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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
34 rmatus cannot tolerate prolonged and extreme cold temperatures (4-6 degrees C) and suggest that aperi
37 re) varieties, long exposures to nonfreezing cold temperatures accelerate flowering time (vernalizati
40 found that pnp translation occurs throughout cold-temperature adaptation, whereas lacZ(+) translation
42 anscriptionally repressed during exposure to cold temperatures, allowing studies of how environmental
44 r extraction of E. coli with methanol:water, cold temperature and a high methanol fraction minimize a
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
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)
53 ressed in shoot tips and buds in response to cold temperatures and day length in a manner that is rel
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
63 ott and his men perished displays persistent cold temperatures at this time of year close to those re
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
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
79 eau or decrease at high latitudes because of cold temperature effects on biogeochemistry and (ii) the
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
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
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
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
95 uniformly cool, but instead has anomalously cold temperatures in the subpolar gyre, warm temperature
97 This finding suggests that stimulation by cold temperatures increases the frequency with which USA
99 eview, we summarize our understanding of how cold temperature induces a switch in the FLC chromatin s
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-
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
113 gion of the period (per) mRNA is enhanced at cold temperatures, leading to more rapid daily increases
116 waters when encountering the combination of cold temperatures (<6 degrees C) and low dissolved oxyge
121 leads to slow growth and hypersensitivity to cold temperature, nutrient limitation, and the IMP dehyd
123 e (TYPE2) is more regional, with significant cold temperatures only noticeable over northwest India.
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
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
138 injury develops after sustained exposure to cold temperatures, resulting in tissue cooling but not f
141 on and characterization of an EMS-generated, cold-temperature-sensitive mutation in Arabidopsis thali
143 profile of room temperature stored (RT) and cold temperature stored (CT) beer differed significantly
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,
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
155 protein kinase mRNA, which is upregulated by cold-temperature treatment, dehydration and abscisic aci
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
162 riods and reduced food supplies, we combined cold temperatures with short days and metabolic challeng
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