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1 ls drastically affects protein export at the cold temperature.
2 is thaliana results in early flowering under cold temperature.
3 Peninsula despite a short growing season and cold temperature.
4 s resulted in a higher threshold response to cold temperature.
5 t that was exacerbated by blunt pressure and cold temperature.
6 rapidly engaged upon exposure to dangerously cold temperature.
7 ns have functions related to the response to cold temperature.
8 ed the viability of yeast cells subjected to cold temperature.
9 cing the performance of GPCRs in response to cold temperatures.
10 M8 exhibit deficient behavioral responses to cold temperatures.
11 mice exhibit strikingly reduced avoidance of cold temperatures.
12 omosomal entanglements and missegregation at cold temperatures.
13 ould be significantly reduced as a result of cold temperatures.
14 s)] exhibit natural variation in response to cold temperatures.
15 ability to resist sweetening when exposed to cold temperatures.
16 urons and are essential for the detection of cold temperatures.
17  low half-saturation constant for Rubisco at cold temperatures.
18 rotection within viral capsids maintained at cold temperatures.
19 some of these targets is greatly enhanced by cold temperatures.
20 ensitivity to mechanical force and innocuous cold temperatures.
21 programs contribute to lifespan extension at cold temperatures.
22 lated") are insensitive to cool to painfully cold temperatures.
23 netic programs actively promote longevity at cold temperatures.
24 he breadth of behavioral responses evoked by cold temperatures.
25 h were minimally perturbed by above freezing cold temperatures.
26 freezing tolerance in preparation for coming cold temperatures.
27 s, and responses to physiologically relevant cold temperatures.
28  nociceptors that respond to harsh touch and cold temperatures.
29 n channel is a major sensor of environmental cold temperatures.
30 , electrical shock, high frequency light and cold temperatures.
31  temperature with minimum risk of morbidity, cold temperatures (1(st) percentile) were associated wit
32 levels of COR14b and DHN5 transcript at mild cold temperatures (12-15 degrees C) than the DV92 allele
33 iative cooling efficiency, causing unusually cold temperatures 2-6 years post-equinox.
34 rmatus cannot tolerate prolonged and extreme cold temperatures (4-6 degrees C) and suggest that aperi
35          Interestingly, the pause density at cold temperatures (7 to 21 degrees C) was five times hig
36 er earlier when exposed for several weeks to cold temperatures, a process called vernalization.
37 re) varieties, long exposures to nonfreezing cold temperatures accelerate flowering time (vernalizati
38                              We suggest that cold temperatures accompanied by reduced photoperiod and
39                 One fundamental component of cold temperature adaptation is the ability to polymerize
40 found that pnp translation occurs throughout cold-temperature adaptation, whereas lacZ(+) translation
41 ce worm genes examined, suggesting a role in cold-temperature adaptation.
42 anscriptionally repressed during exposure to cold temperatures, allowing studies of how environmental
43                                      Because cold temperatures also led to significant reductions of
44 r extraction of E. coli with methanol:water, cold temperature and a high methanol fraction minimize a
45                                              Cold temperature and cold start conditions caused dramat
46 tivates uncoupled respiration in response to cold temperature and contributes to systemic metabolic h
47 itions, including low nutrient availability, cold temperature and freeze-thaw processes, UV and radic
48 s after plants were transferred from warm to cold temperature and in warm-grown plants that constitut
49               Collectively, we identify that cold temperatures and Adrb3 agonists activate distinct c
50 in ecDHFR are involved in TS interactions at cold temperatures and are linked to dynamic motions invo
51 ave been used to trigger a beiging response: cold temperatures and beta3-adrenergic receptor (Adrb3)
52 essing the TRPM8 channel can be activated by cold temperatures and by a cooling agent, menthol.
53 ressed in shoot tips and buds in response to cold temperatures and day length in a manner that is rel
54         Our results demonstrate that despite cold temperatures and low-oxygen conditions, hunter-gath
55      Previous studies have demonstrated that cold temperatures and lower extracellular calcium ion (C
56 flammatory phenotype that is not provoked by cold temperatures and that has different end-organ invol
57 hark's ability to maintain heart function at cold temperatures and their niche expansion into subarct
58 ng in brown fat, rendering mice sensitive to cold temperature, and diminished browning of inguinal wh
59 talizations in Hong Kong was attributable to cold temperatures, and elderly men had greater susceptib
60 plegic arrest is agent specific, feasible at cold temperatures, and may be superior to the use of sta
61                 Episodes of extremely hot or cold temperatures are associated with increased mortalit
62 ng to short cold periods, but is absent when cold temperatures are registered digitally at FLC.
63 ott and his men perished displays persistent cold temperatures at this time of year close to those re
64                                              Cold temperature, Brefeldin A, and monensin, all known t
65 l were more strongly associated with hot and cold temperatures, but gender made no difference.
66 mRNA is generally stabilized upon a shift to cold temperatures, but that a CSR mRNA-specific decay pr
67 de that notothenioid A4-LDHs have adapted to cold temperatures by increases in flexibility in small a
68  stressful environmental conditions, such as cold temperatures, by preventing excess accumulation of
69 pecies show a threshold for calcification at cold temperatures: calcification in P. calcariformata on
70  of the tongue (chorda tympani nerve) from a cold temperature can evoke sweetness, whereas cooling ca
71                                              Cold temperatures can pose direct threats to survival in
72 sion (TGI), alternating non-noxious warm and cold temperatures cause a paradoxical, sometimes painful
73 abolic and enzymic activity, the notion that cold temperature causes free radical production appeared
74                   Here, we show that hot and cold temperature changes cause distinct physiological re
75             In fact, the normal responses to cold temperature could be reversed in the two neuronal s
76  amino acid substitutions that contribute to cold temperature-dependent tubulin polymerization.
77                                              Cold temperature detection involves the process of senso
78                                              Cold temperature did not induce current from other DEG/E
79 eau or decrease at high latitudes because of cold temperature effects on biogeochemistry and (ii) the
80                                              Cold temperature effects on cold start MSAT emissions va
81 cceleration of flowering by a long period of cold temperature, ensures that many plants overwinter ve
82 vernalization (the promotion of flowering by cold temperatures) epigenetically silences FLC expressio
83 e failed to regulate body temperature during cold temperature exposure.
84 S2 were adapted to rapid growth and lysis at cold temperature for a minimum of 50 phage generations a
85 r of amino acid residues can account for the cold temperature function of a polyextremophilic enzyme.
86 ting only a small cohort of sensory neurons, cold temperatures generate a variety of distinct sensati
87                              Mice exposed to cold temperatures had increased levels of circulating NP
88 eratures with pneumonia in the elderly, with cold temperatures having stronger effect estimates.
89 suffer from several abiotic stresses such as cold temperature, high soil salinity, lack of water or h
90 nt in the downstream/upstream gradient where cold temperatures impair growth opportunities in young b
91 mCBF12 and TmCBF15 were up-regulated at mild cold temperatures in G3116 but not in DV92.
92 thol, is the principal molecular detector of cold temperatures in primary sensory neurons of the soma
93 ent for detection and regional adaptation to cold temperatures in the peripheral nervous system that
94  northern European species are responsive to cold temperatures in the previous autumn.
95  uniformly cool, but instead has anomalously cold temperatures in the subpolar gyre, warm temperature
96 ticles, instead of into liquid drops, at the cold temperatures in Titan's atmosphere.
97    This finding suggests that stimulation by cold temperatures increases the frequency with which USA
98                                              Cold temperatures induce formation of beige adipocytes,
99 eview, we summarize our understanding of how cold temperature induces a switch in the FLC chromatin s
100                    Here, we show that PNPase cold-temperature induction involves several post-transcr
101 erature discrimination, detection of noxious cold temperatures, injury-evoked hypersensitivity to col
102 orial convective anomalies is seen advecting cold temperatures into India and maintaining the cold wa
103   TRPM8 activation by CFA was potentiated by cold temperature involving the phosphatidylinositol 4,5-
104                                              Cold temperature is an environmental stimulus that cause
105                                           As cold temperature is associated with reduced metabolic an
106                  Detection and adaptation to cold temperature is crucial to survival.
107        These results suggest that short-term cold temperature is more damaging for branching corals t
108 deling, we found that analog registration of cold temperature is problematic due to impaired analog-t
109 he ecological importance of seed response to cold temperature is well appreciated, the mechanisms und
110  induction of uncoupling protein 1 (Ucp1) by cold temperatures is preceded by rapid downregulation of
111  thermogenesis, when the hypothalamus senses cold temperatures it triggers sympathetic discharge, res
112 t species is accelerated by a long period of cold temperature, known as a vernalization period.
113 gion of the period (per) mRNA is enhanced at cold temperatures, leading to more rapid daily increases
114                             These remarkably cold temperatures likely contributed substantially to th
115 e of stimuli, including menthol, icilin, and cold temperatures (<25 degrees C).
116  waters when encountering the combination of cold temperatures (<6 degrees C) and low dissolved oxyge
117                              When exposed to cold temperatures, mammals undergo remarkable physiologi
118                                We found that cold temperature markedly increased the constitutively a
119                      Mosses grow slowly, but cold temperatures minimize decomposition, facilitating m
120                             The finding that cold temperature modulates DEG/ENaC channel function may
121 leads to slow growth and hypersensitivity to cold temperature, nutrient limitation, and the IMP dehyd
122         In temperate climates, the prolonged cold temperature of winter serves as a seasonal landmark
123 e (TYPE2) is more regional, with significant cold temperatures only noticeable over northwest India.
124  digital artery spasm, often precipitated by cold temperature or emotional stress.
125 hrough exposure of plants to long periods of cold temperature or winter.
126 n response to stressors, such as exposure to cold temperatures or increased physical activity.
127 on (bolting) and flowering after exposure to cold temperatures over winter.
128             Additionally, biodiesel has poor cold-temperature performance and low oxidative stability
129  when these channels were activated by acid, cold temperature potentiated the currents by slowing the
130 issue, Xiao et al. challenge the notion that cold temperatures promote longevity solely through therm
131                          Our results suggest cold temperatures provided a sufficient barrier against
132 d by a variety of noxious stimuli, including cold temperatures, pungent natural compounds, and enviro
133 temperature thermosensor and is activated by cold temperatures ranging from 8 to 25 degrees C and coo
134                                  Exposure to cold temperature rapidly promoted alternative activation
135                  One prominent model is that cold temperatures reduce the rate of chemical reactions,
136                                Transition to cold temperatures requires changes in the partitioning o
137 ed hosts should occur at relatively warm and cold temperatures, respectively.
138  injury develops after sustained exposure to cold temperatures, resulting in tissue cooling but not f
139                                              Cold temperatures robustly activate a small cohort of so
140 l, but nothing is known about how it affects cold temperature sensing.
141 on and characterization of an EMS-generated, cold-temperature-sensitive mutation in Arabidopsis thali
142          This research investigates how this cold temperature signal is perceived by plant cells and
143  profile of room temperature stored (RT) and cold temperature stored (CT) beer differed significantly
144  the proper induction of LDs during heat and cold temperature stress, respectively.
145 at E. sibiricum is constitutively adapted to cold temperatures stressful to mesophiles since little d
146  21 times greater for the cold starts during cold temperature tests than comparable warm temperature
147  pulicaria performed significantly better at cold temperatures than D. ambigua, but by 20 degrees C,
148 d high rates of substrate utilization at the cold temperatures that exist beneath the snow.
149           TRPM8 is the predominant mammalian cold temperature thermosensor and is activated by cold t
150 expressor lines at warm temperatures, and at cold temperatures they accumulated to much higher levels
151 n proposed, but it has been assumed that the cold temperatures they reported encountering on the Ross
152 o the sciatic nerve, and a decrease in their cold temperature threshold.
153              Potato tubers must be stored at cold temperatures to prevent sprouting, minimize disease
154 f wheat, but is not affected by dehydration, cold-temperature treatment or ABA.
155 protein kinase mRNA, which is upregulated by cold-temperature treatment, dehydration and abscisic aci
156                                              Cold temperatures trigger the expression of the CBF fami
157                                              Cold temperatures trigger the expression of the CBF fami
158                                              Cold temperatures trigger the ICE1-CBF-COR transcription
159 RPM8 in thermosensation over a wide range of cold temperatures, validating the hypothesis that TRP ch
160 environmental signals such as photoperiod or cold temperatures (vernalization), flowering time is als
161 channels can be directly activated by hot or cold temperature with high sensitivity.
162 riods and reduced food supplies, we combined cold temperatures with short days and metabolic challeng

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