ライフサイエンスコーパス: heat stress

1 s an evaporative cooling that mitigates crop heat stress.

2 der adverse environmental conditions such as heat stress.

3 d sorghum pistils to be equally sensitive to heat stress.

4 y conserved systems that protect plants from heat stress.

5 age in cool-seeking behaviour during passive heat stress.

6 bolism that contributes to yield loss during heat stress.

7 and is expected to decrease as a response to heat stress.

8 rmline gene expression and totipotency after heat stress.

9 educes fecundity and survival upon prolonged heat stress.

10 3 weeks after exposure to mild or temporary heat stress.

11 ion factor, a pivotal response of the UPR to heat stress.

12 the tolerance their product confers to plant heat stress.

13 upstream regulators directly associated with heat stress.

14 is necessary to maintain PM integrity under heat stress.

15 egates and is essential for surviving severe heat stress.

16 onstress conditions, high light exposure, or heat stress.

17 del for coral community response to frequent heat stress.

18 it our understanding of the full response to heat stress.

19 cepts to combat the negative consequences of heat stress.

20 veness to sympathetic outflow during passive heat stress.

21 GAT4D as a protector of male germ cells from heat stress.

22 stabilizes the digestive vacuole (DV) under heat stress.

23 003 identified as a temporal change point in heat stress.

24 ant association between depth and subsurface heat stress.

25 as induced, whereas TaRca2 was suppressed by heat stress.

26 lesterolaemia on the integrated responses to heat stress.

27 n immunogenic anti-TNF-alpha chimeric Ab, to heat stress.

28 mune tissues, such as the thymus, respond to heat stress.

29 torical temperature variability, rather than heat stress.

30 ites was directly associated with cumulative heat stress.

31 stress, we further subjected individuals to heat stress.

32 make sexual reproduction highly sensitive to heat stress.

33 hesized during heat stress and recovery from heat stress.

34 sis across eudicot and monocot species under heat stress.

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

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

37 ch chloroplast processes are disturbed under heat stress.

38 ile some physiological traits were shaped by heat stress.

39 nd oligogalactolipids were more resistant to heat stress.

40 lthy older adults can achieve during passive heat stress.

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

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

43 eproductive tissues during development under heat stress.

44 with reduced ethylene effects on yield under heat stress.

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

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

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

48 isms have developed mechanisms to respond to heat stress.

49 tures for 5 d and remained high at 4 h after heat stress.

50 intrinsic protector of male germ cells from heat stress.

51 gments cool-seeking behaviour during passive heat stress.

52 olerant pigs and heat-susceptible pigs under heat stress.

53 GAPC accumulates in the nucleus under heat stress.

54 ressing Mgat4d were partially protected from heat stress.

55 two mechanisms that enable plants to survive heat stress.

56 k-induced gene expression to protect against heat stress.

57 l PI(3)P function in DV stabilization during heat stress.

58 sion of somatic genes in the germline during heat stress.

59 ent in cool-seeking behaviour during passive heat stress.

60 erexpression (OE) and knockout mutants under heat stress.

61 tein products were measured during and after heat stress.

62 heat shock protein 70 (HSP70) in response to heat stress.

63 holdase, thereby preventing damage caused by heat stress.

64 expose large populations of adult plants to heat stress.

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

66 nsitivity to lose coral photosynthesis under heat-stress.

67 following pollination was also suppressed by heat-stress.

68 ture treatments: cold stress (18 degrees C), heat stress (32 degrees C), or a control (24 degrees C).

69 ceptible broiler line) were exposed to acute heat stress (35 degrees C) and/or immune simulation with

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

71 : 18 degrees C (day : night) and exposed to heat stress (38 degrees C : 22 degrees C) for up to 5 d

72 BEZ235 or control and subjected to moderate heat stress (45 degrees C for 10 minutes) or control (37

73 adult brood stock in 2016 and 2017 owing to heat stress(6), the amount of larval recruitment decline

74 the DEGs (~3000) specifically responsive to heat stress, ~70% showed time of day (ZT1 or ZT6) occurr

75 Under heat stress, a total of 66 differentially expressed gene

76 oth exercise and temperature-matched passive heat stress ABSTRACT: Acute moderate-intensity exercise

77 Heat stress adversely affects pig growth and reproductio

78 c cells and milk metabolomics indicated that heat stress affected the mammary immune response to simu

79 Specifically, we synthesize how pulse heat stress affects hosts, parasites, and the ecological

80 have employed in situ Hi-C to determine how heat stress affects long-range chromatin conformation in

81 uggest growing resistance to bleaching-level heat stress among coral communities subject to high inte

82 protect against abiotic stressors including heat stress and drought, but there is very little mechan

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

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

85 Heat stress and mastitis are major economic issues in da

86 leached) was positively associated with both heat stress and nitrogen availability for both genera.

87 s eat-3 and fzo-1 are more resistant to both heat stress and oxidative stress.

88 llance helps to maintain cell integrity upon heat stress and protects from proteotoxicity.

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

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

91 Male germ cells are sensitive to heat stress and testes must be maintained outside the bo

92 ditions, increasing species vulnerability to heat stress and water budgets.

93 ing responses was associated with cumulative heat stress and/or local environmental history, includin

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

95 ike scaffolds are robust, even under extreme heat stress, and control over nanocomposite dimensions i

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

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

98 Photosynthesis is impaired during heat stress, and this limitation is often attributed to

99 re markedly more sensitive to the effects of heat stress, and transgenic mice expressing Mgat4d were

100 transcriptionally induced upon growth under heat stress, and we find that positive selection is dete

101 Most experiments examining heat stress are performed during daytime hours, generati

102 pe-derived temperature estimates, suggesting heat stress as a main cause of body size reduction.

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

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

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

106 Heat stress assays carried out in the northern (Hurghada

107 Notably, short-term acute heat stress assays resolved per-colony (genotype) differ

108 conducted a series of 18-hr short-term acute heat stress assays side-by-side with a 21-day long-term

109 ial of mobile, standardized short-term acute heat stress assays to resolve fine-scale differences in

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

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

112 st more than half of its ADCC activity after heat stress at 40 degrees C for 4 months.

113 Upon heat stress, AtBAG7 is sumoylated, proteolytically proce

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

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

116 Heat stress caused decreases in unsaturation indices of

117 In broilers, acute heat stress changed thymic expression responses to LPS a

118 ing targets to improve disease resistance in heat-stressed chickens.

119 tivated Salmonella Enteritidis and a chronic heat stress (CHS).

120 ikelihood that crops will face more frequent heat stress conditions over the coming decades.

121 ression profiles under the thermoneutral and heat stress conditions were documented in heat-tolerant

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

123 development, but also in plant adaptation to heat stress conditions.

124 last-localized PGD3 activity is labile under heat stress conditions.

125 on networks on mRNAs of pigs under different heat-stress conditions using whole transcriptomic RNA-se

126 this gap by identifying the key measures of heat stress, considering both air temperature and near-s

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

128 early morning or late evening hours to lower heat stress damage during flowering.

129 Results from this model show heat stress directly induced a so-far unknown infiltrati

130 events found no meaningful depth refuge from heat stress down to 38 m, and no significant association

131 Increasing heat stress due to global climate change is causing cora

132 ly sensitive model to examine the effects of heat stress due to their intensive metabolic heat produc

133 Heat stress during flowering has differential impact on

134 ing exercise and temperature-matched passive heat stress during isocapnia (i.e. end-tidal PCO2 was he

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

136 r findings demonstrate that a short moderate heat stress during the highly susceptible tetrad stage s

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

138 d a high spatial and temporal variability of heat stress, emphasizing an observed increase in heat ex

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

140 were found to promote cell death induced by heat stress, ER stress, and cell death-inducing molecule

141 Plants are vulnerable to heat stress, especially during reproductive development.

142 ed they are extensively ubiquitylated during heat stress, especially in plants deficient in HSP101 or

143 h-latitude eastern Australia during a global heat stress event in 2016.

144 hing often is spatially variable for a given heat stress event, and drivers of this heterogeneity are

145 ity response to, and recovery from, multiple heat stress events.

146 and 2017 as severe and widespread Caribbean heat-stress events and recognized a change point in 2002

147 Major heat-stress events may be associated with El Nino Southe

148 tures on corals, to indicate the severity of heat stress experienced by corals and to gauge their pos

149 hat corals living in deeper reefs may escape heat stress experienced by shallow corals.

150 assays side-by-side with a 21-day long-term heat stress experiment to assess the ability of both app

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

152 Accumulative heat stress explains 31% of the overall annual rate of c

153 stress results to avoid misrepresentation of heat stress exposure at shallow reefs.

154 re, we assessed three decades (1985-2017) of heat stress exposure in the wider Caribbean at ecoregion

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

156 he consequences of climate change, including heat stress, food scarcity, increases in pollution and v

157 ctic species suggesting optimization for non-heat-stress functional roles.

158 re induced to a lesser extent in Mgat4d[-/-] heat-stressed germ cells (NFkappaB response, TNF and TGF

159 nd 6 miRNAs were differentially expressed in heat-stressed granulosa cells and the corresponding EVs,

160 osphorylation compared with the vehicle plus heat stress group.

161 s of endosymbiotic algae ("bleaching") under heat stress has become a major problem for reef-building

162 kin wetness to cool-seeking behaviour during heat stress has never been established.

163 Heat stress has significant adverse effects on plant pro

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

165 Rca is sensitive to moderate heat stress, however, and becomes progressively inhibite

166 . maxima infection in broiler chickens under heat stress (HS) and mRNA expression of host cytokines t

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

168 rmosusceptible Indian wheat cv. PBW343 under heat stress (HS) at 42 degrees C for 2 h using RNA-seque

169 Follicular cells respond to heat stress (HS) by activating the expression of heat sh

170 of the potential cellular targets of HL and heat stress (HS) combination is PSII because its degree

171 of heat shock proteins (HSPs) in response to heat stress (HS) is indispensable for conferring thermot

172 ant for research into improving reproductive heat stress (HS) tolerance.

173 +/- 5% RH (HIGH), followed by 60 min passive heat stress (HS) where the water temperature in the suit

174 at (DSW) were compared to see the effects of heat stress (HS).

175 polysaccharide (LPS) could be conditioned by heat stress (HS).

176 50% workload max) and (ii) 75 min of passive heat stress (HS; 49 degrees C water-perfused suit) to ma

177 (Arachis hypogaea L.) anther lipidome under heat stress (HT) will aid in understanding the mechanism

178 fy differentially sumoylated proteins during heat stress, hyperosmotic stress, oxidative stress, nitr

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

180 r severe bleaching even under relatively low heat stress implies that mitigating nutrient pollution m

181 rina growth was impaired by the accumulative heat stress imposed by the 3HW treatment.

182 eq to analyze gene-expression changes during heat stress in a coral relative, the sea anemone Aiptasi

183 hange traits being quantified in response to heat stress in a diverse set of rice accessions.

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

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

186 her miRNAs are involved in the regulation of heat stress in B. campestris.

187 unted reflex cutaneous vasodilatation during heat stress in healthy older adults.

188 areas, exposes urban dwellers to additional heat stress in many cities, specially during heat waves.

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

190 ession is likely an acclimation mechanism to heat stress in peanut.

191 is triggered by oxidative stress in cancer, heat stress in plants, and hemorrhagic stroke.

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

193 Several TFs associated with heat stress in previous studies were identified that had

194 t proteasome function was impaired following heat stress in senescent cells, and did not recover upon

195 oduced a new baseline and regionalization of heat stress in the basin that will enhance conservation

196 ediates HCC cell survival caused by moderate heat stress in vitro, but these findings need in vivo va

197 ers hypersensitivity of the male germline to heat stress in vivo.

198 Several pathways activated by heat stress in wild type were induced to a lesser extent

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

200 gments cool-seeking behaviour during passive heat stress independently of differential increases in s

201 Oxidative stress in combination with heat stress induced loss of its Fe-S clusters followed b

202 PI3K/mTOR inhibition prevented moderate heat stress-induced AKT signaling (Z-score, -0.2; P < .0

203 ed pollen and pistil viability will overcome heat stress-induced damage during flowering under curren

204 PI3K/mTOR inhibition prevented moderate heat stress-induced global effects on HCC molecular sign

205 Here, we show that heat stress induces a strong and rapid YAP dephosphoryla

206 Heat stress induces misfolding and aggregation of protei

207 score, 0.4-1.1; P < .001).ConclusionModerate heat stress induces PI3K/mTOR/AKT-dependent global effec

208 In response to heat stress, inner ear tissue releases exosomes that car

209 Heat stress is a critical abiotic stress that reduces th

210 us vascular conductance (CVC) during passive heat stress is unknown.

211 ion to cutaneous vascular conductance during heat stress is unknown.

212 periods: thermoneutral (January to May), and heat stress (July to October).

213 n turnover were significantly upregulated in heat stressed larvae.

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

215 uard that protects proteins against moderate heat stress, likely through a redox-dependent chaperone

216 rmal tolerance were response to experimental heat stress, location on the reef, and thermal microclim

217 Upon heat stress, m(5) C loss leads to ribosome stalling at U

218 Finally, we obtained indication that heat stress may directly alter jejunal tight junction pr

219 combination of insect herbivory and moderate heat stress may exacerbate crop losses.

220 tion of toxic and bacterial compounds during heat stress may have triggered a modulated immune repert

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

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

223 del that included an interaction between two heat stress metrics, the most substantial loss occurring

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

225 ibati, which experience years with prolonged heat stress more frequently than 99% of the world's reef

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

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

228 ry mechanisms and their participation in the heat stress of flowering Chinese cabbage.

229 ther hand, when males were subjected to mild heat stress of the testis (43 degrees C for 25 min), ger

230 g event, we quantified the effects of severe heat stress on 3D reef structural complexity across a gr

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

232 mechanisms, we imposed a moderate transient heat stress on maize (Zea mays) plants at the tetrad sta

233 tion and to evaluate the effects of moderate heat stress on molecular signaling and cellular function

234 ves, thus supporting the influence of direct heat stress on reproductive processes in determining yie

235 This was largely due to heat stress on reproductive processes, especially during

236 Our bovine model indicates direct effects of heat stress on the jejunum of mammals already at moderat

237 growth conditions, the impact of drought and heat stress on the peroxisomes remains unknown.

238 ing them to mitigate the negative effects of heat stress on their physiological activities.

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

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

241 samples collected from the thermoneutral and heat stress periods for gene expression analysis.

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

243 intronic poly(A) sites used in drought- and heat-stressed plants that might play an important role i

244 nces of drought, with reported losses due to heat stress playing a smaller role.

245 umably its induction of genes in response to heat stress) plays an important protective role in coral

246 racted with a different set of proteins upon heat stress, possibly protecting them from heat injuries

247 n the United States, where precipitation and heat stress presents a temporal pattern among growth pha

248 both coral genera, Pocillopora and Acropora, heat stress primarily drove bleaching prevalence (i.e.,

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

250 onal and metabolic pathway genes, as well as heat stress proteins, remained altered even though polle

251 ing exercise and temperature-matched passive heat stress provoked ~16% increases in vertebral artery

252 hat cells may have the ability to respond to heat stress quickly though Hsp70 deacetylation, followed

253 t pollen viability determines seed set under heat stress, recent findings have revealed pearl millet

254 Heat stress reduced feed intake and milk yield by 28 and

255 analysis classified the Caribbean into eight heat-stress regions offering a new regionalization schem

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

257 gent strains were characterized for salt and heat stress resilience as well as antimicrobial and plan

258 ons between disturbance, coral symbioses and heat stress resilience reveal multiple pathways to coral

259 d heat-susceptible pigs under the effects of heat stress, respectively.

260 H4-S47 and H4-T30 in response to osmotic and heat stress, respectively.

261 of them could also be responsive to salt and heat stresses, respectively.

262 f genes and biological mechanisms related to heat stress response in pigs and provide potential bioma

263 ium falciparum Hsp70-x chaperone assists the heat stress response of the malaria parasite.

264 ll as physiological functions of YAP, in the heat stress response.

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

266 ofound role than PRR7 and PRR9 in modulating heat stress responses during the day.

267 latory elements, underpinning new aspects of heat stress responses not previously appreciated.

268 ime and/or the circadian clock contribute to heat stress responses remains largely unknown.

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

270 time of day and/or the clock to differential heat stress responses, we probed wild-type and mutants o

271 ht a significant role for time of day in the heat stress responsive transcriptome, and the clock thro

272 Transient heat stress resulted in reduced starch content, decrease

273 perature data can provide bleaching-relevant heat stress results to avoid misrepresentation of heat s

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

275 c (continuous, i.e., high-intensity) drought-heat stress scenarios in gray poplar (Populusx canescens

276 n the afternoon compared to the morning, and heat stress significantly perturbed the transcriptome.

277 that mediates proteostasis under normal and heat stressed states.

278 r of 10) as well as the ability to withstand heat stress, storage at room temperature, and three free

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

280 sults indicate that with low feed intake and heat stress, there are shifts in rumen VFA dynamics and

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

282 s study utilized the sensitivity of semen to heat stress to discriminate the heat-tolerance ability o

283 Importantly, nitrogen interacted with heat stress to increase bleaching severity up to twofold

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

285 Finally, by applying heat stress to whole seedlings, we address the longstand

286 esults provide a mechanism for improving the heat stress tolerance of photosynthesis in wheat and pot

287 ffinose content in leaves and enhanced plant heat stress tolerance.

288 affinose content in leaves and reduced plant heat stress tolerance.

289 siological studies suggest that HS-activated heat stress transcription factor A1s also positively reg

290 poxia promoted a progressive upregulation of heat stress transcripts, as evidenced by RNAPII binding

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

292 0 h, 1 h, 6 h and 12 h after a 38 degrees C heat-stress treatment.

293 ular mechanisms of C. glabrata adaptation to heat stress via adaptive laboratory evolution.

294 c effects, such as the indirect influence of heat stress via reduced food intake.

295 ity up to twofold when nitrogen was high and heat stress was relatively low.

296 In the second period, indicators of heat stress were significantly different between PF and

297 ances C(3) plant productivity, whereas acute heat stress, which occurs during heat waves, generally e

298 ng of the regulation of C assimilation under heat stress will inform efforts to improve wheat product

299 sed by ~43% during both exercise and passive heat stress, with no change in internal carotid artery b

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