ライフサイエンスコーパス: heat shock

1 n, while U56 is also pseudouridylated during heat shock.

2 i, such as DNA damage, oxidative stress, and heat shock.

3 reduced microbial fitness after exposure to heat shock.

4 a from the cytosol in C2C12 cells exposed to heat shock.

5 anisms such as shear stress, DNA damage, and heat shock.

6 munoglobulin protein (BiP) mRNA (also called heat shock 70-kilodalton protein 5 mRNA) that were not i

7 human CRC tissue exposed to hypoxia, induced heat-shock 70-kDa protein-1-like (HSPA1L) expression sta

8 r histocompatibility complex, flotillin, and heat-shock 70-kDa proteins, are similarly present in all

9 Here we show that heat shock accelerates HIV transcription through inducti

10 und that the oxidative stressor arsenite and heat shock-activated stress responses evident by T-intra

11 Heat shock also caused excessive mitochondrial fragmenta

12 Hormetic heat shock also reduces the progressive accumulation of

13 we found that HSP90 inhibitor PF-4942847 and heat shock also suppress FOXM1.

14 encies are robustly maintained after thermal heat shock and after mimicking the heat-shock response t

15 Railway plants also have strong constitutive heat shock and freezing tolerance compared with mountain

16 types appear independent of the well-studied heat shock and insulin signaling pathways, indicating th

17 f antibiotics and enhance survival following heat shock and membrane stress.

18 We show that a transient heat shock and particularly the concomitant induction of

19 tant forms of MRJ interacted with RBPs after heat shock and prevented their accumulation in aggregate

20 ondrial intermembrane space and matrix after heat shock, and some do so even without stress.

21 Mild heat acclimation and moderate heat shock appear to have different effects on the mitoc

22 estigate how this changes after 10-20 min of heat shock at 42 degrees C.

23 r stress response resembling the response to heat shock, but the transcriptional basis of this respon

24 Upon signal termination, elements of the heat-shock chaperone pathway disaggregate the A-bodies.

25 llelic mutations in DNAJC12, which encodes a heat shock co-chaperone family member that interacts wit

26 interact with tau and heat shock protein 90/heat shock cognate 70 (Hsp90/Hsc70) complexes.

27 A with fatty acid synthase (FAS), filamin-A, heat shock cognate 70-kDa protein, and OGT were confirme

28 chaperones heat shock protein 90 (HSP90) and heat shock cognate protein 70 (HSC70) are nucleating sit

29 Heat shock cognate protein 70 (Hsc70) regulates protein

30 trates that DCB-3503 preferentially binds to heat shock cognate protein 70 (HSC70), which is a determ

31 at least partially mediated through cellular heat shock cognate protein 70 (Hsc70).

32 encoding EBOV minigenomic RNA and identified heat shock cognate protein family A (HSC70) member 8 (HS

33 Heat-shock cognate 70 (HSC-70) and tropomyosin showed Ig

34 Often involved in the regulation of heat shock, cold shock and virulence genes, RNATs consti

35 he molecular chaperone Hsp90 under basal and heat shock conditions, but the effects are opposite and

36 ctioned with GroEL(SR) under both normal and heat-shock conditions.

37 Protein aggregates that form under heat shock contain both cytosolic and mitochondrial prot

38 as found in a region capping the nucleus and heat shock did not affect its location.

39 CtHsfA2b was found to bind to the heat shock element (HSE) on the promoter of AtApx2 and e

40 ch motif that facilitates HSF-1 binding to a heat-shock element (HSE) that is degenerate from the con

41 le cells in response to heat acclimation and heat shock exposure.

42 report that the polycomb protein EZH2, upon heat shock, facilitates transcription of stress-responsi

43 pression of heat shock proteins (HSPs) via a heat shock factor (HSF)-dependent mechanism.

44 Heat shock factor (Hsf1) regulates the expression of mol

45 ated protein kinase kinase signaling control heat shock factor 1 (HSF-1), a conserved stress-activate

46 response pathways, such as those mediated by heat shock factor 1 (HSF1) and nuclear factor-erythroid

47 Activated Heat Shock Factor 1 (HSF1) binds to transcription-primed

48 primary stress response transcription factor heat shock factor 1 (Hsf1) in a highly variable and stoc

49 prime transcriptional responses genome-wide.Heat Shock Factor 1 (HSF1) is a regulator of stress-indu

50 ociation with the heat shock response, yeast heat shock factor 1 (Hsf1) is essential even at low temp

51 In this issue, Qiao et al. demonstrate how heat shock factor 1 (HSF1) uncouples metabolic control f

52 Our data support a model demonstrating that heat shock factor 1 (HSF1), a master transcriptional reg

53 Heat shock factor 1 (HSF1), the "master regulator" of th

54 hanism regulated by the transcription factor heat shock factor 1 (HSF1), which increases the expressi

55 col to analyze the HSR in mice and dissected heat shock factor 1 (HSF1)-dependent and -independent pa

56 distinct regulatory roles for members of the heat shock factor family, including a putative regulator

57 tress, and disruption of genes including the heat shock factor hsf-1, the hypoxia-inducible factor hi

58 es the central heat shock response regulator heat shock factor protein 1 (HSF1) to affect some of its

59 ates transcription factors such as Nrf-1 and heat shock factor-1 and up-regulates gene expression of

60 Heat-shock factor (HSF) is the master transcriptional re

61 -lasting (>3 days) nuclear activation of the heat-shock factor, HSF1.

62 tion, we demonstrated that the modulation of heat-shock factor-1 by knockdown in nCPCs or overexpress

63 One leading candidate pathway is heat-shock factor-1, potentially affecting 8 identified

64 rs of heat shock response in eukaryotes, the heat shock factors (HSFs), have undergone large-scale ge

65 In the Deltadef1 strain, heat shock genes were misregulated, indicating that Def1

66 Remarkably, heat shock (HS)-induced RCD, but not reproductive or vas

67 using a transgenic fish model that exhibits heat-shock (HS) inducible impaired heart regeneration.

68 ic misfolded proteins targeted by Rsp5 after heat-shock (HS).

69 l repression of transcription that follows a heat shock in lower eukaryotes.

70 the genome-wide transcriptional response to heat shock in mammals is rapid and dynamic and results i

71 e a mathematical model of Hsf1 activation by heat shock in which unfolded proteins compete with Hsf1

72 of mammalian cell lines, we found that only heat shock-induced but not basal expression of chaperone

73 required for transcriptional elongation and heat shock-induced chromatin decondensation.

74 tor" of the HSR, controls only a fraction of heat shock-induced genes and does so by increasing RNA p

75 ole for HSF1 in the induction of a subset of heat shock-induced readthrough transcripts.

76 ase boundaries, created from current pulses (heat shocks), invert the polarization of selective domai

77 Exposure of C2C12 muscle cells to heat shock led to apoptotic death featuring activation o

78 thaliana accessions, we identified the small heat shock-like SIEVE ELEMENT-LINING CHAPERONE1 (SLI1).

79 ibitor compound (OS47720) not only elicits a heat-shock-like response but also offers synaptic protec

80 2Av null mutant, chromatin decondensation at heat shock loci is unaffected in the absence of JIL-1 as

81 In addition, we evaluated the effects of heat shock on the localization of melanopsin by immunocy

82 and longevity of animals exposed to hormetic heat shock or HSF-1 overexpression.

83 eadthrough, using nuclear RNA-Seq, comparing heat shock, osmotic stress, and oxidative stress in NIH

84 tive signals, including hypoxia, cold shock, heat shock, oxidative stress, exercise-induced adaptatio

85 Liver heat shock protein (HSP) 70 levels (at 72 hours) and mac

86 n is injured, there is a massive increase of heat shock protein (Hsp) 90alpha inside the wound bed.

87 with fluorescence microscopy to investigate Heat Shock Protein (HSP) gene conformation and 3D nuclea

88 ve neuronal expression of HSP-16.48, a small heat shock protein (HSP) homolog of human alpha-crystall

89 Overexpression of Ssa2, a cytosolic heat shock protein (Hsp)70, was sufficient to partially

90 The 70-kDa heat shock protein (Hsp70) family of chaperones bind cog

91 k protein A2 (HSPA2), a member of the 70 kDa heat shock protein (HSP70) family, plays an important ro

92 The 90-kDa heat shock protein (Hsp90) chaperone system affects the

93 The 90-kDa heat shock protein (Hsp90) is a widely conserved and ubi

94 e81) displayed improved binding to the small heat shock protein (HspB8) in ischemic skeletal muscle c

95 oplasmic aggregates, which contained Hspa1B (heat shock protein 1B hsp70) and ubiquitinated proteins,

96 /-) heart, however, basal phosphorylation of heat shock protein 20 (Hsp20) is significantly decreased

97 ins, myeloid leukemia sequence 1 (Mcl-1) and heat shock protein 27 (HSP27), to block the two proteoly

98 ed by a transient increase of phosphorylated heat shock protein 27, p38 mitogen-activated protein kin

99 We show that overexpression of yeast Heat shock protein 31 (Hsp31), a DJ-1 homolog with robus

100 Here, we demonstrate that cellular heat shock protein 40 (Hsp40/DnaJB1) facilitates the nuc

101 Heat shock protein 47 (HSP47) is an endoplasmic reticulu

102 Two proteins, heat shock protein 47 (Hsp47/SERPINH1) and 65-kDa FK506-

103 s with ABMR expressed fascin1, vimentin, and heat shock protein 47 strongly, whereas those from norma

104 The levels of serum S. japonicum heat shock protein 60 (SjHSP60)-specific IgG and its sub

105 ion induced autoantibodies against dsDNA and heat shock protein 60 as well as antibody accumulation i

106 esponse (mtUPR) as measured by expression of heat shock protein 60, Clp protease, and Lon peptidase 1

107 P. aeruginosa GroEL, a homolog of heat shock protein 60, was identified as one of the fact

108 N)-gamma, CXCL9, Perforin 1, Granzyme B, and heat shock protein 60.

109 Heat shock protein 70 (Hsp70) and Hsp90 are molecular ch

110 Heat shock protein 70 (Hsp70) in complex with bcl2 assoc

111 ith the pharmacochaperone noribogaine or the heat shock protein 70 (HSP70) inhibitor pifithrin-mu suc

112 Stress-inducible heat shock protein 70 (hsp70) interacts with superoxide

113 The highly conserved heat shock protein 70 (Hsp70) is a ubiquitous molecular

114 ING IMMUNOGLOBULIN PROTEIN (BIP), encoding a heat shock protein 70 (HSP70) molecular chaperone, reduc

115 across the substrate binding domain (SBD) of heat shock protein 70 (Hsp70) to pinpoint mechanical uni

116 a42 neurotoxicity through engineering of the Heat shock protein 70 (Hsp70), a chaperone that has demo

117 th gold nanoparticles to sensitively analyze heat shock protein 70 (HSP70), a potential biomarker tha

118 d a robust increase in the folding chaperone heat shock protein 70 (Hsp70), and NAC mitigated this ef

119 tions, which is consistent with conventional heat shock protein 70 (HSP70)-client interaction mechani

120 ate with ATP-dependent chaperones, including heat shock protein 70 (Hsp70).

121 process is facilitated by the mitochondrial heat shock protein 70 (mtHsp70), a chaperone contributin

122 in control DCs, covalently bind to chaperone heat shock protein 70.

123 ity of the auxin co-receptor TIR1, involving HEAT SHOCK PROTEIN 90 (HSP90) [9].

124 was dependent on the chaperoning function of heat shock protein 90 (HSP90) and co-accompanied by the

125 This interaction was stabilized by heat shock protein 90 (HSP90) and followed by proteasoma

126 The chaperones heat shock protein 90 (HSP90) and heat shock cognate pro

127 lysosomal membrane, where it interacts with heat shock protein 90 (HSP90) and stabilizes binding of

128 with molecular targeted agents that inhibit heat shock protein 90 (Hsp90) and/or mammalian target of

129 We found that the heat shock protein 90 (Hsp90) chaperone system of the ye

130 of CK2 and EGFR also caused deactivation of heat shock protein 90 (Hsp90) co-chaperone Cdc37, which

131 The heat shock protein 90 (Hsp90) family of molecular chaper

132 We found that inhibitors of heat shock protein 90 (HSP90) induced apoptosis in BL ce

133 Heat shock protein 90 (HSP90) inhibition is an attractiv

134 Heat shock protein 90 (HSP90) is a molecular chaperone t

135 Heat shock protein 90 (Hsp90) is an essential eukaryotic

136 Na(+) and/or K(+) flux and the activation of heat shock protein 90 (HSP90), a protein required for th

137 nt phenethyl isothiocyanate (PEITC) inhibits heat shock protein 90 (Hsp90), the main negative regulat

138 ivity of these inhibitors was tested against heat shock protein 90 (HSP90), which possesses a similar

139 C-1-interacting proteins that are well-known heat shock protein 90 (Hsp90)-associated co-chaperones:

140 by association with the molecular chaperone heat shock protein 90 (Hsp90).

141 lic androgen receptor (AR) chaperone protein heat shock protein 90 (HSP90).

142 ed by rapid HDAC6-dependent deacetylation of heat shock protein 90 (HSP90).

143 those, we chose to focus on an inhibitor of heat shock protein 90 beta (HSP90beta).

144 is the endoplasmic reticulum resident of the heat shock protein 90 kDa (Hsp90) family of molecular ch

145 protein inhibitor of NOS1 (PIN), calmodulin, heat shock protein 90, and NOS interacting protein.

146 dehydrogenase, alpha-enolase, filamin-A, and heat shock protein 90, were identified in samples of api

147 f RanBP9 to physically interact with tau and heat shock protein 90/heat shock cognate 70 (Hsp90/Hsc70

148 The molecular chaperone heat shock protein A2 (HSPA2), a member of the 70 kDa he

149 d of prestretch and finally treated with the heat shock protein alpha-B crystallin.

150 We have shown previously that the small heat shock protein alphaB-crystallin (alphaB) is exporte

151 The small heat shock protein alphaB-crystallin (CRYAB) has been im

152 Genetic mutations in the human small heat shock protein alphaB-crystallin have been implicate

153 The heat shock protein also seems to regulate the cross-talk

154 The heat shock protein and cell wall component Ssa1 was also

155 egulatory use of an evolutionarily conserved heat shock protein and present a distinctive mechanism f

156 to activate transcription of both the small heat shock protein and the large heat shock protein gene

157 terotetramer stage coinciding with increased heat shock protein association.

158 3-3:serotonin N-acetyltransferase and 14-3-3:heat shock protein beta-6 complexes revealed similaritie

159 en interaction and heterodimer and homodimer heat shock protein complexes.

160 on chromosome 19 that fuses part of the DnaJ heat shock protein family (Hsp40) member B1 gene (DNAJB1

161 MIR21 was shown to target the DnaJ heat shock protein family (Hsp40) member B5 (DNAJB5).

162 n patient biopsy specimens and detected DnaJ heat shock protein family (Hsp40) member B9 (DNAJB9) as

163 cription factor of the so far unstudied DnaJ heat shock protein family (Hsp40) member C22 (Dnajc22).

164 ave determined crystal structures of a small heat shock protein from Salmonella typhimurium in a dime

165 g which the transcript levels of some of the heat shock protein genes significantly reduced in respon

166 h the small heat shock protein and the large heat shock protein genes.

167 Heat shock protein gp96, also known as grp94, is an esse

168 factors DnaJ1, DnaJ2, and GrpE and the small heat shock protein Hsp20.

169 Mutations in the small heat shock protein Hsp27, encoded by the HSPB1 gene, hav

170 The 70 kDa heat shock protein Hsp70 has several essential functions

171 Furthermore, mRNA for the major heat shock protein Hsp70 is transcribed at robust levels

172 Here we show that the small heat shock protein HspB1 (hsp25/27) is phosphorylated in

173 Small heat shock protein HSPB7 is highly expressed in the hear

174 The E. coli heat shock protein HtpG (Hsp90Ec) is the bacterial homol

175 ected and critical role for a specific small heat shock protein in directly modulating actin thin fil

176 rescued with therapeutic application of the heat shock protein in vivo.

177 Heat shock protein levels are often elevated in both car

178 ammatory cytokines, NF-kappaB signaling, and heat shock protein pathway RNA transcripts.

179 AlphaB-crystallin (alphaBC) is a small heat shock protein that is constitutively expressed by p

180 the expression of alphaB-crystallin, a small heat shock protein that is enriched in astrocytes and me

181 FTL578 (ornithine cyclodeaminase), FTL663 (heat shock protein), and FTL1228 (iron-sulfur activator

182 508del, is initiated by binding of the small heat shock protein, Hsp27.

183 ein in the sterol-regulated induction of the heat shock protein, HSP42 and HSP102, mRNAs.

184 ive protein, fibrin degradation product, and heat shock protein-70 improved risk reclassification.

185 ve protein, fibrin degradation products, and heat shock protein-70 representing these 3 pathways was

186 eactive protein, fibrin degradation product, heat shock protein-70, and suPAR were measured in 3278 p

187 ive protein, fibrin degradation product, and heat shock protein-70.

188 Both intracellular and extracellular heat shock protein-90 (Hsp90) family proteins (alpha and

189 Heat shock protein-90 (Hsp90) is an essential molecular

190 onverted to kallikrein because of release of heat shock protein-90 (Hsp90).

191 s an endothelial-cell-specifically expressed heat shock protein.

192 Cytosolic and organelle-based heat-shock protein (HSP) chaperones ensure proper foldin

193 Clustered class-I small heat-shock protein (sHSP) chaperone genes, SlHSP17.6, Sl

194 Heat-shock protein 5 (HSPA5) is a marker for poor progno

195 tern (DAMP) response including elevations in heat-shock protein 70, IL-1, IL-18, and TNFalpha indicat

196 itic RNAs, including Cdg7_FLc_0990, involved heat-shock protein 70-mediated nuclear importing mechani

197 o address this need, we explored the role of heat-shock protein 90 (Hsp90) in opioid-induced MOR sign

198 Inhibition of the chaperone heat-shock protein 90 (HSP90) induces apoptosis, and it

199 The molecular chaperone heat-shock protein 90 (Hsp90) is an essential component

200 directly interacts with PIH1D1, a subunit of heat-shock protein 90 cochaperone R2TP complex, which is

201 PS also stimulated LRP1 shedding, as did the heat-shock protein and LRP1 ligand, calreticulin.

202 d in hetero-oligomer formation between human heat-shock protein family B (small) member 1 (HSPB1) and

203 ry structure and dynamics of the human small heat-shock protein Hsp27 are linked to its molecular cha

204 Heat-shock protein of 90 kDa (Hsp90) is an essential mol

205 in the key proteins in aldose reductase and heat-shock protein-70 within living cancer cells.

206 e and cyclic AMP signaling and a cytoplasmic heat-shock protein.

207 at better maintained phytoene desaturase and heat shock protein70-1 (HSP70-1) inserts in Nicotiana be

208 umulation inhibits the activity of cytosolic HEAT SHOCK PROTEIN90 and, as a consequence, the maturati

209 DP-43 clearance we over-expressed a range of heat shock proteins (HSPs) and identified DNAJB2a (encod

210 nism developed to increase the expression of heat shock proteins (HSPs) via a heat shock factor (HSF)

211 Whether MRP-1 is chaperoned by heat shock proteins (HSPs) was investigated by immunopre

212 s, controls the expression of cytoprotective heat shock proteins (HSPs), molecular chaperones/cochape

213 Small heat shock proteins (sHsps) are a family of ATP-independ

214 Small heat shock proteins (sHsps) are a ubiquitous family of m

215 The ubiquitous small heat shock proteins (sHSPs) are well documented to act i

216 onditions promoting protein unfolding, small heat shock proteins (sHsps) prevent the irreversible agg

217 d protein response (reduced concentration of heat shock proteins 60 and 70).

218 The interaction between the Heat Shock Proteins 70 and 40 is at the core of the ATPa

219 Cellular protein homeostasis depends on heat shock proteins 70 kDa (Hsp70s), a class of ubiquito

220 hermia (MNFH) on the cell death rate and the heat shock proteins 72 (HSP72) induction behavior in ret

221 e encoding ascorbate peroxidase (AtApx2) and heat shock proteins [AtHsp18.1-CI, AtHsp22.0-ER, AtHsp25

222 ly the genes associated with photosynthesis, heat shock proteins and antioxidants impinge on the comp

223 Genes coding for heat shock proteins and pilins were also induced in Delt

224 rradiated whole tumor cells or tumor-derived heat shock proteins can generate tumor-specific immune r

225 ogical role for FOXO-dependent expression of heat shock proteins in vivo.

226 Astrocytic exosomes carry heat shock proteins that can reduce the cellular toxicit

227 uction with increased expression of specific heat shock proteins that was variable across tissues.

228 lation of mitochondrial matrix proteases and heat shock proteins was initially described.

229 A number of heat shock proteins were also elevated.

230 transporters, cytochrome P450, ubiquitin and heat shock proteins were found associated with adaptatio

231 f cytosolic (e.g. glutathione peroxidase and heat shock proteins) and mitochondrial adaptive or stres

232 ected transcription factors, chaperones, and heat shock proteins) were highly expressed in Namikonga.

233 notion that mitochondrial adaptations (e.g. heat shock proteins, antioxidant enzymes and sirtuin-1/P

234 thetic apparatus, the ROS-scavenging system, Heat Shock Proteins, aquaporins, expansins, and desiccat

235 f-antigens, such as apolipoprotein B-100 and heat shock proteins, can contribute to vascular inflamma

236 Previously, we have reported that heat shock proteins, HSP40 and HSP70 reciprocally regula

237 These results indicate that heat shock proteins, in particular Hsp90, stimulate APOB

238 Immune responses primed by endogenous heat shock proteins, specifically gp96, can be varied, a

239 ilies Hsp70, Hsp104, Hsp90, Hsp60, and small heat-shock proteins (sHsps) apparently act as unfolding

240 Small heat-shock proteins (sHSPs) are a conserved group of mol

241 Small heat-shock proteins (sHsps) prevent aggregation of therm

242 ivo, molecular chaperones, such as the small heat-shock proteins (sHsps), normally act to prevent pro

243 ral capsids, virus-like particles, ferritin, heat-shock proteins and chaperonins.

244 This fit well with the identification of heat-shock proteins as a class of antigens that showed o

245 Induction of neuroprotective heat-shock proteins via pharmacological Hsp90 inhibitors

246 uch as Hikeshi, involved in the transport of heat-shock proteins, and NTF2, involved in the transport

247 re commonly observed in experiments on small heat-shock proteins, but their connection to the biologi

248 We have developed an in vivo heat shock protocol to analyze the HSR in mice and disse

249 this association is transiently disrupted by heat shock, providing the first evidence that a chaperon

250 Surprisingly, we found that heat shock represses multiple immune genes in the abdome

251 153/Y155), was dramatically increased by the heat shock response (HSR) in human cells.

252 ides and evaluated their ability to suppress heat shock response (HSR) in MM cells.

253 The heat shock response (HSR) is a mechanism to cope with pr

254 Regulation of the heat shock response (HSR) is essential in all living sys

255 Here, we have characterized the Heat Shock Response (HSR), one branch of this network, a

256 IHSF115 was employed to probe the human heat shock response at the transcriptome level.

257 Here we show that manipulation of the heat shock response by expression of dominant active HSF

258 expression of molecular chaperones and other heat shock response genes.

259 The key transcriptional activators of heat shock response in eukaryotes, the heat shock factor

260 We sought to explore the role for the heat shock response in the clearance of insoluble TDP-43

261 The heat shock response in yeast is regulated by the interac

262 The heat shock response is a stress-responsive protective me

263 terestingly, PGC-1alpha requires the central heat shock response regulator heat shock factor protein

264 one gene induction, the vast majority of the heat shock response was Hsf1 independent.

265 Heat shock response was prioritized over the oxidative s

266 d products and three exhibited the classical heat shock response with expression of HSP70 transcripts

267 t induced a strong cytoplasmic Hsf1-mediated heat shock response, accompanied by attenuation of prote

268 ct group of genes, enriched for roles in the heat shock response, displayed strong activation.

269 ion and metabolism), growth arrest response, heat shock response, DNA recombination, and anaerobiosis

270 istent with the activation of the functional heat shock response, FA strongly elevated the expression

271 Despite its eponymous association with the heat shock response, yeast heat shock factor 1 (Hsf1) is

272 terminants of the extent and duration of the heat shock response.

273 ting similar stress responses, including the heat shock response.

274 d protein aggregation and the HSF1-dependent heat shock response.

275 the master transcriptional regulator of the heat-shock response (HSR) and is essential for stress re

276 ures rapidly induce a genetically programmed heat-shock response (HSR) that is essential to establish

277 Moreover, PafE contributes to the heat-shock response and virulence of Mtb Here, we show t

278 In the absence of Fes1S, the heat-shock response is constitutively induced at normall

279 Although the universally conserved heat-shock response regulated by transcription factor HS

280 r thermal heat shock and after mimicking the heat-shock response transcriptional program at 30 degree

281 utophagy in HSF-1-regulated functions in the heat-shock response, proteostasis and ageing.

282 ation and Ser326 phosphorylation of the main heat shock-responsive transcription factor HSF1, which w

283 rogram at 30 degrees C by overexpressing the heat shock sigma factor encoded by the rpoH gene.

284 independent of chaperone activity during the heat shock stress response.

285 thereby improving its translation following heat shock stress via IRES activation.

286 eased sensitivity to pathogenic bacteria and heat-shock stress.

287 polymerase II occupancy in DoG regions after heat shock, supporting our findings.

288 and extensive changes in transcription upon heat shock that are largely modulated at pause release,

289 rotein folding and pro-survival machinery by heat shock transcription factor 1 (HSF1) ameliorates bio

290 Heat shock transcription factor 1 (HSF1) has been identi

291 We investigated the role that the heat shock transcription factor HSF-1 played in determin

292 tion factor, dFOXO, that works alongside the heat shock transcription factor to activate transcriptio

293 nteraction between a chaperone protein and a heat shock transcription factor, and fine-tuned by phosp

294 We investigated the role that the heat shock transcription factor, HSF-1, and its downstre

295 gulated at the level of mRNA translation via heat-shock transcription factor 1 (HSF1)-induced HuR act

296 iptional response is mediated by a family of heat-shock transcription factors.

297 ion, and the second, with 1.2 x 10(8) cfu of heat shock-treated S. aureus to generate sterile inflamm

298 In addition, heat-shock treatment increased the proportion of cells w

299 n a cellular context, SUBINs largely prevent heat shock-triggered poly-SUMOylation.

300 ment with proteasome and HSP90 inhibitors or heat shock, was the molecular chaperone HSP70.