ライフサイエンスコーパス: cold tolerance

1 to identify 17 genetic loci associated with cold tolerance.

2 cient pathways enabled evolution of seasonal cold tolerance.

3 cold acclimation that lead to an increase in cold tolerance.

4 d its encoded peptides alter desiccation and cold tolerance.

5 tion of endosperm, and the genetic basis for cold tolerance.

6 stent with previous work on cold acclimation/cold tolerance.

7 nic gene expression, energy expenditure, and cold tolerance.

8 K12) regulators of cold-responsive genes and cold tolerance.

9 the transgenic plants did not show increased cold tolerance.

10 ins were newly identified as associated with cold tolerance.

11 and may underlie natural variation in insect cold tolerance.

12 d cold protection clearly dominate inducible cold tolerance.

13 cold stress and the molecular mechanisms of cold tolerance.

14 significant reductions in drought, salt, and cold tolerance.

15 ional activators that have a central role in cold tolerance.

16 er directly or indirectly towards increasing cold tolerance.

17 s studied in two inbred lines of contrasting cold-tolerance.

18 demonstrates high intraspecific diversity in cold-tolerance.

19 elative traits were derived as indicators of cold-tolerance.

20 atic niche shift is mirrored in an increased cold tolerance and a population-specific and functionall

21 A strong negative correlation between basal cold tolerance and developmental acclimation suggests th

22 cid-binding protein, FABP3, is essential for cold tolerance and efficient fatty acid oxidation in mou

23 represses GNC and GNL expression to control cold tolerance and greening, two further physiological p

24 5 can positively regulate drought, salt, and cold tolerance and negatively modulate PR gene expressio

25 gnaling, interactive pathways that influence cold tolerance and phenological development to optimize

26 Thermogenic visceral WAT improves cold tolerance and prevents and reverses insulin resista

27 esult from increased heat loss, because both cold tolerance and response to a beta3-adrenergic agonis

28 a weaker negative correlation between basal cold tolerance and short-term acclimation suggests less

29 expression of iafgp, thereby increasing the cold tolerance and survival of I. scapularis.

30 We conclude A. l. petraea's cold-tolerance and preference for disturbed habitats ena

31 e Northern Hemisphere after the evolution of cold tolerance, and the radiation of northern alpine pla

32 ults showed that dysfunction of RDM4 reduced cold tolerance, as evidenced by decreased survival and i

33 intering structure and to identify potential cold-tolerance-associated biomarkers.

34 Proteins identified as cold-tolerance-associated included molecular chaperones,

35 ar relationship between lipid saturation and cold tolerance at 0 degrees C, an outcome confirmed by d

36 Deletion of Rev-erbalpha markedly improves cold tolerance at 17:00, indicating that overcoming Rev-

37 We found significant increases in cold tolerance at the species' southern limit.

38 sts internal constraints on the evolution of cold tolerance/avoidance strategies.

39 The molecular basis for 'Jonsok'-enhanced cold tolerance can be explained by the constitutive leve

40 rdening (RCH), insects significantly enhance cold tolerance following brief (i.e., minutes to hours)

41 ed in the adaptability of low-temperature of cold tolerance, fungal pathogenicity and specialized hos

42 siological changes associated with increased cold tolerance have been well studied.

43 Furthermore, we argue that the evolution of cold tolerance in certain C(3) lineages is an overlooked

44 While HUFAs may be required for cold tolerance in plants and fish, the primary role of H

45 To identify genes critical for cold tolerance in plants, we screened Arabidopsis thalia

46 tant for cold-responsive gene regulation and cold tolerance in plants.

47 dicate that CRLK1 is a positive regulator of cold tolerance in plants.

48 gulated receptor-like kinase, is crucial for cold tolerance in plants.

49 of PLC1 in an inp51 mutant does not abrogate cold tolerance, indicating that Plc1p-mediated productio

50 The possible function of this protein in cold tolerance is discussed.

51 idence of proteins having a direct effect on cold tolerance is emerging but limited.

52 Cold tolerance is important in defining the distribution

53 an inp51 mutant strain demonstrates that the cold tolerance is strictly due to loss of 5-phosphatase

54 rate trees because of phylogenetic signal in cold tolerance, leading to significantly and substantial

55 volved in physiological processes, including cold tolerance, light-responsiveness and flowering.

56 evelopmental acclimation suggests that basal cold tolerance may constrain developmental acclimation,

57 To gain an understanding of its cold tolerance mechanism, mRNA differential display reve

58 ance that likely serves as a universal plant cold tolerance mechanism.

59 Adult mGPD knockout animals had a normal cold tolerance, normal circadian rhythm in body temperat

60 just 16% of the observed difference between cold tolerance of animals held at 25 degrees C and 10 de

61 r direction and correspondingly modulate the cold tolerance of intact animals.

62 In this study, we characterized cold tolerance of null mutant of RNA-DIRECTED DNA METHYL

63 Cold-tolerance of Attamyces cultivars increases with win

64 studies on mechanisms determining divergent cold-tolerance of inbred maize lines.

65 freezing (-2 degrees C) temperatures on the cold-tolerance of oligochaete worms (Enchytraeus albidus

66 ime control on the one side and greening and cold tolerance on the other that may be governed by the

67 of s/s animals, locomotor activity and acute cold tolerance (partly a measure of shivering thermogene

68 tigation of numerous other phenomena such as cold tolerance, quality as a prey item, and effects of m

69 on, especially underdominance in the case of cold-tolerance related phenotypes.

70 ith the use of diverse larval habitats and a cold tolerance that allows an expanded seasonal activity

71 re environment; to identify genes related to cold tolerance that have been subjected to independent p

72 rom the circadian clock contributes to plant cold tolerance through regulation of the CBF cold-respon

73 sential component of the UPR during heat and cold tolerance, thus confirming the cytoprotective role

74 crystal toxin genes, drought resistance and cold tolerance to extend growth range.

75 atterns of both phenological development and cold tolerance traits in wheat.

76 s (chill-coma) is a common measure of insect cold tolerance used to test central questions in thermal

77 shoot apex development and the induction of cold tolerance was reflected by the gradual up-regulatio

78 a number of other genes important for plant cold tolerance were also affected in the mutants.

79 Distinctive mechanisms for cold tolerance were characterized for two cultivars.

80 Body composition, insulin sensitivity, and cold tolerance were completely normalized in Nse+Syn db/

81 utely activated BAT fuel uptake and enhanced cold tolerance, which resulted in decreased levels of se

82 h is of potential importance in coordinating cold tolerance with growth and development.