensis. |
Q60302270 | Development of transgenic Caenorhabditis elegans expressing human transthyretin as a model for drug screening |
Q28833459 | Developmental Effects of the ToxCast™ Phase I and Phase II Chemicals in Caenorhabditis elegans and Corresponding Responses in Zebrafish, Rats, and Rabbits |
Q30395751 | Developmental Function of the PHR Protein RPM-1 Is Required for Learning in Caenorhabditis elegans |
Q37576470 | Developmental Wiring of Specific Neurons Is Regulated by RET-1/Nogo-A in Caenorhabditis elegans |
Q41806923 | Developmental and Cell Cycle Quiescence Is Mediated by the Nuclear Hormone Receptor Coregulator DIN-1S in the Caenorhabditis elegans Dauer Larva |
Q33809937 | Developmental arrest of Caenorhabditis elegans BRAP-2 mutant exposed to oxidative stress is dependent on BRC-1. |
Q55497322 | Developmental basis for intestinal barrier against the toxicity of graphene oxide. |
Q37691418 | Developmental biomarkers of aging in Caenorhabditis elegans |
Q27306275 | Developmental characterization of the microRNA-specific C. elegans Argonautes alg-1 and alg-2 |
Q34636240 | Developmental defects in a Caenorhabditis elegans model for type III galactosemia |
Q35751693 | Developmental expression of FOG-1/CPEB protein and its control in the Caenorhabditis elegans hermaphrodite germ line |
Q41278623 | Developmental expression pattern screen for genes predicted in the C. elegans genome sequencing project |
Q92001291 | Developmental fidelity is imposed by genetically separable RalGEF activities that mediate opposing signals |
Q36236600 | Developmental genetic analysis of troponin T mutations in striated and nonstriated muscle cells of Caenorhabditis elegans |
Q33772339 | Developmental genetics in primitive chordates |
Q33954683 | Developmental genetics of chromosome I spermatogenesis-defective mutants in the nematode Caenorhabditis elegans |
Q36028965 | Developmental genetics of secretory vesicle acidification during Caenorhabditis elegans spermatogenesis |
Q47069518 | Developmental genetics of the mechanosensory neurons of Caenorhabditis elegans |
Q42608519 | Developmental plasticity and the evolution of parasitism in an unusual nematode, Parastrongyloides trichosuri |
Q39756876 | Developmental programming modulates olfactory behavior in C. elegans via endogenous RNAi pathways |
Q92375631 | Developmental trajectory of Caenorhabditis elegans nervous system governs its structural organization |
Q37457271 | Developmentally programmed germ cell remodelling by endodermal cell cannibalism |
Q36155049 | Dialogue between E. coli free radical pathways and the mitochondria of C. elegans |
Q34539839 | Diapause formation and downregulation of insulin-like signaling via DAF-16/FOXO delays axonal degeneration and neuronal loss |
Q61818318 | Diapause induces functional axonal regeneration after necrotic insult in C. elegans |
Q36548911 | Diapause is associated with a change in the polarity of secretion of insulin-like peptides |
Q40018491 | Dielectrophoresis of Caenorhabditis elegans |
Q45375950 | Diet-dependent depletion of queuosine in tRNAs in Caenorhabditis elegans does not lead to a developmental block |
Q34335946 | Diet-induced developmental acceleration independent of TOR and insulin in C. elegans |
Q27316631 | Dietary restriction during development enlarges intestinal and hypodermal lipid droplets in Caenorhabditis elegans |
Q27320983 | Dietary restriction induced longevity is mediated by nuclear receptor NHR-62 in Caenorhabditis elegans |
Q42672376 | Differences in the genetic control of early egg development and reproduction between C. elegans and its parthenogenetic relative D. coronatus. |
Q42628444 | Different Mechanisms of Longevity in Long-Lived Mouse and Caenorhabditis elegans Mutants Revealed by Statistical Analysis of Mortality Rates |
Q28475938 | Different Mi-2 complexes for various developmental functions in Caenorhabditis elegans |
Q30495874 | Different domains of C. elegans PAR-3 are required at different times in development |
Q40474478 | Different genes influence toluene- and ethanol-induced locomotor impairment in C. elegans. |
Q36837940 | Different isoforms of the C. elegans FGF receptor are required for attraction and repulsion of the migrating sex myoblasts |
Q35548405 | Different roles for Aurora B in condensin targeting during mitosis and meiosis |
Q92622880 | Differential Regulation of Innate and Learned Behavior by Creb1/Crh-1 in Caenorhabditis elegans |
Q34689861 | Differential Regulation of Synaptic Vesicle Tethering and Docking by UNC-18 and TOM-1. |
Q52782412 | Differential centrifugation-based biochemical fractionation of the Drosophila adult CNS. |
Q45300254 | Differential contributions of Caenorhabditis elegans histone deacetylases to huntingtin polyglutamine toxicity. |
Q99726657 | Differential effect of Ayurvedic nootropics on C. elegans models of Parkinson's disease |
Q35880079 | Differential expression and function of synaptotagmin 1 isoforms in Caenorhabditis elegans |
Q36844530 | Differential expression of five tRNA(UAGTrp) amber suppressors in Caenorhabditis elegans |
Q39574195 | Differential expression of individual suppressor tRNA(Trp) gene gene family members in vitro and in vivo in the nematode Caenorhabditis elegans |
Q47069424 | Differential localization of two myosins within nematode thick filaments |
Q37461093 | Differential physiological roles of ESCRT complexes in Caenorhabditis elegans |
Q41185692 | Differential regulation of germ line apoptosis and germ cell differentiation by CPEB family members in C. elegans |
Q33880840 | Differential regulation of polarized synaptic vesicle trafficking and synapse stability in neural circuit rewiring in Caenorhabditis elegans |
Q30485732 | Differential requirements for clathrin in receptor-mediated endocytosis and maintenance of synaptic vesicle pools |
Q46414900 | Differing roles for sur-2/MED23 in C. elegans and C. briggsae vulval development |
Q48257757 | Dihydropyrimidine-Thiones and Clioquinol Synergize To Target β-Amyloid Cellular Pathologies through a Metal-Dependent Mechanism |
Q33326986 | Dimensionality and dynamics in the behavior of C. elegans |
Q37678175 | Dimethyl sulfide protects against oxidative stress and extends lifespan via a methionine sulfoxide reductase A-dependent catalytic mechanism. |
Q36048178 | Direct Visualization Reveals Kinetics of Meiotic Chromosome Synapsis |
Q35283819 | Direct in vivo cellular reprogramming involves transition through discrete, non-pluripotent steps |
Q34056513 | Direct interaction between the WD40 repeat protein WDR-23 and SKN-1/Nrf inhibits binding to target DNA. |
Q34423817 | Direct measurements of drag forces in C. elegans crawling locomotion. |
Q35756667 | Direct profiling of the phospholipid composition of adult Caenorhabditis elegans using whole-body imaging mass spectrometry |
Q35208925 | Direct protein-protein interaction between the intracellular domain of TRA-2 and the transcription factor TRA-1A modulates feminizing activity in C. elegans |
Q36222320 | Direct visualization of specifically modified extracellular glycans in living animals |
Q46171793 | Direct visualization of the movement of the monomeric axonal transport motor UNC-104 along neuronal processes in living Caenorhabditis elegans. |
Q35882321 | Directional Trans-Synaptic Labeling of Specific Neuronal Connections in Live Animals |
Q42270318 | Discovering Functional ERK Substrates Regulating Caenorhabditis elegans Germline Development |
Q37615837 | Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing |
Q27184685 | Discovery of a Natural Microsporidian Pathogen with a Broad Tissue Tropism in Caenorhabditis elegans |
Q33778375 | Discovery of a highly synergistic anthelmintic combination that shows mutual hypersusceptibility |
Q37640990 | Discovery of two GLP-1/Notch target genes that account for the role of GLP-1/Notch signaling in stem cell maintenance |
Q90410907 | Disease-associated tau impairs mitophagy by inhibiting Parkin translocation to mitochondria |
Q34786070 | Disease-related Myotubularins Function in Endocytic Traffic inCaenorhabditis elegans |
Q36238277 | Dishevelled attenuates the repelling activity of Wnt signaling during neurite outgrowth in Caenorhabditis elegans |
Q34184860 | Disruption of Caenorhabditis elegans muscle structure and function caused by mutation of troponin I |
Q34562985 | Disruption of O-GlcNAc Cycling in C. elegans Perturbs Nucleotide Sugar Pools and Complex Glycans |
Q37461014 | Disruption of endocytic pathway regulatory genes activates autophagy in C. elegans |
Q91955757 | Disruption of genes associated with Charcot-Marie-Tooth type 2 lead to common behavioural, cellular and molecular defects in Caenorhabditis elegans |
Q64055984 | Disruption of mitochondrial dynamics affects behaviour and lifespan in Caenorhabditis elegans |
Q27304759 | Disruption of the C. elegans Intestinal Brush Border by the Fungal Lectin CCL2 Phenocopies Dietary Lectin Toxicity in Mammals |
Q96432542 | Disruption of the mutator complex triggers a low penetrance larval arrest phenotype |
Q61207104 | Dissecting a central flip-flop circuit that integrates contradictory sensory cues in C. elegans feeding regulation |
Q33457977 | Dissecting and recording from the C. Elegans neuromuscular junction |
Q27333482 | Dissecting the serotonergic food signal stimulating sensory-mediated aversive behavior in C. elegans |
Q33865361 | Dissecting the signaling mechanisms underlying recognition and preference of food odors |
Q30649514 | Dissection of C. elegans behavioral genetics in 3-D environments |
Q36288349 | Dissection of cell division processes in the one cell stage Caenorhabditis elegans embryo by mutational analysis |
Q33978412 | Dissection of genetic pathways in C. elegans |
Q50322333 | Dissimilar Crystal Proteins Cry5Ca1 and Cry5Da1 Synergistically Act against Meloidogyne incognita and Delay Cry5Ba-Based Nematode Resistance. |
Q35040985 | Distant positioning of proteasomal proteolysis relative to actively transcribed genes |
Q36642250 | Distinct 3-O-sulfated heparan sulfate modification patterns are required for kal-1-dependent neurite branching in a context-dependent manner in Caenorhabditis elegans |
Q58796473 | Distinct CED-10/Rac1 domains confer context-specific functions in development |
Q33915482 | Distinct Caenorhabditis elegans HLH-8/twist-containing dimers function in the mesoderm |
Q36215367 | Distinct Mechanisms Underlie Quiescence during Two Caenorhabditis elegans Sleep-Like States. |
Q47132929 | Distinct Roles of Sensory Neurons in Mediating Pathogen Avoidance and Neuropeptide-Dependent Immune Regulation |
Q36391893 | Distinct activities of the germline and somatic reproductive tissues in the regulation of Caenorhabditis elegans' longevity |
Q34744594 | Distinct and redundant functions of mu1 medium chains of the AP-1 clathrin-associated protein complex in the nematode Caenorhabditis elegans |
Q42219455 | Distinct argonaute-mediated 22G-RNA pathways direct genome surveillance in the C. elegans germline |
Q35644790 | Distinct cell guidance pathways controlled by the Rac and Rho GEF domains of UNC-73/TRIO in Caenorhabditis elegans |
Q36324862 | Distinct conformations of the kinesin Unc104 neck regulate a monomer to dimer motor transition |
Q30479877 | Distinct developmental function of two Caenorhabditis elegans homologs of the cohesin subunit Scc1/Rad21. |
Q88838478 | Distinct effects of tubulin isotype mutations on neurite growth in Caenorhabditis elegans |
Q64797200 | Distinct functional roles of Vps41-mediated neuroprotection in Alzheimer's and Parkinson's disease models of neurodegeneration |
Q90196326 | Distinct functions and temporal regulation of methylated histone H3 during early embryogenesis |
Q36992843 | Distinct isoforms of the RFX transcription factor DAF-19 regulate ciliogenesis and maintenance of synaptic activity |
Q30579957 | Distinct molecular targets including SLO-1 and gap junctions are engaged across a continuum of ethanol concentrations in Caenorhabditis elegans |
Q33729439 | Distinct phases of siRNA synthesis in an endogenous RNAi pathway in C. elegans soma. |
Q36509020 | Distinct protein domains regulate ciliary targeting and function of C. elegans PKD-2. |
Q90414523 | Distinct regions of the intrinsically disordered protein MUT-16 mediate assembly of a small RNA amplification complex and promote phase separation of Mutator foci |
Q39645792 | Distinct requirements for C.elegans TAF(II)s in early embryonic transcription |
Q33969923 | Distinct requirements for somatic and germline expression of a generally expressed Caernorhabditis elegans gene |
Q34363885 | Distinct roles for RDE-1 and RDE-4 during RNA interference in Caenorhabditis elegans |
Q93028804 | Distinct roles for innexin gap junctions and hemichannels in mechanosensation |
Q35029249 | Distinct roles of Rac GTPases and the UNC-73/Trio and PIX-1 Rac GTP exchange factors in neuroblast protrusion and migration in C. elegans |
Q36164634 | Distinct roles of the RasGAP family proteins in C. elegans associative learning and memory |
Q89808006 | Distinct roles of two eIF4E isoforms in the germline of Caenorhabditis elegans |
Q33651724 | Distributed probing of chromatin structure in vivo reveals pervasive chromatin accessibility for expressed and non-expressed genes during tissue differentiation in C. elegans |
Q37070625 | Distribution and transport of cholesterol in Caenorhabditis elegans. |
Q34241406 | Divergent kleisin subunits of cohesin specify mechanisms to tether and release meiotic chromosomes. |
Q27335163 | Divergent mechanisms controlling hypoxic sensitivity and lifespan by the DAF-2/insulin/IGF-receptor pathway |
Q39655700 | Diverse bacteria are pathogens of Caenorhabditis elegans |
Q27317301 | Diverse functions of mRNA metabolism factors in stress defense and aging of Caenorhabditis elegans |
Q27324437 | Diverse host-seeking behaviors of skin-penetrating nematodes |
Q47104913 | Diverse modes of synaptic signaling, regulation, and plasticity distinguish two classes of C. elegans glutamatergic neurons |
Q41825177 | Diverse regulation of sensory signaling by C. elegans nPKC-epsilon/eta TTX-4. |
Q30481735 | Diverse roles of actin in C. elegans early embryogenesis |
Q34625961 | Diverse transcription factor binding features revealed by genome-wide ChIP-seq in C. elegans |
Q34020856 | Diversification of fasting regulated transcription in a cluster of duplicated nuclear hormone receptors in C. elegans |
Q33271915 | Diversity in mating behavior of hermaphroditic and male-female Caenorhabditis nematodes |
Q36936801 | Domain-specific regulation of recombination in Caenorhabditis elegans in response to temperature, age and sex. |
Q36103327 | Domains, amino acid residues, and new isoforms of Caenorhabditis elegans diacylglycerol kinase 1 (DGK-1) important for terminating diacylglycerol signaling in vivo |
Q54965081 | Dominance of P-glycoprotein 12 in phenotypic resistance conversion against ivermectin in Caenorhabditis elegans. |
Q33948873 | Dominant X-chromosome nondisjunction mutants of Caenorhabditis elegans. |
Q33956624 | Dominant maternal-effect mutations causing embryonic lethality in Caenorhabditis elegans |
Q33961860 | Dominant unc-37 mutations suppress the movement defect of a homeodomain mutation in unc-4, a neural specificity gene in Caenorhabditis elegans. |
Q47659329 | Dopa Decarboxylase Modulates Tau Toxicity. |
Q44755356 | Dopamine and glutamate control area-restricted search behavior in Caenorhabditis elegans. |
Q39753173 | Dopamine counteracts octopamine signalling in a neural circuit mediating food response in C. elegans |
Q46305258 | Dopamine induces soluble α-synuclein oligomers and nigrostriatal degeneration. |
Q28535391 | Dopamine modulates acetylcholine release via octopamine and CREB signaling in Caenorhabditis elegans |
Q30476321 | Dopamine modulates the plasticity of mechanosensory responses in Caenorhabditis elegans. |
Q42652303 | Dopamine negatively modulates the NCA ion channels in C. elegans |
Q41652544 | Dopamine receptor DOP-4 modulates habituation to repetitive photoactivation of a C. elegans polymodal nociceptor |
Q34764815 | Dopamine receptors antagonistically regulate behavioral choice between conflicting alternatives in C. elegans |
Q30354575 | Dopamine signaling architecture in Caenorhabditis elegans. |
Q33784944 | Dopamine signaling in C. elegans is mediated in part by HLH-17-dependent regulation of extracellular dopamine levels |
Q31066332 | Dopamine signaling is essential for precise rates of locomotion by C. elegans |
Q28388147 | Dopamine signaling promotes the xenobiotic stress response and protein homeostasis |
Q27332353 | Dopamine signaling regulates fat content through β-oxidation in Caenorhabditis elegans |
Q37725763 | Dopamine signaling tunes spatial pattern selectivity in C. elegans |
Q36861106 | Dopamine transporter/syntaxin 1A interactions regulate transporter channel activity and dopaminergic synaptic transmission |
Q37619225 | Dopamine transporters depolarize neurons by a channel mechanism. |
Q91983046 | Dopamine-dependent, swimming-induced paralysis arises as a consequence of loss of function mutations in the RUNX transcription factor RNT-1 |
Q39755286 | Dopaminergic neurons in the nematodeCaenorhabditis elegans |
Q37315985 | Dopaminergic neurotoxicity of S-ethyl N,N-dipropylthiocarbamate (EPTC), molinate, and S-methyl-N,N-diethylthiocarbamate (MeDETC) in Caenorhabditis elegans |
Q36404769 | Dorsoventral patterning of the C. elegans postembryonic mesoderm requires both LIN-12/Notch and TGFbeta signaling |
Q89623386 | Dose-Dependent Effects of GLD-2 and GLD-1 on Germline Differentiation and Dedifferentiation in the Absence of PUF-8 |
Q34311913 | Dose-dependent control of proliferation and sperm specification by FOG-1/CPEB |
Q35128832 | Double-stranded RNA made in C. elegans neurons can enter the germline and cause transgenerational gene silencing |
Q36380597 | Down regulation of miR-124 in both Werner syndrome DNA helicase mutant mice and mutant Caenorhabditis elegans wrn-1 reveals the importance of this microRNA in accelerated aging |
Q30572576 | Down-regulation of tricarboxylic acid (TCA) cycle genes blocks progression through the first mitotic division in Caenorhabditis elegans embryos |
Q95270052 | Downregulation of eEF1A/EFT3-4 Enhances Dopaminergic Neurodegeneration After 6-OHDA Exposure in C. elegans Model |
Q34043288 | Downregulation of the Hsp90 system causes defects in muscle cells of Caenorhabditis elegans |
Q28589960 | Dpy19l1, a multi-transmembrane protein, regulates the radial migration of glutamatergic neurons in the developing cerebral cortex |
Q35342386 | Dramatic enhancement of genome editing by CRISPR/Cas9 through improved guide RNA design |
Q57139337 | Dramatic evolution of body length due to postembryonic changes in cell size in a newly discovered close relative of |
Q34212718 | Dramatic fertility decline in aging C. elegans males is associated with mating execution deficits rather than diminished sperm quality |
Q40767225 | Drebrin-like protein DBN-1 is a sarcomere component that stabilizes actin filaments during muscle contraction. |
Q28659112 | Drechslerella stenobrocha genome illustrates the mechanism of constricting rings and the origin of nematode predation in fungi |
Q47881346 | Drosophila Nociceptive Sensitization Requires BMP Signaling via the Canonical SMAD Pathway. |
Q46684744 | Drosophila Shep and C. elegans SUP-26 are RNA-binding proteins that play diverse roles in nervous system development |
Q28486802 | Drug absorption efficiency in Caenorhbditis elegans delivered by different methods |
Q27307876 | Drug-dependent behaviors and nicotinic acetylcholine receptor expressions in Caenorhabditis elegans following chronic nicotine exposure. |
Q64269415 | Dual Role of Ribosome-Binding Domain of NAC as a Potent Suppressor of Protein Aggregation and Aging-Related Proteinopathies |
Q37052292 | Dual excitatory and inhibitory serotonergic inputs modulate egg laying in Caenorhabditis elegans |
Q35094575 | Dual roles for ubiquitination in the processing of sperm organelles after fertilization |
Q35946374 | Dual roles of autophagy in the survival of Caenorhabditis elegans during starvation |
Q35230851 | Dual roles of tropomyosin as an F-actin stabilizer and a regulator of muscle contraction in Caenorhabditis elegans body wall muscle |
Q34755256 | Dual sgRNA-directed gene knockout using CRISPR/Cas9 technology in Caenorhabditis elegans |
Q36689628 | Duels without obvious sense: counteracting inductions involved in body wall muscle development in the Caenorhabditis elegans embryo |
Q30579943 | Duplication in the microtubule-actin cross-linking factor 1 gene causes a novel neuromuscular condition |
Q33993451 | Duplications in Caenorhabditis elegans |
Q42360363 | Durotaxis in Nematode Caenorhabditis elegans |
Q50555759 | Dynamic Opposition of Clustered Proteins Stabilizes Cortical Polarity in the C. elegans Zygote. |
Q30608755 | Dynamic SUMO modification regulates mitotic chromosome assembly and cell cycle progression in Caenorhabditis elegans |
Q30157700 | Dynamic analysis identifies novel roles for DLG-1 subdomains in AJM-1 recruitment and LET-413-dependent apical focusing |
Q33660241 | Dynamic chromatin organization during foregut development mediated by the organ selector gene PHA-4/FoxA |
Q28656250 | Dynamic encoding of perception, memory, and movement in a C. elegans chemotaxis circuit |
Q30523072 | Dynamic imaging by fluorescence correlation spectroscopy identifies diverse populations of polyglutamine oligomers formed in vivo |
Q38536445 | Dynamic localization of C. elegans TPR-GoLoco proteins mediates mitotic spindle orientation by extrinsic signaling. |
Q24801581 | Dynamic localization of SPE-9 in sperm: a protein required for sperm-oocyte interactions in Caenorhabditis elegans |
Q30477463 | Dynamic regulation of caveolin-1 trafficking in the germ line and embryo of Caenorhabditis elegans |
Q30597949 | Dynamically-expressed prion-like proteins form a cuticle in the pharynx of Caenorhabditis elegans |
Q64212157 | Dynein Light Chain DLC-1 Facilitates the Function of the Germline Cell Fate Regulator GLD-1 in |
Q48121129 | Dynein and EFF-1 control dendrite morphology by regulating the localization pattern of SAX-7 in epidermal cells |
Q46460507 | Dynein light chain DLC-1 promotes localization and function of the PUF protein FBF-2 in germline progenitor cells |
Q21092488 | Dynein modifiers in C. elegans: light chains suppress conditional heavy chain mutants |
Q37518051 | Dynein-mediated trafficking negatively regulates LET-23 EGFR signaling |
Q24324231 | Dysregulated LRRK2 signaling in response to endoplasmic reticulum stress leads to dopaminergic neuron degeneration in C. elegans |
Q90381677 | Dysregulation of DAF-16/FOXO3A-mediated stress responses accelerates oxidative DNA damage induced aging |
Q64115576 | Dysregulation of Neuronal Gαo Signaling by Graphene Oxide in Nematode Caenorhabditis elegans |
Q47655102 | Dysregulation of the Mitochondrial Unfolded Protein Response Induces Non-Apoptotic Dopaminergic Neurodegeneration in C. elegans Models of Parkinson's Disease. |
Q33352693 | E1 ubiquitin-activating enzyme UBA-1 plays multiple roles throughout C. elegans development |
Q37343806 | E2F coregulates an essential HSF developmental program that is distinct from the heat-shock response |
Q37698652 | E4 ligase-specific ubiquitination hubs coordinate DNA double-strand-break repair and apoptosis |
Q34608708 | EAT-20, a novel transmembrane protein with EGF motifs, is required for efficient feeding in Caenorhabditis elegans. |
Q52349676 | EFF-1 fusogen promotes phagosome sealing during cell process clearance in Caenorhabditis elegans. |
Q46789468 | EFF-1-mediated regenerative axonal fusion requires components of the apoptotic pathway. |
Q36855965 | EFN-4 functions in LAD-2-mediated axon guidance in Caenorhabditis elegans |
Q24794899 | EGF signal propagation during C. elegans vulval development mediated by ROM-1 rhomboid |
Q35176953 | EGF signalling activates the ubiquitin proteasome system to modulate C. elegans lifespan |
Q37401510 | EGFR Cell Survival Signaling Requires Phosphatidylcholine Biosynthesis |
Q35743812 | EGG molecules couple the oocyte-to-embryo transition with cell cycle progression |
Q27322765 | EGL-13/SoxD specifies distinct O2 and CO2 sensory neuron fates in Caenorhabditis elegans |
Q34063804 | EHBP-1 functions with RAB-10 during endocytic recycling in Caenorhabditis elegans |
Q36275271 | ELLI-1, a novel germline protein, modulates RNAi activity and P-granule accumulation in Caenorhabditis elegans. |
Q34706505 | EMB-30: an APC4 homologue required for metaphase-to-anaphase transitions during meiosis and mitosis in Caenorhabditis elegans |
Q35221556 | EMB-4: a predicted ATPase that facilitates lin-12 activity in Caenorhabditis elegans |
Q41979496 | EOL-1, the homolog of the mammalian Dom3Z, regulates olfactory learning in C. elegans |
Q36677308 | ESCRT-Dependent Cell Death in a Caenorhabditis elegans Model of the Lysosomal Storage Disorder Mucolipidosis Type IV. |
Q27346260 | ETS-4 is a transcriptional regulator of life span in Caenorhabditis elegans |
Q35224747 | EVA-1 functions as an UNC-40 Co-receptor to enhance attraction to the MADD-4 guidance cue in Caenorhabditis elegans |
Q35075212 | EZH2 protects glioma stem cells from radiation-induced cell death in a MELK/FOXM1-dependent manner |
Q36001742 | Early Embryogenesis and Anterior-Posterior Axis Formation in the White-Tip Nematode Aphelenchoides besseyi (Nematoda: Aphelenchoididae). |
Q47590831 | Early Pheromone Experience Modifies a Synaptic Activity to Influence Adult Pheromone Responses of C. elegans |
Q49980715 | Early experiences mediate distinct adult gene expression and reproductive programs in Caenorhabditis elegans. |
Q57484781 | East Indian sandalwood ( L.) oil confers neuroprotection and geroprotection in activating SKN-1/Nrf2 signaling pathway |
Q36203731 | Ectopic fat deposition contributes to age-associated pathology in Caenorhabditis elegans |
Q34609004 | Effect of a neuropeptide gene on behavioral states in Caenorhabditis elegans egg-laying |
Q39308359 | Effect of nematodes on rhizosphere colonization by seed-applied bacteria |
Q40239186 | Effect of pulse direct current signals on electrotactic movement of nematodes Caenorhabditis elegans and Caenorhabditis briggsae |
Q34519219 | Effect of the bacterium Serratia marcescens SCBI on the longevity and reproduction of the nematode Caenorhabditis briggsae KT0001. |
Q55283557 | Effect of the diet type and temperature on the C. elegans transcriptome. |
Q70972852 | Effect of the dpy-20 and rol-6 cotransformation markers on alpha-tubulin gene expression in C. elegans transformants |
Q24791911 | Effectiveness of specific RNA-mediated interference through ingested double-stranded RNA in Caenorhabditis elegans |
Q38850783 | Effects and mechanisms of prolongevity induced by Lactobacillus gasseri SBT2055 in Caenorhabditis elegans |
Q61797549 | Effects of Co γ Irradiation on the Reproductive Function of |
Q36184319 | Effects of Microcystin-LR Exposure on Spermiogenesis in Nematode Caenorhabditis elegans |
Q36860942 | Effects of Minor Ginsenosides, Ginsenoside Metabolites, and Ginsenoside Epimers on the Growth of Caenorhabditis elegans |
Q42021872 | Effects of TAT-conjugated platinum nanoparticles on lifespan of mitochondrial electron transport complex I-deficient Caenorhabditis elegans, nuo-1 |
Q64237552 | Effects of Thioflavin T and GSK-3 Inhibition on Lifespan and Motility in a Model of Tauopathy |
Q51941271 | Effects of a Caenorhabditis elegans dauer pheromone ascaroside on physiology and signal transduction pathways. |
Q51545564 | Effects of a bioassay-derived ivermectin lowest observed effect concentration on life-cycle traits of the nematode Caenorhabditis elegans. |
Q28471674 | Effects of genetic mutations and chemical exposures on Caenorhabditis elegans feeding: evaluation of a novel, high-throughput screening assay |
Q57173895 | Effects of liquid cultivation on gene expression and phenotype of C. elegans |
Q37163198 | Effects of long-term continuous cropping on soil nematode community and soil condition associated with replant problem in strawberry habitat |
Q30489322 | Effects of overexpression of huntingtin proteins on mitochondrial integrity |
Q35705666 | Effects of pathogenic proline mutations on myosin assembly |
Q87036608 | Effects of plant extracts on the reversal of glucose-induced impairment of stress-resistance in Caenorhabditis elegans |
Q35038739 | Effects of sex and insulin/insulin-like growth factor-1 signaling on performance in an associative learning paradigm in Caenorhabditis elegans |
Q37098708 | Effects of α-synuclein overexpression in transgenic Caenorhabditis elegans strains |
Q36132227 | Efficient Genome Editing in Caenorhabditis elegans with a Toolkit of Dual-Marker Selection Cassettes |
Q27304977 | Efficient and rapid C. elegans transgenesis by bombardment and hygromycin B selection |
Q27860707 | Efficient gene transfer in C.elegans: extrachromosomal maintenance and integration of transforming sequences |
Q42108619 | Efficient high-resolution deletion discovery in Caenorhabditis elegans by array comparative genomic hybridization |
Q34471658 | Efficient marker-free recovery of custom genetic modifications with CRISPR/Cas9 in Caenorhabditis elegans |
Q56872976 | Efficient proximity labeling in living cells and organisms with TurboID |
Q33281454 | Efficient target-selected mutagenesis in Caenorhabditis elegans: toward a knockout for every gene. |
Q33949428 | Egg-laying defective mutants of the nematode Caenorhabditis elegans |
Q36984952 | Eight genes are required for functional reconstitution of the Caenorhabditis elegans levamisole-sensitive acetylcholine receptor |
Q35697852 | Electrical activity and behavior in the pharynx of Caenorhabditis elegans |
Q43929810 | Electron microscopical reconstruction of the anterior sensory anatomy of the nematodecaenorhabditis elegans |
Q49808079 | Electrophysiological measures of aging pharynx function in C. elegans reveal enhanced organ functionality in older, long-lived mutants. |
Q47148967 | Electrophysiology of the rhythmic defecation program in nematode Heterorhabditis megidis. |
Q35638073 | Elemental bioimaging of Cisplatin in Caenorhabditis elegans by LA-ICP-MS |
Q64987095 | Elemental bioimaging of manganese uptake in C. elegans. |
Q37129478 | Elevated CO2 levels affect development, motility, and fertility and extend life span in Caenorhabditis elegans |
Q35605140 | Elimination of paternal mitochondria through the lysosomal degradation pathway in C. elegans |
Q28607531 | Ellsworth C. Dougherty: A Pioneer in the Selection of Caenorhabditis elegans as a Model Organism |
Q90689207 | Embryo integrity regulates maternal proteostasis and stress resilience |
Q36311980 | Embryogenesis in C. elegans after elimination of individual blastomeres or induced alteration of the cell division order |
Q54187825 | Embryonic gut differentiation in nematodes: endocytosis of macromolecules and its experimental inhibition. |
Q34610993 | Embryonic morphogenesis in Caenorhabditis elegans integrates the activity of LET-502 Rho-binding kinase, MEL-11 myosin phosphatase, DAF-2 insulin receptor and FEM-2 PP2c phosphatase. |
Q37697410 | Embryonic tissue differentiation in Caenorhabditis elegans requires dif-1, a gene homologous to mitochondrial solute carriers |
Q47443193 | Emerging and evolving concepts in gene essentiality. |
Q37505114 | Enabling the Triplet of Tetraphenylethene to Sensitize the Excited State of Europium(III) for Protein Detection and Time-Resolved Luminescence Imaging |
Q34448693 | Endocannabinoid-Goα signalling inhibits axon regeneration in Caenorhabditis elegans by antagonizing Gqα-PKC-JNK signalling |
Q52311781 | Endocannabinoids in Caenorhabditis elegans are essential for the mobilization of cholesterol from internal reserves. |
Q27345025 | Endocytic sorting and recycling require membrane phosphatidylserine asymmetry maintained by TAT-1/CHAT-1 |
Q38999061 | Endogenous RNAi Pathways Are Required in Neurons for Dauer Formation in Caenorhabditis elegans |
Q42159466 | Endogenous syntaxins 2, 3 and 4 exhibit distinct but overlapping patterns of expression at the hepatocyte plasma membrane |
Q42136910 | Endomembrane-associated RSD-3 is important for RNAi induced by extracellular silencing RNA in both somatic and germ cells of Caenorhabditis elegans |
Q55379225 | Endophilin A and B Join Forces With Clathrin to Mediate Synaptic Vesicle Recycling in Caenorhabditis elegans. |
Q57026995 | Endoplasmic Reticulum Homeostasis Is Modulated by the Forkhead Transcription Factor FKH-9 During Infection of |
Q42565864 | Endoplasmic reticulum stress pathway required for immune homeostasis is neurally controlled by arrestin-1. |
Q64903295 | Endoribonuclease ENDU-2 regulates multiple traits including cold tolerance via cell autonomous and nonautonomous controls in Caenorhabditis elegans. |
Q51731940 | Endosome maturation factors Rabenosyn-5/VPS45 and caveolin-1 regulate ciliary membrane and polycystin-2 homeostasis. |
Q28243174 | Engineered endolysin-based "Artilysins" to combat multidrug-resistant gram-negative pathogens |
Q51221666 | Engineered non-Mendelian inheritance of entire parental genomes in C. elegans. |
Q41139907 | Engineering new balancer chromosomes in C. elegans via CRISPR/Cas9 |
Q37680398 | Engineering of a conditional allele reveals multiple roles of XRN2 in Caenorhabditis elegans development and substrate specificity in microRNA turnover |
Q34261458 | Engineering recombinant Orsay virus directly in the metazoan host Caenorhabditis elegans |
Q59134780 | Engulfing cells promote neuronal regeneration and remove neuronal debris through distinct biochemical functions of CED-1 |
Q36379455 | Engulfment pathways promote programmed cell death by enhancing the unequal segregation of apoptotic potential |
Q33346300 | Enhanced Caenorhabditis elegans locomotion in a structured microfluidic environment |
Q36225800 | Enhanced energy metabolism contributes to the extended life span of calorie-restricted Caenorhabditis elegans |
Q33952532 | Enhanced neuronal RNAi in C. elegans using SID-1. |
Q34559649 | Enhancement of actin-depolymerizing factor/cofilin-dependent actin disassembly by actin-interacting protein 1 is required for organized actin filament assembly in the Caenorhabditis elegans body wall muscle |
Q42788396 | Enhancement of odor avoidance regulated by dopamine signaling in Caenorhabditis elegans |
Q33965838 | Enhancers of glp-1, a gene required for cell-signaling in Caenorhabditis elegans, define a set of genes required for germline development |
Q60922133 | Enhancing GABAergic Transmission Improves Locomotion in a Model of Spinal Muscular Atrophy |
Q36012704 | Enrichment of H3K9me2 on Unsynapsed Chromatin in Caenorhabditis elegans Does Not Target de Novo Sites |
Q37238422 | Environmental induction and genetic control of surface antigen switching in the nematode Caenorhabditis elegans |
Q54961421 | Environmental responsiveness of tubulin glutamylation in sensory cilia is regulated by the p38 MAPK pathway. |
Q37581481 | Environmental stresses induce transgenerationally inheritable survival advantages via germline-to-soma communication in Caenorhabditis elegans |
Q33924663 | Environmentally induced changes in correlated responses to selection reveal variable pleiotropy across a complex genetic network |
Q26827462 | Eph receptor signaling in C. elegans |
Q58580316 | Epidermal Remodeling in Dauers Requires the Nidogen Domain Protein DEX-1 |
Q92527683 | Epidermal control of axonal attachment via β-spectrin and the GTPase-activating protein TBC-10 prevents axonal degeneration |
Q37614557 | Epigenetic effect of testosterone in the behavior of C. elegans. A clue to explain androgen-dependent autistic traits? |
Q27302346 | Epigenetic regulation of histone H3 serine 10 phosphorylation status by HCF-1 proteins in C. elegans and mammalian cells |
Q58580309 | Epithelial Shaping by Diverse Apical Extracellular Matrices Requires the Nidogen Domain Protein DEX-1 in |
Q36709963 | Erratum: φXANES: In vivo imaging of metal-protein coordination environments |
Q33547169 | Escherichia coli MW005: lambda Red-mediated recombineering and copy-number induction of oriV-equipped constructs in a single host |
Q57281969 | Escherichia coli mediated resistance of Entamoeba histolytica to oxidative stress is triggered by oxaloacetate |
Q33957117 | Essential genes in the hDf6 region of chromosome I in Caenorhabditis elegans |
Q36946937 | Essential role of ADF/cofilin for assembly of contractile actin networks in the C. elegans somatic gonad |
Q36175303 | Establishing Caenorhabditis elegans as a model for Mycobacterium avium subspecies hominissuis infection and intestinal colonization |
Q36824595 | Establishing a novel C. elegans model to investigate the role of autophagy in amyotrophic lateral sclerosis |
Q100404798 | Establishment and maintenance of motor neuron identity via temporal modularity in terminal selector function |
Q54217543 | Establishment of a Host-to-Host Transmission Model for Mycobacterium avium subsp. hominissuis Using Caenorhabditis elegans and Identification of Colonization-Associated Genes. |
Q34913146 | Establishment of a tissue-specific RNAi system in C. elegans |
Q52205753 | Establishment of left-right asymmetry in the Caenorhabditis elegans embryo: a multistep process involving a series of inductive events |
Q72387014 | Estimation of mutation rates induced by large doses of gamma, proton and neutron irradiation of the X-chromosome of the nematode Panagrellus redivivus |
Q45283836 | Ethanol Stimulates Locomotion via a Gαs-Signaling Pathway in IL2 Neurons in Caenorhabditis elegans. |
Q24632088 | Ethanol metabolism and osmolarity modify behavioral responses to ethanol in C. elegans |
Q33893654 | Ethanol preference in C. elegans |
Q36757345 | Evaluating the pathogenic potential of environmental Escherichia coli by using the Caenorhabditis elegans infection model |
Q87258945 | Evaluation and identification of reliable reference genes for toxicological study in Caenorhabditis elegans |
Q30537891 | Evaluation of Head Movement Periodicity and Irregularity during Locomotion of Caenorhabditis elegans |
Q34389736 | Evaluation of environmental safety concentrations of DMSA Coated Fe2O3-NPs using different assay systems in nematode Caenorhabditis elegans |
Q36935678 | Evaluation of the Fluids Mixing Enclosure System for Life Science Experiments During a Commercial Caenorhabditis elegans Spaceflight Experiment. |
Q41351174 | Evaluation of the long-term memory for thermosensation regulated by neuronal calcium sensor-1 in Caenorhabditis elegans |
Q34146726 | Evaluation of the toxicity of 2-aminoimidazole antibiofilm agents using both cellular and model organism systems |
Q46606749 | Evidence for a role for cyclic AMP in modulating the action of 5-HT and an excitatory neuropeptide, FLP17A, in the pharyngeal muscle of Caenorhabditis elegans |
Q67265327 | Evidence for a transposon in caenorhabditis elegans |
Q36086746 | Evidence for an Opportunistic and Endophytic Lifestyle of the Bursaphelenchus xylophilus-Associated Bacteria Serratia marcescens PWN146 Isolated from Wilting Pinus pinaster |
Q33613864 | Evidence for functional and physical association between Caenorhabditis elegans SEL-10, a Cdc4p-related protein, and SEL-12 presenilin |
Q33961360 | Evidence for parallel processing of sensory information controlling dauer formation in Caenorhabditis elegans |
Q35346808 | Evidence for phosphorylation in the MSP cytoskeletal filaments of amoeboid spermatozoa |
Q34636028 | Evidence for the frequent use of TTG as the translation initiation codon of mitochondrial protein genes in the nematodes, Ascaris suum and Caenorhabditis elegans |
Q70140819 | Evidence in a nematode for regulation of transposon excision by tissue-specific factors |
Q34010321 | Evidence of a mate-finding cue in the hermaphrodite nematode Caenorhabditis elegans |
Q34352055 | Evidence of hermaphroditism and sex ratio distortion in the fungal feeding nematode Bursaphelenchus okinawaensis |
Q30505349 | Evidence that CED-9/Bcl2 and CED-4/Apaf-1 localization is not consistent with the current model for C. elegans apoptosis induction |
Q27319242 | Evidence that masking of synapsis imperfections counterbalances quality control to promote efficient meiosis |
Q36174632 | Evolution and analysis of minimal neural circuits for klinotaxis in Caenorhabditis elegans |
Q98946092 | Evolution and maintenance of microbe-mediated protection under occasional pathogen infection |
Q40100301 | Evolution of Caenorhabditis elegans host defense under selection by the bacterial parasite Serratia marcescens |
Q27308019 | Evolution of New cis-Regulatory Motifs Required for Cell-Specific Gene Expression in Caenorhabditis |
Q33392492 | Evolution of a polymodal sensory response network |
Q34553053 | Evolution of dnmt-2 and mbd-2-like genes in the free-living nematodes Pristionchus pacificus, Caenorhabditis elegans and Caenorhabditis briggsae |
Q36035957 | Evolution of drug-tolerant nematode populations in response to density reduction |
Q30491051 | Evolution of early embryogenesis in rhabditid nematodes |
Q55714897 | Evolution of larger sperm in response to experimentally increased sperm competition in Caenorhabditis elegans. |
Q48193413 | Evolution of mitotic spindle behavior during the first asymmetric embryonic division of nematodes. |
Q74612744 | Evolution of sperm size in nematodes: sperm competition favours larger sperm |
Q96350986 | Evolutionarily conserved regulation of immunity by the splicing factor RNP-6/PUF60 |
Q34119706 | Evolutionarily conserved role of calcineurin in phosphodegron-dependent degradation of phosphodiesterase 4D |
Q36596840 | Evolutionary Conservation of a GPCR-Independent Mechanism of Trimeric G Protein Activation |
Q33729393 | Evolutionary Divergence of the C-terminal Domain of Complexin Accounts for Functional Disparities between Vertebrate and Invertebrate Complexins |
Q27320001 | Evolutionary change within a bipotential switch shaped the sperm/oocyte decision in hermaphroditic nematodes |
Q97423470 | Evolutionary conserved role of neural cell adhesion molecule-1 in memory |
Q41448931 | Excess free histone H3 localizes to centrosomes for proteasome-mediated degradation during mitosis in metazoans |
Q34360039 | Excessive folate synthesis limits lifespan in the C. elegans: E. coli aging model. |
Q33955403 | Excision repair of UV radiation-induced DNA damage in Caenorhabditis elegans |
Q57056958 | Excitable RhoA dynamics drive pulsed contractions in the early embryo |
Q48262160 | Excitatory neurons sculpt GABAergic neuronal connectivity in the C. elegans motor circuit |
Q27339190 | Exercise in an electrotactic flow chamber ameliorates age-related degeneration in Caenorhabditis elegans. |
Q27308745 | Exocyst subunits Exo70 and Exo84 cooperate with small GTPases to regulate behavior and endocytic trafficking in C. elegans |
Q57167694 | Exophiala dermatitidis isolates from various sources: using alternative invertebrate host organisms (Caenorhabditis elegans and Galleria mellonella) to determine virulence |
Q59813418 | Expanded genetic screening in identifies new regulators and an inhibitory role for NAD in axon regeneration |
Q33949349 | Expanded polyglutamines in Caenorhabditis elegans cause axonal abnormalities and severe dysfunction of PLM mechanosensory neurons without cell death |
Q42290242 | Expanding the C. elegans toolbox into a toolshed |
Q36106695 | Expanding the genetic code of Caenorhabditis elegans using bacterial aminoacyl-tRNA synthetase/tRNA pairs |
Q90601698 | Experimental Models to Study Podocyte Biology: Stock-Taking the Toolbox of Glomerular Research |
Q37392791 | Experimental evidence for UNC-6 (netrin) axon guidance by stochastic fluctuations of intracellular UNC-40 (DCC) outgrowth activity. |
Q35535911 | Experimental evolution reveals antagonistic pleiotropy in reproductive timing but not life span in Caenorhabditis elegans |
Q35963009 | Experimental validation of Haldane's hypothesis on the role of infection as an evolutionary force for Metazoans |
Q42373221 | Exploring Potential Germline-Associated Roles of the TRIM-NHL Protein NHL-2 Through RNAi Screening |
Q35986043 | Exploring biology with small organic molecules |
Q34616164 | Exploring the envelope. Systematic alteration in the sex-determination system of the nematode caenorhabditis elegans. |
Q37114819 | Export of RNA silencing from C. elegans tissues does not require the RNA channel SID-1 |
Q98226453 | Exposing a novel genetic interaction between unc-33/CRMP and hmp-2/β-catenin during Caenorhabditis elegans embryogenesis |
Q34881586 | Exposure to Mn/Zn ethylene-bis-dithiocarbamate and glyphosate pesticides leads to neurodegeneration in Caenorhabditis elegans |
Q35785033 | Exposure to glyphosate- and/or Mn/Zn-ethylene-bis-dithiocarbamate-containing pesticides leads to degeneration of γ-aminobutyric acid and dopamine neurons in Caenorhabditis elegans |
Q28553337 | Exposure to the BPA-Substitute Bisphenol S Causes Unique Alterations of Germline Function |
Q39957291 | Exposure to the metabolic inhibitor sodium azide induces stress protein expression and thermotolerance in the nematode Caenorhabditis elegans |
Q47132534 | Expression of CeHSP17 Protein in Response to Heat Shock and Heavy Metal Ions |
Q52544063 | Expression of a Drosophila melanogaster amber suppressor tRNA(Ser) in Caenorhabditis elegans. |
Q34074523 | Expression of an expanded CGG-repeat RNA in a single pair of primary sensory neurons impairs olfactory adaptation in Caenorhabditis elegans |
Q37271606 | Expression of ceramide glucosyltransferases, which are essential for glycosphingolipid synthesis, is only required in a small subset of C. elegans cells |
Q51095155 | Expression of gamma-tubulin during the development of nematode Caenorhabditis elegans. |
Q40317528 | Expression of hepatitis B virus surface antigens induces defective gonad phenotypes in Caenorhabditis elegans |
Q40566579 | Expression of intron-containing C. elegans heat shock genes in mouse cells demonstrates divergence of 3' splice site recognition sequences between nematodes and vertebrates, and an inhibitory effect of heat shock on the mammalian splicing apparatus |
Q33251201 | Expression of mammalian GPCRs in C. elegans generates novel behavioural responses to human ligands. |
Q34765780 | Expression of multiple UNC-13 proteins in the Caenorhabditis elegans nervous system |
Q35115901 | Expression of ram-5 in the structural cell is required for sensory ray morphogenesis in Caenorhabditis elegans male tail |
Q60193030 | Expression of the CCAAT-binding factor NF-Y in Caenorhabditis elegans |
Q34440372 | Expression pattern, regulation, and biological role of runt domain transcription factor, run, in Caenorhabditis elegans |
Q34460106 | Expression profile of Caenorhabditis elegans mutant for the Werner syndrome gene ortholog reveals the impact of vitamin C on development to increase life span. |
Q33263257 | Expression profiling of MAP kinase-mediated meiotic progression in Caenorhabditis elegans |
Q91685792 | Expressional artifact caused by a co-injection marker rol-6 in C. elegans |
Q42698130 | Extended Twilight among Isogenic C. elegans Causes a Disproportionate Scaling between Lifespan and Health |
Q30597014 | Extending the molecular clutch beyond actin-based cell motility |
Q27333224 | Extension of lifespan in C. elegans by naphthoquinones that act through stress hormesis mechanisms |
Q37272940 | Extension of the Caenorhabditis elegans Pharyngeal M1 neuron axon is regulated by multiple mechanisms |
Q83229054 | Extensive intraspecies cryptic variation in an ancient embryonic gene regulatory network |
Q37398041 | Extracellular RNA is transported from one generation to the next in Caenorhabditis elegans |
Q28475323 | Extracellular dopamine potentiates mn-induced oxidative stress, lifespan reduction, and dopaminergic neurodegeneration in a BLI-3-dependent manner in Caenorhabditis elegans |
Q35741923 | Extracellular leucine-rich repeat proteins are required to organize the apical extracellular matrix and maintain epithelial junction integrity in C. elegans |
Q48172143 | Extracellular vesicle budding is inhibited by redundant regulators of TAT-5 flippase localization and phospholipid asymmetry |
Q40676581 | Extrachromosomal DNA transformation of Caenorhabditis elegans |
Q40407487 | Extrachromosomal circular copies of the transposon Tc1. |
Q36264228 | Extrachromosomal copies of transposon Tc1 in the nematode Caenorhabditis elegans |
Q42209149 | Extreme HOT regions are CpG-dense promoters in C. elegans and humans |
Q30847876 | Extrinsic Repair of Injured Dendrites as a Paradigm for Regeneration by Fusion in Caenorhabditis elegans |
Q46397004 | F-Box Protein XREP-4 Is a New Regulator of the Oxidative Stress Response in Caenorhabditis elegans |
Q46340497 | F-actin prevents interaction between sperm DNA and the oocyte meiotic spindle in C. elegans. |
Q58754595 | FACT Sets a Barrier for Cell Fate Reprogramming in Caenorhabditis elegans and Human Cells |
Q27301461 | FAH domain containing protein 1 (FAHD-1) is required for mitochondrial function and locomotion activity in C. elegans |
Q37152671 | FBF and its dual control of gld-1 expression in the Caenorhabditis elegans germline |
Q28478041 | FDA-approved drugs that protect mammalian neurons from glucose toxicity slow aging dependent on cbp and protect against proteotoxicity |
Q37310372 | FER-1/Dysferlin promotes cholinergic signaling at the neuromuscular junction in C. elegans and mice |
Q37124605 | FGF signaling regulates Wnt ligand expression to control vulval cell lineage polarity in C. elegans |
Q34798010 | FGT-1 is a mammalian GLUT2-like facilitative glucose transporter in Caenorhabditis elegans whose malfunction induces fat accumulation in intestinal cells |
Q42104965 | FGT-1-mediated glucose uptake is defective in insulin/IGF-like signaling mutants in Caenorhabditis elegans |
Q36240275 | FIJI Macro 3D ART VeSElecT: 3D Automated Reconstruction Tool for Vesicle Structures of Electron Tomograms |
Q27310260 | FLCN and AMPK Confer Resistance to Hyperosmotic Stress via Remodeling of Glycogen Stores |
Q33335351 | FLI-1 Flightless-1 and LET-60 Ras control germ line morphogenesis in C. elegans |
Q58083909 | FLIRT: fast local infrared thermogenetics for subcellular control of protein function |
Q48322845 | FLP-1 neuropeptides modulate sensory and motor circuits in the nematode Caenorhabditis elegans. |
Q36591412 | FLP-4 neuropeptide and its receptor in a neuronal circuit regulate preference choice through functions of ASH-2 trithorax complex in Caenorhabditis elegans |
Q31140949 | FLR-4, a novel serine/threonine protein kinase, regulates defecation rhythm in Caenorhabditis elegans |
Q47068707 | FMRFamide-like neuropeptides and mechanosensory touch receptor neurons regulate male sexual turning behavior in Caenorhabditis elegans. |
Q46178236 | FMRFamide-like peptides expand the behavioral repertoire of a densely connected nervous system. |
Q42363573 | Facilitation of Endosomal Recycling by an IRG Protein Homolog Maintains Apical Tubule Structure in Caenorhabditis elegans |
Q33748620 | Facioscapulohumeral muscular dystrophy region gene-1 (FRG-1) is an actin-bundling protein associated with muscle-attachment sites |
Q34984054 | Factors regulating the abundance and localization of synaptobrevin in the plasma membrane. |
Q34336516 | Family of FLP Peptides in Caenorhabditis elegans and Related Nematodes |
Q52626888 | Fanconi Anemia FANCM/FNCM-1 and FANCD2/FCD-2 Are Required for Maintaining Histone Methylation Levels and Interact with the Histone Demethylase LSD1/SPR-5 in Caenorhabditis elegans. |
Q64900195 | Fast genetic mapping of complex traits in C. elegans using millions of individuals in bulk. |
Q34848904 | Fast monitoring of in-vivo conformational changes in myosin using single scan polarization-SHG microscopy |
Q93075111 | Fasting prevents hypoxia-induced defects of proteostasis in C. elegans |
Q41962985 | Fat accumulation in Caenorhabditis elegans is mediated by SREBP homolog SBP-1 |
Q33627981 | Fat accumulation in Caenorhabditis elegans triggered by the electrophilic lipid peroxidation product 4-hydroxynonenal (4-HNE). |
Q27657785 | Fatty Acid- and Retinoid-binding Proteins Have Distinct Binding Pockets for the Two Types of Cargo |
Q27322410 | Fatty acid desaturation links germ cell loss to longevity through NHR-80/HNF4 in C. elegans |
Q39776313 | Fatty acids composition of Caenorhabditis elegans using accurate mass GCMS-QTOF |
Q33960729 | Feedback control of sex determination by dosage compensation revealed through Caenorhabditis elegans sdc-3 mutations |
Q39873356 | Feedback from network states generates variability in a probabilistic olfactory circuit. |
Q89677076 | Feedback regulation of BMP signaling by Caenorhabditis elegans cuticle collagens |
Q33413817 | Feeding a ROS-generator to Caenorhabditis elegans leads to increased expression of small heat shock protein HSP-16.2 and hormesis |
Q89169463 | Feeding state regulates pheromone-mediated avoidance behavior via the insulin signaling pathway in Caenorhabditis elegans |
Q27312401 | Feeding state, insulin and NPR-1 modulate chemoreceptor gene expression via integration of sensory and circuit inputs |
Q27321517 | Femtosecond laser ablation reveals antagonistic sensory and neuroendocrine signaling that underlie C. elegans behavior and development |
Q66960317 | Fertilization and sperm competition in the nematodeCaenorhabditis elegans |
Q33827610 | Fertilization in C. elegans requires an intact C-terminal RING finger in sperm protein SPE-42 |
Q57168202 | Field studies reveal a close relative of C. elegans thrives in the fresh figs of Ficus septica and disperses on its Ceratosolen pollinating wasps |
Q39769510 | Filling the gap: adding super-resolution to array tomography for correlated ultrastructural and molecular identification of electrical synapses at the C. elegans connectome |
Q39990540 | Fine tuning of RFX/DAF-19-regulated target gene expression through binding to multiple sites in Caenorhabditis elegans |
Q36958215 | Fine-Scale Crossover Rate Variation on the Caenorhabditis elegans X Chromosome. |
Q33954676 | Fine-structure genetics of ama-1, an essential gene encoding the amanitin-binding subunit of RNA polymerase II in Caenorhabditis elegans |
Q41508221 | Fitness Effects of Thermal Stress Differ Between Outcrossing and Selfing Populations in Caenorhabditis elegans. |
Q57144305 | Flagella-mediated secretion of a novel cytotoxin affecting both vertebrate and invertebrate hosts |
Q33527398 | Flavin adenine dinucleotide rescues the phenotype of frataxin deficiency |
Q41139455 | Flavin monooxygenases regulate Caenorhabditis elegans axon guidance and growth cone protrusion with UNC-6/Netrin signaling and Rac GTPases. |
Q91869418 | Flexible and disposable paper- and plastic-based gel micropads for nematode handling, imaging, and chemical testing |
Q96162535 | Flexible motor sequence generation during stereotyped escape responses |
Q36216689 | Fluorescence visualization of the distribution of microfilaments in gonads and early embryos of the nematode Caenorhabditis elegans |
Q41876139 | Fluorescence-based fixative and vital staining of lipid droplets in Caenorhabditis elegans reveal fat stores using microscopy and flow cytometry approaches |
Q36016032 | Fluorescent Beads Are a Versatile Tool for Staging Caenorhabditis elegans in Different Life Histories |
Q34079552 | Fluoxetine protects against amyloid-beta toxicity, in part via daf-16 mediated cell signaling pathway, in Caenorhabditis elegans |
Q34587786 | Fluoxetine-resistance genes in Caenorhabditis elegans function in the intestine and may act in drug transport |
Q35923574 | Folate Acts in E. coli to Accelerate C. elegans Aging Independently of Bacterial Biosynthesis |
Q36791724 | Folate metabolite profiling of different cell types and embryos suggests variation in folate one-carbon metabolism, including developmental changes in human embryonic brain |
Q27316476 | Folliculin regulates ampk-dependent autophagy and metabolic stress survival |
Q33302941 | Food deprivation attenuates seizures through CaMKII and EAG K+ channels |
Q92955042 | Food deprivation changes chemotaxis behavior in Caenorhabditis elegans |
Q48823976 | Food responsiveness regulates episodic behavioral states in Caenorhabditis elegans. |
Q30498896 | Food sensitizes C. elegans avoidance behaviours through acute dopamine signalling |
Q37568338 | Food, pathogen, signal: The multifaceted nature of a bacterial diet |
Q94553180 | Force microscopy of the Caenorhabditis elegans embryonic eggshell |
Q68511393 | Formaldehyde mutagenesis of the eT1 balanced region in Caenorhabditis elegans: Dose—response curve and the analysis of mutational events |
Q28484462 | Formation of phosphoglycosides in Caenorhabditis elegans: a novel biotransformation pathway |
Q36172263 | Formation of the transition zone by Mks5/Rpgrip1L establishes a ciliary zone of exclusion (CIZE) that compartmentalises ciliary signalling proteins and controls PIP2 ciliary abundance |
Q92859715 | Forward Genetic Screen for Caenorhabditis elegans Mutants with a Shortened Locomotor Healthspan |
Q37401038 | Forward Genetic Screen in Caenorhabditis elegans Suggests F57A10.2 and acp-4 As Suppressors of C9ORF72 Related Phenotypes |
Q33834330 | Forward and reverse mutagenesis in C. elegans |
Q24811127 | Forward genetic analysis of visual behavior in zebrafish |
Q30523972 | Forward genetic analysis to identify determinants of dopamine signaling in Caenorhabditis elegans using swimming-induced paralysis |
Q92609296 | Forward genetic approach for behavioral neuroscience using animal models |
Q30489014 | Forward locomotion of the nematode C. elegans is achieved through modulation of a single gait |
Q88426287 | Four specific immunoglobulin domains in UNC-52/Perlecan function with NID-1/Nidogen during dendrite morphogenesis in Caenorhabditis elegans |
Q30740993 | Fourier transform infrared microspectroscopy for the analysis of the biochemical composition of C. elegans worms |
Q72352558 | Freeze-fracture characterization of the cuticle of adult and dauer forms of Caenorhabditis elegans |
Q43918338 | Freeze-thaw survival of the free-living nematode Caenorhabditis briggsae |
Q57055355 | From "the Worm" to "the Worms" and Back Again: The Evolutionary Developmental Biology of Nematodes |
Q38288095 | From early lessons to new frontiers: the worm as a treasure trove of small RNA biology |
Q36960940 | From genes to function: the C. elegans genetic toolbox |
Q33754689 | From modes to movement in the behavior of Caenorhabditis elegans |
Q39076751 | From the Cover: ZnO Nanoparticles Enhanced Germ Cell Apoptosis in Caenorhabditis elegans, in Comparison with ZnCl2. |
Q35120253 | Full toxicity assessment of Genkwa Flos and the underlying mechanism in nematode Caenorhabditis elegans |
Q24803204 | Function and evolution of the serotonin-synthetic bas-1 gene and other aromatic amino acid decarboxylase genes in Caenorhabditis |
Q28387844 | Function of RSKS-1-AAK-2-DAF-16 signaling cascade in enhancing toxicity of multi-walled carbon nanotubes can be suppressed by mir-259 activation in Caenorhabditis elegans |
Q36295832 | Function of a STIM1 homologue in C. elegans: evidence that store-operated Ca2+ entry is not essential for oscillatory Ca2+ signaling and ER Ca2+ homeostasis. |
Q41963112 | Function of the C. elegans T-box factor TBX-2 depends on interaction with the UNC-37/Groucho corepressor |
Q35650714 | Function of the Caenorhabditis elegans ABC transporter PGP-2 in the biogenesis of a lysosome-related fat storage organelle |
Q33321969 | Function of the PHA-4/FOXA transcription factor during C. elegans post-embryonic development |
Q48179175 | Functional Characterization of Novel Circular RNA Molecule, circzip-2 and Its Synthesizing Gene zip-2 in C. elegans Model of Parkinson's Disease |
Q28551220 | Functional Characterization of a Novel Class of Morantel-Sensitive Acetylcholine Receptors in Nematodes |
Q92649301 | Functional Dissection of C. elegans bZip-Protein CEBP-1 Reveals Novel Structural Motifs Required for Axon Regeneration and Nuclear Import |
Q57036601 | Functional Interactions Between /S6K, /Notch, and Regulators of Fertility and Germline Stem Cell Maintenance |
Q28469504 | Functional Requirements for Heparan Sulfate Biosynthesis in Morphogenesis and Nervous System Development in C. elegans |
Q30856494 | Functional analysis of cytoplasmic dynein heavy chain in Caenorhabditis elegans with fast-acting temperature-sensitive mutations |
Q24802049 | Functional and phylogenetic analysis of the ubiquitylation system in Caenorhabditis elegans: ubiquitin-conjugating enzymes, ubiquitin-activating enzymes, and ubiquitin-like proteins |
Q24303558 | Functional and physical interaction between Bcl-X(L) and a BH3-like domain in Beclin-1 |
Q24798850 | Functional characterization in Caenorhabditis elegans of transmembrane worm-human orthologs |
Q28512067 | Functional characterization of KIN-32, the Caenorhabditis elegans homolog of focal adhesion kinase |
Q30443507 | Functional characterization of TcaA: minimal requirement for teicoplanin susceptibility and role in Caenorhabditis elegans virulence |
Q35080835 | Functional comparison of the nematode Hox gene lin-39 in C. elegans and P. pacificus reveals evolutionary conservation of protein function despite divergence of primary sequences |
Q38327262 | Functional constraint and divergence in the G protein family in Caenorhabditis elegans and Caenorhabditis briggsae |
Q46543895 | Functional differentiation of cooperating kinesin-2 motors orchestrates cargo import and transport in C. elegans cilia |
Q27312406 | Functional dissection of Caenorhabditis elegans CLK-2/TEL2 cell cycle defects during embryogenesis and germline development |
Q33295355 | Functional diversification of the nematode mbd2/3 gene between Pristionchus pacificus and Caenorhabditis elegans |
Q34672587 | Functional domains of LAG-2, a putative signaling ligand for LIN-12 and GLP-1 receptors in Caenorhabditis elegans |
Q34629217 | Functional genomic analysis of the let-7 regulatory network in Caenorhabditis elegans |
Q33754265 | Functional genomics of hsp-90 in parasitic and free-living nematodes |
Q27310570 | Functional loss of two ceramide synthases elicits autophagy-dependent lifespan extension in C. elegans |
Q33932567 | Functional modularity of nuclear hormone receptors in a Caenorhabditis elegans metabolic gene regulatory network |
Q27919691 | Functional modulation of IFT kinesins extends the sensory repertoire of ciliated neurons in Caenorhabditis elegans |
Q34607574 | Functional overlap between the mec-8 gene and five sym genes in Caenorhabditis elegans |
Q34314369 | Functional phenotypic rescue of Caenorhabditis elegans neuroligin-deficient mutants by the human and rat NLGN1 genes |
Q36631120 | Functional redundancy of the B9 proteins and nephrocystins in Caenorhabditis elegans ciliogenesis |
Q35834347 | Functional redundancy of worm spliceosomal proteins U1A and U2B''. |
Q36158589 | Functional relevance of "seed" and "non-seed" sequences in microRNA-mediated promotion of C. elegans developmental progression |
Q34278433 | Functional requirement for histone deacetylase 1 in Caenorhabditis elegans gonadogenesis |
Q34386949 | Functional specialization of sensory cilia by an RFX transcription factor isoform |
Q93055793 | Functional validity, role, and implications of heavy alcohol consumption genetic loci |
Q41781926 | Functionally and spatially distinct modes of munc18-syntaxin 1 interaction |
Q58749293 | Functionally asymmetric motor neurons contribute to coordinating locomotion of |
Q34605683 | Functions of the Caenorhabditis elegans regulatory myosin light chain genes mlc-1 and mlc-2. |
Q41624209 | Further characterization of a temperature-sensitive transformation mutant in Caenorhabditis elegans |
Q47068813 | G alpha(q)-coupled muscarinic acetylcholine receptors enhance nicotinic acetylcholine receptor signaling in Caenorhabditis elegans mating behavior. |
Q47069082 | G protein-coupled receptor kinase-2 (GRK-2) regulates serotonin metabolism through the monoamine oxidase AMX-2 in Caenorhabditis elegans |
Q59125605 | G2019S LRRK2 Increases Stress Susceptibility Through Inhibition of DAF-16 Nuclear Translocation in a 14-3-3 Associated-Manner in Caenorhabditis elegans |
Q44396209 | GABA is dispensable for the formation of junctional GABA receptor clusters in Caenorhabditis elegans. |
Q46294257 | GABA(B) receptor activation mediates frequency-dependent plasticity of developing GABAergic synapses. |
Q35580849 | GABAergic synaptic plasticity during a developmentally regulated sleep-like state in C. elegans |
Q33267334 | GATA transcription factor required for immunity to bacterial and fungal pathogens |
Q36412608 | GCK-3, a newly identified Ste20 kinase, binds to and regulates the activity of a cell cycle-dependent ClC anion channel |
Q36494490 | GCN-2 dependent inhibition of protein synthesis activates osmosensitive gene transcription via WNK and Ste20 kinase signaling |
Q37040651 | GEFs and Rac GTPases control directional specificity of neurite extension along the anterior-posterior axis |
Q27334952 | GEI-8, a homologue of vertebrate nuclear receptor corepressor NCoR/SMRT, regulates gonad development and neuronal functions in Caenorhabditis elegans |
Q40173136 | GFP is a selective non-linear optical sensor of electrophysiological processes in Caenorhabditis elegans |
Q34567223 | GLD-3 and control of the mitosis/meiosis decision in the germline of Caenorhabditis elegans |
Q27313226 | GLD-4-mediated translational activation regulates the size of the proliferative germ cell pool in the adult C. elegans germ line |
Q34664265 | GLOBIN-5-dependent O2 responses are regulated by PDL-1/PrBP that targets prenylated soluble guanylate cyclases to dendritic endings |
Q90504395 | GLP-1 Notch-LAG-1 CSL control of the germline stem cell fate is mediated by transcriptional targets lst-1 and sygl-1 |
Q39757548 | GLP-1 is localized to the mitotic region of the C. elegans germ line |
Q44628444 | GLR-1, a Non-NMDA Glutamate Receptor Homolog, Is Critical for Long-Term Memory inCaenorhabditis elegans |
Q33450594 | GLS-1, a novel P granule component, modulates a network of conserved RNA regulators to influence germ cell fate decisions |
Q30397156 | GMP Synthase Is Required for Virulence Factor Production and Infection by Cryptococcus neoformans. |
Q37152694 | GPC-1, a G protein gamma-subunit, regulates olfactory adaptation in Caenorhabditis elegans |
Q30510175 | GPI-anchor synthesis is indispensable for the germline development of the nematode Caenorhabditis elegans |
Q52716637 | GSK-3 promotes S phase entry and progression in C. elegans germline stem cells to maintain tissue output. |
Q39768366 | GTPase-mediated regulation of the unfolded protein response in Caenorhabditis elegans is dependent on the AAA+ ATPase CDC-48. |
Q57682999 | GTSF-1 is required for formation of a functional RNA-dependent RNA Polymerase complex in |
Q46284217 | Gain and Loss of Small RNA Classes-Characterization of Small RNAs in the Parasitic Nematode Family Strongyloididae |
Q28554020 | Gain-of-Function Alleles in Caenorhabditis elegans Nuclear Hormone Receptor nhr-49 Are Functionally Distinct |
Q34604972 | Gain-of-function mutations in the Caenorhabditis elegans lin-1 ETS gene identify a C-terminal regulatory domain phosphorylated by ERK MAP kinase |
Q33952677 | Gain-of-function mutations of fem-3, a sex-determination gene in Caenorhabditis elegans. |
Q30506498 | Gait Modulation in C. elegans: An Integrated Neuromechanical Model |
Q36217186 | Galactosylated fucose epitopes in nematodes: increased expression in a Caenorhabditis mutant associated with altered lectin sensitivity and occurrence in parasitic species. |
Q41864006 | Gamete-type dependent crossover interference levels in a defined region of Caenorhabditis elegans chromosome V. |
Q35626048 | Gap junctions synchronize action potentials and Ca2+ transients in Caenorhabditis elegans body wall muscle |
Q64883552 | Gastrodin protects dopaminergic neurons via insulin-like pathway in a Parkinson's disease model. |
Q28364603 | Gebiss: an ImageJ plugin for the specification of ground truth and the performance evaluation of 3D segmentation algorithms |
Q37102632 | Gem-1 encodes an SLC16 monocarboxylate transporter-related protein that functions in parallel to the gon-2 TRPM channel during gonad development in Caenorhabditis elegans |
Q24811105 | Gene CATCHR--gene cloning and tagging for Caenorhabditis elegans using yeast homologous recombination: a novel approach for the analysis of gene expression |
Q38812334 | Gene Function Prediction Based on Developmental Transcriptomes of the Two Sexes in C. elegans |
Q34050110 | Gene and information diversity in eukaryotes |
Q35435842 | Gene expression changes of Caenorhabditis elegans larvae during molting and sleep-like lethargus |
Q30487296 | Gene expression profiling to characterize sediment toxicity--a pilot study using Caenorhabditis elegans whole genome microarrays |
Q41170255 | Gene expression profiling to investigate tyrosol-induced lifespan extension in Caenorhabditis elegans. |
Q42909680 | Gene interactions in Caenorhabditis elegans define DPY-31 as a candidate procollagen C-proteinase and SQT-3/ROL-4 as its predicted major target |
Q90006461 | Gene silencing by double-stranded RNA from C. elegans neurons reveals functional mosaicism of RNA interference |
Q34364918 | Gene silencing in Caenorhabditis elegans by transitive RNA interference. |
Q54987165 | Gene-by-environment interactions that disrupt mitochondrial homeostasis cause neurodegeneration in C. elegans Parkinson's models. |
Q46020206 | Gene-diet interactions and aging in C. elegans. |
Q28750043 | Gene-environment interactions: neurodegeneration in non-mammals and mammals |
Q33391345 | Generation of stable transgenic C. elegans using microinjection |
Q55249839 | Genes Activated by Vibrio cholerae upon Exposure to Caenorhabditis elegans Reveal the Mannose-Sensitive Hemagglutinin To Be Essential for Colonization. |
Q33967917 | Genes affecting sensitivity to serotonin in Caenorhabditis elegans |
Q28362102 | Genes affecting the activity of nicotinic receptors involved in Caenorhabditis elegans egg-laying behavior |
Q36233694 | Genes critical for muscle development and function in Caenorhabditis elegans identified through lethal mutations |
Q36076987 | Genes down-regulated in spaceflight are involved in the control of longevity in Caenorhabditis elegans |
Q35847224 | Genes misregulated in C. elegans deficient in Dicer, RDE-4, or RDE-1 are enriched for innate immunity genes |
Q42468230 | Genes necessary for directed axonal elongation or fasciculation in C. elegans |
Q34612379 | Genes regulating touch cell development in Caenorhabditis elegans |
Q33895380 | Genes required for cellular UNC-6/netrin localization in Caenorhabditis elegans |
Q35641438 | Genes required for osmoregulation and apical secretion in Caenorhabditis elegans |
Q41351916 | Genes required for the functions of olfactory AWA neuron regulate the longevity of Caenorhabditis elegans in an insulin/IGF signaling-dependent fashion |
Q27329083 | Genes that act downstream of sensory neurons to influence longevity, dauer formation, and pathogen responses in Caenorhabditis elegans |
Q37737117 | Genes that can be mutated to unmask hidden antigenic determinants in the cuticle of the nematode Caenorhabditis elegans |
Q33834489 | Genes that control a temperature-compensated ultradian clock in Caenorhabditis elegans |
Q34898543 | Genes that control ray sensory neuron axon development in the Caenorhabditis elegans male |
Q33955016 | Genes that implement the hermaphrodite mode of dosage compensation in Caenorhabditis elegans |
Q48078919 | Genesis of an organ: molecular analysis of the pha-1 gene |
Q49791485 | Genetic Identification of Separase Regulators in Caenorhabditis elegans. |
Q33993325 | Genetic Organization in CAENORHABDITIS ELEGANS: Fine-Structure Analysis of the unc-22 Gene |
Q36444015 | Genetic Screen Reveals Link between the Maternal Effect Sterile Gene mes-1 and Pseudomonas aeruginosa-induced Neurodegeneration in Caenorhabditis elegans |
Q48684202 | Genetic Screen for Postembryonic Development in the Zebrafish (Danio rerio): Dominant Mutations Affecting Adult Form. |
Q92856688 | Genetic Silencing of Fatty Acid Desaturases Modulates α-Synuclein Toxicity and Neuronal Loss in Parkinson-Like Models of C. elegans |
Q68081116 | Genetic analysis and complementation by germ-line transformation of lethal mutations in the unc-22 IV region of Caenorhabditis elegans |
Q34616853 | Genetic analysis of Caenorhabditis elegans glp-1 mutants suggests receptor interaction or competition. |
Q93389616 | Genetic analysis of KillerRed in C. elegans identifies a shared role of calcium genes in ROS-mediated neurodegeneration |
Q33958694 | Genetic analysis of a major segment [LGV(left)] of the genome of Caenorhabditis elegans |
Q27312277 | Genetic analysis of a novel tubulin mutation that redirects synaptic vesicle targeting and causes neurite degeneration in C. elegans |
Q33953502 | Genetic analysis of adult-specific surface antigenic differences between varieties of the nematode Caenorhabditis elegans |
Q30485789 | Genetic analysis of crawling and swimming locomotory patterns in C. elegans |
Q36083331 | Genetic analysis of dauer formation in Caenorhabditis briggsae |
Q42961553 | Genetic analysis of defecation in Caenorhabditis elegans |
Q34613365 | Genetic analysis of endocytosis in Caenorhabditis elegans: coelomocyte uptake defective mutants |
Q36508693 | Genetic analysis of hyl-1, the C. elegans homolog of LAG1/LASS1. |
Q36318911 | Genetic analysis of life-span in Caenorhabditis elegans |
Q33877064 | Genetic analysis of lysosomal trafficking in Caenorhabditis elegans |
Q44536512 | Genetic analysis of ryanodine receptor function in Caenorhabditis elegans based on unc-68 revertants |
Q42961395 | Genetic analysis of temperature-sensitive lethal mutants of Salmonella typhimurium. |
Q36571751 | Genetic analysis of the Caenorhabditis elegans GLH family of P-granule proteins |
Q34605401 | Genetic analysis of the Caenorhabditis elegans MAP kinase gene mpk-1 |
Q34569532 | Genetic analysis of the Caenorhabditis elegans pax-6 locus: roles of paired domain-containing and nonpaired domain-containing isoforms |
Q33967910 | Genetic analysis of the roles of daf-28 and age-1 in regulating Caenorhabditis elegans dauer formation |
Q34140720 | Genetic analysis of tissue aging in Caenorhabditis elegans: a role for heat-shock factor and bacterial proliferation. |
Q33994370 | Genetic and Phenotypic Characterization of Roller Mutants of CAENORHABDITIS ELEGANS. |
Q30979942 | Genetic and cellular basis for acetylcholine inhibition of Caenorhabditis elegans egg-laying behavior. |
Q27324772 | Genetic and cellular characterization of Caenorhabditis elegans mutants abnormal in the regulation of many phase II enzymes |
Q47069371 | Genetic and cytological characterization of the recombination protein RAD-51 in Caenorhabditis elegans |
Q44605161 | Genetic and fine structure analysis of unc-26(IV) and adjacent regions in Caenorhabditis elegans |
Q24300674 | Genetic and functional characterization of putative Ras/Raf interaction inhibitors in C. elegans and mammalian cells |
Q36222360 | Genetic and molecular analysis of a Caenorhabditis elegans beta-tubulin that conveys benzimidazole sensitivity |
Q33967305 | Genetic and molecular analysis of spe-27, a gene required for spermiogenesis in Caenorhabditis elegans hermaphrodites |
Q44958129 | Genetic and molecular analysis of thedpy-14 region inCaenorhabditis elegans |
Q33961157 | Genetic and molecular characterization of the Caenorhabditis elegans spermatogenesis-defective gene spe-17 |
Q34605410 | Genetic and molecular characterization of the caenorhabditis elegans gene, mel-26, a postmeiotic negative regulator of mei-1, a meiotic-specific spindle component. |
Q33274205 | Genetic and pharmacological factors that influence reproductive aging in nematodes |
Q33961866 | Genetic and phenotypic studies of hypomorphic lin-12 mutants in Caenorhabditis elegans. |
Q33863714 | Genetic aspects of behavioral neurotoxicology |
Q64068812 | Genetic background modifies phenotypic and transcriptional responses in a C. elegans model of α-synuclein toxicity |
Q34482397 | Genetic characterization of smg-8 mutants reveals no role in C. elegans nonsense mediated decay |
Q33589613 | Genetic control of programmed cell death during animal development |
Q42874188 | Genetic control of temperature preference in the nematode Caenorhabditis elegans |
Q36451316 | Genetic control of vulval development in Caenorhabditis briggsae |
Q41518068 | Genetic deficiency in neuronal peroxisomal fatty acid β-oxidation causes the interruption of dauer development in Caenorhabditis elegans |
Q35830599 | Genetic differences affecting the potency of stereoisomers of halothane |
Q52536430 | Genetic disorders of vision revealed by a behavioral screen of 400 essential loci in zebrafish. |
Q37301677 | Genetic diversity and multihost pathogenicity of clinical and environmental strains of Burkholderia cenocepacia |
Q91800268 | Genetic diversity of laboratory strains and implications for research: The case of Aedes aegypti |
Q36233389 | Genetic identification, sequence, and alternative splicing of the Caenorhabditis elegans alpha 2(IV) collagen gene |
Q30504220 | Genetic interaction between Caenorhabditis elegans teneurin ten-1 and prolyl 4-hydroxylase phy-1 and their function in collagen IV-mediated basement membrane integrity during late elongation of the embryo |
Q37531590 | Genetic interactions affecting touch sensitivity in Caenorhabditis elegans |
Q36439791 | Genetic interactions between UNC-17/VAChT and a novel transmembrane protein in Caenorhabditis elegans |
Q24815740 | Genetic interactions due to constitutive and inducible gene regulation mediated by the unfolded protein response in C. elegans. |
Q34617005 | Genetic loci modulating fitness and life span in Caenorhabditis elegans: categorical trait interval mapping in CL2a x Bergerac-BO recombinant-inbred worms. |
Q99556544 | Genetic modifiers ameliorate endocytic and neuromuscular defects in a model of spinal muscular atrophy |
Q22337102 | Genetic neuroscience of mammalian learning and memory |
Q42975112 | Genetic organization of the region around UNC-15 (I), a gene affecting paramyosin in Caenorhabditis elegans |
Q45069728 | Genetic organization of the unc-22 IV gene and the adjacent region in Caenorhabditis elegans |
Q33953669 | Genetic organization of the unc-60 region in Caenorhabditis elegans |
Q51501534 | Genetic revelation of hexavalent chromium toxicity using Caenorhabditis elegans as a biosensor. |
Q35945665 | Genetic screens for Caenorhabditis elegans mutants defective in left/right asymmetric neuronal fate specification |
Q33960812 | Genetic studies of mei-1 gene activity during the transition from meiosis to mitosis in Caenorhabditis elegans |
Q36083335 | Genetic suppressors of Caenorhabditis elegans pha-4/FoxA identify the predicted AAA helicase ruvb-1/RuvB. |
Q21133806 | Genetically encoded green fluorescent Ca2+ indicators with improved detectability for neuronal Ca2+ signals |
Q36055162 | Genetically separable functions of the MEC-17 tubulin acetyltransferase affect microtubule organization |
Q36719346 | Genetically targeted cell disruption in Caenorhabditis elegans |
Q44683896 | Genetics and Molecular Ethology |
Q36677071 | Genetics of Lipid-Storage Management in Caenorhabditis elegans Embryos |
Q34285676 | Genetics of extracellular matrix remodeling during organ growth using the Caenorhabditis elegans pharynx model |
Q34865200 | Genistein from Vigna angularis Extends Lifespan in Caenorhabditis elegans |
Q26765465 | Genome Editing in C. elegans and Other Nematode Species |
Q33830936 | Genome analysis of Diploscapter coronatus: insights into molecular peculiarities of a nematode with parthenogenetic reproduction |
Q94572519 | Genome editing in the nematode Caenorhabditis briggsae using the CRISPR/Cas9 system |
Q38566890 | Genome integrity is regulated by the Caenorhabditis elegans Rad51D homolog rfs-1 |
Q91958990 | Genome wide analysis reveals heparan sulfate epimerase modulates TDP-43 proteinopathy |
Q36440362 | Genome-Wide Mutational Signature of the Chemotherapeutic Agent Mitomycin C in Caenorhabditis elegans |
Q36310528 | Genome-Wide RNAi Longevity Screens in Caenorhabditis elegans |
Q41385120 | Genome-Wide Screen for Genes Involved in Caenorhabditis elegans Developmentally Timed Sleep |
Q48310744 | Genome-Wide Temporal Expression Profiling in Caenorhabditis elegans Identifies a Core Gene Set Related to Long-Term Memory. |
Q36995333 | Genome-scale spatiotemporal analysis of Caenorhabditis elegans microRNA promoter activity |
Q37016726 | Genome-wide RNAi screen and in vivo protein aggregation reporters identify degradation of damaged proteins as an essential hypertonic stress response |
Q34548324 | Genome-wide analysis of alternative splicing in Caenorhabditis elegans |
Q34591276 | Genome-wide analysis of developmental and sex-regulated gene expression profiles in Caenorhabditis elegans |
Q41886391 | Genome-wide analysis of germ cell proliferation in C.elegans identifies VRK-1 as a key regulator of CEP-1/p53 |
Q28493168 | Genome-wide identification of Pseudomonas aeruginosa virulence-related genes using a Caenorhabditis elegans infection model |
Q36643300 | Genome-wide investigation reveals pathogen-specific and shared signatures in the response of Caenorhabditis elegans to infection |
Q27333095 | Genome-wide microarrray analysis reveals roles for the REF-1 family member HLH-29 in ferritin synthesis and peroxide stress response |
Q34161650 | Genome-wide screening identifies new genes required for stress-induced phase 2 detoxification gene expression in animals. |
Q55446420 | Genome-wide surveys reveal polarity and cytoskeletal regulators mediate LKB1-associated germline stem cell quiescence. |
Q38947969 | Genomewide Association Study of Alcohol Dependence Identifies Risk Loci Altering Ethanol-Response Behaviors in Model Organisms |
Q36166054 | Genomic Scars Generated by Polymerase Theta Reveal the Versatile Mechanism of Alternative End-Joining. |
Q41910269 | Genomic clusters, putative pathogen recognition molecules, and antimicrobial genes are induced by infection of C. elegans with M. nematophilum |
Q59793212 | Genomic identification and functional analysis of essential genes in Caenorhabditis elegans |
Q36382116 | Genomic organization, expression, and analysis of the troponin C gene pat-10 of Caenorhabditis elegans |
Q33533671 | Genomic sequence of a mutant strain of Caenorhabditis elegans with an altered recombination pattern |
Q38930532 | Germ Granules Prevent Accumulation of Somatic Transcripts in the Adult Caenorhabditis elegans Germline |
Q30806560 | Germ-line induction of the Caenorhabditis elegans vulva |
Q90044018 | Germline Maintenance Through the Multifaceted Activities of GLH/Vasa in Caenorhabditis elegans P Granules |
Q36461799 | Germline quality control: eEF2K stands guard to eliminate defective oocytes |
Q37484417 | Germline transformation of Caenorhabditis elegans by injection |
Q35540672 | Giardia duodenalis-induced alterations of commensal bacteria kill Caenorhabditis elegans: a new model to study microbial-microbial interactions in the gut. |
Q34632733 | Glia delimit shape changes of sensory neuron receptive endings in C. elegans |
Q47897846 | Glia initiate brain assembly through noncanonical Chimaerin-Furin axon guidance in C. elegans |
Q35772934 | Glial Expression of the Caenorhabditis elegans Gene swip-10 Supports Glutamate Dependent Control of Extrasynaptic Dopamine Signaling |
Q35245310 | Glial development and function in the nervous system of Caenorhabditis elegans |
Q52339397 | Glial loss of the metallo β-lactamase domain containing protein, SWIP-10, induces age- and glutamate-signaling dependent, dopamine neuron degeneration. |
Q64890665 | Global Proteomic Response of Caenorhabditis elegans Against PemKSa Toxin. |
Q47102107 | Global accumulation of circRNAs during aging in Caenorhabditis elegans |
Q34332382 | Global characterization of the oocyte-to-embryo transition in Caenorhabditis elegans uncovers a novel mRNA clearance mechanism |
Q33797064 | Global effects of the CSR-1 RNA interference pathway on the transcriptional landscape |
Q27312103 | Global functional analyses of cellular responses to pore-forming toxins |
Q43187683 | Global microRNA expression profiling of Caenorhabditis elegans Parkinson's disease models |
Q35669096 | Global transcriptional analysis of Burkholderia pseudomallei high and low biofilm producers reveals insights into biofilm production and virulence |
Q41686906 | Global transcriptional changes caused by an EDMD mutation correlate to tissue specific disease phenotypes in C. elegans |
Q64121194 | Global transcriptional regulation of innate immunity by ATF-7 in C. elegans |
Q27346465 | Glucose induces sensitivity to oxygen deprivation and modulates insulin/IGF-1 signaling and lipid biosynthesis in Caenorhabditis elegans. |
Q64123102 | Glycine promotes longevity in Caenorhabditis elegans in a methionine cycle-dependent fashion |
Q30664220 | Glycogen Fuels Survival During Hyposmotic-Anoxic Stress in Caenorhabditis elegans |
Q33827055 | Glycogen controls Caenorhabditis elegans lifespan and resistance to oxidative stress |
Q27311382 | Glycosyl phosphatidylinositol anchor biosynthesis is essential for maintaining epithelial integrity during Caenorhabditis elegans embryogenesis |
Q34477569 | Glycosylation genes expressed in seam cells determine complex surface properties and bacterial adhesion to the cuticle of Caenorhabditis elegans |
Q35684351 | Glypican Is a Modulator of Netrin-Mediated Axon Guidance |
Q36436710 | Goalpha and diacylglycerol kinase negatively regulate the Gqalpha pathway in C. elegans |
Q34304718 | Goalpha regulates olfactory adaptation by antagonizing Gqalpha-DAG signaling in Caenorhabditis elegans |
Q28366737 | Goalpha regulates volatile anesthetic action in Caenorhabditis elegans |
Q70941967 | Gonadal cell lineages of the nematode Panagrellus redivivus and implications for evolution by the modification of cell lineage |
Q83226132 | Gradient-independent Wnt signaling instructs asymmetric neurite pruning in |
Q42327805 | Graphene Oxide Dysregulates Neuroligin/NLG-1-Mediated Molecular Signaling in Interneurons in Caenorhabditis elegans |
Q36083338 | Gravity force transduced by the MEC-4/MEC-10 DEG/ENaC channel modulates DAF-16/FoxO activity in Caenorhabditis elegans |
Q36334971 | Green Tea Extract Induces the Resistance of Caenorhabditis elegans against Oxidative Stress |
Q92325083 | Green kiwifruit extracts protect motor neurons from death in a spinal muscular atrophy model in Caenorhabditis elegans |
Q51674520 | Group effect in the free-living soil nematode Caenorhabditis elegans exposed to a high ambient temperature. |
Q49972342 | Growth of Caenorhabditis elegans in Defined Media Is Dependent on Presence of Particulate Matter. |
Q43169530 | Guarana (Paullinia cupana Mart.) attenuates methylmercury-induced toxicity in Caenorhabditis elegans |
Q26851850 | Guidance cue netrin-1 and the regulation of inflammation in acute and chronic kidney disease |
Q36560437 | Guidelines on nicotine dose selection for in vivo research. |
Q34341975 | Gαo and Gαq regulate the expression of daf-7, a TGFβ-like gene, in Caenorhabditis elegans |
Q36970729 | H-NS plays a role in expression of Acinetobacter baumannii virulence features. |
Q36676559 | H3K23me2 is a new heterochromatic mark in Caenorhabditis elegans |
Q28477443 | H3K9me2/3 binding of the MBT domain protein LIN-61 is essential for Caenorhabditis elegans vulva development |
Q64092600 | H3K9me3 is required for inheritance of small RNAs that target a unique subset of newly evolved genes |
Q27332118 | HAL-2 promotes homologous pairing during Caenorhabditis elegans meiosis by antagonizing inhibitory effects of synaptonemal complex precursors |
Q41872653 | HAT activity is essential for CBP-1-dependent transcription and differentiation in Caenorhabditis elegans |
Q28611296 | HCP-1, a protein involved in chromosome segregation, is localized to the centromere of mitotic chromosomes in Caenorhabditis elegans |
Q36383113 | HES-Mediated Repression of Pten in Caenorhabditis elegans. |
Q90248594 | HIF-1 Has a Central Role in Caenorhabditis elegans Organismal Response to Selenium |
Q34043275 | HIF-1 and SKN-1 coordinate the transcriptional response to hydrogen sulfide in Caenorhabditis elegans. |
Q35893950 | HIF-1 antagonizes p53-mediated apoptosis through a secreted neuronal tyrosinase |
Q27312348 | HIF-1 modulates dietary restriction-mediated lifespan extension via IRE-1 in Caenorhabditis elegans |
Q38652079 | HIF-1-dependent regulation of lifespan in Caenorhabditis elegans by the acyl-CoA-binding protein MAA-1. |
Q35619440 | HIM-8 binds to the X chromosome pairing center and mediates chromosome-specific meiotic synapsis |
Q37233422 | HIS-24 linker histone and SIR-2.1 deacetylase induce H3K27me3 in the Caenorhabditis elegans germ line |
Q41351670 | HLB-1 functions as a new regulator for the organization and function of neuromuscular junctions in nematode Caenorhabditis elegans |
Q30528663 | HLH-29 regulates ovulation in C. elegans by targeting genes in the inositol triphosphate signaling pathway |
Q37664475 | HLH-30/TFEB-mediated autophagy functions in a cell-autonomous manner for epithelium intrinsic cellular defense against bacterial pore-forming toxin in C. elegans |
Q50024988 | HMP-1/α-catenin promotes junctional mechanical integrity during morphogenesis. |
Q48115090 | HOP-1 Presenilin Deficiency Causes a Late-Onset Notch Signaling Phenotype That Affects Adult Germline Function in Caenorhabditis elegans |
Q36643459 | HOP-1, a Caenorhabditis elegans presenilin, appears to be functionally redundant with SEL-12 presenilin and to facilitate LIN-12 and GLP-1 signaling |
Q90482820 | HRPK-1, a conserved KH-domain protein, modulates microRNA activity during Caenorhabditis elegans development |
Q36768058 | HSF-1 activates the ubiquitin proteasome system to promote non-apoptotic developmental cell death in C. elegans. |
Q41512665 | HSF-1 is a regulator of miRNA expression in Caenorhabditis elegans |
Q35494028 | HSF-1-mediated cytoskeletal integrity determines thermotolerance and life span |
Q33522212 | HSF1-controlled and age-associated chaperone capacity in neurons and muscle cells of C. elegans. |
Q58416239 | HSP-4 endoplasmic reticulum (ER) stress pathway is not activated in a C. elegans model of ethanol intoxication and withdrawal |
Q64056478 | HSP-4/BiP expression in secretory cells is regulated by a developmental program and not by the unfolded protein response |
Q42158356 | HSP43, a small heat-shock protein localized to specific cells of the vulva and spermatheca in the nematode Caenorhabditis elegans |
Q39705533 | HTP-1 coordinates synaptonemal complex assembly with homolog alignment during meiosis in C. elegans |
Q39705513 | HTP-1-dependent constraints coordinate homolog pairing and synapsis and promote chiasma formation during C. elegans meiosis |
Q57788510 | Haematophagic Caenorhabditis elegans |
Q28821267 | HandKAchip - Hands-free killing assay on a chip |
Q37008327 | Handed Asymmetry, Handedness Reversal and Mechanisms of Cell Fate Determination in Nematode Embryos |
Q27329000 | Handedness of a motor program in C. elegans is independent of left-right body asymmetry |
Q64975701 | Harmine suppresses hyper-activated Ras-MAPK pathway by selectively targeting oncogenic mutated Ras/Raf in Caenorhabditis elegans. |
Q64105761 | Hazard potential of perovskite solar cell technology for potential implementation of "safe-by-design" approach |
Q35060018 | Heat avoidance is regulated by transient receptor potential (TRP) channels and a neuropeptide signaling pathway in Caenorhabditis elegans |
Q36217330 | Heat shock and caloric restriction have a synergistic effect on the heat shock response in a sir2.1-dependent manner in Caenorhabditis elegans |
Q64068138 | Heat shock in C. elegans induces downstream of gene transcription and accumulation of double-stranded RNA |
Q35016513 | Heat-shock transcription factor (HSF)-1 pathway required for Caenorhabditis elegans immunity |
Q33817351 | Heparan 2-O-sulfotransferase, hst-2, is essential for normal cell migration in Caenorhabditis elegans. |
Q48340369 | Hepta-Mutant Staphylococcus aureus Sortase A (SrtA7m) as a Tool for in Vivo Protein Labeling in Caenorhabditis elegans. |
Q30486648 | Hereditary spastic paraplegia-associated mutations in the NIPA1 gene and its Caenorhabditis elegans homolog trigger neural degeneration in vitro and in vivo through a gain-of-function mechanism |
Q33872903 | Heritable determinants of male fertilization success in the nematode Caenorhabditis elegans |
Q24601099 | Heritable genome editing in C. elegans via a CRISPR-Cas9 system |
Q64104459 | Heterodimerization of UNC-13/RIM regulates synaptic vesicle release probability but not priming in |
Q39951588 | Heterologous expression in Caenorhabditis elegans as an alternative approach to functional studies in Schistosoma mansoni |
Q28821634 | Heterotaxy in Caenorhabditis: widespread natural variation in left-right arrangement of the major organs |
Q30480572 | Heterotrimeric G protein signaling functions with dynein to promote spindle positioning in C. elegans |
Q34589816 | Heterozygous insertions alter crossover distribution but allow crossover interference in Caenorhabditis elegans |
Q37566924 | Hierarchical assembly of presynaptic components in defined C. elegans synapses |
Q34948860 | High concentration of vitamin E decreases thermosensation and thermotaxis learning and the underlying mechanisms in the nematode Caenorhabditis elegans |
Q24797167 | High copy arrays containing a sequence upstream of mec-3 alter cell migration and axonal morphology in C. elegans |
Q25257076 | High incidence of rapid telomere loss in telomerase-deficient Caenorhabditis elegans |
Q41121841 | High lumenal chloride in the lysosome is critical for lysosome function |
Q34090167 | High molecular weight proteins in the nematode C. elegans bind [3H]ryanodine and form a large conductance channel |
Q37152703 | High nucleotide divergence in developmental regulatory genes contrasts with the structural elements of olfactory pathways in caenorhabditis |
Q41864064 | High resolution transcriptome maps for wild-type and nonsense-mediated decay-defective Caenorhabditis elegans |
Q50094597 | High-Content Microfluidic Screening Platform Used To Identify σ2R/Tmem97 Binding Ligands that Reduce Age-Dependent Neurodegeneration in C. elegans SC_APP Model. |
Q27300484 | High-Throughput All-Optical Analysis of Synaptic Transmission and Synaptic Vesicle Recycling in Caenorhabditis elegans |
Q36245801 | High-Throughput Cloning of Temperature-Sensitive Caenorhabditis elegans Mutants with Adult Syncytial Germline Membrane Architecture Defects |
Q30503329 | High-content behavioral analysis of Caenorhabditis elegans in precise spatiotemporal chemical environments |
Q70190248 | High-frequency excision of transposable element Tc1 in the nematode caenorhabditis elegans is limited to somatic cells |
Q92043665 | High-glucose diets induce mitochondrial dysfunction in Caenorhabditis elegans |
Q83578246 | High-resolution array comparative genomic hybridization analysis reveals unanticipated complexity of genetic deficiencies on chromosome V in Caenorhabditis elegans |
Q42515321 | High-resolution imaging of muscle attachment structures in Caenorhabditis elegans |
Q35756354 | High-resolution multi-photon imaging of morphological structures of caenorhabditis elegans |
Q43038142 | High-resolution temporal analysis reveals a functional timeline for the molecular regulation of cytokinesis. |
Q36631791 | High-throughput and quantitative approaches for measuring circadian rhythms in cyanobacteria using bioluminescence |
Q95818134 | High-throughput capturing and characterization of mutations in essential genes of Caenorhabditis elegans |
Q37621368 | High-throughput expression of C. elegans proteins. |
Q28817960 | High-throughput fluorescence-based isolation of live C. elegans larvae |
Q37318110 | High-throughput imaging of neuronal activity in Caenorhabditis elegans |
Q27334278 | High-throughput in vivo analysis of gene expression in Caenorhabditis elegans |
Q33358028 | High-throughput isolation and mapping of C. elegans mutants susceptible to pathogen infection |
Q34661540 | High-throughput optical quantification of mechanosensory habituation reveals neurons encoding memory in Caenorhabditis elegans |
Q36041627 | High-throughput screening in the C. elegans nervous system |
Q39682609 | High-throughput selection of retrovirus producer cell lines leads to markedly improved efficiency of germ line-transmissible insertions in zebra fish |
Q27334639 | High-throughput, motility-based sorter for microswimmers such as C. elegans |
Q36471335 | Highly Ca2+-selective TRPM channels regulate IP3-dependent oscillatory Ca2+ signaling in the C. elegans intestine |
Q89165861 | Highly efficient RNAi and Cas9-based auto-cloning systems for C. elegans research |
Q40447547 | Highly sensitive isotope-dilution liquid-chromatography-electrospray ionization-tandem-mass spectrometry approach to study the drug-mediated modulation of dopamine and serotonin levels in Caenorhabditis elegans. |
Q27341911 | Histidine protects against zinc and nickel toxicity in Caenorhabditis elegans |
Q27315564 | Histone H3.3 variant dynamics in the germline of Caenorhabditis elegans |
Q64082426 | Histone acetylation promotes long-lasting defense responses and longevity following early life heat stress |
Q27318351 | Histone methylation restrains the expression of subtype-specific genes during terminal neuronal differentiation in Caenorhabditis elegans |
Q33506876 | Homeobox containing genes in the nematode Caenorhabditis elegans |
Q34753563 | Homeostasis in C. elegans sleep is characterized by two behaviorally and genetically distinct mechanisms |
Q64904517 | Homeostatic Feedback Modulates the Development of Two-State Patterned Activity in a Model Serotonin Motor Circuit in Caenorhabditis elegans. |
Q40642162 | Homologous and unique G protein alpha subunits in the nematode Caenorhabditis elegans |
Q34895210 | Homologous recombination is required for genome stability in the absence of DOG-1 in Caenorhabditis elegans |
Q34607526 | Homologs of the Caenorhabditis elegans masculinizing gene her-1 in C. briggsae and the filarial parasite Brugia malayi. |
Q34159059 | Hormetic effect of methylmercury on Caenorhabditis elegans |
Q37651955 | Hormetic heat stress and HSF-1 induce autophagy to improve survival and proteostasis in C. elegans |
Q42241073 | Horvitz and Sulston on Caenorhabditis elegans Cell Lineage Mutants |
Q40174267 | Host cell factor 1 inhibits SKN-1 to modulate oxidative stress responses in Caenorhabditis elegans. |
Q38663589 | Host seeking parasitic nematodes use specific odors to assess host resources. |
Q42132873 | Host translational inhibition by Pseudomonas aeruginosa Exotoxin A Triggers an immune response in Caenorhabditis elegans |
Q51604503 | Host-finding behaviour in the nematode Pristionchus pacificus. |
Q33740873 | How Can We Understand the Genomic Basis of Nematode Parasitism? |
Q90381680 | How Weird is The Worm? Evolution of the Developmental Gene Toolkit in Caenorhabditis elegans |
Q37584846 | How voltage-gated calcium channels gate forms of homeostatic synaptic plasticity |
Q43185602 | Hox Genes Promote Neuronal Subtype Diversification through Posterior Induction in Caenorhabditis elegans |
Q41891353 | Hox Proteins Act as Transcriptional Guarantors to Ensure Terminal Differentiation |
Q35221460 | Hox and a newly identified E2F co-repress cell death in Caenorhabditis elegans |
Q27321279 | Hsp72 (HSPA1A) Prevents Human Islet Amyloid Polypeptide Aggregation and Toxicity: A New Approach for Type 2 Diabetes Treatment |
Q59792755 | Hsp90 Stabilizes SIRT1 Orthologs in Mammalian Cells and |
Q90202329 | Human brain development through the lens of cerebral organoid models |
Q89940643 | Human insulin modulates α-synuclein aggregation via DAF-2/DAF-16 signalling pathway by antagonising DAF-2 receptor in C. elegans model of Parkinson's disease |
Q97418936 | Human organoids: model systems for human biology and medicine |
Q30580304 | Humidity sensation requires both mechanosensory and thermosensory pathways in Caenorhabditis elegans |
Q92006491 | Hybridization promotes asexual reproduction in Caenorhabditis nematodes |
Q30502777 | Hydrodynamic property of the cytoplasm is sufficient to mediate cytoplasmic streaming in the Caenorhabditis elegans embryo |
Q50881619 | Hydrogen peroxide produced by superoxide dismutase SOD-2 activates sperm in Caenorhabditis elegans. |
Q40470026 | Hydrogen peroxide-mediated killing of Caenorhabditis elegans: a common feature of different streptococcal species. |
Q30492639 | Hydrogen sulfide increases hypoxia-inducible factor-1 activity independently of von Hippel-Lindau tumor suppressor-1 in C. elegans |
Q36300148 | Hydrogen sulfide increases thermotolerance and lifespan in Caenorhabditis elegans. |
Q55176673 | Hydrolysis of aromatic β-glucosides by non-pathogenic bacteria confers a chemical weapon against predators. |
Q34568175 | Hydrophobic analogues of rhodamine B and rhodamine 101: potent fluorescent probes of mitochondria in living C. elegans |
Q36237556 | Hydrophobicity variations along the surface of the coiled-coil rod may mediate striated muscle myosin assembly in Caenorhabditis elegans |
Q34105144 | Hyperactive neuroendocrine secretion causes size, feeding, and metabolic defects of C. elegans Bardet-Biedl syndrome mutants |
Q38796581 | Hypergravity hinders axonal development of motor neurons in Caenorhabditis elegans. |
Q35216848 | Hypertonic stress induces rapid and widespread protein damage in C. elegans |
Q36393015 | Hypothesis-based RNAi screening identifies neuroprotective genes in a Parkinson's disease model |
Q36734774 | Hypoxia and the HIF-1 transcriptional pathway reorganize a neuronal circuit for oxygen-dependent behavior in Caenorhabditis elegans |
Q33518501 | Hypoxia and the hypoxic response pathway protect against pore-forming toxins in C. elegans |
Q41686894 | Hypoxia disrupts proteostasis in Caenorhabditis elegans |
Q36543700 | Hypoxia-inducible Factor-1 (HIF-1)-independent hypoxia response of the small heat shock protein hsp-16.1 gene regulated by chromatin-remodeling factors in the nematode Caenorhabditis elegans |
Q56535212 | Hypoxia-inducible factor cell non-autonomously regulates stress responses and behavior via a nuclear receptor |
Q47958364 | IGDB-2, an Ig/FNIII protein, binds the ion channel LGC-34 and controls sensory compartment morphogenesis in C. elegans. |
Q37490727 | INF2- and FHOD-related formins promote ovulation in the somatic gonad of C. elegans |
Q35918401 | IRI-1, a LIN-15B homologue, interacts with inositol-1,4,5-triphosphate receptors and regulates gonadogenesis, defecation, and pharyngeal pumping in Caenorhabditis elegans |
Q36530509 | IRK-1 potassium channels mediate peptidergic inhibition of Caenorhabditis elegans serotonin neurons via a G(o) signaling pathway |
Q37216556 | ITSN-1 controls vesicle recycling at the neuromuscular junction and functions in parallel with DAB-1. |
Q21090965 | Icariin and its derivative icariside II extend healthspan via insulin/IGF-1 pathway in C. elegans |
Q34627357 | Ida-1, the Caenorhabditis elegans orthologue of mammalian diabetes autoantigen IA-2, potentially acts as a common modulator between Parkinson's disease and Diabetes: role of Daf-2/Daf-16 insulin like signalling pathway |
Q42085414 | Identification and Characterization of Mitochondrial Subtypes in Caenorhabditis elegans via Analysis of Individual Mitochondria by Flow Cytometry |
Q28471839 | Identification and characterization of a dual-acting antinematodal agent against the pinewood nematode, Bursaphelenchus xylophilus |
Q34895771 | Identification and classification of genes that act antagonistically to let-60 Ras signaling in Caenorhabditis elegans vulval development |
Q33966197 | Identification and cloning of unc-119, a gene expressed in the Caenorhabditis elegans nervous system |
Q42918976 | Identification and comparative analysis of novel alternatively spliced transcripts of RhoGEF domain encoding gene in C. elegans and C. briggsae |
Q31112675 | Identification and functional characterization of the Caenorhabditis elegans riboflavin transporters rft-1 and rft-2 |
Q34042815 | Identification and functional clustering of genes regulating muscle protein degradation from amongst the known C. elegans muscle mutants |
Q56561565 | Identification and preliminary characterization of Hc-clec-160, a novel C-type lectin domain-containing gene of the strongylid nematode Haemonchus contortus |
Q27320213 | Identification of 526 conserved metazoan genetic innovations exposes a new role for cofactor E-like in neuronal microtubule homeostasis |
Q34454921 | Identification of Burkholderia cenocepacia strain H111 virulence factors using nonmammalian infection hosts. |
Q34602427 | Identification of Caenorhabditis elegans genes required for neuronal differentiation and migration |
Q27318073 | Identification of DVA interneuron regulatory sequences in Caenorhabditis elegans |
Q31026710 | Identification of HMG‐5 as a double‐stranded telomeric DNA‐binding protein in the nematode Caenorhabditis elegans |
Q24337575 | Identification of KIAA1018/FAN1, a DNA repair nuclease recruited to DNA damage by monoubiquitinated FANCD2 |
Q34539806 | Identification of Pseudomonas aeruginosa phenazines that kill Caenorhabditis elegans |
Q89984793 | Identification of Toxicity Effects of Cu2O Materials on C. elegans as a Function of Environmental Ionic Composition |
Q35602800 | Identification of a CREB-dependent serotonergic pathway and neuronal circuit regulating foraging behavior in Caenorhabditis elegans: a useful model for mental disorders and their treatments? |
Q33264967 | Identification of a gonadotropin-releasing hormone receptor orthologue in Caenorhabditis elegans |
Q70176503 | Identification of a large multigene family encoding the major sperm protein of Caenorhabditis elegans |
Q34828717 | Identification of a mariner-like repetitive sequence in C. elegans |
Q24319188 | Identification of a new class of protein kinases represented by eukaryotic elongation factor-2 kinase |
Q35917930 | Identification of a novel ADAMTS9/GON-1 function for protein transport from the ER to the Golgi |
Q34683242 | Identification of a peptide inhibitor of the RPM-1 · FSN-1 ubiquitin ligase complex |
Q27322992 | Identification of a tissue-selective heat shock response regulatory network |
Q37719263 | Identification of an RNA Polymerase III Regulator Linked to Disease-Associated Protein Aggregation |
Q55229208 | Identification of animal behavioral strategies by inverse reinforcement learning. |
Q28476138 | Identification of antifungal compounds active against Candida albicans using an improved high-throughput Caenorhabditis elegans assay |
Q90414665 | Identification of attractive odorants released by preferred bacterial food found in the natural habitats of C. elegans |
Q92350681 | Identification of avoidance genes through neural pathway-specific forward optogenetics |
Q36161305 | Identification of chemical synapses in the pharynx of Caenorhabditis elegans |
Q24796378 | Identification of ciliated sensory neuron-expressed genes in Caenorhabditis elegans using targeted pull-down of poly(A) tails |
Q30496476 | Identification of compounds with bioactivity against the nematode Caenorhabditis elegans by a screen based on the functional genomics of the marine bacterium Pseudoalteromonas tunicata D2. |
Q47068984 | Identification of critical domains and putative partners for the Caenorhabditis elegans spindle component LIN-5. |
Q30418939 | Identification of cross-linked peptides from complex samples. |
Q74606398 | Identification of domains of netrin UNC-6 that mediate attractive and repulsive guidance and responses from cells and growth cones |
Q30586121 | Identification of genes in toxicity pathways of trinucleotide-repeat RNA in C. elegans |
Q37213412 | Identification of genes interacting with rnt-1 through large-scale RNAi screening in Caenorhabditis elegans |
Q46437151 | Identification of genes involved in synaptogenesis using a fluorescent active zone marker in Caenorhabditis elegans. |
Q35055414 | Identification of genes involved in the ciliary trafficking of C. elegans PKD-2. |
Q41868332 | Identification of genes needed for regeneration, stem cell function, and tissue homeostasis by systematic gene perturbation in planaria |
Q34618128 | Identification of genes that regulate a left-right asymmetric neuronal migration in Caenorhabditis elegans |
Q33958810 | Identification of grandchildless loci whose products are required for normal germ-line development in the nematode Caenorhabditis elegans |
Q34588549 | Identification of guanylyl cyclases that function in thermosensory neurons of Caenorhabditis elegans |
Q34604855 | Identification of heterochronic mutants in Caenorhabditis elegans. Temporal misexpression of a collagen::green fluorescent protein fusion gene. |
Q55241384 | Identification of interneurons required for the aversive response of Caenorhabditis elegans to graphene oxide. |
Q37153296 | Identification of key structural elements for neuronal calcium sensor-1 function in the regulation of the temperature-dependency of locomotion in C. elegans |
Q27304753 | Identification of microtubule growth deceleration and its regulation by conserved and novel proteins. |
Q36724340 | Identification of mutations in Caenorhabditis elegans that cause resistance to high levels of dietary zinc and analysis using a genomewide map of single nucleotide polymorphisms scored by pyrosequencing |
Q35221546 | Identification of mutations that delay somatic or reproductive aging of Caenorhabditis elegans |
Q94526205 | Identification of neuroprotective compounds of caenorhabditis elegans dopaminergic neurons against 6-OHDA |
Q35145844 | Identification of nonviable genes affecting touch sensitivity in Caenorhabditis elegans using neuronally enhanced feeding RNA interference. |
Q24337043 | Identification of novel ATP13A2 interactors and their role in α-synuclein misfolding and toxicity |
Q33248011 | Identification of novel antimicrobials using a live-animal infection model |
Q30480412 | Identification of novel chondroitin proteoglycans in Caenorhabditis elegans: embryonic cell division depends on CPG-1 and CPG-2 |
Q50146341 | Identification of novel genes in the carotenogenic and oleaginous yeast Rhodotorula toruloides through genome-wide insertional mutagenesis. |
Q35678558 | Identification of novel genes involved in sarcopenia through RNAi screening in Caenorhabditis elegans |
Q49651475 | Identification of odor blend used by Caenorhabditis elegans for pathogen recognition. |
Q33387396 | Identification of phylogenetically conserved sequence motifs in microRNA 5' flanking sites from C. elegans and C. briggsae |
Q49886755 | Identification of piRNA Binding Sites Reveals the Argonaute Regulatory Landscape of the C. elegans Germline. |
Q50924822 | Identification of regulators of germ stem cell enwrapment by its niche in C. elegans. |
Q34645825 | Identification of residues of the Caenorhabditis elegans LIN-1 ETS domain that are necessary for DNA binding and regulation of vulval cell fates |
Q36436527 | Identification of store-independent and store-operated Ca2+ conductances in Caenorhabditis elegans intestinal epithelial cells |
Q37597371 | Identification of suppressors of mbk-2/DYRK by whole-genome sequencing |
Q42129610 | Identification of the AFD neuron as the site of action of the CREB protein in Caenorhabditis elegans thermotaxis |
Q33279455 | Identification of the C. elegans anaphase promoting complex subunit Cdc26 by phenotypic profiling and functional rescue in yeast |
Q34497400 | Identification of transcription start sites of trans-spliced genes: uncovering unusual operon arrangements |
Q36779966 | Identification of transforming growth factor-beta- regulated genes in caenorhabditis elegans by differential hybridization of arrayed cDNAs |
Q28504857 | Identification of tubulin deglutamylase among Caenorhabditis elegans and mammalian cytosolic carboxypeptidases (CCPs) |
Q30370969 | Identification of vacuoles containing extraintestinal differentiated forms of Legionella pneumophila in colonized Caenorhabditis elegans soil nematodes. |
Q36429779 | Identifying Regulators of Morphogenesis Common to Vertebrate Neural Tube Closure and Caenorhabditis elegans Gastrulation |
Q37168676 | IgCAMs redundantly control axon navigation in Caenorhabditis elegans |
Q34411943 | Ilex paraguariensis Extract Increases Lifespan and Protects Against the Toxic Effects Caused by Paraquat in Caenorhabditis elegans |
Q58699200 | Ilex paraguariensis modulates fat metabolism in Caenorhabditis elegans through purinergic system (ADOR-1) and nuclear hormone receptor (NHR-49) pathways |
Q64281653 | Illuminating Biological Interactions with in Vivo Protein Footprinting |
Q28743708 | Imaging C. elegans embryos using an epifluorescent microscope and open source software |
Q58774848 | Immobility in the sedentary plant-parasitic nematode H. glycines is associated with remodeling of neuromuscular tissue |
Q47384745 | Immobilization of Caenorhabditis elegans to Analyze Intracellular Transport in Neurons |
Q36217044 | Immunochemical localization of myosin heavy chain isoforms and paramyosin in developmentally and structurally diverse muscle cell types of the nematode Caenorhabditis elegans |
Q40964852 | Immunocytochemical localization of two myosins within the same muscle cells in caenorhabditis elegans |
Q36285245 | Immunofluorescence visualization of germ-line-specific cytoplasmic granules in embryos, larvae, and adults of Caenorhabditis elegans |
Q41444639 | Immunohistochemical analysis reveals variations in proteasome tissue expression in C. elegans |
Q40190651 | Impact of a Complex Food Microbiota on Energy Metabolism in the Model Organism Caenorhabditis elegans. |
Q33498516 | Impact of cigarette smoke exposure on innate immunity: a Caenorhabditis elegans model |
Q21133956 | Impact of sublethal levels of environmental pollutants found in sewage sludge on a novel Caenorhabditis elegans model biosensor |
Q37603263 | Impacts of chronic low-level nicotine exposure on Caenorhabditis elegans reproduction: identification of novel gene targets |
Q39697606 | Impaired Coenzyme A metabolism affects histone and tubulin acetylation in Drosophila and human cell models of pantothenate kinase associated neurodegeneration. |
Q30542646 | Impaired complex IV activity in response to loss of LRPPRC function can be compensated by mitochondrial hyperfusion |
Q37365425 | Impaired dense core vesicle maturation in Caenorhabditis elegans mutants lacking Rab2 |
Q42281165 | Impaired mitochondrial respiration promotes dendritic branching via the AMPK signaling pathway |
Q36978345 | Impaired resection of meiotic double-strand breaks channels repair to nonhomologous end joining in Caenorhabditis elegans |
Q36653181 | Imprecise excision of the Caenorhabditis elegans transposon Tc1 creates functional 5' splice sites |
Q34573453 | Imprinting capacity of gamete lineages in Caenorhabditis elegans |
Q92258604 | Improving Signal and Photobleaching Characteristics of Temporal Focusing Microscopy with the Increase in Pulse Repetition Rate |
Q30537143 | Improving spinning disk confocal microscopy by preventing pinhole cross-talk for intravital imaging. |
Q21143895 | In C. elegans, high levels of dsRNA allow RNAi in the absence of RDE-4 |
Q33492754 | In Caenorhabditis elegans nanoparticle-bio-interactions become transparent: silica-nanoparticles induce reproductive senescence |
Q90557911 | In Fimo: A Term Proposed for Excrement Examined Experimentally |
Q64110852 | In Silico Molecular Docking and In Vivo Validation with to Discover Molecular Initiating Events in Adverse Outcome Pathway Framework: Case Study on Endocrine-Disrupting Chemicals with Estrogen and Androgen Receptors |
Q38681317 | In Vivo Delivery and Activation of Masked Fluorogenic Hydrolase Substrates by Endogenous Hydrolases in C. elegans |
Q36876110 | In Vivo Interaction Proteomics in Caenorhabditis elegans Embryos Provides New Insights into P Granule Dynamics |
Q27313835 | In actio optophysiological analyses reveal functional diversification of dopaminergic neurons in the nematode C. elegans. |
Q40773961 | In search of new mutants in cell-signaling systems of the nematode Caenorhabditis elegans. Review |
Q27316596 | In silico molecular comparisons of C. elegans and mammalian pharmacology identify distinct targets that regulate feeding |
Q91973315 | In situ Microfluidic Cryofixation for Cryo Focused Ion Beam Milling and Cryo Electron Tomography |
Q58796380 | In situ analysis of C. elegans vitellogenin fusion gene expression in integrated transgenic strains: effect of promoter mutations on RNA localization |
Q30581020 | In situ imaging in C. elegans reveals developmental regulation of microtubule dynamics |
Q43117068 | In the beginning was the worm ... |
Q41497184 | In vitro aggregating β-lactamase-polyQ chimeras do not induce toxic effects in an in vivo Caenorhabditis elegans model. |
Q38086226 | In vitro and in vivo model systems for studying enteropathogenic Escherichia coli infections |
Q34093167 | In vitro and in vivo reconstitution of the cadherin-catenin-actin complex from Caenorhabditis elegans |
Q36650972 | In vitro mutagenesis of Caenorhabditis elegans cuticle collagens identifies a potential subtilisin-like protease cleavage site and demonstrates that carboxyl domain disulfide bonding is required for normal function but not assembly |
Q24655970 | In vivo analysis of Caenorhabditis elegans noncoding RNA promoter motifs |
Q92527704 | In vivo analysis of FANCD2 recruitment at meiotic DNA breaks in Caenorhabditis elegans |
Q40696210 | In vivo construction of recombinant molecules within the Caenorhabditis elegans germ line using short regions of terminal homology |
Q35567487 | In vivo effects on intron retention and exon skipping by the U2AF large subunit and SF1/BBP in the nematode Caenorhabditis elegans |
Q36467709 | In vivo function of mutated spliced leader RNAs in Caenorhabditis elegans |
Q41929985 | In vivo identification of regulators of cell invasion across basement membranes |
Q40919446 | In vivo imaging of C. elegans ASH neurons: cellular response and adaptation to chemical repellents |
Q42543235 | In vivo imaging of C. elegans endocytosis |
Q40044854 | In vivo imaging of Dauer-specific neuronal remodeling in C. elegans |
Q59799706 | In vivo induction of membrane damage by β-amyloid peptide oligomers |
Q30491435 | In vivo roles for Arp2/3 in cortical actin organization during C. elegans gastrulation |
Q50497285 | In vivo structure-function analyses of Caenorhabditis elegans MEC-4, a candidate mechanosensory ion channel subunit. |
Q92883055 | In-Vivo Quantitative Image Analysis of Age-Related Morphological Changes of C. elegans Neurons Reveals a Correlation between Neurite Bending and Novel Neurite Outgrowths |
Q37214806 | Inactivation of GABAA receptor is related to heat shock stress response in organism model Caenorhabditis elegans |
Q36981507 | Incorporation of a Fluorescent Compound by Live Heterodera glycines. |
Q35904381 | Increased competitiveness of nematode sperm bearing the male X chromosome |
Q34614981 | Increased or decreased levels of Caenorhabditis elegans lon-3, a gene encoding a collagen, cause reciprocal changes in body length. |
Q37681037 | Increased sensitivity and accuracy of a single-stranded DNA splint-mediated ligation assay (sPAT) reveals poly(A) tail length dynamics of developmentally regulated mRNAs |
Q38615476 | Indoles from commensal bacteria extend healthspan. |
Q93107081 | Inducing Mild Traumatic Brain Injury in C. elegans via Cavitation-Free Surface Acoustic Wave-Driven Ultrasonic Irradiation |
Q33600897 | Induction of RNA interference in Caenorhabditis elegans by RNAs derived from plants exhibiting post-transcriptional gene silencing |
Q29614498 | Induction of autophagy by spermidine promotes longevity |
Q36443714 | Induction of cap-independent BiP (hsp-3) and Bcl-2 (ced-9) translation in response to eIF4G (IFG-1) depletion in C. elegans |
Q67060017 | Induction of the alcohol-metabolizing pathway in the nematode Panagrellus redivivus: Phenotypic effects |
Q36981462 | Influence of Lysobacter enzymogenes Strain C3 on Nematodes |
Q35806453 | Information Flow through a Model of the C. elegans Klinotaxis Circuit |
Q64083959 | Infrared-Based Motility Assay Identified New Hits for Nematicide Drug Development |
Q28822538 | Inhibiting poly(ADP-ribosylation) improves axon regeneration |
Q36953159 | Inhibition of CED-3 zymogen activation and apoptosis in Caenorhabditis elegans by caspase homolog CSP-3 |
Q35193777 | Inhibition of Caenorhabditis elegans vulval induction by gap-1 and by let-23 receptor tyrosine kinase |
Q35749188 | Inhibition of Cytohesins Protects against Genetic Models of Motor Neuron Disease. |
Q57021581 | Inhibition of cell fate repressors secures the differentiation of the touch receptor neurons of |
Q30642659 | Inhibition of touch cell fate by egl-44 and egl-46 in C. elegans |
Q36391813 | Inhibition of transcription by the Caenorhabditis elegans germline protein PIE-1: genetic evidence for distinct mechanisms targeting initiation and elongation |
Q33964804 | Inhibitors of LRRK2 kinase attenuate neurodegeneration and Parkinson-like phenotypes in Caenorhabditis elegans and Drosophila Parkinson's disease models |
Q37672064 | Inhibitory peptidergic modulation of C. elegans serotonin neurons is gated by T-type calcium channels |
Q33254080 | Initiation of male sperm-transfer behavior in Caenorhabditis elegans requires input from the ventral nerve cord |
Q33924772 | Innate host defense requires TFEB-mediated transcription of cytoprotective and antimicrobial genes |
Q97420658 | Inoculation With a Microbe Isolated From the Negev Desert Enhances Corn Growth |
Q33938323 | Inositol 1,4,5-trisphosphate signaling regulates mating behavior in Caenorhabditis elegans males |
Q37032079 | Inositol 1,4,5-trisphosphate signaling regulates rhythmic contractile activity of myoepithelial sheath cells in Caenorhabditis elegans |
Q22337099 | Inositol monophosphatase regulates localization of synaptic components and behavior in the mature nervous system of C. elegans |
Q36783201 | Insertion and excision of Caenorhabditis elegans transposable element Tc1. |
Q36688013 | Insertion of part of an intron into the 5' untranslated region of a Caenorhabditis elegans gene converts it into a trans-spliced gene |
Q33725985 | Insertional inactivation of genes encoding the crystalline inclusion proteins of Photorhabdus luminescens results in mutants with pleiotropic phenotypes |
Q38214170 | Insights from the worm: the C. elegans model for innate immunity |
Q33686692 | Insights into species divergence and the evolution of hermaphroditism from fertile interspecies hybrids of Caenorhabditis nematodes |
Q93079618 | Insights into the roles of CMK-1 and OGT-1 in interstimulus interval-dependent habituation in Caenorhabditis elegans |
Q47302045 | Insulin Signaling Deficiency Produces Immobility in Caenorhabditis elegans That Models Diminished Motivation States in Man and Responds to Antidepressants |
Q51747909 | Insulin Signaling Regulates Oocyte Quality Maintenance with Age via Cathepsin B Activity. |
Q27324536 | Insulin signaling and dietary restriction differentially influence the decline of learning and memory with age |
Q36488671 | Insulin signaling in Caenorhabditis elegans regulates both endocrine-like and cell-autonomous outputs |
Q33938012 | Insulin signaling in the aging of healthy and proteotoxically stressed mechanosensory neurons |
Q43037026 | Insulin signaling plays a dual role in Caenorhabditis elegans memory acquisition and memory retrieval |
Q33684279 | Insulin signaling promotes germline proliferation in C. elegans |
Q34153954 | Insulin-like signaling determines survival during stress via posttranscriptional mechanisms in C. elegans |
Q36922585 | Insulin-like signaling pathway functions in integrative response to an olfactory and a gustatory stimuli in Caenorhabditis elegans |
Q40343456 | Insulin-like signalling to the maternal germline controls progeny response to osmotic stress. |
Q27334849 | Insulin/IGF-1 and hypoxia signaling act in concert to regulate iron homeostasis in Caenorhabditis elegans |
Q34735251 | Insulin/IGF-1 signaling, including class II/III PI3Ks, β-arrestin and SGK-1, is required in C. elegans to maintain pharyngeal muscle performance during starvation |
Q37072648 | Insulin/IGF-1-mediated longevity is marked by reduced protein metabolism |
Q37585122 | Insulin/IGF1 signaling inhibits age-dependent axon regeneration |
Q26998238 | Integrated control of protein degradation in C. elegans muscle |
Q28305190 | Integrating the stress response: lessons for neurodegenerative diseases from C. elegans |
Q47879536 | Integration of Plasticity Mechanisms within a Single Sensory Neuron of C. elegans Actuates a Memory |
Q48144374 | Integration of carbohydrate metabolism and redox state controls dauer larva formation in Caenorhabditis elegans |
Q47068896 | Integration of male mating and feeding behaviors in Caenorhabditis elegans. |
Q37278625 | Integration of metabolic and gene regulatory networks modulates the C. elegans dietary response |
Q33880523 | Integrative transformation of Caenorhabditis elegans |
Q42128881 | Integrin acts upstream of netrin signaling to regulate formation of the anchor cell's invasive membrane in C. elegans |
Q34277082 | Integrin α PAT-2/CDC-42 signaling is required for muscle-mediated clearance of apoptotic cells in Caenorhabditis elegans |
Q33762944 | Integrin-linked kinase modulates longevity and thermotolerance in C. elegans through neuronal control of HSF-1. |
Q92960080 | Integrins Have Cell-Type-Specific Roles in the Development of Motor Neuron Connectivity |
Q27308141 | Integrity of Narrow Epithelial Tubes in the C. elegans Excretory System Requires a Transient Luminal Matrix |
Q49788386 | Interaction between the C. elegans centriolar protein SAS-5 and microtubules facilitates organelle assembly. |
Q27324578 | Interaction of ARF-1.1 and neuronal calcium sensor-1 in the control of the temperature-dependency of locomotion in Caenorhabditis elegans |
Q30503202 | Interaction of PAR-6 with CDC-42 is required for maintenance but not establishment of PAR asymmetry in C. elegans |
Q36056356 | Interaction of structure-specific and promiscuous G-protein-coupled receptors mediates small-molecule signaling in Caenorhabditis elegans |
Q36052372 | Interaction of α-catulin with dystrobrevin contributes to integrity of dystrophin complex in muscle |
Q33761415 | Interaction with Shc prevents aberrant Erk activation in the absence of extracellular stimuli |
Q33870828 | Interactions between LHX3- and ISL1-family LIM-homeodomain transcription factors are conserved in Caenorhabditis elegans |
Q61953506 | Interactions between two antagonistic reflexes in the nematode Caenorhabditis elegans |
Q34587853 | Interactions of UNC-34 Enabled with Rac GTPases and the NIK kinase MIG-15 in Caenorhabditis elegans axon pathfinding and neuronal migration |
Q37355860 | Interaxonal interaction defines tiled presynaptic innervation in C. elegans |
Q36340150 | Intercellular calcium signaling in a gap junction-coupled cell network establishes asymmetric neuronal fates in C. elegans |
Q34011581 | Intercistronic region required for polycistronic pre-mRNA processing in Caenorhabditis elegans |
Q91900043 | Interference with Pseudomonas aeruginosa Quorum Sensing and Virulence by the Mycobacterial Pseudomonas Quinolone Signal Dioxygenase AqdC in Combination with the N-Acylhomoserine Lactone Lactonase QsdA |
Q83225755 | Interferon-β-induced miR-1 alleviates toxic protein accumulation by controlling autophagy |
Q99607995 | Intergenerational Pathogen-Induced Diapause in Caenorhabditis elegans Is Modulated by mir-243 |
Q37273465 | Interkingdom adenosine signal reduces Pseudomonas aeruginosa pathogenicity. |
Q36215210 | Intermediate filaments in muscle and epithelial cells of nematodes |
Q27308953 | Intermittent Stem Cell Cycling Balances Self-Renewal and Senescence of the C. elegans Germ Line |
Q30497921 | Internalization of multiple cells during C. elegans gastrulation depends on common cytoskeletal mechanisms but different cell polarity and cell fate regulators |
Q34363355 | Interplay between AAUAAA and the trans-splice site in processing of a Caenorhabditis elegans operon pre-mRNA. |
Q92875181 | Interplay between small RNA pathways shapes chromatin landscapes in C. elegans |
Q28513559 | Interplay between structure-specific endonucleases for crossover control during Caenorhabditis elegans meiosis |
Q37173956 | Interplay between the oxidoreductase PDIA6 and microRNA-322 controls the response to disrupted endoplasmic reticulum calcium homeostasis. |
Q33968512 | Interspecies comparison reveals evolution of control regions in the nematode sex-determining gene tra-2. |
Q34213602 | Interspecies systems biology uncovers metabolites affecting C. elegans gene expression and life history traits |
Q34165686 | Interspecific tests of allelism reveal the evolutionary timing and pattern of accumulation of reproductive isolation mutations. |
Q91787702 | Intertwined Functions of Separase and Caspase in Cell Division and Programmed Cell Death |
Q27308697 | Intestinal Autophagy Improves Healthspan and Longevity in C. elegans during Dietary Restriction |
Q37560029 | Intestinal Enterobacteriaceae that Protect Nematodes from the Effects of Benzimidazoles |
Q36760659 | Intestinal Insulin Signaling Encodes Two Different Molecular Mechanisms for the Shortened Longevity Induced by Graphene Oxide in Caenorhabditis elegans |
Q91721636 | Intestinal peroxisomal fatty acid β-oxidation regulates neural serotonin signaling through a feedback mechanism |
Q89620949 | Intra Strain Variation of the Effects of Gram-Negative ESKAPE Pathogens on Intestinal Colonization, Host Viability, and Host Response in the Model Organism Caenorhabditis elegans |
Q24610113 | Intracellular Phospholipase A1and Acyltransferase, Which Are Involved inCaenorhabditis elegansStem Cell Divisions, Determine thesn-1 Fatty Acyl Chain of Phosphatidylinositol |
Q30485664 | Intracellular amyloid formation in muscle cells of Abeta-transgenic Caenorhabditis elegans: determinants and physiological role in copper detoxification |
Q38386911 | Intracellular and Extracellular Expression of Bacillus thuringiensis Crystal Protein Cry5B in Lactococcus lactis for Use as an Anthelminthic |
Q30497835 | Intracellular organelles mediate cytoplasmic pulling force for centrosome centration in the Caenorhabditis elegans early embryo |
Q28475536 | Intracellular trafficking and synaptic function of APL-1 in Caenorhabditis elegans |
Q24598245 | Intraflagellar transport delivers tubulin isotypes to sensory cilium middle and distal segments |
Q37262305 | Intraflagellar transport/Hedgehog-related signaling components couple sensory cilium morphology and serotonin biosynthesis in Caenorhabditis elegans |
Q37594651 | Intramolecular regulation of presynaptic scaffold protein SYD-2/liprin-α. |
Q42373224 | Intricate and Cell Type-Specific Populations of Endogenous Circular DNA (eccDNA) in Caenorhabditis elegans and Homo sapiens. |
Q39192125 | Intrinsic JNK-MAPK pathway involvement requires daf-16-mediated immune response during Shigella flexneri infection in C. elegans |
Q35918718 | Intrinsic differences between males and females determine sex-specific consequences of inbreeding |
Q26830468 | Introduction to germ cell development in Caenorhabditis elegans |
Q30703677 | Invasive Cell Fate Requires G1 Cell-Cycle Arrest and Histone Deacetylase-Mediated Changes in Gene Expression |
Q90285788 | Invertebrate models of behavioural plasticity and human disease |
Q33508801 | Investigating bacterial sources of toxicity as an environmental contributor to dopaminergic neurodegeneration |
Q35847016 | Investigating the Role of the Host Multidrug Resistance Associated Protein Transporter Family in Burkholderia cepacia Complex Pathogenicity Using a Caenorhabditis elegans Infection Model |
Q58596097 | Investigation of feeding behaviour in C. elegans reveals distinct pharmacological and antibacterial effects of nicotine |
Q41285052 | Investigations on the organization of genetic loci in Drosophila melanogaster: lethal mutations affecting 6-phosphogluconate dehydrogenase and their suppression |
Q41412431 | Involvement of AAT transporters in methylmercury toxicity in Caenorhabditis elegans |
Q37326311 | Involvement of Caenohabditis elegans MAPK Signaling Pathways in Oxidative Stress Response Induced by Silver Nanoparticles Exposure |
Q90226997 | Involvement of Spermidine in the Reduced Lifespan of Caenorhabditis elegans During Vitamin B12 Deficiency |
Q35984238 | Involvement of Vitamin B6 Biosynthesis Pathways in the Insecticidal Activity of Photorhabdus luminescens |
Q88938599 | Involvement of YAP-1, the Homolog of Yes-Associated Protein, in the Wnt-Mediated Neuronal Polarization in Caenorhabditis elegans |
Q24792776 | Involvement of fatty acid pathways and cortical interaction of the pronuclear complex in Caenorhabditis elegans embryonic polarity |
Q40955820 | Involvement of genes required for synaptic function in aging control in C. elegans |
Q27347595 | Involvement of global genome repair, transcription coupled repair, and chromatin remodeling in UV DNA damage response changes during development |
Q36179612 | Involvement of heat shock proteins on Mn-induced toxicity in Caenorhabditis elegans |
Q41369321 | Irisflorentin improves α-synuclein accumulation and attenuates 6-OHDA-induced dopaminergic neuron degeneration, implication for Parkinson's disease therapy |
Q92034745 | Irrational behavior in C. elegans arises from asymmetric modulatory effects within single sensory neurons |
Q46260601 | Is Caenorhabditis elegans representative of freshwater nematode species in toxicity testing? |
Q64993308 | Isolated C. elegans germ nuclei exhibit distinct genomic profiles of histone modification and gene expression. |
Q24543951 | Isolation and Characterization of High-Temperature-Induced Dauer Formation Mutants in Caenorhabditis elegans |
Q35597729 | Isolation and characterization of Caenorhabditis elegans DNA sequences homologous to the v-abl oncogene |
Q47097030 | Isolation and characterization of HepP: a virulence-related Pseudomonas aeruginosa heparinase |
Q34334290 | Isolation and characterization of a nematode transposable element from Panagrellus redivivus |
Q36942238 | Isolation and characterization of a sperm-specific gene family in the nematode Caenorhabditis elegans |
Q33948327 | Isolation and characterization of the activated B-cell factor 1 homolog in Caenorhabditis elegans |
Q67002842 | Isolation and characterization of the cuticle from the free-living nematode Panagrellus silusiae |
Q34283104 | Isolation and genetic characterization of cell-lineage mutants of the nematode Caenorhabditis elegans |
Q42631751 | Isolation and sequence analysis of Caenorhabditis briggsae repetitive elements related to the Caenorhabditis elegans transposon Tc1. |
Q58761320 | Isolation by Miniaturized Culture Chip of an Antarctic bacterium sp. with antimicrobial and anthelmintic activity |
Q89927201 | Isolation of lactic acid bacteria capable of reducing environmental alkyl and fatty acid hydroperoxides, and the effect of their oral administration on oxidative-stressed nematodes and rats |
Q33962115 | Isolation, characterization and epistasis of fluoride-resistant mutants of Caenorhabditis elegans. |
Q28239600 | Isopentenyl-diphosphate isomerase is essential for viability of Caenorhabditis elegans |
Q41949373 | Isotopic ratio outlier analysis global metabolomics of Caenorhabditis elegans |
Q41491522 | Isoxanthohumol, a constituent of hop (Humulus lupulus L.), increases stress resistance in Caenorhabditis elegans dependent on the transcription factor DAF-16. |
Q47103519 | JAK/STAT and TGF-ß activation as potential adverse outcome pathway of TiO2NPs phototoxicity in Caenorhabditis elegans. |
Q52680682 | JMJD-1.2 controls multiple histone post-translational modifications in germ cells and protects the genome from replication stress. |
Q36282697 | JMJD-5/KDM8 regulates H3K36me2 and is required for late steps of homologous recombination and genome integrity |
Q33934548 | JNK regulates lifespan in Caenorhabditis elegans by modulating nuclear translocation of forkhead transcription factor/DAF-16. |
Q27026099 | Japanese studies on neural circuits and behavior of Caenorhabditis elegans |
Q27321836 | Joint molecule resolution requires the redundant activities of MUS-81 and XPF-1 during Caenorhabditis elegans meiosis |
Q24614362 | Joubert syndrome Arl13b functions at ciliary membranes and stabilizes protein transport in Caenorhabditis elegans |
Q30489447 | KDP-1 is a nuclear envelope KASH protein required for cell-cycle progression |
Q34407303 | KEL-8 is a substrate receptor for CUL3-dependent ubiquitin ligase that regulates synaptic glutamate receptor turnover |
Q27336381 | KIAA0556 is a novel ciliary basal body component mutated in Joubert syndrome |
Q35612504 | KIN-29 SIK regulates chemoreceptor gene expression via an MEF2 transcription factor and a class II HDAC. |
Q41889886 | KLB, encoding β-Klotho, is mutated in patients with congenital hypogonadotropic hypogonadism |
Q92185952 | KLF-1 orchestrates a xenobiotic detoxification program essential for longevity of mitochondrial mutants |
Q30486975 | KLP-18, a Klp2 kinesin, is required for assembly of acentrosomal meiotic spindles in Caenorhabditis elegans |
Q27310526 | KLP-7 acts through the Ndc80 complex to limit pole number in C. elegans oocyte meiotic spindle assembly |
Q37669220 | Katanin maintains meiotic metaphase chromosome alignment and spindle structure in vivo and has multiple effects on microtubules in vitro |
Q61816592 | Key role of SMN/SYNCRIP and RNA-Motif 7 in spinal muscular atrophy: RNA-Seq and motif analysis of human motor neurons |
Q34388790 | Killing of Caenorhabditis elegans by Cryptococcus neoformans as a model of yeast pathogenesis |
Q28776658 | Killing of Caenorhabditis elegans by Pseudomonas aeruginosa used to model mammalian bacterial pathogenesis |
Q36477677 | Kinase inhibitors arrest neurodegeneration in cell and C. elegans models of LRRK2 toxicity |
Q28609061 | Kinase suppressor of Ras forms a multiprotein signaling complex and modulates MEK localization |
Q36784741 | Kinesin-1 acts with netrin and DCC to maintain sensory neuron position in Caenorhabditis elegans |
Q37207726 | Kinesin-1 and cytoplasmic dynein act sequentially to move the meiotic spindle to the oocyte cortex in Caenorhabditis elegans |
Q34191608 | Kinesin-1 and dynein at the nuclear envelope mediate the bidirectional migrations of nuclei |
Q38024629 | Kinesin-2 motors transport IFT-particles, dyneins and tubulin subunits to the tips of Caenorhabditis elegans sensory cilia: relevance to vision research? |
Q27331754 | Kinetics and specificity of paternal mitochondrial elimination in Caenorhabditis elegans |
Q90281576 | Kinetochore Recruitment of the Spindle and Kinetochore-Associated (Ska) Complex Is Regulated by Centrosomal PP2A in Caenorhabditis elegans |
Q36531569 | Kinetochores and chromatin diminution in early embryos of Parascaris univalens |
Q34322391 | Klotho interferes with a novel FGF-signalling pathway and insulin/Igf-like signalling to improve longevity and stress resistance in Caenorhabditis elegans |
Q38618355 | Knock-out of a mitochondrial sirtuin protects neurons from degeneration in Caenorhabditis elegans. |
Q39345808 | Knockdown of the C. elegans kinome identifies kinases required for normal protein homeostasis, mitochondrial network structure, and sarcomere structure in muscle |
Q35951411 | Knockout of glial channel ACD-1 exacerbates sensory deficits in a C. elegans mutant by regulating calcium levels of sensory neurons |
Q30300051 | Knockout of the adp gene related with colonization in Bacillus nematocida B16 using customized transcription activator-like effectors nucleases |
Q33870069 | Knockout of the folate transporter folt-1 causes germline and somatic defects in C. elegans |
Q89341432 | Kushui Rose (R. Setate x R. Rugosa) decoction exerts antitumor effects in C. elegans by downregulating Ras/MAPK pathway and resisting oxidative stress |
Q45972001 | KymoAnalyzer: a software tool for the quantitative analysis of intracellular transport in neurons. |
Q50945539 | Kynurenine hydroxylase mutants of the nematode Caenorhabditis elegans. |
Q59809088 | L. (chia) seeds oil extracts reduce lipid accumulation and produce stress resistance in |
Q24294168 | LAAT-1 is the lysosomal lysine/arginine transporter that maintains amino acid homeostasis |
Q36942436 | LAB-1 antagonizes the Aurora B kinase in C. elegans |
Q34395178 | LAB-1 targets PP1 and restricts Aurora B kinase upon entrance into meiosis to promote sister chromatid cohesion. |
Q27321095 | LEM-3 - A LEM domain containing nuclease involved in the DNA damage response in C. elegans |
Q47592676 | LET-413/Erbin acts as a RAB-5 effector to promote RAB-10 activation during endocytic recycling |
Q37702564 | LET-418/Mi2 and SPR-5/LSD1 cooperatively prevent somatic reprogramming of C. elegans germline stem cells |
Q35128372 | LET-711, the Caenorhabditis elegans NOT1 ortholog, is required for spindle positioning and regulation of microtubule length in embryos |
Q43491720 | LET-99 functions in the astral furrowing pathway, where it is required for myosin enrichment in the contractile ring |
Q33840050 | LET-99 inhibits lateral posterior pulling forces during asymmetric spindle elongation in C. elegans embryos |
Q37462389 | LIN-12/Notch regulates lag-1 and lin-12 expression during anchor cell/ventral uterine precursor cell fate specification |
Q37446769 | LIN-23, an E3 Ubiquitin Ligase Component, Is Required for the Repression of CDC-25.2 Activity during Intestinal Development in Caenorhabditis elegans |
Q24569672 | LIN-28 and the poly(U) polymerase PUP-2 regulate let-7 microRNA processing in Caenorhabditis elegans |
Q37592007 | LIN-28 balances longevity and germline stem cell number in Caenorhabditis elegans through let-7/AKT/DAF-16 axis |
Q34075043 | LIN-3/EGF promotes the programmed cell death of specific cells in Caenorhabditis elegans by transcriptional activation of the pro-apoptotic gene egl-1. |
Q41260733 | LIN-32/Atonal Controls Oxygen Sensing Neuron Development in Caenorhabditis elegans |
Q33743662 | LIN-35/Rb causes starvation-induced germ cell apoptosis via CED-9/Bcl2 downregulation in Caenorhabditis elegans |
Q35805454 | LIN-39/Hox triggers cell division and represses EFF-1/fusogen-dependent vulval cell fusion |
Q36716385 | LIN-41 inactivation leads to delayed centrosome elimination and abnormal chromosome behavior during female meiosis in Caenorhabditis elegans |
Q27314880 | LIN-42, the Caenorhabditis elegans PERIOD homolog, negatively regulates microRNA transcription |
Q27320889 | LIN-44/Wnt directs dendrite outgrowth through LIN-17/Frizzled in C. elegans Neurons |
Q35512446 | LIN-5 is a novel component of the spindle apparatus required for chromosome segregation and cleavage plane specification in Caenorhabditis elegans |
Q35844907 | LIN-61, one of two Caenorhabditis elegans malignant-brain-tumor-repeat-containing proteins, acts with the DRM and NuRD-like protein complexes in vulval development but not in certain other biological processes |
Q34767114 | LINKIN, a new transmembrane protein necessary for cell adhesion |
Q42005064 | LRRK2 and RAB7L1 coordinately regulate axonal morphology and lysosome integrity in diverse cellular contexts. |
Q58701452 | LRRK2 kinase regulates α-synuclein propagation via RAB35 phosphorylation |
Q35080550 | LRRK2 modulates vulnerability to mitochondrial dysfunction in Caenorhabditis elegans |
Q40988812 | LYCAT, a homologue of C. elegans acl-8, acl-9, and acl-10, determines the fatty acid composition of phosphatidylinositol in mice |
Q38669973 | Label-free three-dimensional imaging of Caenorhabditis elegans with visible optical coherence microscopy |
Q37215409 | Labeled microRNA pull-down assay system: an experimental approach for high-throughput identification of microRNA-target mRNAs |
Q35853999 | Lactic Acid Bacteria Protects Caenorhabditis elegans from Toxicity of Graphene Oxide by Maintaining Normal Intestinal Permeability under different Genetic Backgrounds |
Q89916726 | Lamina-Dependent Stretching and Unconventional Chromosome Compartments in Early C. elegans Embryos |
Q30513991 | Laminin is required to orient epithelial polarity in the C. elegans pharynx |
Q30482528 | Large P body-like RNPs form in C. elegans oocytes in response to arrested ovulation, heat shock, osmotic stress, and anoxia and are regulated by the major sperm protein pathway |
Q27335383 | Large isoforms of UNC-89 (obscurin) are required for muscle cell architecture and optimal calcium release in Caenorhabditis elegans |
Q67786441 | Large scale cultivation of a free-living nematode (Caenorhabditis elegans) |
Q35027571 | Large-scale detection of in vivo transcription errors |
Q34194189 | Large-scale functional RNAi screen in C. elegans identifies genes that regulate the dysfunction of mutant polyglutamine neurons. |
Q33715279 | Large-scale in vivo femtosecond laser neurosurgery screen reveals small-molecule enhancer of regeneration |
Q28554683 | Large-scale microfluidics providing high-resolution and high-throughput screening of Caenorhabditis elegans poly-glutamine aggregation model |
Q55510726 | Larger sperm outcompete smaller sperm in the nematode Caenorhabditis elegans. |
Q35059332 | Laser microbeam studies of role of amphid receptors in chemosensory behavior of nematodeCaenorhabditis elegans |
Q27304779 | Laterally orienting C. elegans using geometry at microscale for high-throughput visual screens in neurodegeneration and neuronal development studies |
Q41788521 | Latrophilin is required for toxicity of black widow spider venom in Caenorhabditis elegans |
Q33642220 | Latrophilin signaling links anterior-posterior tissue polarity and oriented cell divisions in the C. elegans embryo |
Q40047796 | Leaf Extracts of Selected Gardening Trees Can Attenuate Quorum Sensing and Pathogenicity of Pseudomonas aeruginosa PAO1. |
Q40215765 | Learning in three species of Diptera: the blow fly Phormia regina, the fruit fly Drosophila melanogaster, and the house fly Musca domestica |
Q40286303 | Leeches of the genus Helobdella as model organisms for Evo-Devo studies |
Q36405011 | Left-right olfactory asymmetry results from antagonistic functions of voltage-activated calcium channels and the Raw repeat protein OLRN-1 in C. elegans |
Q27345082 | Leptotene/zygotene chromosome movement via the SUN/KASH protein bridge in Caenorhabditis elegans |
Q33954671 | Lethal and amanitin-resistance mutations in the Caenorhabditis elegans ama-1 and ama-2 genes |
Q28776408 | Lethal paralysis of Caenorhabditis elegans by Pseudomonas aeruginosa |
Q36044037 | Levamisole receptors: a second awakening. |
Q36841732 | Levamisole resistance resolved at the single-channel level in Caenorhabditis elegans. |
Q37286921 | Levels of the ubiquitin ligase substrate adaptor MEL-26 are inversely correlated with MEI-1/katanin microtubule-severing activity during both meiosis and mitosis |
Q35794357 | Library Construction for Mutation Identification by Whole-Genome Sequencing |
Q36942608 | Life Span and Motility Effects of Ethanolic Extracts from Sophora moorcroftiana Seeds on Caenorhabditis elegans |
Q33446005 | Life cycle and population growth rate of Caenorhabditis elegans studied by a new method |
Q35675232 | Life span and stress resistance of Caenorhabditis elegans are differentially affected by glutathione transferases metabolizing 4-hydroxynon-2-enal |
Q36269850 | Life span extensions associated with upregulation of gene expression of antioxidant enzymes in Caenorhabditis elegans; studies of mutation in the age-1, PI3 kinase homologue and short-term exposure to hyperoxia |
Q36269869 | Life span extensions associated with upregulation of gene expression of antioxidant enzymes in Caenorhabdms elegans; studies of mutation in the AGE-1, PI3 kinase homologue and short-term exposure to hyperoxia |
Q35738802 | Life-History Traits of the Model Organism Pristionchus pacificus Recorded Using the Hanging Drop Method: Comparison with Caenorhabditis elegans |
Q36218411 | Lifespan Extending and Stress Resistant Properties of Vitexin from Vigna angularis in Caenorhabditis elegans |
Q42216196 | Lifespan Extension Induced by Caffeine in Caenorhabditis elegans is Partially Dependent on Adenosine Signaling |
Q92970667 | Lifespan Extension in C. elegans Caused by Bacterial Colonization of the Intestine and Subsequent Activation of an Innate Immune Response |
Q33281293 | Lifespan regulation by evolutionarily conserved genes essential for viability |
Q27324080 | Lifespan-extending effects of royal jelly and its related substances on the nematode Caenorhabditis elegans |
Q90643583 | Lifespan-increasing drug nordihydroguaiaretic acid inhibits p300 and activates autophagy |
Q30486359 | Light-sensitive neurons and channels mediate phototaxis in C. elegans |
Q58105676 | Line excitation array detection fluorescence microscopy at 0.8 million frames per second |
Q92487248 | Lineage context switches the function of a C. elegans Pax6 homolog in determining a neuronal fate |
Q35676310 | Linker histone HIS-24 (H1.1) cytoplasmic retention promotes germ line development and influences histone H3 methylation in Caenorhabditis elegans |
Q37234257 | Linking Gene Expression in the Intestine to Production of Gametes Through the Phosphate Transporter PITR-1 in Caenorhabditis elegans |
Q47948608 | Linking the environment, DAF-7/TGFβ signaling and LAG-2/DSL ligand expression in the germline stem cell niche |
Q28483323 | Lipid environment modulates the development of acute tolerance to ethanol in Caenorhabditis elegans |
Q36558343 | Lipid extraction by methyl-tert-butyl ether for high-throughput lipidomics |
Q35970467 | Lipid-mediated regulation of SKN-1/Nrf in response to germ cell absence |
Q47904618 | Lipocalins Are Required for Apical Extracellular Matrix Organization and Remodeling in Caenorhabditis elegans |
Q37379005 | Liprin-α/SYD-2 determines the size of dense projections in presynaptic active zones in C. elegans |
Q30541342 | Live imaging reveals active infiltration of mitotic zone by its stem cell niche |
Q30493096 | Live-cell imaging in Caenorhabditis elegans reveals the distinct roles of dynamin self-assembly and guanosine triphosphate hydrolysis in the removal of apoptotic cells |
Q36639069 | Local cortical pulling-force repression switches centrosomal centration and posterior displacement in C. elegans |
Q36311940 | Localization and segregation of lineage-specific cleavage potential in embryos of Caenorhabditis elegans |
Q27345318 | Localization of a guanylyl cyclase to chemosensory cilia requires the novel ciliary MYND domain protein DAF-25 |
Q35613687 | Localization of the Dual Oxidase BLI-3 and Characterization of Its NADPH Oxidase Domain during Infection of Caenorhabditis elegans |
Q41572746 | Localization of the ribosomal genes in Caenorhabditis elegans chromosomes by in situ hybridization using biotin-labeled probes |
Q35917916 | Localized accumulation of tubulin during semi-open mitosis in the Caenorhabditis elegans embryo |
Q46396995 | Locomotion Behavior Is Affected by the GαS Pathway and the Two-Pore-Domain K+ Channel TWK-7 Interacting in GABAergic Motor Neurons in Caenorhabditis elegans |
Q36045503 | Locomotion control of Caenorhabditis elegans through confinement. |
Q40666309 | Locus encoding a family of small heat shock genes in Caenorhabditis elegans: two genes duplicated to form a 3.8-kilobase inverted repeat |
Q41683416 | Locus-specific integration of extrachromosomal transgenes in C. elegans with the CRISPR/Cas9 system |
Q27346541 | Long astral microtubules and RACK-1 stabilize polarity domains during maintenance phase in Caenorhabditis elegans embryos |
Q48581299 | Long-Term High-Resolution Imaging of Developing C. elegans Larvae with Microfluidics. |
Q47629681 | Long-range correlations and fractal dynamics in C. elegans: Changes with aging and stress. |
Q27327239 | Long-range regulatory polymorphisms affecting a GABA receptor constitute a quantitative trait locus (QTL) for social behavior in Caenorhabditis elegans |
Q35891018 | Long-term recovery from acute cold shock in Caenorhabditis elegans |
Q92527479 | Longevity Effect of Liuwei Dihuang in Both Caenorhabditis Elegans and Aged Mice |
Q51740694 | Longevity and Stress Resistant Property of 6-Gingerol from Zingiber officinale Roscoe in Caenorhabditis elegans. |
Q35254761 | Longevity and stress in Caenorhabditis elegans |
Q37351702 | Longevity determined by developmental arrest genes in Caenorhabditis elegans |
Q41071271 | Longevity effect of a polysaccharide from Chlorophytum borivilianum on Caenorhabditis elegans and Saccharomyces cerevisiae. |
Q92251737 | Longevity is determined by ETS transcription factors in multiple tissues and diverse species |
Q33961955 | Longevity-determining genes in Caenorhabditis elegans: chromosomal mapping of multiple noninteractive loci. |
Q33835054 | Longitudinal imaging of Caenorhabditis elegans in a microfabricated device reveals variation in behavioral decline during aging |
Q27321443 | Loss of Acetylcholine Signaling Reduces Cell Clearance Deficiencies in Caenorhabditis elegans |
Q27301833 | Loss of C. elegans GON-1, an ADAMTS9 Homolog, Decreases Secretion Resulting in Altered Lifespan and Dauer Formation |
Q37696358 | Loss of Caenorhabditis elegans BRCA1 promotes genome stability during replication in smc-5 mutants |
Q30573115 | Loss of MEC-17 leads to microtubule instability and axonal degeneration |
Q36341076 | Loss of Munc18-1 long splice variant in GABAergic terminals is associated with cognitive decline and increased risk of dementia in a community sample |
Q36477139 | Loss of RAB-3/A in Caenorhabditis elegans and the mouse affects behavioral response to ethanol |
Q36383297 | Loss of RAD-23 Protects Against Models of Motor Neuron Disease by Enhancing Mutant Protein Clearance |
Q35828112 | Loss of Sarcomere-associated Formins Disrupts Z-line Organization, but does not Prevent Thin Filament Assembly in Caenorhabditis elegans Muscle |
Q27315375 | Loss of a neural AMP-activated kinase mimics the effects of elevated serotonin on fat, movement, and hormonal secretions |
Q90089208 | Loss of an H3K9me anchor rescues laminopathy-linked changes in nuclear organization and muscle function in an Emery-Dreifuss muscular dystrophy model |
Q30496655 | Loss of dystrophin and the microtubule-binding protein ELP-1 causes progressive paralysis and death of adult C. elegans |
Q89544422 | Loss of flavin adenine dinucleotide (FAD) impairs sperm function and male reproductive advantage in C. elegans |
Q27303689 | Loss of function mutations in HARS cause a spectrum of inherited peripheral neuropathies |
Q34158509 | Loss of individual microRNAs causes mutant phenotypes in sensitized genetic backgrounds in C. elegans |
Q40668798 | Loss of pdr-1/parkin influences Mn homeostasis through altered ferroportin expression in C. elegans |
Q98466600 | Loss of the Major Phosphatidylserine or Phosphatidylethanolamine Flippases Differentially Affect Phagocytosis |
Q34572254 | Loss of the Sec1/Munc18-family proteins VPS-33.2 and VPS-33.1 bypasses a block in endosome maturation in Caenorhabditis elegans |
Q37421035 | Loss of the apical V-ATPase a-subunit VHA-6 prevents acidification of the intestinal lumen during a rhythmic behavior in C. elegans. |
Q33426357 | Loss of the transcriptional repressor PAG-3/Gfi-1 results in enhanced neurosecretion that is dependent on the dense-core vesicle membrane protein IDA-1/IA-2. |
Q37550614 | Loss-of-function genetic tools for animal models: cross-species and cross-platform differences |
Q90649812 | Low Concentrations of Caffeine and Its Analogs Extend the Lifespan of Caenorhabditis elegans by Modulating IGF-1-Like Pathway |
Q54967620 | Lowbush cranberry acts through DAF-16/FOXO signaling to promote increased lifespan and axon branching in aging posterior touch receptor neurons. |
Q41559782 | Luqin-like RYamide peptides regulate food-evoked responses in C. elegans |
Q34517224 | Lysosomal biogenesis and function is critical for necrotic cell death in Caenorhabditis elegans |
Q39914071 | Lysosomal enzyme cathepsin D protects against alpha-synuclein aggregation and toxicity |
Q37035142 | Lysosome biogenesis mediated by vps-18 affects apoptotic cell degradation in Caenorhabditis elegans |
Q33631965 | Lysosome-related organelles in intestinal cells are a zinc storage site in C. elegans |
Q35128197 | MAA-1, a novel acyl-CoA-binding protein involved in endosomal vesicle transport in Caenorhabditis elegans |
Q38254339 | MAB-10/NAB acts with LIN-29/EGR to regulate terminal differentiation and the transition from larva to adult in C. elegans |
Q58790129 | MANF Homolog Is Necessary for the Protection of Dopaminergic Neurons and ER Unfolded Protein Response |
Q37425052 | MAP kinase signaling antagonizes PAR-1 function during polarization of the early Caenorhabditis elegans embryo |
Q50421272 | MAPK signaling couples SCF-mediated degradation of translational regulators to oocyte meiotic progression. |
Q37671514 | MDL-1, a growth- and tumor-suppressor, slows aging and prevents germline hyperplasia and hypertrophy in C. elegans. |
Q36780861 | MEC-10 and MEC-19 Reduce the Neurotoxicity of the MEC-4(d) DEG/ENaC Channel in Caenorhabditis elegans |
Q24299301 | MEC-17 is an alpha-tubulin acetyltransferase |
Q35192719 | MEI-1/MEI-2 katanin-like microtubule severing activity is required for Caenorhabditis elegans meiosis |
Q30541151 | MEMS-based force-clamp analysis of the role of body stiffness in C. elegans touch sensation |
Q36731904 | MES-1, a protein required for unequal divisions of the germline in early C. elegans embryos, resembles receptor tyrosine kinases and is localized to the boundary between the germline and gut cells |
Q37351802 | METT-10, a putative methyltransferase, inhibits germ cell proliferative fate in Caenorhabditis elegans |
Q34082017 | MEX-5 enrichment in the C. elegans early embryo mediated by differential diffusion |
Q52727065 | MIB-1 Is Required for Spermatogenesis and Facilitates LIN-12 and GLP-1 Activity in Caenorhabditis elegans. |
Q35626904 | MIG-10 (Lamellipodin) stabilizes invading cell adhesion to basement membrane and is a negative transcriptional target of EGL-43 in C. elegans |
Q37618684 | MIG-10 (lamellipodin) has netrin-independent functions and is a FOS-1A transcriptional target during anchor cell invasion in C. elegans |
Q35224574 | MIG-15 and ERM-1 promote growth cone directional migration in parallel to UNC-116 and WVE-1. |
Q37081729 | MIG-17/ADAMTS controls cell migration by recruiting nidogen to the basement membrane in C. elegans |
Q42156705 | MIG-32 and SPAT-3A are PRC1 homologs that control neuronal migration in Caenorhabditis elegans |
Q38615508 | MIP-MAP: High Throughput Mapping of Caenorhabditis elegans Temperature-Sensitive Mutants via Molecular Inversion Probes. |
Q27349840 | MISC-1/OGC links mitochondrial metabolism, apoptosis and insulin secretion |
Q60916492 | MIYAIRI 588 Increases the Lifespan and Multiple-Stress Resistance of |
Q41981097 | MK-801 is a potent nematocidal agent. Characterization of MK-801 binding sites in Caenorhabditis elegans |
Q28000044 | MKS and NPHP modules cooperate to establish basal body/transition zone membrane associations and ciliary gate function during ciliogenesis |
Q39487708 | MMAPPR: mutation mapping analysis pipeline for pooled RNA-seq |
Q61814464 | MPK-1/ERK is required for the full activity of resveratrol in extended lifespan and reproduction |
Q54978541 | MPK-1/ERK pathway regulates DNA damage response during development through DAF-16/FOXO. |
Q47984850 | MPK-1/ERK regulatory network controls the number of sperm by regulating timing of sperm-oocyte switch in C. elegans germline. |
Q35932371 | MRG-1 is required for genomic integrity in Caenorhabditis elegans germ cells |
Q33828434 | MSP hormonal control of the oocyte MAP kinase cascade and reactive oxygen species signaling. |
Q30499781 | MSUT2 is a determinant of susceptibility to tau neurotoxicity |
Q36293940 | MUP-4 is a novel transmembrane protein with functions in epithelial cell adhesion in Caenorhabditis elegans |
Q33566414 | MUT-14 and SMUT-1 DEAD box RNA helicases have overlapping roles in germline RNAi and endogenous siRNA formation |
Q36110903 | MUT-16 promotes formation of perinuclear mutator foci required for RNA silencing in the C. elegans germline |
Q47349953 | Machine for rapidly counting and measuring the size of small nematodes |
Q34145653 | Macro-level modeling of the response of C. elegans reproduction to chronic heat stress |
Q33968518 | Macrorestriction analysis of Caenorhabditis elegans genomic DNA. |
Q21128758 | Magnetosensitive neurons mediate geomagnetic orientation in Caenorhabditis elegans |
Q51316473 | Mainstreaming Caenorhabditis elegans in experimental evolution. |
Q35546606 | Maintaining the Constant Exposure Condition for an Acute Caenorhabditis elegans Mortality Test Using Passive Dosing |
Q36998487 | Maintenance of Membrane Integrity and Permeability Depends on a Patched-Related Protein in Caenorhabditis elegans |
Q57044817 | Maintenance of Proteostasis by P Body-Mediated Regulation of eIF4E Availability during Aging in Caenorhabditis elegans |
Q61795756 | Maintenance of cell fates and regulation of the histone variant H3.3 by TLK kinase in |
Q30559458 | Maintenance of muscle myosin levels in adult C. elegans requires both the double bromodomain protein BET-1 and sumoylation |
Q42041726 | Maintenance of neuronal positions in organized ganglia by SAX-7, a Caenorhabditis elegans homologue of L1 |
Q36744063 | Makorin ortholog LEP-2 regulates LIN-28 stability to promote the juvenile-to-adult transition in Caenorhabditis elegans |
Q42958124 | Male Phenotypes and Mating Efficiency in CAENORHABDITIS ELEGANS. |
Q90155516 | Male meiotic spindle features that efficiently segregate paired and lagging chromosomes |
Q36365224 | Manipulation of Karyotype in Caenorhabditis elegans Reveals Multiple Inputs Driving Pairwise Chromosome Synapsis During Meiosis |
Q27347278 | Manipulation of behavioral decline in Caenorhabditis elegans with the Rag GTPase raga-1 |
Q30493862 | Many families of C. elegans microRNAs are not essential for development or viability |
Q34612456 | Many genomic regions are required for normal embryonic programmed cell death in Caenorhabditis elegans |
Q38632705 | Many transcription factors contribute to C. elegans growth and fat storage |
Q36867901 | Mapping Challenging Mutations by Whole-Genome Sequencing |
Q34605663 | Mapping a telomere using the translocation eT1(III;V) in Caenorhabditis elegans. |
Q33960823 | Mapping chromosome rearrangement breakpoints to the physical map of Caenorhabditis elegans by fluorescent in situ hybridization. |
Q33931768 | Mapping muscle protein genes by in situ hybridization using biotin-labeled probes |
Q33966787 | Mapping quantitative trait loci affecting life history traits in the nematode Caenorhabditis elegans |
Q64121843 | Mass Surveilance of -Smartphone-Based DIY Microscope and Machine-Learning-Based Approach for Worm Detection |
Q34190874 | Mass spectrometric comparison of N-glycan profiles from Caenorhabditis elegans mutant embryos |
Q34343340 | Mate searching in Caenorhabditis elegans: a genetic model for sex drive in a simple invertebrate. |
Q37366544 | Mated progeny production is a biomarker of aging in Caenorhabditis elegans |
Q36735339 | Matefin/SUN-1 Phosphorylation on Serine 43 Is Mediated by CDK-1 and Required for Its Localization to Centrosomes and Normal Mitosis in C. elegans Embryos |
Q35037264 | Matefin/SUN-1 is a nuclear envelope receptor for CED-4 during Caenorhabditis elegans apoptosis |
Q27324259 | Matefin/SUN-1 phosphorylation is part of a surveillance mechanism to coordinate chromosome synapsis and recombination with meiotic progression and chromosome movement |
Q33647865 | Material properties of Caenorhabditis elegans swimming at low Reynolds number |
Q46037407 | Maternal MEMI Promotes Female Meiosis II in Response to Fertilization in Caenorhabditis elegans. |
Q91866548 | Maternal Ribosomes Are Sufficient for Tissue Diversification during Embryonic Development in C. elegans |
Q64229870 | Maternal and zygotic gene regulatory effects of endogenous RNAi pathways |
Q36817913 | Maternal mRNAs are regulated by diverse P body-related mRNP granules during early Caenorhabditis elegans development |
Q26823989 | Mating behavior, male sensory cilia, and polycystins in Caenorhabditis elegans |
Q46957319 | Mating induces shrinking and death in Caenorhabditis mothers. |
Q36158140 | Mating worms and the cystic kidney: Caenorhabditis elegans as a model for renal disease |
Q34331714 | Measurements of age-related changes of physiological processes that predict lifespan of Caenorhabditis elegans |
Q33955073 | Measurements of behavioral quiescence in Caenorhabditis elegans |
Q35821046 | Measuring Food Intake and Nutrient Absorption in Caenorhabditis elegans. |
Q36981605 | Measuring Movement to Determine Physiological Roles of Acetylcholinesterase Classes in Caenorhabditis elegans |
Q40919354 | Measuring oxidative stress resistance of Caenorhabditis elegans in 96-well microtiter plates |
Q37627816 | Measuring the effects of bacteria on C. elegans behavior using an egg retention assay |
Q89882162 | Mechanical properties measured by atomic force microscopy define health biomarkers in ageing C. elegans |
Q90100230 | Mechanical stress induces a scalable switch in cortical flow polarization during cytokinesis |
Q24308974 | Mechanism of activation of the Caenorhabditis elegans ras homologue let-60 by a novel, temperature-sensitive, gain-of-function mutation |
Q40109225 | Mechanism of biofilm-mediated stress resistance and lifespan extension in C. elegans |
Q59126308 | Mechanism-based rescue of Munc18-1 dysfunction in varied encephalopathies by chemical chaperones |
Q89418261 | Mechanisms involved in anti-aging effects of guarana (Paullinia cupana) in Caenorhabditis elegans |
Q26771604 | Mechanisms of innate immunity in C. elegans epidermis |
Q34519112 | Mechanosensitive unpaired innexin channels in C. elegans touch neurons |
Q37100427 | Mechanosensory Neuron Aging: Differential Trajectories with Lifespan-Extending Alaskan Berry and Fungal Treatments in Caenorhabditis elegans |
Q28679146 | Mechanosensory inputs influence Caenorhabditis elegans pharyngeal activity via ivermectin sensitivity genes |
Q34705398 | Mechanotransduction: touch and feel at the molecular level as modeled in Caenorhabditis elegans |
Q91800325 | Mediator subunit MDT-15/MED15 and Nuclear Receptor HIZR-1/HNF4 cooperate to regulate toxic metal stress responses in Caenorhabditis elegans |
Q64388942 | Meiotic Double-Strand Break Proteins Influence Repair Pathway Utilization |
Q36673155 | Meiotic HORMA domain proteins prevent untimely centriole disengagement during Caenorhabditis elegans spermatocyte meiosis |
Q33962100 | Meiotic mutants that cause a polar decrease in recombination on the X chromosome in Caenorhabditis elegans |
Q30411914 | Meiotic pairing and imprinted X chromatin assembly in Caenorhabditis elegans |
Q70961682 | Meiotic pairing behavior of two free duplications of linkage group I in Caenorhabditis elegans |
Q36900926 | Meiotic recombination in Caenorhabditis elegans |
Q36322053 | Meiotic recombination modulates the structure and dynamics of the synaptonemal complex during C. elegans meiosis. |
Q36215066 | Membrane and cytoplasmic proteins are transported in the same organelle complex during nematode spermatogenesis |
Q34269080 | Membrane curvature sensing by the C-terminal domain of complexin |
Q36205665 | Membrane flow during nematode spermiogenesis |
Q24633113 | Membrane fusion: grappling with SNARE and SM proteins |
Q27321081 | Membrane invaginations reveal cortical sites that pull on mitotic spindles in one-cell C. elegans embryos |
Q43098302 | Membrane remodeling during embryonic abscission in Caenorhabditis elegans. |
Q34078775 | Membrane transport in Caenorhabditis elegans: an essential role for VPS34 at the nuclear membrane |
Q35868771 | Membrane-associated collagens with interrupted triple-helices (MACITs): evolution from a bilaterian common ancestor and functional conservation in C. elegans |
Q33594817 | Memory of recent oxygen experience switches pheromone valence in Caenorhabditis elegans |
Q36739362 | Mesodermal expression of the C. elegans HMX homolog mls-2 requires the PBC homolog CEH-20 |
Q30512741 | Meta-Analysis of Global Transcriptomics Suggests that Conserved Genetic Pathways are Responsible for Quercetin and Tannic Acid Mediated Longevity in C. elegans. |
Q28485135 | Metabolic labeling of Caenorhabditis elegans primary embryonic cells with azido-sugars as a tool for glycoprotein discovery |
Q37109397 | Metabolic network rewiring of propionate flux compensates vitamin B12 deficiency in C. elegans |
Q28829555 | Metabolic profiling and in vitro assessment of anthelmintic fractions of Picria fel-terrae Lour |
Q35573492 | Metabolic profiling of a transgenic Caenorhabditis elegans Alzheimer model |
Q92713294 | Metabolic regulation of lifespan from a C. elegans perspective |
Q31160447 | Metabolomic signature associated with reproduction-regulated aging in Caenorhabditis elegans |
Q33761840 | Metabolomics analysis uncovers that dietary restriction buffers metabolic changes associated with aging in Caenorhabditis elegans |
Q28608661 | Metabolomics and Natural-Products Strategies to Study Chemical Ecology in Nematodes |
Q35721772 | Metabotropic Glutamate Receptors: MODULATORS OF CONTEXT-DEPENDENT FEEDING BEHAVIOUR IN C. ELEGANS |
Q33761310 | Metallothioneins are required for formation of cross-adaptation response to neurobehavioral toxicity from lead and mercury exposure in nematodes |
Q36293715 | Metaphase to anaphase (mat) transition-defective mutants in Caenorhabditis elegans |
Q21563611 | Metazoan Scc4 homologs link sister chromatid cohesion to cell and axon migration guidance |
Q28472548 | Metformin induces a dietary restriction-like state and the oxidative stress response to extend C. elegans Healthspan via AMPK, LKB1, and SKN-1 |
Q92087089 | Metformin promotes innate immunity through a conserved PMK-1/p38 MAPK pathway |
Q37503122 | Metformin retards aging in C. elegans by altering microbial folate and methionine metabolism. |
Q64940562 | Metformin treatment reduces motor and neuropsychiatric phenotypes in the zQ175 mouse model of Huntington disease. |
Q34436494 | Methionyl-tRNA synthetase from Caenorhabditis elegans: a specific multidomain organization for convergent functional evolution |
Q35160391 | Methods to assess subcellular compartments of muscle in C. elegans |
Q33359886 | Methoxylation enhances stilbene bioactivity in Caenorhabditis elegans |
Q89012051 | Methyl 3,4-Dihydroxybenzoate Enhances Resistance to Oxidative Stressors and Lifespan in C. elegans Partially via daf-2/daf-16 |
Q41850888 | Methyl group donors abrogate adaptive responses to dietary restriction in C. elegans |
Q30411151 | Methylation of histone H3K23 blocks DNA damage in pericentric heterochromatin during meiosis |
Q35050458 | Methylation of ribosomal RNA by NSUN5 is a conserved mechanism modulating organismal lifespan. |
Q37276288 | Methylmercury exposure increases lipocalin related (lpr) and decreases activated in blocked unfolded protein response (abu) genes and specific miRNAs in Caenorhabditis elegans |
Q36528255 | MiR-34 modulates Caenorhabditis elegans lifespan via repressing the autophagy gene atg9. |
Q41882618 | MicroRNA mir-34 provides robustness to environmental stress response via the DAF-16 network in C. elegans |
Q27336009 | MicroRNA predictors of longevity in Caenorhabditis elegans |
Q39028411 | MicroRNA sequence variation potentially contributes to within-species functional divergence in the nematode Caenorhabditis briggsae |
Q27330205 | MicroRNA-encoded behavior in Drosophila |
Q34502279 | MicroRNAs both promote and antagonize longevity in C. elegans. |
Q26801487 | MicroRNAs in Cancer: A Historical Perspective on the Path from Discovery to Therapy |
Q21263170 | Microarray analysis of ncRNA expression patterns in Caenorhabditis elegans after RNAi against snoRNA associated proteins |
Q37257580 | Microbeam irradiation of C. elegans nematode in microfluidic channels |
Q41340386 | Microcystins alter chemotactic behavior in Caenorhabditis elegans by selectively targeting the AWA sensory neuron |
Q34631747 | Microevolution of nematode miRNAs reveals diverse modes of selection |
Q27305248 | Microfabricated polyacrylamide devices for the controlled culture of growing cells and developing organisms |
Q92915730 | Microfluidic Device to Measure the Speed of C. elegans Using the Resistance Change of the Flexible Electrode |
Q30571908 | Microfluidic chamber arrays for whole-organism behavior-based chemical screening |
Q37570204 | Microfluidic tools for developmental studies of small model organisms--nematodes, fruit flies, and zebrafish |
Q41428555 | Microfluidic-based electrotaxis for on-demand quantitative analysis of Caenorhabditis elegans' locomotion |
Q90422730 | Microfluidics for mechanobiology of model organisms |
Q27346627 | Microscopic optical projection tomography in vivo |
Q37242006 | Microsporidia Intracellular Development Relies on Myc Interaction Network Transcription Factors in the Host |
Q54106319 | Microtubule Dynamics Scale with Cell Size to Set Spindle Length and Assembly Timing |
Q93191758 | Microtubule Feedback and LET-99-Dependent Control of Pulling Forces Ensure Robust Spindle Position |
Q34652394 | Microtubule depolymerization in Caenorhabditis elegans touch receptor neurons reduces gene expression through a p38 MAPK pathway |
Q37071743 | Microtubule severing by the katanin complex is activated by PPFR-1-dependent MEI-1 dephosphorylation |
Q30502835 | Microtubule-based localization of a synaptic calcium-signaling complex is required for left-right neuronal asymmetry in C. elegans |
Q38647130 | Microtubule-dependent ribosome localization in C. elegans neurons |
Q36213105 | Microtubules and microtubule-associated proteins from the nematode Caenorhabditis elegans: periodic cross-links connect microtubules in vitro |
Q30480579 | Microtubules are involved in anterior-posterior axis formation in C. elegans embryos |
Q30424058 | Midlife gene expressions identify modulators of aging through dietary interventions. |
Q31082546 | Mimicry of a G protein mutation by pertussis toxin expression in transgenic Caenorhabditis elegans |
Q47223213 | MinION-based long-read sequencing and assembly extends the Caenorhabditis elegans reference genome |
Q37568342 | Mind the gut: Dietary impact on germline stem cells and fertility |
Q41051148 | Mitigating Motor Neuronal Loss in C. elegans Model of ALS8. |
Q33729738 | Mitochondria-localized caveolin in adaptation to cellular stress and injury. |
Q91896603 | Mitochondrial Oxidative Stress Impairs Energy Metabolism and Reduces Stress Resistance and Longevity of C. elegans |
Q37078598 | Mitochondrial Proteostatic Collapse Leads to Hypoxic Injury |
Q63090506 | Mitochondrial ROS generated at the complex-II matrix or intermembrane space microdomain have distinct effects on redox signaling and stress sensitivity in C. elegans |
Q37097856 | Mitochondrial SIRT4-type proteins in Caenorhabditis elegans and mammals interact with pyruvate carboxylase and other acetylated biotin-dependent carboxylases |
Q98735552 | Mitochondrial Signature in Human Monocytes and Resistance to Infection in C. elegans During Fumarate-Induced Innate Immune Training |
Q47137613 | Mitochondrial Stress Restores the Heat Shock Response and Prevents Proteostasis Collapse during Aging. |
Q57177934 | Mitochondrial Subtype Identification and Characterization |
Q47181194 | Mitochondrial Uncoupling Attenuates Age-Dependent Neurodegeneration in C. elegans |
Q33721238 | Mitochondrial dysfunction confers resistance to multiple drugs in Caenorhabditis elegans |
Q40139530 | Mitochondrial dysfunction, oxidative stress, and neurodegeneration elicited by a bacterial metabolite in a C. elegans Parkinson's model |
Q33948518 | Mitochondrial fragmentation leads to intracellular acidification in Caenorhabditis elegans and mammalian cells |
Q37285144 | Mitogen-activated protein kinase pathways defend against bacterial pore-forming toxins. |
Q36653692 | Mitosis-meiosis and sperm-oocyte fate decisions are separable regulatory events |
Q92229730 | Mitotic CDK Promotes Replisome Disassembly, Fork Breakage, and Complex DNA Rearrangements |
Q42741255 | Mitotic Spindle Positioning in the EMS Cell of Caenorhabditis elegans Requires LET-99 and LIN-5/NuMA. |
Q52374566 | Mitotic and Meiotic Functions for the SUMOylation Pathway in the Caenorhabditis elegans Germline. |
Q33957921 | Mode and tempo of molecular evolution in the nematode caenorhabditis: cytochrome oxidase II and calmodulin sequences |
Q27310347 | Model-independent phenotyping of C. elegans locomotion using scale-invariant feature transform |
Q54952915 | Modeling Alzheimer's and Other Age Related Human Diseases in Embryonic Systems. |
Q36938165 | Modeling Alzheimer's disease: from past to future |
Q41971316 | Modeling a congenital disorder of glycosylation type I in C. elegans: a genome-wide RNAi screen for N-glycosylation-dependent loci |
Q37293096 | Modeling molecular and cellular aspects of human disease using the nematode Caenorhabditis elegans |
Q36368904 | Modeling of a negative feedback mechanism explains antagonistic pleiotropy in reproduction in domesticated Caenorhabditis elegans strains |
Q28081157 | Models of germ cell development and their application for toxicity studies |
Q36266144 | Modifiers of solid RNP granules control normal RNP dynamics and mRNA activity in early development |
Q59798385 | Modular Proteoglycan Perlecan/: Mutations, Phenotypes, and Functions |
Q27321178 | Modulating Behavior in C. elegans Using Electroshock and Antiepileptic Drugs |
Q42683255 | Modulation of Alpha-synuclein Expression and Associated Effects by MicroRNA Let-7 in Transgenic C. elegans |
Q33575177 | Modulation of C. elegans touch sensitivity is integrated at multiple levels |
Q36315295 | Modulation of Caenorhabditis elegans infection sensitivity by the LIN-7 cell junction protein |
Q34107344 | Modulation of KSR activity in Caenorhabditis elegans by Zn ions, PAR-1 kinase and PP2A phosphatase |
Q35788386 | Modulation of Locomotion and Reproduction by FLP Neuropeptides in the Nematode Caenorhabditis elegans |
Q54495638 | Modulation of glutamine metabolism by the PI(3)K-PKB-FOXO network regulates autophagy. |
Q34852256 | Modulation of lipid biosynthesis contributes to stress resistance and longevity of C. elegans mutants |
Q37680709 | Modulation of muscle gene expression in Caenorhabditis elegans: differential levels of transcripts, mRNAs, and polypeptides for thick filament proteins during nematode development |
Q92616624 | Modulation of serotonin signaling by the putative oxaloacetate decarboxylase FAHD-1 in Caenorhabditis elegans |
Q41442297 | Modulation of the assay system for the sensory integration of 2 sensory stimuli that inhibit each other in nematode Caenorhabditis elegans |
Q92535130 | Molecular Architecture of Genetically-Tractable GABA Synapses in C. elegans |
Q36251324 | Molecular Control of Innate Immune Response to Pseudomonas aeruginosa Infection by Intestinal let-7 in Caenorhabditis elegans |
Q38908313 | Molecular Determinants of the Regulation of Development and Metabolism by Neuronal eIF2α Phosphorylation in Caenorhabditis elegans |
Q34359578 | Molecular analysis of X chromosome dosage compensation in Caenorhabditis elegans |
Q33938424 | Molecular analysis of mutations in the Caenorhabditis elegans collagen gene dpy-7 |
Q28541664 | Molecular analysis of the cold tolerant Antarctic nematode, Panagrolaimus davidi |
Q59065638 | Molecular analysis of the unc-54 myosin heavy-chain gene of Caenorhabditis elegans |
Q36770644 | Molecular analysis of two genes between let-653 and let-56 in the unc-22(IV) region of Caenorhabditis elegans |
Q47069036 | Molecular analysis of zyg-11, a maternal-effect gene required for early embryogenesis of Caenorhabditis elegans |
Q52664617 | Molecular and biochemical characterization of kettin in Caenorhabditis elegans. |
Q64117692 | Molecular and cellular modulators for multisensory integration in C. elegans |
Q63951811 | Molecular and genetic analyses of a multivariate system specifying behavior and life span |
Q34439145 | Molecular and genetic analyses of the Caenorhabditis elegans dpy-2 and dpy-10 collagen genes: a variety of molecular alterations affect organismal morphology |
Q42117208 | Molecular and genetic analysis of unc-7, a Caenorhabditis elegans gene required for coordinated locomotion |
Q34226928 | Molecular basis for antioxidant enzymes in mediating copper detoxification in the nematode Caenorhabditis elegans |
Q37479275 | Molecular basis for galactosylation of core fucose residues in invertebrates: identification of caenorhabditis elegans N-glycan core alpha1,6-fucoside beta1,4-galactosyltransferase GALT-1 as a member of a novel glycosyltransferase family |
Q39750956 | Molecular basis of loss-of-function mutations in the glp-1 gene of Caenorhabditis elegans |
Q41847623 | Molecular characterization of Pegarn: a Drosophila homolog of UNC-51 kinase |
Q34994075 | Molecular characterization of the Caenorhabditis elegans ALP/Enigma gene alp-1 |
Q36487684 | Molecular characterization of two homologs of the Caenorhabditis elegans cadmium-responsive gene cdr-1: cdr-4 and cdr-6 |
Q36345506 | Molecular cloning and characterization of a matrix metalloproteinase, from Caenorhabditis elegans: employed to identify homologous protein from Angiostrongylus cantonensis |
Q36706269 | Molecular cloning and characterization of the dpy-20 gene of Caenorhabditis elegans |
Q36761409 | Molecular cloning and sequencing of ama-1, the gene encoding the largest subunit of Caenorhabditis elegans RNA polymerase II. |
Q35600121 | Molecular cloning of the muscle gene unc-22 in Caenorhabditis elegans by Tc1 transposon tagging |
Q33244782 | Molecular cloning oflin-29, a heterochronic gene required for the differentiation of hypodermal cells and the cessation of molting inC.elegans |
Q34413740 | Molecular control of TiO₂-NPs toxicity formation at predicted environmental relevant concentrations by Mn-SODs proteins |
Q42060608 | Molecular evidence for the direct involvement of a protein kinase C in developmental and behavioural susceptibility to tumour-promoting phorbol esters in Caenorhabditis elegans |
Q38355590 | Molecular evolution and quantitative variation for chemosensory behaviour in the nematode genus Caenorhabditis |
Q36839397 | Molecular evolution of troponin I and a role of its N-terminal extension in nematode locomotion. |
Q34461607 | Molecular genetics of the Caenorhabditis elegans heterochronic gene lin-14. |
Q26849286 | Molecular machines governing exocytosis of synaptic vesicles |
Q34028189 | Molecular mechanisms of amphetamine actions in Caenorhabditis elegans |
Q48431684 | Molecular physiology of the neural circuit for calcineurin-dependent associative learning in Caenorhabditis elegans. |
Q41641463 | Molecular relationships between closely related strains and species of nematodes |
Q21132397 | Molecular strategies of the Caenorhabditis elegans dauer larva to survive extreme desiccation |
Q40102601 | Molecules on the Surface of Parasitic Nematodes as Probes of the Immune Response in Infection |
Q39431749 | Molting in C. elegans |
Q92615492 | Molybdenum cofactor transfer from bacteria to nematode mediates sulfite detoxification |
Q34321472 | Monascus-fermented dioscorea enhances oxidative stress resistance via DAF-16/FOXO in Caenorhabditis elegans |
Q27318136 | Monoaminergic orchestration of motor programs in a complex C. elegans behavior |
Q30504757 | Monoamines and neuropeptides interact to inhibit aversive behaviour in Caenorhabditis elegans |
Q54972216 | Monoamines differentially modulate neuropeptide release from distinct sites within a single neuron pair. |
Q36214979 | Monoclonal antibodies that recognize a polypeptide antigenic determinant shared by multiple Caenorhabditis elegans sperm-specific proteins |
Q68328721 | More is not better: brood size and population growth in a self-fertilizing nematode |
Q36439857 | More than the sum of its parts: a complex epistatic network underlies natural variation in thermal preference behavior in Caenorhabditis elegans |
Q27309001 | Morphogenesis of the C. elegans Intestine Involves Axon Guidance Genes |
Q57802467 | Morphogenetic degeneracies in the actomyosin cortex |
Q37035950 | Morphological remodeling of C. elegans neurons during aging is modified by compromised protein homeostasis. |
Q35661167 | Morphologically defined sub-stages of C. elegans vulval development in the fourth larval stage |
Q92666119 | Mos1 Element-Mediated CRISPR Integration of Transgenes in Caenorhabditis elegans |
Q35641565 | Mos1 mutagenesis reveals a diversity of mechanisms affecting response of Caenorhabditis elegans to the bacterial pathogen Microbacterium nematophilum |
Q34479071 | Mos1-mediated transgenesis to probe consequences of single gene mutations in variation-rich isolates of Caenorhabditis elegans |
Q33967904 | Mosaic analysis using a ncl-1 (+) extrachromosomal array reveals that lin-31 acts in the Pn.p cells during Caenorhabditis elegans vulval development. |
Q21563452 | Most Caenorhabditis elegans microRNAs are individually not essential for development or viability |
Q33543004 | Motor neuron synapse and axon defects in a C. elegans alpha-tubulin mutant |
Q46246221 | Movement decline across lifespan of Caenorhabditis elegans mutants in the insulin/insulin-like signaling pathway |
Q34353629 | Mulberry leaf polyphenols delay aging and regulate fat metabolism via the germline signaling pathway in Caenorhabditis elegans |
Q36401474 | Multi-Toxic Endpoints of the Foodborne Mycotoxins in Nematode Caenorhabditis elegans |
Q27323213 | Multi-environment model estimation for motility analysis of Caenorhabditis elegans |
Q41079373 | Multi-walled carbon nanotubes-induced alterations in microRNA let-7 and its targets activate a protection mechanism by conferring a developmental timing control. |
Q44241192 | Multicomponent DNA vaccine-encoding Toxoplasma gondii GRA1 and SAG1 primes: anti-Toxoplasma immune response in mice |
Q35999665 | Multigenerational Effects of Heavy Metals on Feeding, Growth, Initial Reproduction and Antioxidants in Caenorhabditis elegans |
Q51283806 | Multigenerational exposure to silver ions and silver nanoparticles reveals heightened sensitivity and epigenetic memory in Caenorhabditis elegans. |
Q37597380 | Multigenic natural variation underlies Caenorhabditis elegans olfactory preference for the bacterial pathogen Serratia marcescens |
Q33777976 | Multimodal RNA-seq using single-strand, double-strand, and CircLigase-based capture yields a refined and extended description of the C. elegans transcriptome |
Q89461686 | Multimodal Stimulation in a Microfluidic Device Facilitates Studies of Interneurons in Sensory Integration in C. elegans |
Q33490736 | Multimodal optical workstation for simultaneous linear, nonlinear microscopy and nanomanipulation: upgrading a commercial confocal inverted microscope |
Q30543273 | Multiparameter behavioral analyses provide insights to mechanisms of cyanide resistance in Caenorhabditis elegans. |
Q30529750 | Multiparameter behavioral profiling reveals distinct thermal response regimes in Caenorhabditis elegans |
Q58753327 | Multiple Aspects of PIP2 Involvement in Gametogenesis |
Q91814121 | Multiple Pathways Act Together To Establish Asymmetry of the Ventral Nerve Cord in Caenorhabditis elegans |
Q47781978 | Multiple Signaling Pathways Coordinately Regulate Forgetting of Olfactory Adaptation through Control of Sensory Responses in Caenorhabditis elegans |
Q28477490 | Multiple Wnts redundantly control polarity orientation in Caenorhabditis elegans epithelial stem cells |
Q41664856 | Multiple conserved cell adhesion protein interactions mediate neural wiring of a sensory circuit in C. elegans. |
Q33573214 | Multiple cytoskeletal pathways and PI3K signaling mediate CDC-42-induced neuronal protrusion in C. elegans |
Q34070518 | Multiple doublesex-related genes specify critical cell fates in a C. elegans male neural circuit |
Q35826438 | Multiple excitatory and inhibitory neural signals converge to fine-tune Caenorhabditis elegans feeding to food availability |
Q42853427 | Multiple forms of histone H2B from the nematode Caenorhabditis elegans |
Q33957915 | Multiple functions of let-23, a Caenorhabditis elegans receptor tyrosine kinase gene required for vulval induction. |
Q34589809 | Multiple genes affect sensitivity of Caenorhabditis elegans to the bacterial pathogen Microbacterium nematophilum. |
Q34182444 | Multiple genetic pathways involving the Caenorhabditis elegans Bloom's syndrome genes him-6, rad-51, and top-3 are needed to maintain genome stability in the germ line |
Q36837043 | Multiple levels of redundant processes inhibit Caenorhabditis elegans vulval cell fates |
Q36949298 | Multiple maternal proteins coordinate to restrict the translation of C. elegans nanos-2 to primordial germ cells |
Q34977321 | Multiple mechanisms actively target the SUN protein UNC-84 to the inner nuclear membrane |
Q34071578 | Multiple phenotypes resulting from a mutagenesis screen for pharynx muscle mutations in Caenorhabditis elegans |
Q35932460 | Multiple potential germ-line helicases are components of the germ-line-specific P granules of Caenorhabditis elegans |
Q92913164 | Multiple sensory neurons mediate starvation-dependent aversive navigation in Caenorhabditis elegans |
Q37738405 | Multiple sites of action of volatile anesthetics in Caenorhabditis elegans |
Q33732230 | Multiple transcription factors directly regulate Hox gene lin-39 expression in ventral hypodermal cells of the C. elegans embryo and larva, including the hypodermal fate regulators LIN-26 and ELT-6. |
Q27307993 | Multisite Phosphorylation of NuMA-Related LIN-5 Controls Mitotic Spindle Positioning in C. elegans |
Q88538771 | Multivariate Analysis of Increase in Life Span of Caenorhabditis elegans Through Intestinal Colonization by Indigenous Probiotic Strains |
Q33654037 | Multivesicular body formation requires OSBP-related proteins and cholesterol |
Q46765636 | Munc13-2-/- baseline secretion defect reveals source of oligomeric mucins in mouse airways |
Q64444850 | Munc18-1 and Syntaxin1: Unraveling the Interactions Between the Dynamic Duo |
Q24557450 | Munc18-1 regulates early and late stages of exocytosis via syntaxin-independent protein interactions |
Q49161494 | Munc18-1 tuning of vesicle merger and fusion pore properties. |
Q36992879 | Munc18a scaffolds SNARE assembly to promote membrane fusion |
Q39925840 | Muscle cell migrations of C. elegans are mediated by the alpha-integrin INA-1, Eph receptor VAB-1, and a novel peptidase homologue MNP-1. |
Q41489967 | Muscle organization in Caenorhabditis elegans: localization of proteins implicated in thin filament attachment and I-band organization |
Q30497873 | Muscle type-specific responses to NAD+ salvage biosynthesis promote muscle function in Caenorhabditis elegans |
Q41080899 | Muscle- and Skin-Derived Cues Jointly Orchestrate Patterning of Somatosensory Dendrites |
Q85042543 | Muscleblind participates in RNA toxicity of expanded CAG and CUG repeats in Caenorhabditis elegans |
Q50945535 | Mutagen sensitivity of kynureninase mutants of the nematode Caenorhabditis elegans. |
Q58543907 | Mutagenesis and Imaging Studies of BMP Signaling Mechanisms in C. elegans |
Q40326687 | Mutagenic consequences of a single G-quadruplex demonstrate mitotic inheritance of DNA replication fork barriers. |
Q67014940 | Mutants affecting paramyosin in Caenorhabditis elegans |
Q36355545 | Mutants altering coordinate synthesis of specific myosins during nematode muscle development |
Q47069294 | Mutants of a temperature-sensitive two-P domain potassium channel. |
Q33654163 | Mutation of a Nopp140 gene dao-5 alters rDNA transcription and increases germ cell apoptosis in C. elegans |
Q36531974 | Mutation of a putative sperm membrane protein in Caenorhabditis elegans prevents sperm differentiation but not its associated meiotic divisions |
Q61795915 | Mutation of a single residue promotes gating of vertebrate and invertebrate two-pore domain potassium channels |
Q33819970 | Mutation of the Drosophila vesicular GABA transporter disrupts visual figure detection |
Q37170303 | Mutation of the Enterohemorrhagic Escherichia coli Core LPS Biosynthesis Enzyme RfaD Confers Hypersusceptibility to Host Intestinal Innate Immunity In vivo |
Q34608399 | Mutational analysis of the Caenorhabditis elegans cell-death gene ced-3. |
Q47155049 | Mutational re-modeling of di-aspartyl intramembrane proteases: uncoupling physiologically-relevant activities from those associated with Alzheimer's disease |
Q34612234 | Mutations affecting nerve attachment of Caenorhabditis elegans |
Q34607228 | Mutations affecting symmetrical migration of distal tip cells in Caenorhabditis elegans |
Q33964180 | Mutations affecting the chemosensory neurons of Caenorhabditis elegans |
Q33957122 | Mutations affecting the meiotic and mitotic divisions of the early Caenorhabditis elegans embryo. |
Q33721212 | Mutations in Caenorhabditis elegans him-19 show meiotic defects that worsen with age. |
Q28554423 | Mutations in Nonessential eIF3k and eIF3l Genes Confer Lifespan Extension and Enhanced Resistance to ER Stress in Caenorhabditis elegans |
Q35650374 | Mutations in a C. elegans Gqalpha gene disrupt movement, egg laying, and viability. |
Q30487651 | Mutations in a beta-tubulin disrupt spindle orientation and microtubule dynamics in the early Caenorhabditis elegans embryo |
Q24670180 | Mutations in beta-spectrin disrupt axon outgrowth and sarcomere structure |
Q27316256 | Mutations in conserved residues of the C. elegans microRNA Argonaute ALG-1 identify separable functions in ALG-1 miRISC loading and target repression |
Q36328437 | Mutations in synaptojanin disrupt synaptic vesicle recycling |
Q35651656 | Mutations in the Caenorhabditis elegans Na,K-ATPase alpha-subunit gene, eat-6, disrupt excitable cell function |
Q27348703 | Mutations in the Caenorhabditis elegans U2AF large subunit UAF-1 alter the choice of a 3' splice site in vivo |
Q38667897 | Mutations in the Caenorhabditis elegans orthologs of human genes required for mitochondrial tRNA modification cause similar electron transport chain defects but different nuclear responses. |
Q30999262 | Mutations in the Caenorhabditis elegans serotonin reuptake transporter MOD-5 reveal serotonin-dependent and -independent activities of fluoxetine. |
Q58555514 | Mutations in the Guanylate Cyclase gcy-28 Neuronally Dissociate Naïve Attraction and Memory Retrieval |
Q37634533 | Mutations in the alpha 2(IV) basement membrane collagen gene of Caenorhabditis elegans produce phenotypes of differing severities. |
Q33958446 | Mutations in the bli-4 (I) locus of Caenorhabditis elegans disrupt both adult cuticle and early larval development |
Q36065954 | Mutations in the pqe-1 gene enhance transgene expression in Caenorhabditis elegans |
Q37570648 | Mutations in the rotated abdomen locus affect muscle development and reveal an intrinsic asymmetry in Drosophila. |
Q33959949 | Mutations in the sup-38 gene of Caenorhabditis elegans suppress muscle-attachment defects in unc-52 mutants |
Q33964176 | Mutations in the unc-52 gene responsible for body wall muscle defects in adult Caenorhabditis elegans are located in alternatively spliced exons |
Q34573160 | Mutations of a redundant alpha-tubulin gene affect Caenorhabditis elegans early embryonic cleavage via MEI-1/katanin-dependent and -independent pathways |
Q34570729 | Mutations that rescue the paralysis of Caenorhabditis elegans ric-8 (synembryn) mutants activate the G alpha(s) pathway and define a third major branch of the synaptic signaling network |
Q35083072 | Mutator phenotype of Caenorhabditis elegans DNA damage checkpoint mutants |
Q34386933 | Mutual antagonism between the anaphase promoting complex and the spindle assembly checkpoint contributes to mitotic timing in Caenorhabditis elegans |
Q36261518 | Myosin Storage Myopathy in C. elegans and Human Cultured Muscle Cells |
Q39814824 | Myosin and paramyosin of Caenorhabditis elegans: Biochemical and structural properties of wild-type and mutant proteins |
Q36323415 | Myosin and the PAR proteins polarize microfilament-dependent forces that shape and position mitotic spindles in Caenorhabditis elegans |
Q52486420 | Myosin heavy chain gene amplification as a suppressor mutation in Caenorhabditis elegans. |
Q39519029 | Myosins exist as homodimers of heavy chains: Demonstration with specific antibody purified by nematode mutant myosin affinity chromatography |
Q36293307 | Myotactin, a novel hypodermal protein involved in muscle-cell adhesion in Caenorhabditis elegans |
Q92824690 | Myrciaria tenella (DC.) O. Berg (Myrtaceae) Leaves as a Source of Antioxidant Compounds |
Q32874792 | Myrf ER-Bound Transcription Factors Drive C. elegans Synaptic Plasticity via Cleavage-Dependent Nuclear Translocation |
Q30317803 | Myricetin-mediated lifespan extension in Caenorhabditis elegans is modulated by DAF-16 |
Q92351156 | N-Glycosylation of the Discoidin Domain Receptor Is Required for Axon Regeneration in Caenorhabditis elegans |
Q37446013 | N-Glycosylation regulates fibroblast growth factor receptor/EGL-15 activity in Caenorhabditis elegans in vivo |
Q34629085 | N-acylethanolamine signalling mediates the effect of diet on lifespan in Caenorhabditis elegans |
Q34730895 | N-glycosylation is required for secretion and mitosis in C. elegans |
Q37461454 | N-terminal acetylation promotes synaptonemal complex assembly in C. elegans |
Q96136141 | N6-adenosine methylation of ribosomal RNA affects lipid oxidation and stress resistance |
Q28554749 | NAD+ Is a Food Component That Promotes Exit from Dauer Diapause in Caenorhabditis elegans |
Q37023627 | NAD+ Supplementation Attenuates Methylmercury Dopaminergic and Mitochondrial Toxicity in Caenorhabditis Elegans |
Q37585797 | NADPH oxidase-mediated redox signaling promotes oxidative stress resistance and longevity through memo-1 in C. elegans |
Q37265148 | NALCN channelopathies: Distinguishing gain-of-function and loss-of-function mutations |
Q46303329 | NCEH-1 modulates cholesterol metabolism and protects against α-synuclein toxicity in a C. elegans model of Parkinson's disease |
Q24683670 | NDC1: a crucial membrane-integral nucleoporin of metazoan nuclear pore complexes |
Q35128017 | NDK-1, the homolog of NM23-H1/H2 regulates cell migration and apoptotic engulfment in C. elegans |
Q48219671 | NECAPs are negative regulators of the AP2 clathrin adaptor complex |
Q83228002 | NHR-14 loss of function couples intestinal iron uptake with innate immunity in through PQM-1 signaling |
Q35382002 | NHR-23 dependent collagen and hedgehog-related genes required for molting. |
Q97529838 | NMDAR-mediated modulation of gap junction circuit regulates olfactory learning in C. elegans |
Q29032831 | NMR spectroscopy of single sub-nL ova with inductive ultra-compact single-chip probes |
Q30495469 | NMY-2 maintains cellular asymmetry and cell boundaries, and promotes a SRC-dependent asymmetric cell division |
Q40691964 | NPR-9 regulates the innate immune response in Caenorhabditis elegans by antagonizing the activity of AIB interneurons |
Q37727615 | NRA-2, a nicalin homolog, regulates neuronal death by controlling surface localization of toxic Caenorhabditis elegans DEG/ENaC channels |
Q34391269 | NRFL-1, the C. elegans NHERF orthologue, interacts with amino acid transporter 6 (AAT-6) for age-dependent maintenance of AAT-6 on the membrane |
Q37137329 | NSBP-1 mediates the effects of cholesterol on insulin/IGF-1 signaling in Caenorhabditis elegans. |
Q40442315 | NUC-1, a caenorhabditis elegans DNase II homolog, functions in an intermediate step of DNA degradation during apoptosis |
Q90493968 | Nanoluciferase-Based Method for Detecting Gene Expression in Caenorhabditis elegans |
Q47136549 | Nanos promotes epigenetic reprograming of the germline by down-regulation of the THAP transcription factor LIN-15B. |
Q46091759 | Nanoscale organization of the MEC-4 DEG/ENaC sensory mechanotransduction channel in Caenorhabditis elegans touch receptor neurons. |
Q35960403 | Natural Genetic Variation Influences Protein Abundances in C. elegans Developmental Signalling Pathways. |
Q37746436 | Natural Genetic Variation in the Caenorhabditis elegans Response to Pseudomonas aeruginosa. |
Q35657447 | Natural Marine and Synthetic Xenobiotics Get on Nematode's Nerves: Neuro-Stimulating and Neurotoxic Findings in Caenorhabditis elegans |
Q35002352 | Natural genetic variation determines susceptibility to aggregation or toxicity in a C. elegans model for polyglutamine disease |
Q35633090 | Natural polymorphisms in C. elegans HECW-1 E3 ligase affect pathogen avoidance behaviour |
Q33784713 | Natural reversal of left-right gut/gonad asymmetry in C. elegans males is independent of embryonic chirality |
Q36602394 | Natural thioallyl compounds increase oxidative stress resistance and lifespan in Caenorhabditis elegans by modulating SKN-1/Nrf |
Q34473095 | Natural variants of C. elegans demonstrate defects in both sperm function and oogenesis at elevated temperatures |
Q33969902 | Natural variation and copulatory plug formation in Caenorhabditis elegans |
Q51889198 | Natural variation in Pristionchus pacificus dauer formation reveals cross-preference rather than self-preference of nematode dauer pheromones. |
Q41872602 | Natural variation in chemosensation: lessons from an island nematode |
Q64098162 | Natural variation in the roles of C. elegans autophagy components during microsporidia infection |
Q33432334 | Natural variation of outcrossing in the hermaphroditic nematode Pristionchus pacificus. |
Q27316095 | Navigational choice between reversal and curve during acidic pH avoidance behavior in Caenorhabditis elegans |
Q64227772 | Necessity and Contingency in Developmental Genetic Screens: EGF, Wnt, and Semaphorin Pathways in Vulval Induction of the Nematode |
Q27311005 | Necrotic Cells Actively Attract Phagocytes through the Collaborative Action of Two Distinct PS-Exposure Mechanisms |
Q37068977 | Negative regulation of Caenorhabditis elegans epidermal damage responses by death-associated protein kinase |
Q35198560 | Negative regulation of male development in Caenorhabditis elegans by a protein-protein interaction between TRA-2A and FEM-3. |
Q24310850 | Negative regulation of the heat shock transcriptional response by HSBP1 |
Q51323100 | NemaCount: quantification of nematode chemotaxis behavior in a browser. |
Q89072309 | NemaFlex: a microfluidics-based technology for standardized measurement of muscular strength of C. elegans |
Q64100805 | Nematicidal actions of the marigold exudate α-terthienyl: oxidative stress-inducing compound penetrates nematode hypodermis |
Q30935415 | Nematicidal activity of Annona crassiflora leaf extract on Caenorhabditis elegans |
Q37913148 | Nematode and snail metallothioneins. |
Q26849700 | Nematode endogenous small RNA pathways |
Q36783860 | Nematode repetitive DNA with ARS and segregation function in Saccharomyces cerevisiae |
Q36430262 | Nematode-bacterium symbioses--cooperation and conflict revealed in the "omics" age. |
Q33883789 | Nematodes: the worm and its relatives |
Q30480880 | Nemo: a computational tool for analyzing nematode locomotion |
Q39786672 | Nerves and genes |
Q92335644 | Nervous system-wide profiling of presynaptic mRNAs reveals regulators of associative memory |
Q24632608 | Netrin (UNC-6) mediates dendritic self-avoidance |
Q78094933 | Netrin UNC-6 and the regulation of branching and extension of motoneuron axons from the ventral nerve cord of Caenorhabditis elegans |
Q27315845 | Netrins and Wnts function redundantly to regulate antero-posterior and dorso-ventral guidance in C. elegans |
Q40517050 | NeuCode Labeling in Nematodes: Proteomic and Phosphoproteomic Impact of Ascaroside Treatment in Caenorhabditis elegans |
Q35537393 | Neural Mechanisms for Evaluating Environmental Variability in Caenorhabditis elegans |
Q35865632 | Neural activity and CaMKII protect mitochondria from fragmentation in aging Caenorhabditis elegans neurons. |
Q30585942 | Neural and genetic degeneracy underlies Caenorhabditis elegans feeding behavior |
Q36914946 | Neural and molecular dissection of a C. elegans sensory circuit that regulates fat and feeding |
Q33290608 | Neural circuits mediate electrosensory behavior in Caenorhabditis elegans |
Q35210793 | Neural integrity is maintained by dystrophin in C. elegans |
Q35863078 | Neural maintenance roles for the matrix receptor dystroglycan and the nuclear anchorage complex in Caenorhabditis elegans |
Q36689215 | Neural regulation of thermotaxis in Caenorhabditis elegans |
Q30448488 | Neurexin and neuroligin mediate retrograde synaptic inhibition in C. elegans |
Q36189451 | Neurite sprouting and synapse deterioration in the aging Caenorhabditis elegans nervous system |
Q27318906 | NeuroChip: a microfluidic electrophysiological device for genetic and chemical biology screening of Caenorhabditis elegans adult and larvae |
Q37151213 | Neurobiological applications of small molecule screening |
Q37759354 | Neurodegenerative disorders: insights from the nematode Caenorhabditis elegans |
Q39407786 | Neuroendocrine Coordination of Mitochondrial Stress Signaling and Proteostasis. |
Q92334304 | Neuroendocrine regulation of fat metabolism by autophagy gene atg-18 in C. elegans dauer larvae |
Q59794156 | Neurohormonal signaling via a sulfotransferase antagonizes insulin-like signaling to regulate a Caenorhabditis elegans stress response |
Q42446057 | Neuroligin modulates the locomotory dopaminergic and serotonergic neuronal pathways of C. elegans |
Q33798705 | Neuroligin-deficient mutants of C. elegans have sensory processing deficits and are hypersensitive to oxidative stress and mercury toxicity |
Q92461952 | Neurological Disorder Brain Model: A Lesson from Marine Worms (Annelida: Polychaeta) |
Q43099242 | Neuron dysfunction is induced by prion protein with an insertional mutation via a Fyn kinase and reversed by sirtuin activation in Caenorhabditis elegans. |
Q37343801 | Neuron type-specific miRNA represses two broadly expressed genes to modulate an avoidance behavior in C. elegans |
Q27319919 | Neuron-specific feeding RNAi in C. elegans and its use in a screen for essential genes required for GABA neuron function |
Q28818674 | Neuron-specific knock-down of SMN1 causes neuron degeneration and death through an apoptotic mechanism |
Q30502208 | Neuron-specific proteotoxicity of mutant ataxin-3 in C. elegans: rescue by the DAF-16 and HSF-1 pathways |
Q33473897 | Neuron-specific regulation of associative learning and memory by MAGI-1 in C. elegans |
Q55179733 | Neuron-specific regulation of superoxide dismutase amid pathogen-induced gut dysbiosis. |
Q91676774 | Neuronal GPCR NPR-8 regulates C. elegans defense against pathogen infection |
Q37408322 | Neuronal GPCR OCTR-1 regulates innate immunity by controlling protein synthesis in Caenorhabditis elegans |
Q27318747 | Neuronal Goα and CAPS regulate behavioral and immune responses to bacterial pore-forming toxins |
Q83230263 | Neuronal TORC1 modulates longevity via AMPK and cell nonautonomous regulation of mitochondrial dynamics in |
Q91863033 | Neuronal XBP-1 Activates Intestinal Lysosomes to Improve Proteostasis in C. elegans |
Q55164268 | Neuronal and non-neuronal signals regulate Caernorhabditis elegans avoidance of contaminated food. |
Q34759983 | Neuronal cell shape and neurite initiation are regulated by the Ndr kinase SAX-1, a member of the Orb6/COT-1/warts serine/threonine kinase family |
Q37733920 | Neuronal function of the mRNA decapping complex determines survival of Caenorhabditis elegans at high temperature through temporal regulation of heterochronic gene expression |
Q47838565 | Neuronal inhibition of the autophagy nucleation complex extends life span in post-reproductive C. elegans. |
Q28657860 | Neuronal migration is regulated by endogenous RNAi and chromatin-binding factor ZFP-1/AF10 in Caenorhabditis elegans |
Q48440701 | Neuronal recognition and synaptogenesis |
Q27320800 | Neuronal reprograming of protein homeostasis by calcium-dependent regulation of the heat shock response |
Q36103669 | Neuronal signaling modulates protein homeostasis in Caenorhabditis elegans post-synaptic muscle cells |
Q27321344 | Neuronal target identification requires AHA-1-mediated fine-tuning of Wnt signaling in C. elegans |
Q45061866 | Neuronal toxicity in Caenorhabditis elegans from an editing site mutant in glutamate receptor channels. |
Q27318339 | Neurons refine the Caenorhabditis elegans body plan by directing axial patterning by Wnts |
Q71971010 | Neuropathology of degenerative cell death in Caenorhabditis elegans |
Q38069826 | Neuropeptide GPCRs in C. elegans |
Q39719034 | Neuropeptide feedback modifies odor-evoked dynamics in Caenorhabditis elegans olfactory neurons |
Q30539729 | Neuropeptide secreted from a pacemaker activates neurons to control a rhythmic behavior. |
Q37206950 | Neuropeptide signaling remodels chemosensory circuit composition in Caenorhabditis elegans |
Q36690118 | Neuropeptidergic Signaling and Active Feeding State Inhibit Nociception in Caenorhabditis elegans |
Q37130942 | Neuropeptides amplify and focus the monoaminergic inhibition of nociception in Caenorhabditis elegans |
Q58753527 | Neuropeptides encoded by modulate locomotion, arousal and egg-laying behaviours in via the receptor SEB-3 |
Q35548900 | Neuroprotective effects of the cultivated Chondrus crispus in a C. elegans model of Parkinson's disease |
Q36395912 | Neurosecretory control of aging in Caenorhabditis elegans |
Q37055480 | Neurotoxic unc-8 mutants encode constitutively active DEG/ENaC channels that are blocked by divalent cations |
Q54293497 | Neurotoxicological evaluation of microcystin-LR exposure at environmental relevant concentrations on nematode Caenorhabditis elegans. |
Q30476174 | Neurotoxin-induced degeneration of dopamine neurons in Caenorhabditis elegans |
Q41011634 | Neurotransmitter signaling through heterotrimeric G proteins: insights from studies in C. elegans |
Q34617669 | New Genes That Interact With lin-35 Rb to Negatively Regulate the let-60 ras Pathway in Caenorhabditis elegans |
Q35821066 | New Insights into the Post-Translational Regulation of DNA Damage Response and Double-Strand Break Repair in Caenorhabditis elegans |
Q35125807 | New genes that extend Caenorhabditis elegans' lifespan in response to reproductive signals |
Q24811634 | New genes tied to endocrine, metabolic, and dietary regulation of lifespan from a Caenorhabditis elegans genomic RNAi screen |
Q36266097 | New genetic regulators question relevance of abundant yolk protein production in C. elegans |
Q37779462 | New haystacks reveal new needles: using Caenorhabditis elegans to identify novel targets for ameliorating body composition changes during human aging |
Q91915881 | New label-free automated survival assays reveal unexpected stress resistance patterns during C. elegans aging |
Q34424915 | New positive regulators of lin-12 activity in Caenorhabditis elegans include the BRE-5/Brainiac glycosphingolipid biosynthesis enzyme. |
Q33518319 | New tools for investigating the comparative biology of Caenorhabditis briggsae and C. elegans |
Q38978311 | Next-Generation Sequencing-Based Approaches for Mutation Mapping and Identification in Caenorhabditis elegans |
Q89489188 | Niche Cell Wrapping Ensures Primordial Germ Cell Quiescence and Protection from Intercellular Cannibalism |
Q37385509 | Nicotinamidase modulation of NAD+ biosynthesis and nicotinamide levels separately affect reproductive development and cell survival in C. elegans |
Q28822035 | Nicotinamide is an endogenous agonist for a C. elegans TRPV OSM-9 and OCR-4 channel |
Q36847553 | Nicotinamide mononucleotide adenylyltransferase promotes hypoxic survival by activating the mitochondrial unfolded protein response |
Q36972561 | Nicotine exposure and transgenerational impact: a prospective study on small regulatory microRNAs |
Q53398764 | Nictation, a dispersal behavior of the nematode Caenorhabditis elegans, is regulated by IL2 neurons. |
Q34778005 | Nidogen is nonessential and not required for normal type IV collagen localization in Caenorhabditis elegans |
Q37678601 | Nitazoxanide: nematicidal mode of action and drug combination studies |
Q35949831 | Nitrate sensing and metabolism modulate motility, biofilm formation, and virulence in Pseudomonas aeruginosa |
Q35065515 | Nitrogen metabolite repression of metabolism and virulence in the human fungal pathogen Cryptococcus neoformans |
Q34515662 | Nitrous oxide (N(2)O) requires the N-methyl-D-aspartate receptor for its action in Caenorhabditis elegans |
Q93215855 | Non-Ionic Surfactants Antagonize Toxicity of Potential Phenolic Endocrine-Disrupting Chemicals, Including Triclosan in Caenorhabditis elegans |
Q35608882 | Non-autonomous DAF-16/FOXO activity antagonizes age-related loss of C. elegans germline stem/progenitor cells |
Q93185875 | Non-canonical activation of CREB mediates neuroprotection in a Caenorhabditis elegans model of excitotoxic necrosis |
Q46473095 | Non-centrosomal epidermal microtubules act in parallel to LET-502/ROCK to promote C. elegans elongation |
Q37581650 | Non-linear impact of glutathione depletion on C. elegans life span and stress resistance |
Q27349046 | Non-lytic, actin-based exit of intracellular parasites from C. elegans intestinal cells |
Q27302293 | Non-microfluidic methods for imaging live C. elegans |
Q42202414 | Non-muscle myosin II is required for correct fate specification in the Caenorhabditis elegans seam cell divisions |
Q46456620 | Non-neuronal cell outgrowth in C. elegans |
Q28487899 | Non-specific protein modifications by a phytochemical induce heat shock response for self-defense |
Q42363578 | Nonautonomous Roles of MAB-5/Hox and the Secreted Basement Membrane Molecule SPON-1/F-Spondin in Caenorhabditis elegans Neuronal Migration |
Q42693068 | Nonautonomous regulation of neuronal migration by insulin signaling, DAF-16/FOXO, and PAK-1 |
Q33973337 | Noncanonical cell death in the nematode Caenorhabditis elegans |
Q42093745 | Noncell- and cell-autonomous G-protein-signaling converges with Ca2+/mitogen-activated protein kinase signaling to regulate str-2 receptor gene expression in Caenorhabditis elegans |
Q34605661 | Nondisjunction Mutants of the Nematode CAENORHABDITIS ELEGANS. |
Q55515706 | Noninvasive Mechanochemical Imaging in Unconstrained Caenorhabditis elegans. |
Q36540356 | Nonmuscle myosin IIB links cytoskeleton to IRE1α signaling during ER stress. |
Q47198829 | Nonsense mRNA suppression via nonstop decay |
Q34506264 | Normal and mutant thermotaxis in the nematode Caenorhabditis elegans |
Q33834326 | Normal ciliogenesis requires synergy between the cystic kidney disease genes MKS-3 and NPHP-4. |
Q30488186 | Normal formation of a subset of intestinal granules in Caenorhabditis elegans requires ATP-binding cassette transporters HAF-4 and HAF-9, which are highly homologous to human lysosomal peptide transporter TAP-like |
Q50420128 | Normal sleep bouts are not essential for C. elegans survival and FoxO is important for compensatory changes in sleep. |
Q41959910 | Notch and Ras promote sequential steps of excretory tube development in C. elegans |
Q34287433 | Notch and the awesome power of genetics |
Q38884385 | Notch is a direct negative regulator of the DNA-damage response |
Q36732362 | Notch signaling and morphogenesis of single-cell tubes in the C. elegans digestive tract |
Q35810761 | Notch signaling is antagonized by SAO-1, a novel GYF-domain protein that interacts with the E3 ubiquitin ligase SEL-10 in Caenorhabditis elegans |
Q35989792 | Novel DLK-independent neuronal regeneration in Caenorhabditis elegans shares links with activity-dependent ectopic outgrowth |
Q43055674 | Novel EGF pathway regulators modulate C. elegans healthspan and lifespan via EGF receptor, PLC-gamma, and IP3R activation |
Q112285152 | Novel Extraction Method for Combined Lipid and Metal Speciation From Caenorhabditis elegans With Focus on Iron Redox Status and Lipid Profiling |
Q59808951 | Novel Findings of Anti-Filarial Drug Target and Structure-Based Virtual Screening for Drug Discovery |
Q64079923 | Novel Genes Involved in Formation of the Tubular Excretory Canals of |
Q33877282 | Novel Mutations in Synaptic Transmission Genes Suppress Neuronal Hyperexcitation in Caenorhabditis elegans |
Q90278121 | Novel Technological Advances in Functional Connectomics in C. elegans |
Q30537740 | Novel acid-activated fluorophores reveal a dynamic wave of protons in the intestine of Caenorhabditis elegans |
Q97528056 | Novel actions of arecoline in the C. elegans motor circuit |
Q27342275 | Novel and conserved protein macoilin is required for diverse neuronal functions in Caenorhabditis elegans |
Q43738966 | Novel antinematodal and antiparasitic agents from Penicillium charlesii. I. Fermentation, isolation and biological activity |
Q38709788 | Novel functions for the RNA-binding protein ETR-1 in Caenorhabditis elegans reproduction and engulfment of germline apoptotic cell corpses |
Q35150105 | Novel functions of lipid-binding protein 5 in Caenorhabditis elegans fat metabolism |
Q36884074 | Novel insertion mutation in Caenorhabditis elegans |
Q42959198 | Novel nematode amber suppressors. |
Q27333876 | Novel polyglutamine model uncouples proteotoxicity from aging |
Q37643848 | Novel role for the yceGH tellurite resistance genes in the pathogenesis of Bacillus anthracis |
Q35665625 | Novel roles of Caenorhabditis elegans heterochromatin protein HP1 and linker histone in the regulation of innate immune gene expression |
Q35862438 | Novel structural arrangement of nematode cystathionine β-synthases: characterization of Caenorhabditis elegans CBS-1. |
Q36976860 | Nuclear Envelope Retention of LINC Complexes Is Promoted by SUN-1 Oligomerization in the Caenorhabditis elegans Germ Line |
Q55362765 | Nuclear Export Inhibition Enhances HLH-30/TFEB Activity, Autophagy, and Lifespan. |
Q24681591 | Nuclear Pore Protein gp210 Is Essential for Viability in HeLa Cells andCaenorhabditis elegans |
Q33778478 | Nuclear entry of a cGMP-dependent kinase converts transient into long-lasting olfactory adaptation |
Q52318700 | Nuclear export of ubiquitinated proteins via the UBIN-POST system. |
Q33899506 | Nuclear pre-mRNA 3'-end processing regulates synapse and axon development in C. elegans |
Q46799501 | Nuclei migrate through constricted spaces using microtubule motors and actin networks in C. elegans hypodermal cells |
Q41900455 | Nucleolar GTPase NOG-1 regulates development, fat storage, and longevity through insulin/IGF signaling in C. elegans |
Q58761890 | Nucleolar fibrillarin is an evolutionarily conserved regulator of bacterial pathogen resistance |
Q27349004 | Nucleolar proteins suppress Caenorhabditis elegans innate immunity by inhibiting p53/CEP-1 |
Q34461760 | Nucleoporins NPP-1, NPP-3, NPP-4, NPP-11 and NPP-13 are required for proper spindle orientation in C. elegans |
Q38738924 | Nucleotide Excision Repair in Caenorhabditis elegans |
Q36549516 | Nucleotide levels regulate germline proliferation through modulating GLP-1/Notch signaling in C. elegans. |
Q34611115 | Null mutations in the lin-31 gene indicate two functions during Caenorhabditis elegans vulval development |
Q36610099 | Number and organization of collagen genes in Caenorhabditis elegans |
Q58754351 | Nutrient-Driven -GlcNAcylation at Promoters Impacts Genome-Wide RNA Pol II Distribution |
Q47988632 | Nutritional Interventions for Mitochondrial OXPHOS Deficiencies: Mechanisms and Model Systems. |
Q42056793 | Nutritional Programming of Lifespan by FOXO Inhibition on Sugar-Rich Diets. |
Q40742097 | Nutritional factors and conditions for the axenic culture of free-living nematodes |
Q37041248 | O2-sensing neurons control CO2 response in C. elegans |
Q64992455 | OFF-responses of interneurons optimize avoidance behaviors depending on stimulus strength via electrical synapses. |
Q34442691 | OSM-9, a novel protein with structural similarity to channels, is required for olfaction, mechanosensation, and olfactory adaptation in Caenorhabditis elegans |
Q37056124 | Octopamine connects nutrient cues to lipid metabolism upon nutrient deprivation. |
Q57291155 | Octopaminergic Signaling Mediates Neural Regulation of Innate Immunity in Caenorhabditis elegans |
Q55096321 | Odor-dependent temporal dynamics in Caenorhabitis elegans adaptation and aversive learning behavior. |
Q61207026 | Odour concentration-dependent olfactory preference change in C. elegans |
Q42415237 | Of fish, flies, worms and men: powerful approaches to neuropsychiatric disease using genetic models |
Q90172835 | Olfaction regulates organismal proteostasis and longevity via microRNA-dependent signaling |
Q40289315 | Olfactory Preferences of the Parasitic Nematode Howardula aoronymphium and its Insect Host Drosophila falleni. |
Q35994965 | Oligoarray comparative genomic hybridization-mediated mapping of suppressor mutations generated in a deletion-biased mutagenesis screen |
Q33305159 | Oligonucleotide Array Comparative Genomic Hybridization (oaCGH) based characterization of genetic deficiencies as an aid to gene mapping in Caenorhabditis elegans |
Q28769794 | On the evolution of early development in the Nematoda. |
Q39175012 | On the nature of in vivo requirements for rde-4 in RNAi and developmental pathways in C. elegans |
Q27333513 | On-Demand Isolation and Manipulation of C. elegans by In Vitro Maskless Photopatterning |
Q47644371 | On-chip functional neuroimaging with mechanical stimulation in Caenorhabditis elegans larvae for studying development and neural circuits |
Q34616610 | One lucky XX male: isolation of the first Caenorhabditis elegans sex-determination mutants |
Q72636515 | Ontogeny of maternal and newly transcribed mRNA analyzed by in situ hybridization during development of Caenorhabditis elegans |
Q24796265 | Oocyte production and sperm utilization patterns in semi-fertile strains of Caenorhabditis elegans |
Q28833838 | Opiates Modulate Noxious Chemical Nociception through a Complex Monoaminergic/Peptidergic Cascade |
Q37015508 | Opposing Wnt pathways orient cell polarity during organogenesis |
Q57136647 | Optical imaging of metabolic dynamics in animals |
Q30500855 | Optical interrogation of neural circuits in Caenorhabditis elegans |
Q48342662 | Optical silencing of body wall muscles induces pumping inhibition in Caenorhabditis elegans. |
Q40690383 | Optimization of ZnO-NPs to Investigate Their Safe Application by Assessing Their Effect on Soil Nematode Caenorhabditis elegans |
Q33410837 | Optimizing dietary restriction for genetic epistasis analysis and gene discovery in C. elegans |
Q39136284 | Optogenetic Random Mutagenesis Using Histone-miniSOG in C. elegans |
Q27323978 | Optogenetic activation of axon guidance receptors controls direction of neurite outgrowth |
Q35160393 | Optogenetic analysis of GABAB receptor signaling in Caenorhabditis elegans motor neurons |
Q58775503 | Optogenetic dissection of mitotic spindle positioning in vivo |
Q27347521 | Optogenetic long-term manipulation of behavior and animal development |
Q30664442 | Optogenetic manipulation of cGMP in cells and animals by the tightly light-regulated guanylyl-cyclase opsin CyclOp |
Q43120887 | Optogenetic mutagenesis in Caenorhabditis elegans |
Q58733576 | Ordered arrangement of dendrites within a sensory nerve bundle |
Q36867969 | Organ Length Control by an ADAMTS Extracellular Protease in Caenorhabditis elegans |
Q82489124 | Organic carbon source in formulated sediments influences life traits and gene expression of Caenorhabditis elegans |
Q92897306 | Organic solvents can influence acetylcholine neurotransmission in Caenorhabditis elegans |
Q36205411 | Organismal regulation of XBP-1-mediated unfolded protein response during development and immune activation |
Q42993272 | Organization and alternative splicing of the Caenorhabditis elegans cAMP-dependent protein kinase catalytic-subunit gene (kin-1). |
Q41254198 | Organization of neuronal microtubules in the nematode Caenorhabditis elegans |
Q35298005 | Organization of the synaptonemal complex during meiosis in Caenorhabditis elegans |
Q55026709 | Organoruthenium(II) Complexes Ameliorates Oxidative Stress and Impedes the Age Associated Deterioration in Caenorhabditis elegans through JNK-1/DAF-16 Signalling. |
Q35926030 | Organotellurium and organoselenium compounds attenuate Mn-induced toxicity in Caenorhabditis elegans by preventing oxidative stress. |
Q35822712 | Oriented Cell Division in the C. elegans Embryo Is Coordinated by G-Protein Signaling Dependent on the Adhesion GPCR LAT-1. |
Q42175755 | Orthosiphon stamineus protects Caenorhabditis elegans against Staphylococcus aureus infection through immunomodulation |
Q36493700 | Oscillatory Ca2+ signaling in the isolated Caenorhabditis elegans intestine: role of the inositol-1,4,5-trisphosphate receptor and phospholipases C beta and gamma |
Q41898432 | Osmotic avoidance defective mutants of the nematode Caenorhabditis elegans |
Q34290559 | Otx-dependent expression of proneural bHLH genes establishes a neuronal bilateral asymmetry in C. elegans. |
Q33811376 | Outcrossing and the maintenance of males within C. elegans populations |
Q35222713 | Overcoming redundancy: an RNAi enhancer screen for morphogenesis genes in Caenorhabditis elegans |
Q52430850 | Overlapping expression patterns and functions of three paralogous P5B ATPases in Caenorhabditis elegans. |
Q26749061 | Overview of Alzheimer's Disease and Some Therapeutic Approaches Targeting Aβ by Using Several Synthetic and Herbal Compounds |
Q34764146 | Oxidoreductases that act as conditional virulence suppressors in Salmonella enterica serovar Typhimurium |
Q35195490 | Oxygen sensing neurons and neuropeptides regulate survival after anoxia in developing C. elegans |
Q54966137 | Oxygen-sensing neurons reciprocally regulate peripheral lipid metabolism via neuropeptide signaling in Caenorhabditis elegans. |
Q34712466 | P granules extend the nuclear pore complex environment in the C. elegans germ line |
Q27312100 | P-type ATPase TAT-2 negatively regulates monomethyl branched-chain fatty acid mediated function in post-embryonic growth and development in C. elegans |
Q35075872 | PAB-1, a Caenorhabditis elegans poly(A)-binding protein, regulates mRNA metabolism in germline by interacting with CGH-1 and CAR-1. |
Q36491719 | PAR proteins direct asymmetry of the cell cycle regulators Polo-like kinase and Cdc25. |
Q42167958 | PAR proteins regulate maintenance-phase myosin dynamics during Caenorhabditis elegans zygote polarization |
Q36783135 | PAR-2, LGL-1 and the CDC-42 GAP CHIN-1 act in distinct pathways to maintain polarity in the C. elegans embryo |
Q30480313 | PAR-3 and PAR-1 inhibit LET-99 localization to generate a cortical band important for spindle positioning in Caenorhabditis elegans embryos |
Q35224029 | PAR-3 oligomerization may provide an actin-independent mechanism to maintain distinct par protein domains in the early Caenorhabditis elegans embryo |
Q33663198 | PAR-4/LKB1 regulates DNA replication during asynchronous division of the early C. elegans embryo |
Q42428878 | PAR-6, but not E-cadherin and β-integrin, is necessary for epithelial polarization in C. elegans |
Q36325026 | PAR-dependent and geometry-dependent mechanisms of spindle positioning |
Q56533458 | PDF-1 neuropeptide signaling regulates sexually dimorphic gene expression in shared sensory neurons of |
Q34358948 | PDHK-2 deficiency is associated with attenuation of lipase-mediated fat consumption for the increased survival of Caenorhabditis elegans dauers |
Q30575316 | PDR-1/hParkin negatively regulates the phagocytosis of apoptotic cell corpses in Caenorhabditis elegans. |
Q92417839 | PETISCO is a novel protein complex required for 21U RNA biogenesis and embryonic viability |
Q36563438 | PGL germ granule assembly protein is a base-specific, single-stranded RNase |
Q24632882 | PGL proteins self associate and bind RNPs to mediate germ granule assembly in C. elegans |
Q35758336 | PHA-4/FoxA cooperates with TAM-1/TRIM to regulate cell fate restriction in the C. elegans foregut |
Q57046164 | PIE-1 Translation in the Germline Lineage Contributes to PIE-1 Asymmetry in the Early Embryo |
Q35078092 | PIE-1 is a bifunctional protein that regulates maternal and zygotic gene expression in the embryonic germ line of Caenorhabditis elegans |
Q99568699 | PIG-1 MELK-dependent phosphorylation of nonmuscle myosin II promotes apoptosis through CES-1 Snail partitioning |
Q92459450 | PIM-Related Kinases Selectively Regulate Olfactory Sensations in Caenorhabditis elegans |
Q36877291 | PKC-1 acts with the ERK MAPK signaling pathway to regulate Caenorhabditis elegans mechanosensory response |
Q100496372 | PLK-1 promotes the merger of the parental genome into a single nucleus by triggering lamina disassembly |
Q39012724 | PLK1 (polo like kinase 1) inhibits MTOR complex 1 and promotes autophagy |
Q39882749 | PPM-1, a PP2Cα/β phosphatase, regulates axon termination and synapse formation in Caenorhabditis elegans |
Q42585902 | PQM-1 complements DAF-16 as a key transcriptional regulator of DAF-2-mediated development and longevity |
Q41663092 | PQN-75 is expressed in the pharyngeal gland cells of Caenorhabditiselegans and is dispensable for germline development |
Q33588098 | PRDE-1 is a nuclear factor essential for the biogenesis of Ruby motif-dependent piRNAs in C. elegans |
Q36943578 | PRG-1 and 21U-RNAs interact to form the piRNA complex required for fertility in C. elegans |
Q34989684 | PRP-17 and the pre-mRNA splicing pathway are preferentially required for the proliferation versus meiotic development decision and germline sex determination in Caenorhabditis elegans |
Q90251987 | PRP-19, a conserved pre-mRNA processing factor and E3 ubiquitin ligase, inhibits the nuclear accumulation of GLP-1/Notch intracellular domain |
Q58601608 | PRY-1/Axin signaling regulates lipid metabolism in Caenorhabditis elegans |
Q33947097 | PS1 N- and C-terminal fragments form a complex that functions in APP processing and Notch signaling |
Q28482319 | PTEN negatively regulates MAPK signaling during Caenorhabditis elegans vulval development |
Q37599085 | PTRN-1, a microtubule minus end-binding CAMSAP homolog, promotes microtubule function in Caenorhabditis elegans neurons |
Q35926411 | PUF-8 Functions Redundantly with GLD-1 to Promote the Meiotic Progression of Spermatocytes in Caenorhabditis elegans |
Q36648653 | PUF-8 and TCER-1 are essential for normal levels of multiple mRNAs in the C. elegans germline |
Q39719162 | PUF-8 negatively regulates RAS/MAPK signalling to promote differentiation of C. elegans germ cells |
Q37076781 | PUF-8 suppresses the somatic transcription factor PAL-1 expression in C. elegans germline stem cells |
Q36297153 | PUF-8, a Pumilio homolog, inhibits the proliferative fate in the Caenorhabditis elegans germline |
Q33874562 | Paired and LIM class homeodomain proteins coordinate differentiation of the C. elegans ALA neuron |
Q64268135 | Pairing of homologous chromosomes in C. elegans meiosis requires DEB-1 - an orthologue of mammalian vinculin |
Q36498331 | Palmitoylation controls DLK localization, interactions and activity to ensure effective axonal injury signaling |
Q36974448 | Pan-neuronal expression of APL-1, an APP-related protein, disrupts olfactory, gustatory, and touch plasticity in Caenorhabditis elegans |
Q33436579 | Parallel use of two behavioral mechanisms for chemotaxis in Caenorhabditis elegans. |
Q37390597 | Parasite neuropeptide biology: Seeding rational drug target selection? |
Q33587754 | Partitioning the C. elegans genome by nucleosome modification, occupancy, and positioning |
Q59092753 | Past experience shapes sexually dimorphic neuronal wiring through monoaminergic signalling |
Q64956272 | Pasteurized Orange Juice Rich in Carotenoids Protects Caenorhabditis elegans against Oxidative Stress and β-Amyloid Toxicity through Direct and Indirect Mechanisms. |
Q34332378 | Paternal RNA contributions in the Caenorhabditis elegans zygote |
Q34418807 | Pathogen-induced Caenorhabditis elegans developmental plasticity has a hormetic effect on the resistance to biotic and abiotic stresses |
Q58795146 | Pathogenesis of the Candida parapsilosis Complex in the Model Host Caenorhabditis elegans |
Q64095606 | Pathogenetic basis of Takenouchi-Kosaki syndrome: Electron microscopy study using platelets in patients and functional studies in a Caenorhabditis elegans model |
Q31101613 | Pathogenicity of Salmonella enterica in Caenorhabditis elegans relies on disseminated oxidative stress in the infected host |
Q48096252 | Pathological phosphorylation of tau and TDP-43 by TTBK1 and TTBK2 drives neurodegeneration |
Q41682254 | Patterns of proteins synthesized during development of Caenorhabditis elegans |
Q99603700 | Peel-1 negative selection promotes screening-free CRISPR-Cas9 genome editing in Caenorhabditis elegans |
Q36035262 | Perilipin-related protein regulates lipid metabolism in C. elegans |
Q33761242 | Perinuclear P granules are the principal sites of mRNA export in adult C. elegans germ cells |
Q42463273 | Perlecan antagonizes collagen IV and ADAMTS9/GON-1 in restricting the growth of presynaptic boutons |
Q41081731 | Persistence of Long-Term Memory in Vitrified and Revived Caenorhabditis elegans |
Q38814024 | Persistent cell migration and adhesion rely on retrograde transport of β(1) integrin. |
Q34151165 | Pervasive and cooperative deadenylation of 3'UTRs by embryonic microRNA families. |
Q27333604 | Phagocytic receptor CED-1 initiates a signaling pathway for degrading engulfed apoptotic cells |
Q30572432 | Phagocytic receptor signaling regulates clathrin and epsin-mediated cytoskeletal remodeling during apoptotic cell engulfment in C. elegans |
Q34769525 | Pharmacological activation of Sirt1 ameliorates polyglutamine-induced toxicity through the regulation of autophagy |
Q90166130 | Pharmacological and functional similarities of the human neuropeptide Y system in C. elegans challenges phylogenetic views on the FLP/NPR system |
Q36280482 | Pharmacological intervention in invertebrate aging. |
Q50061214 | Pharming for genes in neurotransmission: Combining chemical and genetic approaches in C. elegans. |
Q33381873 | Phase-dependent preference of thermosensation and chemosensation during simultaneous presentation assay in Caenorhabditis elegans |
Q95643523 | Phase-separated protein dynamics are affected by fluorescent tag choice |
Q35170726 | Phasor approach to fluorescence lifetime microscopy distinguishes different metabolic states of germ cells in a live tissue |
Q33549702 | Phenotypic covariance of longevity, immunity and stress resistance in the caenorhabditis nematodes |
Q39330009 | Phenotypic plasticity and remodeling in the stress-induced Caenorhabditis elegans dauer |
Q39188232 | Phenotypic, chemical and functional characterization of cyclic nucleotide phosphodiesterase 4 (PDE4) as a potential anthelmintic drug target |
Q36381604 | Pheromone-sensing neurons regulate peripheral lipid metabolism in Caenorhabditis elegans |
Q35045199 | Phorbol esters and neurotransmitter release: more than just protein kinase C? |
Q33655594 | Phosphatidylinositol 4,5-bisphosphate and loss of PLCgamma activity inhibit TRPM channels required for oscillatory Ca2+ signaling |
Q54979740 | Phosphatidylinositol-5-Phosphate 4-Kinases Regulate Cellular Lipid Metabolism By Facilitating Autophagy. |
Q58799570 | Phosphatidylserine exposure mediated by ABC transporter activates the integrin signaling pathway promoting axon regeneration |
Q47154641 | Phosphatidylserine save-me signals drive functional recovery of severed axons in Caenorhabditis elegans |
Q50348631 | Phospholipase D functional ablation has a protective effect in an Alzheimer's disease Caenorhabditis elegans model. |
Q30579987 | Phospholipids that contain polyunsaturated fatty acids enhance neuronal cell mechanics and touch sensation |
Q36953702 | Phosphorylation of FEZ1 by Microtubule Affinity Regulating Kinases regulates its function in presynaptic protein trafficking. |
Q27347875 | Phosphorylation of the conserved transcription factor ATF-7 by PMK-1 p38 MAPK regulates innate immunity in Caenorhabditis elegans |
Q47313631 | Phosphorylation of the synaptonemal complex protein SYP-1 promotes meiotic chromosome segregation |
Q35802054 | Phosphorylation of α-synuclein protein at Ser-129 reduces neuronal dysfunction by lowering its membrane binding property in Caenorhabditis elegans |
Q30499509 | Phosphorylation promotes neurotoxicity in a Caenorhabditis elegans model of TDP-43 proteinopathy |
Q50198893 | Photoswitchable diacylglycerols enable optical control of protein kinase C. |
Q35070424 | Phthalates induce neurotoxicity affecting locomotor and thermotactic behaviors and AFD neurons through oxidative stress in Caenorhabditis elegans |
Q42809553 | Phycoerythrin averts intracellular ROS generation and physiological functional decline in eukaryotes under oxidative stress. |
Q41806990 | Phycoerythrin extends life span and health span of Caenorhabditis elegans |
Q42445069 | Phylogenetic, expression, and functional analyses of anoctamin homologs in Caenorhabditis elegans |
Q90644667 | Physical and functional interaction between SET1/COMPASS complex component CFP-1 and a Sin3S HDAC complex in C. elegans |
Q34355649 | Physical and functional interactions between the histone H3K4 demethylase KDM5A and the nucleosome remodeling and deacetylase (NuRD) complex |
Q28478056 | Physiological IRE-1-XBP-1 and PEK-1 signaling in Caenorhabditis elegans larval development and immunity |
Q90424738 | Physiological Starvation Promotes Caenorhabditis elegans Vulval Induction |
Q41868219 | Physiological and Immunological Regulations in Caenorhabditis elegans Infected with Salmonella enterica serovar Typhi |
Q37076806 | Pioneer Axon Navigation Is Controlled by AEX-3, a Guanine Nucleotide Exchange Factor for RAB-3 in Caenorhabditis elegans |
Q90706662 | Planar Asymmetries in the C. elegans Embryo Emerge by Differential Retention of aPARs at Cell-Cell Contacts |
Q42580440 | Plastin increases cortical connectivity to facilitate robust polarization and timely cytokinesis. |
Q42149368 | Polarization of the C. elegans zygote proceeds via distinct establishment and maintenance phases |
Q36245121 | Polarized Rac-dependent protrusions drive epithelial intercalation in the embryonic epidermis of C. elegans |
Q47256910 | Polo-like Kinase Couples Cytoplasmic Protein Gradients in the C. elegans Zygote |
Q33305160 | Poly-G/poly-C tracts in the genomes of Caenorhabditis |
Q50438573 | Polyadenylation is the key aspect of GLD-2 function in C. elegans. |
Q30420542 | Polyglutamine aggregate structure in vitro and in vivo; new avenues for coherent anti-Stokes Raman scattering microscopy |
Q35746858 | Polyglutamine aggregates alter protein folding homeostasis in Caenorhabditis elegans |
Q79948907 | Polyglutamine proteins at the pathogenic threshold display neuron-specific aggregation in a pan-neuronal Caenorhabditis elegans model |
Q39918678 | Polymerase theta-mediated end joining of replication-associated DNA breaks in C. elegans. |
Q35814233 | Polymerase Θ is a key driver of genome evolution and of CRISPR/Cas9-mediated mutagenesis |
Q37640182 | Polymodal Responses in C. elegans Phasmid Neurons Rely on Multiple Intracellular and Intercellular Signaling Pathways |
Q45240224 | Polymodal sensory function of the Caenorhabditis elegans OCR-2 channel arises from distinct intrinsic determinants within the protein and is selectively conserved in mammalian TRPV proteins. |
Q33484977 | Polymorphic segmental duplication in the nematode Caenorhabditis elegans |
Q92619938 | Polyphenols and Metabolites Enhance Survival in Rodents and Nematodes-Impact of Mitochondria |
Q33993852 | Polyploids and sex determination in Caenorhabditis elegans |
Q36489111 | Polyunsaturated fatty acids influence synaptojanin localization to regulate synaptic vesicle recycling |
Q91988466 | Pomegranate juice and extract extended lifespan and reduced intestinal fat deposition in Caenorhabditis elegans |
Q37290090 | Position of UNC-13 in the active zone regulates synaptic vesicle release probability and release kinetics |
Q37385906 | Positive and negative tissue-specific signaling by a nematode epidermal growth factor receptor |
Q42534346 | Positive selection of Caenorhabditis elegans mutants with increased stress resistance and longevity. |
Q41751562 | Post-developmental microRNA expression is required for normal physiology, and regulates aging in parallel to insulin/IGF-1 signaling in C. elegans |
Q37383242 | Post-transcriptional control of executioner caspases by RNA-binding proteins |
Q33960393 | Post-transcriptional regulation of RNA polymerase II levels in Caenorhabditis elegans. |
Q37381631 | Post-transcriptional regulation of sex determination in Caenorhabditis elegans: widespread expression of the sex-determining gene fem-1 in both sexes |
Q34642010 | Post-transcriptional regulation of the E/Daughterless ortholog HLH-2, negative feedback, and birth order bias during the AC/VU decision in C. elegans |
Q36455332 | Post-translational O-GlcNAcylation is essential for nuclear pore integrity and maintenance of the pore selectivity filter |
Q30155412 | Post-translational modification of Cu/Zn superoxide dismutase under anaerobic conditions |
Q33297427 | Postembryonic RNAi in Heterorhabditis bacteriophora: a nematode insect parasite and host for insect pathogenic symbionts |
Q36172273 | Postmitotic diversification of olfactory neuron types is mediated by differential activities of the HMG-box transcription factor SOX-2. |
Q30532148 | Postsynaptic ERG potassium channels limit muscle excitability to allow distinct egg-laying behavior states in Caenorhabditis elegans. |
Q33769630 | Potential role of Diploscapter sp. strain LKC25, a bacterivorous nematode from soil, as a vector of food-borne pathogenic bacteria to preharvest fruits and vegetables |
Q35022073 | Power law relationship between cell cycle duration and cell volume in the early embryonic development of Caenorhabditis elegans |
Q58753546 | Powerful and interpretable behavioural features for quantitative phenotyping of |
Q24315670 | Pre-fibrillar alpha-synuclein variants with impaired beta-structure increase neurotoxicity in Parkinson's disease models |
Q39634533 | Precise regulation of the guidance receptor DMA-1 by KPC-1/Furin instructs dendritic branching decisions |
Q90580737 | Precoce and opposite response of proteasome activity after acute or chronic exposure of C. elegans to γ-radiation |
Q51738183 | Predator-secreted sulfolipids induce defensive responses in C. elegans. |
Q51837124 | Predicting mutation outcome from early stochastic variation in genetic interaction partners. |
Q33285034 | Predictive modeling of signaling crosstalk during C. elegans vulval development |
Q51760837 | Predominant gut Lactobacillus murinus strain mediates anti-inflammaging effects in calorie-restricted mice. |
Q31112644 | Premature sperm activation and defective spermatogenesis caused by loss of spe-46 function in Caenorhabditis elegans |
Q41477059 | Presumptive TRP channel CED-11 promotes cell volume decrease and facilitates degradation of apoptotic cells in Caenorhabditis elegans |
Q50225769 | Preventing Illegitimate Extrasynaptic Acetylcholine Receptor Clustering Requires the RSU-1 Protein. |
Q27350248 | PrimerMapper: high throughput primer design and graphical assembly for PCR and SNP detection |
Q35780637 | Pristionchus uniformis, should I stay or should I go? Recent host range expansion in a European nematode |
Q37090144 | Pro-crossover factors regulate damage-dependent apoptosis in the Caenorhabditis elegans germ line |
Q62609576 | Pro-oxidant and lifespan extension effects of caffeine and related methylxanthines in Caenorhabditis elegans |
Q34646681 | Probing single-cell micromechanics in vivo: the microrheology of C. elegans developing embryos |
Q92659591 | Probiotic Bacillus subtilis Protects against α-Synuclein Aggregation in C. elegans |
Q55345844 | Probiotic Lactobacillus fermentum strain JDFM216 stimulates the longevity and immune response of Caenorhabditis elegans through a nuclear hormone receptor. |
Q33849961 | Processed Panax ginseng, sun ginseng, inhibits the differentiation and proliferation of 3T3-L1 preadipocytes and fat accumulation in Caenorhabditis elegans |
Q42619945 | Prodomain-dependent tissue targeting of an ADAMTS protease controls cell migration in Caenorhabditis elegans |
Q92258649 | Production of YP170 Vitellogenins Promotes Intestinal Senescence in Caenorhabditis elegans |
Q86721187 | Production of nematocidal compounds by hairy root cultures of Tagetes patula L |
Q34048830 | Products of the Parkinson's disease-related glyoxalase DJ-1, D-lactate and glycolate, support mitochondrial membrane potential and neuronal survival |
Q50542077 | Profiling changes to natively-bound metals during Caenorhabditis elegans development. |
Q27304403 | Profiling of the mammalian mitotic spindle proteome reveals an ER protein, OSTD-1, as being necessary for cell division and ER morphology |
Q35049409 | Profiling the RNA editomes of wild-type C. elegans and ADAR mutants |
Q34489256 | Programmed cell death mediated by ced-3 and ced-4 protects Caenorhabditis elegans from Salmonella typhimurium-mediated killing |
Q36157242 | Programmed elimination of cells by caspase-independent cell extrusion in C. elegans |
Q33719898 | Progression from a stem cell-like state to early differentiation in the C. elegans germ line |
Q64387580 | Progression of Meiosis Is Coordinated by the Level and Location of MAPK Activation Via OGR-2 in |
Q37717607 | Progressive degeneration of dopaminergic neurons through TRP channel-induced cell death. |
Q92757520 | Prolonged exposure to multi-walled carbon nanotubes dysregulates intestinal mir-35 and its direct target MAB-3 in nematode Caenorhabditis elegans |
Q92088136 | Prolonged quiescence delays somatic stem cell-like divisions in Caenorhabditis elegans and is controlled by insulin signaling |
Q33963876 | Prolyl 4-hydroxylase is an essential procollagen-modifying enzyme required for exoskeleton formation and the maintenance of body shape in the nematode Caenorhabditis elegans |
Q35692955 | Prolyl 4-hydroxylase is required for viability and morphogenesis in Caenorhabditis elegans |
Q36240758 | Promoters recognized by forkhead proteins exist for individual 21U-RNAs |
Q36875574 | Promotion of Homologous Recombination by SWS-1 in Complex with RAD-51 Paralogs in Caenorhabditis elegans. |
Q27311143 | Promotion of bone morphogenetic protein signaling by tetraspanins and glycosphingolipids |
Q30633193 | Propensity of undulatory swimmers, such as worms, to go against the flow |
Q42260665 | Proper cyclin B3 dosage is important for precision of metaphase-to-anaphase onset timing in Caenorhabditis elegans |
Q40820100 | Proper expression of myosin genes in transgenic nematodes |
Q41906912 | Properties of a class of genes required for ray morphogenesis in Caenorhabditis elegans |
Q44666821 | Properties of a strain of free-living nematode, Rhabditidae sp.: Life cycle and age-related mortality |
Q37385660 | Propionyl-CoA and adenosylcobalamin metabolism in Caenorhabditis elegans: evidence for a role of methylmalonyl-CoA epimerase in intermediary metabolism |
Q30528736 | Proprioceptive coupling within motor neurons drives C. elegans forward locomotion |
Q93110819 | Prostaglandin signals from adult germ stem cells delay somatic aging of Caenorhabditis elegans |
Q35205667 | Proteasomal ubiquitin receptor RPN-10 controls sex determination in Caenorhabditis elegans |
Q64933175 | Proteasome regulation of the chromodomain protein MRG-1 controls the balance between proliferative fate and differentiation in the C. elegans germ line. |
Q36817904 | Protection of specific maternal messenger RNAs by the P body protein CGH-1 (Dhh1/RCK) during Caenorhabditis elegans oogenesis |
Q34701335 | Protective efficacy of selenite against lead-induced neurotoxicity in Caenorhabditis elegans |
Q34190184 | Protein Misfolding Induces Hypoxic Preconditioning via a Subset of the Unfolded Protein Response Machinery |
Q53434430 | Protein instability, haploinsufficiency, and cortical hyper-excitability underlie STXBP1 encephalopathy. |
Q35283856 | Protein phosphatase 2A cooperates with the autophagy-related kinase UNC-51 to regulate axon guidance in Caenorhabditis elegans |
Q89289778 | Protein phosphatase 2A is crucial for sarcomere organization in Caenorhabditis elegans striated muscle |
Q27313309 | Protein phosphatase 4 promotes chromosome pairing and synapsis, and contributes to maintaining crossover competence with increasing age |
Q30503929 | Protein phosphatase 5 is a negative regulator of separase function during cortical granule exocytosis in C. elegans |
Q37341788 | Protein structural domains in the Caenorhabditis elegans unc-54 myosin heavy chain gene are not separated by introns |
Q30651736 | Proteogenomic database construction driven from large scale RNA-seq data |
Q50517209 | Proteoglycan distribution pattern during aging in the nematode Caenorhabditis elegans: an ultrastructural histochemical study. |
Q34042438 | Proteomic analysis reveals CACN-1 is a component of the spliceosome in Caenorhabditis elegans |
Q36162952 | Proteomic analysis uncovers a metabolic phenotype in C. elegans after nhr-40 reduction of function |
Q58797518 | Proteomic and evolutionary analyses of sperm activation identify uncharacterized genes in Caenorhabditis nematodes |
Q30481350 | Protons act as a transmitter for muscle contraction in C. elegans |
Q39529678 | Pseudomonas aeruginosa PAO1 kills Caenorhabditis elegans by cyanide poisoning |
Q37185887 | Pseudomonas aeruginosa killing of Caenorhabditis elegans used to identify P. aeruginosa virulence factors |
Q27318409 | Pseudomonas aeruginosa suppresses host immunity by activating the DAF-2 insulin-like signaling pathway in Caenorhabditis elegans |
Q37405354 | Pseudomonas brassicacearum strain DF41 kills Caenorhabditis elegans through biofilm-dependent and biofilm-independent mechanisms |
Q64936358 | Pseudomonas donghuensis HYS virulence towards Caenorhabditis elegans is regulated by the Cbr/Crc system. |
Q36864661 | Pseudomonas fluorescens NZI7 repels grazing by C. elegans, a natural predator |
Q33779559 | Pseudosynapsis and decreased stringency of meiotic repair pathway choice on the hemizygous sex chromosome of Caenorhabditis elegans males |
Q27310269 | PtdIns(4,5)P₂ and PtdIns3P coordinate to regulate phagosomal sealing for apoptotic cell clearance |
Q27333057 | Pulsed irradiation improves target selectivity of infrared laser-evoked gene operator for single-cell gene induction in the nematode C. elegans |
Q33789108 | Purging deleterious mutations under self fertilization: paradoxical recovery in fitness with increasing mutation rate in Caenorhabditis elegans |
Q42008104 | Purification and characterization of protein kinase C from the nematode Caenorhabditis elegans |
Q36218914 | Purified thick filaments from the nematode Caenorhabditis elegans: evidence for multiple proteins associated with core structures |
Q40795509 | Putative calcium-binding domains of the Caenorhabditis elegans BK channel are dispensable for intoxication and ethanol activation |
Q35611478 | Pyrrolnitrin and Hydrogen Cyanide Production by Pseudomonas chlororaphis Strain PA23 Exhibits Nematicidal and Repellent Activity against Caenorhabditis elegans |
Q58783573 | QsRNA-seq: a method for high-throughput profiling and quantifying small RNAs |
Q50025148 | Quantifying Salmonella population dynamics in water and biofilms. |
Q47157463 | Quantifying male and female pheromone-based mate choice in Caenorhabditis nematodes using a novel microfluidic technique |
Q49841698 | Quantitating transcription factor redundancy: The relative roles of the ELT-2 and ELT-7 GATA factors in the C. elegans endoderm. |
Q38926478 | Quantitative Analysis of Synthetic Cell Lineage Tracing Using Nuclease Barcoding |
Q35107326 | Quantitative analysis and modeling probe polarity establishment in C. elegans embryos |
Q27334746 | Quantitative analysis of cytokinesis in situ during C. elegans postembryonic development |
Q33355988 | Quantitative image analysis reveals distinct structural transitions during aging in Caenorhabditis elegans tissues |
Q30491423 | Quantitative mapping of a digenic behavioral trait implicates globin variation in C. elegans sensory behaviors |
Q57279143 | Quantitative proteomics by amino acid labeling in C. elegans |
Q33597953 | Quantitative proteomics by metabolic labeling of model organisms |
Q36746367 | Quantitative screening of genes regulating tryptophan hydroxylase transcription in Caenorhabditis elegans using microfluidics and an adaptive algorithm |
Q36305244 | Quantitative trait loci controlling halothane sensitivity in Caenorhabditis elegans |
Q89977391 | Quercetin and Its Mixture Increase the Stress Resistance of Caenorhabditis elegans to UV-B |
Q36545935 | Quinic acid could be a potential rejuvenating natural compound by improving survival of Caenorhabditis elegans under deleterious conditions |
Q53400377 | Quinolinic acid and glutamatergic neurodegeneration in Caenorhabditis elegans. |
Q35758927 | Quorum quenching quandary: resistance to antivirulence compounds |
Q27308784 | RAB-10 Promotes EHBP-1 Bridging of Filamentous Actin and Tubular Recycling Endosomes |
Q27310002 | RAB-10 Regulates Dendritic Branching by Balancing Dendritic Transport |
Q34407310 | RAB-10 is required for endocytic recycling in the Caenorhabditis elegans intestine |
Q36212719 | RAB-10-GTPase-mediated regulation of endosomal phosphatidylinositol-4,5-bisphosphate |
Q30482098 | RAB-11 permissively regulates spindle alignment by modulating metaphase microtubule dynamics in Caenorhabditis elegans early embryos |
Q36414834 | RAB-5 and RAB-10 cooperate to regulate neuropeptide release in Caenorhabditis elegans |
Q27304603 | RAB-5 controls the cortical organization and dynamics of PAR proteins to maintain C. elegans early embryonic polarity |
Q36599717 | RAB-5- and DYNAMIN-1-Mediated Endocytosis of EFF-1 Fusogen Controls Cell-Cell Fusion |
Q34673172 | RAB-5- and RAB-11-dependent vesicle-trafficking pathways are required for plasma membrane repair after attack by bacterial pore-forming toxin. |
Q34257541 | RAB-7 antagonizes LET-23 EGFR signaling during vulva development in Caenorhabditis elegans |
Q33761243 | RACK-1 acts with Rac GTPase signaling and UNC-115/abLIM in Caenorhabditis elegans axon pathfinding and cell migration |
Q30486461 | RACK-1 directs dynactin-dependent RAB-11 endosomal recycling during mitosis in Caenorhabditis elegans |
Q33953160 | RACK-1 regulates let-7 microRNA expression and terminal cell differentiation in Caenorhabditis elegans |
Q30780655 | RAD-51-dependent and -independent roles of a Caenorhabditis elegans BRCA2-related protein during DNA double-strand break repair |
Q24305945 | RAE-1, a novel PHR binding protein, is required for axon termination and synapse formation in Caenorhabditis elegans |
Q36149403 | RAL-1 controls multivesicular body biogenesis and exosome secretion |
Q40695755 | RBD-1, a nucleolar RNA-binding protein, is essential for Caenorhabditis elegans early development through 18S ribosomal RNA processing |
Q57182249 | RBM-5 modulates U2AF large subunit-dependent alternative splicing in C. elegans |
Q24543937 | RDE-4 preferentially binds long dsRNA and its dimerization is necessary for cleavage of dsRNA to siRNA. |
Q36084332 | REC-1 and HIM-5 distribute meiotic crossovers and function redundantly in meiotic double-strand break formation in Caenorhabditis elegans. |
Q28236857 | REST and stress resistance in ageing and Alzheimer's disease |
Q86847638 | RETRACTED ARTICLE: Suspended animation: effects on short-term and long-term positive associative memory in Hypsibius dujardini |
Q34740838 | RETRACTED: The second RNA chaperone, Hfq2, is also required for survival under stress and full virulence of Burkholderia cenocepacia J2315. |
Q34581023 | RHGF-1/PDZ-RhoGEF and retrograde DLK-1 signaling drive neuronal remodeling on microtubule disassembly |
Q92983620 | RHO-1 and the Rho GEF RHGF-1 interact with UNC-6/Netrin signaling to regulate growth cone protrusion and microtubule organization in Caenorhabditis elegans |
Q27335077 | RIC-7 promotes neuropeptide secretion |
Q28344728 | RIC-8 (Synembryn): a novel conserved protein that is required for G(q)alpha signaling in the C. elegans nervous system |
Q90148455 | RIMB-1/RIM-Binding Protein and UNC-10/RIM Redundantly Regulate Presynaptic Localization of the Voltage-Gated Calcium Channel in Caenorhabditis elegans |
Q34264041 | RIP-chip-SRM--a new combinatorial large-scale approach identifies a set of translationally regulated bantam/miR-58 targets in C. elegans |
Q36274493 | RMD-1, a novel microtubule-associated protein, functions in chromosome segregation in Caenorhabditis elegans |
Q33937385 | RME-8, a conserved J-domain protein, is required for endocytosis in Caenorhabditis elegans. |
Q41380855 | RNA Binding Protein Vigilin Collaborates with miRNAs To Regulate Gene Expression for Caenorhabditis elegans Larval Development |
Q33593407 | RNA as a target of double-stranded RNA-mediated genetic interference in Caenorhabditis elegans |
Q34608015 | RNA interference can target pre-mRNA: consequences for gene expression in a Caenorhabditis elegans operon |
Q21146750 | RNA interference in nematodes and the chance that favored Sydney Brenner |
Q41828589 | RNA interference links oxidative stress to the inhibition of heat stress adaptation. |
Q64058173 | RNA interference may result in unexpected phenotypes in Caenorhabditis elegans |
Q91932666 | RNA processing errors triggered by cadmium and integrator complex disruption are signals for environmental stress |
Q37234074 | RNA recognition by the Caenorhabditis elegans oocyte maturation determinant OMA-1. |
Q35991558 | RNA surveillance is required for endoplasmic reticulum homeostasis |
Q40486717 | RNA-Seq Reveals Acute Manganese Exposure Increases Endoplasmic Reticulum Related and Lipocalin mRNAs in Caenorhabditis elegans |
Q34781501 | RNA-seq in the tetraploid Xenopus laevis enables genome-wide insight in a classic developmental biology model organism |
Q36732466 | RNA-seq-based mapping and candidate identification of mutations from forward genetic screens |
Q35964313 | RNASeq in C. elegans Following Manganese Exposure |
Q40903136 | RNAi Interrogation of Dietary Modulation of Development, Metabolism, Behavior, and Aging in C. elegans |
Q37163073 | RNAi Screen Identifies Novel Regulators of RNP Granules in the Caenorhabditis elegans Germ Line |
Q90428483 | RNAi pathways repress reprogramming of C. elegans germ cells during heat stress |
Q33786725 | RNAi screen of DAF-16/FOXO target genes in C. elegans links pathogenesis and dauer formation |
Q34579574 | RNAi screening of human glycogene orthologs in the nematode Caenorhabditis elegans and the construction of the C. elegans glycogene database |
Q34165740 | RNAi screening to identify postembryonic phenotypes in C. elegans |
Q30823962 | RNAi-Based Suppressor Screens Reveal Genetic Interactions Between the CRL2LRR-1 E3-Ligase and the DNA Replication Machinery in Caenorhabditis elegans |
Q40786122 | RNF-121 is an endoplasmic reticulum-membrane E3 ubiquitin ligase involved in the regulation of beta-integrin |
Q41831887 | ROP, the Drosophila Sec1 homolog, interacts with syntaxin and regulates neurotransmitter release in a dosage-dependent manner. |
Q37289169 | ROP-1, an RNA quality-control pathway component, affects Caenorhabditis elegans dauer formation |
Q89136425 | ROS is the major player in regulating altered autophagy and lifespan in sin-3 mutants of C. elegans |
Q38449056 | RPM-1 is localized to distinct subcellular compartments and regulates axon length in GABAergic motor neurons. |
Q50639977 | RPM-1, a Caenorhabditis elegans protein that functions in presynaptic differentiation, negatively regulates axon outgrowth by controlling SAX-3/robo and UNC-5/UNC5 activity. |
Q46942610 | RPN-6 determines C. elegans longevity under proteotoxic stress conditions |
Q30492826 | RSBP-1 is a membrane-targeting subunit required by the Galpha(q)-specific but not the Galpha(o)-specific R7 regulator of G protein signaling in Caenorhabditis elegans |
Q34573419 | RTCB-1 mediates neuroprotection via XBP-1 mRNA splicing in the unfolded protein response pathway |
Q24309568 | RTEL1 maintains genomic stability by suppressing homologous recombination |
Q50299304 | Rab GTPases mature the LC3-associated midbody phagosome. |
Q31063785 | Rabx-5 regulates RAB-5 early endosomal compartments and synaptic vesicles in C. elegans |
Q37429828 | Rac1/RhoA antagonism defines cell-to-cell heterogeneity during epidermal morphogenesis in nematodes. |
Q33948818 | Radiation-sensitive mutants of Caenorhabditis elegans |
Q106957270 | Radiolabeled Cobaltabis(dicarbollide) Anion–Graphene Oxide Nanocomposites for In Vivo Bioimaging and Boron Delivery |
Q28271536 | Raloxifene attenuates Pseudomonas aeruginosa pyocyanin production and virulence |
Q33705128 | RamA, a member of the AraC/XylS family, influences both virulence and efflux in Salmonella enterica serovar Typhimurium. |
Q34018995 | Random and targeted transgene insertion in Caenorhabditis elegans using a modified Mos1 transposon |
Q37174167 | Random mutagenesis of the mouse genome: a strategy for discovering gene function and the molecular basis of disease |
Q56530863 | Rap2 and TNIK control Plexin-dependent tiled synaptic innervation in |
Q52565557 | Rapid Integration of Multi-copy Transgenes Using Optogenetic Mutagenesis in Caenorhabditis elegans. |
Q38680638 | Rapid and Direct VHH and Target Identification by Staphylococcal Surface Display Libraries |
Q34066898 | Rapid and accurate developmental stage recognition of C. elegans from high-throughput image data |
Q35050871 | Rapid and precise engineering of the Caenorhabditis elegans genome with lethal mutation co-conversion and inactivation of NHEJ repair |
Q27308937 | Rapid and tunable control of protein stability in Caenorhabditis elegans using a small molecule |
Q37532863 | Rapid creation of forward-genetics tools for C. briggsae using TALENs: lessons for nonmodel organisms |
Q33784954 | Rapid evolution of phenotypic plasticity and shifting thresholds of genetic assimilation in the nematode Caenorhabditis remanei |
Q35542015 | Rapid mapping and identification of mutations in Caenorhabditis elegans by restriction site-associated DNA mapping and genomic interval pull-down sequencing. |
Q39392068 | Rapid phenotypic changes in Caenorhabditis elegans under uranium exposure |
Q92765412 | Rapid population-wide declines in stem cell number and activity during reproductive aging in C. elegans |
Q33481617 | Rapid selection of cyclic peptides that reduce alpha-synuclein toxicity in yeast and animal models |
Q37398886 | Rapid sequence evolution of transcription factors controlling neuron differentiation in Caenorhabditis |
Q37291326 | Rapid sublethal toxicity assessment using bioluminescent Caenorhabditis elegans, a novel whole-animal metabolic biosensor |
Q34434642 | Ras farnesyltransferase inhibitors suppress the phenotype resulting from an activated ras mutation in Caenorhabditis elegans |
Q91783151 | Ras-Dependent Cell Fate Decisions Are Reinforced by the RAP-1 Small GTPase in Caenorhabditis elegans |
Q50009387 | Ratiometric Calcium Imaging of Individual Neurons in Behaving Caenorhabditis Elegans. |
Q48448814 | Rational design of a high-affinity, fast, red calcium indicator R-CaMP2. |
Q30500476 | Real Time FRET Based Detection of Mechanical Stress in Cytoskeletal and Extracellular Matrix Proteins |
Q35294109 | Real-time multimodal optical control of neurons and muscles in freely behaving Caenorhabditis elegans |
Q28552649 | Recent Duplication and Functional Divergence in Parasitic Nematode Levamisole-Sensitive Acetylcholine Receptors |
Q36956321 | Receptor-mediated endocytosis in the Caenorhabditis elegans oocyte. |
Q30528880 | Receptors and other signaling proteins required for serotonin control of locomotion in Caenorhabditis elegans |
Q36587654 | Recognition of familiar food activates feeding via an endocrine serotonin signal in Caenorhabditis elegans |
Q33417666 | Recombinational landscape and population genomics of Caenorhabditis elegans |
Q92254348 | Recompleting the Caenorhabditis elegans genome |
Q42014454 | Reconstruction of Spatial Thermal Gradient Encoded in Thermosensory Neuron AFD in Caenorhabditis elegans |
Q27313580 | Recovery from an acute infection in C. elegans requires the GATA transcription factor ELT-2 |
Q92896770 | Recruitment of mRNAs to P granules by condensation with intrinsically-disordered proteins |
Q90594776 | Redox-mediated regulation of aging and healthspan by an evolutionarily conserved transcription factor HLH-2/Tcf3/E2A |
Q35221614 | Reduced dosage of pos-1 suppresses Mex mutants and reveals complex interactions among CCCH zinc-finger proteins during Caenorhabditis elegans embryogenesis |
Q30519553 | Reduced expression of BTBD10, an Akt activator, leads to motor neuron death |
Q41382843 | Reduced muscle contraction and a relaxed posture during sleep-like Lethargus |
Q35000937 | Reduced sleep-like quiescence in both hyperactive and hypoactive mutants of the Galphaq Gene egl-30 during lethargus in Caenorhabditis elegans |
Q92235387 | Reducing INS-IGF1 signaling protects against non-cell autonomous vesicle rupture caused by SNCA spreading |
Q33807965 | Reduction in chromosome mobility accompanies nuclear organization during early embryogenesis in Caenorhabditis elegans |
Q90123490 | Reduction of mRNA export unmasks different tissue sensitivities to low mRNA levels during Caenorhabditis elegans development |
Q27310363 | Reduction of mitoferrin results in abnormal development and extended lifespan in Caenorhabditis elegans |
Q36588951 | Redundant canonical and noncanonical Caenorhabditis elegans p21-activated kinase signaling governs distal tip cell migrations |
Q34589627 | Reevaluation of the role of the med-1 and med-2 genes in specifying the Caenorhabditis elegans endoderm |
Q36770724 | Reevaluation of whether a soma-to-germ-line transformation extends lifespan in Caenorhabditis elegans |
Q47128336 | Region-specific irradiation system with heavy-ion microbeam for active individuals of Caenorhabditis elegans. |
Q39540658 | Regulated disruption of inositol 1,4,5-trisphosphate signaling in Caenorhabditis elegans reveals new functions in feeding and embryogenesis |
Q58722669 | Regulated nuclear accumulation of a histone methyltransferase times the onset of heterochromatin formation in embryos |
Q37105901 | Regulated proteolysis of DNA polymerase eta during the DNA-damage response in C. elegans |
Q47674857 | Regulation of Axon Guidance by the Wnt Receptor Ror/CAM-1 in the PVT Guidepost Cell in Caenorhabditis elegans. |
Q34356028 | Regulation of C. elegans fat uptake and storage by acyl-CoA synthase-3 is dependent on NR5A family nuclear hormone receptor nhr-25. |
Q34386115 | Regulation of C. elegans presynaptic differentiation and neurite branching via a novel signaling pathway initiated by SAM-10. |
Q33834486 | Regulation of CED-3 caspase localization and activation by C. elegans nuclear-membrane protein NPP-14. |
Q33279466 | Regulation of Caenorhabditis elegans body size and male tail development by the novel gene lon-8 |
Q37011390 | Regulation of Caenorhabditis elegans male mate searching behavior by the nuclear receptor DAF-12. |
Q33958809 | Regulation of Caenorhabditis elegans vitellogenesis by DAF-2/IIS through separable transcriptional and posttranscriptional mechanisms |
Q46244949 | Regulation of Crossover Frequency and Distribution during Meiotic Recombination. |
Q37467624 | Regulation of DAF-16-mediated Innate Immunity in Caenorhabditis elegans |
Q27316903 | Regulation of DCC localization by HTZ-1/H2A.Z and DPY-30 does not correlate with H3K4 methylation levels |
Q36429947 | Regulation of DLK-1 kinase activity by calcium-mediated dissociation from an inhibitory isoform |
Q33661396 | Regulation of Dauer formation by O-GlcNAcylation in Caenorhabditis elegans. |
Q27309016 | Regulation of Gap Junction Dynamics by UNC-44/ankyrin and UNC-33/CRMP through VAB-8 in C. elegans Neurons |
Q52373738 | Regulation of Glutamate Signaling in the Sensorimotor Circuit by CASY-1A/Calsyntenin in Caenorhabditis elegans. |
Q24313264 | Regulation of MBK-2/DYRK by CDK-1 and the pseudophosphatases EGG-4 and EGG-5 during the oocyte-to-embryo transition |
Q36480286 | Regulation of Neuronal Oxygen Responses in C. elegans Is Mediated through Interactions between Globin 5 and the H-NOX Domains of Soluble Guanylate Cyclases. |
Q34975931 | Regulation of RNA granule dynamics by phosphorylation of serine-rich, intrinsically disordered proteins in C. elegans |
Q42359773 | Regulation of UNC-130/FOXD-mediated mesodermal patterning in C. elegans |
Q40952507 | Regulation of WNT Signaling at the Neuromuscular Junction by the Immunoglobulin Superfamily Protein RIG-3 in Caenorhabditis elegans |
Q35900717 | Regulation of acid-base transporters by reactive oxygen species following mitochondrial fragmentation |
Q33713496 | Regulation of age-related structural integrity in neurons by protein with tau-like repeats (PTL-1) is cell autonomous. |
Q41350965 | Regulation of aging by unc-13 and sbt-1 in Caenorhabditis elegans is temperature-dependent |
Q34714959 | Regulation of anoxic death in Caenorhabditis elegans by mammalian apoptosis signal-regulating kinase (ASK) family proteins |
Q33794429 | Regulation of asymmetric positioning of nuclei by Wnt and Src signaling and its roles in POP-1/TCF nuclear asymmetry in Caenorhabditis elegans |
Q34614580 | Regulation of axonal midline guidance by prolyl 4-hydroxylation in Caenorhabditis elegans |
Q54188370 | Regulation of chromatin states and gene expression during HSN neuronal maturation is mediated by EOR-1/PLZF, MAU-2/cohesin loader, and SWI/SNF complex. |
Q46736369 | Regulation of developmental rate and germ cell proliferation in Caenorhabditis elegans by the p53 gene network |
Q36632596 | Regulation of endocytic recycling by C. elegans Rab35 and its regulator RME-4, a coated-pit protein |
Q37418580 | Regulation of endosomal clathrin and retromer-mediated endosome to Golgi retrograde transport by the J-domain protein RME-8. |
Q86026553 | Regulation of experience-dependent bidirectional chemotaxis by a neural circuit switch in Caenorhabditis elegans |
Q28540665 | Regulation of extracellular matrix organization by BMP signaling in Caenorhabditis elegans |
Q35212298 | Regulation of fat storage and reproduction by Krüppel-like transcription factor KLF3 and fat-associated genes in Caenorhabditis elegans |
Q33596760 | Regulation of genes affecting body size and innate immunity by the DBL-1/BMP-like pathway in Caenorhabditis elegans |
Q33497905 | Regulation of heterochromatin assembly on unpaired chromosomes during Caenorhabditis elegans meiosis by components of a small RNA-mediated pathway |
Q35160819 | Regulation of intermuscular electrical coupling by the Caenorhabditis elegans innexin inx-6. |
Q35212150 | Regulation of lipoprotein assembly, secretion and fatty acid β-oxidation by Krüppel-like transcription factor, klf-3. |
Q35799651 | Regulation of longevity in Caenorhabditis elegans by heat shock factor and molecular chaperones |
Q35044834 | Regulation of mechanosensation in C. elegans through ubiquitination of the MEC-4 mechanotransduction channel |
Q42714619 | Regulation of membrane trafficking by a novel Cdc42-related protein in Caenorhabditis elegans epithelial cells. |
Q34171603 | Regulation of neuronal APL-1 expression by cholesterol starvation |
Q43540459 | Regulation of neurotransmitter vesicles by the homeodomain protein UNC-4 and its transcriptional corepressor UNC-37/groucho in Caenorhabditis elegans cholinergic motor neurons. |
Q27932881 | Regulation of nicotinic receptor trafficking by the transmembrane Golgi protein UNC-50. |
Q41849547 | Regulation of proteinase levels in the nematode Caenorhabditis elegans. Preferential depression by acute or chronic starvation |
Q36391785 | Regulation of serotonin biosynthesis by the G proteins Galphao and Galphaq controls serotonin signaling in Caenorhabditis elegans |
Q35804099 | Regulation of sex-specific differentiation and mating behavior in C. elegans by a new member of the DM domain transcription factor family |
Q38352378 | Regulation of sperm gene expression by the GATA factor ELT-1. |
Q37599421 | Regulation of sperm-specific proteins by IFE-1, a germline-specific homolog of eIF4E, in C. elegans |
Q34197648 | Regulation of synaptic extracellular matrix composition is critical for proper synapse morphology |
Q30608522 | Regulation of synaptic transmission at the Caenorhabditis elegans M4 neuromuscular junction by an antagonistic relationship between two calcium channels. |
Q34132410 | Regulation of the Caenorhabditis elegans oxidative stress defense protein SKN-1 by glycogen synthase kinase-3. |
Q41947665 | Regulation of the Caenorhabditis elegans posterior Hox gene egl-5 by microRNA and the polycomb-like gene sop-2. |
Q37348005 | Regulation of the MEI-1/MEI-2 Microtubule-Severing Katanin Complex in Early Caenorhabditis elegans Development |
Q49206676 | Regulation of the Response of Caenorhabditis elegans to Simulated Microgravity by p38 Mitogen-Activated Protein Kinase Signaling. |
Q77874508 | Regulation of the UNC-18-Caenorhabditis elegans syntaxin complex by UNC-13 |
Q41543407 | Regulation of the mec-3 gene by the C.elegans homeoproteins UNC-86 and MEC-3 |
Q36965113 | Regulation of vitellogenin gene expression in transgenic Caenorhabditis elegans: short sequences required for activation of the vit-2 promoter |
Q33518456 | Regulators of AWC-mediated olfactory plasticity in Caenorhabditis elegans |
Q37693518 | Regulators of Lysosome Function and Dynamics in Caenorhabditis elegans |
Q42429601 | Regulatory analysis of the C. elegans genome with spatiotemporal resolution |
Q36850528 | Regulatory myosin light-chain genes of Caenorhabditis elegans |
Q83226143 | Reliability of an interneuron response depends on an integrated sensory state |
Q27304998 | Reliable Screening of Dye Phototoxicity by Using a Caenorhabditis elegans Fast Bioassay |
Q35127528 | Reliable reference miRNAs for quantitative gene expression analysis of stress responses in Caenorhabditis elegans |
Q93389084 | Remodeling of the endoplasmic reticulum in Caenorhabditis elegans oocytes is regulated by CGH-1 |
Q33741138 | Removing bias against short sequences enables northern blotting to better complement RNA-seq for the study of small RNAs |
Q35914599 | Replication blocking lesions present a unique substrate for homologous recombination |
Q35791458 | Replication-coupled chromatin assembly generates a neuronal bilateral asymmetry in C. elegans |
Q33889851 | Repression by the 3' UTR of fem-3, a sex-determining gene, relies on a ubiquitous mog-dependent control in Caenorhabditis elegans |
Q64055118 | Repression of Germline Genes in Somatic Tissues by H3K9 Dimethylation of Their Promoters |
Q34136391 | Repression of Wnt signaling by a Fer-type nonreceptor tyrosine kinase |
Q27334743 | Repression of a potassium channel by nuclear hormone receptor and TGF-β signaling modulates insulin signaling in Caenorhabditis elegans |
Q35987521 | Repression of the Heat Shock Response Is a Programmed Event at the Onset of Reproduction |
Q27309712 | Reproductive Aging Drives Protein Accumulation in the Uterus and Limits Lifespan in C. elegans |
Q44608913 | Reproductive Fitness and Quinone Content of Caenorhabditis elegans clk-1 Mutants Fed Coenzyme Q Isoforms of Varying Length |
Q35787971 | Reproductive Mode and the Evolution of Genome Size and Structure in Caenorhabditis Nematodes |
Q35610594 | Reproductive toxicity and meiotic dysfunction following exposure to the pesticides Maneb, Diazinon and Fenarimol |
Q34779351 | Requirements of multiple domains of SLI-1, a Caenorhabditis elegans homologue of c-Cbl, and an inhibitory tyrosine in LET-23 in regulating vulval differentiation |
Q39102707 | Reserpine requires the D2-type receptor, dop-3, and the exoribonuclease, eri-1, to extend the lifespan in C. elegans. |
Q34569837 | Resistance to volatile anesthetics by mutations enhancing excitatory neurotransmitter release in Caenorhabditis elegans |
Q36221428 | Restoring de novo coenzyme Q biosynthesis in Caenorhabditis elegans coq-3 mutants yields profound rescue compared to exogenous coenzyme Q supplementation |
Q27348721 | Restricting dosage compensation complex binding to the X chromosomes by H2A.Z/HTZ-1 |
Q92020770 | Restriction of Cellular Plasticity of Differentiated Cells Mediated by Chromatin Modifiers, Transcription Factors and Protein Kinases |
Q42948884 | Resveratrol Attenuates Radiation Damage in Caenorhabditis elegans by Preventing Oxidative Stress |
Q50448610 | Resveratrol reduces amyloid-beta (Aβ₁₋₄₂)-induced paralysis through targeting proteostasis in an Alzheimer model of Caenorhabditis elegans. |
Q35169840 | Revelations from the Nematode Caenorhabditis elegans on the Complex Interplay of Metal Toxicological Mechanisms |
Q34521584 | Reversal of age-dependent nuclear morphology by inhibition of prenylation does not affect lifespan in Caenorhabditis elegans |
Q41167129 | Reversal of salt preference is directed by the insulin/PI3K and Gq/PKC signaling in Caenorhabditis elegans |
Q37190073 | Reverse genetic analysis of Caenorhabditis elegans presenilins reveals redundant but unequal roles for sel-12 and hop-1 in Notch-pathway signaling |
Q37286312 | Review of the results from the International C. elegans first experiment (ICE-FIRST). |
Q36278501 | Revising the standard wisdom of C. elegans natural history: ecology of longevity |
Q36287834 | Revisiting the X:A signal that specifies Caenorhabditis elegans sexual fate |
Q91943247 | Rhizobium induces DNA damage in Caenorhabditis elegans intestinal cells |
Q67288417 | Rhizocticin A, an antifungal phosphono-oligopeptide of Bacillus subtilis ATCC 6633: biological properties |
Q28482363 | Rhn1, a nuclear protein, is required for suppression of meiotic mRNAs in mitotically dividing fission yeast |
Q42566354 | Rho is a presynaptic activator of neurotransmitter release at pre-existing synapses in C. elegans |
Q83231103 | Rhodoquinone biosynthesis in requires precursors generated by the kynurenine pathway |
Q71009316 | Ribosomal DNA of Caenorhabditis elegans |
Q39017738 | Rice husks and their hydrochars cause unexpected stress response in the nematode Caenorhabditis elegans: reduced transcription of stress-related genes. |
Q27331645 | Rictor/TORC2 regulates Caenorhabditis elegans fat storage, body size, and development through sgk-1 |
Q49790650 | Robo and Ror function in a common receptor complex to regulate Wnt-mediated neurite outgrowth in Caenorhabditis elegans. |
Q36071246 | Robust Distal Tip Cell Pathfinding in the Face of Temperature Stress Is Ensured by Two Conserved microRNAS in Caenorhabditis elegans |
Q58741935 | Robust Genome Editing with Short Single-Stranded and Long, Partially Single-Stranded DNA Donors in |
Q28541321 | Rogue sperm indicate sexually antagonistic coevolution in nematodes |
Q89036467 | Role of Caenorhabditis elegans AKT-1/2 and SGK-1 in Manganese Toxicity |
Q93155640 | Role of KASH domain lengths in the regulation of LINC complexes |
Q64095835 | Role of Low-Affinity Calcium System Member Fig1 Homologous Proteins in Conidiation and Trap-Formation of Nematode-trapping Fungus Arthrobotrys oligospora |
Q91894405 | Role of PRY-1/Axin in heterochronic miRNA-mediated seam cell development |
Q58704340 | Role of Presenilin in Mitochondrial Oxidative Stress and Neurodegeneration in |
Q35751951 | Role of T-box gene tbx-2 for anterior foregut muscle development in C. elegans |
Q30805155 | Role of a class DHC1b dynein in retrograde transport of IFT motors and IFT raft particles along cilia, but not dendrites, in chemosensory neurons of living Caenorhabditis elegans |
Q36885434 | Role of oxygen consumption in hypoxia protection by translation factor depletion. |
Q38631377 | Role of phase variation in the resistance of Myxococcus xanthus fruiting bodies to Caenorhabditis elegans predation |
Q38411480 | Role of protein kinase C β and vascular endothelial growth factor receptor in malignant pleural mesothelioma: Therapeutic implications and the usefulness of Caenorhabditis elegans model organism |
Q36994763 | Role of the Caenorhabditis elegans Shc adaptor protein in the c-Jun N-terminal kinase signaling pathway |
Q36287771 | Role of the Caenorhabditis elegans multidrug resistance gene, mrp-4, in gut granule differentiation |
Q64980501 | Role of tyramine in calcium dynamics of GABAergic neurons and escape behavior in Caenorhabditis elegans. |
Q34614445 | Roles for Caenorhabditis elegans rad-51 in meiosis and in resistance to ionizing radiation during development |
Q34938094 | Roles for class IIA phosphatidylinositol transfer protein in neurotransmission and behavioral plasticity at the sensory neuron synapses of Caenorhabditis elegans |
Q34772500 | Roles for netrin signaling outside of axon guidance: a view from the worm |
Q38566924 | Roller mutants of the nematode Caenorhabditis elegans |
Q39481696 | Rosmarinus officinalis L. increases Caenorhabditis elegans stress resistance and longevity in a DAF-16, HSF-1 and SKN-1-dependent manner. |
Q27322778 | Rotational manipulation of single cells and organisms using acoustic waves. |
Q61807408 | RppH can faithfully replace TAP to allow cloning of 5′-triphosphate carrying small RNAs |
Q34612399 | Rules of nonallelic noncomplementation at the synapse in Caenorhabditis elegans. |
Q42361205 | Run-on of germline apoptosis promotes gonad senescence in C. elegans |
Q24630269 | Running with the Red Queen: host-parasite coevolution selects for biparental sex |
Q38543667 | S-Adenosyl methionine synthetase 1 limits fat storage in Caenorhabditis elegans |
Q54966655 | S-allylmercapto-N-acetylcysteine protects against oxidative stress and extends lifespan in Caenorhabditis elegans. |
Q35741892 | S6K links cell fate, cell cycle and nutrient response in C. elegans germline stem/progenitor cells |
Q51736955 | SAC-1 ensures epithelial endocytic recycling by restricting ARF-6 activity. |
Q36466328 | SACY-1 DEAD-Box helicase links the somatic control of oocyte meiotic maturation to the sperm-to-oocyte switch and gamete maintenance in Caenorhabditis elegans |
Q47139287 | SAP97 Binding Partner CRIPT Promotes Dendrite Growth In Vitro and In Vivo. |
Q27312016 | SAS-1 is a C2 domain protein critical for centriole integrity in C. elegans |
Q34036844 | SAX-7/L1CAM and HMR-1/cadherin function redundantly in blastomere compaction and non-muscle myosin accumulation during Caenorhabditis elegans gastrulation |
Q30558402 | SEB-3, a CRF receptor-like GPCR, regulates locomotor activity states, stress responses and ethanol tolerance in Caenorhabditis elegans |
Q34442163 | SEC-10 and RAB-10 coordinate basolateral recycling of clathrin-independent cargo through endosomal tubules in Caenorhabditis elegans |
Q41814175 | SEL-5, a serine/threonine kinase that facilitates lin-12 activity in Caenorhabditis elegans |
Q35170564 | SEL-8, a nuclear protein required for LIN-12 and GLP-1 signaling in Caenorhabditis elegans |
Q34587157 | SER-7, a Caenorhabditis elegans 5-HT7-like receptor, is essential for the 5-HT stimulation of pharyngeal pumping and egg laying |
Q52324560 | SFT-4/Surf4 control ER export of soluble cargo proteins and participate in ER exit site organization. |
Q25257790 | SGCEdb: a flexible database and web interface integrating experimental results and analysis for structural genomics focusing on Caenorhabditis elegans |
Q47125851 | SID-1 Domains Important for dsRNA Import in Caenorhabditis elegans |
Q60957747 | SIN-3 as a key determinant of lifespan and its sex dependent differential role on healthspan in C |
Q38797285 | SIR-2.1 integrates metabolic homeostasis with the reproductive neuromuscular excitability in early aging male Caenorhabditis elegans |
Q34034672 | SKIP is an indispensable factor for Caenorhabditis elegans development |
Q90243928 | SKN-1 Is a Negative Regulator of DAF-16 and Somatic Stress Resistance in Caenorhabditis elegans |
Q42069628 | SKN-1 and Nrf2 couples proline catabolism with lipid metabolism during nutrient deprivation |
Q39896060 | SKN-1 links C. elegans mesendodermal specification to a conserved oxidative stress response |
Q34413384 | SKN-1/Nrf2 inhibits dopamine neuron degeneration in a Caenorhabditis elegans model of methylmercury toxicity |
Q37060597 | SKR-1, a homolog of Skp1 and a member of the SCF(SEL-10) complex, regulates sex-determination and LIN-12/Notch signaling in C. elegans |
Q33957125 | SL1 trans splicing and 3'-end formation in a novel class of Caenorhabditis elegans operon |
Q28910400 | SLC30A10 is a cell surface-localized manganese efflux transporter, and parkinsonism-causing mutations block its intracellular trafficking and efflux activity |
Q34052546 | SLC6 family transporter SNF-10 is required for protease-mediated activation of sperm motility in C. elegans |
Q34524707 | SLI-1 Cbl inhibits the engulfment of apoptotic cells in C. elegans through a ligase-independent function |
Q27310064 | SLO BK Potassium Channels Couple Gap Junctions to Inhibition of Calcium Signaling in Olfactory Neuron Diversification |
Q57132107 | SLO potassium channels antagonize premature decision making in |
Q30541399 | SLO-2 isoforms with unique Ca(2+) - and voltage-dependence characteristics confer sensitivity to hypoxia in C. elegans |
Q34395310 | SLX-1 is required for maintaining genomic integrity and promoting meiotic noncrossovers in the Caenorhabditis elegans germline |
Q52655080 | SMAD Transcription Factor, Sma-9, Attunes TGF-β Signaling Cascade Towards Modulating Amyloid Beta Aggregation and Associated Outcome in Transgenic C. elegans. |
Q30895194 | SMF-1, SMF-2 and SMF-3 DMT1 orthologues regulate and are regulated differentially by manganese levels in C. elegans |
Q37349465 | SMG-1 is a phosphatidylinositol kinase-related protein kinase required for nonsense-mediated mRNA Decay in Caenorhabditis elegans |
Q34463782 | SMG-5, required for C.elegans nonsense-mediated mRNA decay, associates with SMG-2 and protein phosphatase 2A. |
Q36119514 | SMK-1/PPH-4.1-mediated silencing of the CHK-1 response to DNA damage in early C. elegans embryos |
Q35663992 | SMU-2 and SMU-1, Caenorhabditis elegans homologs of mammalian spliceosome-associated proteins RED and fSAP57, work together to affect splice site choice |
Q37583652 | SNEVhPrp19/hPso4 Regulates Adipogenesis of Human Adipose Stromal Cells |
Q37598953 | SNX-1 and RME-8 oppose the assembly of HGRS-1/ESCRT-0 degradative microdomains on endosomes |
Q27309073 | SPARC Promotes Cell Invasion In Vivo by Decreasing Type IV Collagen Levels in the Basement Membrane |
Q36287786 | SPD-3 is required for spindle alignment in Caenorhabditis elegans embryos and localizes to mitochondria |
Q24310765 | SPE-39 family proteins interact with the HOPS complex and function in lysosomal delivery |
Q34263090 | SPE-44 implements sperm cell fate |
Q35206632 | SPE-8, a protein-tyrosine kinase, localizes to the spermatid cell membrane through interaction with other members of the SPE-8 group spermatid activation signaling pathway in C. elegans |
Q34550044 | SPK-1, an SR protein kinase, inhibits programmed cell death in Caenorhabditis elegans |
Q35149495 | SPR-5 is a histone H3K4 demethylase with a role in meiotic double-strand break repair |
Q35037849 | SQV-7, a protein involved in Caenorhabditis elegans epithelial invagination and early embryogenesis, transports UDP-glucuronic acid, UDP-N- acetylgalactosamine, and UDP-galactose |
Q33925166 | SRC-1 mediates UNC-5 signaling in Caenorhabditis elegans |
Q35949117 | STAM and Hrs down-regulate ciliary TRP receptors |
Q36411169 | STAR family RNA-binding protein ASD-2 regulates developmental switching of mutually exclusive alternative splicing in vivo |
Q91970454 | STEFTR: A Hybrid Versatile Method for State Estimation and Feature Extraction From the Trajectory of Animal Behavior |
Q37727808 | STITCHER 2.0: primer design for overlapping PCR applications |
Q35562769 | STR-33, a novel G protein-coupled receptor that regulates locomotion and egg laying in Caenorhabditis elegans |
Q30492693 | SUMO regulates the assembly and function of a cytoplasmic intermediate filament protein in C. elegans |
Q37406766 | SUN-1 and ZYG-12, mediators of centrosome-nucleus attachment, are a functional SUN/KASH pair in Caenorhabditis elegans |
Q24319015 | SUT-2 potentiates tau-induced neurotoxicity in Caenorhabditis elegans |
Q35189880 | SWI/SNF chromatin remodeling regulates alcohol response behaviors in Caenorhabditis elegans and is associated with alcohol dependence in humans |
Q47302328 | SYGL-1 and LST-1 link niche signaling to PUF RNA repression for stem cell maintenance in Caenorhabditis elegans |
Q35945636 | SYP-3 restricts synaptonemal complex assembly to bridge paired chromosome axes during meiosis in Caenorhabditis elegans |
Q92501231 | Salmonella biofilms program innate immunity for persistence in Caenorhabditis elegans |
Q27939376 | Sar1, a Novel Regulator of ER-Mitochondrial Contact Sites |
Q35967428 | Sarcomeres Pattern Proprioceptive Sensory Dendritic Endings through UNC-52/Perlecan in C. elegans |
Q37041560 | Sarcomeric actin organization is synergistically promoted by tropomodulin, ADF/cofilin, AIP1 and profilin in C. elegans |
Q36908578 | Sarcopenia in the Caenorhabditis elegans pharynx correlates with muscle contraction rate over lifespan |
Q88548203 | Satiety behavior is regulated by ASI/ASH reciprocal antagonism |
Q30485759 | Scoring diverse cellular morphologies in image-based screens with iterative feedback and machine learning |
Q36380265 | Screening and Characterization of Lactic Acid Bacteria Strains with Anti-inflammatory Activities through in vitro and Caenorhabditis elegans Model Testing |
Q52443157 | Screening for a new generation of anthelminthic compounds. In vitro selection of the nematode Caenorhabditis elegans for ivermectin resistance. |
Q35993596 | Screening of toxic potential of graphene family nanomaterials using in vitro and alternative in vivo toxicity testing systems |
Q46488616 | Sec61β facilitates the maintenance of endoplasmic reticulum homeostasis by associating microtubules |
Q98177986 | Secoisolariciresinol Diglucoside Delays the Progression of Aging-Related Diseases and Extends the Lifespan of Caenorhabditis elegans via DAF-16 and HSF-1 |
Q30504512 | Second-generation high-throughput forward genetic screen in mice to isolate subtle behavioral mutants |
Q46324287 | Sedimentation Velocity Analysis with Fluorescence Detection of Mutant Huntingtin Exon 1 Aggregation in Drosophila melanogaster and Caenorhabditis elegans. |
Q34338341 | Segregation of holocentric chromosomes at meiosis in the nematode, Caenorhabditis elegans |
Q37856873 | Selectable genetic markers for nematode transgenesis. |
Q39444633 | Selected elements of herpes simplex virus accessory factor HCF are highly conserved in Caenorhabditis elegans |
Q79428556 | Selection against males in Caenorhabditis elegans under two mutational treatments |
Q34614701 | Selection and maintenance of androdioecy in Caenorhabditis elegans |
Q28731290 | Selection of reliable reference genes in Caenorhabditis elegans for analysis of nanotoxicity |
Q27308116 | Selection on a Subunit of the NURF Chromatin Remodeler Modifies Life History Traits in a Domesticated Strain of Caenorhabditis elegans |
Q41074700 | Selective targeting of primary and secondary nucleation pathways in Aβ42 aggregation using a rational antibody scanning method |
Q30500560 | Selective toxicity of the anthelmintic emodepside revealed by heterologous expression of human KCNMA1 in Caenorhabditis elegans |
Q36243584 | Selenium induces cholinergic motor neuron degeneration in Caenorhabditis elegans |
Q64883455 | Selenium species-dependent toxicity, bioavailability and metabolic transformations in Caenorhabditis elegans. |
Q35014192 | Semaphorin and Eph receptor signaling guide a series of cell movements for ventral enclosure in C. elegans |
Q36585509 | Semaphorin controls epidermal morphogenesis by stimulating mRNA translation via eIF2alpha in Caenorhabditis elegans |
Q36466343 | Semaphorin-1 and netrin signal in parallel and permissively to position the male ray 1 sensillum in Caenorhabditis elegans |
Q36412842 | Semi-permeable Diffusion Barriers Enhance Patterning Robustness in the C. elegans Germline |
Q36981485 | Sensitive PCR Detection of Meloidogyne arenaria, M. incognita, and M. javanica Extracted from Soil. |
Q36111729 | Sensitive detection of lysosomal membrane permeabilization by lysosomal galectin puncta assay. |
Q36839619 | Sensitive red protein calcium indicators for imaging neural activity |
Q27310752 | Sensory Neurons Arouse C. elegans Locomotion via Both Glutamate and Neuropeptide Release |
Q27919709 | Sensory ciliogenesis in Caenorhabditis elegans: assignment of IFT components into distinct modules based on transport and phenotypic profiles |
Q33944222 | Sensory experience and sensory activity regulate chemosensory receptor gene expression in Caenorhabditis elegans. |
Q35863095 | Sensory organ remodeling in Caenorhabditis elegans requires the zinc-finger protein ZTF-16. |
Q33349445 | Sensory perception of food and insulin-like signals influence seizure susceptibility |
Q36787837 | Sensory regulation of the C. elegans germline through TGF-β-dependent signaling in the niche |
Q38226537 | Sensory systems: their impact on C. elegans survival |
Q58553548 | Sentryn Acts with a Subset of Active Zone Proteins To Optimize the Localization of Synaptic Vesicles in |
Q58553556 | Sentryn and SAD Kinase Link the Guided Transport and Capture of Dense Core Vesicles in |
Q35969218 | Separable Roles for a Caenorhabditis elegans RMI1 Homolog in Promoting and Antagonizing Meiotic Crossovers Ensure Faithful Chromosome Inheritance. |
Q47653350 | Separate transcriptionally regulated pathways specify distinct classes of sister dendrites in a nociceptive neuron |
Q48051775 | Separation, Sizing, and Quantitation of Engineered Nanoparticles in an Organism Model Using Inductively Coupled Plasma Mass Spectrometry and Image Analysis. |
Q36162821 | Sequence Complexity of Chromosome 3 in Caenorhabditis elegans |
Q36236952 | Sequence and transmembrane topology of MEC-4, an ion channel subunit required for mechanotransduction in Caenorhabditis elegans |
Q38434567 | Sequence determinants of the Caenhorhabditis elegans dopamine transporter dictating in vivo axonal export and synaptic localization |
Q40547351 | Sequence identity between an inverted repeat family of transposable elements in Drosophila and Caenorhabditis |
Q35678088 | Sequence of theC. eleganstransposable element Tcl |
Q33961648 | Sequence requirements for myosin gene expression and regulation in Caenorhabditis elegans |
Q30574571 | Sequential breakdown of 3-phosphorylated phosphoinositides is essential for the completion of macropinocytosis |
Q33734515 | Sequential rounds of RNA-dependent RNA transcription drive endogenous small-RNA biogenesis in the ERGO-1/Argonaute pathway |
Q33676129 | Sequestration of polyunsaturated fatty acids in membrane phospholipids of Caenorhabditis elegans dauer larva attenuates eicosanoid biosynthesis for prolonged survival |
Q27331883 | Serotonergic chemosensory neurons modify the C. elegans immune response by regulating G-protein signaling in epithelial cells |
Q43238127 | Serotonergic neurosecretory synapse targeting is controlled by netrin-releasing guidepost neurons in Caenorhabditis elegans |
Q30703360 | Serotonergic signalling suppresses ataxin 3 aggregation and neurotoxicity in animal models of Machado-Joseph disease |
Q34572365 | Serotonin (5HT), fluoxetine, imipramine and dopamine target distinct 5HT receptor signaling to modulate Caenorhabditis elegans egg-laying behavior |
Q38842451 | Serotonin Regulates the Feeding and Reproductive Behaviors of Pratylenchus penetrans |
Q36295271 | Serotonin activates overall feeding by activating two separate neural pathways in Caenorhabditis elegans |
Q61810629 | Serotonin and neuropeptides are both released by the HSN command neuron to initiate Caenorhabditis elegans egg laying |
Q27303703 | Serotonin control of thermotaxis memory behavior in nematode Caenorhabditis elegans |
Q91686582 | Serotonin modulates behavior-related neural activity of RID interneuron in Caenorhabditis elegans |
Q27305034 | Serotonin promotes exploitation in complex environments by accelerating decision-making |
Q30837852 | Serotonin-dependent kinetics of feeding bursts underlie a graded response to food availability in C. elegans. |
Q48192684 | Sesamin extends lifespan through pathways related to dietary restriction in Caenorhabditis elegans |
Q36671213 | Several Grassland Soil Nematode Species Are Insensitive to RNA-Mediated Interference |
Q36180956 | Sex Attraction and Mating in Bursaphelenchus okinawaensis and B. xylophilus |
Q27309673 | Sex Pheromones of C. elegans Males Prime the Female Reproductive System and Ameliorate the Effects of Heat Stress |
Q33952308 | Sex determination in the nematode C. elegans: analysis of tra-3 suppressors and characterization of fem genes. |
Q34613155 | Sex determination in the parasitic nematode Strongyloides ratti |
Q28483655 | Sex differences in carbohydrate metabolism are linked to gene expression in Caenorhabditis elegans |
Q47560315 | Sex- and Gamete-Specific Patterns of X Chromosome Segregation in a Trioecious Nematode |
Q34895019 | Sex-dependent resistance to the pathogenic fungus Cryptococcus neoformans |
Q36896657 | Sex-specific pruning of neuronal synapses in Caenorhabditis elegans |
Q50421437 | Sex-specific regulation of aging in Caenorhabditis elegans. |
Q38220875 | Sexual modulation of neural circuits and behavior in Caenorhabditis elegans. |
Q34280305 | Sexual partners for the stressed: facultative outcrossing in the self-fertilizing nematode Caenorhabditis elegans |
Q93110642 | Sexually Dimorphic Regulation of Behavioral States by Dopamine in Caenorhabditis elegans |
Q50076274 | Sexually Dimorphic unc-6/Netrin Expression Controls Sex-Specific Maintenance of Synaptic Connectivity. |
Q37603778 | Sexually dimorphic control of gene expression in sensory neurons regulates decision-making behavior in C. elegans. |
Q41785202 | Shank is a dose-dependent regulator of Cav1 calcium current and CREB target expression. |
Q24293442 | Shared as well as distinct roles of EHD proteins revealed by biochemical and functional comparisons in mammalian cells and C. elegans |
Q64088194 | Shared behavioral mechanisms underlie aggregation and swarming |
Q35585632 | Shared gene expression in distinct neurons expressing common selector genes |
Q37508663 | Shengmai Formula suppressed over-activated Ras/MAPK pathway in C. elegans by opening mitochondrial permeability transition pore via regulating cyclophilin D. |
Q28534968 | Shifts in the distribution of mass densities is a signature of caloric restriction in Caenorhabditis elegans |
Q28542808 | Shigella flexneri infection in Caenorhabditis elegans: cytopathological examination and identification of host responses |
Q41682734 | Short-term nicotine exposure induces long-lasting modulation of gustatory plasticity in Caenorhabditis elegans |
Q64882898 | Short-term starvation stress at young adult stages enhances meiotic activity of germ cells to maintain spermatogenesis in aged male Caenorhabditis elegans. |
Q57189944 | Shugoshin Is Essential for Meiotic Prophase Checkpoints in C. elegans |
Q38358191 | Signalling through RHEB-1 mediates intermittent fasting-induced longevity in C. elegans |
Q28478034 | Signalogs: orthology-based identification of novel signaling pathway components in three metazoans |
Q46322055 | Silencing of Repetitive DNA Is Controlled by a Member of an Unusual Caenorhabditis elegans Gene Family |
Q55228818 | Silencing of Syntaxin 1A in the Dopaminergic Neurons Decreases the Activity of the Dopamine Transporter and Prevents Amphetamine-Induced Behaviors in C. elegans. |
Q33225632 | Similar patterns of mitochondrial vulnerability and rescue induced by genetic modification of alpha-synuclein, parkin, and DJ-1 in Caenorhabditis elegans |
Q35899515 | Similar requirements for CDC-42 and the PAR-3/PAR-6/PKC-3 complex in diverse cell types |
Q90202659 | Similarities and differences in the biotransformation and transcriptomic responses of Caenorhabditis elegans and Haemonchus contortus to five different benzimidazole drugs |
Q35029517 | Single nucleotide polymorphisms in wild isolates of Caenorhabditis elegans. |
Q36342458 | Single swim sessions in C. elegans induce key features of mammalian exercise |
Q38349287 | Single-cell transcriptional analysis of taste sensory neuron pair in Caenorhabditis elegans |
Q30579989 | Single-molecule analysis of cell surface dynamics in Caenorhabditis elegans embryos. |
Q64979453 | Single-molecule dynamics of the P granule scaffold MEG-3 in the Caenorhabditis elegans zygote. |
Q34118162 | Single/low-copy integration of transgenes in Caenorhabditis elegans using an ultraviolet trimethylpsoralen method |
Q55636051 | Sir-2.1 mediated attenuation of α-synuclein expression by Alaskan bog blueberry polyphenols in a transgenic model of Caenorhabditis elegans. |
Q36660763 | Site-selected insertion of the transposon Tc1 into a Caenorhabditis elegans myosin light chain gene |
Q27490914 | Six RNA Viruses and Forty-One Hosts: Viral Small RNAs and Modulation of Small RNA Repertoires in Vertebrate and Invertebrate Systems |
Q34100473 | Six and Eya promote apoptosis through direct transcriptional activation of the proapoptotic BH3-only gene egl-1 in Caenorhabditis elegans |
Q59794878 | Sleep Counteracts Aging Phenotypes to Survive Starvation-Induced Developmental Arrest in C. elegans |
Q36875603 | Sleep and Development in Genetically Tractable Model Organisms |
Q36723404 | Sleep-active neuron specification and sleep induction require FLP-11 neuropeptides to systemically induce sleep |
Q33618993 | Small DNA pieces in C. elegans are intermediates of DNA fragmentation during apoptosis |
Q41096952 | Small GTPases promote actin coat formation on microsporidian pathogens traversing the apical membrane of Caenorhabditis elegans intestinal cells |
Q91863777 | Small Molecule Modifiers of In Vitro Manganese Transport Alter Toxicity In Vivo |
Q37461155 | Small RNA in situ hybridization in Caenorhabditis elegans, combined with RNA-seq, identifies germline-enriched microRNAs |
Q50082693 | Small RNA-mediated Cry toxin silencing allows Bacillus thuringiensis to evade Caenorhabditis elegans avoidance behavioral defenses. |
Q34299392 | Small heat-shock proteins protect from heat-stroke-associated neurodegeneration |
Q57292355 | Small molecule inhibits α-synuclein aggregation, disrupts amyloid fibrils, and prevents degeneration of dopaminergic neurons |
Q27305142 | Small molecule injection into single-cell C. elegans embryos via carbon-reinforced nanopipettes |
Q37645771 | Small molecule modulator of sigma 2 receptor is neuroprotective and reduces cognitive deficits and neuroinflammation in experimental models of Alzheimer's disease |
Q38602469 | Small nucleoli are a cellular hallmark of longevity |
Q89518731 | Small-RNA-mediated transgenerational silencing of histone genes impairs fertility in piRNA mutants |
Q34567291 | Small-molecule-mediated axonal branching in Caenorhabditis elegans |
Q61804389 | Smart scanning for low-illumination and fast RESOLFT nanoscopy in vivo |
Q33760246 | SnAvi--a new tandem tag for high-affinity protein-complex purification |
Q57377899 | Sodium sulfite is a potential hypoxia inducer that mimics hypoxic stress in Caenorhabditis elegans |
Q35913560 | Soil Nitrogen Status Modifies Rice Root Response to Nematode-Bacteria Interactions in the Rhizosphere |
Q80386245 | Soil nematodes mediate positive interactions between legume plants and rhizobium bacteria |
Q93335917 | Soma-germ line interactions and a role for muscle in the regulation of C. elegans sperm motility |
Q72064826 | Somatic damage to the X chromosome of the nematode Caenorhabditis elegans induced by gamma radiation |
Q36914456 | Somatic excision of transposable element Tc1 from the Bristol genome of Caenorhabditis elegans |
Q40882330 | Somatic expression of unc-54 and vha-6 mRNAs declines but not pan-neuronal rgef-1 and unc-119 expression in aging Caenorhabditis elegans |
Q37465080 | Somatic increase of CCT8 mimics proteostasis of human pluripotent stem cells and extends C. elegans lifespan |
Q37271689 | Somatically expressed germ-granule components, PGL-1 and PGL-3, repress programmed cell death in C. elegans |
Q35130721 | Some C. elegans class B synthetic multivulva proteins encode a conserved LIN-35 Rb-containing complex distinct from a NuRD-like complex |
Q35663393 | Some, but not all, retromer components promote morphogenesis of C. elegans sensory compartments |
Q30402051 | Sonogenetics is a non-invasive approach to activating neurons in Caenorhabditis elegans |
Q48092080 | Sophisticated lessons from simple organisms: appreciating the value of curiosity-driven research |
Q39114156 | Sorbus alnifolia protects dopaminergic neurodegeneration in Caenorhabditis elegans |
Q47339817 | Sorting nexin 3 mutation impairs development and neuronal function in Caenorhabditis elegans |
Q35392007 | Spastin binds to lipid droplets and affects lipid metabolism |
Q37580008 | Spatial and Temporal Analysis of Active ERK in the C. elegans Germline |
Q41524804 | Spatial control of active CDC-42 during collective migration of hypodermal cells in Caenorhabditis elegans. |
Q41612718 | Spatial function of the oxidative DNA damage response in radiation induced bystander effects in intra- and inter-system of Caenorhabditis elegans |
Q37603781 | Spatial patterning of P granules by RNA-induced phase separation of the intrinsically-disordered protein MEG-3 |
Q35221476 | Spatial regulation of lag-2 transcription during vulval precursor cell fate patterning in Caenorhabditis elegans |
Q64054756 | Spatial regulation of the polarity kinase PAR-1 by parallel inhibitory mechanisms |
Q39069162 | Spatiotemporal coupling and decoupling of gene transcription with DNA replication origins during embryogenesis in C. elegans |
Q35943942 | Spatiotemporal localization of D-amino acid oxidase and D-aspartate oxidases during development in Caenorhabditis elegans |
Q38694774 | Spatiotemporal regulation of autophagy during Caenorhabditis elegans aging |
Q27309068 | Specific RNA Interference in Caenorhabditis elegans by Ingested dsRNA Expressed in Bacillus subtilis |
Q34007934 | Specific alpha- and beta-tubulin isotypes optimize the functions of sensory Cilia in Caenorhabditis elegans |
Q36635861 | Specific conserved C-terminal amino acids of Caenorhabditis elegans HMP-1/α-catenin modulate F-actin binding independently of vinculin |
Q42622243 | Specific insulin-like peptides encode sensory information to regulate distinct developmental processes |
Q43179779 | Specific microRNAs regulate heat stress responses in Caenorhabditis elegans |
Q34613123 | Specification of germ cell fates by FOG-3 has been conserved during nematode evolution |
Q40482438 | Spectral insights into the transformation and distribution of CdSe quantum dots in microorganisms during food-chain transport. |
Q70884053 | Spectrum of 32P-induced mutants of Caenorbabditis elegans |
Q35604035 | Spectrum of variations in dog-1/FANCJ and mdf-1/MAD1 defective Caenorhabditis elegans strains after long-term propagation |
Q34606820 | Sperm competition in the absence of fertilization in Caenorhabditis elegans. |
Q35644773 | Sperm development and motility are regulated by PP1 phosphatases in Caenorhabditis elegans |
Q47789760 | Sperm isolation and biochemical analysis of the major sperm protein from Caenorhabditis elegans |
Q41364343 | Sperm morphogenesis in wild-type and fertilization-defective mutants of Caenorhabditis elegans |
Q71994587 | Sperm precedence in a hermaphroditic nematode (Caenorhabditis elegans) is due to competitive superiority of male sperm |
Q35620409 | Sperm status regulates sexual attraction in Caenorhabditis elegans |
Q33348988 | Spermatogenesis-defective (spe) mutants of the nematode Caenorhabditis elegans provide clues to solve the puzzle of male germline functions during reproduction |
Q33495558 | Spermatogenesis-specific features of the meiotic program in Caenorhabditis elegans |
Q36618653 | Spermidine promotes mating and fertilization efficiency in model organisms |
Q30369463 | Spermidine protects against α-synuclein neurotoxicity. |
Q92099227 | Sphingolipidomic Analysis of C. elegans reveals Development- and Environment-dependent Metabolic Features |
Q58748929 | Sphingosine Kinase Activates the Mitochondrial Unfolded Protein Response and Is Targeted to Mitochondria by Stress |
Q36570686 | Spindle assembly checkpoint gene mdf-1 regulates germ cell proliferation in response to nutrition signals in C. elegans |
Q30497012 | Spindle assembly checkpoint genes reveal distinct as well as overlapping expression that implicates MDF-2/Mad2 in postembryonic seam cell proliferation in Caenorhabditis elegans |
Q36210732 | Spindle assembly checkpoint proteins regulate and monitor meiotic synapsis in C. elegans |
Q52717063 | Spindle assembly checkpoint strength is linked to cell fate in the C. elegans embryo. |
Q28611303 | Spindle dynamics and the role of gamma-tubulin in early Caenorhabditis elegans embryos |
Q36119905 | Splicing Machinery Facilitates Post-Transcriptional Regulation by FBFs and Other RNA-Binding Proteins in Caenorhabditis elegans Germline |
Q27316202 | Splicing factors control C. elegans behavioural learning in a single neuron by producing DAF-2c receptor |
Q36659894 | Splicing in Caenorhabditis elegans does not require an AG at the 3' splice acceptor site |
Q83231047 | Splicing in a single neuron is coordinately controlled by RNA binding proteins and transcription factors |
Q36556958 | Splicing removes the Caenorhabditis elegans transposon Tc1 from most mutant pre-mRNAs |
Q52723971 | Split cGAL, an intersectional strategy using a split intein for refined spatiotemporal transgene control in Caenorhabditis elegans. |
Q27324147 | Spreading of a prion domain from cell-to-cell by vesicular transport in Caenorhabditis elegans |
Q50355391 | Spt4 selectively regulates the expression of C9orf72 sense and antisense mutant transcripts. |
Q30444256 | Stabilization of RAD-51-DNA filaments via an interaction domain in Caenorhabditis elegans BRCA2 |
Q35880035 | Stabilization of RNT-1 protein, runt-related transcription factor (RUNX) protein homolog of Caenorhabditis elegans, by oxidative stress through mitogen-activated protein kinase pathway |
Q30478491 | Stabilization of cell polarity by the C. elegans RING protein PAR-2. |
Q46770214 | Stabilization of nontoxic Aβ-oligomers: insights into the mechanism of action of hydroxyquinolines in Alzheimer's disease |
Q51133234 | Stable Heritable Germline Silencing Directs Somatic Silencing at an Endogenous Locus. |
Q38601965 | Stable-isotope labeling with amino acids in nematodes. |
Q90070141 | Stage-specific combinations of opposing poly(A) modifying enzymes guide gene expression during early oogenesis |
Q36885612 | Stage-specific patterns of collagen gene expression during development of Caenorhabditis elegans |
Q30445078 | Staphylococcal biofilm exopolysaccharide protects against Caenorhabditis elegans immune defenses |
Q31142975 | Staphylococcus aureus virulence factors identified by using a high-throughput Caenorhabditis elegans-killing model |
Q50712938 | Starvation induces cAMP response element-binding protein-dependent gene expression through octopamine-Gq signaling in Caenorhabditis elegans. |
Q30651780 | Starvation-induced collective behavior in C. elegans |
Q89496650 | Statins Induce a DAF-16/Foxo-dependent Longevity Phenotype via JNK-1 through Mevalonate Depletion in C. elegans |
Q35938123 | Staufen Negatively Modulates MicroRNA Activity in Caenorhabditis elegans |
Q38755568 | Stem cells: the new "model organism". |
Q43033371 | Step response analysis of thermotaxis in Caenorhabditis elegans. |
Q33213374 | Step-response analysis of chemotaxis in Caenorhabditis elegans. |
Q28468527 | Stereotypical Escape Behavior in Caenorhabditis elegans Allows Quantification of Effective Heat Stimulus Level |
Q39874356 | Sterilization and growth inhibition of Caenorhabditis elegans by 5-fluorodeoxyuridine |
Q24792967 | Sterol-derived hormone(s) controls entry into diapause in Caenorhabditis elegans by consecutive activation of DAF-12 and DAF-16 |
Q27333654 | Stimulation of host immune defenses by a small molecule protects C. elegans from bacterial infection |
Q30495978 | Stimulation of movement in a quiescent, hibernation-like form of Caenorhabditis elegans by dopamine signaling |
Q36296637 | Stochastic assembly produces heterogeneous communities in the Caenorhabditis elegans intestine |
Q35200126 | Stochastic blockmodeling of the modules and core of the Caenorhabditis elegans connectome |
Q47111902 | Stochastic loss and gain of symmetric divisions in the C. elegans epidermis perturbs robustness of stem cell number. |
Q99613302 | Stoichiometric interactions explain spindle dynamics and scaling across 100 million years of nematode evolution |
Q34328154 | Stomatin inhibits pannexin-1-mediated whole-cell currents by interacting with its carboxyl terminal |
Q38572873 | Strain evolution in Caenorhabditis elegans: transposable elements as markers of interstrain evolutionary history |
Q35618284 | Strain-specific telomere length revealed by single telomere length analysis in Caenorhabditis elegans |
Q64388663 | Strategies for Efficient Genome Editing Using CRISPR-Cas9 |
Q37238402 | Strategies for automated analysis of C. elegans locomotion |
Q53685393 | Streptothricin acetyl transferase 2 (Sat2): A dominant selection marker for Caenorhabditis elegans genome editing. |
Q97528365 | Stress and timing associated with Caenorhabditis elegans immobilization methods |
Q33293515 | Stress generation and filament turnover during actin ring constriction |
Q30828424 | Stress response in Caenorhabditis elegans caused by optical tweezers: wavelength, power, and time dependence |
Q47703549 | Stress-Induced Sleep After Exposure to Ultraviolet Light Is Promoted by p53 in Caenorhabditis elegans |
Q28510624 | Stressed-induced TMEM135 protein is part of a conserved genetic network involved in fat storage and longevity regulation in Caenorhabditis elegans |
Q36274367 | Structural Complexity of Early Embryos: A Study on the Nematode Caenorhabditis elegans |
Q27676598 | Structural Insights into Apoptotic DNA Degradation by CED-3 Protease Suppressor-6 (CPS-6) from Caenorhabditis elegans |
Q27683864 | Structural and Functional Characterization of the α-Tubulin Acetyltransferase MEC-17 |
Q38607680 | Structural and functional characterization of the α-catenin·β-catenin binding interface in Caenorhabditis elegans reveals conserved requirements for cell-cell adhesion in metazoans. |
Q41376858 | Structural and functional diversity in the neuronal microtubules of Caenorhabditis elegans |
Q33974916 | Structural and functional evaluation of C. elegans filamins FLN-1 and FLN-2. |
Q27683827 | Structural and functional implications of the QUA2 domain on RNA recognition by GLD-1 |
Q36956243 | Structural basis and function of XRN2 binding by XTB domains |
Q41633223 | Structural basis for CRMP2-induced axonal microtubule formation |
Q27700128 | Structural basis for Na(+) transport mechanism by a light-driven Na(+) pump |
Q36013308 | Structural components of the nonstriated contractile apparatuses in the Caenorhabditis elegans gonadal myoepithelial sheath and their essential roles for ovulation |
Q30482884 | Structural determinants underlying the temperature-sensitive nature of a Galpha mutant in asymmetric cell division of Caenorhabditis elegans |
Q35921707 | Structural domains required for Caenorhabditis elegans G protein-coupled receptor kinase 2 (GRK-2) function in vivo |
Q36392594 | Structural insight into the mechanism of synergistic autoinhibition of SAD kinases |
Q33641456 | Structural maintenance of chromosomes (SMC) proteins promote homolog-independent recombination repair in meiosis crucial for germ cell genomic stability |
Q34608024 | Structural requirements for the tissue-specific and tissue-general functions of the Caenorhabditis elegans epidermal growth factor LIN-3. |
Q27681244 | Structural study of TTR-52 reveals the mechanism by which a bridging molecule mediates apoptotic cell engulfment |
Q57179631 | Structure and conserved function of iso-branched sphingoid bases from the nematode |
Q42076666 | Structure and evolution of a family of interspersed repetitive DNA sequences in Caenorhabditis elegans |
Q72893160 | Structure and function relationships among calmodulins and troponin C-like proteins from divergent eukaryotic organisms |
Q37591298 | Structure and physiological activity of the motoneurons of the nematode Ascaris |
Q36064950 | Structure, evolution and properties of a novel repetitive DNA family in Caenorhabditis elegans |
Q27938882 | Structure-based functional analysis reveals a role for the SM protein Sly1p in retrograde transport to the endoplasmic reticulum |
Q34704137 | Structure-function study of mammalian Munc18-1 and C. elegans UNC-18 implicates domain 3b in the regulation of exocytosis |
Q36844952 | Structures of spontaneous deletions in Caenorhabditis elegans |
Q24814026 | Studies on Acanthocheilonema viteae cystatin: genomic organization, promoter studies and expression in Caenorhabditis elegans |
Q91868263 | Studies on the antifungal and serotonin receptor agonist activities of the secondary metabolites from piezotolerant deep-sea fungus Ascotricha sp |
Q36749672 | Studying polyglutamine aggregation in Caenorhabditis elegans using an analytical ultracentrifuge equipped with fluorescence detection. |
Q33863500 | Subcellular in vivo time-lapse imaging and optical manipulation of Caenorhabditis elegans in standard multiwell plates |
Q35908495 | Sublethal Toxicity Endpoints of Heavy Metals to the Nematode Caenorhabditis elegans |
Q27318584 | Subunit composition of a DEG/ENaC mechanosensory channel of Caenorhabditis elegans |
Q88726156 | Subunits of the DNA polymerase alpha-primase complex promote Notch-mediated proliferation with discrete and shared functions in C. elegans germline |
Q27318485 | Sumoylated NHR-25/NR5A regulates cell fate during C. elegans vulval development |
Q30663031 | Super-resolution mapping of glutamate receptors in C. elegans by confocal correlated PALM |
Q38891467 | Superoxide dismutase SOD-1 modulates C. elegans pathogen avoidance behavior |
Q35889471 | Superoxide dismutase is dispensable for normal animal lifespan |
Q33810396 | Superresolution microscopy reveals the three-dimensional organization of meiotic chromosome axes in intact Caenorhabditis elegans tissue |
Q27320962 | Suppression of RNAi by dsRNA-degrading RNaseIII enzymes of viruses in animals and plants |
Q40256638 | Suppression of transcriptional drift extends C. elegans lifespan by postponing the onset of mortality |
Q36533561 | Suppressor mutations identify amino acids in PAA-1/PR65 that facilitate regulatory RSA-1/B″ subunit targeting of PP2A to centrosomes in C. elegans |
Q30360903 | Suppressor mutations suggest a surface on PAT-4 (Integrin-linked Kinase) that interacts with UNC-112 (Kindlin). |
Q28623285 | Suppressors of a lin-12 hypomorph define genes that interact with both lin-12 and glp-1 in Caenorhabditis elegans |
Q33961962 | Suppressors of glp-1, a gene required for cell communication during development in Caenorhabditis elegans, define a set of interacting genes |
Q35757666 | Suppressors of spindle checkpoint defect (such) mutants identify new mdf-1/MAD1 interactors in Caenorhabditis elegans |
Q36990715 | Suppressors of the cdc-25.1(gf)-associated intestinal hyperplasia reveal important maternal roles for prp-8 and a subset of splicing factors in C. elegans |
Q33967312 | Suppressors of the unc-73 gene of Caenorhabditis elegans. |
Q34610754 | Suppressors of transforming growth factor-beta pathway mutants in the Caenorhabditis elegans dauer formation pathway |
Q35844840 | Suppressors of zyg-1 define regulators of centrosome duplication and nuclear association in Caenorhabditis elegans |
Q27324179 | Surveillance-Activated Defenses Block the ROS–Induced Mitochondrial Unfolded Protein Response |
Q30495199 | Suspended animation extends survival limits of Caenorhabditis elegans and Saccharomyces cerevisiae at low temperature |
Q39033268 | Sustained centrosome-cortical contact ensures robust polarization of the one-cell C. elegans embryo |
Q38948100 | Sydney Brenner on the Genetics of Caenorhabditis elegans. |
Q92539178 | Sydney Brenner: The birth of a model organism and the worm's connection to reproductive biology |
Q94515540 | Sydney Brenner—a personal perspective |
Q30494245 | Symmetry breaking and polarization of the C. elegans zygote by the polarity protein PAR-2 |
Q41882631 | Synapse location during growth depends on glia location |
Q27346352 | Synapse-Assembly Proteins Maintain Synaptic Vesicle Cluster Stability and Regulate Synaptic Vesicle Transport in Caenorhabditis elegans |
Q35205580 | Synapsis and chiasma formation in Caenorhabditis elegans require HIM-3, a meiotic chromosome core component that functions in chromosome segregation |
Q35945640 | Synapsis-defective mutants reveal a correlation between chromosome conformation and the mode of double-strand break repair during Caenorhabditis elegans meiosis |
Q35804006 | Synapsis-dependent and -independent mechanisms stabilize homolog pairing during meiotic prophase in C. elegans |
Q30840162 | Synaptic UNC13A protein variant causes increased neurotransmission and dyskinetic movement disorder |
Q35221490 | Synaptic activity regulates the abundance and binding of complexin |
Q22336987 | Synaptic polarity depends on phosphatidylinositol signaling regulated by myo-inositol monophosphatase in Caenorhabditis elegans |
Q30547814 | Synaptic polarity of the interneuron circuit controlling C. elegans locomotion |
Q26269869 | Synaptic vesicle exocytosis |
Q52348681 | Synaptogenesis Is Modulated by Heparan Sulfate in Caenorhabditis elegans. |
Q35190971 | Synaptogenesis in the CNS: an odyssey from wiring together to firing together |
Q30009179 | Synaptojanin cooperates in vivo with endophilin through an unexpected mechanism |
Q39412683 | Synaptonemal Complex Components Are Required for Meiotic Checkpoint Function in Caenorhabditis elegans |
Q35218991 | Synaptotagmin 1 directs repetitive release by coupling vesicle exocytosis to the Rab3 cycle |
Q58586491 | Syncytial germline architecture is actively maintained by contraction of an internal actomyosin corset |
Q37518043 | Syndapin/SDPN-1 is required for endocytic recycling and endosomal actin association in the C. elegans intestine |
Q28388500 | Synergistic effects induced by a low dose of diesel particulate extract and ultraviolet-A in Caenorhabditis elegans: DNA damage-triggered germ cell apoptosis |
Q36734003 | Syntaxin opening by the MUN domain underlies the function of Munc13 in synaptic-vesicle priming |
Q42088439 | Synthesis of paucimannose N-glycans by Caenorhabditis elegans requires prior actions of UDP-N-acetyl-D-glucosamine:alpha-3-D-mannoside beta1,2-N-acetylglucosaminyltransferase I, alpha3,6-mannosidase II and a specific membrane-bound beta-N-acetylgluc |
Q28829473 | Synthetic Ligands of Cannabinoid Receptors Affect Dauer Formation in the Nematode Caenorhabditis elegans |
Q49788245 | Systematic Functional Characterization of Human 21st Chromosome Orthologs in Caenorhabditis elegans. |
Q47728022 | Systematic Proteogenomic Approach To Exploring a Novel Function for NHERF1 in Human Reproductive Disorder: Lessons for Exploring Missing Proteins. |
Q34471570 | Systematic analyses of rpm-1 suppressors reveal roles for ESS-2 in mRNA splicing in Caenorhabditis elegans |
Q47766760 | Systematic analysis of DNA crosslink repair pathways during development and aging in Caenorhabditis elegans |
Q37314308 | Systematic analysis of dynamic miRNA-target interactions during C. elegans development. |
Q28468287 | Systematic development of small molecules to inhibit specific microscopic steps of Aβ42 aggregation in Alzheimer's disease |
Q60916829 | Systematic evaluation of C. elegans lincRNAs with CRISPR knockout mutants |
Q33388643 | Systematic identification of gene activities promoting hypoxic death |
Q30541649 | Systematic profiling of Caenorhabditis elegans locomotive behaviors reveals additional components in G-protein Gαq signaling |
Q34572464 | Systematic, RNA-interference-mediated identification of mus-101 modifier genes in Caenorhabditis elegans |
Q30482661 | Systemic RNAi mediated gene silencing in the anhydrobiotic nematode Panagrolaimus superbus |
Q27311127 | Systemic Regulation of RAS/MAPK Signaling by the Serotonin Metabolite 5-HIAA |
Q37075691 | Systemic regulation of starvation response in Caenorhabditis elegans |
Q46154053 | Systems level circuit model of C. elegans undulatory locomotion: mathematical modeling and molecular genetics. |
Q94521055 | TALPID3 and ANKRD26 selectively orchestrate FBF1 localization and cilia gating |
Q33784334 | TBC-2 is required for embryonic yolk protein storage and larval survival during L1 diapause in Caenorhabditis elegans |
Q33948559 | TBC-2 regulates RAB-5/RAB-7-mediated endosomal trafficking in Caenorhabditis elegans |
Q27333769 | TBC-8, a putative RAB-2 GAP, regulates dense core vesicle maturation in Caenorhabditis elegans |
Q34807584 | TDP-1, the Caenorhabditis elegans ortholog of TDP-43, limits the accumulation of double-stranded RNA. |
Q34829446 | TDP-43 neurotoxicity and protein aggregation modulated by heat shock factor and insulin/IGF-1 signaling |
Q92493386 | TDP2 negatively regulates axon regeneration by inducing SUMOylation of an Ets transcription factor |
Q33554213 | TEG-1 CD2BP2 controls miRNA levels by regulating miRISC stability in C. elegans and human cells |
Q36304336 | TEG-1 CD2BP2 regulates stem cell proliferation and sex determination in the C. elegans germ line and physically interacts with the UAF-1 U2AF65 splicing factor |
Q33521309 | TGF-beta Sma/Mab signaling mutations uncouple reproductive aging from somatic aging |
Q34782904 | TGF-β signaling can act from multiple tissues to regulate C. elegans body size |
Q26850420 | TGF-β signaling in C. elegans |
Q61806923 | TIAM-1/GEF can shape somatosensory dendrites independently of its GEF activity by regulating F-actin localization |
Q33260760 | TILLING is an effective reverse genetics technique for Caenorhabditis elegans |
Q37424724 | TORC2 signaling antagonizes SKN-1 to induce C. elegans mesendodermal embryonic development |
Q83228113 | TRAIP drives replisome disassembly and mitotic DNA repair synthesis at sites of incomplete DNA replication |
Q27309241 | TRIP13PCH-2 promotes Mad2 localization to unattached kinetochores in the spindle checkpoint response |
Q30578892 | TRPM channels modulate epileptic-like convulsions via systemic ion homeostasis |
Q30587013 | TRPV channel-mediated calcium transients in nociceptor neurons are dispensable for avoidance behaviour |
Q93335822 | TRPV1 pore turret dictates distinct DkTx and capsaicin gating |
Q27335531 | TRY-5 is a sperm-activating protease in Caenorhabditis elegans seminal fluid |
Q30316454 | TSG (2,3,5,4'-Tetrahydroxystilbene-2-O- β -D-glucoside) from the Chinese Herb Polygonum multiflorum Increases Life Span and Stress Resistance of Caenorhabditis elegans |
Q40235744 | Taking advantage of reduced droplet-surface interaction to optimize transport of bioanalytes in digital microfluidics |
Q37381857 | Talin requires beta-integrin, but not vinculin, for its assembly into focal adhesion-like structures in the nematode Caenorhabditis elegans |
Q52242543 | Tandemly duplicated Caenorhabditis elegans collagen genes differ in their modes of splicing |
Q99555935 | Targeted Central Nervous System Irradiation of Caenorhabditis elegans Induces a Limited Effect on Motility |
Q89294641 | Targeted Chromosomal Rearrangements via Combinatorial Use of CRISPR/Cas9 and Cre/LoxP Technologies in Caenorhabditis elegans |
Q36365219 | Targeted Chromosomal Translocations and Essential Gene Knockout Using CRISPR/Cas9 Technology in Caenorhabditis elegans |
Q24671860 | Targeted cell killing by reconstituted caspases |
Q37493438 | Targeted gene knockout reveals a role in meiotic recombination for ZHP-3, a Zip3-related protein in Caenorhabditis elegans |
Q28074694 | Targeted genome engineering in Caenorhabditis elegans |
Q46945596 | Targeted mutagenesis in a human-parasitic nematode |
Q90696326 | Targeted thermal stimulation and high-content phenotyping reveal that the C. elegans escape response integrates current behavioral state and past experience |
Q35676920 | Targeting Homologous Recombination in Notch-Driven C. elegans Stem Cell and Human Tumors |
Q27301090 | Tau mutant A152T, a risk factor for FTD/PSP, induces neuronal dysfunction and reduced lifespan independently of aggregation in a C. elegans Tauopathy model |
Q35005293 | Tc1 transposition and mutator activity in a Bristol strain of Caenorhabditis elegans |
Q37483933 | Tc4, a Caenorhabditis elegans transposable element with an unusual fold-back structure |
Q36262543 | Tea polyphenols as an antivirulence compound Disrupt Quorum-Sensing Regulated Pathogenicity of Pseudomonas aeruginosa |
Q43078935 | Technical report: exploring the basis of congenital myasthenic syndromes in an undergraduate course, using the model organism, Caenorhabditis elegans |
Q36128245 | Telomere maintenance through recruitment of internal genomic regions |
Q35148883 | Telomeric Position Effect Variegation in Saccharomyces cerevisiae by Caenorhabditis elegans Linker Histones Suggests a Mechanistic Connection between Germ Line and Telomeric Silencing |
Q43742053 | Temperature dependent binding of mebendazole to tubulin in benzimidazole-susceptible and -resistant strains of Trichostrongylus colubriformis and Caenorhabditis elegans |
Q35045354 | Temperature, oxygen, and salt-sensing neurons in C. elegans are carbon dioxide sensors that control avoidance behavior. |
Q27308150 | Temperature- and touch-sensitive neurons couple CNG and TRPV channel activities to control heat avoidance in Caenorhabditis elegans |
Q33950484 | Temperature-sensitive lethal mutations on yeast chromosome I appear to define only a small number of genes |
Q47849134 | Temperature-sensitive mutation affecting myofilament assembly in Caenorhabditis elegans |
Q80441480 | Temporal activity patterns in thermosensory neurons of freely moving Caenorhabditis elegans encode spatial thermal gradients |
Q28776675 | Temporal and spatial expression patterns of the small heat shock (hsp16) genes in transgenic Caenorhabditis elegans |
Q47108673 | Temporal dynamics of gene expression in heat-stressed Caenorhabditis elegans. |
Q36990499 | Temporal dynamics of outcrossing and host mortality rates in host-pathogen experimental coevolution |
Q46732435 | Temporal regulation of cuticle synthesis during development of Caenorhabditis elegans |
Q41662098 | Temporal regulation of epithelium formation mediated by FoxA, MKLP1, MgcRacGAP, and PAR-6. |
Q33258828 | Temporal regulation of foregut development by HTZ-1/H2A.Z and PHA-4/FoxA |
Q30519548 | Temporally-regulated quick activation and inactivation of Ras is important for olfactory behaviour |
Q57008747 | Terminal uridylyltransferases target RNA viruses as part of the innate immune system |
Q42790926 | Terrain following and applications: Caenorhabditis elegans swims along the floor using a bump and undulate strategy |
Q27311391 | Tertiary siRNAs mediate paramutation in C. elegans |
Q47069117 | Tests for parental imprinting in the nematode Caenorhabditis elegans |
Q54382204 | Tetramethylpyrazine analogue CXC195 protects against cerebral ischemia/reperfusion-induced apoptosis through PI3K/Akt/GSK3β pathway in rats. |
Q28542478 | Tetraspanin (TSP-17) protects dopaminergic neurons against 6-OHDA-induced neurodegeneration in C. elegans |
Q27331504 | Tetraspanin is required for generation of reactive oxygen species by the dual oxidase system in Caenorhabditis elegans |
Q30828185 | TfAP-2 is required for night sleep in Drosophila. |
Q30741759 | The 14-3-3 protein PAR-5 regulates the asymmetric localization of the LET-99 spindle positioning protein. |
Q24298486 | The AAA-ATPase VCP/p97 promotes 53BP1 recruitment by removing L3MBTL1 from DNA double-strand breaks |
Q33249990 | The AFD sensory neurons encode multiple functions underlying thermotactic behavior in Caenorhabditis elegans. |
Q55037040 | The AFF-1 exoplasmic fusogen is required for endocytic scission and seamless tube elongation. |
Q37175375 | The ALP-Enigma protein ALP-1 functions in actin filament organization to promote muscle structural integrity in Caenorhabditis elegans |
Q30497242 | The AP-1 clathrin adaptor facilitates cilium formation and functions with RAB-8 in C. elegans ciliary membrane transport. |
Q27308855 | The AP-2 Transcription Factor APTF-2 Is Required for Neuroblast and Epidermal Morphogenesis in Caenorhabditis elegans Embryogenesis |
Q35621969 | The AP2 clathrin adaptor protein complex regulates the abundance of GLR-1 glutamate receptors in the ventral nerve cord of Caenorhabditis elegans |
Q41822656 | The Adhesion Molecule KAL-1/anosmin-1 Regulates Neurite Branching through a SAX-7/L1CAM-EGL-15/FGFR Receptor Complex. |
Q37691095 | The Adverse Effects of Triptolide on the Reproductive System of Caenorhabditis elegans: Oogenesis Impairment and Decreased Oocyte Quality |
Q27303959 | The Amyloid Precursor Protein Controls PIKfyve Function |
Q36282013 | The Analysis of Gene Expression on Fertility Decline in Caenorhabditis elegans after the Treatment with 5-Fluorouracil |
Q36903333 | The Anaphase-Promoting Complex (APC) ubiquitin ligase affects chemosensory behavior in C. elegans |
Q40010489 | The Anaphase-Promoting Complex (APC) ubiquitin ligase regulates GABA transmission at the C. elegans neuromuscular junction |
Q41682166 | The Annona muricata leaf ethanol extract affects mobility and reproduction in mutant strain NB327 Caenorhabditis elegans |
Q27312637 | The ArfGEF GBF-1 Is Required for ER Structure, Secretion and Endocytic Transport in C. elegans |
Q36837028 | The Arp2/3 activators WAVE and WASP have distinct genetic interactions with Rac GTPases in Caenorhabditis elegans axon guidance |
Q30490986 | The Arp2/3 complex, UNC-115/abLIM, and UNC-34/Enabled regulate axon guidance and growth cone filopodia formation in Caenorhabditis elegans |
Q36724064 | The Ascaris suum nicotinic receptor, ACR-16, as a drug target: Four novel negative allosteric modulators from virtual screening. |
Q38429066 | The Atypical MAP Kinase SWIP-13/ERK8 Regulates Dopamine Transporters Through a Rho-Dependent Mechanism. |
Q52589292 | The Atypical Rho GTPase CHW-1 Works with SAX-3/Robo To Mediate Axon Guidance in Caenorhabditis elegans. |
Q37323153 | The BCL-2-like protein CED-9 of C. elegans promotes FZO-1/Mfn1,2- and EAT-3/Opa1-dependent mitochondrial fusion |
Q35061925 | The BLI-3/TSP-15/DOXA-1 dual oxidase complex is required for iodide toxicity in Caenorhabditis elegans |
Q90438658 | The Balance between Mono- and NEDD8-Chains Controlled by NEDP1 upon DNA Damage Is a Regulatory Module of the HSP70 ATPase Activity |
Q58616987 | The Bermuda Triangle: The Pragmatics, Policies, and Principles for Data Sharing in the History of the Human Genome Project |
Q35571482 | The Bicoid class homeodomain factors ceh-36/OTX and unc-30/PITX cooperate in C. elegans embryonic progenitor cells to regulate robust development |
Q58765231 | The C-terminal coiled-coil domain of Corynebacterium diphtheriae DIP0733 is crucial for interaction with epithelial cells and pathogenicity in invertebrate animal model systems |
Q53436292 | The C-terminal of CASY-1/Calsyntenin regulates GABAergic synaptic transmission at the Caenorhabditis elegans neuromuscular junction. |
Q92518188 | The C. elegans CHP1 homolog, pbo-1, functions in innate immunity by regulating the pH of the intestinal lumen |
Q34393555 | The C. elegans CSR-1 argonaute pathway counteracts epigenetic silencing to promote germline gene expression |
Q27302364 | The C. elegans Chp/Wrch Ortholog CHW-1 Contributes to LIN-18/Ryk and LIN-17/Frizzled Signaling in Cell Polarity |
Q35177728 | The C. elegans Crumbs family contains a CRB3 homolog and is not essential for viability |
Q27333780 | The C. elegans D2-like dopamine receptor DOP-3 decreases behavioral sensitivity to the olfactory stimulus 1-octanol |
Q36226742 | The C. elegans Discoidin Domain Receptor DDR-2 Modulates the Met-like RTK-JNK Signaling Pathway in Axon Regeneration |
Q33385013 | The C. elegans EMAP-like protein, ELP-1 is required for touch sensation and associates with microtubules and adhesion complexes |
Q30485746 | The C. elegans F-spondin family protein SPON-1 maintains cell adhesion in neural and non-neural tissues |
Q27334177 | The C. elegans H3K27 demethylase UTX-1 is essential for normal development, independent of its enzymatic activity |
Q27334834 | The C. elegans Homolog of RBBP6 (RBPL-1) regulates fertility through controlling cell proliferation in the germline and nutrient synthesis in the intestine |
Q33643773 | The C. elegans Hox gene ceh-13 regulates cell migration and fusion in a non-colinear way. Implications for the early evolution of Hox clusters |
Q47672508 | The C. elegans Intestine As a Model for Intercellular Lumen Morphogenesis and In Vivo Polarized Membrane Biogenesis at the Single-cell Level: Labeling by Antibody Staining, RNAi Loss-of-function Analysis and Imaging |
Q36404895 | The C. elegans L1CAM homologue LAD-2 functions as a coreceptor in MAB-20/Sema2 mediated axon guidance |
Q40649340 | The C. elegans LIM homeobox gene lin-11 specifies multiple cell fates during vulval development |
Q35629132 | The C. elegans Myt1 ortholog is required for the proper timing of oocyte maturation |
Q35132398 | The C. elegans NR4A nuclear receptor gene nhr-6 promotes cell cycle progression in the spermatheca lineage |
Q28748241 | The C. elegans RSA complex localizes protein phosphatase 2A to centrosomes and regulates mitotic spindle assembly |
Q42984279 | The C. elegans SNAPc component SNPC-4 coats piRNA domains and is globally required for piRNA abundance |
Q38515423 | The C. elegans TGF-beta Dauer pathway regulates longevity via insulin signaling |
Q27320804 | The C. elegans TPR Containing Protein, TRD-1, Regulates Cell Fate Choice in the Developing Germ Line and Epidermis |
Q30489372 | The C. elegans Tailless/TLX transcription factor nhr-67 controls neuronal identity and left/right asymmetric fate diversification |
Q68464595 | The C. elegans Trans-spliced leader RNA is bound to Sm and has a trimethylguanosine cap |
Q36110308 | The C. elegans UNC-23 protein, a member of the BCL-2-associated athanogene (BAG) family of chaperone regulators, interacts with HSP-1 to regulate cell attachment and maintain hypodermal integrity |
Q33830458 | The C. elegans VAPB homolog VPR-1 is a permissive signal for gonad development |
Q34154691 | The C. elegans adult male germline: stem cells and sexual dimorphism |
Q27321293 | The C. elegans cGMP-dependent protein kinase EGL-4 regulates nociceptive behavioral sensitivity |
Q38418633 | The C. elegans dauer larva as a paradigm to study metabolic suppression and desiccation tolerance |
Q34515312 | The C. elegans dosage compensation complex mediates interphase X chromosome compaction |
Q30497313 | The C. elegans homolog of Drosophila Lethal giant larvae functions redundantly with PAR-2 to maintain polarity in the early embryo |
Q41890082 | The C. elegans homolog of the mammalian tumor suppressor Dep-1/Scc1 inhibits EGFR signaling to regulate binary cell fate decisions |
Q27329754 | The C. elegans male exercises directional control during mating through cholinergic regulation of sex-shared command interneurons |
Q34266474 | The C. elegans microRNA mir-71 acts in neurons to promote germline-mediated longevity through regulation of DAF-16/FOXO |
Q41843809 | The C. elegans mitochondrial K+(ATP) channel: a potential target for preconditioning |
Q28071970 | The C. elegans model in toxicity testing |
Q41916654 | The C. elegans p38 MAPK pathway regulates nuclear localization of the transcription factor SKN-1 in oxidative stress response |
Q36151083 | The C. elegans protein CEH-30 protects male-specific neurons from apoptosis independently of the Bcl-2 homolog CED-9. |
Q37424516 | The C. elegans tailless/Tlx homolog nhr-67 regulates a stage-specific program of linker cell migration in male gonadogenesis |
Q42621442 | The C. elegans unc-104 4 gene encodes a putative kinesin heavy chain-like protein |
Q34090580 | The C.elegans MAPK phosphatase LIP-1 is required for the G(2)/M meiotic arrest of developing oocytes |
Q46412377 | The CDK8 Complex and Proneural Proteins Together Drive Neurogenesis from a Mesodermal Lineage |
Q89693413 | The CHORD protein CHP-1 regulates EGF receptor trafficking and signaling in C. elegans and in human cells |
Q34587861 | The CRAL/TRIO and GOLD domain protein CGR-1 promotes induction of vulval cell fates in Caenorhabditis elegans and interacts genetically with the Ras signaling pathway |
Q33729305 | The CRL2LRR-1 ubiquitin ligase regulates cell cycle progression during C. elegans development |
Q30368429 | The CSN/COP9 signalosome regulates synaptonemal complex assembly during meiotic prophase I of Caenorhabditis elegans. |
Q37374551 | The Ca(2+)-dependent activator protein for secretion CAPS: do I dock or do I prime? |
Q36603128 | The Ca2+/Mn2+ ion-pump PMR1 links elevation of cytosolic Ca(2+) levels to α-synuclein toxicity in Parkinson's disease models |
Q27308477 | The CaM Kinase CMK-1 Mediates a Negative Feedback Mechanism Coupling the C. elegans Glutamate Receptor GLR-1 with Its Own Transcription |
Q34568854 | The Caenorhabditis elegans ABL-1 tyrosine kinase is required for Shigella flexneri pathogenesis |
Q35190195 | The Caenorhabditis elegans APC-related gene apr-1 is required for epithelial cell migration and Hox gene expression. |
Q24557446 | The Caenorhabditis elegans Aurora B kinase AIR-2 phosphorylates and is required for the localization of a BimC kinesin to meiotic and mitotic spindles |
Q33729115 | The Caenorhabditis elegans CDT-2 ubiquitin ligase is required for attenuation of EGFR signalling in vulva precursor cells |
Q30167815 | The Caenorhabditis elegans EGL-15 signaling pathway implicates a DOS-like multisubstrate adaptor protein in fibroblast growth factor signal transduction |
Q27334778 | The Caenorhabditis elegans Eph receptor activates NCK and N-WASP, and inhibits Ena/VASP to regulate growth cone dynamics during axon guidance |
Q36677319 | The Caenorhabditis elegans Ephrin EFN-4 Functions Non-cell Autonomously with Heparan Sulfate Proteoglycans to Promote Axon Outgrowth and Branching |
Q35102641 | The Caenorhabditis elegans GARP complex contains the conserved Vps51 subunit and is required to maintain lysosomal morphology |
Q37571891 | The Caenorhabditis elegans IMPAS gene, imp-2, is essential for development and is functionally distinct from related presenilins |
Q92518364 | The Caenorhabditis elegans INX-4/Innexin is required for the fine-tuning of temperature orientation in thermotaxis behavior |
Q27324417 | The Caenorhabditis elegans JNK signaling pathway activates expression of stress response genes by derepressing the Fos/HDAC repressor complex |
Q40561456 | The Caenorhabditis elegans MAPK phosphatase VHP-1 mediates a novel JNK-like signaling pathway in stress response |
Q27316318 | The Caenorhabditis elegans Myc-Mondo/Mad complexes integrate diverse longevity signals |
Q37353585 | The Caenorhabditis elegans NR4A nuclear receptor is required for spermatheca morphogenesis |
Q88670499 | The Caenorhabditis elegans Ortholog of TDP-43 Regulates the Chromatin Localization of the Heterochromatin Protein 1 Homolog HPL-2 |
Q27308887 | The Caenorhabditis elegans Protein FIC-1 Is an AMPylase That Covalently Modifies Heat-Shock 70 Family Proteins, Translation Elongation Factors and Histones |
Q34569329 | The Caenorhabditis elegans Ror RTK CAM-1 inhibits EGL-20/Wnt signaling in cell migration |
Q61455359 | The Caenorhabditis elegans SCC-3 homologue is required for meiotic synapsis and for proper chromosome disjunction in mitosis and meiosis |
Q35191574 | The Caenorhabditis elegans SH2 domain-containing protein tyrosine phosphatase PTP-2 participates in signal transduction during oogenesis and vulval development |
Q90286307 | The Caenorhabditis elegans SMOC-1 Protein Acts Cell Nonautonomously To Promote Bone Morphogenetic Protein Signaling |
Q34166897 | The Caenorhabditis elegans SUN protein UNC-84 interacts with lamin to transfer forces from the cytoplasm to the nucleoskeleton during nuclear migration |
Q33627241 | The Caenorhabditis elegans Ste20-related kinase and Rac-type small GTPase regulate the c-Jun N-terminal kinase signaling pathway mediating the stress response |
Q27339317 | The Caenorhabditis elegans T-box factor MLS-1 requires Groucho co-repressor interaction for uterine muscle specification |
Q27324679 | The Caenorhabditis elegans THO complex is required for the mitotic cell cycle and development |
Q33763733 | The Caenorhabditis elegans UNC-14 RUN domain protein binds to the kinesin-1 and UNC-16 complex and regulates synaptic vesicle localization |
Q36234657 | The Caenorhabditis elegans UNC-87 protein is essential for maintenance, but not assembly, of bodywall muscle |
Q33523009 | The Caenorhabditis elegans Werner syndrome protein functions upstream of ATR and ATM in response to DNA replication inhibition and double-strand DNA breaks. |
Q34049748 | The Caenorhabditis elegans aristaless orthologue, alr-1, is required for maintaining the functional and structural integrity of the amphid sensory organs |
Q33885210 | The Caenorhabditis elegans bus-2 mutant reveals a new class of O-glycans affecting bacterial resistance |
Q34214723 | The Caenorhabditis elegans cell death gene ced-4 encodes a novel protein and is expressed during the period of extensive programmed cell death |
Q47069382 | The Caenorhabditis elegans choline transporter CHO-1 sustains acetylcholine synthesis and motor function in an activity-dependent manner. |
Q34611147 | The Caenorhabditis elegans dosage compensation machinery is recruited to X chromosome DNA attached to an autosome |
Q36515754 | The Caenorhabditis elegans ekl (enhancer of ksr-1 lethality) genes include putative components of a germline small RNA pathway |
Q52580548 | The Caenorhabditis elegans gene ham-1 regulates daughter cell size asymmetry primarily in divisions that produce a small anterior daughter cell. |
Q35189396 | The Caenorhabditis elegans gene ham-2 links Hox patterning to migration of the HSN motor neuron |
Q27332402 | The Caenorhabditis elegans gene mfap-1 encodes a nuclear protein that affects alternative splicing |
Q33955478 | The Caenorhabditis elegans gene sdc-2 controls sex determination and dosage compensation in XX animals |
Q42536961 | The Caenorhabditis elegans gene unc-25 encodes glutamic acid decarboxylase and is required for synaptic transmission but not synaptic development. |
Q24312342 | The Caenorhabditis elegans gene unc-76 and its human homologs define a new gene family involved in axonal outgrowth and fasciculation |
Q36530182 | The Caenorhabditis elegans hif-1 gene encodes a bHLH-PAS protein that is required for adaptation to hypoxia |
Q28474884 | The Caenorhabditis elegans homolog of Gen1/Yen1 resolvases links DNA damage signaling to DNA double-strand break repair |
Q90592035 | The Caenorhabditis elegans homolog of the Evi1 proto-oncogene, egl-43, coordinates G1 cell cycle arrest with pro-invasive gene expression during anchor cell invasion |
Q34698220 | The Caenorhabditis elegans homologue of deleted in azoospermia is involved in the sperm/oocyte switch |
Q37375791 | The Caenorhabditis elegans homologue of the extracellular calcium binding protein SPARC/osteonectin affects nematode body morphology and mobility |
Q34360677 | The Caenorhabditis elegans homologue of the proto-oncogene ect-2 positively regulates RAS signalling during vulval development |
Q37102607 | The Caenorhabditis elegans ing-3 gene regulates ionizing radiation-induced germ-cell apoptosis in a p53-associated pathway |
Q35068251 | The Caenorhabditis elegans interneuron ALA is (also) a high-threshold mechanosensor |
Q35105757 | The Caenorhabditis elegans iodotyrosine deiodinase ortholog SUP-18 functions through a conserved channel SC-box to regulate the muscle two-pore domain potassium channel SUP-9. |
Q51121883 | The Caenorhabditis elegans matrix non-peptidase MNP-1 is required for neuronal cell migration and interacts with the Ror receptor tyrosine kinase CAM-1. |
Q37596039 | The Caenorhabditis elegans microtubule minus-end binding homolog PTRN-1 stabilizes synapses and neurites |
Q34785872 | The Caenorhabditis elegans microtubule-severing complex MEI-1/MEI-2 katanin interacts differently with two superficially redundant beta-tubulin isotypes |
Q34047933 | The Caenorhabditis elegans mucolipin-like gene cup-5 is essential for viability and regulates lysosomes in multiple cell types |
Q24673193 | The Caenorhabditis elegans muscle-affecting gene unc-87 encodes a novel thin filament-associated protein |
Q36491758 | The Caenorhabditis elegans nephrocystins act as global modifiers of cilium structure |
Q37349505 | The Caenorhabditis elegans nuclear receptor gene nhr-25 regulates epidermal cell development |
Q28345584 | The Caenorhabditis elegans odr-2 gene encodes a novel Ly-6-related protein required for olfaction |
Q36323071 | The Caenorhabditis elegans p120 catenin homologue, JAC-1, modulates cadherin-catenin function during epidermal morphogenesis |
Q40776029 | The Caenorhabditis elegans p38 MAPK Gene plays a key role in protection from mycobacteria |
Q35102638 | The Caenorhabditis elegans paxillin orthologue, PXL-1, is required for pharyngeal muscle contraction and for viability |
Q34504049 | The Caenorhabditis elegans pericentriolar material components SPD-2 and SPD-5 are monomeric in the cytoplasm before incorporation into the PCM matrix |
Q42425399 | The Caenorhabditis elegans protein SAS-5 forms large oligomeric assemblies critical for centriole formation |
Q35175988 | The Caenorhabditis elegans rhy-1 gene inhibits HIF-1 hypoxia-inducible factor activity in a negative feedback loop that does not include vhl-1. |
Q36708252 | The Caenorhabditis elegans rol-6 gene, which interacts with the sqt-1 collagen gene to determine organismal morphology, encodes a collagen |
Q33967319 | The Caenorhabditis elegans sel-1 gene, a negative regulator of lin-12 and glp-1, encodes a predicted extracellular protein. |
Q33937907 | The Caenorhabditis elegans sex determining gene fem-3 is regulated post-transcriptionally |
Q34698077 | The Caenorhabditis elegans snf-11 gene encodes a sodium-dependent GABA transporter required for clearance of synaptic GABA. |
Q34618536 | The Caenorhabditis elegans spe-39 Gene Is Required for Intracellular Membrane Reorganization During Spermatogenesis |
Q33970144 | The Caenorhabditis elegans spe-5 gene is required for morphogenesis of a sperm-specific organelle and is associated with an inherent cold-sensitive phenotype |
Q27335341 | The Caenorhabditis elegans synthetic multivulva genes prevent ras pathway activation by tightly repressing global ectopic expression of lin-3 EGF |
Q33961013 | The Caenorhabditis elegans unc-31 gene affects multiple nervous system-controlled functions. |
Q47068893 | The Caenorhabditis elegans unc-60 gene encodes proteins homologous to a family of actin-binding proteins |
Q36872521 | The Caenorhabditis elegans unc-64 locus encodes a syntaxin that interacts genetically with synaptobrevin |
Q30494543 | The Caenorhabditis elegans unc-78 gene encodes a homologue of actin-interacting protein 1 required for organized assembly of muscle actin filaments |
Q30982840 | The Caenorhabditis elegans unc-93 gene encodes a putative transmembrane protein that regulates muscle contraction. |
Q36381451 | The Caenorhabditis elegans vab-10 spectraplakin isoforms protect the epidermis against internal and external forces |
Q36893929 | The Caenorhabditis elegans vitellogenin gene family includes a gene encoding a distantly related protein |
Q40936759 | The Caenorhabditis elegans voltage-gated calcium channel subunits UNC-2 and UNC-36 and the calcium-dependent kinase UNC-43/CaMKII regulate neuromuscular junction morphology |
Q34392836 | The Caenorhabditis elegans vulval morphogenesis gene sqv-4 encodes a UDP-glucose dehydrogenase that is temporally and spatially regulated |
Q37819497 | The Caenorhabiditis elegans model as a reliable tool in neurotoxicology |
Q27311025 | The Causative Gene in Chanarian Dorfman Syndrome Regulates Lipid Droplet Homeostasis in C. elegans |
Q35782942 | The Cell Death Pathway Regulates Synapse Elimination through Cleavage of Gelsolin in Caenorhabditis elegans Neurons |
Q58795929 | The Claudin-like Protein HPO-30 Is Required to Maintain LAChRs at the Neuromuscular Junction |
Q49886711 | The Coding Regions of Germline mRNAs Confer Sensitivity to Argonaute Regulation in C. elegans. |
Q35770831 | The Conserved G-Protein Coupled Receptor FSHR-1 Regulates Protective Host Responses to Infection and Oxidative Stress |
Q39757006 | The Core Molecular Machinery Used for Engulfment of Apoptotic Cells Regulates the JNK Pathway Mediating Axon Regeneration in Caenorhabditis elegans |
Q27312444 | The DAF-16 FOXO transcription factor regulates natc-1 to modulate stress resistance in Caenorhabditis elegans, linking insulin/IGF-1 signaling to protein N-terminal acetylation |
Q27332405 | The DAF-16/FOXO transcription factor functions as a regulator of epidermal innate immunity |
Q39864475 | The DAF-7 TGF-beta signaling pathway regulates chemosensory receptor gene expression in C. elegans |
Q33638256 | The DEAD Box RNA helicase VBH-1 is a new player in the stress response in C. elegans |
Q33469989 | The DEAD-box protein MEL-46 is required in the germ line of the nematode Caenorhabditis elegans |
Q37165659 | The DEG/ENaC cation channel protein UNC-8 drives activity-dependent synapse removal in remodeling GABAergic neurons |
Q35212132 | The DEG/ENaC protein MEC-10 regulates the transduction channel complex in Caenorhabditis elegans touch receptor neurons |
Q33796268 | The DEP domain-containing protein TOE-2 promotes apoptosis in the Q lineage of C. elegans through two distinct mechanisms |
Q27022343 | The DLK signalling pathway--a double-edged sword in neural development and regeneration |
Q33963768 | The DM domain transcription factor MAB-3 regulates male hypersensitivity to oxidative stress in Caenorhabditis elegans |
Q48502725 | The DSL ligand APX-1 is required for normal ovulation in C. elegans. |
Q35852560 | The Deubiquitylase MATH-33 Controls DAF-16 Stability and Function in Metabolism and Longevity. |
Q59351000 | The Dietary Restriction-Like ( Gene, a Putative Serine/Threonine Kinase, is Essential for Orsay Virus Infection in |
Q33304884 | The Drosophila Perlecan gene trol regulates multiple signaling pathways in different developmental contexts |
Q34611336 | The Dunce cAMP phosphodiesterase PDE-4 negatively regulates G alpha(s)-dependent and G alpha(s)-independent cAMP pools in the Caenorhabditis elegans synaptic signaling network |
Q36648746 | The E2F-DP1 Transcription Factor Complex Regulates Centriole Duplication in Caenorhabditis elegans. |
Q54315987 | The E3 Ubiquitin Ligase MIB-1 Is Necessary To Form the Nuclear Halo in Caenorhabditis elegans Sperm. |
Q36926613 | The E3 ubiquitin ligase mind bomb 1 ubiquitinates and promotes the degradation of survival of motor neuron protein |
Q27308807 | The EARP Complex and Its Interactor EIPR-1 Are Required for Cargo Sorting to Dense-Core Vesicles |
Q41974694 | The EBAX-type Cullin-RING E3 ligase and Hsp90 guard the protein quality of the SAX-3/Robo receptor in developing neurons |
Q35092727 | The EEL-1 ubiquitin ligase promotes DNA damage-induced germ cell apoptosis in C. elegans |
Q27331300 | The EFF-1A Cytoplasmic Domain Influences Hypodermal Cell Fusions in C. elegans But Is Not Dependent on 14-3-3 Proteins |
Q34618883 | The EGL-13 SOX domain transcription factor affects the uterine pi cell lineages in Caenorhabditis elegans. |
Q44376549 | The EGL-21 carboxypeptidase E facilitates acetylcholine release at Caenorhabditis elegans neuromuscular junctions. |
Q36969602 | The EGL-4 PKG acts with KIN-29 salt-inducible kinase and protein kinase A to regulate chemoreceptor gene expression and sensory behaviors in Caenorhabditis elegans |
Q34144633 | The ERK-MAPK pathway regulates longevity through SKN-1 and insulin-like signaling in Caenorhabditis elegans |
Q39975748 | The ESCRT-II proteins are involved in shaping the sarcoplasmic reticulum in C. elegans |
Q37682356 | The ETS-5 transcription factor regulates activity states in Caenorhabditis elegans by controlling satiety |
Q64900497 | The Effect of Hemicellulose and Lignin on Properties of Polysaccharides in Lentinus edodes and Their Antioxidant Evaluation. |
Q33993444 | The Effect of Temperature and Parental Age on Recombination and Nondisjunction in CAENORHABDITIS ELEGANS |
Q64886413 | The Effects of Age and Reproduction on the Lipidome of Caenorhabditis elegans. |
Q90752831 | The Enigmatic Canal-Associated Neurons Regulate Caenorhabditis elegans Larval Development Through a cAMP Signaling Pathway |
Q27310362 | The Evolutionarily Conserved LIM Homeodomain Protein LIM-4/LHX6 Specifies the Terminal Identity of a Cholinergic and Peptidergic C. elegans Sensory/Inter/Motor Neuron-Type |
Q34618765 | The Evolutionary Duplication and Probable Demise of an Endodermal GATA Factor in Caenorhabditis elegans |
Q34634709 | The F-box protein MEC-15 (FBXW9) promotes synaptic transmission in GABAergic motor neurons in C. elegans |
Q39012662 | The FGD homologue EXC-5 regulates apical trafficking in C. elegans tubules |
Q34828352 | The FLYWCH transcription factors FLH-1, FLH-2, and FLH-3 repress embryonic expression of microRNA genes in C. elegans |
Q33759468 | The FMRFamide-Like Peptide Family in Nematodes |
Q41770483 | The FMRFamide-related neuropeptide FLP-20 is required in the mechanosensory neurons during memory for massed training in C. elegans |
Q24680328 | The Facioscapulohumeral muscular dystrophy region on 4qter and the homologous locus on 10qter evolved independently under different evolutionary pressure |
Q34221742 | The Flamingo ortholog FMI-1 controls pioneer-dependent navigation of follower axons in C. elegans |
Q40002173 | The FoxF/FoxC factor LET-381 directly regulates both cell fate specification and cell differentiation in C. elegans mesoderm development |
Q37115248 | The G protein-coupled receptor FSHR-1 is required for the Caenorhabditis elegans innate immune response |
Q39646764 | The G-protein gamma subunit gpc-1 of the nematode C.elegans is involved in taste adaptation |
Q44590307 | The G-protein-coupled serotonin receptor SER-1 regulates egg laying and male mating behaviors in Caenorhabditis elegans. |
Q35588925 | The GATA factor elt-1 regulates C. elegans developmental timing by promoting expression of the let-7 family microRNAs |
Q34524678 | The GATA transcription factor egl-27 delays aging by promoting stress resistance in Caenorhabditis elegans |
Q35093137 | The GATA transcription factor/MTA-1 homolog egr-1 promotes longevity and stress resistance in Caenorhabditis elegans |
Q35005742 | The GEX-2 and GEX-3 proteins are required for tissue morphogenesis and cell migrations in C. elegans |
Q35108098 | The GLD-2 poly(A) polymerase activates gld-1 mRNA in the Caenorhabditis elegans germ line |
Q34296958 | The GPS motif is a molecular switch for bimodal activities of adhesion class G protein-coupled receptors. |
Q35222275 | The Galpha12-RGS RhoGEF-RhoA signalling pathway regulates neurotransmitter release in C. elegans |
Q36257348 | The Genetics of Axon Guidance and Axon Regeneration in Caenorhabditis elegans |
Q47372758 | The Germline-Specific Factor OEF-1 Facilitates Coordinated Progression Through Germ Cell Development in Caenorhabditis elegans |
Q40464821 | The Groucho ortholog UNC-37 interacts with the short Groucho-like protein LSY-22 to control developmental decisions in C. elegans |
Q27313660 | The HLH-6 transcription factor regulates C. elegans pharyngeal gland development and function |
Q41373535 | The Helicase Aquarius/EMB-4 Is Required to Overcome Intronic Barriers to Allow Nuclear RNAi Pathways to Heritably Silence Transcription. |
Q90074266 | The Hox Gene egl-5 Acts as a Terminal Selector for VD13 Development via Wnt Signaling |
Q36365268 | The Importance of cGMP Signaling in Sensory Cilia for Body Size Regulation in Caenorhabditis elegans |
Q36668084 | The Influence of Competition Among C. elegans Small RNA Pathways on Development |
Q36000559 | The Integral Role of Genetic Variation in the Evolution of Outcrossing in the Caenorhabditis elegans-Serratia marcescens Host-Parasite System |
Q38066189 | The Intersection of Aging, Longevity Pathways, and Learning and Memory in C. elegans |
Q27312208 | The Invertebrate Lysozyme Effector ILYS-3 Is Systemically Activated in Response to Danger Signals and Confers Antimicrobial Protection in C. elegans |
Q34584084 | The Janthinobacterium sp. HH01 genome encodes a homologue of the V. cholerae CqsA and L. pneumophila LqsA autoinducer synthases |
Q27302867 | The KLP-7 Residue S546 Is a Putative Aurora Kinase Site Required for Microtubule Regulation at the Centrosome in C. elegans |
Q89985578 | The Kinesin-3 motor, KLP-4, mediates axonal organization and cholinergic signaling in Caenorhabditis elegans |
Q42257809 | The L-type cyclin CYL-1 and the heat-shock-factor HSF-1 are required for heat-shock-induced protein expression in Caenorhabditis elegans |
Q36323697 | The L-type voltage-dependent Ca2+ channel EGL-19 controls body wall muscle function in Caenorhabditis elegans |
Q34714971 | The LIN-15A and LIN-56 transcriptional regulators interact to negatively regulate EGF/Ras signaling in Caenorhabditis elegans vulval cell-fate determination |
Q39045655 | The Lipocalin LPR-1 Cooperates with LIN-3/EGF Signaling To Maintain Narrow Tube Integrity in Caenorhabditis elegans |
Q39445420 | The Liprin homology domain is essential for the homomeric interaction of SYD-2/Liprin-α protein in presynaptic assembly |
Q41849034 | The Longevity Properties of 1,2,3,4,6-Penta-O-Galloyl-β-D-Glucose from Curcuma longa in Caenorhabditis elegans |
Q36723456 | The MAP kinase pathway coordinates crossover designation with disassembly of synaptonemal complex proteins during meiosis |
Q37097037 | The MIG-15 NIK kinase acts cell-autonomously in neuroblast polarization and migration in C. elegans |
Q47099823 | The MXL-3/SBP-1 Axis Is Responsible for Glucose-Dependent Fat Accumulation in C. elegans. |
Q48263996 | The MYST family histone acetyltransferase complex regulates stress resistance and longevity through transcriptional control of DAF-16/FOXO transcription factors. |
Q58414109 | The Machado-Joseph disease deubiquitylase ATX-3 couples longevity and proteostasis |
Q28271572 | The Mediator Kinase Module Restrains Epidermal Growth Factor Receptor Signaling and Represses Vulval Cell Fate Specification in Caenorhabditis elegans |
Q21145049 | The Mediator subunit MDT-15 confers metabolic adaptation to ingested material |
Q50001924 | The Microbial Zoo in the C. elegans Intestine: Bacteria, Fungi and Viruses. |
Q42381532 | The Mitotic Spindle in the One-Cell C. elegans Embryo Is Positioned with High Precision and Stability |
Q27675937 | The Myosin Chaperone UNC-45 Is Organized in Tandem Modules to Support Myofilament Formation in C. elegans |
Q35536520 | The N- or C-terminal domains of DSH-2 can activate the C. elegans Wnt/beta-catenin asymmetry pathway |
Q33707693 | The N-terminal extension domain of the C. elegans half-molecule ABC transporter, HMT-1, is required for protein-protein interactions and function |
Q36381062 | The NC1/endostatin domain of Caenorhabditis elegans type XVIII collagen affects cell migration and axon guidance. |
Q48096263 | The NCA-1 and NCA-2 Ion Channels Function Downstream of Gq and Rho To Regulate Locomotion in Caenorhabditis elegans |
Q38961642 | The NCLX-type Na+/Ca2+ Exchanger NCX-9 Is Required for Patterning of Neural Circuits in Caenorhabditis elegans. |
Q37540380 | The NHR-8 nuclear receptor regulates cholesterol and bile acid homeostasis in C. elegans |
Q37431751 | The NemaGENETAG initiative: large scale transposon insertion gene-tagging in Caenorhabditis elegans |
Q30513474 | The Nematode Caenorhabditis elegans, Stress and Aging: Identifying the Complex Interplay of Genetic Pathways Following the Treatment with Humic Substances |
Q42741247 | The Neuropeptides FLP-2 and PDF-1 Act in Concert To Arouse Caenorhabditis elegans Locomotion |
Q35980925 | The Nkx5/HMX homeodomain protein MLS-2 is required for proper tube cell shape in the C. elegans excretory system |
Q37172089 | The Nrf2/SKN-1-dependent glutathione S-transferase π homologue GST-1 inhibits dopamine neuron degeneration in a Caenorhabditis elegans model of manganism |
Q36251122 | The Nuclear Receptor HIZR-1 Uses Zinc as a Ligand to Mediate Homeostasis in Response to High Zinc |
Q57294358 | The Oxidative Stress Response Requires the NHR-49 Transcription Factor |
Q36397272 | The Oxidative Stress Response in Caenorhabditis elegans Requires the GATA Transcription Factor ELT-3 and SKN-1/Nrf2. |
Q36242750 | The P granule component PGL-1 promotes the localization and silencing activity of the PUF protein FBF-2 in germline stem cells |
Q34036901 | The PAM-1 aminopeptidase regulates centrosome positioning to ensure anterior-posterior axis specification in one-cell C. elegans embryos |
Q34644841 | The PGL family proteins associate with germ granules and function redundantly in Caenorhabditis elegans germline development |
Q35910997 | The PLEXIN PLX-2 and the ephrin EFN-4 have distinct roles in MAB-20/Semaphorin 2A signaling in Caenorhabditis elegans morphogenesis |
Q41915924 | The POU transcription factor UNC-86 controls the timing and ventral guidance of Caenorhabditis elegans axon growth |
Q37015850 | The PUF binding landscape in metazoan germ cells |
Q36839557 | The Paired-box protein PAX-3 regulates the choice between lateral and ventral epidermal cell fates in C. elegans |
Q27301328 | The Parallel Worm Tracker: a platform for measuring average speed and drug-induced paralysis in nematodes |
Q38743414 | The Prevalence and Distribution of Neurodegenerative Compound-Producing Soil Streptomyces spp. |
Q34618751 | The Promotion of Gonadal Cell Divisions by the Caenorhabditis elegans TRPM Cation Channel GON-2 Is Antagonized by GEM-4 Copine |
Q97420198 | The Protective Effect of Adenosine-Preconditioning on Paraquat-Induced Damage in Caenorhabditis elegans |
Q55402112 | The Protein Arginine Methyltransferase PRMT-5 Regulates SER-2 Tyramine Receptor-Mediated Behaviors in Caenorhabditis elegans. |
Q91863841 | The Pseudomonas aeruginosa accessory genome elements influence virulence towards Caenorhabditis elegans |
Q33840061 | The Puf RNA-binding proteins FBF-1 and FBF-2 inhibit the expression of synaptonemal complex proteins in germline stem cells |
Q38723242 | The R148.3 Gene Modulates Caenorhabditis elegans Lifespan and Fat Metabolism |
Q92969123 | The R941L mutation in MYH14 disrupts mitochondrial fission and associates with peripheral neuropathy |
Q41268124 | The RGM protein DRAG-1 positively regulates a BMP-like signaling pathway in Caenorhabditis elegans |
Q27350466 | The RHO-1 RhoGTPase modulates fertility and multiple behaviors in adult C. elegans |
Q35209458 | The RING finger/B-box factor TAM-1 and a retinoblastoma-like protein LIN-35 modulate context-dependent gene silencing in Caenorhabditis elegans |
Q30822165 | The RNA-binding protein ATX-2 regulates cytokinesis through PAR-5 and ZEN-4 |
Q36671956 | The RNase PARN-1 Trims piRNA 3' Ends to Promote Transcriptome Surveillance in C. elegans |
Q27334152 | The Rac GTP exchange factor TIAM-1 acts with CDC-42 and the guidance receptor UNC-40/DCC in neuronal protrusion and axon guidance |
Q27308898 | The Receptor-Bound Guanylyl Cyclase DAF-11 Is the Mediator of Hydrogen Peroxide-Induced cGMP Increase in Caenorhabditis elegans [corrected] |
Q40131951 | The RhlR quorum-sensing receptor controls Pseudomonas aeruginosa pathogenesis and biofilm development independently of its canonical homoserine lactone autoinducer. |
Q92702470 | The Role of Ca2+ Signaling in Aging and Neurodegeneration: Insights from Caenorhabditis elegans Models |
Q26768120 | The Role of Dafachronic Acid Signaling in Development and Longevity in Caenorhabditis elegans: Digging Deeper Using Cutting-Edge Analytical Chemistry |
Q89473436 | The Role of pkc-3 and Genetic Suppressors in Caenorhabditis elegans Epithelial Cell Junction Formation |
Q48104463 | The Role of the UNC-82 Protein Kinase in Organizing Myosin Filaments in Striated Muscle of Caenorhabditis elegans. |
Q35239082 | The Rosetteless gene controls development in the choanoflagellate S. rosetta |
Q34775852 | The SAX-3 receptor stimulates axon outgrowth and the signal sequence and transmembrane domain are critical for SAX-3 membrane localization in the PDE neuron of C. elegans |
Q41384749 | The SEK-1 p38 MAP Kinase Pathway Modulates Gq Signaling in Caenorhabditis elegans |
Q30008996 | The SH3 domain of UNC-89 (obscurin) interacts with paramyosin, a coiled-coil protein, in Caenorhabditis elegans muscle |
Q33779545 | The SKPO-1 peroxidase functions in the hypodermis to protect Caenorhabditis elegans from bacterial infection |
Q37127286 | The SM protein Car/Vps33A regulates SNARE-mediated trafficking to lysosomes and lysosome-related organelles |
Q24540364 | The SQV-1 UDP-glucuronic acid decarboxylase and the SQV-7 nucleotide-sugar transporter may act in the Golgi apparatus to affect Caenorhabditis elegans vulval morphogenesis and embryonic development |
Q24653713 | The STAR protein QKI-6 is a translational repressor |
Q33890297 | The STAR protein, GLD-1, is a translational regulator of sexual identity in Caenorhabditis elegans |
Q30584661 | The SUN protein UNC-84 is required only in force-bearing cells to maintain nuclear envelope architecture |
Q33734500 | The Shift of the Intestinal Microbiome in the Innate Immunity-Deficient Mutant rde-1 Strain of C. elegans upon Orsay Virus Infection |
Q36173010 | The Skp1 Homologs SKR-1/2 Are Required for the Caenorhabditis elegans SKN-1 Antioxidant/Detoxification Response Independently of p38 MAPK |
Q50048940 | The Small GTPase RAC1/CED-10 Is Essential in Maintaining Dopaminergic Neuron Function and Survival Against α-Synuclein-Induced Toxicity. |
Q36780830 | The Stress Granule RNA-Binding Protein TIAR-1 Protects Female Germ Cells from Heat Shock in Caenorhabditis elegans |
Q64076738 | The Stress-Chip: A microfluidic platform for stress analysis in Caenorhabditis elegans |
Q28345297 | The T-box factor MLS-1 acts as a molecular switch during specification of nonstriated muscle in C. elegans |
Q36724365 | The T-box gene tbx-2, the homeobox gene egl-5 and the asymmetric cell division gene ham-1 specify neural fate in the HSN/PHB lineage |
Q37113467 | The T-box transcription factor SEA-1 is an autosomal element of the X:A signal that determines C. elegans sex. |
Q37399413 | The TFEB orthologue HLH-30 regulates autophagy and modulates longevity in Caenorhabditis elegans |
Q27314628 | The TRIM-NHL protein LIN-41 controls the onset of developmental plasticity in Caenorhabditis elegans |
Q61455477 | The TRIM-NHL protein NHL-2 is a co-factor in the nuclear and somatic RNAi pathways in . e |
Q33982824 | The TRiC/CCT chaperone is implicated in Alzheimer's disease based on patient GWAS and an RNAi screen in Aβ-expressing Caenorhabditis elegans. |
Q33955005 | The Tc3 family of transposable genetic elements in Caenorhabditis elegans |
Q36740430 | The Tc5 family of transposable elements in Caenorhabditis elegans |
Q27311563 | The Tumor Suppressor BCL7B Functions in the Wnt Signaling Pathway |
Q30539764 | The UBXN-2/p37/p47 adaptors of CDC-48/p97 regulate mitosis by limiting the centrosomal recruitment of Aurora A. |
Q36118132 | The UNC-45 chaperone mediates sarcomere assembly through myosin degradation in Caenorhabditis elegans |
Q30617477 | The UNC-6/Netrin receptors UNC-40/DCC and UNC-5 inhibit growth cone filopodial protrusion via UNC-73/Trio, Rac-like GTPases and UNC-33/CRMP. |
Q52621010 | The UPRmt Protects Caenorhabditis elegans from Mitochondrial Dysfunction by Upregulating Specific Enzymes of the Mevalonate Pathway. |
Q60922622 | The USTC co-opts an ancient machinery to drive piRNA transcription in |
Q33606931 | The Ubiquitin Ligase CHIP Integrates Proteostasis and Aging by Regulation of Insulin Receptor Turnover |
Q37379153 | The Use of the Nematode Caenorhabditis elegans to Evaluate the Adverse Effects of Epoxiconazole Exposure on Spermatogenesis |
Q36117665 | The V0-ATPase mediates apical secretion of exosomes containing Hedgehog-related proteins in Caenorhabditis elegans |
Q28548328 | The Validation of Nematode-Specific Acetylcholine-Gated Chloride Channels as Potential Anthelmintic Drug Targets |
Q33598282 | The Vasa Homolog RDE-12 engages target mRNA and multiple argonaute proteins to promote RNAi in C. elegans |
Q27324781 | The Vps33a gene regulates behavior and cerebellar Purkinje cell number |
Q30485568 | The WAVE/SCAR complex promotes polarized cell movements and actin enrichment in epithelia during C. elegans embryogenesis |
Q37192059 | The WD40 repeat protein WDR-23 functions with the CUL4/DDB1 ubiquitin ligase to regulate nuclear abundance and activity of SKN-1 in Caenorhabditis elegans |
Q37563461 | The WD40-repeat proteins WDR-20 and WDR-48 bind and activate the deubiquitinating enzyme USP-46 to promote the abundance of the glutamate receptor GLR-1 in the ventral nerve cord of Caenorhabditis elegans |
Q27310399 | The Wnt Frizzled Receptor MOM-5 Regulates the UNC-5 Netrin Receptor through Small GTPase-Dependent Signaling to Determine the Polarity of Migrating Cells |
Q33528971 | The Wnt pathway controls cell death engulfment, spindle orientation, and migration through CED-10/Rac |
Q27314681 | The Wnt receptor Ryk reduces neuronal and cell survival capacity by repressing FOXO activity during the early phases of mutant huntingtin pathogenicity |
Q35247850 | The Wnt/beta-catenin asymmetry pathway patterns the atonal ortholog lin-32 to diversify cell fate in a Caenorhabditis elegans sensory lineage |
Q37200232 | The ZFP-1(AF10)/DOT-1 complex opposes H2B ubiquitination to reduce Pol II transcription |
Q34729441 | The accessory helix of complexin functions by stabilizing central helix secondary structure |
Q33836936 | The actin-binding protein UNC-115/abLIM controls formation of lamellipodia and filopodia and neuronal morphogenesis in Caenorhabditis elegans |
Q46278755 | The addition of a developmental factor, unc-62, to already long-lived worms increases lifespan and healthspan |
Q92682672 | The adhesion modulation domain of Caenorhabditis elegans α-catenin regulates actin binding during morphogenesis |
Q33966277 | The age-1 and daf-2 genes function in a common pathway to control the lifespan of Caenorhabditis elegans |
Q40819143 | The aging process of the nematodeCaenorhabditis elegansin bacterial and axenic culture |
Q28489013 | The alkaloid compound harmane increases the lifespan of Caenorhabditis elegans during bacterial infection, by modulating the nematode's innate immune response |
Q37375722 | The alpha and beta subunits of nematode actin capping protein function in yeast |
Q35378929 | The alpha1 subunit EGL-19, the alpha2/delta subunit UNC-36, and the beta subunit CCB-1 underlie voltage-dependent calcium currents in Caenorhabditis elegans striated muscle |
Q36215260 | The alteration of myosin isoform compartmentation in specific mutants of Caenorhabditis elegans |
Q92650897 | The amphipod crustacean Parhyale hawaiensis: An emerging comparative model of arthropod development, evolution, and regeneration |
Q24321690 | The amyotrophic lateral sclerosis 8 protein VAPB is cleaved, secreted, and acts as a ligand for Eph receptors |
Q28473873 | The anticonvulsant ethosuximide disrupts sensory function to extend C. elegans lifespan |
Q36376790 | The apical ECM preserves embryonic integrity and distributes mechanical stress during morphogenesis. |
Q30495483 | The arf-like GTPase Arl8 mediates delivery of endocytosed macromolecules to lysosomes in Caenorhabditis elegans |
Q39942092 | The atRA-responsive gene neuron navigator 2 functions in neurite outgrowth and axonal elongation |
Q42565688 | The atm-1 gene is required for genome stability in Caenorhabditis elegans |
Q27334407 | The atypical calpains: evolutionary analyses and roles in Caenorhabditis elegans cellular degeneration |
Q28213756 | The aurora kinase AIR-2 functions in the release of chromosome cohesion in Caenorhabditis elegans meiosis |
Q91891080 | The autophagy receptor p62/SQST-1 promotes proteostasis and longevity in C. elegans by inducing autophagy |
Q67316253 | The avoidance of D-tryptophan by the nematodeCaenorhabditis elegans |
Q37287574 | The axial element protein HTP-3 promotes cohesin loading and meiotic axis assembly in C. elegans to implement the meiotic program of chromosome segregation |
Q34139157 | The balanced regulation of Hsc70 by DNJ-13 and UNC-23 is required for muscle functionality. |
Q42440871 | The basement membrane components nidogen and type XVIII collagen regulate organization of neuromuscular junctions in Caenorhabditis elegans. |
Q34466190 | The beginning of connectomics: a commentary on White et al. (1986) 'The structure of the nervous system of the nematode Caenorhabditis elegans'. |
Q37931862 | The behavioral genetics of Caenorhabditis elegans |
Q36076959 | The branched actin nucleator Arp2/3 promotes nuclear migrations and cell polarity in the C. elegans zygote |
Q42095834 | The broad-spectrum antibiotic, zeamine, kills the nematode worm Caenorhabditis elegans. |
Q47069099 | The bromodomain protein LEX-1 acts with TAM-1 to modulate gene expression in C. elegans |
Q27349703 | The burrowing behavior of the nematode Caenorhabditis elegans: a new assay for the study of neuromuscular disorders |
Q33674391 | The cAMP-PKA pathway-mediated fat mobilization is required for cold tolerance in C. elegans |
Q36607166 | The candidate MAP kinase phosphorylation substrate DPL-1 (DP) promotes expression of the MAP kinase phosphatase LIP-1 in C. elegans germ cells |
Q36063101 | The canonical eIF4E isoform of C. elegans regulates growth, embryogenesis, and germline sex-determination |
Q39758649 | The cat-1 gene of Caenorhabditis elegans encodes a vesicular monoamine transporter required for specific monoamine-dependent behaviors |
Q37310259 | The cation diffusion facilitator gene cdf-2 mediates zinc metabolism in Caenorhabditis elegans |
Q30157505 | The cell signaling adaptor protein EPS-8 is essential for C. elegans epidermal elongation and interacts with the ankyrin repeat protein VAB-19. |
Q53394853 | The cellular geometry of growth drives the amino acid economy of Caenorhabditis elegans. |
Q34854482 | The chromosomal passenger complex and centralspindlin independently contribute to contractile ring assembly |
Q52691422 | The cisd gene family regulates physiological germline apoptosis through ced-13 and the canonical cell death pathway in Caenorhabditis elegans. |
Q61917624 | The co-chaperone UNC45A is essential for the expression of mitotic kinase NEK7 and tumorigenesis |
Q116674737 | The compact genome of Caenorhabditis niphades n. sp., isolated from a wood-boring weevil, Niphades variegatus |
Q55221543 | The conserved LEM-3/Ankle1 nuclease is involved in the combinatorial regulation of meiotic recombination repair and chromosome segregation in Caenorhabditis elegans. |
Q41937140 | The conserved Mediator subunit MDT-15 is required for oxidative stress responses in Caenorhabditis elegans |
Q24658101 | The conserved NAD(H)-dependent corepressor CTBP-1 regulates Caenorhabditis elegans life span |
Q37644126 | The conserved SNARE SEC-22 localizes to late endosomes and negatively regulates RNA interference in Caenorhabditis elegans |
Q33979402 | The conserved miR-51 microRNA family is redundantly required for embryonic development and pharynx attachment in Caenorhabditis elegans |
Q36470529 | The conserved proteins CHE-12 and DYF-11 are required for sensory cilium function in Caenorhabditis elegans |
Q37507620 | The conserved transmembrane RING finger protein PLR-1 downregulates Wnt signaling by reducing Frizzled, Ror and Ryk cell-surface levels in C. elegans |
Q34568579 | The cooperation of FGF receptor and Klotho is involved in excretory canal development and regulation of metabolic homeostasis in Caenorhabditis elegans. |
Q27319353 | The core apoptotic executioner proteins CED-3 and CED-4 promote initiation of neuronal regeneration in Caenorhabditis elegans |
Q35208591 | The coronin-like protein POD-1 is required for anterior-posterior axis formation and cellular architecture in the nematode caenorhabditis elegans |
Q35120879 | The cyclin-dependent kinase inhibitors, cki-1 and cki-2, act in overlapping but distinct pathways to control cell cycle quiescence during C. elegans development |
Q36359272 | The cystic-fibrosis-associated ΔF508 mutation confers post-transcriptional destabilization on the C. elegans ABC transporter PGP-3. |
Q34313050 | The cytoplasmic poly(A) polymerases GLD-2 and GLD-4 promote general gene expression via distinct mechanisms |
Q34520955 | The dauerlarva, a post-embryonic developmental variant of the nematode Caenorhabditis elegans |
Q36218775 | The decapping scavenger enzyme DCS-1 controls microRNA levels in Caenorhabditis elegans |
Q48013887 | The dense-core vesicle maturation protein CCCP-1 binds RAB-2 and membranes through its C-terminal domain |
Q34886654 | The deubiquitinating enzyme USP-46 negatively regulates the degradation of glutamate receptors to control their abundance in the ventral nerve cord of Caenorhabditis elegans |
Q34273890 | The development of sexual dimorphism: studies of the Caenorhabditis elegans male |
Q39757304 | The directed migration of gonadal distal tip cells in Caenorhabditis elegans requires NGAT-1, a ß1,4-N-acetylgalactosaminyltransferase enzyme. |
Q37467688 | The divalent metal transporter homologues SMF-1/2 mediate dopamine neuron sensitivity in caenorhabditis elegans models of manganism and parkinson disease |
Q34613210 | The divergent Caenorhabditis elegans beta-catenin proteins BAR-1, WRM-1 and HMP-2 make distinct protein interactions but retain functional redundancy in vivo |
Q34619185 | The divergent orphan nuclear receptor ODR-7 regulates olfactory neuron gene expression via multiple mechanisms in Caenorhabditis elegans |
Q49666338 | The double-stranded RNA binding protein RDE-4 can act cell autonomously during feeding RNAi in C. elegans. |
Q30533916 | The doublecortin-related gene zyg-8 is a microtubule organizer in Caenorhabditis elegans neurons |
Q35694176 | The dynamics of replication licensing in live Caenorhabditis elegans embryos. |
Q33519519 | The dystrophin complex controls bk channel localization and muscle activity in Caenorhabditis elegans |
Q28291406 | The eEF2 kinase confers resistance to nutrient deprivation by blocking translation elongation |
Q27004910 | The early bird catches the worm: new technologies for the Caenorhabditis elegans toolkit |
Q34083670 | The early-onset torsion dystonia-associated protein, torsinA, is a homeostatic regulator of endoplasmic reticulum stress response |
Q38527894 | The ecology and biodemography of Caenorhabditis elegans |
Q33831372 | The ecology of sexual reproduction |
Q42850433 | The effect of a selective octopamine antagonist, epinastine, on pharyngeal pumping in Caenorhabditis elegans |
Q34412205 | The effect of environmental conditions on biofilm formation of Burkholderia pseudomallei clinical isolates |
Q93013799 | The effect of metal mixture composition on toxicity to C. elegans at individual and population levels |
Q38279572 | The effects of pdr1, djr1.1 and pink1 loss in manganese-induced toxicity and the role of α-synuclein in C. elegans |
Q34686025 | The effects of transient starvation persist through direct interactions between CaMKII and ether-a-go-go K+ channels in C. elegans males |
Q41644122 | The embryonic cell lineage of Caenorhabditis elegans: A modern hieroglyph: The best way to acquire knowledge in Developmental Biology is to learn how this knowledge was derived |
Q36643272 | The embryonic muscle transcriptome of Caenorhabditis elegans |
Q24337665 | The evolutionarily conserved longevity determinants HCF-1 and SIR-2.1/SIRT1 collaborate to regulate DAF-16/FOXO |
Q27325648 | The evolutionarily conserved mediator subunit MDT-15/MED15 links protective innate immune responses and xenobiotic detoxification |
Q92916397 | The exocyst complex and Rab5 are required for abscission by localizing ESCRT III subunits to the cytokinetic bridge |
Q92804058 | The fatty acid oleate is required for innate immune activation and pathogen defense in Caenorhabditis elegans |
Q34775392 | The fatty acid synthase fasn-1 acts upstream of WNK and Ste20/GCK-VI kinases to modulate antimicrobial peptide expression in C. elegans epidermis |
Q40444900 | The forkhead domain gene unc-130 generates chemosensory neuron diversity in C. elegans |
Q24536542 | The function and expansion of the Patched- and Hedgehog-related homologs in C. elegans |
Q36597434 | The function and regulation of the GATA factor ELT-2 in the C. elegans endoderm |
Q33467385 | The function of a spindle checkpoint gene bub-1 in C. elegans development |
Q73107324 | The fundamental role of pirouettes in Caenorhabditis elegans chemotaxis |
Q33962108 | The generation and genetic analysis of suppressors of lethal mutations in the Caenorhabditis elegans rol-3(V) gene. |
Q29617240 | The genetics of caloric restriction in Caenorhabditis elegans |
Q42963840 | The genetics of feeding in Caenorhabditis elegans. |
Q39090716 | The genetics of isoflurane-induced developmental neurotoxicity. |
Q41967970 | The genetics of levamisole resistance in the nematode Caenorhabditis elegans |
Q24544640 | The genome of bacteriophage T4: an archeological dig. |
Q36096537 | The genome-wide role of HSF-1 in the regulation of gene expression in Caenorhabditis elegans |
Q27339558 | The germinal center kinase GCK-1 is a negative regulator of MAP kinase activation and apoptosis in the C. elegans germline |
Q34300974 | The global regulator Ler is necessary for enteropathogenic Escherichia coli colonization of Caenorhabditis elegans |
Q28748302 | The glutaredoxin GLRX-21 functions to prevent selenium-induced oxidative stress in Caenorhabditis elegans |
Q34673999 | The glutathione reductase GSR-1 determines stress tolerance and longevity in Caenorhabditis elegans |
Q28833466 | The glyoxylate shunt is essential for desiccation tolerance in C. elegans and budding yeast |
Q43843024 | The growth factor SVH-1 regulates axon regeneration in C. elegans via the JNK MAPK cascade |
Q35091535 | The heterochronic genes lin-28a and lin-28b play an essential and evolutionarily conserved role in early zebrafish development |
Q35852721 | The hitchhiker's guide to Xenopus genetics |
Q36804080 | The hmsHFRS operon of Xenorhabdus nematophila is required for biofilm attachment to Caenorhabditis elegans |
Q33945482 | The homeobox protein CEH-23 mediates prolonged longevity in response to impaired mitochondrial electron transport chain in C. elegans |
Q34069391 | The homeodomain protein hmbx-1 maintains asymmetric gene expression in adult C. elegans olfactory neurons |
Q28540122 | The homologous carboxyl-terminal domains of microtubule-associated protein 2 and TAU induce neuronal dysfunction and have differential fates in the evolution of neurofibrillary tangles |
Q91753122 | The human ABCB6 protein is the functional homologue of HMT-1 proteins mediating cadmium detoxification |
Q37191828 | The hydrolethalus syndrome protein HYLS-1 regulates formation of the ciliary gate |
Q92281758 | The hypoxia-response pathway modulates RAS/MAPK-mediated cell fate decisions in Caenorhabditis elegans |
Q34569711 | The identities of sym-2, sym-3 and sym-4, three genes that are synthetically lethal with mec-8 in Caenorhabditis elegans |
Q42796960 | The immunoglobulin super family protein RIG-3 prevents synaptic potentiation and regulates Wnt signaling |
Q28476319 | The influence of bacterial diet on fat storage in C. elegans |
Q71720215 | The integration of antagonistic reflexes revealed by laser ablation of identified neurons determines habituation kinetics of the Caenorhabditis elegans tap withdrawal response |
Q35410579 | The integrin-adhesome is required to maintain muscle structure, mitochondrial ATP production, and movement forces in Caenorhabditis elegans |
Q33942926 | The interplay of biology and technology |
Q36275033 | The interplay of stiffness and force anisotropies drives embryo elongation. |
Q33727929 | The intestinal TORC2 signaling pathway contributes to associative learning in Caenorhabditis elegans |
Q90069318 | The involvement of McpB chemoreceptor from Pseudomonas aeruginosa PAO1 in virulence |
Q37168885 | The ire-1 ER stress-response pathway is required for normal secretory-protein metabolism in C. elegans |
Q30524916 | The kinesin-3 family motor KLP-4 regulates anterograde trafficking of GLR-1 glutamate receptors in the ventral nerve cord of Caenorhabditis elegans |
Q70598101 | The kinetochores of Caenorhabditis elegans |
Q38389240 | The laboratory domestication of Caenorhabditis elegans. |
Q30540862 | The large GTPase dynamin associates with the spindle midzone and is required for cytokinesis |
Q33957342 | The let-60 locus controls the switch between vulval and nonvulval cell fates in Caenorhabditis elegans |
Q28270307 | The let-7 MicroRNA family members mir-48, mir-84, and mir-241 function together to regulate developmental timing in Caenorhabditis elegans |
Q34606099 | The levels of the RoRNP-associated Y RNA are dependent upon the presence of ROP-1, the Caenorhabditis elegans Ro60 protein |
Q53398723 | The lifespan-extending effects of Nymphaea hybrid root extract in the nematode Caenorhabditis elegans. |
Q34441969 | The lin-15 locus encodes two negative regulators of Caenorhabditis elegans vulval development |
Q33283088 | The lin-35/Rb and RNAi pathways cooperate to regulate a key cell cycle transition in C. elegans |
Q41434168 | The lin-4 microRNA targets the LIN-14 transcription factor to inhibit netrin-mediated axon attraction |
Q67259849 | The linkage mapping of cloned restriction fragment length differences in Caenorabditis elegans |
Q30776009 | The lipid binding pleckstrin homology domain in UNC-104 kinesin is necessary for synaptic vesicle transport in Caenorhabditis elegans |
Q35112722 | The longevity of Caenorhabditis elegans in soil |
Q36145402 | The loss of LRPPRC function induces the mitochondrial unfolded protein response |
Q30410713 | The lysosomal cathepsin protease CPL-1 plays a leading role in phagosomal degradation of apoptotic cells in Caenorhabditis elegans |
Q30353125 | The lysosomal membrane protein SCAV-3 maintains lysosome integrity and adult longevity. |
Q51764427 | The mTOR-S6 kinase pathway promotes stress granule assembly. |
Q68721793 | The major gut esterase locus in the nematode Caenorhabditis elegans |
Q93064022 | The marginal cells of the Caenorhabditis elegans pharynx scavenge cholesterol and other hydrophobic small molecules |
Q34250574 | The mbk-2 kinase is required for inactivation of MEI-1/katanin in the one-cell Caenorhabditis elegans embryo |
Q33938156 | The mec-7 beta-tubulin gene of Caenorhabditis elegans is expressed primarily in the touch receptor neurons |
Q89490812 | The mechanoreceptor DEG-1 regulates cold tolerance in Caenorhabditis elegans |
Q33959501 | The meiotic behavior of an inversion in Caenorhabditis elegans |
Q34432602 | The membrane-associated proteins FCHo and SGIP are allosteric activators of the AP2 clathrin adaptor complex |
Q34419977 | The metabolite α-ketoglutarate extends lifespan by inhibiting ATP synthase and TOR. |
Q37052315 | The metal transporter SMF-3/DMT-1 mediates aluminum-induced dopamine neuron degeneration |
Q34192883 | The miR-35-41 family of microRNAs regulates RNAi sensitivity in Caenorhabditis elegans |
Q50437960 | The microRNA machinery regulates fasting-induced changes in gene expression and longevity in Caenorhabditis elegans. |
Q33922400 | The microRNA miR-124 controls gene expression in the sensory nervous system of Caenorhabditis elegans |
Q27332210 | The microRNA mir-71 inhibits calcium signaling by targeting the TIR-1/Sarm1 adaptor protein to control stochastic L/R neuronal asymmetry in C. elegans |
Q36009192 | The microRNA pathway controls germ cell proliferation and differentiation in C. elegans |
Q28708987 | The microarchitecture of C. elegans behavior during lethargus: homeostatic bout dynamics, a typical body posture, and regulation by a central neuron |
Q37297856 | The midbody ring scaffolds the abscission machinery in the absence of midbody microtubules |
Q34783904 | The million mutation project: a new approach to genetics in Caenorhabditis elegans |
Q40820116 | The minor myosin heavy chain, mhcA, of Caenorhabditis elegans is necessary for the initiation of thick filament assembly |
Q21134575 | The mir-51 family of microRNAs functions in diverse regulatory pathways in Caenorhabditis elegans |
Q33959081 | The mitochondrial genomes of two nematodes, Caenorhabditis elegans and Ascaris suum |
Q47237663 | The modERN Resource: Genome-Wide Binding Profiles for Hundreds of Drosophila and Caenorhabditis elegans Transcription Factors |
Q33960734 | The mog-1 gene is required for the switch from spermatogenesis to oogenesis in Caenorhabditis elegans. |
Q90082884 | The molecular basis of LST-1 self-renewal activity and its control of stem cell pool size |
Q34422621 | The monoaminergic modulation of sensory-mediated aversive responses in Caenorhabditis elegans requires glutamatergic/peptidergic cotransmission |
Q36631199 | The mood stabilizer valproate inhibits both inositol- and diacylglycerol-signaling pathways in Caenorhabditis elegans |
Q38105458 | The multiple faces of calcineurin signaling in Caenorhabditis elegans: development, behaviour and aging |
Q37375862 | The multipurpose 15-protofilament microtubules in C. elegans have specific roles in mechanosensation |
Q33969908 | The mup-4 locus in Caenorhabditis elegans is essential for hypodermal integrity, organismal morphogenesis and embryonic body wall muscle position |
Q36995989 | The myosin-binding UCS domain but not the Hsp90-binding TPR domain of the UNC-45 chaperone is essential for function in Caenorhabditis elegans |
Q33966210 | The ncl-1 gene and genetic mosaics of Caenorhabditis elegans. |
Q38591559 | The near demise and subsequent revival of classical genetics for investigating Caenorhabditis elegans embryogenesis: RNAi meets next-generation DNA sequencing |
Q40958117 | The nematode C. elegans as a complex viscoelastic fluid |
Q36700088 | The nematode Caenorhabditis elegans as a tool to predict chemical activity on mammalian development and identify mechanisms influencing toxicological outcome |
Q28367224 | The nematode Caenorhabditis elegans synthesizes unusual O-linked glycans: identification of glucose-substituted mucin-type O-glycans and short chondroitin-like oligosaccharides |
Q33777641 | The nematode homologue of Mediator complex subunit 28, F28F8.5, is a critical regulator of C. elegans development. |
Q27317381 | The nephronophthisis-related gene ift-139 is required for ciliogenesis in Caenorhabditis elegans |
Q30540534 | The netrin receptor DCC focuses invadopodia-driven basement membrane transmigration in vivo |
Q42204186 | The neural network for chemotaxis to tastants in Caenorhabditis elegans is specialized for temporal differentiation |
Q36219774 | The neuroethology of C. elegans escape |
Q28288745 | The neuroprotective drug riluzole acts via small conductance Ca2+-activated K+ channels to ameliorate defects in spinal muscular atrophy models |
Q27306806 | The new anthelmintic tribendimidine is an L-type (levamisole and pyrantel) nicotinic acetylcholine receptor agonist |
Q35506248 | The nonmuscle myosin regulatory light chain gene mlc-4 is required for cytokinesis, anterior-posterior polarity, and body morphology during Caenorhabditis elegans embryogenesis |
Q34998152 | The novel hydroxylamine derivative NG-094 suppresses polyglutamine protein toxicity in Caenorhabditis elegans |
Q33818160 | The novel intestinal filament organizer IFO-1 contributes to epithelial integrity in concert with ERM-1 and DLG-1. |
Q37557464 | The novel secreted factor MIG-18 acts with MIG-17/ADAMTS to control cell migration in Caenorhabditis elegans |
Q34679993 | The nphp-2 and arl-13 genetic modules interact to regulate ciliogenesis and ciliary microtubule patterning in C. elegans |
Q36784726 | The nuclear argonaute NRDE-3 contributes to transitive RNAi in Caenorhabditis elegans |
Q61812007 | The nuclear hormone receptor NHR-86 controls anti-pathogen responses in C. elegans |
Q37311435 | The nuclear receptor NHR-25 cooperates with the Wnt/beta-catenin asymmetry pathway to control differentiation of the T seam cell in C. elegans |
Q35936761 | The nucleolus of Caenorhabditis elegans |
Q93049674 | The nucleoside diphosphate kinase NDK-1/NME1 promotes phagocytosis in concert with DYN-1/Dynamin |
Q40497197 | The nucleotide sequences of 5S rRNAs from a rotifer, Brachionus plicatilis, and two nematodes, Rhabditis tokai and Caenorhabditis elegans |
Q64065434 | The nutritional requirements of Caenorhabditis elegans |
Q30578006 | The olfactory neuron AWC promotes avoidance of normally palatable food following chronic dietary restriction |
Q37475787 | The onset of C. elegans dosage compensation is linked to the loss of developmental plasticity |
Q37247474 | The ortholog of human solute carrier family 35 member B1 (UDP-galactose transporter-related protein 1) is involved in maintenance of ER homeostasis and essential for larval development in Caenorhabditis elegans |
Q42032097 | The ortholog of the human proto-oncogene ROS1 is required for epithelial development in C. elegans |
Q73344684 | The pathway of myofibrillogenesis determines the interrelationship between myosin and paramyosin synthesis inCaenorhabditis elegans |
Q28538226 | The periplasmic enzyme, AnsB, of Shigella flexneri modulates bacterial adherence to host epithelial cells |
Q28596855 | The pesticidal Cry6Aa toxin from Bacillus thuringiensis is structurally similar to HlyE-family alpha pore-forming toxins |
Q47069393 | The pha-4 gene is required to generate the pharyngeal primordium of Caenorhabditis elegans |
Q34602382 | The phenotype of mes-2, mes-3, mes-4 and mes-6, maternal-effect genes required for survival of the germline in Caenorhabditis elegans, is sensitive to chromosome dosage |
Q99595515 | The physiological function of long-noncoding RNAs |
Q90027731 | The polarity protein VANG-1 antagonizes Wnt signaling by facilitating Frizzled endocytosis |
Q57454033 | The polarity-induced force imbalance in Caenorhabditis elegans embryos is caused by asymmetric binding rates of dynein to the cortex |
Q34218631 | The postembryonic cell lineages of the hermaphrodite and male gonads in Caenorhabditis elegans |
Q41880093 | The potassium chloride cotransporter KCC-2 coordinates development of inhibitory neurotransmission and synapse structure in Caenorhabditis elegans |
Q52358034 | The presynaptic machinery at the synapse of C. elegans. |
Q38698124 | The protection of novel 2-arylethenylquinoline derivatives against impairment of associative learning memory induced by neural Aβ in C. elegans Alzheimer's disease model |
Q37020576 | The protein L-isoaspartyl-O-methyltransferase functions in the Caenorhabditis elegans stress response |
Q37633312 | The putative multidrug resistance protein MRP-7 inhibits methylmercury-associated animal toxicity and dopaminergic neurodegeneration in Caenorhabditis elegans |
Q55383892 | The receptor protein tyrosine phosphatase CLR-1 is required for synaptic partner recognition. |
Q41912038 | The recycling endosome protein RAB-10 promotes autophagic flux and localization of the transmembrane protein ATG-9. |
Q35297715 | The response of Caenorhabditis elegans to hydrogen sulfide and hydrogen cyanide |
Q27314666 | The response to high CO2 levels requires the neuropeptide secretion component HID-1 to promote pumping inhibition |
Q33939646 | The retrograde IFT machinery of C. elegans cilia: two IFT dynein complexes? |
Q24300619 | The ribosomal protein RACK1 is required for microRNA function in both C. elegans and humans |
Q39287886 | The robustness of Caenorhabditis elegans male mating behavior depends on the distributed properties of ray sensory neurons and their output through core and male-specific targets |
Q36531751 | The role of Candida albicans AP-1 protein against host derived ROS in in vivo models of infection. |
Q36311977 | The role of eggshell and underlying vitelline membrane for normal pattern formation in the early C. elegans embryo |
Q90221394 | The role of poly(ADP-ribose) polymerases in manganese exposed Caenorhabditis elegans |
Q37117060 | The role of protein phosphatase 4 in regulating microtubule severing in the Caenorhabditis elegans embryo |
Q33956125 | The role of sdc-1 in the sex determination and dosage compensation decisions in Caenorhabditis elegans |
Q33239140 | The role of the AFD neuron in C. elegans thermotaxis analyzed using femtosecond laser ablation |
Q37420016 | The role of the formin gene fhod-1 in C. elegans embryonic morphogenesis |
Q27339997 | The roles and acting mechanism of Caenorhabditis elegans DNase II genes in apoptotic dna degradation and development |
Q33521391 | The roles of EGF and Wnt signaling during patterning of the C. elegans Bgamma/delta Equivalence Group |
Q35091288 | The same but different: worms reveal the pervasiveness of developmental system drift |
Q34565972 | The scaffolding protein SYD-2/Liprin-α regulates the mobility and polarized distribution of dense-core vesicles in C. elegans motor neurons |
Q33830454 | The secreted MSP domain of C. elegans VAPB homolog VPR-1 patterns the adult striated muscle mitochondrial reticulum via SMN-1 |
Q34733633 | The secretory pathway calcium ATPase PMR-1/SPCA1 has essential roles in cell migration during Caenorhabditis elegans embryonic development |
Q59134935 | The sensory amphidial structures of Caenorhabditis elegans are involved in macrocyclic lactone uptake and anthelmintic resistance |
Q35020039 | The short coiled-coil domain-containing protein UNC-69 cooperates with UNC-76 to regulate axonal outgrowth and normal presynaptic organization in Caenorhabditis elegans |
Q26770155 | The short-lived African turquoise killifish: an emerging experimental model for ageing |
Q34668519 | The significance of alternative transcripts for Caenorhabditis elegans transcription factor genes, based on expression pattern analysis |
Q36368745 | The slicing activity of miRNA-specific Argonautes is essential for the miRNA pathway in C. elegans |
Q88499137 | The small GTPase ARF-1.2 is a regulator of unicellular tube formation in Caenorhabditis elegans |
Q34806985 | The small GTPase Arf1 modulates mitochondrial morphology and function |
Q58716051 | The small GTPase RAB-35 defines a third pathway that is required for the recognition and degradation of apoptotic cells |
Q36404856 | The small GTPase Rab2 functions in the removal of apoptotic cells in Caenorhabditis elegans. |
Q28000022 | The small GTPases ARL-13 and ARL-3 coordinate intraflagellar transport and ciliogenesis |
Q37582784 | The small ubiquitin-like modifier (SUMO) is required for gonadal and uterine-vulval morphogenesis in Caenorhabditis elegans |
Q42646097 | The small, secreted immunoglobulin protein ZIG-3 maintains axon position in Caenorhabditis elegans |
Q27323319 | The somatic reproductive tissues of C. elegans promote longevity through steroid hormone signaling |
Q57802373 | The spatial and temporal dynamics of nuclear RNAi-targeted retrotransposon transcripts in |
Q27313726 | The specification and global reprogramming of histone epigenetic marks during gamete formation and early embryo development in C. elegans |
Q35914578 | The sperm surface localization of the TRP-3/SPE-41 Ca2+ -permeable channel depends on SPE-38 function in Caenorhabditis elegans |
Q34888218 | The spindle assembly function of Caenorhabditis elegans katanin does not require microtubule-severing activity |
Q44540931 | The sterol modifying enzyme LET-767 is essential for growth, reproduction and development in Caenorhabditis elegans. |
Q33822501 | The stress response factor daf-16/FOXO is required for multiple compound families to prolong the function of neurons with Huntington's disease |
Q36586994 | The sup-7(st5) X gene of Caenorhabditis elegans encodes a tRNATrpUAG amber suppressor |
Q54217793 | The surveillance of pre-mRNA splicing is an early step in C. elegans RNAi of endogenous genes. |
Q36190026 | The survival motor neuron gene smn-1 interacts with the U2AF large subunit gene uaf-1 to regulate Caenorhabditis elegans lifespan and motor functions |
Q28818150 | The synaptonemal complex has liquid crystalline properties and spatially regulates meiotic recombination factors |
Q34131609 | The synaptonemal complex shapes the crossover landscape through cooperative assembly, crossover promotion and crossover inhibition during Caenorhabditis elegans meiosis |
Q36645873 | The synaptonemal complexes of caenorhabditis elegans: comparison of wild-type and mutant strains and pachytene karyotype analysis of wild-type |
Q34643275 | The sys-1 and sys-3 genes cooperate with Wnt signaling to establish the proximal-distal axis of the Caenorhabditis elegans gonad |
Q28542476 | The tau tubulin kinases TTBK1/2 promote accumulation of pathological TDP-43 |
Q27437622 | The thioredoxin TRX-1 modulates the function of the insulin-like neuropeptide DAF-28 during dauer formation in Caenorhabditis elegans |
Q29619760 | The threshold for polyglutamine-expansion protein aggregation and cellular toxicity is dynamic and influenced by aging in Caenorhabditis elegans |
Q36796834 | The torsin-family AAA+ protein OOC-5 contains a critical disulfide adjacent to Sensor-II that couples redox state to nucleotide binding |
Q50146173 | The toxicity of a mixture of two antiseptics, triclosan and triclocarban, on reproduction and growth of the nematode Caenorhabditis elegans. |
Q35907418 | The tra-3 sex determination gene of Caenorhabditis elegans encodes a member of the calpain regulatory protease family. |
Q38274190 | The transcription factor HLH-2/E/Daughterless regulates anchor cell invasion across basement membrane in C. elegans |
Q64215121 | The transcription factor NHR-8: A new target to increase ivermectin efficacy in nematodes |
Q55542149 | The transcription factor SKN-1 and detoxification gene ugt-22 alter albendazole efficacy in Caenorhabditis elegans. |
Q28493171 | The transcriptional regulator CzcR modulates antibiotic resistance and quorum sensing in Pseudomonas aeruginosa |
Q34714372 | The transgenerational effects of heat stress in the nematode Caenorhabditis remanei are negative and rapidly eliminated under direct selection for increased stress resistance in larvae |
Q27314756 | The translational regulators GCN-1 and ABCF-3 act together to promote apoptosis in C. elegans |
Q34282154 | The tripartite motif protein MADD-2 functions with the receptor UNC-40 (DCC) in Netrin-mediated axon attraction and branching. |
Q37518034 | The tubulin repertoire of C. elegans sensory neurons and its context-dependent role in process outgrowth |
Q30479702 | The twisted pharynx phenotype in C. elegans |
Q27314620 | The two Caenorhabditis elegans UDP-glucose:glycoprotein glucosyltransferase homologues have distinct biological functions |
Q35083442 | The two actin-interacting protein 1 genes have overlapping and essential function for embryonic development in Caenorhabditis elegans |
Q46104742 | The two isoforms of the Caenorhabditis elegans leukocyte-common antigen related receptor tyrosine phosphatase PTP-3 function independently in axon guidance and synapse formation. |
Q42175607 | The type 2 secretion Pseudopilin, gspJ, is required for multihost pathogenicity of Burkholderia cenocepacia AU1054 |
Q35120803 | The type II poly(A)-binding protein PABP-2 genetically interacts with the let-7 miRNA and elicits heterochronic phenotypes in Caenorhabditis elegans |
Q43182438 | The ubc-2 gene of Caenorhabditis elegans encodes a ubiquitin-conjugating enzyme involved in selective protein degradation |
Q37375173 | The ubiquitin ligase CRL2ZYG11 targets cyclin B1 for degradation in a conserved pathway that facilitates mitotic slippage. |
Q92741126 | The ubiquitin-conjugating enzyme UBE2QL1 coordinates lysophagy in response to endolysosomal damage |
Q34601947 | The ubiquitin-fold modifier 1 (Ufm1) cascade of Caenorhabditis elegans |
Q41788416 | The unc-22(IV) region of Caenorhabditis elegans: genetic analysis of lethal mutations |
Q48174545 | The unc-53 gene negatively regulates rac GTPases to inhibit unc-5 activity during Distal tip cell migrations in C. elegans. |
Q37407936 | The unfolded protein response in a pair of sensory neurons promotes entry of C. elegans into dauer diapause |
Q46982604 | The use of elements as a substitute for biomass in toxicokinetic studies in small organisms |
Q34280972 | The use of functional genomics in C. elegans for studying human development and disease |
Q27313266 | The vesicle protein SAM-4 regulates the processivity of synaptic vesicle transport |
Q42460741 | The von Hippel Lindau tumor suppressor limits longevity |
Q34316697 | The worm in the world and the world in the worm |
Q41785447 | The zinc matrix metalloproteinase ZMP-2 increases survival of Caenorhabditis elegans through interference with lipoprotein absorption |
Q55257517 | The zinc transporter ZIPT-7.1 regulates sperm activation in nematodes. |
Q44433252 | TheC. elegansG-protein-coupled receptor SRA-13 inhibits RAS/MAPK signalling during olfaction and vulval development |
Q47069469 | TheCaenorhabditis elegansnonmuscle myosin genesnmy-1andnmy-2function as redundant components of thelet-502/Rho-binding kinase andmel-11/myosin phosphatase pathway during embryonic morphogenesis |
Q34088101 | Theory of the locomotion of nematodes: Dynamics of undulatory progression on a surface |
Q30762087 | Thermal avoidance in Caenorhabditis elegans: an approach to the study of nociception |
Q30566713 | Thermotaxis is a robust mechanism for thermoregulation in Caenorhabditis elegans nematodes |
Q26827313 | Thermotaxis of C. elegans as a model for temperature perception, neural information processing and neural plasticity |
Q34569881 | Thiamine pyrophosphate biosynthesis and transport in the nematode Caenorhabditis elegans |
Q39691121 | Thinking about the brain / F. H. C. Crick. - (9.1979). |
Q56534524 | Thioredoxin shapes the sensory response to produced nitric oxide |
Q36162972 | Three distinct amine receptors operating at different levels within the locomotory circuit are each essential for the serotonergic modulation of chemosensation in Caenorhabditis elegans |
Q42964179 | Three new classes of mutations in the Caenorhabditis elegans muscle gene sup-9. |
Q22008748 | Three proteins involved in Caenorhabditis elegans vulval invagination are similar to components of a glycosylation pathway |
Q34542019 | Three sorting nexins drive the degradation of apoptotic cells in response to PtdIns(3)P signaling |
Q89567836 | Three-dimensional behavioural phenotyping of freely moving C. elegans using quantitative light field microscopy |
Q36104570 | Three-dimensional fluorescent microscopy via simultaneous illumination and detection at multiple planes |
Q49120995 | Threshold chemosensitivity and hypothetical chemoreceptor function of the nematodeCaenorhabditis elegans. |
Q40091006 | Thymol has antifungal activity against Candida albicans during infection and maintains the innate immune response required for function of the p38 MAPK signaling pathway in Caenorhabditis elegans. |
Q34012620 | Time-lapse microscopy of early embryogenesis in Caenorhabditis elegans |
Q27339158 | Timing of locomotor activity circadian rhythms in Caenorhabditis elegans |
Q48846335 | Tissue and Species Specificity for Phorbol Ester Receptors |
Q35863085 | Tissue architecture in the Caenorhabditis elegans gonad depends on interactions among fibulin-1, type IV collagen and the ADAMTS extracellular protease |
Q27311477 | Tissue expression pattern of PMK-2 p38 MAPK is established by the miR-58 family in C. elegans |
Q37145916 | Tissue homogeneity requires inhibition of unequal gene silencing during development |
Q49168064 | Tissue treatment for whole mount internal lectin staining in the nematodes Caenorhabditis elegans, Panagrolaimus superbus and Acrobeloides maximus |
Q36113113 | Tissue- and Time-Specific Expression of Otherwise Identical tRNA Genes |
Q54112891 | Tissue-Specific Functions of fem-2/PP2c Phosphatase and fhod-1/formin During Caenorhabditiselegans Embryonic Morphogenesis. |
Q42613799 | Tissue-specific activities of an immune signaling module regulate physiological responses to pathogenic and nutritional bacteria in C. elegans |
Q58798740 | Tissue-specific degradation of essential centrosome components reveals distinct microtubule populations at microtubule organizing centers |
Q40587321 | Tissue-specific direct targets of Caenorhabditis elegans Rb/E2F dictate distinct somatic and germline programs |
Q39021067 | Tissue-specific regulation of alternative polyadenylation represses expression of a neuronal ankyrin isoform in C. elegans epidermal development |
Q36274015 | Toll-like Receptor Signaling Promotes Development and Function of Sensory Neurons Required for a C. elegans Pathogen-Avoidance Behavior |
Q92435639 | Toll-like receptor homolog TOL-1 regulates Bifidobacterium infantis-elicited longevity and behavior in Caenorhabditis elegans |
Q33551382 | Tomatidine enhances lifespan and healthspan in C. elegans through mitophagy induction via the SKN-1/Nrf2 pathway |
Q46437143 | Torsin-mediated protection from cellular stress in the dopaminergic neurons of Caenorhabditis elegans. |
Q37566119 | TorsinA rescues ER-associated stress and locomotive defects in C. elegans models of ALS. |
Q36730299 | Touch sensitivity in Caenorhabditis elegans |
Q41445222 | Toward Universal Forward Genetics: Using a Draft Genome Sequence of the Nematode Oscheius tipulae To Identify Mutations Affecting Vulva Development |
Q35176354 | Toward a better understanding of human eye disease insights from the zebrafish, Danio rerio. |
Q28770084 | Toward improving Caenorhabditis elegans phenome mapping with an ORFeome-based RNAi library |
Q57466104 | Toxic Effects of Size-tunable Gold Nanoparticles on Caenorhabditis elegans Development and Gene Regulation |
Q31168602 | Toxic-selenium and low-selenium transcriptomes in Caenorhabditis elegans: toxic selenium up-regulates oxidoreductase and down-regulates cuticle-associated genes |
Q64935097 | Toxicity Assay for Citrinin, Zearalenone and Zearalenone-14-Sulfate Using the Nematode Caenorhabditis elegans as Model Organism. |
Q55003393 | Toxicity evaluation of Wanzhou watershed of Yangtze Three Gorges Reservior in the flood season in Caenorhabditis elegans. |
Q41522614 | Toxicity evaluation of boron nitride nanospheres and water-soluble boron nitride in Caenorhabditis elegans |
Q37545351 | Toxicity of bioactive and probiotic marine bacteria and their secondary metabolites in Artemia sp. and Caenorhabditis elegans as eukaryotic model organisms. |
Q28393689 | Toxicity of quantum dots and cadmium salt to Caenorhabditis elegans after multigenerational exposure |
Q92599293 | Traditional tonifying polyherbal infusion, Jatu-Phala-Tiga, exerts antioxidant activities and extends lifespan of Caenorhabditis elegans |
Q37403265 | Trafficking of heme and porphyrins in metazoa. |
Q34403732 | Trans-cellular introduction of HIV-1 protein Nef induces pathogenic response in Caenorhabditis elegans |
Q91632758 | Trans-splicing of the C. elegans let-7 primary transcript developmentally regulates let-7 microRNA biogenesis and let-7 family microRNA activity |
Q37327342 | Transcript expression patterns illuminate the mechanistic background of hormesis in caenorhabditis elegans maupas |
Q36285399 | Transcription factor redundancy and tissue-specific regulation: evidence from functional and physical network connectivity |
Q38595946 | Transcription of class III genes in cell-free extracts from the nematode Caenorhabditis elegans |
Q64089932 | Transcriptional alterations in Caenorhabditis elegans following exposure to an anthelmintic fraction of the plant Picria fel-terrae Lour |
Q36661884 | Transcriptional control of cell-cycle quiescence during C. elegans development |
Q47129438 | Transcriptional control of non-apoptotic developmental cell death in C. elegans |
Q33351781 | Transcriptional profiling in C. elegans suggests DNA damage dependent apoptosis as an ancient function of the p53 family |
Q37464821 | Transcriptional profiling of C. elegans DAF-19 uncovers a ciliary base-associated protein and a CDK/CCRK/LF2p-related kinase required for intraflagellar transport |
Q37111132 | Transcriptional regulation and stabilization of left-right neuronal identity in C. elegans |
Q27331769 | Transcriptional repression of Hox genes by C. elegans HP1/HPL and H1/HIS-24 |
Q33987754 | Transcriptional upregulation of both egl-1 BH3-only and ced-3 caspase is required for the death of the male-specific CEM neurons |
Q42088994 | Transcriptionally regulated cell adhesion network dictates distal tip cell directionality |
Q89314606 | Transcriptome Analysis of C. elegans Reveals Novel Targets for DON Cytotoxicity |
Q41677454 | Transcriptome analysis reveals molecular anthelmintic effects of procyanidins in C. elegans |
Q91851115 | Transcriptome resilience predicts thermotolerance in Caenorhabditis elegans |
Q33760468 | Transgene-mediated co-suppression of DNA topoisomerase-1 gene in Caenorhabditis elegans |
Q42264027 | Transgenerational Diapause as an Avoidance Strategy against Bacterial Pathogens in Caenorhabditis elegans |
Q48201499 | Transgenesis by microparticle bombardment for live imaging of fluorescent proteins in Pristionchus pacificus germline and early embryos |
Q35751448 | Transgenic nematodes as biosensors for metal stress in soil pore water samples |
Q92782432 | Transient Receptor Potential V Channels Are Essential for Glucose Sensing by Aldolase and AMPK |
Q52691762 | Transient and Partial Nuclear Lamina Disruption Promotes Chromosome Movement in Early Meiotic Prophase. |
Q33552126 | Translation of a small subset of Caenorhabditis elegans mRNAs is dependent on a specific eukaryotic translation initiation factor 4E isoform |
Q41366279 | Translation readthrough mitigation. |
Q92147739 | Translational Regulation of Non-autonomous Mitochondrial Stress Response Promotes Longevity |
Q47069366 | Translational control of maternal glp-1 mRNA by POS-1 and its interacting protein SPN-4 in Caenorhabditis elegans |
Q34636227 | Translational control of the oogenic program by components of OMA ribonucleoprotein particles in Caenorhabditis elegans |
Q30537573 | Transmembrane protein OSTA-1 shapes sensory cilia morphology via regulation of intracellular membrane trafficking in C. elegans |
Q27310200 | Transmembrane proteoglycans control stretch-activated channels to set cytosolic calcium levels |
Q36969541 | Transmission dynamics of heritable silencing induced by double-stranded RNA in Caenorhabditis elegans |
Q82851452 | Trap induction and trapping in eight nematode-trapping fungi (Orbiliaceae) as affected by juvenile stage of Caenorhabditis elegans |
Q91994955 | Treatment of Caenorhabditis elegans with Small Selenium Species Enhances Antioxidant Defense Systems |
Q35293750 | Trimethylation of Lys36 on H3 restricts gene expression change during aging and impacts life span |
Q35046098 | Trimethylpsoralen induces small deletion mutations in Caenorhabditis elegans |
Q60908258 | Trodusquemine enhances Aβ aggregation but suppresses its toxicity by displacing oligomers from cell membranes |
Q34359408 | Tropomyosin and troponin are required for ovarian contraction in the Caenorhabditis elegans reproductive system |
Q24673007 | Tropomyosin inhibits ADF/cofilin-dependent actin filament dynamics |
Q30494196 | Troponin I controls ovulatory contraction of non-striated actomyosin networks in the C. elegans somatic gonad |
Q89266446 | Tubular Excretory Canal Structure Depends on Intermediate Filaments EXC-2 and IFA-4 in Caenorhabditis elegans |
Q36933702 | Tudor domain ERI-5 tethers an RNA-dependent RNA polymerase to DCR-1 to potentiate endo-RNAi |
Q70483180 | Tumor promoters specifically and reversibly disturb development and behavior of Caenorhabditis elegans |
Q47559208 | Tumor suppressor APC is an attenuator of spindle-pulling forces during C. elegans asymmetric cell division. |
Q90573581 | Tumour travel tours - Why circulating cancer cells value company |
Q90431025 | Turnover in local parasite populations temporarily favors host outcrossing over self-fertilization during experimental evolution |
Q42174578 | Twitchin kinase inhibits muscle activity. |
Q35754884 | Twitchin kinase interacts with MAPKAP kinase 2 in Caenorhabditis elegans striated muscle |
Q34042679 | Two Golgi-resident 3'-Phosphoadenosine 5'-phosphosulfate transporters play distinct roles in heparan sulfate modifications and embryonic and larval development in Caenorhabditis elegans |
Q36095693 | Two LIM domain proteins and UNC-96 link UNC-97/pinch to myosin thick filaments in Caenorhabditis elegans muscle |
Q34383750 | Two Leucobacter strains exert complementary virulence on Caenorhabditis including death by worm-star formation |
Q27320328 | Two PI 3-kinases and one PI 3-phosphatase together establish the cyclic waves of phagosomal PtdIns(3)P critical for the degradation of apoptotic cells |
Q36244417 | Two Paralogous Tetraspanins TSP-12 and TSP-14 Function with the ADAM10 Metalloprotease SUP-17 to Promote BMP Signaling in Caenorhabditis elegans |
Q38938096 | Two Rab2 interactors regulate dense-core vesicle maturation |
Q41868764 | Two Wnts instruct topographic synaptic innervation in C. elegans |
Q30582807 | Two actin-interacting protein 1 isoforms function redundantly in the somatic gonad and are essential for reproduction in Caenorhabditis elegans |
Q35942369 | Two alternative mechanisms that regulate the presentation of apoptotic cell engulfment signal in Caenorhabditis elegans |
Q37425018 | Two distinct roles for EGL-9 in the regulation of HIF-1-mediated gene expression in Caenorhabditis elegans |
Q42224388 | Two forms of death in ageing Caenorhabditis elegans |
Q47102060 | Two functional domains in C. elegans glypican LON-2 can independently inhibit BMP-like signaling |
Q48355416 | Two functionally distinct E2/E3 pairs coordinate sequential ubiquitination of a common substrate in Caenorhabditis elegans development. |
Q24643890 | Two heteromeric kinesin complexes in chemosensory neurons and sensory cilia of Caenorhabditis elegans |
Q40538629 | Two highly conserved transcribed regions in the 5S DNA repeats of the nematodes Caenorhabditis elegans and Caenorhabditis briggsae |
Q43242512 | Two insulin-like peptides antagonistically regulate aversive olfactory learning in C. elegans. |
Q33969590 | Two neuronal G proteins are involved in chemosensation of the Caenorhabditis elegans Dauer-inducing pheromone |
Q37013669 | Two novel DEG/ENaC channel subunits expressed in glia are needed for nose-touch sensitivity in Caenorhabditis elegans |
Q51444288 | Two organobromines trigger lifespan, growth, reproductive and transcriptional changes in Caenorhabditis elegans. |
Q34605166 | Two pleiotropic classes of daf-2 mutation affect larval arrest, adult behavior, reproduction and longevity in Caenorhabditis elegans. |
Q48057176 | Two populations of cytoplasmic dynein contribute to spindle positioning in C. elegans embryos |
Q37461949 | Two thioredoxin reductases, trxr-1 and trxr-2, have differential physiological roles in Caenorhabditis elegans |
Q33961146 | Two types of sites required for meiotic chromosome pairing in Caenorhabditis elegans |
Q33527395 | Two very long chain fatty acid acyl-CoA synthetase genes, acs-20 and acs-22, have roles in the cuticle surface barrier in Caenorhabditis elegans |
Q30832370 | Type II platelet-activating factor-acetylhydrolase is essential for epithelial morphogenesis in Caenorhabditis elegans |
Q36262020 | Type IV collagen is detectable in most, but not all, basement membranes of Caenorhabditis elegans and assembles on tissues that do not express it |
Q42819776 | Tyramine and octopamine independently inhibit serotonin-stimulated aversive behaviors in Caenorhabditis elegans through two novel amine receptors. |
Q34365217 | UAP56 levels affect viability and mRNA export in Caenorhabditis elegans |
Q93177704 | UDP-N-acetylglucosamine-dolichyl-phosphate N-acetylglucosaminephosphotransferase is indispensable for oogenesis, oocyte-to-embryo transition, and larval development of the nematode Caenorhabditis elegans |
Q35990615 | UNC-1 regulates gap junctions important to locomotion in C. elegans |
Q37365420 | UNC-108/RAB-2 and its effector RIC-19 are involved in dense core vesicle maturation in Caenorhabditis elegans. |
Q36739860 | UNC-108/Rab2 regulates postendocytic trafficking in Caenorhabditis elegans |
Q24647131 | UNC-11, a Caenorhabditis elegans AP180 homologue, regulates the size and protein composition of synaptic vesicles |
Q24652483 | UNC-129 regulates the balance between UNC-40 dependent and independent UNC-5 signaling pathways |
Q37417587 | UNC-13 and UNC-10/rim localize synaptic vesicles to specific membrane domains. |
Q43240851 | UNC-13 is required for synaptic vesicle fusion in C. elegans |
Q37094524 | UNC-13L, UNC-13S, and Tomosyn form a protein code for fast and slow neurotransmitter release in Caenorhabditis elegans |
Q27346293 | UNC-16 (JIP3) Acts Through Synapse-Assembly Proteins to Inhibit the Active Transport of Cell Soma Organelles to Caenorhabditis elegans Motor Neuron Axons |
Q55383005 | UNC-16/JIP3 and UNC-76/FEZ1 limit the density of mitochondria in C. elegans neurons by maintaining the balance of anterograde and retrograde mitochondrial transport. |
Q47169436 | UNC-16/JIP3 regulates early events in synaptic vesicle protein trafficking via LRK-1/LRRK2 and AP complexes. |
Q47933065 | UNC-18 and Tomosyn Antagonistically Control Synaptic Vesicle Priming Downstream of UNC-13 in Caenorhabditis elegans |
Q37034998 | UNC-18 modulates ethanol sensitivity in Caenorhabditis elegans |
Q36854983 | UNC-18 promotes both the anterograde trafficking and synaptic function of syntaxin |
Q47068719 | UNC-31 (CAPS) is required for dense-core vesicle but not synaptic vesicle exocytosis in Caenorhabditis elegans. |
Q43147479 | UNC-33 (CRMP) and ankyrin organize microtubules and localize kinesin to polarize axon-dendrite sorting |
Q35978913 | UNC-4 antagonizes Wnt signaling to regulate synaptic choice in the C. elegans motor circuit |
Q35615975 | UNC-4 represses CEH-12/HB9 to specify synaptic inputs to VA motor neurons in C. elegans |
Q35208880 | UNC-4/UNC-37-dependent repression of motor neuron-specific genes controls synaptic choice in Caenorhabditis elegans |
Q27335586 | UNC-41/stonin functions with AP2 to recycle synaptic vesicles in Caenorhabditis elegans |
Q51646975 | UNC-55, an orphan nuclear hormone receptor, orchestrates synaptic specificity among two classes of motor neurons in Caenorhabditis elegans. |
Q30586748 | UNC-6 (netrin) stabilizes oscillatory clustering of the UNC-40 (DCC) receptor to orient polarity |
Q40345230 | UNC-6/Netrin induces neuronal asymmetry and defines the site of axon formation |
Q24635896 | UNC-6/netrin and its receptors UNC-5 and UNC-40/DCC modulate growth cone protrusion in vivo in C. elegans |
Q41442490 | UNC-64 and RIC-4, the plasma membrane-associated SNAREs syntaxin and SNAP-25, regulate fat storage in nematode Caenorhabditis elegans |
Q34483508 | UNC-83 IS a KASH protein required for nuclear migration and is recruited to the outer nuclear membrane by a physical interaction with the SUN protein UNC-84 |
Q33677404 | UNC-83 coordinates kinesin-1 and dynein activities at the nuclear envelope during nuclear migration |
Q36091809 | UNC-89 (obscurin) binds to MEL-26, a BTB-domain protein, and affects the function of MEI-1 (katanin) in striated muscle of Caenorhabditis elegans |
Q35147435 | UNC50 prompts G1/S transition and proliferation in HCC by regulation of epidermal growth factor receptor trafficking |
Q24324707 | Ubiquilin and p97/VCP bind erasin, forming a complex involved in ERAD |
Q33292491 | Ubiquitin conjugating enzymes participate in polyglutamine protein aggregation |
Q100456054 | Ubiquitin-dependent regulation of a conserved DMRT protein controls sexually dimorphic synaptic connectivity and behavior |
Q27324783 | Ubiquitin-mediated response to microsporidia and virus infection in C. elegans |
Q27932043 | Ubiquitin-related modifier Urm1 acts as a sulphur carrier in thiolation of eukaryotic transfer RNA. |
Q30515046 | Ubiquitination is involved in secondary growth, not initial formation of polyglutamine protein aggregates in C. elegans. |
Q26269856 | Ultrahigh-resolution imaging reveals formation of neuronal SNARE/Munc18 complexes in situ |
Q37219535 | Ultraviolet-A triggers photoaging in model nematode Caenorhabditis elegans in a DAF-16 dependent pathway. |
Q36218364 | Unc-1: a stomatin homologue controls sensitivity to volatile anesthetics in Caenorhabditis elegans |
Q36256331 | Unc-45 mutations in Caenorhabditis elegans implicate a CRO1/She4p-like domain in myosin assembly |
Q52315637 | Unconventional function of an Achaete-Scute homolog as a terminal selector of nociceptive neuron identity. |
Q41323838 | Uncoupling Protein, UCP-4 May Be Involved in Neuronal Defects During Aging and Resistance to Pathogens in Caenorhabditis elegans |
Q24811849 | Uncoupling of longevity and telomere length in C. elegans |
Q26738368 | Understanding Synaptogenesis and Functional Connectome in C. elegans by Imaging Technology |
Q92316218 | Understanding lipidomic basis of iron limitation induced chemosensitization of drug-resistant Mycobacterium tuberculosis |
Q36045461 | Undulatory locomotion of Caenorhabditis elegans on wet surfaces |
Q36427428 | Unexpected Variation in Neuroanatomy among Diverse Nematode Species |
Q89863572 | Unexpected cell type-dependent effects of autophagy on polyglutamine aggregation revealed by natural genetic variation in C. elegans |
Q42397809 | Unfolded protein response genes regulated by CED-1 are required for Caenorhabditis elegans innate immunity |
Q42247505 | Unique Structural Features of Membrane-Bound C-Terminal Domain Motifs Modulate Complexin Inhibitory Function |
Q55449967 | Unique patterns of trimethylation of histone H3 lysine 4 are prone to changes during aging in Caenorhabditis elegans somatic cells. |
Q37289368 | Unraveling flp-11/flp-32 dichotomy in nematodes |
Q35840153 | Unraveling the mechanisms of synapse formation and axon regeneration: the awesome power of C. elegans genetics |
Q35527130 | Unsaturated fatty acids induce non-canonical autophagy |
Q34897837 | Unusual DNA structures associated with germline genetic activity in Caenorhabditis elegans |
Q36215085 | Unusual forms of low density lipoprotein receptors in hamster cell mutants with defects in the receptor structural gene |
Q35145730 | Unusual regulation of splicing of the cholinergic locus in Caenorhabditis elegans |
Q24652552 | Upregulation of the let-7 microRNA with precocious development in lin-12/Notch hypermorphic Caenorhabditis elegans mutants |
Q38677014 | Uridine monophosphate synthetase enables eukaryotic de novo NAD+ biosynthesis from quinolinic acid |
Q38253642 | Use of Caenorhabditis elegans as a model to study Alzheimer's disease and other neurodegenerative diseases |
Q89896229 | Use of Phycobiliproteins from Atacama Cyanobacteria as Food Colorants in a Dairy Beverage Prototype |
Q24810874 | Use of SNPs to determine the breakpoints of complex deficiencies, facilitating gene mapping in Caenorhabditis elegans |
Q33761720 | Use of an activated beta-catenin to identify Wnt pathway target genes in caenorhabditis elegans, including a subset of collagen genes expressed in late larval development |
Q37111234 | Use of cDNA subtraction and RNA interference screens in combination reveals genes required for germ-line development in Caenorhabditis elegans |
Q37185724 | Use of non-mammalian alternative models for neurotoxicological study |
Q28552737 | Using C. elegans Forward and Reverse Genetics to Identify New Compounds with Anthelmintic Activity |
Q35726417 | Using C. elegans for aging research |
Q33936475 | Using C. elegans for antimicrobial drug discovery |
Q35218763 | Using C. elegans to identify the protease targets of serpins in vivo |
Q41875981 | Using Caenorhabditis elegans as a model organism for evaluating extracellular signal-regulated kinase docking domain inhibitors |
Q41234866 | Using Multiple Phenotype Assays and Epistasis Testing to Enhance the Reliability of RNAi Screening and Identify Regulators of Muscle Protein Degradation. |
Q34046877 | Using RNA interference to identify genes required for RNA interference |
Q37310263 | Using RNA interference to identify specific modifiers of a temperature-sensitive, embryonic-lethal mutation in the Caenorhabditis elegans ubiquitin-like Nedd8 protein modification pathway E1-activating gene rfl-1 |
Q90374432 | Using Transcriptomes as Mutant Phenotypes Reveals Functional Regions of a Mediator Subunit in Caenorhabditis elegans |
Q33817389 | Using a health-rating system to evaluate the usefulness of Caenorhabditis elegans as a model for anthelmintic study |
Q92690748 | Using genetics to understand biology |
Q61799981 | Using the drug-protein interactome to identify anti-ageing compounds for humans |
Q36460071 | Utility of an improved model of amyloid-beta (Aβ₁₋₄₂) toxicity in Caenorhabditis elegans for drug screening for Alzheimer's disease |
Q30515861 | V-ATPase V1 sector is required for corpse clearance and neurotransmission in Caenorhabditis elegans |
Q35176665 | VAB-10 spectraplakin acts in cell and nuclear migration in Caenorhabditis elegans |
Q34988024 | VAPB/ALS8 MSP ligands regulate striated muscle energy metabolism critical for adult survival in caenorhabditis elegans |
Q34329148 | VHA-19 is essential in Caenorhabditis elegans oocytes for embryogenesis and is involved in trafficking in oocytes |
Q58284047 | VIG-1 is required for maintenance of genome stability in Caenorhabditis elegans |
Q42018471 | Validated Liquid Culture Monitoring System for Lifespan Extension of Caenorhabditis elegans through Genetic and Dietary Manipulations |
Q46772888 | Valproic acid extends Caenorhabditis elegans lifespan. |
Q89595586 | Variability in β-catenin pulse dynamics in a stochastic cell fate decision in C. elegans |
Q28552620 | Variable Temperature Stress in the Nematode Caenorhabditis elegans (Maupas) and Its Implications for Sensitivity to an Additional Chemical Stressor |
Q28256325 | Vesicular neurotransmitter transporters. Potential sites for the regulation of synaptic function |
Q33966257 | Viable maternal-effect mutations that affect the development of the nematode Caenorhabditis elegans |
Q54233787 | Viable-but-Nonculturable Listeria monocytogenes and Salmonella enterica Serovar Thompson Induced by Chlorine Stress Remain Infectious. |
Q50803639 | Video camera-computer tracking of nematodeCaenorhabditis elegans to record behavioral responses. |
Q40032948 | Vigorous motor activity in Caenorhabditis elegans requires efficient clearance of dopamine mediated by synaptic localization of the dopamine transporter DAT-1. |
Q36532718 | Vinculin is essential for muscle function in the nematode |
Q26784521 | Violacein: Properties and Production of a Versatile Bacterial Pigment |
Q36992204 | Virgin Caenorhabditis remanei females are attracted to a coital pheromone released by con-specific copulating males |
Q58089902 | Virulence behavior of uropathogenic Escherichia coli strains in the host model Caenorhabditis elegans |
Q34132052 | Virulence effect of Enterococcus faecalis protease genes and the quorum-sensing locus fsr in Caenorhabditis elegans and mice |
Q36746663 | Virulence of Leucobacter chromiireducens subsp. solipictus to Caenorhabditis elegans: characterization of a novel host-pathogen interaction |
Q30439292 | Virulence of Staphylococcus aureus small colony variants in the Caenorhabditis elegans infection model |
Q99579728 | Virulence phenotypes result from interactions between pathogen ploidy and genetic background |
Q42376698 | Virulence test using nematodes to prescreen Nocardia species capable of inducing neurodegeneration and behavioral disorders |
Q36712646 | Viscoelastic properties of the nematode Caenorhabditis elegans, a self-similar, shear-thinning worm |
Q90167250 | Visualization and Quantification of Transposon Activity in Caenorhabditis elegans RNAi Pathway Mutants |
Q30978149 | Visualization and dissemination of multidimensional proteomics data comparing protein abundance during Caenorhabditis elegans development |
Q33246039 | Visualization of C. elegans transgenic arrays by GFP |
Q36015483 | Visualization of Caenorhabditis elegans cuticular structures using the lipophilic vital dye DiI. |
Q46718490 | Visualizing Calcium Flux in Freely Moving Nematode Embryos |
Q41890231 | Visualizing neuroblast cytokinesis during C. elegans embryogenesis |
Q90628355 | Vitamin B12 Regulates Glial Migration and Synapse Formation through Isoform-Specific Control of PTP-3/LAR PRTP Expression |
Q41262106 | Vitamin B12 deficiency in Caenorhabditis elegans results in loss of fertility, extended life cycle, and reduced lifespan. |
Q42369211 | Vitamin B12 deficiency results in severe oxidative stress, leading to memory retention impairment in Caenorhabditis elegans. |
Q30407475 | WAVE binds Ena/VASP for enhanced Arp2/3 complex-based actin assembly |
Q42090364 | WAVE/SCAR promotes endocytosis and early endosome morphology in polarized C. elegans epithelia |
Q33675132 | WDR23 regulates NRF2 independently of KEAP1. |
Q33538090 | WWP-1 is a novel modulator of the DAF-2 insulin-like signaling network involved in pore-forming toxin cellular defenses in Caenorhabditis elegans |
Q30393822 | Ways and means of coping with uncertainties of the relationship of the genetic blue print to protein structure and function in the cell |
Q50103667 | What Can We Learn About Human Disease from the Nematode C. elegans? |
Q39666433 | What genetic model organisms offer the study of behavior and neural circuits |
Q42138075 | Whole apple extracts increase lifespan, healthspan and resistance to stress in Caenorhabditis elegans |
Q30823060 | Whole exome sequencing of Rett syndrome-like patients reveals the mutational diversity of the clinical phenotype |
Q88645437 | Whole-Genome Analysis of Bacillus thuringiensis Revealing Partial Genes as a Source of Novel Cry Toxins |
Q34093437 | Whole-animal chemical screen identifies colistin as a new immunomodulator that targets conserved pathways. |
Q69404038 | Whole-animal connectomes of both Caenorhabditis elegans sexes |
Q38973407 | Whole-animal mounts of Caenorhabditis elegans for 3D imaging using atomic force microscopy |
Q24599852 | Whole-genome profiling of mutagenesis in Caenorhabditis elegans |
Q34614500 | Why are there males in the hermaphroditic species Caenorhabditis elegans? |
Q27321065 | Why do sleeping nematodes adopt a hockey-stick-like posture? |
Q36782218 | Why do worms go against the flow? C. elegans behaviors explained by simple physics |
Q33979803 | Withania somnifera root extract extends lifespan of Caenorhabditis elegans. |
Q42153268 | Wnt Ligands Differentially Regulate Toxicity and Translocation of Graphene Oxide through Different Mechanisms in Caenorhabditis elegans |
Q59333345 | Wnt Secretion Is Regulated by the Tetraspan Protein HIC-1 through Its Interaction with Neurabin/NAB-1 |
Q92022778 | Wnt Signaling Drives Ectopic Gene Expression and Larval Arrest in the Absence of the Caenorhabditis elegans DREAM Repressor Complex |
Q41499175 | Wnt and EGF pathways act together to induce C. elegans male hook development |
Q35202988 | Wnt pathway components orient a mitotic spindle in the early Caenorhabditis elegans embryo without requiring gene transcription in the responding cell |
Q33310139 | Wnt signal from multiple tissues and lin-3/EGF signal from the gonad maintain vulval precursor cell competence in Caenorhabditis elegans |
Q34293036 | Wnt signaling controls the stem cell-like asymmetric division of the epithelial seam cells during C. elegans larval development |
Q33911219 | Wnt signaling drives WRM-1/beta-catenin asymmetries in early C. elegans embryos |
Q36825237 | Wnt signaling in Pristionchus pacificus gonadal arm extension and the evolution of organ shape |
Q36418931 | Wnt signals can function as positional cues in establishing cell polarity |
Q40266207 | Wnt-Ror signaling to SIA and SIB neurons directs anterior axon guidance and nerve ring placement in C. elegans |
Q55450116 | Wnts Promote Synaptic Assembly Through T-Cell Specific Transcription Factors in Caenorhabditis elegans. |
Q35567444 | Wobble base-pairing slows in vivo translation elongation in metazoans |
Q30498190 | Worm Phenotype Ontology: integrating phenotype data within and beyond the C. elegans community |
Q89996447 | Worm-Based Alternate Assessment of Probiotic Intervention against Gut Barrier Infection |
Q34194372 | Worm-stars and half-worms: Novel dangers and novel defense |
Q34070082 | WormBase 2012: more genomes, more data, new website |
Q34382790 | WormBase 2014: new views of curated biology |
Q28269956 | WormBase 2016: expanding to enable helminth genomic research |
Q29541022 | WormBook: WormBiology for the 21st Century |
Q34211906 | WormScan: a technique for high-throughput phenotypic analysis of Caenorhabditis elegans |
Q39493266 | Wormpath: searching for molecular interaction networks in Caenorhabditis elegans |
Q34361733 | Worms need microbes too: microbiota, health and aging in Caenorhabditis elegans |
Q31051911 | Worms taste bitter: ASH neurons, QUI-1, GPA-3 and ODR-3 mediate quinine avoidance in Caenorhabditis elegans |
Q37397469 | Worms with a single functional sensory cilium generate proper neuron-specific behavioral output. |
Q27028078 | Worms, bacteria, and micronutrients: an elegant model of our diet |
Q35070715 | Worms, flies and four-legged friends: the applicability of biological models to the understanding of intestinal inflammatory diseases |
Q92128854 | Wrapping culture plates with Parafilm M® increases Caenorhabditis elegans growth |
Q37485543 | X Chromosome Crossover Formation and Genome Stability in Caenorhabditis elegans Are Independently Regulated by xnd-1. |
Q30412367 | X-chromosome silencing in the germline of C. elegans |
Q27667259 | X-ray Crystal Structure of the UCS Domain-Containing UNC-45 Myosin Chaperone from Drosophila melanogaster |
Q91960771 | XBP-1 Remodels Lipid Metabolism to Extend Longevity |
Q30478329 | XBX-1 encodes a dynein light intermediate chain required for retrograde intraflagellar transport and cilia assembly in Caenorhabditis elegans |
Q27307853 | XRN2 Autoregulation and Control of Polycistronic Gene Expresssion in Caenorhabditis elegans |
Q34360631 | Yersinia pestis kills Caenorhabditis elegans by a biofilm-independent process that involves novel virulence factors |
Q70241295 | Yolk proteins of Caenorhabditis elegans |
Q36085279 | Z-line formins promote contractile lattice growth and maintenance in striated muscles of C. elegans |
Q27313630 | ZHP-3 acts at crossovers to couple meiotic recombination with synaptonemal complex disassembly and bivalent formation in C. elegans |
Q57753918 | ZNFX-1 Functions within Perinuclear Nuage to Balance Epigenetic Signals |
Q92535141 | ZPD-2, a Small Compound That Inhibits α-Synuclein Amyloid Aggregation and Its Seeded Polymerization |
Q34350963 | ZTF-8 interacts with the 9-1-1 complex and is required for DNA damage response and double-strand break repair in the C. elegans germline |
Q36758443 | ZYX-1, the unique zyxin protein of Caenorhabditis elegans, is involved in dystrophin-dependent muscle degeneration |
Q36503151 | Zebrafish: a model system for the study of eye genetics |
Q27313811 | Zinc Levels Modulate Lifespan through Multiple Longevity Pathways in Caenorhabditis elegans |
Q50889958 | Zinc mediates the SREBP-SCD axis to regulate lipid metabolism in Caenorhabditis elegans. |
Q92181348 | Zn homeostasis in genetic models of Parkinson's disease in Caenorhabditis elegans |
Q41461248 | aPKC Cycles between Functionally Distinct PAR Protein Assemblies to Drive Cell Polarity |
Q47768387 | acn-1, a C. elegans homologue of ACE, genetically interacts with the let-7 microRNA and other heterochronic genes |
Q34945410 | acr-23 Encodes a monepantel-sensitive channel in Caenorhabditis elegans |
Q36717354 | akirin is required for diakinesis bivalent structure and synaptonemal complex disassembly at meiotic prophase I |
Q36741195 | apl-1, a Caenorhabditis elegans gene encoding a protein related to the human beta-amyloid protein precursor |
Q58597565 | as a Model Host to Monitor the Infection Processes |
Q36254841 | beta-Filagenin, a newly identified protein coassembling with myosin and paramyosin in Caenorhabditis elegans |
Q30986475 | cDNA cloning of a novel heterogeneous nuclear ribonucleoprotein gene homologue in Caenorhabditis elegans using hamster prion protein cDNA as a hybridization probe |
Q40418342 | cGAL, a temperature-robust GAL4-UAS system for Caenorhabditis elegans |
Q30831282 | cdc-25.4, a Caenorhabditis elegans Ortholog of cdc25, Is Required for Male Mating Behavior |
Q37520983 | cel-mir-237 and its homologue, hsa-miR-125b, modulate the cellular response to ionizing radiation. |
Q41825913 | cin-4, a gene with homology to topoisomerase II, is required for centromere resolution by cohesin removal from sister kinetochores during mitosis |
Q35200613 | clr-1 encodes a receptor tyrosine phosphatase that negatively regulates an FGF receptor signaling pathway in Caenorhabditis elegans |
Q37622610 | dad-1, an endogenous programmed cell death suppressor in Caenorhabditis elegans and vertebrates. |
Q27312521 | daf-31 encodes the catalytic subunit of N alpha-acetyltransferase that regulates Caenorhabditis elegans development, metabolism and adult lifespan |
Q27309551 | dbl-1/TGF-β and daf-12/NHR Signaling Mediate Cell-Nonautonomous Effects of daf-16/FOXO on Starvation-Induced Developmental Arrest |
Q47069276 | dmd-3, a doublesex-related gene regulated by tra-1, governs sex-specific morphogenesis in C. elegans. |
Q27318821 | dnc-1/dynactin 1 knockdown disrupts transport of autophagosomes and induces motor neuron degeneration |
Q34609789 | dpy-18 encodes an alpha-subunit of prolyl-4-hydroxylase in caenorhabditis elegans |
Q34020669 | drr-2 encodes an eIF4H that acts downstream of TOR in diet-restriction-induced longevity of C. elegans |
Q57245808 | eIF5A is required for autophagy by mediating ATG3 translation |
Q24617775 | ePAT: a simple method to tag adenylated RNA to measure poly(A)-tail length and other 3' RACE applications |
Q38333549 | elt-1, an embryonically expressed Caenorhabditis elegans gene homologous to the GATA transcription factor family |
Q35297761 | emb-1 encodes the APC16 subunit of the Caenorhabditis elegans anaphase-promoting complex |
Q35221634 | emb-4 is a conserved gene required for efficient germline-specific chromatin remodeling during Caenorhabditis elegans embryogenesis |
Q48117247 | emb-5, a gene required for the correct timing of gut precursor cell division during gastrulation in Caenorhabditis elegans, encodes a protein similar to the yeast nuclear protein SPT6. |
Q36237200 | emo-1, a Caenorhabditis elegans Sec61p gamma homologue, is required for oocyte development and ovulation |
Q35195151 | end-1 encodes an apparent GATA factor that specifies the endoderm precursor in Caenorhabditis elegans embryos |
Q33956541 | fog-1, a regulatory gene required for specification of spermatogenesis in the germ line of Caenorhabditis elegans |
Q21146385 | fog-2 and the evolution of self-fertile hermaphroditism in Caenorhabditis |
Q33954044 | fog-2, a germ-line-specific sex determination gene required for hermaphrodite spermatogenesis in Caenorhabditis elegans |
Q36585340 | glh-1, a germ-line putative RNA helicase from Caenorhabditis, has four zinc fingers |
Q36936847 | glo-3, a novel Caenorhabditis elegans gene, is required for lysosome-related organelle biogenesis |
Q34411576 | gon-14 functions with class B and class C synthetic multivulva genes to control larval growth in Caenorhabditis elegans |
Q35906149 | hch-1, a gene required for normal hatching and normal migration of a neuroblast in C. elegans, encodes a protein related to TOLLOID and BMP-1. |
Q37041104 | hunchback and Ikaros-like zinc finger genes control reproductive system development in Caenorhabditis elegans |
Q36749030 | ifet-1 is a broad-scale translational repressor required for normal P granule formation in C. elegans |
Q28539863 | ins-7 Gene expression is partially regulated by the DAF-16/IIS signaling pathway in Caenorhabditis elegans under celecoxib intervention |
Q28359738 | jkk-1 and mek-1 regulate body movement coordination and response to heavy metals through jnk-1 in Caenorhabditis elegans |
Q39757556 | lag-2 may encode a signaling ligand for the GLP-1 and LIN-12 receptors of C. elegans |
Q36358538 | large-scale screening for targeted knockouts in the Caenorhabditis elegans genome |
Q38445788 | let-65 is cytoplasmic methionyl tRNA synthetase in C. elegans |
Q47103765 | let-7 miRNA controls CED-7 homotypic adhesion and EFF-1-mediated axonal self-fusion to restore touch sensation following injury. |
Q34589802 | lin-8, which antagonizes Caenorhabditis elegans Ras-mediated vulval induction, encodes a novel nuclear protein that interacts with the LIN-35 Rb protein |
Q34606840 | lir-2, lir-1 and lin-26 encode a new class of zinc-finger proteins and are organized in two overlapping operons both in Caenorhabditis elegans and in Caenorhabditis briggsae |
Q94518377 | mRNA decapping is an evolutionarily conserved modulator of neuroendocrine signaling that controls development and ageing |
Q64934077 | mRNA profiling reveals significant transcriptional differences between a multipotent progenitor and its differentiated sister. |
Q33650318 | mab-31 and the TGF-beta pathway act in the ray lineage to pattern C. elegans male sensory rays |
Q37397473 | mec-15 encodes an F-box protein required for touch receptor neuron mechanosensation, synapse formation and development |
Q37661686 | miRNAs cooperate in apoptosis regulation during C. elegans development |
Q37379479 | microRNAs Involved in the Control of Innate Immunity in Candida Infected Caenorhabditis elegans |
Q27321558 | mir-233 modulates the unfolded protein response in C. elegans during Pseudomonas aeruginosa infection |
Q36000094 | mir-35 is involved in intestine cell G1/S transition and germ cell proliferation in C. elegans |
Q43720972 | mir-355 Functions as An Important Link between p38 MAPK Signaling and Insulin Signaling in the Regulation of Innate Immunity |
Q27334018 | n-butylidenephthalide protects against dopaminergic neuron degeneration and α-synuclein accumulation in Caenorhabditis elegans models of Parkinson's disease |
Q36255131 | ncl-1 is required for the regulation of cell size and ribosomal RNA synthesis in Caenorhabditis elegans |
Q83227749 | neurons have functional dendritic spines |
Q37161408 | nhl-2 Modulates microRNA activity in Caenorhabditis elegans |
Q36300854 | p21-activated kinase interacts with Wnt signaling to regulate tissue polarity and gene expression |
Q28619405 | p24 proteins and quality control of LIN-12 and GLP-1 trafficking in Caenorhabditis elegans |
Q27315174 | p38 MAPK regulates expression of immune response genes and contributes to longevity in C. elegans |
Q44750222 | pWormgatePro enables promoter-driven knockdown by hairpin RNA interference of muscle and neuronal gene products in Caenorhabditis elegans |
Q37460702 | par-1, atypical pkc, and PP2A/B55 sur-6 are implicated in the regulation of exocyst-mediated membrane trafficking in Caenorhabditis elegans |
Q35553959 | par-2, a gene required for blastomere asymmetry in Caenorhabditis elegans, encodes zinc-finger and ATP-binding motifs |
Q33959251 | par-4, a gene required for cytoplasmic localization and determination of specific cell types in Caenorhabditis elegans embryogenesis |
Q35204451 | pha-4, an HNF-3 homolog, specifies pharyngeal organ identity in Caenorhabditis elegans |
Q36298021 | piRNAs can trigger a multigenerational epigenetic memory in the germline of C. elegans |
Q36684944 | piRNAs initiate an epigenetic memory of nonself RNA in the C. elegans germline |
Q27341372 | pix-1 controls early elongation in parallel with mel-11 and let-502 in Caenorhabditis elegans |
Q47069280 | pop-1 Encodes an HMG box protein required for the specification of a mesoderm precursor in Early C. elegans embryos |
Q35988888 | pxn-1 and pxn-2 May Interact Negatively during Neuronal Development and Aging in C. elegans |
Q28512956 | sel-10, a negative regulator of lin-12 activity in Caenorhabditis elegans, encodes a member of the CDC4 family of proteins |
Q33620956 | skn-1 is required for interneuron sensory integration and foraging behavior in Caenorhabditis elegans |
Q35176036 | sli-3 negatively regulates the LET-23/epidermal growth factor receptor-mediated vulval induction pathway in Caenorhabditis elegans |
Q36574846 | smg mutants affect the expression of alternatively spliced SR protein mRNAs in Caenorhabditis elegans |
Q34606258 | smg-7 is required for mRNA surveillance in Caenorhabditis elegans. |
Q24323124 | soc-2 encodes a leucine-rich repeat protein implicated in fibroblast growth factor receptor signaling |
Q24545800 | spe-10 encodes a DHHC-CRD zinc-finger membrane protein required for endoplasmic reticulum/Golgi membrane morphogenesis during Caenorhabditis elegans spermatogenesis |
Q34606827 | spe-12 encodes a sperm cell surface protein that promotes spermiogenesis in Caenorhabditis elegans |
Q34611179 | spe-29 encodes a small predicted membrane protein required for the initiation of sperm activation in Caenorhabditis elegans |
Q52687070 | spe-43 is required for sperm activation in C. elegans. |
Q35848041 | spr-2, a suppressor of the egg-laying defect caused by loss of sel-12 presenilin in Caenorhabditis elegans, is a member of the SET protein subfamily |
Q34941722 | sqv mutants of Caenorhabditis elegans are defective in vulval epithelial invagination |
Q44610934 | sup-9, sup-10, and unc-93 may encode components of a two-pore K+ channel that coordinates muscle contraction in Caenorhabditis elegans. |
Q34592502 | synMuv B proteins antagonize germline fate in the intestine and ensure C. elegans survival |
Q36480389 | toca-1 is in a novel pathway that functions in parallel with a SUN-KASH nuclear envelope bridge to move nuclei in Caenorhabditis elegans |
Q24551644 | trans splicing of polycistronic Caenorhabditis elegans pre-mRNAs: analysis of the SL2 RNA |
Q89747950 | trans-Fatty acids facilitate DNA damage-induced apoptosis through the mitochondrial JNK-Sab-ROS positive feedback loop |
Q27322661 | ttm-1 encodes CDF transporters that excrete zinc from intestinal cells of C. elegans and act in a parallel negative feedback circuit that promotes homeostasis |
Q36990693 | unc-3-dependent repression of specific motor neuron fates in Caenorhabditis elegans |
Q36969594 | unc-44 Ankyrin and stn-2 gamma-syntrophin regulate sax-7 L1CAM function in maintaining neuronal positioning in Caenorhabditis elegans |
Q36328696 | unc-94 encodes a tropomodulin in Caenorhabditis elegans |
Q34610168 | xnd-1 regulates the global recombination landscape in Caenorhabditis elegans. |
Q35072948 | α Integrin cytoplasmic tails have tissue-specific roles during C. elegans development |
Q36231028 | α-actinin is required for the proper assembly of Z-disk/focal-adhesion-like structures and for efficient locomotion in Caenorhabditis elegans |
Q36263751 | β-Integrin de-phosphorylation by the Density-Enhanced Phosphatase DEP-1 attenuates EGFR signaling in C. elegans. |
Q38932129 | β-Phenylethylamine requires the dopamine transporter to increase extracellular dopamine in Caenorhabditis elegans dopaminergic neurons. |
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