scholarly article | Q13442814 |
P356 | DOI | 10.1016/0012-1606(83)90201-4 |
P8608 | Fatcat ID | release_5ojun5we6bawtm67cff6vugv7i |
P3181 | OpenCitations bibliographic resource ID | 458444 |
P698 | PubMed publication ID | 6684600 |
P2093 | author name string | J G White | |
J E Sulston | |||
J N Thomson | |||
E Schierenberg | |||
P433 | issue | 1 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | tail spike morphogenesis | Q22298821 |
Caenorhabditis elegans | Q91703 | ||
P1104 | number of pages | 56 | |
P304 | page(s) | 64-119 | |
P577 | publication date | 1983-11-01 | |
P1433 | published in | Developmental Biology | Q3025402 |
P1476 | title | The embryonic cell lineage of the nematode Caenorhabditis elegans | |
P478 | volume | 100 |
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Q34610776 | Calcium/calmodulin-dependent protein kinase II regulates Caenorhabditis elegans locomotion in concert with a G(o)/G(q) signaling network. |
Q34445959 | Caloric restriction and lifespan: a role for protein turnover? |
Q33903791 | Cancer models in Caenorhabditis elegans |
Q47069436 | Candidate adaptor protein CED-6 promotes the engulfment of apoptotic cells in C. elegans. |
Q38125960 | Canonical RTK-Ras-ERK signaling and related alternative pathways |
Q58757966 | Caspase Is Required for Asymmetric Divisions That Generate Cells Programmed To Die |
Q34384760 | Caspase-mediated activation of Caenorhabditis elegans CED-8 promotes apoptosis and phosphatidylserine externalization |
Q37302731 | Caspases in apoptosis and beyond |
Q92554661 | Caudal-dependent cell positioning directs morphogenesis of the C. elegans ventral epidermis |
Q35184459 | Cdk1 phosphorylates SPAT-1/Bora to trigger PLK-1 activation and drive mitotic entry in C. elegans embryos |
Q35756670 | Ce-emerin and LEM-2: essential roles in Caenorhabditis elegans development, muscle function, and mitosis |
Q36152597 | CeNDR, the Caenorhabditis elegans natural diversity resource |
Q39042190 | Cell Biology of the Caenorhabditis elegans Nucleus |
Q90622887 | Cell Biology of the Tardigrades: Current Knowledge and Perspectives |
Q37550296 | Cell Death in C. elegans Development |
Q36525471 | Cell Fate Decision Making through Oriented Cell Division |
Q92085462 | Cell Non-autonomous Function of daf-18/PTEN in the Somatic Gonad Coordinates Somatic Gonad and Germline Development in C. elegans Dauer Larvae |
Q28184418 | Cell Polarity and the Cytoskeleton in theCaenorhabditis ElegansZygote |
Q57980365 | Cell Polarity in One-Cell C. elegans Embryos: Ensuring an Accurate and Precise Spatial Axis During Development |
Q34003205 | Cell architecture: surrounding muscle cells shape gland cell morphology in the Caenorhabditis elegans pharynx |
Q36235652 | Cell contacts orient some cell division axes in the Caenorhabditis elegans embryo |
Q41556728 | Cell cycle arrest of proliferating neuronal cells by serum deprivation can result in either apoptosis or differentiation. |
Q38554864 | Cell cycle timing regulation during asynchronous divisions of the early C. elegans embryo |
Q35179382 | Cell cycle: check for asynchrony |
Q34511145 | Cell death and sexual differentiation of behavior: worms, flies, and mammals. |
Q38350731 | Cell death in development: Signaling pathways and core mechanisms |
Q24644733 | Cell death specification in C. elegans |
Q40872590 | Cell death/apoptosis: normal, chemically induced, and teratogenic effect |
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 |
Q40430871 | Cell fate decisions in the early embryo of the nematode Caenorhabditis elegans. |
Q41065675 | Cell fate specification and differentiation in the nervous system of Caenorhabditis elegans |
Q28271574 | Cell fate specification in the C. elegans embryo |
Q39977879 | Cell identification and cell lineage analysis |
Q27320530 | Cell interactions and patterned intercalations shape and link epithelial tubes in C. elegans |
Q42155894 | Cell interactions coordinate the development of the C. elegans egg-laying system |
Q35998167 | Cell intercalation from top to bottom |
Q39700277 | Cell lineage analysis in mammalian embryogenesis |
Q37820053 | Cell lineage and cell death: Caenorhabditis elegans and cancer research |
Q68989090 | Cell lineage in development |
Q97557528 | Cell lineage-dependent chiral actomyosin flows drive cellular rearrangements in early C. elegans development |
Q71731120 | Cell mixing during early epiboly in the zebrafish embryo |
Q34754380 | Cell nonautonomy of C. elegans daf-2 function in the regulation of diapause and life span |
Q34632447 | Cell plasticity in Caenorhabditis elegans: from induced to natural cell reprogramming. |
Q33712553 | Cell polarity in the early Caenorhabditis elegans embryo |
Q41585919 | Cell polarity: par for the polar course |
Q34488124 | Cell proliferation and growth in C. elegans |
Q53113184 | Cell proliferation patterns in early zebrafish development. |
Q28548446 | Cell-Autonomous Gβ Signaling Defines Neuron-Specific Steady State Serotonin Synthesis in Caenorhabditis elegans |
Q36774754 | Cell-cell fusion |
Q68262743 | Cell-cell interactions in the guidance of late-developing neurons in Caenorhabditis elegans |
Q72531737 | Cell-cell interactions. Receiving signals in the nematode embryo |
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 |
Q37211993 | Cell-nonautonomous inhibition of radiation-induced apoptosis by dynein light chain 1 in Caenorhabditis elegans |
Q39745837 | Cell-specific gene expression in the nematode |
Q36570593 | Cell-specific microarray profiling experiments reveal a comprehensive picture of gene expression in the C. elegans nervous system |
Q27310046 | Cell-to-cell heterogeneity in cortical tension specifies curvature of contact surfaces in Caenorhabditis elegans embryos |
Q46707781 | Cell-type specific regulation of serotonergic identity by the C. elegans LIM-homeodomain factor LIM-4. |
Q35864744 | Cell-type-specific nuclei purification from whole animals for genome-wide expression and chromatin profiling. |
Q35001866 | Cellular analyses of the mitotic region in the Caenorhabditis elegans adult germ line |
Q89559683 | Cellular development of a nematode: 3-D computer reconstruction of living embryos |
Q33319913 | Cellular pattern formation, establishment of polarity and segregation of colored cytoplasm in embryos of the nematode Romanomermis culicivorax |
Q37412642 | Cellular symmetry breaking during Caenorhabditis elegans development |
Q33567057 | Centriolar remodeling underlies basal body maturation during ciliogenesis in Caenorhabditis elegans |
Q42512894 | Centriole translocation and degeneration during ciliogenesis in Caenorhabditis elegans neurons. |
Q33769568 | Centrioles initiate cilia assembly but are dispensable for maturation and maintenance in C. elegans. |
Q36147639 | Centrosome movement in the early divisions of Caenorhabditis elegans: a cortical site determining centrosome position |
Q40443426 | Chapter 14 Methods for the Study of Cell Death in the Nematode Caenorhabditis elegans |
Q61953427 | Chapter 3.3.5 Caenorhabditis elegans and the genetics of learning |
Q43852175 | Characterization of RSF-1, the Caenorhabditis elegans homolog of the Ras-association domain family protein 1. |
Q47069562 | Characterization of a novel gene expressed in neuromuscular tissues and centrosomes in Caenorhabditis elegans. |
Q40292806 | Characterization of a novel protein kinase D: Caenorhabditis elegans DKF-1 is activated by translocation-phosphorylation and regulates movement and growth in vivo |
Q36235730 | Characterization of beta pat-3 heterodimers, a family of essential integrin receptors in C. elegans |
Q46874149 | Characterization of loss-of-function and gain-of-function Eph receptor tyrosine kinase signaling in C. elegans axon targeting and cell migration |
Q47069267 | Characterization of the C. elegans gap-2 gene encoding a novel Ras-GTPase activating protein and its possible role in larval development |
Q37366639 | Characterization of the effects of methylmercury on Caenorhabditis elegans |
Q33538327 | Characterization of the octamer, a cis-regulatory element that modulates excretory cell gene-expression in Caenorhabditis elegans |
Q37866234 | Chemistry and the worm: Caenorhabditis elegans as a platform for integrating chemical and biological research |
Q47069555 | Chemosensory neurons function in parallel to mediate a pheromone response in C. elegans |
Q33239290 | Chemosensory neurons with overlapping functions direct chemotaxis to multiple chemicals in C. elegans |
Q42411795 | Chiral forces organize left-right patterning in C. elegans by uncoupling midline and anteroposterior axis |
Q45943868 | Chromatin accessibility dynamics reveal novel functional enhancers in C. elegans. |
Q52249900 | Chromatin diminution and early cleavage in Parascaris univalens (Nematoda). |
Q33855919 | Chromatin silencing and the maintenance of a functional germline in Caenorhabditis elegans |
Q55433216 | Chromosomal barcoding as a tool for multiplexed phenotypic characterization of laboratory evolved lineages. |
Q36480375 | Chromosomal clustering and GATA transcriptional regulation of intestine-expressed genes in C. elegans |
Q34698580 | Ciliopathy proteins establish a bipartite signaling compartment in a C. elegans thermosensory neuron |
Q39752816 | Cis-regulatory mechanisms of left/right asymmetric neuron-subtype specification in C. elegans |
Q44323322 | Cleavage pattern, gastrulation, and neurulation in the appendicularian, Oikopleura dioica |
Q52247906 | Clonal origins of cells in the pigmented retina of the zebrafish eye. |
Q41768044 | Clusters of identical new mutations can account for the "overdispersed" molecular clock. |
Q89431281 | Cnidarians layer up |
Q37095287 | Co-expression of Foxa.a, Foxd and Fgf9/16/20 defines a transient mesendoderm regulatory state in ascidian embryos |
Q58648625 | Coelomocytes: Biology and Possible Immune Functions in Invertebrates with Special Remarks on Nematodes |
Q38485000 | Collaborative regulation of development but independent control of metabolism by two epidermis-specific transcription factors in Caenorhabditis elegans |
Q90391698 | Combinatorial Contact Cues Specify Cell Division Orientation by Directing Cortical Myosin Flows |
Q38750070 | Combinatorial decoding of the invariant C. elegans embryonic lineage in space and time |
Q35129174 | Comparative RNA-Seq analysis reveals pervasive tissue-specific alternative polyadenylation in Caenorhabditis elegans intestine and muscles |
Q42778223 | Comparative Transcriptomics of Steinernema and Caenorhabditis Single Embryos Reveals Orthologous Gene Expression Convergence during Late Embryogenesis |
Q30488223 | Comparative analysis of embryonic cell lineage between Caenorhabditis briggsae and Caenorhabditis elegans |
Q52109044 | Comparative and experimental embryogenesis of Plectidae (Nematoda). |
Q38703734 | Comparative genetic, proteomic and phosphoproteomic analysis of C. elegans embryos with a focus on ham-1/STOX and pig-1/MELK in dopaminergic neuron development. |
Q36083006 | Comparative genomics of Steinernema reveals deeply conserved gene regulatory networks |
Q41152938 | Comparative genomics of the tardigrades Hypsibius dujardini and Ramazzottius varieornatus. |
Q27324018 | Comparing algorithms that reconstruct cell lineage trees utilizing information on microsatellite mutations |
Q50530775 | Compensatory embryonic response to allele-specific inactivation of the murine X-linked gene Hcfc1. |
Q30542170 | Completion of cytokinesis in C. elegans requires a brefeldin A-sensitive membrane accumulation at the cleavage furrow apex |
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 |
Q47135374 | Comprehensive functional genomics using Caenorhabditis elegans as a model organism |
Q48695478 | Comprehensive single cell-resolution analysis of the role of chromatin regulators in early C. elegans embryogenesis. |
Q38619221 | Comprehensive single-cell transcriptional profiling of a multicellular organism. |
Q47143344 | Connectomics, the Final Frontier |
Q41058884 | Conservation of anatomically restricted glycosaminoglycan structures in divergent nematode species |
Q24312091 | Conservation of the centromere/kinetochore protein ZW10 |
Q46466764 | Conserved Ankyrin Repeat Proteins and Their NIMA Kinase Partners Regulate Extracellular Matrix Remodeling and Intracellular Trafficking in Caenorhabditis elegans |
Q38674857 | Conserved gene regulatory module specifies lateral neural borders across bilaterians. |
Q33760559 | Conserved genes act as modifiers of invertebrate SMN loss of function defects |
Q27316391 | Contrasting responses within a single neuron class enable sex-specific attraction in Caenorhabditis elegans |
Q30975928 | Contribution of neurons to habituation to mechanical stimulation in Caenorhabditis elegans |
Q45960530 | Control of alternative behavioral states by serotonin in Caenorhabditis elegans. |
Q27333582 | Control of apoptosis by asymmetric cell division |
Q36742440 | Control of cell cycle timing during C. elegans embryogenesis |
Q48110372 | Control of cell fates in the central body region of C. elegans by the homeobox gene lin-39. |
Q33744987 | Control of cell migration during Caenorhabditis elegans development |
Q33964428 | Control of cleavage spindle orientation in Caenorhabditis elegans: the role of the genes par-2 and par-3. |
Q28215106 | Control of developmental timing in animals |
Q70121859 | Control of larval development by chemosensory neurons in Caenorhabditis elegans |
Q74243892 | Control of neural development and function in a thermoregulatory network by the LIM homeobox gene lin-11 |
Q34874075 | Control of neuronal subtype identity by the C. elegans ARID protein CFI-1. |
Q36151090 | Control of sex-specific apoptosis in C. elegans by the BarH homeodomain protein CEH-30 and the transcriptional repressor UNC-37/Groucho |
Q50769000 | Convergent genetic programs regulate similarities and differences between related motor neuron classes in Caenorhabditis elegans. |
Q39729704 | Coordinates, DNA content and heterogeneity of cell nuclei and segments of the Caenorhabditis elegans intestine |
Q27319972 | Coordination of cell proliferation and cell fate determination by CES-1 snail |
Q93086449 | Core Concept: Cells nibble one another via the under-appreciated process of trogocytosis |
Q46194826 | Correct Hox gene expression established independently of position in Caenorhabditis elegans |
Q28270015 | Cortical and cytoplasmic flow polarity in early embryonic cells of Caenorhabditis elegans |
Q36000713 | Coupling between cytoplasmic concentration gradients through local control of protein mobility in the Caenorhabditis elegans zygote |
Q42556969 | Culture and manipulation of embryonic cells |
Q36095552 | Culture conditions for bovine embryonic stem cell-like cells isolated from blastocysts after external fertilization |
Q77646485 | Cuticle chirality and body handedness in Caenorhabditis elegans |
Q41715971 | Cyclin B3 and dynein heavy chain cooperate to increase fitness in the absence of mdf-1/MAD1 in Caenorhabditis elegans |
Q47864345 | Cyclin D involvement demarcates a late transition in C. elegans embryogenesis |
Q34806301 | Cyclin D regulation of a sexually dimorphic asymmetric cell division |
Q47068705 | Cyclin E expression during development in Caenorhabditis elegans |
Q36567048 | Cyclin-dependent kinase inhibitors in yeast, animals, and plants: a functional comparison |
Q36499304 | Cyclin-dependent kinases in C. elegans |
Q30442050 | Cytoplasmic dynein is required for distinct aspects of MTOC positioning, including centrosome separation, in the one cell stage Caenorhabditis elegans embryo |
Q33948186 | Cytoplasmic dynein light intermediate chain is required for discrete aspects of mitosis in Caenorhabditis elegans |
Q38375486 | Cytoplasmic localization and asymmetric division in the early embryo of Caenorhabditis elegans |
Q30487217 | DEX-1 and DYF-7 establish sensory dendrite length by anchoring dendritic tips during cell migration |
Q33948509 | DLG-1 is a MAGUK similar to SAP97 and is required for adherens junction formation |
Q34525913 | DNA double-strand break repair in Caenorhabditis elegans |
Q38290939 | DPY-30, a nuclear protein essential early in embryogenesis for Caenorhabditis elegans dosage compensation |
Q45270370 | DRP-1-mediated mitochondrial fragmentation during EGL-1-induced cell death in C. elegans |
Q30576952 | De novo inference of systems-level mechanistic models of development from live-imaging-based phenotype analysis. |
Q37611164 | Deceptively simple but simply deceptive--Caenorhabditis elegans lifespan studies: considerations for aging and antioxidant effects |
Q34783303 | Deconvolution of gene expression from cell populations across the C. elegans lineage |
Q52559040 | Deep Reinforcement Learning of Cell Movement in the Early Stage of C. elegans Embryogenesis. |
Q83225462 | Deep sampling of Hawaiian reveals high genetic diversity and admixture with global populations |
Q73672839 | Deficiency screen based on the monoclonal antibody MH27 to identify genetic loci required for morphogenesis of the Caenorhabditis elegans embryo |
Q35221163 | Defining the transcriptional redundancy of early bodywall muscle development in C. elegans: evidence for a unified theory of animal muscle development |
Q47069352 | Deletion of the Caenorhabditis elegans homologues of the CLN3 gene, involved in human juvenile neuronal ceroid lipofuscinosis, causes a mild progeric phenotype. |
Q42728547 | Dendritic tree extraction from noisy maximum intensity projection images in C. elegans |
Q27321332 | Depletion of the C. elegans NAC engages the unfolded protein response, resulting in increased chaperone expression and apoptosis |
Q110669023 | Description of a new and two known species of the insect–associated genus Oigolaimella Paramonov, 1952 (Nematoda: Diplogastridae) with a note on the biology, biogeography and relationship with congeners |
Q42075632 | Detecting apoptotic cells and monitoring their clearance in the nematode 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 |
Q24644275 | Determination of cell fate selection during phage lambda infection |
Q27314802 | Determinative developmental cell lineages are robust to cell deaths |
Q102059106 | Determining the effector response to cell death |
Q70993637 | Developing Caenorhabditis elegans neurons may contain both cell-death protective and killer activities |
Q81187791 | Development and validation of computational models of cellular interaction |
Q36075874 | Development of Caenorhabditis elegans pharynx, with emphasis on its nervous system. |
Q46916834 | Development of an intestinal cell culture model to obtain smooth muscle cells and myenteric neurones. |
Q38186647 | Development of left/right asymmetry in the Caenorhabditis elegans nervous system: from zygote to postmitotic neuron |
Q42074002 | Development of the enteric nervous system in the moth. I. Diversity of cell types and the embryonic expression of FMRFamide-related neuropeptides |
Q42074000 | Development of the enteric nervous system in the moth. II. Stereotyped cell migration precedes the differentiation of embryonic neurons |
Q64067931 | Developmental Control of the Cell Cycle: Insights from Caenorhabditis elegans |
Q35512401 | Developmental alterations of the C. elegans male anal depressor morphology and function require sex-specific cell autonomous and cell non-autonomous interactions |
Q35318010 | Developmental and abnormal cell death in C. elegans |
Q36403386 | Developmental apoptosis in C. elegans: a complex CEDnario |
Q33417276 | Developmental biology and databases: how to archive, find and query gene expression patterns using the world wide web. |
Q52232113 | Developmental biology. Lighting up Drosophila |
Q52191683 | Developmental biology. The worm keeps turning. |
Q38003249 | Developmental decisions: balancing genetics and the environment by C. elegans |
Q41848655 | Developmental effect of polyamine depletion in Caenorhabditis elegans |
Q41278623 | Developmental expression pattern screen for genes predicted in the C. elegans genome sequencing project |
Q36236600 | Developmental genetic analysis of troponin T mutations in striated and nonstriated muscle cells of Caenorhabditis elegans |
Q48930860 | Developmental genetics of Caenorhabditis elegans sex determination. |
Q33327418 | Developmental genetics of the C. elegans pharyngeal neurons NSML and NSMR. |
Q38254969 | Developmental genetics of the Caenorhabditis elegans pharynx |
Q47069285 | Developmental patterning in the Caenorhabditis elegans hindgut |
Q38588717 | Developmental robustness in the Caenorhabditis elegans embryo |
Q92375631 | Developmental trajectory of Caenorhabditis elegans nervous system governs its structural organization |
Q43963465 | Developmental transition to bilaterally symmetric cell divisions is regulated by Pax-mediated transcription in embryos of the leech Helobdella austinensis. |
Q37457271 | Developmentally programmed germ cell remodelling by endodermal cell cannibalism |
Q45375950 | Diet-dependent depletion of queuosine in tRNAs in Caenorhabditis elegans does not lead to a developmental block |
Q49080737 | Different roads to form the same gut in nematodes. |
Q37532849 | Differential expression of conserved germ line markers and delayed segregation of male and female primordial germ cells in a hermaphrodite, the leech helobdella |
Q34926423 | Differential requirement for the nonhelical tailpiece and the C terminus of the myosin rod in Caenorhabditis elegans muscle |
Q52256898 | Differentiated parental DNA strands confer developmental asymmetry on daughter cells in fission yeast. |
Q92885924 | Digging deeper: methodologies for high-content phenotyping in Caenorhabditis elegans |
Q36434656 | Digital development: a database of cell lineage differentiation in C. elegans with lineage phenotypes, cell-specific gene functions and a multiscale model |
Q35208636 | Direct cell lineage analysis in Drosophila melanogaster by time-lapse, three-dimensional optical microscopy of living embryos |
Q38117122 | Direct cellular reprogramming in Caenorhabditis elegans: facts, models, and promises for regenerative medicine |
Q58775874 | Direct visualization of a native Wnt in vivo reveals that a long-range Wnt gradient forms by extracellular dispersal |
Q35718550 | Direct visualization of the elt-2 gut-specific GATA factor binding to a target promoter inside the living Caenorhabditis elegans embryo |
Q57468222 | Disassembly of dying cells in diverse organisms |
Q38906169 | Discovering sparse transcription factor codes for cell states and state transitions during development |
Q64055984 | Disruption of mitochondrial dynamics affects behaviour and lifespan in Caenorhabditis elegans |
Q35065169 | Disruption of the ATP-binding cassette B7 (ABTM-1/ABCB7) induces oxidative stress and premature cell death in Caenorhabditis elegans |
Q31150980 | Dissecting Drosophila embryonic brain development using photoactivated gene expression |
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 |
Q33915482 | Distinct Caenorhabditis elegans HLH-8/twist-containing dimers function in the mesoderm |
Q35091279 | Distinct DNA binding sites contribute to the TCF transcriptional switch in C. elegans and Drosophila. |
Q30479612 | Distinct IFT mechanisms contribute to the generation of ciliary structural diversity in C. elegans |
Q54200063 | Distinct chromatin organization in the germ line founder cell of the Caenorhabditis elegans embryo. |
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 |
Q33969923 | Distinct requirements for somatic and germline expression of a generally expressed Caernorhabditis elegans gene |
Q47069293 | Distinct signaling pathways mediate touch and osmosensory responses in a polymodal sensory neuron. |
Q97597495 | Diversity of activator of G-Protein signaling (AGS)-family proteins and their impact on asymmetric cell division across taxa |
Q30476321 | Dopamine modulates the plasticity of mechanosensory responses in Caenorhabditis elegans. |
Q57139337 | Dramatic evolution of body length due to postembryonic changes in cell size in a newly discovered close relative of |
Q36689628 | Duels without obvious sense: counteracting inductions involved in body wall muscle development in the Caenorhabditis elegans embryo |
Q42360363 | Durotaxis in Nematode Caenorhabditis elegans |
Q38424104 | Dynamic and persistent effects of ethanol exposure on development: an in vivo analysis during and after embryonic ethanol exposure in Caenorhabditis elegans |
Q37867601 | Dynamic lineage analysis of embryonic morphogenesis using transgenic quail and 4D multispectral imaging |
Q30597949 | Dynamically-expressed prion-like proteins form a cuticle in the pharynx of Caenorhabditis elegans |
Q52183446 | Dynamics and ultrastructure of developmental cell fusions in the Caenorhabditis elegans hypodermis. |
Q33552348 | Dynamics of Delta/Notch signaling on endomesoderm segregation in the sea urchin embryo |
Q59129034 | Dynein links engulfment and execution of apoptosis via CED-4/Apaf1 in C. elegans |
Q27302969 | E3 ubiquitin ligases promote progression of differentiation during C. elegans embryogenesis |
Q42579625 | EAT-4, a homolog of a mammalian sodium-dependent inorganic phosphate cotransporter, is necessary for glutamatergic neurotransmission in caenorhabditis elegans |
Q36431850 | EGF homologous sequences encoded in the genome of Drosophila melanogaster, and their relation to neurogenic genes |
Q27322765 | EGL-13/SoxD specifies distinct O2 and CO2 sensory neuron fates in Caenorhabditis elegans |
Q33396126 | ELT-2 is the predominant transcription factor controlling differentiation and function of the C. elegans intestine, from embryo to adult. |
Q44301511 | EXT gene family member rib-2 is essential for embryonic development and heparan sulfate biosynthesis in Caenorhabditis elegans |
Q36001742 | Early Embryogenesis and Anterior-Posterior Axis Formation in the White-Tip Nematode Aphelenchoides besseyi (Nematoda: Aphelenchoididae). |
Q37068237 | Early determinative events in Caenorhabditis elegans |
Q27318527 | Early development of the root-knot nematode Meloidogyne incognita. |
Q40519531 | Early embryogenesis of the pinewood nematode Bursaphelenchus xylophilus |
Q40914938 | Early events in higher-plant embryogenesis |
Q35895941 | Early neural cell death: dying to become neurons |
Q34609004 | Effect of a neuropeptide gene on behavioral states in Caenorhabditis elegans egg-laying |
Q35381658 | Effect of temperature pre-exposure on the locomotion and chemotaxis of C. elegans |
Q38438551 | Effects of developmental exposure to ethanol on Caenorhabditis elegans |
Q56872976 | Efficient proximity labeling in living cells and organisms with TurboID |
Q31127143 | Efficient single-cell transgene induction in Caenorhabditis elegans using a pulsed infrared laser |
Q49808079 | Electrophysiological measures of aging pharynx function in C. elegans reveal enhanced organ functionality in older, long-lived mutants. |
Q35605140 | Elimination of paternal mitochondria through the lysosomal degradation pathway in C. elegans |
Q91378063 | Embryo timelapses can be compiled and quantified to understand canonical histone dynamics across multiple cell cycles |
Q36311980 | Embryogenesis in C. elegans after elimination of individual blastomeres or induced alteration of the cell division order |
Q36246634 | Embryogenesis in the parasitic nematode Heterodera glycines is independent of host-derived hatching stimulation |
Q34986576 | Embryogenesis of Romanomermis culicivorax: an alternative way to construct a nematode |
Q37052906 | Embryonic Methamphetamine Exposure Inhibits Methamphetamine Cue Conditioning and Reduces Dopamine Concentrations in Adult N2 Caenorhabditis elegans |
Q47867924 | Embryonic cell lineage of the marine nematode Pellioditis marina |
Q34038380 | Embryonic polarity: protein stability in asymmetric cell division |
Q37697410 | Embryonic tissue differentiation in Caenorhabditis elegans requires dif-1, a gene homologous to mitochondrial solute carriers |
Q37505114 | Enabling the Triplet of Tetraphenylethene to Sensitize the Excited State of Europium(III) for Protein Detection and Time-Resolved Luminescence Imaging |
Q38060994 | Encoding asymmetry within neural circuits. |
Q35125443 | Endoderm development in Caenorhabditis elegans: the synergistic action of ELT-2 and -7 mediates the specification→differentiation transition |
Q51221666 | Engineered non-Mendelian inheritance of entire parental genomes in C. elegans. |
Q57939426 | Engulfment genes cooperate with ced-3 to promote cell death in Caenorhabditis elegans |
Q36379455 | Engulfment pathways promote programmed cell death by enhancing the unequal segregation of apoptotic potential |
Q31020226 | Enzymes involved in the biogenesis of the nematode cuticle |
Q26827462 | Eph receptor signaling in C. elegans |
Q36788759 | Eric Davidson: Steps to a gene regulatory network for development |
Q46345898 | Essential embryonic roles of the CKI-1 cyclin-dependent kinase inhibitor in cell-cycle exit and morphogenesis in C elegans. |
Q52641927 | Establishment of Signaling Interactions with Cellular Resolution for Every Cell Cycle of Embryogenesis. |
Q104111142 | Establishment of a morphological atlas of the Caenorhabditis elegans embryo using deep-learning-based 4D segmentation |
Q52205753 | Establishment of left-right asymmetry in the Caenorhabditis elegans embryo: a multistep process involving a series of inductive events |
Q21145377 | Estimating cell depth from somatic mutations |
Q34902504 | Ethanol-induced differential gene expression and acetyl-CoA metabolism in a longevity model of the nematode Caenorhabditis elegans |
Q49168982 | Evaluation of fixation methods for ultrastructural study of Caenorhabditis elegans embryos. |
Q36622852 | Evidence for compensatory upregulation of expressed X-linked genes in mammals, Caenorhabditis elegans and Drosophila melanogaster |
Q47997795 | Evidence for crucial role of hindgut expansion in directing proper migration of primordial germ cells in mouse early embryogenesis |
Q52232706 | Evidence from mosaic analysis of the masculinizing gene her-1 for cell interactions in C. elegans sex determination. |
Q34614025 | Evidence from reversal of handedness in C. elegans embryos for early cell interactions determining cell fates |
Q70140819 | Evidence in a nematode for regulation of transposon excision by tissue-specific factors |
Q38003840 | Evo-devo of the germline and somatic gonad in nematodes. |
Q91650607 | Evolution and Developmental System Drift in the Endoderm Gene Regulatory Network of Caenorhabditis and Other Nematodes |
Q41601027 | Evolution of cell lineage |
Q35013179 | Evolution of development in closely related species of flies and worms |
Q38727266 | Evolution of embryonic development in nematodes |
Q38416508 | Evolution of germline segregation processes in animal development |
Q33964038 | Evolution of nematode development |
Q45984175 | Evolution of neuronal patterning in free-living rhabditid nematodes I: Sex-specific serotonin-containing neurons. |
Q57165476 | Evolution of the bilaterian mouth and anus |
Q33633041 | Evolutionary change in the functional specificity of genes |
Q41126145 | Evolutionary conservation of a genetic pathway of programmed cell death |
Q36106695 | Expanding the genetic code of Caenorhabditis elegans using bacterial aminoacyl-tRNA synthetase/tRNA pairs |
Q35880465 | Experience Modulates the Reproductive Response to Heat Stress in C. elegans via Multiple Physiological Processes |
Q35115901 | Expression of ram-5 in the structural cell is required for sensory ray morphogenesis in Caenorhabditis elegans male tail |
Q58493889 | Expression of the UNC-5 guidance receptor in the touch neurons of C. elegans steers their axons dorsally |
Q67487964 | Expression of the polyubiquitin-encoding gene (ubq-1) in transgenic Caenorhabditis elegans |
Q71794026 | Expression patterns of predicted genes from the C. elegans genome sequence visualized by FISH in whole organisms |
Q36654524 | Extending from PARs in Caenorhabditis elegans to homologues in Haemonchus contortus and other parasitic nematodes. |
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 |
Q35741923 | Extracellular leucine-rich repeat proteins are required to organize the apical extracellular matrix and maintain epithelial junction integrity in C. elegans |
Q22010738 | F1Aalpha, a death receptor-binding protein homologous to the Caenorhabditis elegans sex-determining protein, FEM-1, is a caspase substrate that mediates apoptosis |
Q35400294 | FBN-1, a fibrillin-related protein, is required for resistance of the epidermis to mechanical deformation during C. elegans embryogenesis |
Q42363573 | Facilitation of Endosomal Recycling by an IRG Protein Homolog Maintains Apical Tubule Structure in Caenorhabditis elegans |
Q33772658 | Fate maps old and new. |
Q33689786 | Fate specification and tissue-specific cell cycle control of the Caenorhabditis elegans intestine |
Q35787386 | Ferreting out stem cells from their niches |
Q35079239 | Fine mapping of Rcr1 and analyses of its effect on transcriptome patterns during infection by Plasmodiophora brassicae |
Q37225630 | Fishing lines, time-delayed guideposts, and other tricks used by developing pharyngeal neurons in Caenorhabditis elegans |
Q36216689 | Fluorescence visualization of the distribution of microfilaments in gonads and early embryos of the nematode Caenorhabditis elegans |
Q58213310 | Fluorescent Nanodiamond – A Novel Nanomaterial for In Vivo Applications |
Q67713645 | Fluorescent dextran clonal markers |
Q34587786 | Fluoxetine-resistance genes in Caenorhabditis elegans function in the intestine and may act in drug transport |
Q97681463 | Following the fate of cells in vivo |
Q50782405 | Food Search Strategy Changes in Caenorhabditis elegans under Chronic Starvation Conditions. |
Q48823976 | Food responsiveness regulates episodic behavioral states in Caenorhabditis elegans. |
Q30974711 | Form of the worm: genetics of epidermal morphogenesis in C. elegans |
Q57055355 | From "the Worm" to "the Worms" and Back Again: The Evolutionary Developmental Biology of Nematodes |
Q47356373 | From Reductionism to Holism: Toward a More Complete View of Development Through Genome Engineering. |
Q35094105 | From genes to integrative physiology: ion channel and transporter biology in Caenorhabditis elegans |
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 |
Q36677147 | Functional Interplay of Two Paralogs Encoding SWI/SNF Chromatin-Remodeling Accessory Subunits During Caenorhabditis elegans Development |
Q39112060 | Functional analysis of leucine aminopeptidase in Caenorhabditis elegans |
Q44677506 | Functional analysis of the domains of the C elegans Ror receptor tyrosine kinase CAM-1. |
Q27312406 | Functional dissection of Caenorhabditis elegans CLK-2/TEL2 cell cycle defects during embryogenesis and germline development |
Q48262345 | Functional elements and domains inferred from sequence comparisons of a heat shock gene in two nematodes |
Q47068768 | Functional genomic analysis of apoptotic DNA degradation in C. elegans. |
Q31385984 | Functional genomics |
Q92187401 | Funerals and Feasts: The Immunological Rites of Cell Death |
Q33924982 | Fusomorphogenesis: cell fusion in organ formation |
Q60948018 | G Proteins and GPCRs in C. elegans Development: A Story of Mutual Infidelity |
Q47069506 | G alphas-induced neurodegeneration in Caenorhabditis elegans. |
Q38353856 | G proteins are required for spatial orientation of early cell cleavages in C. elegans embryos. |
Q33938676 | GLIA: listening and talking to the synapse |
Q90395620 | Game of Tissues: How the Epidermis Thrones C. elegans Shape |
Q46710963 | Gametic selection, developmental trajectories, and extrinsic heterogeneity in Haldane's rule |
Q98180485 | Gap junctions deliver malonyl-CoA from soma to germline to support embryogenesis 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 |
Q90024169 | Gene Cascade Finder: A tool for identification of gene cascades and its application in Caenorhabditis elegans |
Q90006461 | Gene silencing by double-stranded RNA from C. elegans neurons reveals functional mosaicism of RNA interference |
Q37080795 | Gene transcription is coordinated with, but not dependent on, cell divisions during C. elegans embryonic fate specification |
Q36700594 | Generation and modulation of chemosensory behaviors in C. elegans |
Q38651031 | Generation of cell diversity during early embryogenesis in the nematode Caenorhabditis elegans. |
Q36233694 | Genes critical for muscle development and function in Caenorhabditis elegans identified through lethal mutations |
Q34612379 | Genes regulating touch cell development in Caenorhabditis elegans |
Q48078919 | Genesis of an organ: molecular analysis of the pha-1 gene |
Q64916668 | Genetic Analysis of Nuclear Migration and Anchorage to Study LINC Complexes During Development of Caenorhabditis elegans. |
Q33958694 | Genetic analysis of a major segment [LGV(left)] of the genome of Caenorhabditis elegans |
Q33877064 | Genetic analysis of lysosomal trafficking in Caenorhabditis elegans |
Q34140720 | Genetic analysis of tissue aging in Caenorhabditis elegans: a role for heat-shock factor and bacterial proliferation. |
Q35764318 | Genetic and pharmacological suppression of polyglutamine-dependent neuronal dysfunction in Caenorhabditis elegans |
Q33863714 | Genetic aspects of behavioral neurotoxicology |
Q24642910 | Genetic control of cell division patterns in the Drosophila embryo |
Q38607199 | Genetic control of differentiation of the Caenorhabditis elegans touch receptor neurons |
Q30479203 | Genetic control of fusion pore expansion in the epidermis of Caenorhabditis elegans |
Q37028387 | Genetic control of nucleolar size: An evolutionary perspective |
Q41604606 | Genetic control of programmed cell death and aging in the nematode Caenorhabditis elegans. |
Q33589613 | Genetic control of programmed cell death during animal development |
Q37110384 | Genetic dissection of neural circuits |
Q34350636 | Genetic models of mechanotransduction: the nematode Caenorhabditis elegans |
Q35739145 | Genetic networks in the early development of Caenorhabditis elegans |
Q45986590 | Genetic redundancy in endoderm specification within the genus Caenorhabditis. |
Q35945665 | Genetic screens for Caenorhabditis elegans mutants defective in left/right asymmetric neuronal fate specification |
Q52182134 | Genetics of RAS signaling in C. elegans. |
Q41515240 | Genetics of apoptosis |
Q36314245 | Genetics of graviperception in animals. |
Q40835187 | Genetics of programmed cell death in C. elegans: past, present and future. |
Q26765465 | Genome Editing in C. elegans and Other Nematode Species |
Q51840886 | Genome Editing of C. elegans. |
Q36310528 | Genome-Wide RNAi Longevity Screens in Caenorhabditis elegans |
Q47575778 | Genome-scale analysis of in vivo spatiotemporal promoter activity in Caenorhabditis elegans. |
Q34591276 | Genome-wide analysis of developmental and sex-regulated gene expression profiles in Caenorhabditis elegans |
Q21563514 | Genomic variability within an organism exposes its cell lineage tree |
Q38032802 | Germ cell specification |
Q34007885 | Germ plasm and molecular determinants of germ cell fate |
Q30806560 | Germ-line induction of the Caenorhabditis elegans vulva |
Q34026926 | Getting signals crossed in C. elegans |
Q79268095 | Gland-specific expression of C. elegans hlh-6 requires the combinatorial action of three distinct promoter elements |
Q47897846 | Glia initiate brain assembly through noncanonical Chimaerin-Furin axon guidance in C. elegans |
Q40429780 | Glia-derived neurons are required for sex-specific learning in C. elegans |
Q36294286 | Glia-neuron interactions in nervous system function and development |
Q35245310 | Glial development and function in the nervous system of Caenorhabditis elegans |
Q36825936 | Gliogenesis and glial pathology in depression |
Q61460364 | Global cell sorting in the C. elegans embryo defines a new mechanism for pattern formation |
Q83180021 | Global cell sorting is mediated by local cell-cell interactions in the C. elegans embryo |
Q27316426 | Global linking of cell tracks using the Viterbi algorithm |
Q40776320 | Gonad establishment during asexual reproduction in the annelid Pristina leidyi. |
Q51927296 | Google 'EarthWorm'. |
Q57064641 | Greater coverage of the phylum Nematoda in SSU rDNA studies |
Q27027374 | Gutsy moves in mice: cellular and molecular dynamics of endoderm morphogenesis |
Q92433185 | H3K27me3 suppresses sister-lineage somatic gene expression in late embryonic germline cells of the ascidian, Halocynthia roretzi |
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 |
Q34795822 | Heads or tails: cell polarity and axis formation in the early Caenorhabditis elegans embryo |
Q52272168 | Heterochronic mutants of the nematode Caenorhabditis elegans. |
Q92471557 | Heterogeneity of primordial germ cells |
Q28821634 | Heterotaxy in Caenorhabditis: widespread natural variation in left-right arrangement of the major organs |
Q24797167 | High copy arrays containing a sequence upstream of mec-3 alter cell migration and axonal morphology in C. elegans |
Q30500041 | High resolution cell lineage tracing reveals developmental variability in leech |
Q51862878 | High sensitivity of C. elegans vulval precursor cells to the dose of posterior Wnts. |
Q58616010 | High-Throughput Analysis of Behavior Under the Control of Optogenetics in Caenorhabditis elegans |
Q70190248 | High-frequency excision of transposable element Tc1 in the nematode caenorhabditis elegans is limited to somatic cells |
Q95818134 | High-throughput capturing and characterization of mutations in essential genes of Caenorhabditis elegans |
Q27334278 | High-throughput in vivo analysis of gene expression in Caenorhabditis elegans |
Q33283982 | High-throughput screening of small molecules for bioactivity and target identification in Caenorhabditis elegans |
Q27333859 | Highly asynchronous and asymmetric cleavage divisions accompany early transcriptional activity in pre-blastula medaka embryos |
Q92765296 | How cells fuse |
Q39995724 | How targets select activation or repression in response to Wnt. |
Q34355988 | How the worm removes corpses: the nematode C. elegans as a model system to study engulfment. |
Q45058913 | How to Make a Worm Twitch |
Q44109052 | Hox Gene Loss during Dynamic Evolution of the Nematode Cluster |
Q43185602 | Hox Genes Promote Neuronal Subtype Diversification through Posterior Induction in Caenorhabditis elegans |
Q60086336 | Hox genes misled by local environments |
Q46471273 | Http://C. elegans: mining the functional genomic landscape |
Q50047285 | Hub connectivity, neuronal diversity, and gene expression in the Caenorhabditis elegans connectome. |
Q97418936 | Human organoids: model systems for human biology and medicine |
Q58581622 | I Spy in the Developing Fly a Multitude of Ways to Die |
Q28507741 | Ich-1, an Ice/ced-3-related gene, encodes both positive and negative regulators of programmed cell death |
Q42085414 | Identification and Characterization of Mitochondrial Subtypes in Caenorhabditis elegans via Analysis of Individual Mitochondria by Flow Cytometry |
Q47068792 | Identification of CHE-13, a novel intraflagellar transport protein required for cilia formation |
Q34602427 | Identification of Caenorhabditis elegans genes required for neuronal differentiation and migration |
Q30837912 | Identification of genes driving lineage divergence from single-cell gene expression data in C. elegans. |
Q68273724 | Identification of genes required for cytoplasmic localization in early C. elegans embryos |
Q34618128 | Identification of genes that regulate a left-right asymmetric neuronal migration in Caenorhabditis elegans |
Q48330068 | Identification of human FEM1A, the ortholog of a C. elegans sex-differentiation gene |
Q38333481 | Identification of lineage-specific zygotic transcripts in early Caenorhabditis elegans embryos |
Q38721411 | Identifying Adult Stem Cells Using Cre-Mediated Lineage Tracing |
Q36429779 | Identifying Regulators of Morphogenesis Common to Vertebrate Neural Tube Closure and Caenorhabditis elegans Gastrulation |
Q43219256 | If you don't want them shed them |
Q37168676 | IgCAMs redundantly control axon navigation in Caenorhabditis elegans |
Q28082141 | Illuminating neural circuits and behaviour in Caenorhabditis elegans with optogenetics |
Q60227338 | Illumination of neural development by in vivo clonal analysis. |
Q28743708 | Imaging C. elegans embryos using an epifluorescent microscope and open source software |
Q48728400 | Imaging dynamic cell-cell junctional coupling in vivo using Trojan-LAMP. |
Q37780838 | Imaging of mitotic spindle dynamics in Caenorhabditis elegans embryos |
Q36217044 | Immunochemical localization of myosin heavy chain isoforms and paramyosin in developmentally and structurally diverse muscle cell types of the nematode Caenorhabditis elegans |
Q52255478 | Immunocytochemical localization of neurosecretory amines and peptides in the free-living nematode, Goodeyus ulmi. |
Q47069295 | Importance of the basement membrane protein SPARC for viability and fertility in Caenorhabditis elegans |
Q33492754 | In Caenorhabditis elegans nanoparticle-bio-interactions become transparent: silica-nanoparticles induce reproductive senescence |
Q40773961 | In search of new mutants in cell-signaling systems of the nematode Caenorhabditis elegans. Review |
Q33313180 | In vivo imaging of cellular structures in Caenorhabditis elegans by combined TPEF, SHG and THG microscopy. |
Q54278436 | Inactivation of wild-type and rad mutant Caenorhabditis elegans by 8-methoxypsoralen and near ultraviolet radiation. |
Q73105711 | Induction of apoptosis in HL-60 cells by eicosapentaenoic acid (EPA) is associated with downregulation of bcl-2 expression |
Q52231446 | Induction of gut in Caenorhabditis elegans embryos |
Q36633936 | Induction of neuronal branching in Caenorhabditis elegans |
Q91928931 | Inference of single-cell phylogenies from lineage tracing data using Cassiopeia |
Q40142959 | Inferring average generation via division-linked labeling |
Q42320266 | Inferring cell differentiation processes based on phylogenetic analysis of genome-wide epigenetic information: hematopoiesis as a model case |
Q30835788 | Infrared laser-induced gene expression for tracking development and function of single C. elegans embryonic neurons |
Q34114831 | Initiation and early patterning of the endoderm |
Q33254080 | Initiation of male sperm-transfer behavior in Caenorhabditis elegans requires input from the ventral nerve cord |
Q35616802 | Insight into transcription factor gene duplication from Caenorhabditis elegans Promoterome-driven expression patterns. |
Q37826364 | Insights from Caenorhabditis elegans on the role of metals in neurodegenerative diseases |
Q46627365 | Insulin-like signaling negatively regulates muscle arm extension through DAF-12 in Caenorhabditis elegans |
Q55012943 | Integrated Microfluidic Device for Drug Studies of Early C. Elegans Embryogenesis. |
Q28301622 | Integrative analysis of the Caenorhabditis elegans genome by the modENCODE project |
Q34277082 | Integrin α PAT-2/CDC-42 signaling is required for muscle-mediated clearance of apoptotic cells in Caenorhabditis elegans |
Q47069211 | Interaction and regulation of the Caenorhabditis elegans death protease CED-3 by CED-4 and CED-9. |
Q36069223 | Interactome modeling |
Q37355860 | Interaxonal interaction defines tiled presynaptic innervation in C. elegans |
Q74403354 | Interference between the PHA-4 and PEB-1 transcription factors in formation of the Caenorhabditis elegans pharynx |
Q37479445 | Intermediate filaments in Caenorhabditis elegans. |
Q36215210 | Intermediate filaments in muscle and epithelial cells of nematodes |
Q30497921 | Internalization of multiple cells during C. elegans gastrulation depends on common cytoskeletal mechanisms but different cell polarity and cell fate regulators |
Q43224791 | Intestinal tube formation in Caenorhabditis elegans requires vang-1 and egl-15 signaling. |
Q36634138 | Invertebrate models of dystonia |
Q34050117 | Inverted selective plane illumination microscopy (iSPIM) enables coupled cell identity lineaging and neurodevelopmental imaging in Caenorhabditis elegans |
Q49031802 | Investigating the ecology and evolution of cryptic marine nematode species through quantitative real-time PCR of the ribosomal ITS region. |
Q27347595 | Involvement of global genome repair, transcription coupled repair, and chromatin remodeling in UV DNA damage response changes during development |
Q35597729 | Isolation and characterization of Caenorhabditis elegans DNA sequences homologous to the v-abl oncogene |
Q36942238 | Isolation and characterization of a sperm-specific gene family in the nematode Caenorhabditis elegans |
Q58285264 | Isolation and characterization of lethal mutation near theunc‐29(LG I) region ofCaenorhabditis elegans |
Q33894819 | Isolation and culture of larval cells from C. elegans |
Q35396163 | Isolation of specific neurons from C. elegans larvae for gene expression profiling |
Q45983560 | Isolation ofCaenorhabditis elegans mutants lacking alcohol dehydrogenase activity |
Q30650981 | Isolation, characterization and immunolocalization of phosphorylcholine-substituted glycolipids in developmental stages of Caenorhabditis elegans |
Q28239600 | Isopentenyl-diphosphate isomerase is essential for viability of Caenorhabditis elegans |
Q27312169 | It's all in your mind: determining germ cell fate by neuronal IRE-1 in C. elegans |
Q27026099 | Japanese studies on neural circuits and behavior of Caenorhabditis elegans |
Q37349399 | Key players in chromosome segregation in Caenorhabditis elegans |
Q36784741 | Kinesin-1 acts with netrin and DCC to maintain sensory neuron position in Caenorhabditis elegans |
Q34191608 | Kinesin-1 and dynein at the nuclear envelope mediate the bidirectional migrations of nuclei |
Q37111025 | Knockdown of SKN-1 and the Wnt effector TCF/POP-1 reveals differences in endomesoderm specification in C. briggsae as compared with C. elegans |
Q37702564 | LET-418/Mi2 and SPR-5/LSD1 cooperatively prevent somatic reprogramming of C. elegans germline stem cells |
Q37446769 | LIN-23, an E3 Ubiquitin Ligase Component, Is Required for the Repression of CDC-25.2 Activity during Intestinal Development in Caenorhabditis elegans |
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 |
Q35512446 | LIN-5 is a novel component of the spindle apparatus required for chromosome segregation and cleavage plane specification in Caenorhabditis elegans |
Q30513991 | Laminin is required to orient epithelial polarity in the C. elegans pharynx |
Q37372540 | Large-scale sorting of C. elegans embryos reveals the dynamics of small RNA expression |
Q33223645 | Larval and adult brains |
Q36787590 | Laser killing of cells in Caenorhabditis elegans |
Q34121093 | Laser microsurgery in Caenorhabditis elegans |
Q46932244 | Lateral inhibition during vulval induction in Caenorhabditis elegans |
Q33642220 | Latrophilin signaling links anterior-posterior tissue polarity and oriented cell divisions in the C. elegans embryo |
Q34770342 | Left-right asymmetry in the nervous system: the Caenorhabditis elegans model |
Q37867503 | Left-right patterning in the C. elegans embryo: Unique mechanisms and common principles |
Q33446005 | Life cycle and population growth rate of Caenorhabditis elegans studied by a new method |
Q47439483 | Limitation of the size of the vulval primordium of Caenorhabditis elegans by lin-15 expression in surrounding hypodermis |
Q47698225 | LinMap: visualizing complexity gradients in evolutionary landscapes |
Q64236774 | Lineage Tracing: Computational Reconstruction Goes Beyond the Limit of Imaging |
Q89559275 | Lineage analysis of transplanted individual cells in embryos of Drosophila melanogaster : I. The method |
Q92487248 | Lineage context switches the function of a C. elegans Pax6 homolog in determining a neuronal fate |
Q34149240 | Lineage programming: navigating through transient regulatory states via binary decisions |
Q51868339 | Lineage specific trimethylation of H3 on lysine 4 during C. elegans early embryogenesis. |
Q90814608 | Lineage tracing meets single-cell omics: opportunities and challenges |
Q50440790 | Link of Zygotic Genome Activation and Cell Cycle Control. |
Q37215105 | Linking asymmetric cell division to the terminal differentiation program of postmitotic neurons in C. elegans |
Q42585551 | Lipocalin signaling controls unicellular tube development in the Caenorhabditis elegans excretory system |
Q26751216 | Live Imaging of Adult Neural Stem Cells in Rodents |
Q33226509 | Live imaging and morphometric analysis of embryonic development in the ascidian Ciona intestinalis |
Q50239529 | Live imaging of cellular dynamics during Caenorhabditis elegans postembryonic development. |
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 |
Q36311940 | Localization and segregation of lineage-specific cleavage potential in embryos of Caenorhabditis elegans |
Q27321533 | Long-term imaging of Caenorhabditis elegans using nanoparticle-mediated immobilization |
Q33908342 | Long-term time-lapse microscopy of C. elegans post-embryonic development |
Q36626409 | Long-term, high-resolution confocal time lapse imaging of Arabidopsis cotyledon epidermis during germination |
Q27321443 | Loss of Acetylcholine Signaling Reduces Cell Clearance Deficiencies in Caenorhabditis elegans |
Q30502448 | Loss of intestinal nuclei and intestinal integrity in aging C. elegans |
Q30416737 | Loss of the RhoGAP SRGP-1 promotes the clearance of dead and injured cells 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 |
Q37425052 | MAP kinase signaling antagonizes PAR-1 function during polarization of the early Caenorhabditis elegans embryo |
Q35748546 | MED GATA factors promote robust development of the C. elegans endoderm |
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 |
Q47069183 | MEX-3 is a KH domain protein that regulates blastomere identity in early C. elegans embryos |
Q41680284 | MIG-13 positions migrating cells along the anteroposterior body axis of C. elegans |
Q35224574 | MIG-15 and ERM-1 promote growth cone directional migration in parallel to UNC-116 and WVE-1. |
Q42156705 | MIG-32 and SPAT-3A are PRC1 homologs that control neuronal migration in Caenorhabditis elegans |
Q28613384 | MOM-4, a MAP kinase kinase kinase-related protein, activates WRM-1/LIT-1 kinase to transduce anterior/posterior polarity signals in C. elegans |
Q46029130 | MOM-5 frizzled regulates the distribution of DSH-2 to control C. elegans asymmetric neuroblast divisions. |
Q44100008 | MRG-1, a mortality factor-related chromodomain protein, is required maternally for primordial germ cells to initiate mitotic proliferation in C. elegans |
Q36293940 | MUP-4 is a novel transmembrane protein with functions in epithelial cell adhesion in Caenorhabditis elegans |
Q46287591 | Magnetic resonance microscopy of embryonic cell lineages and movements |
Q34569012 | Malignant worms: what cancer research can learn from C. elegans |
Q41097496 | Mammalian homologues of C. elegans PAR-1 are asymmetrically localized in epithelial cells and may influence their polarity |
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 |
Q69895691 | Mapping the distribution of differentiation potential for intestine, muscle, and hypodermis during early development in Caenorhabditis elegans |
Q64228033 | Maps of variability in cell lineage trees |
Q33335080 | Marking cell layers with spectinomycin provides a new tool for monitoring cell fate during leaf development |
Q34190874 | Mass spectrometric comparison of N-glycan profiles from Caenorhabditis elegans mutant embryos |
Q47070377 | Maternal Pumilio acts together with Nanos in germline development in Drosophila embryos |
Q91866548 | Maternal Ribosomes Are Sufficient for Tissue Diversification during Embryonic Development in C. elegans |
Q42598422 | Maternal deployment of the embryonic SKN-1-->MED-1,2 cell specification pathway in C. elegans |
Q49023846 | Maternal effect of low temperature on handedness determination in C. elegans embryos. |
Q47626606 | Maternal effects of microRNAs in early embryogenesis |
Q51887793 | Maximum parsimony analysis of gene expression profiles permits the reconstruction of developmental cell lineage trees. |
Q52668776 | Mechanical forces drive neuroblast morphogenesis and are required for epidermal closure. |
Q34638690 | Mechanisms for the control of gene activity during development |
Q64103888 | Mechanisms of Spindle Positioning: Lessons from Worms and Mammalian Cells |
Q39038829 | Mechanisms of Vertebrate Germ Cell Determination |
Q36749996 | Mechanisms of asymmetric cell division: Two Bs or not two Bs, that is the question |
Q37269833 | Mechanisms of ephrin receptor protein kinase-independent signaling in amphid axon guidance in Caenorhabditis elegans |
Q38132385 | Mechanisms of plasticity in a Caenorhabditis elegans mechanosensory circuit |
Q43986595 | Mechanosensitive Ion Channels in Caenorhabditis elegans |
Q81568754 | Med-type GATA factors and the evolution of mesendoderm specification in nematodes |
Q44155294 | Medical significance of Caenorhabditis elegans. |
Q33402686 | Medium- and high-throughput screening of neurotoxicants using C. elegans |
Q50514847 | Membrane extensions are associated with proper anterior migration of muscle cells during Caenorhabditis elegans embryogenesis. |
Q26999431 | Membrane trafficking and phagosome maturation during the clearance of apoptotic cells |
Q46299366 | Mesoderm and ectoderm lineages in the crustacean Parhyale hawaiensis display intra-germ layer compensation |
Q41416332 | Meta-Boolean models of asymmetric division patterns in the C. elegans intestinal lineage: Implications for the posterior boundary of intestinal twist |
Q92713294 | Metabolic regulation of lifespan from a C. elegans perspective |
Q33807271 | Metabolome and proteome changes with aging in Caenorhabditis elegans |
Q34548376 | Metazoan motor models: kinesin superfamily in C. elegans |
Q38104184 | Methods for detection and analysis of apoptosis signaling in the C. elegans germline. |
Q40929025 | Methods of studying behavioral plasticity in Caenorhabditis elegans. |
Q39114147 | Micro-connectomics: probing the organization of neuronal networks at the cellular scale |
Q26774739 | MicroRNAs: Not "Fine-Tuners" but Key Regulators of Neuronal Development and Function |
Q34356120 | Microevolutionary studies in nematodes: a beginning |
Q54106319 | Microtubule Dynamics Scale with Cell Size to Set Spindle Length and Assembly Timing |
Q36213105 | Microtubules and microtubule-associated proteins from the nematode Caenorhabditis elegans: periodic cross-links connect microtubules in vitro |
Q46532458 | Migrations of the Caenorhabditis elegans HSNs are regulated by egl-43, a gene encoding two zinc finger proteins |
Q41051148 | Mitigating Motor Neuronal Loss in C. elegans Model of ALS8. |
Q44993538 | Mitotic entry: The interplay between Cdk1, Plk1 and Bora |
Q38558261 | Model organisms illuminate human genetics and disease. |
Q41682413 | Model organisms in evo-devo: promises and pitfalls of the comparative approach |
Q34082590 | Model organisms: comparative physiology or just physiology? |
Q37293096 | Modeling molecular and cellular aspects of human disease using the nematode Caenorhabditis elegans |
Q42039744 | Modeling the establishment of PAR protein polarity in the one-cell C. elegans embryo |
Q33558314 | Models of global gene expression define major domains of cell type and tissue identity |
Q38429811 | Modularity and anti-modularity in networks with arbitrary degree distribution |
Q41365143 | Molecular cloning and in vitro expression of C. elegans and parasitic nematode ionotropic receptors |
Q35531971 | Molecular conservation of metazoan gut formation: evidence from expression of endomesoderm genes in Capitella teleta (Annelida) |
Q92463016 | Molecular evolution across developmental time reveals rapid divergence in early embryogenesis |
Q33974169 | Molecular evolution of cyclin proteins in animals and fungi |
Q38722464 | Molecular genetic approaches to the study of motility in Caenorhabditis elegans |
Q41100020 | Molecular genetics of asymmetric cleavage in the early Caenorhabditis elegans embryo |
Q52441096 | Molecular markers for identified neuroblasts and ganglion mother cells in the Drosophila central nervous system |
Q47567494 | Molecular markers of differentiation in Caenorhabditis elegans obtained by promoter trapping. |
Q57076476 | Molecular memoirs of a cellular family |
Q35586708 | Molecular networks controlling epithelial cell polarity in development |
Q92000983 | Molecular recording of mammalian embryogenesis |
Q40060283 | Monitoring the clearance of apoptotic and necrotic cells in the nematode Caenorhabditis elegans |
Q27309001 | Morphogenesis of the C. elegans Intestine Involves Axon Guidance Genes |
Q33967904 | Mosaic analysis using a ncl-1 (+) extrachromosomal array reveals that lin-31 acts in the Pn.p cells during Caenorhabditis elegans vulval development. |
Q37682753 | Movers and shakers or anchored: Caenorhabditis elegans nuclei achieve it with KASH/SUN. |
Q27323213 | Multi-environment model estimation for motility analysis of Caenorhabditis elegans |
Q104289900 | Multi-tissue patterning drives anterior morphogenesis of the C. elegans embryo |
Q52723294 | Multi-view light-sheet imaging and tracking with the MaMuT software reveals the cell lineage of a direct developing arthropod limb. |
Q39628462 | Multidimensional regulation of gene expression in the C. elegans embryo |
Q91814121 | Multiple Pathways Act Together To Establish Asymmetry of the Ventral Nerve Cord in Caenorhabditis elegans |
Q34070518 | Multiple doublesex-related genes specify critical cell fates in a C. elegans male neural circuit |
Q47068752 | Multiple enhancers contribute to expression of the NK-2 homeobox gene ceh-22 in C. elegans pharyngeal muscle |
Q73353794 | Multiple ephrins control cell organization in C. elegans using kinase-dependent and -independent functions of the VAB-1 Eph receptor |
Q52236554 | Multiple intercellular signalling systems control the development of the Caenorhabditis elegans vulva. |
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 |
Q47255056 | Multiple regulatory elements with spatially and temporally distinct activities control the expression of the epithelial differentiation gene lin-26 in C. elegans |
Q27307993 | Multisite Phosphorylation of NuMA-Related LIN-5 Controls Mitotic Spindle Positioning in C. elegans |
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 |
Q47069580 | Mutations affecting embryonic cell migrations in Caenorhabditis elegans |
Q51585826 | Mutations affecting sensitivity to ethanol in the nematode, Caenorhabditis elegans. |
Q33964180 | Mutations affecting the chemosensory neurons of Caenorhabditis elegans |
Q47068817 | Mutations in the Caenorhabditis elegans unc-4 gene alter the synaptic input to ventral cord motor neurons |
Q35754139 | Myogenic conversion and transcriptional profiling of embryonic blastomeres in Caenorhabditis elegans |
Q36232555 | Myosin and paramyosin of Caenorhabditis elegans embryos assemble into nascent structures distinct from thick filaments and multi-filament assemblages |
Q36293307 | Myotactin, a novel hypodermal protein involved in muscle-cell adhesion in Caenorhabditis elegans |
Q83975473 | N-ethylmaleimide sensitive factor is required for fusion of the C. elegans uterine anchor cell |
Q73525906 | N-tosyl-L-phenylalanyl-chloromethylketone reduces hypoxic-ischemic brain injury in rat pups |
Q35128017 | NDK-1, the homolog of NM23-H1/H2 regulates cell migration and apoptotic engulfment in C. elegans |
Q40442315 | NUC-1, a caenorhabditis elegans DNase II homolog, functions in an intermediate step of DNA degradation during apoptosis |
Q27311005 | Necrotic Cells Actively Attract Phagocytes through the Collaborative Action of Two Distinct PS-Exposure Mechanisms |
Q35837231 | Negative regulators of programed cell death |
Q38117100 | Nematode model systems in evolution and development |
Q36402736 | Nematode neurons: anatomy and anatomical methods in Caenorhabditis elegans |
Q33883789 | Nematodes: the worm and its relatives |
Q30480880 | Nemo: a computational tool for analyzing nematode locomotion |
Q78094933 | Netrin UNC-6 and the regulation of branching and extension of motoneuron axons from the ventral nerve cord of Caenorhabditis elegans |
Q36254400 | Network inference of pal-1 lineage-specific regulation in the C. elegans embryo by structural equation modeling |
Q28067266 | Neural circuit rewiring: insights from DD synapse remodeling |
Q27334196 | Neural development features: spatio-temporal development of the Caenorhabditis elegans neuronal network |
Q35210793 | Neural integrity is maintained by dystrophin in C. elegans |
Q46263952 | Neural lineage tracing in the mammalian brain |
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 |
Q36402745 | Neural specification and differentiation |
Q42723189 | Neurite extension: starting at the finish line |
Q35057663 | Neuroblast migration along the anteroposterior axis of C. elegans is controlled by opposing gradients of Wnts and a secreted Frizzled-related protein |
Q46309571 | Neurodegeneration Induced by Metals in Caenorhabditis elegans |
Q30369071 | Neuroendocrine modulation sustains the C. elegans forward motor state. |
Q73781256 | Neurogenetics of synaptic transmission in Caenorhabditis elegans |
Q90435636 | Neuron ID dataset facilitates neuronal annotation for whole-brain activity imaging of C. elegans |
Q28818674 | Neuron-specific knock-down of SMN1 causes neuron degeneration and death through an apoptotic mechanism |
Q38775274 | Neuronal cell fate decisions: O2 and CO2 sensing neurons require egl-13/Sox5. |
Q46326031 | Neuronal cell-type classification: challenges, opportunities and the path forward |
Q71236697 | Neuronal localization of serotonin in the nematode Ascaris suum |
Q28657860 | Neuronal migration is regulated by endogenous RNAi and chromatin-binding factor ZFP-1/AF10 in Caenorhabditis elegans |
Q27318339 | Neurons refine the Caenorhabditis elegans body plan by directing axial patterning by Wnts |
Q38069826 | Neuropeptide GPCRs in C. elegans |
Q52169678 | New approach to cell lineage analysis in mammals using the Cre-loxP system. |
Q33518319 | New tools for investigating the comparative biology of Caenorhabditis briggsae and C. elegans |
Q40783600 | New ways to look at axons in Caenorhabditis elegans |
Q37682750 | Non-apoptotic cell death in Caenorhabditis elegans |
Q46473095 | Non-centrosomal epidermal microtubules act in parallel to LET-502/ROCK to promote C. elegans elongation |
Q41462929 | Non-coding stem-bulge RNAs are required for cell proliferation and embryonic development in C. elegans |
Q46456620 | Non-neuronal cell outgrowth in C. elegans |
Q42693068 | Nonautonomous regulation of neuronal migration by insulin signaling, DAF-16/FOXO, and PAK-1 |
Q33973337 | Noncanonical cell death in the nematode Caenorhabditis elegans |
Q37147746 | Noncanonical cell death programs in the nematode Caenorhabditis elegans |
Q34286367 | Not being the wrong size |
Q41959910 | Notch and Ras promote sequential steps of excretory tube development in C. elegans |
Q64079923 | Novel Genes Involved in Formation of the Tubular Excretory Canals of |
Q90278121 | Novel Technological Advances in Functional Connectomics in C. elegans |
Q47069105 | Novel genes controlling ventral cord asymmetry and navigation of pioneer axons in C. elegans |
Q34461760 | Nucleoporins NPP-1, NPP-3, NPP-4, NPP-11 and NPP-13 are required for proper spindle orientation in C. elegans |
Q50650519 | OMA-1 is a P granules-associated protein that is required for germline specification in Caenorhabditis elegans embryos. |
Q90622860 | Oikopleura dioica: An Emergent Chordate Model to Study the Impact of Gene Loss on the Evolution of the Mechanisms of Development |
Q28769794 | On the evolution of early development in the Nematoda. |
Q34085749 | Oncogenic potential of a C.elegans cdc25 gene is demonstrated by a gain-of-function allele |
Q27321162 | Opposing activities of LIT-1/NLK and DAF-6/patched-related direct sensory compartment morphogenesis in C. elegans |
Q58733576 | Ordered arrangement of dendrites within a sensory nerve bundle |
Q36534977 | Orientation of spindle axis and distribution of plasma membrane proteins during cell division in polarized MDCKII cells |
Q35822712 | Oriented Cell Division in the C. elegans Embryo Is Coordinated by G-Protein Signaling Dependent on the Adhesion GPCR LAT-1. |
Q35990171 | Other model organisms for sarcomeric muscle diseases |
Q34290559 | Otx-dependent expression of proneural bHLH genes establishes a neuronal bilateral asymmetry in C. elegans. |
Q48839998 | Ovarian differentiation and human embryo quality. 1. Molecular and morphogenetic homologies between oocytes and embryos in Drosophila, C. elegans, Xenopus and mammals. |
Q35222713 | Overcoming redundancy: an RNAi enhancer screen for morphogenesis genes in Caenorhabditis elegans |
Q35939502 | Overlapping cell population expression profiling and regulatory inference in C. elegans |
Q36491719 | PAR proteins direct asymmetry of the cell cycle regulators Polo-like kinase and Cdc25. |
Q73341305 | PAR proteins regulate microtubule dynamics at the cell cortex in C. elegans |
Q42428878 | PAR-6, but not E-cadherin and β-integrin, is necessary for epithelial polarization in C. elegans |
Q50441731 | PCP and SAX-3/Robo Pathways Cooperate to Regulate Convergent Extension-Based Nerve Cord Assembly in C. elegans. |
Q35758336 | PHA-4/FoxA cooperates with TAM-1/TRIM to regulate cell fate restriction in the C. elegans foregut |
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 |
Q74150651 | POP-1 and anterior-posterior fate decisions in C. elegans embryos |
Q36496248 | Pairing of competitive and topologically distinct regulatory modules enhances patterned gene expression. |
Q27322762 | Pan-neuronal imaging in roaming Caenorhabditis elegans |
Q45965930 | Partially compromised specification causes stochastic effects on gut development in C. elegans. |
Q28384357 | Pathophysiology of manganese-associated neurotoxicity |
Q28304067 | Pattern formation during vulval development in C. elegans |
Q33702220 | Patterning the C. elegans embryo: moving beyond the cell lineage. |
Q45788160 | Patterns of cell lineage, movement, and migration from germ layer specification to gastrulation in the amphipod crustacean Parhyale hawaiensis |
Q28540040 | Pervasive divergence of transcriptional gene regulation in Caenorhabditis nematodes |
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 |
Q24602890 | Phagosome maturation during the removal of apoptotic cells: receptors lead the way |
Q38974724 | Pharmacological Tools to Study the Role of Astrocytes in Neural Network Functions. |
Q35792598 | Pharyngeal pumping continues after laser killing of the pharyngeal nervous system of C. elegans |
Q39330009 | Phenotypic plasticity and remodeling in the stress-induced Caenorhabditis elegans dauer |
Q37091672 | Phosphorylation of RNA polymerase II is independent of P-TEFb in the C. elegans germline |
Q41842603 | Phylogenetic analysis of developmental and postnatal mouse cell lineages. |
Q34482326 | Phylogenetic fate mapping |
Q36470545 | Phylogenetic fate mapping: theoretical and experimental studies applied to the development of mouse fibroblasts |
Q38609404 | Physical determinants of asymmetric cell divisions in the early development of Caenorhabditis elegans |
Q28727320 | Plectus - a stepping stone in embryonic cell lineage evolution of nematodes |
Q28236847 | Polarity and cell fate specification in the control of Caenorhabditis elegans gastrulation |
Q30654911 | Polarity controls forces governing asymmetric spindle positioning in the Caenorhabditis elegans embryo |
Q36245121 | Polarized Rac-dependent protrusions drive epithelial intercalation in the embryonic epidermis of C. elegans |
Q38189357 | Polarized cells, polarized views: asymmetric cell division in hematopoietic cells. |
Q37381631 | Post-transcriptional regulation of sex determination in Caenorhabditis elegans: widespread expression of the sex-determining gene fem-1 in both sexes |
Q34086564 | Postembryonic expression of Caenorhabditis elegans mab-21 and its requirement in sensory ray differentiation |
Q37541721 | Postembryonic segregation of the germ line in sea urchins in relation to indirect development |
Q27860867 | Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans |
Q35022073 | Power law relationship between cell cycle duration and cell volume in the early embryonic development of Caenorhabditis elegans |
Q33452181 | Precise observation of C. elegans dynamic behaviours under controlled thermal stimulus using a mobile phone-based microscope. |
Q41477059 | Presumptive TRP channel CED-11 promotes cell volume decrease and facilitates degradation of apoptotic cells in Caenorhabditis elegans |
Q41088732 | Probing and rearranging the transcription factor network controlling the C. elegans endoderm |
Q41851342 | Programmed Cell Death During Caenorhabditis elegans Development |
Q39029856 | Programmed cell clearance: From nematodes to humans |
Q38799151 | Programmed cell death and clearance of cell corpses in Caenorhabditis elegans |
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 |
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 |
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 |
Q47069576 | Properties and partial purification of choline acetyltransferase from the nematode Caenorhabditis elegans |
Q28074596 | Prospects and challenges of CRISPR/Cas genome editing for the study and control of neglected vector-borne nematode diseases |
Q35283856 | Protein phosphatase 2A cooperates with the autophagy-related kinase UNC-51 to regulate axon guidance in Caenorhabditis elegans |
Q27333057 | Pulsed irradiation improves target selectivity of infrared laser-evoked gene operator for single-cell gene induction in the nematode C. elegans |
Q28598341 | Quantifying Mosaic Development: Towards an Evo-Devo Postmodern Synthesis of the Evolution of Development via Differentiation Trees of Embryos |
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 |
Q35815971 | Quantitative Differences in Nuclear β-catenin and TCF Pattern Embryonic Cells in C. elegans |
Q82562472 | Quantitative analysis of germline mitosis in adult C. elegans |
Q34618912 | Quantitative classification and natural clustering of Caenorhabditis elegans behavioral phenotypes. |
Q30525795 | Quantitative semi-automated analysis of morphogenesis with single-cell resolution in complex embryos |
Q30502527 | Quantitative time-lapse fluorescence microscopy in single cells |
Q30482098 | RAB-11 permissively regulates spindle alignment by modulating metaphase microtubule dynamics in Caenorhabditis elegans early embryos |
Q33579078 | RNA Interference in Caenorhabditis elegans. |
Q41490235 | RNA target specificity of the embryonic cell fate determinant POS-1. |
Q40441230 | Rapidly evolving homing CRISPR barcodes |
Q40022135 | Ras is required for a limited number of cell fates and not for general proliferation in Caenorhabditis elegans |
Q37696431 | Recent advances in understanding the molecular mechanisms regulating C. elegans transcription |
Q35633530 | Reciprocal asymmetry of SYS-1/beta-catenin and POP-1/TCF controls asymmetric divisions in Caenorhabditis elegans |
Q48098846 | Reciprocal signaling by Wnt and Notch specifies a muscle precursor in the C. elegans embryo. |
Q33327362 | Reconstruction of cell lineage trees in mice |
Q30497703 | Reconstruction of rat retinal progenitor cell lineages in vitro reveals a surprising degree of stochasticity in cell fate decisions. |
Q58049916 | Reconstruction of the pharyngeal corpus of Aphelenchus avenae (Nematoda: Tylenchomorpha), with implications for phylogenetic congruence |
Q28296496 | Reconstruction of zebrafish early embryonic development by scanned light sheet microscopy |
Q93086985 | Recording development with single cell dynamic lineage tracing |
Q34575336 | Redefinition of lymphoid progenitors |
Q34589627 | Reevaluation of the role of the med-1 and med-2 genes in specifying the Caenorhabditis elegans endoderm |
Q88664208 | Regeneration of the germline in the annelid Capitella teleta |
Q39540658 | Regulated disruption of inositol 1,4,5-trisphosphate signaling in Caenorhabditis elegans reveals new functions in feeding and embryogenesis |
Q46621417 | Regulation of C. elegans longevity by specific gustatory and olfactory neurons |
Q42359773 | Regulation of UNC-130/FOXD-mediated mesodermal patterning in C. elegans |
Q52477724 | Regulation of anterior cell-specific mec-3 expression during asymmetric cell division in C. elegans |
Q46210314 | Regulation of cellular responsiveness to inductive signals in the developing C. elegans nervous system |
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. |
Q36882039 | Regulation of interneuron function in the C. elegans thermoregulatory pathway by the ttx-3 LIM homeobox gene |
Q38319731 | Regulation of metallothionein gene transcription. Identification of upstream regulatory elements and transcription factors responsible for cell-specific expression of the metallothionein genes from Caenorhabditis elegans |
Q47069067 | Regulation of neuronal lineage decisions by the HES-related bHLH protein REF-1. |
Q43540459 | Regulation of neurotransmitter vesicles by the homeodomain protein UNC-4 and its transcriptional corepressor UNC-37/groucho in Caenorhabditis elegans cholinergic motor neurons. |
Q37348005 | Regulation of the MEI-1/MEI-2 Microtubule-Severing Katanin Complex in Early Caenorhabditis elegans Development |
Q42429601 | Regulatory analysis of the C. elegans genome with spatiotemporal resolution |
Q24319026 | Related F-box proteins control cell death in Caenorhabditis elegans and human lymphoma |
Q41070697 | Remodelling germ cells by intercellular cannibalism |
Q36802245 | Replication in UV-irradiated Caenorhabditis elegans embryos |
Q112717509 | Replication stress promotes cell elimination by extrusion |
Q35791458 | Replication-coupled chromatin assembly generates a neuronal bilateral asymmetry in C. elegans |
Q34136391 | Repression of Wnt signaling by a Fer-type nonreceptor tyrosine kinase |
Q47915934 | Repression of gene expression in the embryonic germ lineage of C. elegans |
Q68686836 | Repressive Gene Regulation Synchronizes Development with Cellular Metabolism |
Q52138163 | Reproductive isolation in Caenorhabditis: terminal phenotypes of hybrid embryos. |
Q35212031 | Reprogramming of early embryonic blastomeres into endodermal progenitors by a Caenorhabditis elegans GATA factor |
Q27346396 | Repurposing an endogenous degradation system for rapid and targeted depletion of C. elegans proteins |
Q36432857 | Residual body removal during spermatogenesis in C. elegans requires genes that mediate cell corpse clearance |
Q58049917 | Resolving phylogenetic incongruence to articulate homology and phenotypic evolution: a case study from Nematoda |
Q46047227 | Restriction of mesendoderm to a single blastomere by the combined action of SKN-1 and a GSK-3beta homolog is mediated by MED-1 and -2 in C. elegans |
Q34424934 | Restriction of vaccinia virus replication by a ced-3 and ced-4-dependent pathway in Caenorhabditis elegans |
Q28743441 | Revealing developmental networks by comparative transcriptomics |
Q35169840 | Revelations from the Nematode Caenorhabditis elegans on the Complex Interplay of Metal Toxicological Mechanisms |
Q34032017 | Rewritable digital data storage in live cells via engineered control of recombination directionality |
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 |
Q36110365 | Robust tracking and quantification of C. elegans body shape and locomotion through coiling, entanglement, and omega bends |
Q35751951 | Role of T-box gene tbx-2 for anterior foregut muscle development in C. elegans |
Q37845410 | Role of cell death in the formation of sexual dimorphism in the Drosophila central nervous system |
Q36287771 | Role of the Caenorhabditis elegans multidrug resistance gene, mrp-4, in gut granule differentiation |
Q37989861 | Role of the ubiquitin-proteasome system in nervous system function and disease: using C. elegans as a dissecting tool |
Q64980501 | Role of tyramine in calcium dynamics of GABAergic neurons and escape behavior in Caenorhabditis elegans. |
Q33788171 | Roles of the Wnt effector POP-1/TCF in the C. elegans endomesoderm specification gene network |
Q34036844 | SAX-7/L1CAM and HMR-1/cadherin function redundantly in blastomere compaction and non-muscle myosin accumulation during Caenorhabditis elegans gastrulation |
Q34524707 | SLI-1 Cbl inhibits the engulfment of apoptotic cells in C. elegans through a ligase-independent function |
Q47068740 | SMA-1 spectrin has essential roles in epithelial cell sheet morphogenesis in C. elegans. |
Q34550044 | SPK-1, an SR protein kinase, inhibits programmed cell death in Caenorhabditis elegans |
Q28584654 | SSBD: a database of quantitative data of spatiotemporal dynamics of biological phenomena |
Q38271464 | SUN proteins and nuclear envelope spacing |
Q37363084 | SUN-domain and KASH-domain proteins during development, meiosis and disease. |
Q33885880 | Saturation of the human phenome |
Q44597384 | Searching WormBase for information about Caenorhabditis elegans |
Q47068875 | Secretion of a novel class of iFABPs in nematodes: coordinate use of the Ascaris/Caenorhabditis model systems |
Q30455390 | Segregation of fate during cleavage of frog (Xenopus laevis) blastomeres |
Q33963846 | Selective lineage specification by mab-19 during Caenorhabditis elegans male peripheral sense organ development |
Q35014192 | Semaphorin and Eph receptor signaling guide a series of cell movements for ventral enclosure in C. elegans |
Q34619554 | Senescence and apoptosis: dueling or complementary cell fates? |
Q34392782 | Sensation in a single neuron pair represses male behavior in hermaphrodites |
Q37226697 | Sensory neuron fates are distinguished by a transcriptional switch that regulates dendrite branch stabilization. |
Q61797996 | Sensory neuron lineage mapping and manipulation in the Drosophila olfactory system |
Q35072790 | Sensory roles of neuronal cilia: cilia development, morphogenesis, and function in C. elegans |
Q41103383 | Sensory signaling in Caenorhabditis elegans |
Q36742107 | Sensory signaling-dependent remodeling of olfactory cilia architecture in C. elegans |
Q50441741 | Sequential Rosettes Drive C. elegans Ventral Nerve Cord Assembly. |
Q46269433 | Sequential signalling during Caenorhabditis elegans vulval induction |
Q34572365 | Serotonin (5HT), fluoxetine, imipramine and dopamine target distinct 5HT receptor signaling to modulate Caenorhabditis elegans egg-laying behavior |
Q43824672 | Serotonin modulates locomotory behavior and coordinates egg-laying and movement in Caenorhabditis elegans |
Q30430208 | Setting up a simple light sheet microscope for in toto imaging of C. elegans development |
Q33927280 | Sex in the wormcounting and compensating X-chromosome dose |
Q36896657 | Sex-specific pruning of neuronal synapses in Caenorhabditis elegans |
Q52682499 | Sexual Dimorphism and Sex Differences in Caenorhabditis elegans Neuronal Development and Behavior. |
Q52087513 | Sexual and temporal dynamics of molecular evolution in C. elegans development. |
Q39015304 | Sexual modulation of sex-shared neurons and circuits in Caenorhabditis elegans |
Q40594382 | Signal molecules involved in plant embryogenesis |
Q83230580 | Silencing the alternative |
Q35899515 | Similar requirements for CDC-42 and the PAR-3/PAR-6/PKC-3 complex in diverse cell types |
Q27309155 | Single Cell Quantification of Reporter Gene Expression in Live Adult Caenorhabditis elegans Reveals Reproducible Cell-Specific Expression Patterns and Underlying Biological Variation |
Q101166072 | Single-cell RNA profiling links ncRNAs to spatiotemporal gene expression during C. elegans embryogenesis |
Q96431676 | Single-cell lineage tracing by integrating CRISPR-Cas9 mutations with transcriptomic data |
Q34360540 | Single-cell sequencing-based technologies will revolutionize whole-organism science |
Q34100473 | Six and Eya promote apoptosis through direct transcriptional activation of the proapoptotic BH3-only gene egl-1 in Caenorhabditis elegans |
Q34422777 | Small micromeres contribute to the germline in the sea urchin |
Q50470918 | Small-molecule mechanism of action studies in Caenorhabditis elegans. |
Q33185042 | Social feeding in Caenorhabditis elegans is induced by neurons that detect aversive stimuli |
Q35965867 | Somatic gonad sheath cells and Eph receptor signaling promote germ-cell death in C. elegans |
Q26829162 | Somatic muscle specification during embryonic and post-embryonic development in the nematode C. elegans |
Q51664841 | Somatic sexual differentiation in Caenorhabditis elegans. |
Q37271689 | Somatically expressed germ-granule components, PGL-1 and PGL-3, repress programmed cell death in C. elegans |
Q45981171 | Spatial and temporal controls target pal-1 blastomere-specification activity to a single blastomere lineage in C. elegans embryos. |
Q33965821 | Spatial and temporal patterns of lin-12 expression during C. elegans hermaphrodite development |
Q33927380 | Spatially isotropic four-dimensional imaging with dual-view plane illumination microscopy |
Q34986880 | Spatio-temporal reference model of Caenorhabditis elegans embryogenesis with cell contact maps |
Q39069162 | Spatiotemporal coupling and decoupling of gene transcription with DNA replication origins during embryogenesis in C. elegans |
Q33899196 | Spatiotemporal expression profiling of long intervening noncoding RNAs in Caenorhabditis elegans |
Q35178248 | Spatiotemporal transcriptomics reveals the evolutionary history of the endoderm germ layer |
Q42251598 | Specific roles for the GATA transcription factors end-1 and end-3 during C. elegans E-lineage development. |
Q39750144 | Specification of thermosensory neuron fate in C. elegans requires ttx-1, a homolog of otd/Otx |
Q34136096 | Spectrin: the ghost in the machine |
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 |
Q52717063 | Spindle assembly checkpoint strength is linked to cell fate in the C. elegans embryo. |
Q46410421 | Stage- and tissue-specific patterns of cell division in embryonic and larval tissues of amphioxus during normal development |
Q84595952 | Staging worms for next-generation analysis |
Q40438232 | Stem cells, clonal progenitors, and commitment to the three lymphocyte linages: T, B, and NK Cells |
Q42101666 | Stochasticity and stereotypy in the Ciona notochord |
Q37238402 | Strategies for automated analysis of C. elegans locomotion |
Q104286529 | Stressful development: Integrating endoderm development, stress, and longevity |
Q36274367 | Structural Complexity of Early Embryos: A Study on the Nematode Caenorhabditis elegans |
Q36567783 | Structural uniformity of neocortex, revisited |
Q37263501 | Structure and evolution of the C. elegans embryonic endomesoderm network |
Q36487490 | Student learning of early embryonic development via the utilization of research resources from the nematode Caenorhabditis elegans |
Q58049904 | Sudhausia aristotokia n. gen., n. sp. and S. crassa n. gen., n. sp. (Nematoda: Diplogastridae): viviparous new species with precocious gonad development |
Q35088163 | Super models |
Q45973814 | Suppression of CED-3-independent apoptosis by mitochondrial betaNAC in Caenorhabditis elegans. |
Q40256638 | Suppression of transcriptional drift extends C. elegans lifespan by postponing the onset of mortality |
Q41882631 | Synapse location during growth depends on glia location |
Q59062681 | Synaptic code for sensory modalities revealed by C. elegans GLR-1 glutamate receptor |
Q21184163 | Synthetic lethal analysis of Caenorhabditis elegans posterior embryonic patterning genes identifies conserved genetic interactions |
Q30572441 | Systematic quantification of developmental phenotypes at single-cell resolution during embryogenesis. |
Q38996854 | Systems-level quantification of division timing reveals a common genetic architecture controlling asynchrony and fate asymmetry |
Q37424724 | TORC2 signaling antagonizes SKN-1 to induce C. elegans mesendodermal embryonic development |
Q36005254 | Tales of cannibalism, suicide, and murder: Programmed cell death in C. elegans |
Q34360673 | Targets of TGF beta-related signaling in Caenorhabditis elegans |
Q28776675 | Temporal and spatial expression patterns of the small heat shock (hsp16) genes in transgenic 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 |
Q38505668 | The ANISEED database: digital representation, formalization, and elucidation of a chordate developmental program. |
Q40010489 | The Anaphase-Promoting Complex (APC) ubiquitin ligase regulates GABA transmission at the C. elegans neuromuscular junction |
Q35027948 | The Arf GAP CNT-2 regulates the apoptotic fate in C. elegans asymmetric neuroblast divisions |
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 |
Q39751647 | The C. elegans Frizzled CFZ-2 is required for cell migration and interacts with multiple Wnt signaling pathways |
Q36404895 | The C. elegans L1CAM homologue LAD-2 functions as a coreceptor in MAB-20/Sema2 mediated axon guidance |
Q28204737 | The C. elegans PH domain protein CED-12 regulates cytoskeletal reorganization via a Rho/Rac GTPase signaling pathway |
Q30489372 | The C. elegans Tailless/TLX transcription factor nhr-67 controls neuronal identity and left/right asymmetric fate diversification |
Q33830458 | The C. elegans VAPB homolog VPR-1 is a permissive signal for gonad development |
Q47068900 | The C. elegans cell corpse engulfment gene ced-7 encodes a protein similar to ABC transporters. |
Q34515312 | The C. elegans dosage compensation complex mediates interphase X chromosome compaction |
Q92254340 | The C. elegans embryonic transcriptome with tissue, time, and alternative splicing resolution |
Q46696437 | The C. elegans eyes absent ortholog EYA-1 is required for tissue differentiation and plays partially redundant roles with PAX-6. |
Q47069345 | The C. elegans ezrin-radixin-moesin protein ERM-1 is necessary for apical junction remodelling and tubulogenesis in the intestine |
Q52009166 | The C. elegans gene dig-1 encodes a giant member of the immunoglobulin superfamily that promotes fasciculation of neuronal processes. |
Q47069049 | The C. elegans gene lin-44, which controls the polarity of certain asymmetric cell divisions, encodes a Wnt protein and acts cell nonautonomously |
Q31115435 | The C. elegans genome sequencing project: a beginning |
Q50639441 | The C. elegans glycosyltransferase BUS-8 has two distinct and essential roles in epidermal morphogenesis. |
Q46824595 | The C. elegans histone deacetylase HDA-1 is required for cell migration and axon pathfinding |
Q41890082 | The C. elegans homolog of the mammalian tumor suppressor Dep-1/Scc1 inhibits EGFR signaling to regulate binary cell fate decisions |
Q46730392 | The C. elegans lethal gut-obstructed gob-1 gene is trehalose-6-phosphate phosphatase |
Q30155605 | The C. elegans nck-1 gene encodes two isoforms and is required for neuronal guidance |
Q46719795 | The C. elegans nuclear receptor gene fax-1 and homeobox gene unc-42 coordinate interneuron identity by regulating the expression of glutamate receptor subunits and other neuron-specific genes |
Q36151083 | The C. elegans protein CEH-30 protects male-specific neurons from apoptosis independently of the Bcl-2 homolog CED-9. |
Q28272159 | The C. elegans protein EGL-1 is required for programmed cell death and interacts with the Bcl-2-like protein CED-9 |
Q46412377 | The CDK8 Complex and Proneural Proteins Together Drive Neurogenesis from a Mesodermal Lineage |
Q47068931 | The CSL transcription factor LAG-1 directly represses hlh-6 expression in C. elegans |
Q35190195 | The Caenorhabditis elegans APC-related gene apr-1 is required for epithelial cell migration and Hox gene expression. |
Q62820160 | The Caenorhabditis elegans CED-9 protein does not directly inhibit the caspase CED-3, in vitro nor in yeast |
Q36875639 | The Caenorhabditis elegans Excretory System: A Model for Tubulogenesis, Cell Fate Specification, and Plasticity |
Q37493976 | The Caenorhabditis elegans F-box protein SEL-10 promotes female development and may target FEM-1 and FEM-3 for degradation by the proteasome |
Q38656542 | The Caenorhabditis elegans Female State: Decoupling the Transcriptomic Effects of Aging and Sperm-Status |
Q34569329 | The Caenorhabditis elegans Ror RTK CAM-1 inhibits EGL-20/Wnt signaling in cell migration |
Q34166897 | The Caenorhabditis elegans SUN protein UNC-84 interacts with lamin to transfer forces from the cytoplasm to the nucleoskeleton during nuclear migration |
Q47069316 | The Caenorhabditis elegans Skp1-related gene family: diverse functions in cell proliferation, morphogenesis, and meiosis |
Q36234657 | The Caenorhabditis elegans UNC-87 protein is essential for maintenance, but not assembly, of bodywall muscle |
Q34049748 | The Caenorhabditis elegans aristaless orthologue, alr-1, is required for maintaining the functional and structural integrity of the amphid sensory organs |
Q34214723 | The Caenorhabditis elegans cell death gene ced-4 encodes a novel protein and is expressed during the period of extensive programmed cell death |
Q47069551 | The Caenorhabditis elegans distal-less ortholog ceh-43 is required for development of the anterior hypodermis |
Q36515754 | The Caenorhabditis elegans ekl (enhancer of ksr-1 lethality) genes include putative components of a germline small RNA pathway |
Q38094080 | The Caenorhabditis elegans epidermis as a model skin. I: development, patterning, and growth |
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 |
Q43696096 | The Caenorhabditis elegans gene lin-10 is broadly expressed while required specifically for the determination of vulval cell fates |
Q48061840 | The Caenorhabditis elegans gene sem-4 controls neuronal and mesodermal cell development and encodes a zinc finger protein |
Q34306496 | The Caenorhabditis elegans genes ced-3 and ced-4 act cell autonomously to cause programmed cell death |
Q33924971 | The Caenorhabditis elegans gonad: a test tube for cell and developmental biology |
Q34683627 | The Caenorhabditis elegans heterochronic gene lin-14 encodes a nuclear protein that forms a temporal developmental switch |
Q36530182 | The Caenorhabditis elegans hif-1 gene encodes a bHLH-PAS protein that is required for adaptation to hypoxia |
Q39298926 | The Caenorhabditis elegans homeobox gene ceh-19 is required for MC motorneuron function |
Q47069560 | The Caenorhabditis elegans innexin INX-3 is localized to gap junctions and is essential for embryonic development |
Q38116926 | The Caenorhabditis elegans intestine |
Q46386492 | The Caenorhabditis elegans lev-8 gene encodes a novel type of nicotinic acetylcholine receptor alpha subunit |
Q47068869 | The Caenorhabditis elegans lin-12 gene encodes a transmembrane protein with overall similarity to Drosophila Notch |
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. |
Q34645190 | The Caenorhabditis elegans pvl-5 gene protects hypodermal cells from ced-3-dependent, ced-4-independent cell death |
Q37819497 | The Caenorhabiditis elegans model as a reliable tool in neurotoxicology |
Q64888204 | The CeNGEN Project: The Complete Gene Expression Map of an Entire Nervous System. |
Q35193758 | The DAF-3 Smad protein antagonizes TGF-beta-related receptor signaling in the Caenorhabditis elegans dauer pathway |
Q39864475 | The DAF-7 TGF-beta signaling pathway regulates chemosensory receptor gene expression 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 |
Q33264001 | The ELT-2 GATA-factor and the global regulation of transcription in the C. elegans intestine |
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 |
Q39012662 | The FGD homologue EXC-5 regulates apical trafficking in C. elegans tubules |
Q36765041 | The GABAergic nervous system of Caenorhabditis elegans |
Q35005742 | The GEX-2 and GEX-3 proteins are required for tissue morphogenesis and cell migrations in C. elegans |
Q27313660 | The HLH-6 transcription factor regulates C. elegans pharyngeal gland development and function |
Q33710905 | The HMX/NKX homeodomain protein MLS-2 specifies the identity of the AWC sensory neuron type via regulation of the ceh-36 Otx gene in C. elegans |
Q30652335 | The Homeobox Genes of Caenorhabditis elegans and Insights into Their Spatio-Temporal Expression Dynamics during Embryogenesis |
Q88755638 | The Inherent Asymmetry of DNA Replication |
Q38066189 | The Intersection of Aging, Longevity Pathways, and Learning and Memory in C. elegans |
Q64054749 | The Kinetochore-Microtubule Coupling Machinery Is Repurposed in Sensory Nervous System Morphogenesis |
Q37429363 | The LIM and POU homeobox genes ttx-3 and unc-86 act as terminal selectors in distinct cholinergic and serotonergic neuron types |
Q45819556 | The LIM homeobox gene ceh-14 is required for phasmid function and neurite outgrowth |
Q37097037 | The MIG-15 NIK kinase acts cell-autonomously in neuroblast polarization and migration in C. elegans |
Q90420096 | The Making of Hematopoiesis: Developmental Ancestry and Environmental Nurture |
Q83232114 | The Makorin and the lncRNA regulate to schedule sexual maturation of the nervous system |
Q50001924 | The Microbial Zoo in the C. elegans Intestine: Bacteria, Fungi and Viruses. |
Q37242505 | The NF-Y complex negatively regulates Caenorhabditis elegans tbx-2 expression |
Q37314402 | The NK-2 class homeodomain factor CEH-51 and the T-box factor TBX-35 have overlapping function in C. elegans mesoderm development |
Q35980925 | The Nkx5/HMX homeodomain protein MLS-2 is required for proper tube cell shape in the C. elegans excretory system |
Q50457814 | The PAF1 complex is involved in embryonic epidermal morphogenesis in Caenorhabditis elegans. |
Q47069462 | The PIE-1 protein and germline specification in C. elegans embryos |
Q52005375 | The Pax2/5/8 gene egl-38 coordinates organogenesis of the C. elegans egg-laying system. |
Q42629326 | The RFX-type transcription factor DAF-19 regulates sensory neuron cilium formation in C. elegans |
Q50255148 | The Rho guanine exchange factor RHGF-2 acts through the Rho-binding kinase LET-502 to mediate embryonic elongation in C. elegans. |
Q38739786 | The Role of Maternal-Effect Genes in Mammalian Development: Are Mammalian Embryos Really an Exception? |
Q22337105 | The Structure of the Nervous System of the Nematode Caenorhabditis elegans |
Q28345297 | The T-box factor MLS-1 acts as a molecular switch during specification of nonstriated muscle in C. elegans |
Q47069121 | The T-box factor TBX-2 and the SUMO conjugating enzyme UBC-9 are required for ABa-derived pharyngeal 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 |
Q47822426 | The TBP-like factor CeTLF is required to activate RNA polymerase II transcription during C. elegans embryogenesis. |
Q38321297 | The TRA-1A sex determination protein of C. elegans regulates sexually dimorphic cell deaths by repressing the egl-1 cell death activator gene |
Q47069018 | The UNC-3 Olf/EBF protein represses alternate neuronal programs to specify chemosensory neuron identity |
Q28264908 | The VAB-1 Eph receptor tyrosine kinase functions in neural and epithelial morphogenesis in C. elegans |
Q35621372 | The age of model organisms |
Q92998004 | The amino acid transporter SLC-36.1 cooperates with PtdIns3P 5-kinase to control phagocytic lysosome reformation |
Q40185917 | The antiparasitic activity of avenacosides against intestinal nematodes. |
Q34126620 | The art and design of genetic screens: 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'. |
Q59072157 | The best supporting actors |
Q33893322 | The caenorhabditis elegans fate-determining gene mab-9 encodes a T-box protein required to pattern the posterior hindgut |
Q33908341 | The ced-8 gene controls the timing of programmed cell deaths in C. elegans. |
Q41461117 | The cellular basis of sea urchin gastrulation |
Q53394853 | The cellular geometry of growth drives the amino acid economy of Caenorhabditis elegans. |
Q58413846 | The central nervous system of the ascidian larva: mitotic history of cells forming the neural tube in late embryonic Ciona intestinalis |
Q37305286 | The central role of neuroinformatics in the National Academy of Engineering's grandest challenge: reverse engineer the brain |
Q30513497 | The characterization of the Caenorhabditis elegans mitochondrial thioredoxin system uncovers an unexpected protective role of thioredoxin reductase 2 in β-amyloid peptide toxicity |
Q41306445 | The ciliary transition zone functions in cell adhesion but is dispensable for axoneme assembly in C. elegans |
Q47188342 | The combinatorial control of alternative splicing in C. elegans |
Q46563375 | The combined action of two intercellular signaling pathways specifies three cell fates during vulval induction in C. elegans |
Q35685996 | The concept of space and competition in immune regulation |
Q33979402 | The conserved miR-51 microRNA family is redundantly required for embryonic development and pharynx attachment in Caenorhabditis elegans |
Q42632954 | The conserved nuclear receptor Ftz-F1 is required for embryogenesis, moulting and reproduction in Caenorhabditis elegans |
Q47068906 | The conserved zinc finger protein VAB-23 is an essential regulator of epidermal morphogenesis in Caenorhabditis elegans |
Q47068886 | The coordinate regulation of pharyngeal development in C. elegans by lin-35/Rb, pha-1, and ubc-18. |
Q36709968 | The draft genome and transcriptome of Panagrellus redivivus are shaped by the harsh demands of a free-living lifestyle |
Q28611336 | The dynactin complex is required for cleavage plane specification in early Caenorhabditis elegans embryos |
Q27004910 | The early bird catches the worm: new technologies for the Caenorhabditis elegans toolkit |
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 |
Q36102482 | The end of "naive reductionism": rise of systems biology or renaissance of physiology? |
Q35912786 | The engulfment process of programmed cell death in caenorhabditis elegans |
Q28141789 | The ephrin VAB-2/EFN-1 functions in neuronal signaling to regulate epidermal morphogenesis in C. elegans |
Q36434045 | The ever-expanding neuropeptide gene families in the nematode Caenorhabditis elegans |
Q34277353 | The evolution of developmental mechanisms |
Q27023095 | The evolution of early neurogenesis |
Q40728688 | The exoskeleton collagens in Caenorhabditis elegans are modified by prolyl 4-hydroxylases with unique combinations of subunits |
Q40872645 | The expression of two P-glycoprotein (pgp) genes in transgenic Caenorhabditis elegans is confined to intestinal cells |
Q33964433 | The fog-3 gene and regulation of cell fate in the germ line of Caenorhabditis elegans |
Q33208041 | The forces that position a mitotic spindle asymmetrically are tethered until after the time of spindle assembly |
Q40444900 | The forkhead domain gene unc-130 generates chemosensory neuron diversity in C. elegans |
Q28275485 | The four cdc25 genes from the nematode Caenorhabditis elegans |
Q89554679 | The full-length transcriptome of C. elegans using direct RNA sequencing |
Q36597434 | The function and regulation of the GATA factor ELT-2 in the C. elegans endoderm |
Q28291207 | The generation of diversity and pattern in animal development |
Q35944695 | The genetics of hiding the corpse: engulfment and degradation of apoptotic cells in C. elegans and D. melanogaster. |
Q22065318 | The genome of Romanomermis culicivorax: revealing fundamental changes in the core developmental genetic toolkit in Nematoda |
Q34114793 | The germline in C. elegans: origins, proliferation, and silencing |
Q37898072 | The glia of Caenorhabditis elegans |
Q64084839 | The glutathione system and the related thiol network in Caenorhabditis elegans |
Q45937044 | The identification of a Caenorhabditis elegans homolog of p34cdc2 kinase. |
Q34569711 | The identities of sym-2, sym-3 and sym-4, three genes that are synthetically lethal with mec-8 in Caenorhabditis elegans |
Q40585908 | The ins and outs of programmed cell death during C. elegans development |
Q71720215 | The integration of antagonistic reflexes revealed by laser ablation of identified neurons determines habituation kinetics of the Caenorhabditis elegans tap withdrawal response |
Q36275033 | The interplay of stiffness and force anisotropies drives embryo elongation. |
Q21146093 | The left-right polarity puzzle: determining embryonic handedness |
Q34264575 | The lin-12 locus specifies cell fates in Caenorhabditis elegans |
Q50690805 | The lineaging of fluorescently-labeled Caenorhabditis elegans embryos with StarryNite and AceTree. |
Q68721793 | The major gut esterase locus in the nematode Caenorhabditis elegans |
Q38328399 | The many glia of a tiny nematode: studying glial diversity using Caenorhabditis elegans |
Q45984975 | The maternal-to-zygotic transition in embryonic patterning of Caenorhabditis elegans. |
Q24672515 | The microRNAs of Caenorhabditis elegans |
Q40820116 | The minor myosin heavy chain, mhcA, of Caenorhabditis elegans is necessary for the initiation of thick filament assembly |
Q37540119 | The molecular basis of organ formation: insights from the C. elegans foregut |
Q34897748 | The molecular identities of the Caenorhabditis elegans intraflagellar transport genes dyf-6, daf-10 and osm-1 |
Q33834236 | The molecular mechanism of programmed cell death in C. elegans |
Q36402754 | The motor circuit |
Q38105458 | The multiple faces of calcineurin signaling in Caenorhabditis elegans: development, behaviour and aging |
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 |
Q61950353 | The natural history of Caenorhabditis elegans research |
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 |
Q36700088 | The nematode Caenorhabditis elegans as a tool to predict chemical activity on mammalian development and identify mechanisms influencing toxicological outcome |
Q38093212 | The nematode Pristionchus pacificus as a model system for integrative studies in evolutionary biology. |
Q36057305 | The nematode stoma: Homology of cell architecture with improved understanding by confocal microscopy of labeled cell boundaries |
Q36854753 | The neuron classification problem |
Q30815397 | The nongenotoxic carcinogens naphthalene and para-dichlorobenzene suppress apoptosis in Caenorhabditis elegans |
Q35506248 | The nonmuscle myosin regulatory light chain gene mlc-4 is required for cytokinesis, anterior-posterior polarity, and body morphology during Caenorhabditis elegans embryogenesis |
Q33818160 | The novel intestinal filament organizer IFO-1 contributes to epithelial integrity in concert with ERM-1 and DLG-1. |
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 |
Q93049674 | The nucleoside diphosphate kinase NDK-1/NME1 promotes phagocytosis in concert with DYN-1/Dynamin |
Q37475787 | The onset of C. elegans dosage compensation is linked to the loss of developmental plasticity |
Q38798014 | The origin and evolution of cell types |
Q33965273 | The ornithine decarboxylase gene of Caenorhabditis elegans: cloning, mapping and mutagenesis. |
Q38548506 | The perfect C. elegans project: an initial report |
Q33374514 | The perfect storm of tiny RNAs |
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 |
Q43115568 | The polycomb complex protein mes-2/E(z) promotes the transition from developmental plasticity to differentiation in C. elegans embryos. |
Q34607278 | The primary sex determination signal of Caenorhabditis elegans |
Q33923419 | The rich club of the C. elegans neuronal connectome |
Q38645411 | The rise and fall of basal bodies in the nematode Caenorhabditis elegans. |
Q34017450 | The role of C. elegans Ena/VASP homolog UNC-34 in neuronal polarity and motility |
Q89527531 | The role of cell lineage in the development of neuronal circuitry and function |
Q36311977 | The role of eggshell and underlying vitelline membrane for normal pattern formation in the early C. elegans embryo |
Q35174458 | The role of mitochondria in the life of the nematode, Caenorhabditis elegans |
Q43454297 | The role of oxygen intermediates in the retention time of diacetyl adaptation in the nematode Caenorhabditis elegans |
Q37117060 | The role of protein phosphatase 4 in regulating microtubule severing in the Caenorhabditis elegans embryo |
Q36310130 | The role of stress in ageing: research on the nematode, Caenorhabditis elegans |
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 |
Q34733633 | The secretory pathway calcium ATPase PMR-1/SPCA1 has essential roles in cell migration during Caenorhabditis elegans embryonic development |
Q51980295 | The simplicity of metazoan cell lineages. |
Q24675812 | The size of the nucleus increases as yeast cells grow |
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. |
Q28647396 | The study of Priapulus caudatus reveals conserved molecular patterning underlying different gut morphogenesis in the Ecdysozoa. |
Q33527545 | The synapsin gene family in basal chordates: evolutionary perspectives in metazoans |
Q22037733 | The tardigrade Hypsibius dujardini, a new model for studying the evolution of development |
Q28588455 | The timing of cortical neurogenesis is encoded within lineages of individual progenitor cells |
Q27314756 | The translational regulators GCN-1 and ABCF-3 act together to promote apoptosis in C. elegans |
Q48545872 | The trickiest family tree in biology. |
Q34117126 | The type I membrane protein EFF-1 is essential for developmental cell fusion |
Q30540553 | The union of somatic gonad precursors and primordial germ cells during Caenorhabditis elegans embryogenesis |
Q36385085 | The use of Caenorhabditis elegans in parasitic nematode research |
Q34280972 | The use of functional genomics in C. elegans for studying human development and disease |
Q35633177 | The worm's sense of smell. Development of functional diversity in the chemosensory system of Caenorhabditis elegans |
Q38568827 | Theory and Practice of Lineage Tracing |
Q34542019 | Three sorting nexins drive the degradation of apoptotic cells in response to PtdIns(3)P signaling |
Q67862538 | Thymocyte Activation and Death: a Mechanism for Molding the T Cell Repertoire |
Q60922548 | Timing mechanism of sexually dimorphic nervous system differentiation |
Q73211895 | Timing of CNS cell generation: a programmed sequence of neuron and glial cell production from isolated murine cortical stem cells |
Q30780782 | Timing of Tissue-specific Cell Division Requires a Differential Onset of Zygotic Transcription during Metazoan Embryogenesis |
Q37145916 | Tissue homogeneity requires inhibition of unequal gene silencing during development |
Q54112891 | Tissue-Specific Functions of fem-2/PP2c Phosphatase and fhod-1/formin During Caenorhabditiselegans Embryonic Morphogenesis. |
Q46366442 | Tissue-specific activities of C. elegans DAF-16 in the regulation of lifespan |
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 |
Q40775385 | Touch receptor development and function in Caenorhabditis elegans |
Q36730299 | Touch sensitivity in Caenorhabditis elegans |
Q28682854 | Toward 959 nematode genomes |
Q36508939 | Toward a global picture of development: lessons from genome-scale analysis in Caenorhabditis elegans embryonic development |
Q36073702 | Toward an understanding of the molecular mechanisms of physiological cell death. |
Q34016126 | Toward understanding the functional role of Ss-RIOK-1, a RIO protein kinase-encoding gene of Strongyloides stercoralis |
Q26853226 | Towards 3D in silico modeling of the sea urchin embryonic development |
Q34942459 | Towards a Tralfamadorian view of the embryo: multidimensional imaging of development |
Q26782656 | Towards understanding the roles of position and geometry on cell fate decisions during preimplantation development |
Q31913870 | Toxicity of the dithiocarbamate fungicide mancozeb to the nontarget soil nematode, Caenorhabditis elegans |
Q34354294 | Tracing the lineage of tracing cell lineages |
Q40340502 | Tracking and Quantifying Developmental Processes in C. elegans Using Open-source Tools |
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 |
Q45284298 | Transcriptional control and patterning of the pho-1 gene, an essential acid phosphatase expressed in the C. elegans intestine |
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 |
Q34388176 | Transcriptional regulator of programmed cell death encoded by Caenorhabditis elegans gene ces-2. |
Q33987754 | Transcriptional upregulation of both egl-1 BH3-only and ced-3 caspase is required for the death of the male-specific CEM neurons |
Q34386523 | Transdifferentiation and remodeling of post-embryonic C. elegans cells by a single transcription factor |
Q35751448 | Transgenic nematodes as biosensors for metal stress in soil pore water samples |
Q38752205 | Translational Control of Germ Cell Decisions |
Q47069366 | Translational control of maternal glp-1 mRNA by POS-1 and its interacting protein SPN-4 in Caenorhabditis elegans |
Q50652230 | Translational repression restricts expression of the C. elegans Nanos homolog NOS-2 to the embryonic germline. |
Q37578034 | Transorganogenesis and transdifferentiation in C. elegans are dependent on differentiated cell identity |
Q47068976 | Trithorax, Hox, and TALE-class homeodomain proteins ensure cell survival through repression of the BH3-only gene egl-1. |
Q90776762 | Twenty million years of evolution: The embryogenesis of four Caenorhabditis species are indistinguishable despite extensive genome divergence |
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 |
Q35942369 | Two alternative mechanisms that regulate the presentation of apoptotic cell engulfment signal in Caenorhabditis elegans |
Q36774418 | Two novel transmembrane protein tyrosine kinases expressed during Caenorhabditis elegans hypodermal development |
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 |
Q47069426 | UNC-39, the C. elegans homolog of the human myotonic dystrophy-associated homeodomain protein Six5, regulates cell motility and differentiation |
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 |
Q44275086 | UNC-85, a C. elegans homolog of the histone chaperone Asf1, functions in post-embryonic neuroblast replication |
Q100456054 | Ubiquitin-dependent regulation of a conserved DMRT protein controls sexually dimorphic synaptic connectivity and behavior |
Q52663455 | Ultra-structural time-course study in the C. elegans model for Duchenne muscular dystrophy highlights a crucial role for sarcomere-anchoring structures and sarcolemma integrity in the earliest steps of the muscle degeneration process. |
Q74023749 | Ultrastructure of the post-corpus of Zeldia punctata (Cephalobina) for analysis of the evolutionary framework of nematodes related to Caenorhabditis elegans (Rhabditina) |
Q52315637 | Unconventional function of an Achaete-Scute homolog as a terminal selector of nociceptive neuron identity. |
Q35236830 | Uncoupling different characteristics of the C. elegans E lineage from differentiation of intestinal markers |
Q50868215 | Understanding cell migration guidance: lessons from sex myoblast migration in C. elegans. |
Q37689079 | Understanding the role of asymmetric cell division in cancer using C. elegans |
Q91130628 | Unravelling cellular relationships during development and regeneration using genetic lineage tracing |
Q38122046 | Unravelling stem cell dynamics by lineage tracing |
Q36610073 | Untwisting the Caenorhabditis elegans embryo |
Q52062732 | Unusual cleavage and gastrulation in a freshwater nematode: developmental and phylogenetic implications. |
Q34552932 | Use of somatic mutations to quantify random contributions to mouse development |
Q42715239 | Use of transgenic GFP reporter strains of the nematode Caenorhabditis elegans to investigate the patterns of stress responses induced by pesticides and by organic extracts from agricultural soils |
Q77435125 | Using Caenorhabditis elegans to study vesicular transport |
Q33825826 | Using Stage- and Slit-Scanning to Improve Contrast and Optical Sectioning in Dual-View Inverted Light Sheet Microscopy (diSPIM). |
Q45984496 | Using the nematode Caenorhabditis elegans to predict mammalian acute lethality to metallic salts. |
Q30515861 | V-ATPase V1 sector is required for corpse clearance and neurotransmission in Caenorhabditis elegans |
Q34604343 | VAB-8, UNC-73 and MIG-2 regulate axon polarity and cell migration functions of UNC-40 in C. elegans |
Q89595586 | Variability in β-catenin pulse dynamics in a stochastic cell fate decision in C. elegans |
Q59094299 | Variable cell number in nematodes |
Q38271151 | Variation in transcriptome size: are we getting the message? |
Q46009509 | Variations on a theme: Imaging cytokinetic and stable rings in situ using Caenorhabditis elegans. |
Q33966257 | Viable maternal-effect mutations that affect the development of the nematode Caenorhabditis elegans |
Q36532718 | Vinculin is essential for muscle function in the nematode |
Q46718490 | Visualizing Calcium Flux in Freely Moving Nematode Embryos |
Q41890231 | Visualizing neuroblast cytokinesis during C. elegans embryogenesis |
Q28613336 | WRM-1 activates the LIT-1 protein kinase to transduce anterior/posterior polarity signals in C. elegans |
Q42871447 | Watching nuclei move: Insights into how kinesin-1 and dynein function together |
Q50103667 | What Can We Learn About Human Disease from the Nematode C. elegans? |
Q36215907 | Whole-Organism Developmental Expression Profiling Identifies RAB-28 as a Novel Ciliary GTPase Associated with the BBSome and Intraflagellar Transport |
Q24801913 | Whole-genome analysis of temporal gene expression during foregut development |
Q34528428 | Whole-organism lineage tracing by combinatorial and cumulative genome editing |
Q30593069 | Widespread genomic incompatibilities in Caenorhabditis elegans. |
Q34502088 | Wiring optimization can relate neuronal structure and function |
Q35202988 | Wnt pathway components orient a mitotic spindle in the early Caenorhabditis elegans embryo without requiring gene transcription in the responding cell |
Q39758271 | Wnt signaling polarizes an early C. elegans blastomere to distinguish endoderm from mesoderm |
Q38132717 | Wnt signaling through the Ror receptor in the nervous system |
Q30497437 | Wnt/Frizzled signaling controls C. elegans gastrulation by activating actomyosin contractility |
Q35158576 | WormBase: a cross-species database for comparative genomics |
Q34284591 | WormBase: a multi-species resource for nematode biology and genomics |
Q24608819 | WormBase: network access to the genome and biology of Caenorhabditis elegans |
Q41653878 | Worming your way through the genome |
Q37397469 | Worms with a single functional sensory cilium generate proper neuron-specific behavioral output. |
Q64334712 | Wound healing, cellular regeneration and plasticity: the elegans way |
Q54313380 | X-ray inactivation of Caenorhabditis elegans embryos or larvae. |
Q37429057 | You are what you eat: multifaceted functions of autophagy during C. elegans development |
Q36085279 | Z-line formins promote contractile lattice growth and maintenance in striated muscles of C. elegans |
Q50144720 | ZYG-1 promotes limited centriole amplification in the C. elegans seam lineage. |
Q27026019 | Zygotic genome activation during the maternal-to-zygotic transition |
Q52585083 | Zygotic loss of ZEN-4/MKLP1 results in disruption of epidermal morphogenesis in the C. elegans embryo. |
Q34025380 | cdk-7 Is required for mRNA transcription and cell cycle progression in Caenorhabditis elegans embryos |
Q35125298 | ced-4 and proto-oncogene tfg-1 antagonistically regulate cell size and apoptosis in C. elegans |
Q36567824 | cis regulatory requirements for hypodermal cell-specific expression of the Caenorhabditis elegans cuticle collagen gene dpy-7. |
Q33825382 | clk-1, mitochondria, and physiological rates |
Q24336422 | cul-1 is required for cell cycle exit in C. elegans and identifies a novel gene family |
Q37622610 | dad-1, an endogenous programmed cell death suppressor in Caenorhabditis elegans and vertebrates. |
Q37566224 | egl-1: a key activator of apoptotic cell death in C. elegans |
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 |
Q47069132 | eor-1 and eor-2 are required for cell-specific apoptotic death in C. elegans |
Q36936847 | glo-3, a novel Caenorhabditis elegans gene, is required for lysosome-related organelle biogenesis |
Q33971145 | gon-2, a gene required for gonadogenesis 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. |
Q36358538 | large-scale screening for targeted knockouts in the Caenorhabditis elegans genome |
Q45943348 | lin-17 mutations of Caenorhabditis elegans disrupt certain asymmetric cell divisions. |
Q64934077 | mRNA profiling reveals significant transcriptional differences between a multipotent progenitor and its differentiated sister. |
Q34560342 | mec-3, a homeobox-containing gene that specifies differentiation of the touch receptor neurons in C. elegans |
Q37661686 | miRNAs cooperate in apoptosis regulation during C. elegans development |
Q47068867 | pha-2 encodes the C. elegans ortholog of the homeodomain protein HEX and is required for the formation of the pharyngeal isthmus |
Q35204451 | pha-4, an HNF-3 homolog, specifies pharyngeal organ identity in Caenorhabditis elegans |
Q47069280 | pop-1 Encodes an HMG box protein required for the specification of a mesoderm precursor in Early C. elegans embryos |
Q47068717 | rpm-1, a conserved neuronal gene that regulates targeting and synaptogenesis in C. elegans |
Q34941722 | sqv mutants of Caenorhabditis elegans are defective in vulval epithelial invagination |
Q34592502 | synMuv B proteins antagonize germline fate in the intestine and ensure C. elegans survival |
Q39750794 | tcl-2 encodes a novel protein that acts synergistically with Wnt signaling pathways in C. elegans |
Q34414566 | unc-8, a DEG/ENaC family member, encodes a subunit of a candidate mechanically gated channel that modulates C. elegans locomotion |
Q44825556 | vab-8 is a key regulator of posteriorly directed migrations in C. elegans and encodes a novel protein with kinesin motor similarity |
Q28073716 | β-catenin-driven binary cell fate decisions in animal development |
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