ライフサイエンスコーパス: cold temperature

1 ns have functions related to the response to cold temperature.

2 ed the viability of yeast cells subjected to cold temperature.

3 ls drastically affects protein export at the cold temperature.

4 at warm temperature over those increased at cold temperature.

5 TENOID DIOXYGENASE 3 (NCED3), in response to cold temperature.

6 MTA3 transcriptional activity in response to cold temperature.

7 rapidly engaged upon exposure to dangerously cold temperature.

8 is thaliana results in early flowering under cold temperature.

9 Peninsula despite a short growing season and cold temperature.

10 s resulted in a higher threshold response to cold temperature.

11 t that was exacerbated by blunt pressure and cold temperature.

12 he breadth of behavioral responses evoked by cold temperatures.

13 h were minimally perturbed by above freezing cold temperatures.

14 freezing tolerance in preparation for coming cold temperatures.

15 s, and responses to physiologically relevant cold temperatures.

16 nociceptors that respond to harsh touch and cold temperatures.

17 n channel is a major sensor of environmental cold temperatures.

18 , electrical shock, high frequency light and cold temperatures.

19 M8 exhibit deficient behavioral responses to cold temperatures.

20 mice exhibit strikingly reduced avoidance of cold temperatures.

21 omosomal entanglements and missegregation at cold temperatures.

22 ould be significantly reduced as a result of cold temperatures.

23 ability to resist sweetening when exposed to cold temperatures.

24 ctrical spread or extended it beyond that at cold temperatures.

25 eratures and low rates at warm and extremely cold temperatures.

26 genes/operons to enable their expression at cold temperatures.

27 t shelf-life or necessitate storage at ultra-cold temperatures.

28 lignified polar oi1 barrier formation under cold temperatures.

29 ing fast motional regimes, even at extremely cold temperatures.

30 temperatures and strongly bounded by minimum cold temperatures.

31 mposable phenotypic defects upon exposure to cold temperatures.

32 levant and sex-specific sensor of moderately cold temperatures.

33 terized, little is known about those sensing cold temperatures.

34 nhanced sensorimotor behavior when tested at cold temperatures.

35 tle touch of animals raised in and tested at cold temperatures.

36 cing the performance of GPCRs in response to cold temperatures.

37 s)] exhibit natural variation in response to cold temperatures.

38 urons and are essential for the detection of cold temperatures.

39 low half-saturation constant for Rubisco at cold temperatures.

40 me induced during growth on n-alkanes and in cold temperatures.

41 te chemistry that will be most pronounced in cold temperatures.

42 rotection within viral capsids maintained at cold temperatures.

43 some of these targets is greatly enhanced by cold temperatures.

44 ensitivity to mechanical force and innocuous cold temperatures.

45 programs contribute to lifespan extension at cold temperatures.

46 lated") are insensitive to cool to painfully cold temperatures.

47 netic programs actively promote longevity at cold temperatures.

48 temperature with minimum risk of morbidity, cold temperatures (1(st) percentile) were associated wit

49 levels of COR14b and DHN5 transcript at mild cold temperatures (12-15 degrees C) than the DV92 allele

50 iative cooling efficiency, causing unusually cold temperatures 2-6 years post-equinox.

51 described a distinct thermometer circuit for cold temperature.(3) Together, the results demonstrate t

52 part freezing tolerance in plants exposed to cold temperature (4 degrees C).

53 ficant spectral changes than those stored at cold temperature (4 degrees C).

54 rmatus cannot tolerate prolonged and extreme cold temperatures (4-6 degrees C) and suggest that aperi

55 elative difference, including when tested at cold temperature (5 degrees C).

56 Interestingly, the pause density at cold temperatures (7 to 21 degrees C) was five times hig

57 The avoidance of cold temperatures, a particular challenge in ectotherms,

58 er earlier when exposed for several weeks to cold temperatures, a process called vernalization.

59 re) varieties, long exposures to nonfreezing cold temperatures accelerate flowering time (vernalizati

60 We suggest that cold temperatures accompanied by reduced photoperiod and

61 One fundamental component of cold temperature adaptation is the ability to polymerize

62 found that pnp translation occurs throughout cold-temperature adaptation, whereas lacZ(+) translation

63 ce worm genes examined, suggesting a role in cold-temperature adaptation.

64 anscriptionally repressed during exposure to cold temperatures, allowing studies of how environmental

65 Cold temperature also impacts AstC levels in other Droso

66 Because cold temperatures also led to significant reductions of

67 r extraction of E. coli with methanol:water, cold temperature and a high methanol fraction minimize a

68 Cold temperature and cold start conditions caused dramat

69 tivates uncoupled respiration in response to cold temperature and contributes to systemic metabolic h

70 al, nonselective cation channel activated by cold temperature and cooling agents that plays a critica

71 itions, including low nutrient availability, cold temperature and freeze-thaw processes, UV and radic

72 s after plants were transferred from warm to cold temperature and in warm-grown plants that constitut

73 Collectively, we identify that cold temperatures and Adrb3 agonists activate distinct c

74 in ecDHFR are involved in TS interactions at cold temperatures and are linked to dynamic motions invo

75 ave been used to trigger a beiging response: cold temperatures and beta3-adrenergic receptor (Adrb3)

76 essing the TRPM8 channel can be activated by cold temperatures and by a cooling agent, menthol.

77 RPM8) channels are well known as sensors for cold temperatures and cooling agents such as menthol and

78 bital openings correlated significantly with cold temperatures and cranial size, suggesting not only

79 ressed in shoot tips and buds in response to cold temperatures and day length in a manner that is rel

80 lands is driven by reduced local exposure to cold temperatures and enhanced by abiotic microclimatic

81 in motor neuron number of animals raised in cold temperatures and for their enhanced sensorimotor be

82 mechanism with implications in adaptation to cold temperatures and high-calorie diets.

83 te process, with maximal rates at relatively cold temperatures and low rates at warm and extremely co

84 Our results demonstrate that despite cold temperatures and low-oxygen conditions, hunter-gath

85 Previous studies have demonstrated that cold temperatures and lower extracellular calcium ion (C

86 , with Sungir being strongly associated with cold temperatures and Mladec with warm-to-hot temperatur

87 Postharvest storage assays suggested that cold temperatures and relative humidity affect the avoca

88 flammatory phenotype that is not provoked by cold temperatures and that has different end-organ invol

89 hark's ability to maintain heart function at cold temperatures and their niche expansion into subarct

90 ige adipogenesis) upon the first exposure to cold temperatures and then interconvert between "dormant

91 ng in brown fat, rendering mice sensitive to cold temperature, and diminished browning of inguinal wh

92 talizations in Hong Kong was attributable to cold temperatures, and elderly men had greater susceptib

93 zation, caused by low wintertime irradiance, cold temperatures, and insufficient micronutrients.

94 plegic arrest is agent specific, feasible at cold temperatures, and may be superior to the use of sta

95 lated dinosaurs were already well adapted to cold temperatures, and not only survived but also underw

96 Episodes of extremely hot or cold temperatures are associated with increased mortalit

97 ng to short cold periods, but is absent when cold temperatures are registered digitally at FLC.

98 cells, working in a wide operation window of cold temperatures, are developed.

99 ott and his men perished displays persistent cold temperatures at this time of year close to those re

100 To overwinter, animals must detect constant cold temperatures before adapting their behavior accordi

101 it can be transported over long distances at cold temperatures before decomposing thermally to releas

102 ~ 35 km away where they experienced similar cold temperatures before returning to the aggregation si

103 Cold temperature, Brefeldin A, and monensin, all known t

104 l were more strongly associated with hot and cold temperatures, but gender made no difference.

105 mRNA is generally stabilized upon a shift to cold temperatures, but that a CSR mRNA-specific decay pr

106 ing humans, and sensitizes their response to cold temperature by inducing a leftward shift in the vol

107 de that notothenioid A4-LDHs have adapted to cold temperatures by increases in flexibility in small a

108 stressful environmental conditions, such as cold temperatures, by preventing excess accumulation of

109 pecies show a threshold for calcification at cold temperatures: calcification in P. calcariformata on

110 of the tongue (chorda tympani nerve) from a cold temperature can evoke sweetness, whereas cooling ca

111 mogenesis (NST) from skeletal muscle so that cold temperatures can be tolerated.

112 Cold temperatures can pose direct threats to survival in

113 sion (TGI), alternating non-noxious warm and cold temperatures cause a paradoxical, sometimes painful

114 abolic and enzymic activity, the notion that cold temperature causes free radical production appeared

115 Here, we show that hot and cold temperature changes cause distinct physiological re

116 This study employed previously established cold temperature conditioning treatments for ripening of

117 ndance of various AS events under normal and cold temperature conditions in Arabidopsis.

118 In fact, the normal responses to cold temperature could be reversed in the two neuronal s

119 When exposed to cold temperatures, cpn60alpha2 mutants accumulate less c

120 ude marine environments are characterized by cold temperatures, dark winters and a strong seasonal cy

121 amino acid substitutions that contribute to cold temperature-dependent tubulin polymerization.

122 Cold temperature detection involves the process of senso

123 Cold temperature did not induce current from other DEG/E

124 A3 and CAMTA3(334) to induce target genes at cold temperature did not involve increased levels of the

125 The cold temperature did not significantly affect the peak i

126 iption and translation inhibitors (TTis) and cold temperatures during isolation.

127 Dormancy is enhanced by cold temperatures during seed development by affecting s

128 while equilibrium H(2)O sorption is high at cold temperatures (e.g., -20 degrees C), the effect of h

129 eau or decrease at high latitudes because of cold temperature effects on biogeochemistry and (ii) the

130 Cold temperature effects on cold start MSAT emissions va

131 cceleration of flowering by a long period of cold temperature, ensures that many plants overwinter ve

132 vernalization (the promotion of flowering by cold temperatures) epigenetically silences FLC expressio

133 e failed to regulate body temperature during cold temperature exposure.

134 ire a genetically pre-determined duration of cold-temperature exposure to induce autocatalytic system

135 n development is highly sensitive to hot and cold temperature extremes, reliable methods to evaluate

136 S2 were adapted to rapid growth and lysis at cold temperature for a minimum of 50 phage generations a

137 r of amino acid residues can account for the cold temperature function of a polyextremophilic enzyme.

138 Upon exposure to cold temperatures, GA levels fall to low levels in the p

139 ting only a small cohort of sensory neurons, cold temperatures generate a variety of distinct sensati

140 Mice exposed to cold temperatures had increased levels of circulating NP

141 Hot and cold temperatures have a different impact on fly activit

142 eratures with pneumonia in the elderly, with cold temperatures having stronger effect estimates.

143 suffer from several abiotic stresses such as cold temperature, high soil salinity, lack of water or h

144 sent extreme physiological challenges due to cold temperatures, high physical exertion, and 24-hour d

145 ar for north Florida due to its tolerance to cold temperatures; however, guidelines on how N manageme

146 nt in the downstream/upstream gradient where cold temperatures impair growth opportunities in young b

147 ses information about long-lasting, absolute cold temperature in Drosophila.

148 mCBF12 and TmCBF15 were up-regulated at mild cold temperatures in G3116 but not in DV92.

149 thol, is the principal molecular detector of cold temperatures in primary sensory neurons of the soma

150 tures yet enables this prophage to excise at cold temperatures in Shewanella oneidensis.

151 sis supports a key role for GluK2 in sensing cold temperatures in somatosensory DRG neurons in the pe

152 ent for detection and regional adaptation to cold temperatures in the peripheral nervous system that

153 northern European species are responsive to cold temperatures in the previous autumn.

154 uniformly cool, but instead has anomalously cold temperatures in the subpolar gyre, warm temperature

155 ticles, instead of into liquid drops, at the cold temperatures in Titan's atmosphere.

156 gents, and is highly sensitive to moderately cold temperatures, in a temperature range at which TRPM8

157 ns (e.g. high salt brines, high pressure and cold temperatures) including the ability to synthesize t

158 This finding suggests that stimulation by cold temperatures increases the frequency with which USA

159 Cold temperatures induce formation of beige adipocytes,

160 ipocyte progenitor cells (APCs) can generate cold temperature-induced thermogenic beige adipocytes wi

161 The physiological responses of pear to cold-temperature-induced ripening have been well charact

162 eview, we summarize our understanding of how cold temperature induces a switch in the FLC chromatin s

163 llenge of prolonged noncircadian exposure to cold temperature induces circadian induction of SREBP1 t

164 Here, we show that PNPase cold-temperature induction involves several post-transcr

165 parately encodes and relays absolute hot and cold temperature information, show how patterns of sleep

166 erature discrimination, detection of noxious cold temperatures, injury-evoked hypersensitivity to col

167 orial convective anomalies is seen advecting cold temperatures into India and maintaining the cold wa

168 TRPM8 activation by CFA was potentiated by cold temperature involving the phosphatidylinositol 4,5-

169 Cold temperature is an environmental stimulus that cause

170 As cold temperature is associated with reduced metabolic an

171 Detection and adaptation to cold temperature is crucial to survival.

172 These results suggest that short-term cold temperature is more damaging for branching corals t

173 Cold temperature is prevalent across the biosphere and s

174 deling, we found that analog registration of cold temperature is problematic due to impaired analog-t

175 he ecological importance of seed response to cold temperature is well appreciated, the mechanisms und

176 induction of uncoupling protein 1 (Ucp1) by cold temperatures is preceded by rapid downregulation of

177 thermogenesis, when the hypothalamus senses cold temperatures it triggers sympathetic discharge, res

178 t species is accelerated by a long period of cold temperature, known as a vernalization period.

179 gion of the period (per) mRNA is enhanced at cold temperatures, leading to more rapid daily increases

180 These remarkably cold temperatures likely contributed substantially to th

181 e of stimuli, including menthol, icilin, and cold temperatures (<25 degrees C).

182 waters when encountering the combination of cold temperatures (<6 degrees C) and low dissolved oxyge

183 When exposed to cold temperatures, mammals undergo remarkable physiologi

184 We found that cold temperature markedly increased the constitutively a

185 Warm and cold temperatures masculinize fish with mid-range condit

186 Mosses grow slowly, but cold temperatures minimize decomposition, facilitating m

187 The finding that cold temperature modulates DEG/ENaC channel function may

188 leads to slow growth and hypersensitivity to cold temperature, nutrient limitation, and the IMP dehyd

189 ction of mango fruit tolerance to suboptimal cold temperature of 7 or 10 degrees C after postharvest

190 In temperate climates, the prolonged cold temperature of winter serves as a seasonal landmark

191 The strong effect of cold temperatures on many physiological processes has re

192 e (TYPE2) is more regional, with significant cold temperatures only noticeable over northwest India.

193 digital artery spasm, often precipitated by cold temperature or emotional stress.

194 hat EYES ABSENT (EYA) shows higher levels in cold temperature or short photoperiod and promotes winte

195 hrough exposure of plants to long periods of cold temperature or winter.

196 n response to stressors, such as exposure to cold temperatures or increased physical activity.

197 Fs in thermogenic tissues of mice exposed to cold temperatures or treated with the beta-adrenergic re

198 ng these warm blobs, also causing abnormally cold temperatures over North America during the cold sea

199 on (bolting) and flowering after exposure to cold temperatures over winter.

200 Additionally, biodiesel has poor cold-temperature performance and low oxidative stability

201 when these channels were activated by acid, cold temperature potentiated the currents by slowing the

202 Organisms that thrive at cold temperatures produce ice-binding proteins to manage

203 issue, Xiao et al. challenge the notion that cold temperatures promote longevity solely through therm

204 Our results suggest cold temperatures provided a sufficient barrier against

205 d by a variety of noxious stimuli, including cold temperatures, pungent natural compounds, and enviro

206 temperature thermosensor and is activated by cold temperatures ranging from 8 to 25 degrees C and coo

207 Exposure to cold temperature rapidly promoted alternative activation

208 One prominent model is that cold temperatures reduce the rate of chemical reactions,

209 otic associations, each grown under warm and cold temperature regimes.

210 The ability of plants to withstand cold temperatures relies on their photosynthetic activit

211 Transition to cold temperatures requires changes in the partitioning o

212 ed hosts should occur at relatively warm and cold temperatures, respectively.

213 injury develops after sustained exposure to cold temperatures, resulting in tissue cooling but not f

214 show that growing Xenopus laevis embryos at cold temperatures results in an increase in the number o

215 Cold temperatures robustly activate a small cohort of so

216 TRPM8 is a polymodal TRP channel involved in cold temperature sensing, thermoregulation, and cold pai

217 l, but nothing is known about how it affects cold temperature sensing.

218 on and characterization of an EMS-generated, cold-temperature-sensitive mutation in Arabidopsis thali

219 olyte leakage assays show that PRR7 enhances cold temperature sensitivity, supported by ChIP-qPCR at

220 n to certain environmental stresses, such as cold temperatures, short chain alcohols, and high magnes

221 This research investigates how this cold temperature signal is perceived by plant cells and

222 development-to be generally less tolerant to cold temperatures, since they are confined to attacking

223 profile of room temperature stored (RT) and cold temperature stored (CT) beer differed significantly

224 During cold temperature stress, accumulation of the gene encodi

225 the proper induction of LDs during heat and cold temperature stress, respectively.

226 Under cold-temperature stress, both sexes were less active and

227 d the resistance of cytoskeleton proteins to cold-temperature stress.

228 at E. sibiricum is constitutively adapted to cold temperatures stressful to mesophiles since little d

229 However, cold temperatures strongly induce the expression of the

230 predetermines the sensitivity of AML LSCs to cold temperature, suggesting that cold sensitivity could

231 21 times greater for the cold starts during cold temperature tests than comparable warm temperature

232 pulicaria performed significantly better at cold temperatures than D. ambigua, but by 20 degrees C,

233 ffer from severe limitations when applied to cold temperatures that characterize Arctic environments.

234 d high rates of substrate utilization at the cold temperatures that exist beneath the snow.

235 TRPM8 is the predominant mammalian cold temperature thermosensor and is activated by cold t

236 ocomotory muscle power is often depressed at cold temperatures, these sharks remain capable of captur

237 expressor lines at warm temperatures, and at cold temperatures they accumulated to much higher levels

238 n proposed, but it has been assumed that the cold temperatures they reported encountering on the Ross

239 o the sciatic nerve, and a decrease in their cold temperature threshold.

240 Potato tubers must be stored at cold temperatures to minimize sprouting and losses due t

241 Potato tubers must be stored at cold temperatures to prevent sprouting, minimize disease

242 f wheat, but is not affected by dehydration, cold-temperature treatment or ABA.

243 protein kinase mRNA, which is upregulated by cold-temperature treatment, dehydration and abscisic aci

244 Cold temperatures trigger the expression of the CBF fami

245 Cold temperatures trigger the expression of the CBF fami

246 Cold temperatures trigger the ICE1-CBF-COR transcription

247 RPM8 in thermosensation over a wide range of cold temperatures, validating the hypothesis that TRP ch

248 environmental signals such as photoperiod or cold temperatures (vernalization), flowering time is als

249 le for the transduction of prolonged extreme cold temperatures, where tissue damage causes pan-nocice

250 channels can be directly activated by hot or cold temperature with high sensitivity.

251 riods and reduced food supplies, we combined cold temperatures with short days and metabolic challeng

252 ial deficits in cold avoidance at moderately cold temperatures, with a strength of the phenotype simi