Stress resistance and signal fidelity independent of nuclear MAPK function
about
Hyperosmotic stress-induced ATF-2 activation through Polo-like kinase 3 in human corneal epithelial cellsSynthetic biology: lessons from engineering yeast MAPK signalling pathwaysYeast mRNA cap-binding protein Cbc1/Sto1 is necessary for the rapid reprogramming of translation after hyperosmotic shock.Down-regulation of TORC2-Ypk1 signaling promotes MAPK-independent survival under hyperosmotic stressSphingolipid biosynthesis upregulation by TOR complex 2-Ypk1 signaling during yeast adaptive response to acetic acid stressPlasma membrane aminoglycerolipid flippase function is required for signaling competence in the yeast mating pheromone response pathwayHog1 mitogen-activated protein kinase (MAPK) interrupts signal transduction between the Kss1 MAPK and the Tec1 transcription factor to maintain pathway specificity.Specific α-arrestins negatively regulate Saccharomyces cerevisiae pheromone response by down-modulating the G-protein-coupled receptor Ste2.Different polarisome components play distinct roles in Slt2p-regulated cortical ER inheritance in Saccharomyces cerevisiae.The yeast Hot1 transcription factor is critical for activating a single target gene, STL1Pathway connectivity and signaling coordination in the yeast stress-activated signaling network.Adaptive Posttranslational Control in Cellular Stress Response Pathways and Its Relationship to Toxicity Testing and Safety AssessmentDesign, synthesis, and characterization of a highly effective Hog1 inhibitor: a powerful tool for analyzing MAP kinase signaling in yeastOsmostress-induced cell volume loss delays yeast Hog1 signaling by limiting diffusion processes and by Hog1-specific effectsBasic Properties of the p38 Signaling Pathway in Response to Hyperosmotic ShockReconstruction of the High-Osmolarity Glycerol (HOG) Signaling Pathway from the Halophilic Fungus Wallemia ichthyophaga in Saccharomyces cerevisiaeNuclear relocation of Kss1 contributes to the specificity of the mating responseA quantitative study of the Hog1 MAPK response to fluctuating osmotic stress in Saccharomyces cerevisiae.Automated ensemble modeling with modelMaGe: analyzing feedback mechanisms in the Sho1 branch of the HOG pathway.Multiple means to the same end: the genetic basis of acquired stress resistance in yeast.Identification and characterization of a salt stress-inducible zinc finger protein from Festuca arundinacea.A systems biology analysis of long and short-term memories of osmotic stress adaptation in fungiOsmotic stress-induced phosphorylation of H2AX by polo-like kinase 3 affects cell cycle progression in human corneal epithelial cellsOsmostress induces autophosphorylation of Hog1 via a C-terminal regulatory region that is conserved in p38αTORC2-dependent protein kinase Ypk1 phosphorylates ceramide synthase to stimulate synthesis of complex sphingolipids.Quantitative analysis of glycerol accumulation, glycolysis and growth under hyper osmotic stress.Phosphoproteomic analyses reveal novel cross-modulation mechanisms between two signaling pathways in yeastThe Dynamical Systems Properties of the HOG Signaling Cascade.Hyperosmotic stress-induced corneal epithelial cell death through activation of Polo-like kinase 3 and c-Jun.Control analysis of the eukaryotic cell cycle using gene copy-number series in yeast tetraploidsThe Hog1 mitogen-activated protein kinase mediates a hypoxic response in Saccharomyces cerevisiae.Delayed Turnover of Unphosphorylated Ssk1 during Carbon Stress Activates the Yeast Hog1 Map Kinase Pathway.Vacuolar H+-ATPase works in parallel with the HOG pathway to adapt Saccharomyces cerevisiae cells to osmotic stressDynamic processes at stress promoters regulate the bimodal expression of HOG response genes.MAPK feedback encodes a switch and timer for tunable stress adaptation in yeast.Linking the signaling cascades and dynamic regulatory networks controlling stress responses.Assembly, molecular organization, and membrane-binding properties of development-specific septinsGenetic networks inducing invasive growth in Saccharomyces cerevisiae identified through systematic genome-wide overexpressionSignalling pathways in the pathogenesis of Cryptococcus.Native cysteine residues are dispensable for the structure and function of all five yeast mitotic septins
P2860
Q24307842-A97903AB-2AEA-4942-84EC-22949ED54D96Q26991913-4334B8DD-549D-42C2-953F-F73F56E668F1Q27929949-74D53BE1-214D-4B7C-96B1-6CC6A155E464Q27931435-ABD9EE77-F734-483B-AA67-09D4190F3734Q27932351-570EC4D4-2632-4CC3-900C-0F685CF4ED8DQ27932915-9011A84F-8349-4D56-826D-A333BCE77243Q27933210-8D1EE112-4A37-4578-821B-52EA2F4E9076Q27934739-A7D525C2-36BA-4BEF-AE2E-DFA43F8DB967Q27935784-0C0E34FA-63A1-4F5C-927D-F3AA77A13B32Q27936363-C3156EC3-5BE2-4931-B2AC-E2A6E7352977Q27937397-E84CC570-1296-4D1C-89BA-FA0695CCE453Q28383566-27E3A1E4-5D78-41C6-873F-4769CADE132DQ28478363-A9862485-01C7-4D38-847E-82AB5B0674E5Q28535284-472783A7-B318-43DE-9AB7-C3514DB56B99Q28547726-12AA679A-2D40-4DDF-BC2D-77CAFF77D553Q30008896-BD3BA94A-C45B-49FB-AE1F-D452CD45AA76Q30840668-EE929B0A-12E4-4453-91BA-1F402B4DF4D6Q33538019-401F8615-80F8-42AC-979E-EE2294E4801AQ33869009-CDF83452-1D41-486E-9C91-198F9C2FB51DQ34079179-C89F0075-2450-4BE7-B2CE-3CF5C57F6469Q34137985-6A569DB5-D32C-4AD1-8E17-E86BFA687CE5Q34282739-3F062FC3-29CC-4819-9E62-44775C3E7B34Q34396857-7361189C-3088-4DAC-BA07-15AC1BAEA700Q34416082-4ED87FC3-C035-4218-837A-7C168A353DCFQ34440056-BB3308A0-A287-44AF-8F85-EF227AB38543Q34769244-A024FF33-97FB-47A8-A666-16FCCD78CF8EQ34990551-0A60DF08-055E-4CD6-B0D6-213F23A38439Q34999282-6EDCC633-35A9-4620-97CB-75C723C7B762Q35027536-FC81A7DE-CEF8-4503-B645-4B285F33DB42Q35029588-8BC4CCCF-8F0D-4EC8-8AD7-EAE8B4BB9347Q35065482-E0B6EB07-E996-447C-8710-631C268191F6Q35764555-C245D28D-1754-44EB-8079-3AD882BFB804Q35804688-2883D0A0-203B-4E97-B494-AC40CB75226BQ35836166-78817034-0D96-4AF7-AE82-3547605A8CCCQ35861696-9C5216FF-39C5-42C3-8CC3-622A15C2B3CBQ36580599-46DC33C3-49D5-4797-889D-4FBD718312FCQ36634715-1B780B99-093C-4AA7-9E4C-8595036DC649Q36709972-B9A6BEAA-CD83-431F-B144-14623848A263Q37377961-C01AAE53-0D00-4E9C-98C5-4F86A19EF712Q37431107-1D05E15C-686E-4358-A590-46511E8A727C
P2860
Stress resistance and signal fidelity independent of nuclear MAPK function
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
Stress resistance and signal fidelity independent of nuclear MAPK function
@en
type
label
Stress resistance and signal fidelity independent of nuclear MAPK function
@en
prefLabel
Stress resistance and signal fidelity independent of nuclear MAPK function
@en
P2093
P2860
P356
P1476
Stress resistance and signal fidelity independent of nuclear MAPK function
@en
P2093
Jeremy Thorner
Jesse C Patterson
Patrick J Westfall
Raymond E Chen
P2860
P304
12212-12217
P356
10.1073/PNAS.0805797105
P407
P577
2008-08-21T00:00:00Z