The HOG pathway dictates the short-term translational response after hyperosmotic shock.
about
Genome-Wide Transcriptional Response of Saccharomyces cerevisiae to Stress-Induced PerturbationsCheckpoints in a yeast differentiation pathway coordinate signaling during hyperosmotic stressYeast mRNA cap-binding protein Cbc1/Sto1 is necessary for the rapid reprogramming of translation after hyperosmotic shock.Control of Cdc28 CDK1 by a stress-induced lncRNAScaffold Protein Ahk1, Which Associates with Hkr1, Sho1, Ste11, and Pbs2, Inhibits Cross Talk Signaling from the Hkr1 Osmosensor to the Kss1 Mitogen-Activated Protein KinasePathway connectivity and signaling coordination in the yeast stress-activated signaling network.Characterization of the proteostasis roles of glycerol accumulation, protein degradation and protein synthesis during osmotic stress in C. elegansOsmostress-induced cell volume loss delays yeast Hog1 signaling by limiting diffusion processes and by Hog1-specific effectsDynamic transcriptome analysis measures rates of mRNA synthesis and decay in yeastAn evolutionarily conserved RNase-based mechanism for repression of transcriptional positive autoregulation.Heat shock response in yeast involves changes in both transcription rates and mRNA stabilitiesApparent ploidy effects on silencing are post-transcriptional at HML and telomeres in Saccharomyces cerevisiae.Delayed Ras/PKA signaling augments the unfolded protein responseNonsense-mediated mRNA decay controls the changes in yeast ribosomal protein pre-mRNAs levels upon osmotic stressThe significance of translation regulation in the stress response.Metabolic respiration induces AMPK- and Ire1p-dependent activation of the p38-Type HOG MAPK pathway.Stress granule-defective mutants deregulate stress responsive transcripts.Expression of RCK2 MAPKAP (MAPK-activated protein kinase) rescues yeast cells sensitivity to osmotic stress.Vacuolar H+-ATPase works in parallel with the HOG pathway to adapt Saccharomyces cerevisiae cells to osmotic stressIRES-dependent translated genes in fungi: computational prediction, phylogenetic conservation and functional association.Circadian clock regulation of mRNA translation through eukaryotic elongation factor eEF-2Response to hyperosmotic stressHog1: 20 years of discovery and impact.A dynamic model of proteome changes reveals new roles for transcript alteration in yeast.Osmostress-induced gene expression--a model to understand how stress-activated protein kinases (SAPKs) regulate transcriptionRewiring yeast osmostress signalling through the MAPK network reveals essential and non-essential roles of Hog1 in osmoadaptation.An Analog-sensitive Version of the Protein Kinase Slt2 Allows Identification of Novel Targets of the Yeast Cell Wall Integrity Pathway.Microbial response to environmental stresses: from fundamental mechanisms to practical applications.mRNA decay: an adaptation tool for the environmental fungal pathogen Cryptococcus neoformans.Ask yeast how to burn your fats: lessons learned from the metabolic adaptation to salt stress.Proteomic analysis of Trichoderma atroviride reveals independent roles for transcription factors BLR-1 and BLR-2 in light and darkness.Cellular stress induces cytoplasmic RNA granules in fission yeast.The Hog1 stress-activated protein kinase targets nucleoporins to control mRNA export upon stress.An mRNA decapping mutant deficient in P body assembly limits mRNA stabilization in response to osmotic stress.Regulation of transcriptome, translation, and proteome in response to environmental stress in fission yeast.Analysis of the 5' untranslated region (5'UTR) of the alcohol oxidase 1 (AOX1) gene in recombinant protein expression in Pichia pastoris.Multilayered control of peroxisomal activity upon salt stress in Saccharomyces cerevisiae.Genomics of cellular proliferation in periodic environmental fluctuations.Genome and physiology of the ascomycete filamentous fungusXeromyces bisporus, the most xerophilic organism isolated to date
P2860
Q26765664-D7A882E8-941F-40C0-9396-687558FC9DFEQ27335270-344F52BC-BCFB-483C-85F0-526A9904A4C3Q27929949-5B30328B-E83D-403C-934D-7D2385991BA3Q27932241-9B8F62A3-5821-4FD8-BFC5-1EACBE72D17EQ27934789-8892C588-B5C9-4DD4-84B6-27A9B62E352FQ27937397-ED8520E6-1AFC-4AF6-828C-6D20E52ED014Q28481692-8A629254-E42A-4087-9A56-44FD1E8A7A08Q28535284-75B2F691-6A48-4233-AB00-752FCBD43278Q30498341-906617C8-AE0B-4AC4-B78E-FC31604EDA11Q33768399-3A5175AD-C372-4723-A1A1-DBDBFDD36F2AQ33833790-A7B601F2-B6DD-4649-9B98-1D57FC6FF80DQ34335649-9E11726F-2269-482D-85FA-51A0768785B2Q34384031-735EBD06-9741-41C0-B85B-6AF5C60F0E00Q34688707-2D7694AA-F87A-40DD-9333-AADF6E01DF80Q34975771-7BADE311-C89B-4759-A86E-A3934D2C34E3Q35376992-6B37BAF7-89C5-427F-84E7-9034599CAAF9Q35398740-C8C81AD2-4B64-4814-9251-D3BD25A00746Q35730785-A55DA39E-C42A-4177-AF9D-74396C39B3CDQ35804688-B1465DFC-6B45-4069-A202-DBCA42BAB0EDQ35868482-08B6B1DE-BF5A-40C5-BADF-D0B318D6374EQ37213851-9CB45F6B-8B4E-4E62-A897-D355AF7373B3Q38048770-CAD13EA4-4C48-42FA-B727-C0217204529FQ38250197-9EFA2F4E-69AF-4B29-B28B-8F59C9A913D1Q38253819-277DB9D2-A599-4F6A-8E87-22A26493138DQ38276110-D2E2E868-E0EC-4843-8861-99E97CF64F3AQ38753265-DF2ECA1A-6B91-4805-83C3-EE9995B876F8Q38915696-109C9616-9A9B-490A-BC24-50CC99185715Q39242521-FFECA9CD-34E4-4130-936B-D155152A11B4Q39317871-4CB2CB0F-7F07-4C15-B2D8-06AC0BCA091BQ39384878-5E982D8C-1718-4259-B0AA-DCCE8EB5E82BQ40322501-9854C582-4C9E-4032-B546-AE22C3A084DBQ41221209-FC9B03E7-25BC-4E96-84A2-D5332FE47096Q42155215-796E20FA-5388-4AA8-B5E9-6A285F1ACC27Q42270200-1B240264-90BA-4050-8459-D5C5E24CB0A3Q42326263-736DF592-F3DA-45AA-833E-BB3C3776EAFBQ42526446-02DF94EB-294A-4EFB-A054-F4F5CAA525B6Q47944422-CF698FBC-E1DF-4AAA-B229-0E6915133576Q55137338-D6F91B0D-3744-44AA-948F-8CC6A5814184Q59140410-32151FC5-88C7-4FF1-9E1F-C4994379206F
P2860
The HOG pathway dictates the short-term translational response after hyperosmotic shock.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
2010年论文
@zh
2010年论文
@zh-cn
name
The HOG pathway dictates the short-term translational response after hyperosmotic shock.
@en
The HOG pathway dictates the short-term translational response after hyperosmotic shock.
@nl
type
label
The HOG pathway dictates the short-term translational response after hyperosmotic shock.
@en
The HOG pathway dictates the short-term translational response after hyperosmotic shock.
@nl
prefLabel
The HOG pathway dictates the short-term translational response after hyperosmotic shock.
@en
The HOG pathway dictates the short-term translational response after hyperosmotic shock.
@nl
P2093
P2860
P356
P1476
The HOG pathway dictates the short-term translational response after hyperosmotic shock.
@en
P2093
Francesc Posas
Jonas Warringer
Malin Hult
Sergi Regot
P2860
P304
P356
10.1091/MBC.E10-01-0006
P577
2010-06-29T00:00:00Z