about
Genes confer similar robustness to environmental, stochastic, and genetic perturbations in yeast"Myc'ed messages": myc induces transcription of E2F1 while inhibiting its translation via a microRNA polycistronFacilitated variation: how evolution learns from past environments to generalize to new environmentsPrion switching in response to environmental stressHeat shock protein-90-alpha, a prolactin-STAT5 target gene identified in breast cancer cells, is involved in apoptosis regulationComparative genomics and evolution of the HSP90 family of genes across all kingdoms of organismsProgressive, transgenerational changes in offspring phenotype and epigenotype following nutritional transitionNetwork hubs buffer environmental variation in Saccharomyces cerevisiaeTHE EVOLUTION OF THE EVOLVABILITY PROPERTIES OF THE YEAST PRION [PSI + ]The frailty of adaptive hypotheses for the origins of organismal complexityThe theory of facilitated variationGenetic predisposition to cancer — insights from population geneticsHsp90: a specialized but essential protein-folding toolThe heat shock protein 90-CDC37 chaperone complex is required for signaling by types I and II interferonsQuantitative analysis of HSP90-client interactions reveals principles of substrate recognitionWaddington's canalization revisited: developmental stability and evolution.Near-neutrality in evolution of genes and gene regulationThe Bacillus subtilis sin operon: an evolvable network motifCryptic genetic variation is enriched for potential adaptationsDevelopment of bat flight: morphologic and molecular evolution of bat wing digitsGenetic analysis of viable Hsp90 alleles reveals a critical role in Drosophila spermatogenesisDrosophila Piwi functions in Hsp90-mediated suppression of phenotypic variationNetworked buffering: a basic mechanism for distributed robustness in complex adaptive systemsMutational robustness can facilitate adaptationRobustness and evolvabilityHsp70 chaperones: cellular functions and molecular mechanismRobustness: mechanisms and consequencesRobustness and evolvability: a paradox resolvedMolecular clock: an anti-neo-Darwinian legacyMutations leading to loss of sporulation ability in Bacillus subtilis are sufficiently frequent to favor genetic canalizationThe 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 translationWhither genomics?Channelling evolution: canalization and the nervous systemEvolution of genetic potential.Mechanisms of Hsp90 regulationMultifunctional Microtubule-Associated Proteins in PlantsHazards inherent in interdisciplinary behavioral researchProtein Folding and Mechanisms of ProteostasisMolecular mechanisms of robustness in plantsEpistasis and quantitative traits: using model organisms to study gene-gene interactions
P2860
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P2860
description
1998 nî lūn-bûn
@nan
1998 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Hsp90 as a capacitor for morphological evolution
@ast
Hsp90 as a capacitor for morphological evolution
@en
Hsp90 as a capacitor for morphological evolution
@nl
type
label
Hsp90 as a capacitor for morphological evolution
@ast
Hsp90 as a capacitor for morphological evolution
@en
Hsp90 as a capacitor for morphological evolution
@nl
prefLabel
Hsp90 as a capacitor for morphological evolution
@ast
Hsp90 as a capacitor for morphological evolution
@en
Hsp90 as a capacitor for morphological evolution
@nl
P3181
P356
P1433
P1476
Hsp90 as a capacitor for morphological evolution
@en
P2093
S L Rutherford
S Lindquist
P2888
P304
P3181
P356
10.1038/24550
P407
P577
1998-11-26T00:00:00Z
P5875
P6179
1032477985