ライフサイエンスコーパス: heat stress

1 enhanced tolerance, respectively, to extreme heat stress.

2 sponse, leading to PM integrity defects upon heat stress.

3 rity plays a key role in cell survival under heat stress.

4 mics in tolerance of skeletal muscle against heat stress.

5 system (UPS)-mediated proteolysis following heat stress.

6 sweating and cutaneous vasodilatation during heat stress.

7 nd aggregated proteins during aging, but not heat stress.

8 (HREs), which cause their activation during heat stress.

9 erance, and ATP turnover of S. mutans during heat stress.

10 h which Saccharomyces cerevisiae responds to heat stress.

11 iological factors that reduce sensitivity to heat stress.

12 to warmer temperatures (29 degrees C) before heat stress.

13 oteome of yeast continuously exposed to mild heat stress.

14 he temporal response of the broiler liver to heat stress.

15 ut when cardiac pre-load is increased during heat stress.

16 cells undergo such an arrest in response to heat stress.

17 upon Hsp90 inhibition or stress foci during heat stress.

18 ch chloroplast processes are disturbed under heat stress.

19 creases in sympathetic nerve activity during heat stress.

20 responses of S. mutans during physiological heat stress.

21 d aged individuals during whole-body passive heat stress.

22 ubpopulations that are reversibly damaged by heat stress.

23 further exacerbated under osmotic, salt, or heat stress.

24 ress treatments, but only accumulated during heat stress.

25 h the duration of the syncytial stage during heat stress.

26 ns significantly associated with response to heat stress.

27 differential regulation of AS in response to heat stress.

28 entify the poplar members most responsive to heat stress.

29 reflex cutaneous vasodilatation with passive heat stress.

30 nts and reactive oxygen species during early heat stress.

31 well as new genes that can be implicated in heat stress.

32 of the two reporters were up-regulated upon heat stress.

33 number of down-regulated genes in 10 min of heat stress.

34 was significantly modulated within 10 min of heat stress.

35 ion of HSFA1 genes and other HSF genes under heat stress.

36 ) and follows the inactivation of PSII under heat stress.

37 ated proteins to promote cell survival after heat stress.

38 PSII inactivation and photobleaching under heat stress.

39 ctivity triggered elongation pausing without heat stress.

40 hesized during heat stress and recovery from heat stress.

41 ile some physiological traits were shaped by heat stress.

42 nd oligogalactolipids were more resistant to heat stress.

43 lthy older adults can achieve during passive heat stress.

44 tterns between cell types and in response to heat stress.

45 ar stripped roots, as well as in response to heat stress.

46 eproductive tissues during development under heat stress.

47 with reduced ethylene effects on yield under heat stress.

48 salt stress, heat stress, and recovery from heat stress.

49 al start sites, one of which is exclusive to heat stress.

50 t directly or indirectly with HSP22E/F under heat stress.

51 sis across eudicot and monocot species under heat stress.

52 r glutathione peptides that have experienced heat stress.

53 rtant role in plant resistance to aphids and heat stress.

54 that healthy older adults can achieve during heat stress.

55 in vivo, but lost this association following heat stress.

56 id metabolism drives TAG accumulation during heat stress.

57 varied depending on cultivar and accumulated heat stress.

58 well as the observed increase in GPC due to heat stress.

59 nsitivity to lose coral photosynthesis under heat-stress.

60 following pollination was also suppressed by heat-stress.

61 increased levels of light-stress elicited by heat-stress.

62 sion of those SET genes responds to cold and heat stresses.

63 rotects the mosquito against desiccation and heat stresses.

64 previously reported that clinically relevant heat-stress (37-41 degrees C) resulted in a classical he

65 The spatial patterns of SST and heat stress across the Coral Triangle reflect the comple

66 ipatory response, parents subject to a prior heat stress actually produce offspring that are less abl

67 ght temperature are common choice of forcing heat stress algorithms, current parameterizations in mos

68 When a second heat stress (also 32 degrees C for 10 days) was applied

69 Reef-building corals are vulnerable to heat stress and are facing widespread losses due to clim

70 type, the rcf2-1 mutant is hypersensitive to heat stress and because the reduced thermotolerance is c

71 e antisense RNA gene is only expressed after heat stress and dependent on the activity of HSFA1a/HSFA

72 cal for pollen fertility under conditions of heat stress and drought.

73 may include heat-related disorders, such as heat stress and economic consequences of reduced work ca

74 HSP22E/F strongly accumulate during heat stress and form high molecular mass complexes.

75 NL-44, will minimize the negative impact of heat stress and increase global food productivity, benef

76 th of populations experiencing environmental heat stress and our understanding of impacts at the leve

77 cutaneous blood flow during exercise-induced heat stress and provide direction for future research ex

78 ify and quantify proteins synthesized during heat stress and recovery from heat stress.

79 stigate specifically the early events in the heat stress and recovery response.

80 id not directly correlate with resilience to heat stress and suggested that each species may have a d

81 EMD 57033-binding protects myosin against heat stress and thermal denaturation.

82 uction of the luciferase gene in response to heat stress and was more sensitive to high temperature t

83 B subunits became partially insoluble during heat stress and, in the CI and CII RNAi lines, showed re

84 to cells lacking ClpP, are not sensitive to heat-stress and do not accumulate protein aggregates sho

85 ve increased tree mortality through drought, heat stress, and insect attacks, with manifold impacts o

86 of light stress, osmotic shock, salt stress, heat stress, and recovery from heat stress.

87 rtant candidate genes related to drought and heat stress, and revealed important genomic regions poss

88 ve advantage over the mammals in response to heat stress, and therefore, mammals with testicular desc

89 ad a general growth defect, was sensitive to heat stress, and was attenuated for growth in mice.

90 s extreme weather events (e.g., drought- and heat-stress, and flooding), should also be considered in

91 Cardiovascular adjustments to heat stress are attenuated in healthy aged individuals,

92 Cardiovascular adjustments during heat stress are generally attenuated in healthy aged hum

93 The details of the sphingolipid responses to heat stress are important, because they guide some of th

94 hat increases in sympathetic activity during heat stress are not attenuated in healthy aged humans.

95 mapped 25 loci linked to growth traits under heat stress, arsenite, and paraquat, the majority of whi

96 talytic PDX1 homologs that do not respond to heat stress as demonstrated for rice (Oryza sativa) and

97 tant seedlings were more sensitive to severe heat stress, as indicated by a more dramatic decline of

98 dystachion to single salinity, drought, and heat stresses, as well as their double and triple stress

99 Heat stress assays carried out in the northern (Hurghada

100 report that Arabidopsis plants subjected to heat stress at 37 degrees C show much higher frequencies

101 s by CRISPR/Cas9 in Citrus plants exposed to heat stress at 37 degrees C.

102 rance, recorded as decreased mortality under heat stress at 40 +/- 1 degrees C (down from 80% to 55%)

103 ray at three time points--post 10 and 60 min heat stress at 42 degrees C and 30 min recovery at 26 de

104 ntal datasets with two wheat cultivars under heat stress at anthesis and grain filling stages.

105 Heat stress at anthesis reduced observed grain numbers p

106 ees C day/26 degrees C night with additional heat stress at anthesis) for a suite of traits including

107 ees C day/21 degrees C night with additional heat stress at anthesis; 34 degrees C day/26 degrees C n

108 FA1d are involved in thermotolerance to mild heat stress at temperatures as low as 27 degrees C.

109 Upon heat stress, AtBAG7 is sumoylated, proteolytically proce

110 pid volume loading, performed during passive heat stress, augments both cutaneous vasodilatation and

111 We address these questions by scrutinizing heat stress, because the frequency of extremely hot weat

112 However, in response to heat stress, both root hairs and stripped roots showed h

113 of MSNA remained greater in the aged during heat stress (burst frequency: Y: 47 +/- 6 vs. A: 63 +/-

114 ation of AtPARK13 transcripts are induced by heat stress but not by other stress conditions, includin

115 the mitochondrial regulome, demonstrate that heat stress can impair respiration by disturbing cytopla

116 In heat-stressed cardiomyocytes expression of the stress-ma

117 Furthermore, after heat stress, CI sHSPs showed increased retention in the

118 osylated therapeutic protein under different heat stress conditions and aggregation states.

119 o stabilization of the catalytic PDX1s under heat stress conditions, which would serve to maintain vi

120 mRNA stability of heat-inducible genes under heat stress conditions.

121 markers to extreme response to post anthesis heat stress conditions.

122 Under heat-stress conditions, up-regulation of ethylene biosyn

123 it-set and seed development under normal and heat-stress conditions.

124 In heat-stressed conditions, differential regulation of HSP

125 As heat stress continued, gasping was evoked in both groups

126 ing climate projections, we show that future heat stress could reduce the forest edge growth enhancem

127 on, ripening APX6-deficient seeds exposed to heat stress displayed reduced germination vigor.

128 r unit area and individual grain size, while heat stress during grain filling mainly decreased the si

129 dels require improvements in the response to heat stress during grain filling, but all models need im

130 ter than that in the interior in response to heat stress during the growing season.

131 he yield variability, with precipitation and heat stress during the late vegetative and early reprodu

132 High temperature (heat) stress during grain filling is a major problem in

133 t all models need improvements in simulating heat stress effects on grain set during anthesis.

134 egrees C water bath to create an accelerated heat stressed environment.

135 ture climate change will bring more frequent heat stress events and pose an increasing risk to global

136 Heat-stress events are more frequent during La Nina even

137 Whole-body heat stress evoked similar SSNA activation in CHF patien

138 dict the coral host response in a short-term heat stress experiment.

139 uctivity but are rarely tested with observed heat stress experimental datasets.

140 , Nigeria, and Shanghai, China) could become heat stressed, exposing more than 350 million more peopl

141 Heat stress factors (HSFs) are a class of transcription

142 iverse wheat elite lines and landraces under heat-stressed field conditions.

143 adaptation they maintain an active memory of heat stress for several days that promotes a more effici

144 t will remain generally higher than that for heat stress for the next half century, the relative impo

145 was more sensitive to drought stress than to heat stress for the US Midwest since the 1980s, and this

146 the major stress factor, clearly separating heat-stressed from non-heat-stressed plants.

147 ferential expression between the control and heat stressed groups.

148 onal acclimatization on coral sensitivity to heat-stress, has received limited attention despite diff

149 roRNA pathway in the adaptation to recurring heat stress (HS memory) at the physiological and molecul

150 re, our objectives were to examine how acute heat stress (HS) alters intestinal integrity and metabol

151 ydomonas reinhardtii acclimates to long-term heat stress (HS) and recovers from it.

152 e response, although the roles of PMEs under heat stress (HS) are poorly understood.

153 e reproductive tissues are more sensitive to heat stress (HS) compared to vegetative tissues, but the

154 esponse, which is often accompanied by fever/heat stress (HS).

155 ) drought acclimation (DA) or to (transient) heat stress (HS).

156 Most of the crop models tended to reproduce heat stress impacts better during grain filling than at

157 Environmental heat stress impacts on the physiology and viability of m

158 observed flowering dates and disaggregating heat-stress impacts, both pre- and postflowering stages

159 lated in reproductive tissues in response to heat stress in a manner to optimize resource allocation

160 role for this lethal pathway in response to heat stress in Arabidopsis thaliana The similarity of fe

161 SNA) that control the skin blood flow during heat stress in CHF patients.

162 ve lesions and ubiquitinated proteins during heat stress in CWD clams.

163 hat attenuated cardiovascular adjustments to heat stress in healthy aged individuals are unlikely to

164 tic nerve activity during whole-body passive heat stress in humans.

165 oduction and cutaneous vasodilatation during heat stress in humans; however, the mechanism by which h

166 scriptomics studies of thermal adaptation to heat stress in metazoans and compare these results with

167 e substrates with which they interact during heat stress in order to understand which chloroplast pro

168 ROS and abscisic acid regulates rapid SAA to heat stress in plants.

169 eration in mammals and is also implicated in heat stress in plants.

170 ell's survival and energy generation against heat stress in S. mutans.

171 e of ENSO and other climatic oscillations to heat stress in the Coral Triangle, we use a 5-km resolut

172 B2a RNAs were also present in the absence of heat stress in the female gametophyte.

173 gnificantly reduced in response to prolonged heat stress in the lhr1 mutant.

174 We show that transient, mild heat stress in the nematode Caenorhabditis elegans resul

175 Heat stress increased core temperature to a similar exte

176 s for mitigation and adaptation to projected heat stress increases in rapidly urbanizing India.

177 by both warm and cold fluid ingestion during heat stress, independently of differences in core and sk

178 by both warm and cold fluid ingestion during heat stress, independently of differences in core and sk

179 This investigation of heat stress-induced cellular senescence elucidates the m

180 NA breaks was found to be a primary cause of heat stress-induced cellular senescence in these cells.

181 ribution also is critical for the capture of heat stress-induced cytosolic protein aggregates and the

182 adiodurans, the Ro ortholog Rsr functions in heat-stress-induced ribosomal RNA (rRNA) maturation and

183 Here, we demonstrate that heat stress induces p21-dependent cellular senescence-li

184 The reprogramming of gene expression in heat stress is a key determinant to organism survival.

185 Climate-driven heat stress is a key factor affecting forest plantation

186 Heat stress is a major environmental constraint for crop

187 Heat stress is a severe environmental factor that signif

188 In addition, heat stress is found to be as important for yield as pre

189 of broiler self-regulation mechanisms under heat stress is important for the modern scale of poultry

190 t SSNA activation during a modest whole-body heat stress is not attenuated in CHF.

191 Heat stress is one of the best-studied cellular stress f

192 After about 30 minutes, heat stress is still in effect and the enzyme activity p

193 ow and cutaneous vascular conductance during heat stress is substantially attenuated in chronic heart

194 r Caribbean reef corals to similar light and heat-stress levels.

195 A quantitative proteomic comparison between heat-stressed LVS and the isogenic Lon-deficient mutant

196 107 of the heavy chain was identified in the heat-stressed mAb sample.

197 tion excipients in both light-irradiated and heat-stressed mAb samples.

198 an air temperature is nonlinearly related to heat stress, meaning that the same future warming as rea

199 a wide variety of different proteins against heat stress-mediated unfolding in vitro and in vivo.

200 e and phosphoglycerate kinase play a role in heat-stress-mediated protection of bitter gourd.

201 We show that this heat stress memory requires the activity of the FORGETTE

202 nd ISWI families, which also display reduced heat stress memory.

203 This nonlinearity is higher for heat stress metrics that integrate the effect of rising

204 cessful pollination and ovule fertilization, heat-stress modified PsACS and PsACO transcript profiles

205 ange in near UV-visible light-irradiated and heat-stressed monoclonal antibody (mAb) drug product in

206 Additionally, embryos from heat-stressed mothers displayed increased sensitivity to

207 etic variability in the response of wheat to heat stress needs to be considered through cultivar para

208 from the nucleolus to the nucleoplasm during heat stress; nucleolar pools are replenished during reco

209 The observed impact of heat stress on grain filling duration, total aboveground

210 circle retention and abrogated the effect of heat stress on longevity.

211 hondrial function, we combined the effect of heat stress on respiratory capacity with the discovery p

212 thogen in the tropical environment imposes a heat stress on the wearer that is itself a safety risk.

213 therefore provides a co-benefit of reducing heat stress on urban residents.

214 , to determine the severity of the impact of heat-stress on coral physiology, but also the dependence

215 of Caenorhabditis elegans following hormetic heat stress or HSF-1 overexpression.

216 cal for survival in all organisms exposed to heat stress or other conditions that alter the folding o

217 Pretreatment with mild heat stress or overexpression of Hsp70 protected cells f

218 Several regions experienced little to no heat stress over the entire period.

219 (PDAT1) were unable to accumulate TAGs after heat stress, phosphatidylcholine appears to be the major

220 sense-mediated mRNA decay (NMD)-impaired and heat-stressed plants shared a set of retained introns as

221 Transcriptomes of NMD-impaired and heat-stressed plants shared a set of retained introns as

222 r, clearly separating heat-stressed from non-heat-stressed plants.

223 To respond to and cope with heat stress, plants synthesize heat shock proteins (HSPs

224 is thaliana) seedlings indicated that during heat stress, polyunsaturated fatty acids from thylakoid

225 t matched either by endogenous sHSPs in both heat-stressed poplar plants and field-grown adult trees.

226 Here, we investigated how heat stress promotes longevity in yeast.

227 is-allelic variation for response to cold or heat stress provided an opportunity to study the basis f

228 ments and defined metabolic sensitivities to heat stress, providing evidence that metabolic enzyme th

229 uced by high ambient temperatures, below the heat-stress range, is collectively called thermomorphoge

230 Although heat stress reduces seed size in rice (Oryza sativa), li

231 the defects of QK in tolerance to different heat stress regimes, and to hydrogen peroxide, but not t

232 ne (SET) production in wheat under long-term heat stress remain unexplored.

233 We report here that quiescence induced by heat stress requires ALA depolarization and release of F

234 ng mechanism, (2) it shows that lifespan and heat stress resistance are separable, and (3) it strengt

235 as a model.We surprisingly discovered marked heat stress resistance in yeast ectopically expressing h

236 enetic variation) was high for oxidative and heat stress resistance, low (but significant) for longev

237 mediated stress response and is required for heat stress resistance.

238 The contribution of HsfA2 in heat stress response (HSR) and thermotolerance was inves

239 Heat stress response (HSR) is a conserved mechanism deve

240 Our findings revealed an important heat stress response and tolerance mechanism involving p

241 The divergence of the heat stress response exceeds that observed in the respon

242 Transcriptome analysis showed that heat stress response genes are differentially regulated

243 TFs of different families suggests that the heat stress response in rice involves integration of var

244 ence of anticipatory parental effects in the heat stress response in the highly polymorphic nematode

245 At sublethal concentrations, the heat stress response is crucial to overcome allicin stre

246 gether, these results provide evidence for a heat stress response pathway in pollen that connects a c

247 ic variation for longevity and oxidative and heat stress response, as well as an informative model fo

248 gely stabilizes RpoH and thereby induces the heat stress response.

249 factors (HSFs) are central regulators of the heat stress response.

250 panied by the induction of the oxidative and heat stress response.

251 pollen have attenuated expression of several heat-stress response genes, including two heat shock tra

252 ss (37-41 degrees C) resulted in a classical heat-stress response with up-regulation of cellular chap

253 monstrate the extent of heterogeneity of the heat-stress response within populations of yeast cells a

254 While HSFs are central in heat stress responses, their role in the response to amb

255 membrane permeability and the oxidative and heat stress responses.

256 in stabilizing the mRNAs of several crucial heat stress responsive genes under high temperature.

257 RCF3 is an important upstream regulator for heat stress-responsive gene expression and thermotoleran

258 cold stress tolerance, RCF2 is required for heat stress-responsive gene regulation and thermotoleran

259 re responsible for the transcription of many heat stress-responsive genes including those encoding he

260 At a cellular level, the moderate heat stress resulted in precocious endosperm cellulariza

261 ing a classic model system for understanding heat stresses - rocky intertidal shores.

262 finity purification of CI and CII sHSPs from heat-stressed seedlings recovered eukaryotic translation

263 us endosperm cellularization, whereas severe heat-stressed seeds failed to cellularize.

264 leaching despite the presence of significant heat stress, such as in the Banda Sea.

265 ant impairs the survival of Leishmania under heat stress, supporting the central role of the chaperon

266 RCP scenarios, whereas high temperature and heat stress take over the dominant stress of drought on

267 Cold, frost, and wet conditions, and high heat-stress tended to induce earlier dormancy of deciduo

268 The nac019 mutant is more sensitive to heat stress than the wild type, and chromatin immunoprec

269 idae, and Acroporidae) are more sensitive to heat stress than their hosts, exhibiting differential sy

270 erved in the way that S. mutans responded to heat stress that included 66 transcription factors for t

271 the appropriate PPE for filoviruses and the heat stress that it imposes.

272 diator to HSP promoters in response to acute heat stress through cooperative physical and/or function

273 h confidence with chloroplast HSP22E/F under heat stress thus revealing chloroplast processes affecte

274 ic post-menopausal women underwent a passive heat stress to induce hot flushes at baseline and follow

275 t 26 degrees C following 60 min 42 degrees C heat stress to investigate specifically the early events

276 lated in reproductive tissues in response to heat stress to modulate resource allocation dynamics.

277 We examined the effects of a modest heat stress to test the hypothesis that SSNA responses c

278 eubiquitinases associate more with Rsp5 upon heat-stress to prevent the assembly of K63-linked ubiqui

279 plays a positive role in salt, drought, and heat stress tolerance by stress-specific gene regulation

280 lar replication, full virulence in mice, and heat stress tolerance.

281 he rglg1rglg2 double mutant conferred better heat-stress tolerance and had resulted in higher endogen

282 Heat stress transcription factor A2s (HsfA2s) are key re

283 Expression of genes encoding heat stress transcription factors (HSF genes) and heat s

284 Heat stress transcription factors (HSFs) are central reg

285 Heat stress transcription factors (Hsfs) regulate the tr

286 ular chaperones and are under the control of heat stress transcription factors (HSFs).

287 eveloped a coexpression network of rice from heat stress transcriptome data.

288 ent with a model in which, upon the onset of heat stress, translation is rapidly reprogrammed to enha

289 ate (34 degrees C) and a high (42 degrees C) heat stress treatment on developing rice seeds during th

290 ese genes are rapidly induced in response to heat stress treatment.

291 We conducted cold and heat stress treatments on the branching coral Acropora y

292 me footprinting, we show that 2 hr of severe heat stress triggers global pausing of translation elong

293 Autophagy activated by heat stress was also found to be partially dependent on

294 A heat stress was found to increase concentrations of 3',5

295 The mechanistic basis of tolerance to heat stress was investigated in Oryza sativa and two wil

296 BAM1, which is transcriptionally induced by heat stress, was about 10 degrees C higher than that of

297 se in odds of survival of coral larvae under heat stress when their parents come from a warmer lower-

298 It acquires isoAsp rapidly during heat stress, which eliminates RNA unwinding (but not rew

299 recovery to the soluble cell fraction after heat stress, which was also dependent on HSP101.

300 d that rapid volume loading performed during heat stress would increase cardiac output in older adult