scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1032477985 |
P356 | DOI | 10.1038/24550 |
P3181 | OpenCitations bibliographic resource ID | 326141 |
P698 | PubMed publication ID | 9845070 |
P5875 | ResearchGate publication ID | 13442806 |
P2093 | author name string | S Lindquist | |
S L Rutherford | |||
P2860 | cites work | Mutations in Hsp83 and cdc37 impair signaling by the sevenless receptor tyrosine kinase in Drosophila. | Q45975761 |
Ras1 and a putative guanine nucleotide exchange factor perform crucial steps in signaling by the sevenless protein tyrosine kinase. | Q46027909 | ||
Effect of polymorphism in the Drosophila regulatory gene Ultrabithorax on homeotic stability | Q48066973 | ||
Naturally occurring genetic variation affects Drosophila photoreceptor determination. | Q50901453 | ||
CANALIZATION OF DEVELOPMENT AND THE INHERITANCE OF ACQUIRED CHARACTERS | Q59064935 | ||
Coevolution of functionally constrained characters: prerequisites for adaptive versatility | Q71421129 | ||
Mammalian p50Cdc37 is a protein kinase-targeting subunit of Hsp90 that binds and stabilizes Cdk4 | Q24322569 | ||
The human cytosolic molecular chaperones hsp90, hsp70 (hsc70) and hdj-1 have distinct roles in recognition of a non-native protein and protein refolding | Q24562938 | ||
Inhibition of heat shock protein HSP90-pp60v-src heteroprotein complex formation by benzoquinone ansamycins: essential role for stress proteins in oncogenic transformation | Q24564127 | ||
Mutational analysis of Hsp90 function: interactions with a steroid receptor and a protein kinase | Q27932967 | ||
In vivo functions of the Saccharomyces cerevisiae Hsp90 chaperone | Q27937958 | ||
Repression of heat shock transcription factor HSF1 activation by HSP90 (HSP90 complex) that forms a stress-sensitive complex with HSF1 | Q28118304 | ||
HSP90 interacts with and regulates the activity of heat shock factor 1 in Xenopus oocytes | Q33776598 | ||
The heat shock protein 83 (Hsp83) is required for Raf-mediated signalling in Drosophila | Q33886429 | ||
Transient interaction of Hsp90 with early unfolding intermediates of citrate synthase. Implications for heat shock in vivo | Q34307813 | ||
A role for Hsp90 in retinoid receptor signal transduction | Q34454414 | ||
Heat-shock protein hsp90 governs the activity of pp60v-src kinase | Q36449591 | ||
Protein folding and the regulation of signaling pathways | Q40655622 | ||
A role for Hsp90 in cell cycle control: Wee1 tyrosine kinase activity requires interaction with Hsp90. | Q40794316 | ||
Reduced levels of hsp90 compromise steroid receptor action in vivo | Q45391521 | ||
P433 | issue | 6709 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | capacitor | Q5322 |
P304 | page(s) | 336-42 | |
P577 | publication date | 1998-11-26 | |
P1433 | published in | Nature | Q180445 |
P1476 | title | Hsp90 as a capacitor for morphological evolution | |
P478 | volume | 396 |
Q21145225 | "Myc'ed messages": myc induces transcription of E2F1 while inhibiting its translation via a microRNA polycistron |
Q59077589 | . . . but yeast prion offers clues about evolution |
Q27683567 | 300-Fold Increase in Production of the Zn2+-Dependent Dechlorinase TrzN in Soluble Form via Apoenzyme Stabilization |
Q37110334 | A Caenorhabditis elegans genetic-interaction map wiggles into view |
Q30616556 | A DPP-mediated feed-forward loop canalizes morphogenesis during Drosophila dorsal closure |
Q28552332 | A High Temperature-Dependent Mitochondrial Lipase EXTRA GLUME1 Promotes Floral Phenotypic Robustness against Temperature Fluctuation in Rice (Oryza sativa L.) |
Q34631852 | A cellular perspective on conformational disease: the role of genetic background and proteostasis networks |
Q28252463 | A chaperome subnetwork safeguards proteostasis in aging and neurodegenerative disease |
Q37000945 | A conformational switch in the ligand-binding domain regulates the dependence of the glucocorticoid receptor on Hsp90. |
Q73561207 | A critical role for the proteasome activator PA28 in the Hsp90-dependent protein refolding |
Q33847031 | A gene's ability to buffer variation is predicted by its fitness contribution and genetic interactions |
Q30443642 | A generalized combinatorial approach for detecting gene-by-gene and gene-by-environment interactions with application to nicotine dependence |
Q52175078 | A genetic analysis of the relationship between life-history variation and heat-shock tolerance in Drosophila buzzatii. |
Q28755549 | A genetic code alteration generates a proteome of high diversity in the human pathogen Candida albicans |
Q40969134 | A genomics approach to the chaperone network of Arabidopsis thaliana |
Q73977972 | A glucosinolate mutant of Arabidopsis is thermosensitive and defective in cytosolic Hsp90 expression after heat stress |
Q40631570 | A high-affinity conformation of Hsp90 confers tumour selectivity on Hsp90 inhibitors |
Q34692567 | A highly charged region in the middle domain of plant endoplasmic reticulum (ER)-localized heat-shock protein 90 is required for resistance to tunicamycin or high calcium-induced ER stresses. |
Q37291878 | A mother's sacrifice: what is she keeping for herself? |
Q52701895 | A naturally occurring variant of Hsp90 that is associated with decanalization. |
Q28539763 | A network characteristic that correlates environmental and genetic robustness |
Q42158646 | A novel chaperone-activity-reducing mechanism of the 90-kDa molecular chaperone HSP90. |
Q27930628 | A novel mode of chaperone action: heme activation of Hap1 by enhanced association of Hsp90 with the repressed Hsp70-Hap1 complex. |
Q33682731 | A population threshold for functional polymorphisms |
Q38041770 | A prescription for 'stress'--the role of Hsp90 in genome stability and cellular adaptation |
Q51974966 | A primary role of developmental instability in sexual selection. |
Q31042817 | A protein evolution model with independent sites that reproduces site-specific amino acid distributions from the Protein Data Bank |
Q33831051 | A proteomics approach to decipher the molecular nature of planarian stem cells |
Q28533944 | A purine analog synergizes with chloroquine (CQ) by targeting Plasmodium falciparum Hsp90 (PfHsp90) |
Q37216954 | A rheostat model for a rapid and reversible form of imprinting-dependent evolution |
Q39236769 | A rhizosphere fungus enhances Arabidopsis thermotolerance through production of an HSP90 inhibitor |
Q46294002 | A role for LAX2 in regulating xylem development and lateral-vein symmetry in the leaf |
Q91627037 | A role for epigenetic adaption in evolution |
Q35668881 | A screen for enhancers of clearance identifies huntingtin as a heat shock protein 90 (Hsp90) client protein. |
Q52607470 | A sibling method for identifying vQTLs. |
Q33267330 | A single basis for developmental buffering of Drosophila wing shape |
Q34416447 | A subclass of plant heat shock cognate 70 chaperones carries a motif that facilitates trafficking through plasmodesmata. |
Q39019558 | A systematic survey of in vivo obligate chaperonin-dependent substrates |
Q34731338 | A systems biological view of intracellular pathogens |
Q38664570 | A toxic imbalance of Hsp70s in Saccharomyces cerevisiae is caused by competition for cofactors. |
Q35890257 | A trans-acting Variant within the Transcription Factor RIM101 Interacts with Genetic Background to Determine its Regulatory Capacity |
Q28140932 | A yeast prion provides a mechanism for genetic variation and phenotypic diversity |
Q38934775 | Accounting for genetic interactions improves modeling of individual quantitative trait phenotypes in yeast |
Q27851585 | Activity of IPI-504, a novel heat-shock protein 90 inhibitor, in patients with molecularly defined non-small-cell lung cancer |
Q37229448 | Adaptive Genetic Robustness of Escherichia coli Metabolic Fluxes |
Q33302100 | Adaptive evolution of a stress response protein |
Q38839639 | Adenomatous polyposis coli mutants dominantly activate Hsf1-dependent cell stress pathways through inhibition of microtubule dynamics |
Q90479296 | Adiponectin Paradox in Alzheimer's Disease; Relevance to Amyloidogenic Evolvability? |
Q50636467 | Alleviation of deleterious effects of protein mutation through inactivation of molecular chaperones. |
Q50491064 | Altered Transcription and Neofunctionalization of Duplicated Genes Rescue the Harmful Effects of a Chimeric Gene in Brassica napus. |
Q34543463 | Alternative modes of client binding enable functional plasticity of Hsp70. |
Q36360700 | Alternative splicing of Drosophila Nmnat functions as a switch to enhance neuroprotection under stress |
Q28237753 | An RNA aptamer perturbs heat shock transcription factor activity in Drosophila melanogaster |
Q35865381 | An erythroid chaperone that facilitates folding of alpha-globin subunits for hemoglobin synthesis |
Q44048499 | An evaluation of Hsp90 as a mediator of cortical patterning in Tetrahymena |
Q34627252 | An evolutionary perspective on epistasis and the missing heritability |
Q39244663 | An overview on molecular chaperones enhancing solubility of expressed recombinant proteins with correct folding |
Q74381639 | Analysing phenotypic variation: when old-fashioned means up-to-date |
Q34185278 | Ancestors and variants: tales from the cryptic |
Q42033067 | Aneuploidy underlies rapid adaptive evolution of yeast cells deprived of a conserved cytokinesis motor |
Q47883626 | Antibodies specific for heat shock proteins in human and murine malaria |
Q40178192 | Antiviral activity and RNA polymerase degradation following Hsp90 inhibition in a range of negative strand viruses |
Q35185548 | Apoptosis, necrosis and cellular senescence: chaperone occupancy as a potential switch |
Q27011896 | Asparagine repeats in Plasmodium falciparum proteins: good for nothing? |
Q36182585 | Assisted reproduction: the epigenetic perspective |
Q34631335 | Asymmetric flies: the control of developmental noise in Drosophila. |
Q40822867 | Bag1-Hsp70 mediates a physiological stress signalling pathway that regulates Raf-1/ERK and cell growth. |
Q64113359 | Basal and dynamics mRNA expression of muscular HSP108, HSP90, HSF-1 and HSF-2 in thermally manipulated broilers during embryogenesis |
Q35097340 | Between genotype and phenotype: protein chaperones and evolvability |
Q26824767 | Beyond genotype to phenotype: why the phenotype of an individual cannot always be predicted from their genome sequence and the environment that they experience |
Q50237935 | Beyond mean allelic effects: A locus at the major color gene MC1R associates also with differing levels of phenotypic and genetic (co)variance for coloration in barn owls. |
Q36949785 | Beyond orchids and dandelions: testing the 5-HTT "risky" allele for evidence of phenotypic capacitance and frequency-dependent selection |
Q38086999 | Beyond transposons: the epigenetic and somatic functions of the Piwi-piRNA mechanism |
Q37132799 | Bimodal protein solubility distribution revealed by an aggregation analysis of the entire ensemble of Escherichia coli proteins |
Q38373921 | Bimodality of stable and plastic traits in plants |
Q84267290 | Binding mechanism between Hsp90 and Sgt1 explored by homology modeling and molecular dynamics simulations in rice |
Q74573004 | Biochemical networking contributes more to genetic buffering in human and mouse metabolic pathways than does gene duplication |
Q42364021 | Biofilm Formation and Heat Stress Induce Pyomelanin Production in Deep-Sea Pseudoalteromonas sp. SM9913. |
Q53203863 | Biological constraints that limit compensation of a common skeletal trait variant lead to inequivalence of tibial function among healthy young adults. |
Q37634372 | Biological noise to get a sense of direction: an analogy between chemotaxis and stress response |
Q29617468 | Biological robustness |
Q28730028 | Biological robustness: paradigms, mechanisms, and systems principles |
Q36144688 | Biphasic patterns of diversification and the emergence of modules |
Q34446471 | Birth defects and anti-heat shock protein 70 antibodies in early pregnancy |
Q46229590 | Body size patterns in Drosophila inhabiting a mesocosm: interactive effects of spatial variation in temperature and abundance |
Q43572431 | Both the N- and C-terminal chaperone sites of Hsp90 participate in protein refolding |
Q45015767 | Brassinosteroid nuclear signaling recruits HSP90 activity. |
Q38997863 | Bridging the physical scales in evolutionary biology: from protein sequence space to fitness of organisms and populations |
Q33296879 | Buffering mechanisms in aging: a systems approach toward uncovering the genetic component of aging |
Q51504173 | CHIP buffers heterogeneous Bcl-2 expression levels to prevent augmentation of anticancer drug-resistant cell population. |
Q50208902 | Caenorhabditis elegans Genes Affecting Interindividual Variation in Life-span Biomarker Gene Expression. |
Q51358334 | Can evolution of sexual dimorphism be triggered by developmental temperatures? |
Q57086237 | Canalization and developmental stability in the Brachyrrhine mouse |
Q53987291 | Canalization by Selection of de Novo Induced Mutations. |
Q51469680 | Canalization in the critical states of highly connected networks of competing Boolean nodes. |
Q46270612 | Canalization of Tomato Fruit Metabolism |
Q36493258 | Canalization of development by microRNAs |
Q28474898 | Canalization of gene expression and domain shifts in the Drosophila blastoderm by dynamical attractors |
Q28475017 | Canalization of gene expression in the Drosophila blastoderm by gap gene cross regulation |
Q36501656 | Canalization of genetic and pharmacological perturbations in developing primary neuronal activity patterns |
Q34637648 | Canalization of segmentation and its evolution in Drosophila. |
Q28583715 | Canalization, developmental stability, and morphological integration in primate limbs |
Q35194013 | Cancer as robust intrinsic state of endogenous molecular-cellular network shaped by evolution |
Q58993941 | Cause and effect in evolution |
Q35588824 | Cdc37 goes beyond Hsp90 and kinases |
Q47121267 | Cdc7-Dbf4-mediated phosphorylation of HSP90-S164 stabilizes HSP90-HCLK2-MRN complex to enhance ATR/ATM signaling that overcomes replication stress in cancer |
Q39645338 | Cell cycle transition under stress conditions controlled by vertebrate heat shock factors |
Q33771248 | Cellular proteomes have broad distributions of protein stability |
Q91344872 | CgSTE11 mediates cross tolerance to multiple environmental stressors in Candida glabrata |
Q33692244 | Chance favors the prepared genome |
Q34668840 | Changes in the transcriptome of the malaria parasite Plasmodium falciparum during the initial phase of transmission from the human to the mosquito |
Q24804271 | Channelling evolution: canalization and the nervous system |
Q36642450 | Chaperone and anti-chaperone: two-faced synuclein as stimulator of synaptic evolution |
Q92024438 | Chaperone biomarkers of lifespan and penetrance track the dosages of many other proteins |
Q47596318 | Chaperone overload is a possible contributor to 'civilization diseases'. |
Q34815474 | Chaperones and aging: role in neurodegeneration and in other civilizational diseases |
Q34966121 | Chaperones come of age. |
Q41565850 | Chaperones rescue the energetic landscape of mutant CFTR at single molecule and in cell. |
Q57027551 | Chaperones, Canalization, and Evolution of Animal Forms |
Q40183775 | Chaperones: needed for both the good times and the bad times |
Q43068402 | Chaperonin GroEL/GroES Over-Expression Promotes Aminoglycoside Resistance and Reduces Drug Susceptibilities in Escherichia coli Following Exposure to Sublethal Aminoglycoside Doses. |
Q28247346 | Chaperonin overexpression promotes genetic variation and enzyme evolution |
Q48069881 | Chaperoning epigenetics: FKBP51 decreases the activity of DNMT1 and mediates epigenetic effects of the antidepressant paroxetine |
Q44315461 | Characterization of a plant homolog of hop, a cochaperone of hsp90. |
Q34645228 | Characterization of conditionally expressed mutants affecting age-specific survival in inbred lines of Drosophila melanogaster: lethal conditions and temperature-sensitive periods. |
Q29012569 | Characterization of the 105-kDa molecular chaperone |
Q89876909 | Chemical Biology Framework to Illuminate Proteostasis |
Q36655158 | Chemical Tools to Investigate Mechanisms Associated with HSP90 and HSP70 in Disease |
Q41971592 | Chemical chaperones assist intracellular folding to buffer mutational variations. |
Q34152568 | Chromatin regulators as capacitors of interspecies variations in gene expression |
Q41472536 | Chromatin regulators shape the genotype-phenotype map. |
Q37707546 | Chromatin regulators, phenotypic robustness, and autism risk |
Q43220563 | Circumventing HSP90 inhibitors via apoptosis block |
Q37677249 | Cloning and expression of a cytosolic HSP90 gene in Chlorella vulgaris |
Q39691708 | Co-chaperones are limiting in a depleted chaperone network |
Q36814334 | Co-expression of chaperones from P. furiosus enhanced the soluble expression of the recombinant hyperthermophilic α-amylase in E. coli |
Q35930811 | Combined HSP90 and kinase inhibitor therapy: Insights from The Cancer Genome Atlas. |
Q92677800 | Commensal Gut Bacteria Buffer the Impact of Host Genetic Variants on Drosophila Developmental Traits under Nutritional Stress |
Q21266601 | Comparative genomics and evolution of the HSP90 family of genes across all kingdoms of organisms |
Q55438167 | Comparisons of Expression Levels of Heat Shock Proteins (hsp70 and hsp90) From Anaphothrips obscurus (Thysanoptera: Thripidae) in Polymorphic Adults Exposed to Different Heat Shock Treatments. |
Q34060169 | Competing views on cancer |
Q40110092 | Complexity of Hsp90 in organelle targeting. |
Q90029099 | Comprehensive fitness maps of Hsp90 show widespread environmental dependence |
Q47362539 | Computational Analysis of the Chaperone Interaction Networks |
Q47561894 | Computing the Extended Synthesis: Mapping the Dynamics and Conceptual Structure of the Evolvability Research Front |
Q37854116 | Conformational dynamics of the molecular chaperone Hsp90 |
Q39627392 | Constant, cycling, hot and cold thermal environments: strong effects on mean viability but not on genetic estimates. |
Q33944549 | Contribution of individual random mutations to genotype-by-environment interactions in Escherichia coli |
Q33267332 | Control of canalization and evolvability by Hsp90 |
Q34984598 | Converging concepts of protein folding in vitro and in vivo |
Q41812975 | Conversion of a chaperonin GroEL-independent protein into an obligate substrate |
Q50233779 | Cooperativity of Negative Autoregulation Confers Increased Mutational Robustness. |
Q57191467 | Coping with predator stress: interclonal differences in induction of heat-shock proteins in the water flea Daphnia magna |
Q52062053 | Craniofacial variability and morphological integration in mice susceptible to cleft lip and palate. |
Q34675896 | Cross signaling, cell specificity, and physiology |
Q51536828 | Crouching variation revealed. |
Q37057427 | Cryptic Genetic Variation in Evolutionary Developmental Genetics |
Q47741423 | Cryptic clues revealed |
Q47382840 | Cryptic genetic variation and body size evolution in threespine stickleback. |
Q24545852 | Cryptic genetic variation is enriched for potential adaptations |
Q34189506 | Cryptic genetic variation promotes rapid evolutionary adaptation in an RNA enzyme |
Q46849730 | Cryptic genetic variation uncovers evolution of environmentally sensitive parameters in Caenorhabditis vulval development |
Q36534143 | Cryptic genetic variation: evolution's hidden substrate |
Q33638416 | Cryptic variation between species and the basis of hybrid performance |
Q34391913 | Cryptic variation in morphological evolution: HSP90 as a capacitor for loss of eyes in cavefish. |
Q45127910 | Cryptic variation in vulva development by cis-regulatory evolution of a HAIRY-binding site |
Q36336642 | Current ideas about applications of heat shock proteins in vaccine design and immunotherapy |
Q38222613 | Current understanding of the formation and adaptation of metabolic systems based on network theory |
Q89567300 | Cyclin G and the Polycomb Repressive complexes PRC1 and PR-DUB cooperate for developmental stability |
Q33981313 | DAF-12 regulates a connected network of genes to ensure robust developmental decisions. |
Q38488673 | Darwin's legacy II: why biology is not physics, or why it has taken a century to see the dependence of genes on the environment |
Q35655390 | Dearth of polymorphism associated with a sustained response to selection for flowering time in maize |
Q36551570 | Decanalization of wing development accompanied the evolution of large wings in high-altitude Drosophila |
Q88641892 | Decanalizing thinking on genetic canalization |
Q26810004 | Deciphering morphology in Triatominae: the evolutionary signals |
Q51839556 | Deficiency mapping of the genomic regions associated with effects on developmental stability in Drosophila melanogaster. |
Q39558750 | Deficiency screening for genomic regions with effects on environmental sensitivity of the sensory bristles of Drosophila melanogaster |
Q34438056 | Defining and interpreting intraspecific molecular variation |
Q28673578 | Degeneracy allows for both apparent homogeneity and diversification in populations |
Q40292207 | Depletion of hsp90beta induces multiple defects in B cell receptor signaling. |
Q27312600 | Destabilizing protein polymorphisms in the genetic background direct phenotypic expression of mutant SOD1 toxicity |
Q35065527 | Detecting major genetic loci controlling phenotypic variability in experimental crosses |
Q27314802 | Determinative developmental cell lineages are robust to cell deaths |
Q31108274 | Development of a purine-scaffold novel class of Hsp90 binders that inhibit the proliferation of cancer cells and induce the degradation of Her2 tyrosine kinase |
Q24546686 | Development of bat flight: morphologic and molecular evolution of bat wing digits |
Q35901753 | Developmental Patterning as a Quantitative Trait: Genetic Modulation of the Hoxb6 Mutant Skeletal Phenotype |
Q58750848 | Developmental Plasticity and Robustness of a Nematode Mouth-Form Polyphenism |
Q51980251 | Developmental expression of Hsp90, Hsp70 and HSF during morphogenesis in the vetigastropod Haliotis asinina. |
Q52118951 | Developmental genetics: buffer zone. |
Q36333337 | Developmental instability as an estimator of genetic stress. |
Q50717903 | Developmental instability is genetically correlated with phenotypic plasticity, constraining heritability, and fitness. |
Q36837933 | Developmental mechanisms underlying variable, invariant and plastic phenotypes. |
Q35143386 | Developmental noise, ageing and cancer |
Q46246522 | Developmental nonlinearity drives phenotypic robustness. |
Q28749056 | Developmental plasticity and the evolution of animal complex life cycles |
Q33265021 | Developmental plasticity mirrors differences among taxa in spadefoot toads linking plasticity and diversity |
Q31036657 | Developmental stability: a major role for cyclin G in drosophila melanogaster |
Q55498494 | Diet and hormonal manipulation reveal cryptic genetic variation: implications for the evolution of novel feeding strategies. |
Q33942363 | Difference in the distribution pattern of substrate enzymes in the metabolic network of Escherichia coli, according to chaperonin requirement |
Q35597014 | Differences in performance and transcriptome-wide gene expression associated with Rhagoletis (Diptera: Tephritidae) larvae feeding in alternate host fruit environments |
Q52781556 | Different effects of paternal trans-generational immune priming on survival and immunity in step and genetic offspring. |
Q36677331 | Differential Masking of Natural Genetic Variation by miR-9a in Drosophila |
Q41897731 | Differential Regulation of Cryptic Genetic Variation Shapes the Genetic Interactome Underlying Complex Traits |
Q35579665 | Differential dependence on N-glycosylation of anthrax toxin receptors CMG2 and TEM8 |
Q33849171 | Differential effects of developmental thermal plasticity across three generations of guppies (Poecilia reticulata): canalization and anticipatory matching |
Q90611727 | Differential gene expression during substrate probing in larvae of the Caribbean coral Porites astreoides |
Q28238796 | Direct activation of HSP90A transcription by c-Myc contributes to c-Myc-induced transformation |
Q55025456 | Direct measurement of pervasive weak repression by microRNAs and their role at the network level. |
Q33299477 | Direct selection on genetic robustness revealed in the yeast transcriptome. |
Q57092294 | Directional selection reduces developmental canalization against genetic and environmental perturbations in Drosophila wings |
Q37095239 | Discovering susceptibility genes for asthma and allergy |
Q50482111 | Disintegrating the fly: A mutational perspective on phenotypic integration and covariation. |
Q28140363 | Disruption of hsp90 function results in degradation of the death domain kinase, receptor-interacting protein (RIP), and blockage of tumor necrosis factor-induced nuclear factor-kappaB activation |
Q46113733 | Dissection of the ATP-induced conformational cycle of the molecular chaperone Hsp90. |
Q36974987 | Diverse genetic architectures lead to the same cryptic phenotype in a yeast cross |
Q36178618 | Diversify or die: generation of diversity in response to stress. |
Q36983160 | DnaK-Dependent Accelerated Evolutionary Rate in Prokaryotes |
Q36095587 | Do plants and animals differ in phenotypic plasticity? |
Q35213567 | Do the different parental 'heteromes' cause genomic shock in newly formed allopolyploids? |
Q28252644 | Do we need an extended evolutionary synthesis? |
Q35923107 | Does stress induce (para)sex? Implications for Candida albicans evolution |
Q34389862 | Does the central dogma still stand? |
Q35132025 | Down-regulation of heat shock protein HSP90ab1 in radiation-damaged lung cells other than mast cells |
Q34043288 | Downregulation of the Hsp90 system causes defects in muscle cells of Caenorhabditis elegans |
Q52838896 | Downregulation of the evolutionary capacitor Hsp90 is mediated by social cues. |
Q46695979 | Dramatic changes in leaf development of the native Capsicum chinense from the Seychelles at temperatures below 24 degrees C. |
Q24600056 | Drosophila Piwi functions in Hsp90-mediated suppression of phenotypic variation |
Q28303213 | Drugging the cancer chaperone HSP90: combinatorial therapeutic exploitation of oncogene addiction and tumor stress |
Q28254233 | Drugging the cancer kinome: progress and challenges in developing personalized molecular cancer therapeutics |
Q37117696 | Dynamic duo takes down fungal villains |
Q36574555 | Dynamics of Dark-Fly Genome Under Environmental Selections |
Q29619032 | EGF-ERBB signalling: towards the systems level |
Q34494155 | Eco-Evo-Devo: developmental symbiosis and developmental plasticity as evolutionary agents |
Q52654283 | Ecologically relevant stress resistance: from microarrays and quantitative trait loci to candidate genes - a research plan and preliminary results using Drosophila as a model organism and climatic and genetic stress as model stresses. |
Q34588948 | Effect of E(sev) and Su(Raf) Hsp83 mutants and trans-heterozygotes on bristle trait means and variation in Drosophila melanogaster |
Q52106778 | Effect of heat shock, pretreatment and hsp70 copy number on wing development in Drosophila melanogaster. |
Q37307182 | Effects of HIV protease inhibitor ritonavir on Akt-regulated cell proliferation in breast cancer |
Q37514523 | Effects of larval crowding on quantitative variation for development time and viability in Drosophila melanogaster |
Q33693917 | Effects of small Hsp genes on developmental stability and microenvironmental canalization |
Q48210380 | Efficacy of Onalespib, a Long-Acting Second-Generation HSP90 Inhibitor, as a Single Agent and in Combination with Temozolomide against Malignant Gliomas |
Q92039391 | Efficient conversion of chemical energy into mechanical work by Hsp70 chaperones |
Q35629412 | Embryo stability and vulnerability in an always changing world |
Q89673807 | Embryonic geometry underlies phenotypic variation in decanalized conditions |
Q37899277 | Emerging model systems in eco-evo-devo: the environmentally responsive spadefoot toad |
Q36788747 | Empirical laws of survival and evolution: their universality and implications |
Q27332084 | Encoding asymmetry of the N-glycosylation motif facilitates glycoprotein evolution |
Q37415449 | Endocrine disruptors in female reproductive tract development and carcinogenesis |
Q28218794 | Endosymbiotic bacteria: groEL buffers against deleterious mutations |
Q29615326 | Engineering stability in gene networks by autoregulation |
Q30480122 | Environmental and genetic modifiers of squint penetrance during zebrafish embryogenesis. |
Q33772654 | Environmental conditions in water storage drums and influences on Aedes aegypti in Trinidad, West Indies. |
Q33782545 | Environmental disruption of host-microbe co-adaptation as a potential driving force in evolution |
Q37764210 | Environmental duress and epistasis: how does stress affect the strength of selection on new mutations? |
Q37587846 | Environmental influences on epigenetic profiles. |
Q36176440 | Environmental signaling and evolutionary change: can exposure of pregnant mammals to environmental estrogens lead to epigenetically induced evolutionary changes in embryos? |
Q44539402 | Environmental stress increases variability in the expression of dental cusps |
Q33889139 | Environmental stress-dependent effects of deletions encompassing Hsp70Ba on canalization and quantitative trait asymmetry in Drosophila melanogaster. |
Q50123026 | Environmentally constrained mutation and adaptive evolution in Salmonella. |
Q83345313 | Epialleles via DNA methylation: consequences for plant evolution |
Q55506430 | Epigenetic control of variation and stochasticity in metabolic disease. |
Q28748764 | Epigenetic effects on the mouse mandible: common features and discrepancies in remodeling due to muscular dystrophy and response to food consistency |
Q29394941 | Epigenetic mechanisms of character origination |
Q35910463 | Epigenetic mechanisms underlying developmental plasticity in horned beetles |
Q59049636 | Epigenetic regulation of translation reveals hidden genetic variation to produce complex traits |
Q35115421 | Epigenetics as an answer to Darwin's "special difficulty," Part 2: natural selection of metastable epialleles in honeybee castes. |
Q34618183 | Epigenomic plasticity within populations: its evolutionary significance and potential. |
Q26824140 | Epistasis and quantitative traits: using model organisms to study gene-gene interactions |
Q35093983 | Essential gene disruptions reveal complex relationships between phenotypic robustness, pleiotropy, and fitness |
Q33760114 | Etiology of fibrous dysplasia and McCune-Albright syndrome |
Q52111267 | Evidence for an epigenetic mechanism by which Hsp90 acts as a capacitor for morphological evolution. |
Q52655578 | Evidence for canalization of Distal-less function in the leg of Drosophila melanogaster. |
Q100526205 | Evidence for secondary-variant genetic burden and non-random distribution across biological modules in a recessive ciliopathy |
Q33967135 | Evidence for the adaptive evolution of mutation rates |
Q35124513 | Evidence for the possible involvement of calmodulin in regulation of steady state levels of Hsp90 family members (Hsp87 and Hsp85) in response to heat shock in sorghum |
Q57685946 | Evolution AfterandBefore Gene Duplication? |
Q41046825 | Evolution of Escherichia coli for growth at high temperatures |
Q47576447 | Evolution of Hsp90 expression in Tetrahymena thermophila (Protozoa, Ciliata) populations exposed to thermally variable environments |
Q50278905 | Evolution of Immunity and Pathogens. |
Q47714195 | Evolution of anatomy and gene control |
Q36099001 | Evolution of animal Piwi-interacting RNAs and prokaryotic CRISPRs |
Q35013179 | Evolution of development in closely related species of flies and worms |
Q42021004 | Evolution of dominance in metabolic pathways. |
Q24816827 | Evolution of genetic potential |
Q35040941 | Evolution of mutational robustness |
Q57093037 | Evolution of the developmental plasticity and a coupling between left mechanosensory neuromasts and an adaptive foraging behavior |
Q52113964 | Evolution of yellow gene regulation and pigmentation in Drosophila. |
Q36825575 | Evolution under canalization and the dual roles of microRNAs: a hypothesis |
Q34671764 | Evolutionary capacitance and control of protein stability in protein-protein interaction networks |
Q28191006 | Evolutionary capacitance as a general feature of complex gene networks |
Q34576553 | Evolutionary capacitance may be favored by natural selection |
Q60620314 | Evolutionary consequences of cryptic genetic variation |
Q52164984 | Evolutionary novelties in islands: Drosophila santomea, a new melanogaster sister species from São Tomé. |
Q35960653 | Evolutionary origins of invasive populations |
Q27627101 | Evolutionary transition pathways for changing peptide ligand specificity and structure |
Q50034432 | Evolvability of Amyloidogenic Proteins in Human Brain. |
Q59090104 | Evolving evolvability |
Q28655926 | Explaining bathymetric diversity patterns in marine benthic invertebrates and demersal fishes: physiological contributions to adaptation of life at depth |
Q35015487 | Explaining intraspecific diversity in plant secondary metabolites in an ecological context |
Q58802587 | Exploiting vulnerabilities in cancer signalling networks to combat targeted therapy resistance |
Q95721479 | Exposure of Caenorhabditis elegans to extremely low frequency high magnetic fields induces stress responses |
Q42997233 | Expression of AeaHsp26 and AeaHsp83 in Aedes aegypti (Diptera: Culicidae) larvae and pupae in response to heat shock stress |
Q37490567 | Expression of a unique drug-resistant Hsp90 ortholog by the nematode Caenorhabditis elegans |
Q42175832 | Expression of hsp70, hsp90 and hsf1 in the reef coral Acropora digitifera under prospective acidified conditions over the next several decades |
Q42576148 | Expression of hsp90 mediates cytoprotective effects in the gastrodermis of planarians. |
Q35083342 | Expression of the small heat-shock protein alphaB-crystallin in tauopathies with glial pathology |
Q33948624 | Expression pattern of heat shock protein 90 gene of humphead snapper Lutjanus sanguineus during pathogenic Vibrio harveyi stress |
Q28679262 | External and internal shell formation in the ramshorn snail Marisa cornuarietis are extremes in a continuum of gradual variation in development |
Q51955760 | Extreme temperatures increase the deleterious consequences of inbreeding under laboratory and semi-natural conditions. |
Q21145369 | Facilitated variation: how evolution learns from past environments to generalize to new environments |
Q37729435 | Factors That Shape Eukaryotic tRNAomes: Processing, Modification and Anticodon-Codon Use |
Q28607448 | Fitness Trade-Offs Determine the Role of the Molecular Chaperonin GroEL in Buffering Mutations |
Q55554499 | Fitness Trade-Offs and Environmentally Induced Mutation Buffering in Isogenic C. elegans |
Q36623195 | Fluctuating asymmetry and developmental instability in evolutionary biology: past, present and future |
Q34575572 | Fluctuating asymmetry as an indicator of fitness: can we bridge the gap between studies? |
Q52111470 | Fluctuating asymmetry--indicator of what? |
Q34594841 | Fluctuation and response in biology |
Q37609461 | Folate modulates Hox gene-controlled skeletal phenotypes. |
Q73679852 | Folding and binding: problems with proteins |
Q30482962 | Foundations for engineering biology |
Q37865526 | From Waddington's epigenetic landscape to small noncoding RNA: some important milestones in the history of epigenetics research |
Q33925704 | From genotype to phenotype: buffering mechanisms and the storage of genetic information |
Q37236447 | From oncogene to network addiction: the new frontier of cancer genomics and therapeutics |
Q80014413 | From worm genetic networks to complex human diseases |
Q40893718 | Function of 90-kDa heat shock protein in cellular differentiation of human embryonal carcinoma cells |
Q35078839 | Functional interactions among morphologic and tissue quality traits define bone quality |
Q93053264 | Functions and mechanisms of epigenetic inheritance in animals |
Q36864694 | Fungal Hsp90: a biological transistor that tunes cellular outputs to thermal inputs |
Q28361532 | Geldanamycin: the prototype of a class of antitumor drugs targeting the heat shock protein 90 family of molecular chaperones |
Q33697209 | Gene expression in the placenta: maternal stress and epigenetic responses |
Q34505897 | Gene expression profiles of cytosolic heat shock proteins Hsp70 and Hsp90 from symbiotic dinoflagellates in response to thermal stress: possible implications for coral bleaching |
Q39969375 | Gene expression profiles of necrosis and apoptosis induced by 5-fluoro-2'-deoxyuridine |
Q47259561 | Gene expression regulation by heat-shock proteins: the cardinal roles of HSF1 and Hsp90. |
Q40126638 | Gene expression stasis and plasticity following migration into a foreign environment. |
Q51983943 | Gene network polymorphism is the raw material of natural selection: the selfish gene network hypothesis. |
Q34649576 | Generators of phenotypic diversity in the evolution of pathogenic microorganisms |
Q21091148 | Genes confer similar robustness to environmental, stochastic, and genetic perturbations in yeast |
Q35574849 | Genetic Architecture of Micro-Environmental Plasticity in Drosophila melanogaster |
Q35078594 | Genetic analysis of speciation by means of introgression into Drosophila melanogaster |
Q24548039 | Genetic analysis of viable Hsp90 alleles reveals a critical role in Drosophila spermatogenesis |
Q27345471 | Genetic and Environmental Control of Neurodevelopmental Robustness in Drosophila |
Q28681527 | Genetic and environmental factors affecting cryptic variations in gene regulatory networks |
Q30992984 | Genetic assimilation: a review of its potential proximate causes and evolutionary consequences |
Q42031257 | Genetic basis of adaptive evolution of a polyphenism by genetic accommodation |
Q99411829 | Genetic buffering and potentiation in metabolism |
Q35845515 | Genetic code evolution reveals the neutral emergence of mutational robustness, and information as an evolutionary constraint |
Q34698874 | Genetic constraints on protein evolution |
Q34489534 | Genetic defects in N-glycosylation and cellular diversity in mammals |
Q44497610 | Genetic dissection of p23, an Hsp90 cochaperone, reveals a distinct surface involved in estrogen receptor signaling |
Q28731289 | Genetic divergence between freshwater and marine morphs of alewife (Alosa pseudoharengus): a 'next-generation' sequencing analysis |
Q40301483 | Genetic instability and divergence of clonal populations in colon cancer cells in vitro. |
Q22122022 | Genetic predisposition to cancer — insights from population genetics |
Q34610326 | Genetic screens for factors involved in the notum bristle loss of interspecific hybrids between Drosophila melanogaster and D. simulans |
Q38104420 | Genetic susceptibility and mechanisms for refractive error |
Q34614118 | Genetic variation for phenotypically invariant traits detected in teosinte: implications for the evolution of novel forms. |
Q34331502 | Genetic variation in cancer predisposition: mutational decay of a robust genetic control network |
Q47288161 | Genetic variation in variability: Phenotypic variability of fledging weight and its evolution in a songbird population. |
Q33379081 | Genetical genomics: spotlight on QTL hotspots |
Q35157836 | Genetically determined phenotype covariation networks control bone strength |
Q34192551 | Genetics and the making of Homo sapiens |
Q38747548 | Genetics of Genome-Wide Recombination Rate Evolution in Mice from an Isolated Island |
Q28394588 | Genetics of healthy aging and longevity |
Q35963002 | Genetics of microenvironmental canalization in Arabidopsis thaliana |
Q39726084 | Genome sequence of Saccharomyces carlsbergensis, the world's first pure culture lager yeast. |
Q34845890 | Genome-scale co-evolutionary inference identifies functions and clients of bacterial Hsp90 |
Q34894739 | Genome-wide analysis of the Populus Hsp90 gene family reveals differential expression patterns, localization, and heat stress responses |
Q51753273 | Genome-wide high-frequency non-Mendelian loss of heterozygosity in rice. |
Q34405735 | Genome-wide non-mendelian inheritance of extra-genomic information in Arabidopsis |
Q50085780 | Genomic buffering mitigates the effects of deleterious mutations in bacteria. |
Q64963172 | Genomic clustering of fitness-affecting mutations favors the evolution of chromosomal instability. |
Q37117012 | Genomic consequences of background effects on scalloped mutant expressivity in the wing of Drosophila melanogaster |
Q101051150 | Genotype by environment interaction for gene expression in Drosophila melanogaster |
Q38077445 | Genotype to phenotype: lessons from model organisms for human genetics |
Q52099216 | Genotype-specific responses of fluctuating asymmetry and of preadult survival to the effects of lead and temperature stress in Drosophila melanogaster |
Q34153590 | Glycoprotein folding in the endoplasmic reticulum |
Q38764474 | Goldfish morphology as a model for evolutionary developmental biology. |
Q41990114 | Group II archaeal chaperonin recognition of partially folded human γD-crystallin mutants |
Q42480755 | HEAT SHOCK PROTEIN 90C is a bona fide Hsp90 that interacts with plastidic HSP70B in Chlamydomonas reinhardtii |
Q42380877 | HSP90 Inhibition and Cellular Stress Elicits Phenotypic Plasticity in Hematopoietic Differentiation |
Q92519795 | HSP90 Molecular Chaperones, Metabolic Rewiring, and Epigenetics: Impact on Tumor Progression and Perspective for Anticancer Therapy |
Q38953212 | HSP90 Shapes the Consequences of Human Genetic Variation |
Q36183675 | HSP90 Stabilizes Auxin-Responsive Phenotypes by Masking a Mutation in the Auxin Receptor TIR1. |
Q36498432 | HSP90 affects the expression of genetic variation and developmental stability in quantitative traits |
Q29617504 | HSP90 and the chaperoning of cancer |
Q34482045 | HSP90 as a new therapeutic target for cancer therapy: the story unfolds |
Q29616824 | HSP90 at the hub of protein homeostasis: emerging mechanistic insights |
Q50517360 | HSP90 canonical content organizes a molecular scaffold mechanism to progress flowering. |
Q34793260 | HSP90 empowers evolution of resistance to hormonal therapy in human breast cancer models |
Q36377911 | HSP90 stabilizes auxin receptor TIR1 and ensures plasticity of auxin responses |
Q47734561 | HSP90, a capacitor of behavioral variation |
Q36498436 | HSP90-buffered genetic variation is common in Arabidopsis thaliana |
Q38584468 | HSP90AB1: Helping the good and the bad. |
Q34510091 | HSP90α plays an important role in piRNA biogenesis and retrotransposon repression in mouse |
Q36279553 | Hallmarks of therapeutic management of the cystic fibrosis functional landscape. |
Q26774064 | Hazards inherent in interdisciplinary behavioral research |
Q40925552 | Heat Shock Protein 90 regulates encystation in Entamoeba |
Q90080306 | Heat Shock Proteins Are Essential Components in Transformation and Tumor Progression: Cancer Cell Intrinsic Pathways and Beyond |
Q37013952 | Heat Shock Proteins Promote Cancer: It's a Protection Racket |
Q48331448 | Heat shock and developmental expression of hsp83 in the filarial nematode Brugia pahangi |
Q36834709 | Heat shock genes - integrating cell survival and death |
Q37547517 | Heat shock protein 83 plays pleiotropic roles in embryogenesis, longevity, and fecundity of the pea aphid Acyrthosiphon pisum |
Q34351999 | Heat shock protein 90 as a drug target against protozoan infections: biochemical characterization of HSP90 from Plasmodium falciparum and Trypanosoma evansi and evaluation of its inhibitor as a candidate drug |
Q38357729 | Heat shock protein 90 function is essential for Plasmodium falciparum growth in human erythrocytes. |
Q39230727 | Heat shock protein 90 homeostasis controls stage differentiation in Leishmania donovani |
Q38971900 | Heat shock protein 90 maintains the stability and function of transcription factor Broad Z7 by interacting with its Broad-Complex-Tramtrack-Bric-a-brac domain. |
Q36362840 | Heat shock protein 90 mediates macrophage activation by Taxol and bacterial lipopolysaccharide |
Q52708029 | Heat shock protein 90: a capacitor or a mutator? |
Q36834685 | Heat shock protein 90: the cancer chaperone |
Q35038788 | Heat shock protein and proteasome targeting agents |
Q35916107 | Heat shock protein-90 dampens and directs signaling stimulated by insulin-like growth factor-1 and insulin |
Q21195216 | Heat shock protein-90-alpha, a prolactin-STAT5 target gene identified in breast cancer cells, is involved in apoptosis regulation |
Q37777181 | Heat shock proteins (chaperones) in fish and shellfish and their potential role in relation to fish health: a review |
Q34479725 | Heat shock proteins and Drosophila aging |
Q50567847 | Heat shock proteins and cancer: intracellular chaperones or extracellular signalling ligands? |
Q28272905 | Heat shock proteins and heat shock factor 1 in carcinogenesis and tumor development: an update |
Q26864311 | Heat shock proteins at the crossroads between cancer and Alzheimer's disease |
Q64264862 | Heat shock proteins create a signature to predict the clinical outcome in breast cancer |
Q35070272 | Heat shock proteins in breast cancer progression--a suitable case for treatment? |
Q35210928 | Heat shock proteins in relation to heat stress tolerance of creeping bentgrass at different N levels |
Q38737242 | Heat-Shock Protein 90-Targeted Nano Anticancer Therapy |
Q33259824 | Heat-shock promoters: targets for evolution by P transposable elements in Drosophila |
Q36066038 | Heat-shock protein 90 inhibitors as novel cancer chemotherapeutics - an update |
Q36004744 | Heat-shock treatment-mediated increase in transduction by recombinant adeno-associated virus 2 vectors is independent of the cellular heat-shock protein 90 |
Q28510837 | Hectd1 is required for development of the junctional zone of the placenta |
Q92471557 | Heterogeneity of primordial germ cells |
Q60054363 | Heterologous Hsp90 promotes phenotypic diversity through network evolution |
Q50656194 | Hidden genetic variation evolves with ecological specialization: the genetic basis of phenotypic plasticity in Arctic charr ecomorphs. |
Q51406685 | High temperatures reveal cryptic genetic variation in a polymorphic female sperm storage organ. |
Q96609310 | Highly parallel lab evolution reveals that epistasis can curb the evolution of antibiotic resistance |
Q31130020 | Histone variant HTZ1 shows extensive epistasis with, but does not increase robustness to, new mutations |
Q33861840 | Hormesis: an adaptive expectation with emphasis on ionizing radiation |
Q36780484 | Hormetic modulation of aging and longevity by mild heat stress |
Q41671786 | Host proteostasis modulates influenza evolution. |
Q42940088 | How do eubacterial organisms manage aggregation-prone proteome? |
Q38982331 | How plasticity, genetic assimilation and cryptic genetic variation may contribute to adaptive radiations. |
Q55191686 | Hsf1 Phosphorylation Generates Cell-to-Cell Variation in Hsp90 Levels and Promotes Phenotypic Plasticity. |
Q73500917 | Hsp70 (DnaK)--an evolution facilitator? |
Q58477233 | Hsp70 and Hsp90 change their expression and subcellular localization after microspore embryogenesis induction in Brassica napus L |
Q39956857 | Hsp70 and thermal pretreatment mitigate developmental damage caused by mitotic poisons in Drosophila |
Q24644472 | Hsp70 chaperones: cellular functions and molecular mechanism |
Q84551753 | Hsp70 molecular chaperones are required to support p53 tumor suppressor activity under stress conditions |
Q33632917 | Hsp90 & Co. - a holding for folding |
Q59792755 | Hsp90 Stabilizes SIRT1 Orthologs in Mammalian Cells and |
Q37214963 | Hsp90 affecting chromatin remodeling might explain transgenerational epigenetic inheritance in Drosophila |
Q33607477 | Hsp90 and co-chaperones twist the functions of diverse client proteins |
Q36088933 | Hsp90 and environmental impacts on epigenetic states: a model for the trans-generational effects of diethylstibesterol on uterine development and cancer |
Q34157465 | Hsp90 and environmental stress transform the adaptive value of natural genetic variation |
Q29618584 | Hsp90 as a capacitor of phenotypic variation |
Q36635195 | Hsp90 as a target for drug development |
Q36581399 | Hsp90 at the crossroads of genetics and epigenetics |
Q34173907 | Hsp90 depletion goes wild |
Q35823157 | Hsp90 inhibitors and drug resistance in cancer: the potential benefits of combination therapies of Hsp90 inhibitors and other anti-cancer drugs |
Q37277287 | Hsp90 inhibitors and the reduction of anti-cancer drug resistance by non-genetic and genetic mechanisms |
Q34583912 | Hsp90 inhibitors as novel cancer chemotherapeutic agents |
Q34173374 | Hsp90 is important for fecundity, longevity, and buffering of cryptic deleterious variation in wild fly populations. |
Q34427556 | Hsp90 modulates CAG repeat instability in human cells |
Q92501257 | Hsp90 of E. coli modulates assembly of FtsZ, the bacterial tubulin homolog |
Q28475988 | Hsp90 orchestrates stress response signaling governing fungal drug resistance |
Q41995021 | Hsp90 orchestrates temperature-dependent Candida albicans morphogenesis via Ras1-PKA signaling |
Q34539771 | Hsp90 orchestrates transcriptional regulation by Hsf1 and cell wall remodelling by MAPK signalling during thermal adaptation in a pathogenic yeast |
Q28204780 | Hsp90 phosphorylation is linked to its chaperoning function. Assembly of the reovirus cell attachment protein |
Q28284142 | Hsp90 phosphorylation, Wee1 and the cell cycle |
Q28269868 | Hsp90 prevents phenotypic variation by suppressing the mutagenic activity of transposons |
Q34740694 | Hsp90 promotes kinase evolution |
Q43141228 | Hsp90 reaches new heights. Conference on the Hsp90 chaperone machine |
Q27314993 | Hsp90 selectively modulates phenotype in vertebrate development |
Q53820041 | Hsp90 shapes protein and RNA evolution to balance trade-offs between protein stability and aggregation. |
Q33659713 | Hsp90's secrets unfold: new insights from structural and functional studies |
Q36934856 | Hsp90--from signal transduction to cell transformation. |
Q28243562 | Hsp90: a chaperone for HIV-1 |
Q34473659 | Hsp90: a chaperone for protein folding and gene regulation |
Q24291482 | Hsp90: a specialized but essential protein-folding tool |
Q34319594 | Hsp90: chaperoning signal transduction |
Q81093207 | Hsp90: from structure to phenotype |
Q35913771 | Hsp90: the vulnerable chaperone |
Q35155106 | Human immunodeficiency virus (HIV) type 1 transframe protein can restore activity to a dimerization-deficient HIV protease variant. |
Q40704635 | Identification of Hsp90 as a stimulatory host factor involved in influenza virus RNA synthesis |
Q27940260 | Identification of SSF1, CNS1, and HCH1 as multicopy suppressors of a Saccharomyces cerevisiae Hsp90 loss-of-function mutation |
Q37152621 | Identification of common and unique modifiers of zebrafish midline bifurcation and cyclopia |
Q33867547 | Identification of conserved residues required for the binding of a tetratricopeptide repeat domain to heat shock protein 90. |
Q31036694 | Identification of novel in vivo obligate GroEL/ES substrates based on data from a cell-free proteomics approach. |
Q63433250 | Identifying Extrinsic versus Intrinsic Drivers of Variation in Cell Behavior in Human iPSC Lines from Healthy Donors |
Q33508608 | Identifying protein stabilizing ligands using GroEL. |
Q35170976 | Impact of a stress-inducible switch to mutagenic repair of DNA breaks on mutation in Escherichia coli |
Q27320086 | Impact of gut microbiota on the fly's germ line |
Q30838235 | In silico genetic robustness analysis of microRNA secondary structures: potential evidence of congruent evolution in microRNA |
Q26810029 | Inbreeding and sex: canalization, plasticity and sexual selection |
Q34267911 | Inbreeding-stress interactions: evolutionary and conservation consequences |
Q52169686 | Independence between developmental stability and canalization in the skull of the house mouse. |
Q57150594 | Induced mutations alter patterns of quantitative variation, phenotypic integration, and plasticity to elevated CO in Arabidopsis thaliana |
Q40580807 | Induction of Hsp90 protein expression in malignant melanomas and melanoma metastases |
Q35458609 | Inferring regulatory mechanisms from patterns of evolutionary divergence |
Q34686189 | Infrared laser-induced gene expression in targeted single cells of Caenorhabditis elegans |
Q34372353 | Inheritance beyond plain heritability: variance-controlling genes in Arabidopsis thaliana. |
Q42458582 | Inherited adaptation of genome-rewired cells in response to a challenging environment. |
Q37192047 | Inherited human sex reversal due to impaired nucleocytoplasmic trafficking of SRY defines a male transcriptional threshold |
Q33533806 | Insect evolution: Redesigning the fruitfly |
Q40443440 | Insights into function and regulation of small heat shock protein 25 (HSPB1) in a mouse model with targeted gene disruption |
Q51471195 | Insulin signalling underlies both plasticity and divergence of a reproductive trait in Drosophila. |
Q42928663 | Integrating high-throughput genetic interaction mapping and high-content screening to explore yeast spindle morphogenesis |
Q37532887 | Integration of two ancestral chaperone systems into one: the evolution of eukaryotic molecular chaperones in light of eukaryogenesis |
Q33803992 | Intracellular proteolysis |
Q36155338 | Intramolecular phenotypic capacitance in a modular RNA molecule |
Q58459479 | Investigating Coral Reef Degradation at Alina's Reef in the Florida Keys: Cellular Physiology of White Grunt (Haemulon plumieri) as a Biological Indicator |
Q28575256 | Involvement of cell surface HSP90 in cell migration reveals a novel role in the developing nervous system |
Q81277082 | Involvement of the TRAP-1 homologue, Dd-TRAP1, in spore differentiation during Dictyostelium development |
Q37710778 | Is canalization more than just a beautiful idea? |
Q51697895 | Is evolvability evolvable? |
Q45188577 | Isolation and characterization of an immunogenic fragment of heat shock protein 60 from Trichophyton mentagrophytes. |
Q57129851 | It's not magic - Hsp90 and its effects on genetic and epigenetic variation |
Q80400951 | Key issues in achieving an integrative perspective on stress |
Q40070747 | Lack of tailless leads to an increase in expression variability in Drosophila embryos. |
Q57578017 | Language as ergonomic perfection |
Q73713207 | Large accumulation of mRNA and DNA point modifications in a plant senescent tissue |
Q64227762 | Layers of Cryptic Genetic Variation Underlie a Yeast Complex Trait |
Q38206169 | Left-right asymmetry of the gnathostome skull: its evolutionary, developmental, and functional aspects |
Q64056947 | Leishmania donovani 90 kD Heat Shock Protein - Impact of Phosphosites on Parasite Fitness, Infectivity and Casein Kinase Affinity |
Q34481875 | Lessons from model organisms: phenotypic robustness and missing heritability in complex disease |
Q47765923 | Limb development takes a measured step toward systems analysis |
Q48183899 | Little effect of HSP90 inhibition on the quantitative wing traits variation in Drosophila melanogaster |
Q36904964 | Local adaptation and evolutionary potential along a temperature gradient in the fungal pathogen Rhynchosporium commune |
Q34310595 | Low level genome mistranslations deregulate the transcriptome and translatome and generate proteotoxic stress in yeast. |
Q91405200 | Lowering the culture temperature corrects collagen abnormalities caused by HSP47 gene knockout |
Q30659534 | Macroevolution is more than repeated rounds of microevolution |
Q33344233 | Maize sex determination and abaxial leaf fates are canalized by a factor that maintains repressed epigenetic states |
Q35729999 | Mammalian mRNA splice-isoform selection is tightly controlled. |
Q60461538 | Mapping phenotypes: canalization, plasticity and developmental stability |
Q28481516 | Mapping the Hsp90 genetic interaction network in Candida albicans reveals environmental contingency and rewired circuitry |
Q34124519 | Maturation of steroid receptors: an example of functional cooperation among molecular chaperones and their associated proteins |
Q38718647 | Mccrearamycins A-D, Geldanamycin-Derived Cyclopentenone Macrolactams from an Eastern Kentucky Abandoned Coal Mine Microbe. |
Q33580440 | Measurements of translation initiation from all 64 codons in E. coli |
Q55040050 | Mechanism of evolution by genetic assimilation : Equivalence and independence of genetic mutation and epigenetic modulation in phenotypic expression. |
Q36976462 | Mechanisms and evolution of environmental responses in Caenorhabditis elegans |
Q26741834 | Mechanisms of Hsp90 regulation |
Q28082759 | Mechanisms of mutational robustness in transcriptional regulation |
Q28080783 | Mechanistic Asymmetry in Hsp90 Dimers |
Q51973924 | Mesosternal bristle number in a cosmopolitan drosophilid: an X-linked variable trait independent of sternopleural bristles. |
Q52754615 | Metabolomic analysis of the selection response of Drosophila melanogaster to environmental stress: are there links to gene expression and phenotypic traits? |
Q54137723 | MicroRNAs Establish Uniform Traits during the Architecture of Vertebrate Embryos. |
Q34017534 | MicroRNAs and their roles in developmental canalization |
Q28252446 | Microbial cell individuality and the underlying sources of heterogeneity |
Q28681825 | Microsatellite-encoded domain in rodent Sry functions as a genetic capacitor to enable the rapid evolution of biological novelty |
Q36875674 | Mitonuclear Epistasis for Development Time and Its Modification by Diet in Drosophila |
Q91577731 | Mitonuclear conflict and cooperation govern the integration of genotypes, phenotypes and environments |
Q36188406 | Modifiers of the Genotype-Phenotype Map: Hsp90 and Beyond |
Q33267333 | Modularity and intrinsic evolvability of Hsp90-buffered change |
Q37903182 | Molecular and structural antioxidant defenses against oxidative stress in animals |
Q85213922 | Molecular biology: Choose your protein partners |
Q48222243 | Molecular chaperone Hsp90 associates with resistance protein N and its signaling proteins SGT1 and Rar1 to modulate an innate immune response in plants |
Q36496399 | Molecular chaperones and selection against mutations |
Q47785215 | Molecular chaperones and the stress of oncogenesis |
Q37343873 | Molecular chaperones in pathogen virulence: emerging new targets for therapy. |
Q29547715 | Molecular chaperones in protein folding and proteostasis |
Q34165962 | Molecular chaperones--cellular machines for protein folding |
Q33632311 | Molecular chaperones: the busy life of Hsp90. |
Q80400955 | Molecular chaperones: the modular evolution of cellular networks |
Q51357657 | Molecular characterization of three Hsp90 from Pieris and expression patterns in response to cold and thermal stress in summer and winter diapause of Pieris melete. |
Q24671662 | Molecular clock: an anti-neo-Darwinian legacy |
Q48068499 | Molecular cloning and characterization of four heat shock protein genes from Macrocentrus cingulum (Hymenoptera: Braconidae). |
Q50867385 | Molecular evolutionary mechanisms driving functional diversification of the HSP90A family of heat shock proteins in eukaryotes. |
Q51046987 | Molecular genetics: Chaperone protein gets personal. |
Q33445336 | Molecular identification of differentially regulated genes in the hydrothermal-vent species Bathymodiolus thermophilus and Paralvinella pandorae in response to temperature |
Q46269622 | Molecular investigation of genetic assimilation during the rapid adaptive radiations of East African cichlid fishes |
Q36837925 | Molecular mechanisms governing differential robustness of development and environmental responses in plants |
Q41932080 | Molecular mechanisms of anti-aging hormetic effects of mild heat stress on human cells. |
Q40208649 | Molecular mechanisms of canalization: Hsp90 and beyond |
Q38174591 | Molecular mechanisms of paralogous compensation and the robustness of cellular networks |
Q26822913 | Molecular mechanisms of robustness in plants |
Q89486514 | Morphological novelty emerges from pre-existing phenotypic plasticity |
Q64251984 | Mouse Skull Mean Shape and Shape Robustness Rely on Different Genetic Architectures and Different Loci |
Q35962309 | Multi-locus Genotypes Underlying Temperature Sensitivity in a Mutationally Induced Trait |
Q33400248 | Multidimensional analysis of Drosophila wing variation in Evolution Canyon |
Q26752489 | Multifunctional Microtubule-Associated Proteins in Plants |
Q39528389 | Multiple capacitors for natural genetic variation in Drosophila melanogaster |
Q36885382 | Mutation rate variation in multicellular eukaryotes: causes and consequences |
Q24624037 | Mutational robustness can facilitate adaptation |
Q24685246 | Mutations leading to loss of sporulation ability in Bacillus subtilis are sufficiently frequent to favor genetic canalization |
Q34055320 | Mutator suppression and escape from replication error-induced extinction in yeast |
Q34655913 | NAD synthase NMNAT acts as a chaperone to protect against neurodegeneration. |
Q36038362 | NMNAT2:HSP90 Complex Mediates Proteostasis in Proteinopathies. |
Q35002352 | Natural genetic variation determines susceptibility to aggregation or toxicity in a C. elegans model for polyglutamine disease |
Q37136710 | Natural product inhibitors of Hsp90: potential leads for drug discovery |
Q24541501 | Near-neutrality in evolution of genes and gene regulation |
Q35582253 | Near-neutrality, robustness, and epigenetics |
Q46812108 | Negative Epistasis in Experimental RNA Fitness Landscapes. |
Q35844781 | Negative feedback confers mutational robustness in yeast transcription factor regulation |
Q35144915 | Nematode Hsp90: highly conserved but functionally diverse |
Q64235552 | Network hubs affect evolvability |
Q21563565 | Network hubs buffer environmental variation in Saccharomyces cerevisiae |
Q24615100 | Networked buffering: a basic mechanism for distributed robustness in complex adaptive systems |
Q36103669 | Neuronal signaling modulates protein homeostasis in Caenorhabditis elegans post-synaptic muscle cells |
Q36899148 | Neurospora crassa heat shock factor 1 Is an essential gene; a second heat shock factor-like gene, hsf2, is required for asexual spore formation. |
Q41888198 | New microRNAs in Drosophila--birth, death and cycles of adaptive evolution. |
Q27308766 | Nitric oxide acts as a positive regulator to induce metamorphosis of the ascidian Herdmania momus |
Q59050717 | Noise rules |
Q28681260 | Non-coding RNAs: multi-tasking molecules in the cell |
Q28708799 | Non-local competition drives both rapid divergence and prolonged stasis in a model of speciation in populations with degenerate resource consumption |
Q37117023 | Nonadditive expression of homoeologous genes is established upon polyploidization in hexaploid wheat |
Q35991123 | Nonlinear Dynamics in Gene Regulation Promote Robustness and Evolvability of Gene Expression Levels |
Q45360855 | Novel arrangement and comparative analysis of hsp90 family genes in three thermotolerant species of Stratiomyidae (Diptera). |
Q52836209 | Novel genetic capacitors and potentiators for the natural genetic variation of sensory bristles and their trait specificity in Drosophila melanogaster. |
Q37813152 | Novel therapeutic strategies in multiple myeloma: role of the heat shock protein inhibitors |
Q28569589 | Odorants as cell-type specific activators of a heat shock response in the rat olfactory mucosa |
Q35664375 | On the Nature and Evolutionary Impact of Phenotypic Robustness Mechanisms. |
Q61449485 | On the Reciprocally Causal and Constructive Nature of Developmental Plasticity and Robustness |
Q55559653 | Oncogenic addiction to high 26S proteasome level. |
Q38093796 | Opportunities and challenges for molecular chaperone modulation to treat protein-conformational brain diseases |
Q34456547 | Opposing effects of folding and assembly chaperones on evolvability of Rubisco |
Q31924315 | Opposite effects of the Hsp90 inhibitor Geldanamycin: induction of apoptosis in PC12, and differentiation in N2A cells |
Q73564976 | Organization and structure of the Giardia genome |
Q38092221 | Origin of evolutionary change in avian clutch size |
Q53384664 | Origin of the neutral and nearly neutral theories of evolution. |
Q39478378 | Overexpression of AtHsp90.2, AtHsp90.5 and AtHsp90.7 in Arabidopsis thaliana enhances plant sensitivity to salt and drought stresses. |
Q48448556 | PHOX2B germline and somatic mutations in late-onset central hypoventilation syndrome. |
Q34039572 | PIWI proteins and PIWI-interacting RNAs in the soma |
Q38425435 | Parental identity influences progeny responses to incubation thermal stress in sockeye salmon Onchorhynchus nerka |
Q29618887 | Pathways of chaperone-mediated protein folding in the cytosol |
Q34271971 | Perspective: Evolution and detection of genetic robustness |
Q38549040 | Pervasive robustness in biological systems. |
Q78732204 | Pharmacogenomics in cancer drug discovery and development: inhibitors of the Hsp90 molecular chaperone |
Q44202026 | Pharmacological prevention of Parkinson disease in Drosophila. |
Q34998365 | Phenotypic and genetic consequences of protein damage |
Q35762881 | Phenotypic convergence in bacterial adaptive evolution to ethanol stress |
Q28469256 | Phenotypic diversity and altered environmental plasticity in Arabidopsis thaliana with reduced Hsp90 levels |
Q39393652 | Phenotypic diversity, population structure and stress protein-based capacitoring in populations of Xeropicta derbentina, a heat-tolerant land snail species |
Q50704325 | Phenotypic heterogeneity can enhance rare-cell survival in 'stress-sensitive' yeast populations. |
Q37115037 | Phenotypic integration of skeletal traits during growth buffers genetic variants affecting the slenderness of femora in inbred mouse strains |
Q38177306 | Phenotypic plasticity and epigenetic marking: an assessment of evidence for genetic accommodation |
Q29614515 | Phenotypic plasticity and the epigenetics of human disease |
Q33787403 | Phenotypic plasticity can facilitate adaptive evolution in gene regulatory circuits |
Q33733118 | Phenotypic plasticity facilitates recurrent rapid adaptation to introduced predators |
Q33274208 | Phenotypic plasticity in Drosophila pigmentation caused by temperature sensitivity of a chromatin regulator network |
Q33662766 | Phenotypic plasticity in the range-margin population of the lycaenid butterfly Zizeeria maha |
Q47331678 | Phenotypic plasticity of body size in a temperate population of Drosophila melanogaster: when the temperature-size rule does not apply |
Q51875929 | Phenotypic robustness can increase phenotypic variability after nongenetic perturbations in gene regulatory circuits. |
Q44769960 | Phylogenetic analysis of eukaryotes using heat-shock protein Hsp90. |
Q35435973 | Physics and the canalization of morphogenesis: a grand challenge in organismal biology |
Q28755485 | Physiological Diversity in Insects: Ecological and Evolutionary Contexts |
Q30042023 | Plasmodium falciparum heat shock protein 110 stabilizes the asparagine repeat-rich parasite proteome during malarial fevers |
Q48470373 | Plastic flies: the regulation and evolution of trait variability in Drosophila. |
Q36834689 | Polyglutamine expansion in Drosophila: thermal stress and Hsp70 as selective agents |
Q39844194 | Population responses to anthropogenic disturbance: lessons from three‐spined sticklebacksGasterosteus aculeatusin eutrophic habitats |
Q36875232 | Population transcriptomics uncovers the regulation of gene expression variation in adaptation to changing environment |
Q50522799 | Post-embryonic functions of HSP90 in Tribolium castaneum include the regulation of compound eye development. |
Q34606166 | Post-transcriptional repair of a split heat shock protein 90 gene by mRNA trans-splicing |
Q55513021 | Post-translational buffering leads to convergent protein expression levels between primates. |
Q34811520 | Potential genetic variance and the domestication of maize |
Q56927558 | Potential role of the heat shock protein 90 (hsp90) in buffering mutations to favour cyclical parthenogenesis in the peach potato aphid Myzus persicae (Aphididae, Hemiptera) |
Q36368879 | Power provides protection: Genetic robustness in yeast depends on the capacity to generate energy |
Q51837124 | Predicting mutation outcome from early stochastic variation in genetic interaction partners. |
Q21145845 | Prion switching in response to environmental stress |
Q48425764 | Prions and chaperones: Outside the fold. |
Q40300772 | Profiling of Brevibacillus borstelensis transcriptome exposed to high temperature shock |
Q34189462 | Progress and potential of Drosophila protein interaction maps |
Q51752072 | Progress and prospects for targeting Hsp90 to treat fungal infections. |
Q34074075 | Progress on canalization |
Q21560899 | Progressive, transgenerational changes in offspring phenotype and epigenotype following nutritional transition |
Q73255932 | Prokaryote and eukaryote evolvability |
Q28189476 | Proliferation, cell cycle and apoptosis in cancer |
Q34205949 | Promoter nucleosome organization shapes the evolution of gene expression |
Q34611621 | Proposal for a role of the Hsp90/Hsp70-based chaperone machinery in making triage decisions when proteins undergo oxidative and toxic damage |
Q26801512 | Protein Folding and Mechanisms of Proteostasis |
Q34225700 | Protein aggregation and aggregate toxicity: new insights into protein folding, misfolding diseases and biological evolution |
Q58700273 | Protein evolution speed depends on its stability and abundance and on chaperone concentrations |
Q33570364 | Protein evolution via amino acid and codon elimination |
Q35761364 | Protein expression parallels thermal tolerance and ecologic changes in the diversification of a diving beetle species complex |
Q34152827 | Protein folding in the cytoplasm and the heat shock response |
Q42724601 | Protein folding taking shape. Workshop on molecular chaperones |
Q37832796 | Protein folding, protein homeostasis, and cancer. |
Q36109387 | Protein homeostasis in models of aging and age-related conformational disease |
Q33728820 | Protein misfolding and degradation in genetic diseases. |
Q92950813 | Protein quality control machinery in intracellular protozoan parasites: hopes and challenges for therapeutic targeting |
Q52699324 | Proteomic characterization of a temperature-sensitive conditional lethal in Drosophila melanogaster. |
Q28286034 | Proteomic data from human cell cultures refine mechanisms of chaperone-mediated protein homeostasis |
Q29614783 | Proteotoxic stress and inducible chaperone networks in neurodegenerative disease and aging |
Q50454192 | Proton Gradient Regulation5-Like1-Mediated Cyclic Electron Flow Is Crucial for Acclimation to Anoxia and Complementary to Nonphotochemical Quenching in Stress Adaptation. |
Q26853052 | Quality control and fate determination of Hsp90 client proteins |
Q28709615 | Quantifying the decanalizing effects of spontaneous mutations in rhabditid nematodes |
Q35904778 | Quantitative Genetics Identifies Cryptic Genetic Variation Involved in the Paternal Regulation of Seed Development |
Q37609932 | Quantitative Trait Loci and Antagonistic Associations for Two Developmentally Related Traits in the Drosophila Head |
Q24297748 | Quantitative analysis of HSP90-client interactions reveals principles of substrate recognition |
Q52602086 | Quantitative epigenetics. |
Q37089359 | Quantitative trait symmetry independent of Hsp90 buffering: distinct modes of genetic canalization and developmental stability |
Q30373007 | RNA chaperones buffer deleterious mutations in E. coli. |
Q33784954 | Rapid evolution of phenotypic plasticity and shifting thresholds of genetic assimilation in the nematode Caenorhabditis remanei |
Q57898739 | Re-evaluating the environment in developmental evolution |
Q92859230 | Rebalancing Protein Homeostasis Enhances Tumor Antigen Presentation |
Q59808502 | Redundancy, Feedback, and Robustness in the Gene Family |
Q50114108 | Redundant and incoherent regulations of multiple phenotypes suggest microRNAs' role in stability control. |
Q41514448 | Regulated noise in the epigenetic landscape of development and disease |
Q46675520 | Regulation of gene expression via retrotransposon insertions and the noncoding RNA 4.5S RNAH. |
Q73878472 | Regulation of metamorphosis in ascidians involves NO/cGMP signaling and HSP90 |
Q38086397 | Regulation of molecular chaperones through post-translational modifications: decrypting the chaperone code |
Q37638939 | Regulation of organismal proteostasis by transcellular chaperone signaling |
Q34190284 | Regulatory circuitry governing fungal development, drug resistance, and disease. |
Q37509533 | Relaxed selection in the wild |
Q33565358 | Remodeling of Proteostasis Upon Transition to Adulthood is Linked to Reproduction Onset |
Q27933130 | Remodeling of yeast genome expression in response to environmental changes |
Q68686836 | Repressive Gene Regulation Synchronizes Development with Cellular Metabolism |
Q34061520 | Reproducibility and consistency of proteomic experiments on natural populations of a non-model aquatic insect |
Q37592774 | Research on inbreeding in the 'omic' era. |
Q36762412 | Resistance to HSP90 inhibition involving loss of MCL1 addiction. |
Q59077597 | Results may not fit well with current theories . . |
Q34787768 | Review. The genotype-phenotype link |
Q41845109 | Ribosome profiling reveals post-transcriptional buffering of divergent gene expression in yeast. |
Q24634833 | Robustness and evolvability |
Q37858278 | Robustness and evolvability in the B-system of flower development |
Q24657364 | Robustness and evolvability: a paradox resolved |
Q47306214 | Robustness versus evolvability analysis for regulatory feed-forward loops |
Q39217320 | Robustness, evolvability, and neutrality |
Q24646806 | Robustness: mechanisms and consequences |
Q27320539 | Role of pleiotropy in the evolution of a cryptic developmental variation in Caenorhabditis elegans |
Q35955737 | Roles for microRNAs in conferring robustness to biological processes |
Q34576423 | Roles of heat-shock proteins in innate and adaptive immunity |
Q33336944 | SHEPHERD is the Arabidopsis GRP94 responsible for the formation of functional CLAVATA proteins |
Q59044179 | Safeguards and spurs |
Q36170641 | Selection Transforms the Landscape of Genetic Variation Interacting with Hsp90. |
Q37215211 | Selection for chaperone-like mediated genetic robustness at low mutation rate: impact of drift, epistasis and complexity |
Q57272349 | Selection for distinct gene expression properties favours the evolution of mutational robustness in gene regulatory networks |
Q44081409 | Selective apoptosis of tandemly duplicated FLT3-transformed leukemia cells by Hsp90 inhibitors |
Q39651070 | Selective pressures on genomes in molecular evolution |
Q37626776 | Sensitive periods in epigenetics: bringing us closer to complex behavioral phenotypes |
Q28143497 | Sensitivity of mature Erbb2 to geldanamycin is conferred by its kinase domain and is mediated by the chaperone protein Hsp90 |
Q39336891 | Sequence and domain conservation of the coelacanth Hsp40 and Hsp90 chaperones suggests conservation of function |
Q58698878 | Sexual selection contributes to partial restoration of phenotypic robustness in a butterfly |
Q34134393 | Shadow enhancers foster robustness of Drosophila gastrulation |
Q90098376 | Shaping the regulation of the p53 mRNA tumour suppressor: the co-evolution of genetic signatures |
Q39365428 | Silencing of Transposable Elements by piRNAs in Drosophila: An Evolutionary Perspective |
Q77209190 | Simulation of the evolution of genomic complexity |
Q63544601 | Single-nucleotide variations in the genes encoding the mitochondrial Hsp60/Hsp10 chaperone system and their disease-causing potential |
Q91585979 | Snails in the sun: Strategies of terrestrial gastropods to cope with hot and dry conditions |
Q38479707 | Species-specific color-pattern modifications of butterfly wings |
Q37397927 | Splice site strength-dependent activity and genetic buffering by poly-G runs |
Q37710717 | Stationary phase in gram-negative bacteria. |
Q47111902 | Stochastic loss and gain of symmetric divisions in the C. elegans epidermis perturbs robustness of stem cell number. |
Q40647234 | Stochastic variation in Cardamine hirsuta petal number |
Q36095581 | Stochasticity or the fatal 'imperfection' of cloning |
Q33706890 | Stress and the cell nucleus: dynamics of gene expression and structural reorganization. |
Q34049943 | Stress and transposable elements: co-evolution or useful parasites? |
Q35031242 | Stress proteins and glial functions: possible therapeutic targets for neurodegenerative disorders |
Q34022656 | Stress, genomes, and evolution |
Q28767873 | Stress-induced variation in evolution: from behavioural plasticity to genetic assimilation |
Q104286529 | Stressful development: Integrating endoderm development, stress, and longevity |
Q46776796 | Strong and parallel salinity-induced phenotypic plasticity in one generation of threespine stickleback |
Q33840745 | Structure and in vivo function of Hsp90. |
Q34116190 | Structure, function, and mechanism of the Hsp90 molecular chaperone |
Q40125671 | Studies of stability mechanisms of early embryonal development of fruit fly Drosophila |
Q38338129 | Supersaturation is a major driving force for protein aggregation in neurodegenerative diseases |
Q37576646 | Susan Lindquist: Visionary scientist and peerless mentor |
Q34010599 | Synthesis and preliminary evaluation steroidal antiestrogen-geldanamycin conjugates |
Q34151015 | Synthetic lethality: general principles, utility and detection using genetic screens in human cells |
Q55554520 | Systematic mapping of genetic interactions in Caenorhabditis elegans identifies common modifiers of diverse signaling pathways |
Q92932138 | Systemic signalling and local effectors in developmental stability, body symmetry, and size |
Q33302931 | Systems analysis of chaperone networks in the malarial parasite Plasmodium falciparum |
Q83051409 | Systems biology spins off a new model for the study of canalization |
Q22065711 | THE EVOLUTION OF THE EVOLVABILITY PROPERTIES OF THE YEAST PRION [PSI + ] |
Q36379365 | Targeting chaperones in transformed systems--a focus on Hsp90 and cancer |
Q35125859 | Temperature stress mediates decanalization and dominance of gene expression in Drosophila melanogaster |
Q47189342 | Temperature-induced shifts in associations of longevity with body size in Drosophila melanogaster |
Q34145693 | Temperature-sensitive RB mutations linked to incomplete penetrance of familial retinoblastoma in 12 families |
Q39143127 | Temperature-sensitive phenotype caused by natural mutation in Capsicum latescent in two tropical regions. |
Q57615351 | Temperature-specific acclimation effects on adult locomotor performance of inbred and crossbredDrosophila melanogaster |
Q35910431 | The "Special" crystal-Stellate System in Drosophila melanogaster Reveals Mechanisms Underlying piRNA Pathway-Mediated Canalization. |
Q34767044 | The 2008 Genetics Society of America Medal. Susan Lindquist |
Q24544957 | The Bacillus subtilis sin operon: an evolvable network motif |
Q40181125 | The Baldwin effect and genetic assimilation: revisiting two mechanisms of evolutionary change mediated by phenotypic plasticity |
Q55041195 | The Chlamydomonas genome reveals its secrets: chaperone genes and the potential roles of their gene products in the chloroplast. |
Q37092783 | The EDGE hypothesis: epigenetically directed genetic errors in repeat-containing proteins (RCPs) involved in evolution, neuroendocrine signaling, and cancer |
Q28138074 | The Fas-induced apoptosis analyzed by high throughput proteome analysis |
Q58230560 | The Genetic Architecture of Fluctuating Asymmetry of Mandible Size and Shape in a Population of Mice: Another Look |
Q51042630 | The HSP90 chaperone machinery. |
Q28280296 | The HSP90 family of genes in the human genome: insights into their divergence and evolution |
Q42660287 | The HTL1 gene (YCR020W-b) of Saccharomyces cerevisiae is necessary for growth at 37 degrees C, and for the conservation of chromosome stability and fertility |
Q36259352 | The Hsp27 gene is not required for Drosophila development but its activity is associated with starvation resistance |
Q36961678 | The Hsp90 capacitor, developmental remodeling, and evolution: the robustness of gene networks and the curious evolvability of metamorphosis |
Q42040986 | The Hsp90 chaperone complex A potential target for cancer therapy? |
Q28361507 | The Hsp90 family of proteins in Arabidopsis thaliana |
Q36845743 | The Hsp90-Sti1 interaction is critical for Leishmania donovani proliferation in both life cycle stages |
Q34472616 | The Hsp90-dependent proteome is conserved and enriched for hub proteins with high levels of protein-protein connectivity |
Q37234274 | The Interplay of Temperature and Genotype on Patterns of Alternative Splicing in Drosophila melanogaster |
Q47985263 | The La and related RNA-binding proteins (LARPs): structures, functions, and evolving perspectives. |
Q52673300 | The Molecular Chaperone HSP90 Promotes Notch Signaling in the Germline of Caenorhabditis elegans. |
Q35850146 | The Multi-allelic Genetic Architecture of a Variance-Heterogeneity Locus for Molybdenum Concentration in Leaves Acts as a Source of Unexplained Additive Genetic Variance |
Q54560706 | The Paradoxides puzzle resolved: the appearance of the oldest paradoxidines and its bearing on the Cambrian Series 3 lower boundary |
Q33757213 | The Role of DAF-21/Hsp90 in Mouth-Form Plasticity in Pristionchus pacificus |
Q84549159 | The adaptive potential of a plant pathogenic fungus, Rhizoctonia solani AG-3, under heat and fungicide stress |
Q33209779 | The analysis of large-scale gene expression correlated to the phase changes of the migratory locust |
Q36731446 | The association of Hsp90 expression induced by aspirin with anti-stress damage in chicken myocardial cells. |
Q46892205 | The brachymorph mouse and the developmental-genetic basis for canalization and morphological integration |
Q58570246 | The causes of evolvability and their evolution |
Q50493069 | The chlorate-resistant and photomorphogenesis-defective mutant cr88 encodes a chloroplast-targeted HSP90. |
Q58733939 | The complex underpinnings of genetic background effects |
Q28268061 | The concept of synthetic lethality in the context of anticancer therapy |
Q34213206 | The consequences of rare sexual reproduction by means of selfing in an otherwise clonally reproducing species |
Q42488505 | The cytosolic/nuclear HSC70 and HSP90 molecular chaperones are important for stomatal closure and modulate abscisic acid-dependent physiological responses in Arabidopsis. |
Q34347326 | The development and evolution of crossveins in insect wings |
Q38570432 | The developmental genetics of biological robustness. |
Q88758108 | The developmental-genetics of canalization |
Q35083617 | The distribution of heat shock proteins in the nervous system of the unstressed mouse embryo suggests a role in neuronal and non-neuronal differentiation |
Q56920071 | The dynamics of evolutionary stasis |
Q35811177 | The effect of chaperonin buffering on protein evolution |
Q46167922 | The effects of Hsp90 expression alteration on spinal metastases of breast carcinoma |
Q45120597 | The effects of stabilizing and directional selection on phenotypic and genotypic variation in a population of RNA enzymes |
Q34531292 | The emerging conceptual framework of evolutionary developmental biology |
Q47980910 | The environmental and genetic regulation of obake expressivity: morphogenetic fields as evolvable systems. |
Q29617486 | The epigenetic progenitor origin of human cancer |
Q37075845 | The evolution of fungal drug resistance: modulating the trajectory from genotype to phenotype. |
Q38268475 | The evolution of protein moonlighting: adaptive traps and promiscuity in the chaperonins. |
Q36710753 | The evolution of sex: empirical insights into the roles of epistasis and drift |
Q38992195 | The evolutionary capacitor HSP90 buffers the regulatory effects of mammalian endogenous retroviruses. |
Q24796988 | The expression of HSP83 genes in Leishmania infantum is affected by temperature and by stage-differentiation and is regulated at the levels of mRNA stability and translation |
Q22066346 | The frailty of adaptive hypotheses for the origins of organismal complexity |
Q40786951 | The future of evolutionary developmental biology |
Q24294462 | The heat shock protein 90-CDC37 chaperone complex is required for signaling by types I and II interferons |
Q36804122 | The hemopexin domain of MMP3 is responsible for mammary epithelial invasion and morphogenesis through extracellular interaction with HSP90β |
Q33217402 | The histidine kinase Hik34 is involved in thermotolerance by regulating the expression of heat shock genes in synechocystis |
Q34474861 | The importance of sequence diversity in the aggregation and evolution of proteins |
Q35910095 | The key role of epigenetics in the persistence of asexual lineages. |
Q28534944 | The maternal-to-zygotic transition targets actin to promote robustness during morphogenesis |
Q30391567 | The molecular chaperone DnaK is a source of mutational robustness |
Q42722777 | The mysterious steps in carcinogenesis |
Q44945432 | The nature of nurture and the future of evodevo: toward a theory of developmental evolution |
Q34143477 | The origins of cancer robustness and evolvability. |
Q38270618 | The peculiarities of piRNA expression upon heat shock exposure in Drosophila melanogaster. |
Q30854397 | The periplasmic Escherichia coli peptidylprolyl cis,trans-isomerase FkpA. I. Increased functional expression of antibody fragments with and without cis-prolines. |
Q42266350 | The polymorphisms in the promoter of HSP90 gene and their association with heat tolerance of bay scallop |
Q35990059 | The population genetic theory of hidden variation and genetic robustness. |
Q36709964 | The protein chaperone HSP90 can facilitate the divergence of gene duplicates |
Q36089277 | The relationship between evolutionary and physiological variation in hemoglobin |
Q42713350 | The relevance of heat shock regulation in fungal pathogens of humans |
Q33723746 | The role of HSP90 in evolution |
Q51701073 | The role of developmental plasticity in evolutionary innovation. |
Q28728733 | The role of genes domesticated from LTR retrotransposons and retroviruses in mammals |
Q45913880 | The role of stress proteins in responses of a montane willow leaf beetle to environmental temperature variation. |
Q28315755 | The significance and scope of evolutionary developmental biology: a vision for the 21st century |
Q53254709 | The sources of adaptive variation. |
Q34181891 | The stress of protein misfolding: from single cells to multicellular organisms |
Q22066347 | The theory of facilitated variation |
Q35650889 | The unfolded protein response supports cellular robustness as a broad-spectrum compensatory pathway |
Q35080182 | The unfolding story of three-dimensional domain swapping. |
Q34520452 | The utility of prions |
Q26824333 | The yeast prions [PSI+] and [URE3] are molecular degenerative diseases |
Q35791991 | Therapeutic and diagnostic implications of Hsp90 activation |
Q36499222 | Therapeutic aspects of chaperones/heat-shock proteins in neuro-oncology |
Q31131552 | Thermal stress depletes energy reserves in Drosophila |
Q47833878 | Three-dimensional structure of heat shock protein 90 from Plasmodium falciparum: molecular modelling approach to rational drug design against malaria. |
Q33633023 | Too late for the midwife toad: stress, variability and Hsp90. |
Q33335863 | Total synthesis of the Hsp90 inhibitor geldanamycin |
Q35814227 | Transcriptional Derepression Uncovers Cryptic Higher-Order Genetic Interactions |
Q33592605 | Transcriptomic analysis of maternally provisioned cues for phenotypic plasticity in the annual killifish, Austrofundulus limnaeus |
Q28543649 | Transhydrogenase promotes the robustness and evolvability of E. coli deficient in NADPH production |
Q36976476 | Transient exposure to low levels of insecticide affects metabolic networks of honeybee larvae |
Q33687526 | Transposable elements in cancer as a by-product of stress-induced evolvability |
Q33935404 | Transposons, environmental changes, and heritable induced phenotypic variability. |
Q33838803 | Triggers of the HSP70 stress response: environmental responses and laboratory manipulation in an Antarctic marine invertebrate (Nacella concinna) |
Q37078937 | Trithorax requires Hsp90 for maintenance of active chromatin at sites of gene expression |
Q42722265 | Tumor heterogeneity, clonal evolution, and therapy resistance: an opportunity for multitargeting therapy |
Q35889629 | Uncovering cryptic genetic variation. |
Q89863572 | Unexpected cell type-dependent effects of autophagy on polyglutamine aggregation revealed by natural genetic variation in C. elegans |
Q35362020 | Unifying genetic canalization, genetic constraint, and genotype-by-environment interaction: QTL by genomic background by environment interaction of flowering time in Boechera stricta |
Q57004511 | Upper thermal limits in terrestrial ectotherms: how constrained are they? |
Q48212979 | Variability in a Short Tandem Repeat Mediates Complex Epistatic Interactions in Arabidopsis thaliana. |
Q33717980 | Variability in gene expression underlies incomplete penetrance |
Q36724648 | Variation and constraint in plant evolution and development |
Q52697947 | Variations in morphological and life-history traits under extreme temperatures in Drosophila ananassae. |
Q33952911 | Visualizing high error levels during gene expression in living bacterial cells. |
Q50219668 | Waddington Redux: De Novo Mutations Underlie the Genetic Assimilation of Stress-Induced Phenocopies in Drosophila melanogaster. |
Q24533552 | Waddington's canalization revisited: developmental stability and evolution |
Q34075802 | Was Wright right? The canonical genetic code is an empirical example of an adaptive peak in nature; deviant genetic codes evolved using adaptive bridges |
Q53278492 | What history tells us II. The discovery of chaperone function. |
Q36988221 | What's Luck Got to Do with It: Single Cells, Multiple Fates, and Biological Nondeterminism |
Q24804052 | Whither genomics? |
Q38583423 | Why molecular chaperones buffer mutational damage: a case study with a yeast Hsp40/70 system. |
Q61444108 | Widespread inter-individual gene expression variability in |
Q36059814 | Wild worm embryogenesis harbors ubiquitous polygenic modifier variation |
Q46707609 | Within-strain variation in behavior differs consistently between common inbred strains of mice |
Q64517233 | Worming into genetic instability |
Q60930362 | Y-chromosomes can constrain adaptive evolution via epistatic interactions with other chromosomes |
Q35848258 | ZAP-70 is a novel conditional heat shock protein 90 (Hsp90) client: inhibition of Hsp90 leads to ZAP-70 degradation, apoptosis, and impaired signaling in chronic lymphocytic leukemia |
Q42715572 | Zebrafish Hsp70 is required for embryonic lens formation |
Q38712393 | Zebrafish as a Model for the Study of Chaperonopathies |
Q81455816 | [HSP86, germ cells and yolk sac tumor] |
Q48082512 | cDNA cloning, heat shock regulation and developmental expression of the hsp83 gene in the Mediterranean fruit fly Ceratitis capitata. |
Q35683507 | daf-41/p23: A Small Protein Heating Up Lifespan Regulation |
Q34160394 | miRNA regulation of Sdf1 chemokine signaling provides genetic robustness to germ cell migration |
Q33975084 | p50(Cdc37) can buffer the temperature-sensitive properties of a mutant of Hck. |
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