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1 an effective strategy for increasing alfalfa cold tolerance.
2 lation by stabilizing SK2, thereby improving cold tolerance.
3 characterize candidate genes responsible for cold tolerance.
4 cific fatty acid synthase knockout decreased cold tolerance.
5 yotic pathway, which coincides with impaired cold tolerance.
6 JA biosynthesis is key for CsHSFA1d-mediated cold tolerance.
7 file, which likely play a role in increasing cold tolerance.
8 t of insect nutritional status and weight on cold tolerance.
9 ysis to explore the mechanism underlying its cold tolerance.
10 longbing, HLB) and other major diseases, and cold tolerance.
11 putao might contribute to the enhancement of cold tolerance.
12 rifying the molecular mechanisms involved in cold tolerance.
13 pulation overall, but the latter has greater cold tolerance.
14 ng candidates for breeding programs aimed at cold tolerance.
15 e, which provides crop breeding for improved cold tolerance.
16 in-regulated hepatic glucose production, and cold tolerance.
17  planting dates for genotypes and sources of cold tolerance.
18 emperate ortholog, were sufficient to confer cold tolerance.
19 ts (i.e. 'antifreeze') and exhibited greater cold tolerance.
20  to identify 17 genetic loci associated with cold tolerance.
21 cient pathways enabled evolution of seasonal cold tolerance.
22  break, early blooming in winter, and strong cold tolerance.
23 cold acclimation that lead to an increase in cold tolerance.
24 d its encoded peptides alter desiccation and cold tolerance.
25 tion of endosperm, and the genetic basis for cold tolerance.
26 stent with previous work on cold acclimation/cold tolerance.
27 nic gene expression, energy expenditure, and cold tolerance.
28 es; c. 5% of articles consider both heat and cold tolerance.
29 K12) regulators of cold-responsive genes and cold tolerance.
30 the transgenic plants did not show increased cold tolerance.
31 ins were newly identified as associated with cold tolerance.
32 and may underlie natural variation in insect cold tolerance.
33 d cold protection clearly dominate inducible cold tolerance.
34  cold stress and the molecular mechanisms of cold tolerance.
35 significant reductions in drought, salt, and cold tolerance.
36 ional activators that have a central role in cold tolerance.
37 er directly or indirectly towards increasing cold tolerance.
38 elative traits were derived as indicators of cold-tolerance.
39 s studied in two inbred lines of contrasting cold-tolerance.
40 demonstrates high intraspecific diversity in cold-tolerance.
41 al limits and gene expression may facilitate cold tolerance across a species range, whereas high temp
42 atic niche shift is mirrored in an increased cold tolerance and a population-specific and functionall
43  A strong negative correlation between basal cold tolerance and developmental acclimation suggests th
44 cid-binding protein, FABP3, is essential for cold tolerance and efficient fatty acid oxidation in mou
45           With the aim to add new sources of cold tolerance and elucidate mechanism of cold-tolerance
46 e were compared for potential differences in cold tolerance and energy metabolism.
47 lthough both sexes showed similar changes in cold tolerance and gene expression in response to cold t
48  represses GNC and GNL expression to control cold tolerance and greening, two further physiological p
49 eaction norms reflecting a trade-off between cold tolerance and growth.
50                              This results in cold tolerance and increased energy expenditure, protect
51 t mice generated by using Fabp4-Cre improves cold tolerance and increases energy expenditure and prot
52 ey found that range-edge frogs had increased cold tolerance and longer legs associated with better di
53 5 can positively regulate drought, salt, and cold tolerance and negatively modulate PR gene expressio
54 gnaling, interactive pathways that influence cold tolerance and phenological development to optimize
55            Thermogenic visceral WAT improves cold tolerance and prevents and reverses insulin resista
56 dipose-specific ACOX2 knockout also impaired cold tolerance and promoted diet-induced obesity and ins
57 esult from increased heat loss, because both cold tolerance and response to a beta3-adrenergic agonis
58  a weaker negative correlation between basal cold tolerance and short-term acclimation suggests less
59 ard commercial hybrid known for its seedling cold tolerance and some cold susceptible breeding lines
60  expression of iafgp, thereby increasing the cold tolerance and survival of I. scapularis.
61 mically extensive database on plant heat and cold tolerances and used this dataset to test for therma
62                  We conclude A. l. petraea's cold-tolerance and preference for disturbed habitats ena
63 increased basal rectal temperature, enhanced cold tolerance, and improved glucose homeostasis.
64 e Northern Hemisphere after the evolution of cold tolerance, and the radiation of northern alpine pla
65 found support for several expected patterns: Cold tolerances are more variable and exhibit steeper la
66 ults showed that dysfunction of RDM4 reduced cold tolerance, as evidenced by decreased survival and i
67 rotrimeric G-protein gamma subunit, AGG3, in cold tolerance, as newly predicted from our environmenta
68 ere may provide a foundation for discovering cold tolerance-associated genome-wide variations in prio
69 intering structure and to identify potential cold-tolerance-associated biomarkers.
70                       Proteins identified as cold-tolerance-associated included molecular chaperones,
71 ar relationship between lipid saturation and cold tolerance at 0 degrees C, an outcome confirmed by d
72   Deletion of Rev-erbalpha markedly improves cold tolerance at 17:00, indicating that overcoming Rev-
73            We found significant increases in cold tolerance at the species' southern limit.
74 sts internal constraints on the evolution of cold tolerance/avoidance strategies.
75 t cold acclimation is effective in enhancing cold tolerance but benefits only cold-tolerant (CT) geno
76 ly contributed to variation in both heat and cold tolerances but that their relative importance diffe
77 disordered regions plays an adaptive role in cold tolerance by concentrating enzymes and substrates t
78                           The enhancement of cold tolerance by OsCAF1B in transgenic rice seedlings i
79    The molecular basis for 'Jonsok'-enhanced cold tolerance can be explained by the constitutive leve
80         Upland switchgrass exhibits superior cold tolerance compared to the lowland ecotype, but the
81                        However, no effect on cold tolerance could be determined using supercooling po
82     Then, we measured the heat (CT(max)) and cold tolerance (CT(min)) of worker ants in summer and sp
83 is factor Pex16 (Pex16-AKO) in mice impaired cold tolerance, decreased energy expenditure, and increa
84 bolism, and membrane stabilization as key to cold tolerance during PR and FR phases. The current stud
85 rdening (RCH), insects significantly enhance cold tolerance following brief (i.e., minutes to hours)
86 vailable on shade, drought, waterlogging and cold tolerance for 799 northern hemisphere woody species
87 ed in the adaptability of low-temperature of cold tolerance, fungal pathogenicity and specialized hos
88                                              Cold tolerance has evolved more quickly than heat tolera
89 siological changes associated with increased cold tolerance have been well studied.
90 monas reinhardtii to show that NTRC mediates cold tolerance in a redox-dependent manner.
91  Furthermore, we argue that the evolution of cold tolerance in certain C(3) lineages is an overlooked
92                       However, a decrease in cold tolerance in early spring seriously affects regrowt
93 ycerophospholipid metabolism affects alfalfa cold tolerance in early spring.
94 red riboflavin as an enhancer of postharvest cold tolerance in fruits inducing antioxidant defense me
95                        Ants acclimated their cold tolerance in line with seasonal changes, but heat t
96 ions and gene expression are associated with cold tolerance in mangrove species.
97              While HUFAs may be required for cold tolerance in plants and fish, the primary role of H
98 hether altered FAX1 abundance contributes to cold tolerance in plants remains unclear.
99               To identify genes critical for cold tolerance in plants, we screened Arabidopsis thalia
100 tant for cold-responsive gene regulation and cold tolerance in plants.
101 dicate that CRLK1 is a positive regulator of cold tolerance in plants.
102 gulated receptor-like kinase, is crucial for cold tolerance in plants.
103 by the Exportin-1 inhibitor KPT-330 enhances cold tolerance in pre-diabetic obese mice, and greatly p
104 ls of Ghd8 delayed heading date and enhanced cold tolerance in rice.
105 roviding a good candidate gene for improving cold tolerance in rice.
106                      Genetic variability for cold tolerance in sorghum has been evaluated by characte
107 ere, we investigate behavioral mechanisms of cold tolerance in the snow fly (Chionea spp.), a flightl
108 of cold tolerance and elucidate mechanism of cold-tolerance in wild species of chickpea, the present
109 of PLC1 in an inp51 mutant does not abrogate cold tolerance, indicating that Plc1p-mediated productio
110     The possible function of this protein in cold tolerance is discussed.
111 idence of proteins having a direct effect on cold tolerance is emerging but limited.
112                                              Cold tolerance is important in defining the distribution
113 an inp51 mutant strain demonstrates that the cold tolerance is strictly due to loss of 5-phosphatase
114 rate trees because of phylogenetic signal in cold tolerance, leading to significantly and substantial
115 volved in physiological processes, including cold tolerance, light-responsiveness and flowering.
116 d in cold paleoclimates have presently lower cold tolerance limits than those with warm thermal ances
117 evelopmental acclimation suggests that basal cold tolerance may constrain developmental acclimation,
118              To gain an understanding of its cold tolerance mechanism, mRNA differential display reve
119 ance that likely serves as a universal plant cold tolerance mechanism.
120     Adult mGPD knockout animals had a normal cold tolerance, normal circadian rhythm in body temperat
121                                 The enhanced cold tolerance observed in the CT genotypes is likely at
122  just 16% of the observed difference between cold tolerance of animals held at 25 degrees C and 10 de
123 r and spring lows in the canopy exceeded the cold tolerance of ants nesting there.
124  a critical role for the epitranscriptome in cold tolerance of Arabidopsis.
125 hat most thermal tolerance research examines cold tolerance of cultivated species; c. 5% of articles
126 r direction and correspondingly modulate the cold tolerance of intact animals.
127              In this study, we characterized cold tolerance of null mutant of RNA-DIRECTED DNA METHYL
128 xpression of Ghd8, thus conferring increased cold tolerance of rice seedlings.
129                                              Cold-tolerance of Attamyces cultivars increases with win
130  studies on mechanisms determining divergent cold-tolerance of inbred maize lines.
131  freezing (-2 degrees C) temperatures on the cold-tolerance of oligochaete worms (Enchytraeus albidus
132 ime control on the one side and greening and cold tolerance on the other that may be governed by the
133 of s/s animals, locomotor activity and acute cold tolerance (partly a measure of shivering thermogene
134 tigation of numerous other phenomena such as cold tolerance, quality as a prey item, and effects of m
135 on, especially underdominance in the case of cold-tolerance related phenotypes.
136                                              Cold tolerance scaled weakly with both dimensions.
137                          Thus, screening for cold tolerance should not be limited to early seedling c
138                  While theory often predicts cold tolerance should track environmental temperatures,
139 ugh this species can utilise two alternative cold tolerance strategies with diapause for overwinterin
140 ith the use of diverse larval habitats and a cold tolerance that allows an expanded seasonal activity
141 re environment; to identify genes related to cold tolerance that have been subjected to independent p
142  wild relatives of chickpea exhibit enhanced cold tolerance, their molecular responses to freezing st
143 trate phosphocholine is sufficient to induce cold tolerance, thermogenic gene expression, and allied
144 rom the circadian clock contributes to plant cold tolerance through regulation of the CBF cold-respon
145 sential component of the UPR during heat and cold tolerance, thus confirming the cytoprotective role
146          Ants from both strata adapted their cold tolerance to cope with winter cold, while heat tole
147  crystal toxin genes, drought resistance and cold tolerance to extend growth range.
148 atterns of both phenological development and cold tolerance traits in wheat.
149 s (chill-coma) is a common measure of insect cold tolerance used to test central questions in thermal
150 ity of arbuscular mycorrhizal fungi, whereas cold tolerance was associated with lower fungal richness
151 ance of the m(6) A epitranscriptome on plant cold tolerance was further assessed using the mta mutant
152  with a defect in thermogenesis, an impaired cold tolerance was observed in fat-specific Afadin knock
153  shoot apex development and the induction of cold tolerance was reflected by the gradual up-regulatio
154  a number of other genes important for plant cold tolerance were also affected in the mutants.
155                   Distinctive mechanisms for cold tolerance were characterized for two cultivars.
156   Body composition, insulin sensitivity, and cold tolerance were completely normalized in Nse+Syn db/
157 erance, and previously selected for seedling cold tolerance were used.
158 is study advances our understanding of plant cold tolerance, which provides crop breeding for improve
159 utely activated BAT fuel uptake and enhanced cold tolerance, which resulted in decreased levels of se
160 h is of potential importance in coordinating cold tolerance with growth and development.
161 dipocyte specific Mypt1 deficiency increases cold tolerance with higher Ucp1 levels in subcutaneous w
162 le checks, but noticeably between sources of cold tolerance, with the Ethiopian highland sources havi

 
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