ライフサイエンスコーパス: heat tolerance

1 e.g. immunity, reproduction, development and heat tolerance).

2 to chloroplasts as the basis of differential heat tolerance.

3 endoplasmic reticulum (ER)-related genes in heat tolerance.

4 the non-photorespiratory release of CO(2) in heat tolerance.

5 o play a role in genotype-specific nocturnal heat tolerance.

6 perform targeted assessments of drought and heat tolerance.

7 will aid in understanding the mechanisms of heat tolerance.

8 demonstrating a substantial genetic basis of heat tolerance.

9 ted loci matched the phenotypic variation in heat tolerance.

10 orals to survive such heatwaves, i.e., their heat tolerance.

11 etabolism and signaling that result in plant heat tolerance.

12 ant cereal crop worldwide and shows superior heat tolerance.

13 hroughput methodologies for the screening of heat tolerance.

14 ostimulant treatments manifested in improved heat tolerance.

15 WP-RK transcription factors and ER system in heat tolerance.

16 ting in an increased level of photosynthetic heat tolerance.

17 is often used as a proxy for photosynthetic heat tolerance.

18 r new roles in chromatic regulation of plant heat tolerance.

19 loping genotypes with greater photosynthetic heat tolerance.

20 way for genomic predictive models of corals heat tolerance.

21 few naive purebreds with exceptionally high heat tolerance.

22 didate genes, and haplotypes associated with heat tolerance.

23 keletal muscle transcriptome associated with heat tolerance.

24 n urgent need to develop crops with enhanced heat tolerance.

25 atural variations have adaptive functions in heat tolerance.

26 sts to have a range of intraspecific natural heat tolerance.

27 imited data and the complex genetic basis of heat tolerance.

28 criptional regulation of HsfA2 for improving heat tolerance.

29 growth, development, disease resistance and heat tolerance.

30 Oryza meridionalis exhibited intermediate heat tolerance.

31 er within regulatory modules associated with heat tolerance.

32 lly modify cool-season species for improving heat tolerance.

33 ved a correlation between flowering time and heat tolerance.

34 -based signaling pathway that contributes to heat tolerance.

35 ors have also been reported to contribute to heat tolerance.

36 ized small heat shock proteins (CP-sHSPs) in heat tolerance.

37 ession change that is congruent with greater heat tolerance, a putatively adaptive state in warmer ur

38 of semen to heat stress to discriminate the heat-tolerance ability of pigs.

39 ted to their thermal environment and inherit heat tolerance across generations.

40 rpins the development of markers and maps of heat tolerance across seascapes and ocean warming scenar

41 ad a severely diminished capacity to acquire heat tolerance after mild conditioning pretreatments.

42 oduced from the warmest reef had the highest heat tolerance, although gene expression responses to he

43 over genetic markers potentially involved in heat tolerance among large populations without prior inf

44 Variation in heat tolerance among populations can determine whether a

45 outline an efficient strategy for screening heat tolerance and accentuate the need to focus on reduc

46 dations for the future incorporation of PSII heat tolerance and acclimation into models of the therma

47 as adaptation, contributed about equally to heat tolerance and are reflected in patterns of gene exp

48 iModulons to increase protein productivity, heat tolerance and fructose utilization; (ii) an iModulo

49 have a remarkable ability to maintain their heat tolerance and health despite acclimation to 3-6 deg

50 Additionally, a new way of interpreting both heat tolerance and heat resistance was developed, differ

51 erant Arabidopsis accessions confers greater heat tolerance and induces less cell death compared with

52 n concentration in the cell, enhancing plant heat tolerance and inhibiting plant growth.

53 ive genomic resource revealing insights into heat tolerance and laying a foundation for generating mo

54 rant crop leaf atlas revealing insights into heat tolerance and laying a foundation for generating mo

55 e findings deepen our understanding of plant heat tolerance and significantly impact the scientific c

56 affected the gene expression associated with heat tolerance and SVs surrounding ER-related genes shap

57 on may result in the underestimation of PSII heat tolerance and that the extent of acclimation can be

58 than HSP gene can be used for improvement of heat tolerance and that the improvement is possible in a

59 at color and horn development in Ankole, and heat tolerance and tick resistance across African cattle

60 ion of one RWP-RK gene led to enhanced plant heat tolerance and transactivated ER-related genes quick

61 Surprisingly, 35S:ERF1 also showed enhanced heat tolerance and up-regulation of heat tolerance genes

62 could have a significant impact on improving heat tolerance and yield of different crops subjected to

63 ing canopy architecture, improving enzymatic heat tolerance, and (re)engineering key metabolic pathwa

64 mays L) this protein has been implicated in heat tolerance, and it has been hypothesized that EF-Tu

65 ined nine traits related to leaf drought and heat tolerance, and leaf economics across 58 species fro

66 eversed G1 arrest, its fortified cell walls, heat tolerance, and longevity.

67 7%-10% of plants altered in leaf morphology, heat tolerance, and mitochondrial genome stability.

68 n greatly reduced aphid fecundity, decreased heat tolerance, and modified aphid body color, from ligh

69 e of heritable genetic variation in mosquito heat tolerance, and phenotypic trade-offs in tolerance t

70 ping functions in the negative regulation of heat tolerance, and their loss of function singly or in

71 These include immune-, heat-tolerance- and reproduction-related genes.

72 Conversely, heat tolerance appears unrelated to climate ancestry.

73 is is that the microbial community and coral heat tolerance are causally linked.

74 on to maintain a balance of plant growth and heat tolerance are poorly understood.

75 ddress this, we measured leaf photosynthetic heat tolerance as the critical temperatures at which pho

76 uces accumulation of complex I, and enhances heat tolerance, as is seen in shot1 mutants.

77 aped by 'snapshot' measurements that capture heat tolerance at a single point in time.

78 sed for indentifying and confirming QTLs for heat tolerance at flowering stage.

79 cal C4 heat-tolerant crop, has mechanisms of heat tolerance at the cellular level which remain unclea

80 AN2 to IAN6) is responsible for variation in heat tolerance at the reproductive stage in Arabidopsis

81 uracy of current estimates of photosynthetic heat tolerance based on snapshot measurements.

82 ates cured of the virus are unable to confer heat tolerance, but heat tolerance is restored after the

83 ort the hypothesis that EF-Tu contributes to heat tolerance by acting as a molecular chaperone and pr

84 it has been hypothesized that EF-Tu confers heat tolerance by acting as a molecular chaperone and pr

85 hypothesis that maize EF-Tu plays a role in heat tolerance by acting as a molecular chaperone and pr

86 ole of heat stress memory genes in enhancing heat tolerance by promoting the clearance of reactive ox

87 We hypothesized that CR would increase heat tolerance by reducing cellular stress and subsequen

88 give insight into the strategies to improve heat tolerance by targeting one or some of the TaCLPB ge

89 could theoretically be leveraged to enhance heat tolerance by up to 1 degrees C-week within one gene

90 A new study shows that coral heat tolerance can result from selection on a suite of g

91 strains with stably inherited differences in heat tolerance caused by bacterial endosymbionts and sho

92 n nocturnal CO2 fixation, stomatal movement, heat tolerance, circadian clock, and carbohydrate metabo

93 genes that largely correlate with decreased heat tolerance, consistent with maladaptive regulatory r

94 ng evapotranspiration, light reflection, and heat tolerance, control of development, and providing an

95 several QTLs with small effects and stronger heat tolerance could be attained through pyramiding vali

96 rees C), but nursery web spiders had limited heat tolerance (CTM50 = 34 degrees C).

97 ld tolerance to cope with winter cold, while heat tolerance did not change, in line with previous evi

98 unding ER-related genes shaped adaptation to heat tolerance during domestication in the population.

99 more, HopI1-expressing plants have increased heat tolerance, establishing that HopI1 can engage the p

100 e demonstrated how oxygen limitation can set heat tolerance for some aquatic ectotherms, but only at

101 ssing two budding yeast strains of different heat tolerance for up to 12 generations.

102 enhanced heat tolerance and up-regulation of heat tolerance genes compared with the wild type.

103 Often deemed a selective advantage for heat tolerance, high body temperatures also limits birds

104 ctors (HSFs) are pivotal in regulating plant heat tolerance; however, the mechanisms HSFs employ in r

105 CPF reduced the heat tolerance; however, this was buffered by latitude-s

106 his work sheds light on the genomic basis of heat tolerance in a complete subterrestrial eukaryotic g

107 crit) and m(1) were associated with measured heat tolerance in adult plants, highlighting their usabi

108 Ectopic expression of CtHsfA2b improved heat tolerance in Arabidopsis and restored heat-sensitiv

109 conclude that HSP101 plays a pivotal role in heat tolerance in Arabidopsis.

110 e the expression of heat-inducible genes and heat tolerance in Arabidopsis.

111 ge of how acclimation and symbiosis modulate heat tolerance in coral early life-history stages.

112 nder heat may afford new ways of engineering heat tolerance in crop plants.

113 Summer heat did not approach ants' heat tolerance in either stratum, but winter and spring

114 Cold tolerance has evolved more quickly than heat tolerance in endotherms and ectotherms.

115 ial targets for enhancing quality traits and heat tolerance in future wheat improvement programs.

116 important to understand the genetic basis of heat tolerance in hexaploid wheat.

117 1 impaired fungal development, virulence and heat tolerance in M. robertsii.

118 ve experimental approach to rapidly quantify heat tolerance in many samples yet the role of key metho

119 Here, we test if parent corals retain their heat tolerance in nursery settings, if simple proxies pr

120 Further investigation of the enhanced heat tolerance in plants lacking tylAPX, using mutants d

121 ults from different populations suggest that heat tolerance in rice at flowering stage is controlled

122 d could be an important source for enhancing heat tolerance in rice at flowering stage.

123 s on reduced rates of respiration to improve heat tolerance in rice.

124 Stress indices indicated strong heat tolerance in the genotype YR x Ksu110-240, which sh

125 We attribute heat tolerance in the wild species to thermal stability

126 ted selection in breeding wheat for improved heat tolerance in Ventnor or Karl 92 genetic background.

127 nclude the essential components of nocturnal heat tolerance in wheat are uncoupled from resilience to

128 l thermal sensitivity and ability to acquire heat tolerance, including in corals harboring naturally

129 ing parent colonies for high rather than low heat tolerance increased the tolerance of adult offsprin

130 Our finding on the heritability of coral heat tolerance indicates that selective breeding could b

131 overexpression of ZmHSF12-1 decreases plant heat tolerance, indicating the distinct functions of the

132 change, in line with previous evidence that heat tolerance is a less labile trait.

133 Developing new rice varieties with heat tolerance is an essential way to sustain rice produ

134 Heat tolerance is an important characteristic in pigs, a

135 ects of plant cells and thus enhancing plant heat tolerance is critical for crop production.

136 Experiments have shown heat tolerance is dependent not just on the magnitude of

137 Our current understanding of PSII heat tolerance is predominantly shaped by 'snapshot' mea

138 rus are unable to confer heat tolerance, but heat tolerance is restored after the virus is reintroduc

139 One measure of photosynthetic heat tolerance is T(crit) - the critical temperature at

140 f the strongest markers of intergenerational heat tolerance is the saturation state of DGCC betaine l

141 at tolerance, suggests that more emphasis on heat tolerance is warranted in breeding programs.

142 ing variation in heat limits, revealing that heating tolerance is effectively fixed within a species

143 Increased heat tolerance may prove beneficial by conferring the ab

144 mechanisms underlying both acute and chronic heat tolerances may help to refine predictions regarding

145 ed for their usability for forecasting adult heat tolerance, measured as the vegetative heat toleranc

146 n singly or in combination confers increased heat tolerance, measured by a lower number of barren sil

147 The virus-infected fungus confers heat tolerance not only to its native monocot host but a

148 rmed data-imputation approach to predict the heat tolerance of 60% of amphibian species and assessed

149 We detected substantial variation in heat tolerance of a randomly selected set of indica rice

150 t heat tolerance, measured as the vegetative heat tolerance of adult rice plants through visual (stay

151 Improving the heat tolerance of cotton is a major concern for breeding

152 the costs of hybrid breeding and improve the heat tolerance of flowering plants by avoiding higher te

153 Moreover, the influence of infections on the heat tolerance of hosts has rarely been investigated wit

154 rovides valuable insights into enhancing the heat tolerance of LAB.

155 that CR reduces cellular injury and improves heat tolerance of old animals by lowering radical produc

156 Consequently, ClpG largely contributes to heat tolerance of P. aeruginosa primarily in stationary

157 Buchnera), which has dramatic effects on the heat tolerance of pea aphid hosts (Acyrthosiphon pisum).

158 HSF12-2 in Arabidopsis not only improved the heat tolerance of plants but also compensated for the gr

159 Overexpression of GAPC enhances heat tolerance of seedlings and the expression of heat-i

160 The heat tolerance of shot1 emphasizes the importance of mit

161 ng system of photosystem II and to a reduced heat tolerance of the oxygen-evolving system, particular

162 The results strongly suggest that heat tolerance of wheat, and possibly other crop plants,

163 affected environments is often linked to the heat tolerance or heat-/chemical-induced germination of

164 n recovery capacity and acclimatory gains in heat tolerance over an individual's lifespan.

165 s with local environmental temperatures than heat tolerances overall.

166 mperature stress can be used as a vegetative heat tolerance phenotype.

167 oved genomic prediction accuracy of multiple heat tolerance phenotypes by ~11%.

168 In new data of 45 K cattle with heat tolerance phenotypes, the FAEMI score demonstrates

169 ein synthesis gene (RARS) is associated with heat tolerance plasticity within urban heat islands and

170 Despite accounting for heat-tolerance plasticity, a 4 degrees C global temperat

171 Thus, the Arabidopsis IAN genes repress heat tolerance, probably through the HSR and UPR and by

172 uld be attained through pyramiding validated heat tolerance QTLs.

173 and Xgwm 577, which were strongly linked to heat tolerance related traits.

174 c regions carrying morphology-, immune-, and heat-tolerance-related genes underwent divergent selecti

175 er, the underlying metabolomic mechanisms of heat tolerance remain poorly understood.

176 n was intensified for drought, freezing, and heat tolerance, respectively.

177 overexpression plants show slightly enhanced heat tolerance suggesting that TE-mediated control of AP

178 ce IAN1 gene function also leads to enhanced heat tolerance, suggesting a conserved function of plant

179 rait changes are in the direction of greater heat tolerance suggests that consistent exposure to extr

180 likely high degree of genetic variability in heat tolerance, suggests that more emphasis on heat tole

181 ht mean that physiological limits related to heat tolerance (survival) will be reached regularly and

182 abitats, with pond species exhibiting higher heat tolerance than stream species.

183 vironmental temperatures and display greater heat tolerance than their forest counterparts.

184 s in the northern Red Sea have a much higher heat tolerance than their prevailing temperature regime

185 revealed that: (a) predators exhibit higher heat tolerances than prey (~4 C), a trend which remained

186 ty may allow some reefs to have an inherited heat tolerance that is higher or lower than predicted ba

187 ns and instead a legacy effect may exist for heat tolerance that is rarely reported.

188 n 2 years, acclimatization achieves the same heat tolerance that we would expect from strong natural

189 ttest reefs in the world transfer sufficient heat tolerance to a naive population sufficient to withs

190 he heat; rather, they apply their impressive heat tolerance to avoid competitors and predators.

191 es solubilize aggregated proteins and confer heat tolerance to cells.

192 aptive laboratory evolution to improve their heat tolerance to ensure nearly complete cell survivabil

193 enotypes and harness germplasm with enhanced heat tolerance to mitigate the impact of rising heat str

194 However, only heat tolerance traits (critical thermal maximum and knoc

195 ae may offset the negative effects of CPF on heat tolerance under warming, unless the expected DTF in

196 t is unknown whether they can maintain their heat tolerance upon larval dispersal or translocation to

197 on traits relating to drought, freezing, and heat tolerance using a diverse combination of Arabidopsi

198 In contrast, plant heat tolerances vary mainly as a result of biogeographic

199 Variation in heat tolerance was associated with daytime respiration b

200 Heat tolerance was characterised by the critical thermal

201 genomic variation associated with prolonged heat tolerance was clustered in several regions of the g

202 tolerance in line with seasonal changes, but heat tolerance was more phylogenetically constrained.

203 Heat tolerance was primarily influenced by leaf habit, w

204 Leaf heat tolerance was quantified using the temperature at w

205 Also the chlorpyrifos-induced reduction in heat tolerance was stronger when the pesticide pulse fol

206 -induced GAPC nuclear accumulation and plant heat tolerance were reduced in Arabidopsis phospholipase

207 n of MBF1c has a dominant-negative effect on heat tolerance when constitutively expressed in plants,

208 rate of evolutionary adaptation in mosquito heat tolerance will exceed the projected rate of climate

209 economics is central to linking drought and heat tolerance, with leaf habit as a key influencing fac

210 mber 2 (SERP2), was identified as underlying heat tolerance, with the lead variant (rs383130643) asso

211 en species, while they were linked more with heat tolerance within deciduous species.

212 begun to explore variation in body size and heat tolerance within species, our understanding of thes

213 sing ZmHSF12-1 and ZmHSF12-2 to improve crop heat tolerance without causing growth retardation and yi