ライフサイエンスコーパス: heat-sensitive

1 r, the slowest reactions tend to be the most heat-sensitive.

2 Heat-sensitive 3'-protected derivatives of 2'-deoxyribon

3 ky clones containing the fragment secreted a heat-sensitive activity that induced competence in Wicky

4 All heat-sensitive afferents (n = 16) were insensitive to me

5 The heat-sensitive allele arises through a single base delet

6 Characterizations of the heat-sensitive allele demonstrate that mutants are also

7 Mutants for a heat-sensitive allele, called mup-2(e2346ts), and for a

8 icate that the pre-U1 processing activity is heat sensitive and that an RNA component is required.

9 both temperatures, and 1, ts25, was strongly heat sensitive and was unable to form plaques at 39 degr

10 SOAF comprises discrete, heat-sensitive and -stable components (referred to here

11 Unlike LPS, the activity of EDA was heat-sensitive and persisted in the presence of the LPS-

12 tion of proliferation was pathogen specific, heat sensitive, and multiplicity of infection dependent

13 The G-protein activator was heat-sensitive, and the magnitude of its action was rela

14 that have complex geometries, those that are heat-sensitive, and those bearing complex sample matrice

15 s from cells not expressing the protein were heat-sensitive at 60 degreesC.

16 lease is regulated by formalin-resistant and heat-sensitive bacterial surface factors distinct from u

17 e sudA gene, an extragenic suppressor of the heat-sensitive bimD6 mutation and showed that it coded f

18 We have been studying the heat-sensitive bimD6 mutation of Aspergillus nidulans.

19 Frequency of the heat-sensitive Buchnera allele is negatively correlated

20 tein 3 (VRL3, also known as TRPV3), which is heat-sensitive but capsaicin-insensitive.

21 the cutaneous receptive field of 43 mechano-heat-sensitive C-fiber (CMH) nociceptors.

22 the prevalence of mechanically insensitive, heat-sensitive C-fibers (CH) that contain the heat trans

23 t stimuli and that mechanically insensitive, heat-sensitive C-fibers (CHs) that contain TRPV1 increas

24 ral excitation through the activation of the heat-sensitive capsaicin receptor TRPV1 by magnetic nano

25 ring activation threshold temperature of the heat-sensitive capsaicin receptor TRPV1 ion channel, lea

26 avior with that of its distant relative, the heat-sensitive capsaicin-gated transient receptor potent

27 roidal neovascularization (CNV) by injecting heat-sensitive carboxyfluorescein liposomes intravenousl

28 ertani (LB) medium to strains containing the heat-sensitive cell division mutation ftsZ84.

29 mediate TLR2-dependent activation, whereas a heat-sensitive cell-associated mycobacterial factor medi

30 to assessed their functional roles using the heat-sensitive channel dTRPA1.

31 nd irreversibly activates the capsaicin- and heat-sensitive channel, TRPV1.

32 usly, we have shown that snakes co-opt a non-heat-sensitive channel, vertebrate TRPA1 (transient rece

33 ther with our previous identification of the heat-sensitive channels VR1 and VRL-1, demonstrate that

34 The heat-sensitive component of viable E. chaffeensis cells

35 (GC-FID and GC-MS), while quantitation of a heat-sensitive compound, isofuranodiene, known for its a

36 st that the protective epitope(s) on OspC is heat sensitive/conformational, a finding which has impli

37 aching conditions changes the microbiome for heat-sensitive corals, but not for heat-tolerant corals

38 mber mutations can conditionally correct the heat-sensitive defect in three mutant forms of the repre

39 d heat tolerance in Arabidopsis and restored heat-sensitive defects of Arabidopsis hsfa2 mutant, whic

40 termine the mortality projection of specific heat-sensitive diseases to provide more detailed informa

41 ntiinflammatory effects of a small (<3-kDa), heat-sensitive factor(s) that is not lipopolysaccharide,

42 ow temperature so that it is compatible with heat-sensitive flexible materials like papers and textil

43 A heat-sensitive glycoprotein fraction of Melosira EPS acc

44 e to impaired ubiquitin ligase activity, the heat-sensitive growth defect of the spa1-1 mutant is sup

45 5 degrees C but display pronounced cold- and heat-sensitive growth phenotypes.

46 substrate-bound, developmentally regulated, heat-sensitive guidance cues preserved in the cryostat s

47 ts from other enteropathogens and requires a heat-sensitive H. pylori component and the DC-intrinsic

48 We identified approximately 1100 heat-sensitive HEK293 proteins, 12% of which could be is

49 ity present in BSN-CM indicates that it is a heat-sensitive, heparin-binding factor with a probable m

50 nts being cold sensitive in some species and heat sensitive in others, with varying and non-coinciden

51 r potential vanilloid subtype 1 (TRPV1) is a heat-sensitive ion channel also involved in pain sensati

52 r potential vanilloid subtype 1 (TRPV1) is a heat-sensitive ion channel that plays a key role in enha

53 Transcripts undergoing heat-sensitive IR are mostly involved in specific functi

54 growth, allowing direct implementation into heat-sensitive large-area devices.

55 1 receptors have classically been defined as heat-sensitive, ligand-gated, nonselective cation channe

56 duct of ApHsp26.2m did not accumulate in the heat-sensitive line.

57 Carboxyfluorescein was encapsulated in heat-sensitive liposomes and injected intravenously in r

58 thalocyanine tetrasulfonate, encapsulated in heat-sensitive liposomes, was administered intravenously

59 ulation, and those spores that did form were heat sensitive, lysed extensively, and were highly irreg

60 A shift towards heat-sensitive M. vaginatus could ultimately destabilize

61 nd to possess a non-dialyzable, trypsin- and heat-sensitive material capable of generating ROS in res

62 ild conditions provide an entry to acid- and heat-sensitive members of this theoretically intriguing

63 temperatures makes them unsuitable to study heat-sensitive membrane proteins like cytochrome-P450 an

64 A1 channels, we have identified two portable heat-sensitive modules within the ankyrin repeat-rich am

65 Furthermore, shot1-2 suppresses other heat-sensitive mutants, and shot1-2 alone is more heat t

66 he translation of proline codons; and (iv) a heat-sensitive mutation in trmD, whose product catalyzes

67 charomyces cerevisiae SEN1 gene results in a heat-sensitive mutation that alters the cellular abundan

68 I is in good agreement with data on noxious, heat-sensitive neurons in the dorsal horn.

69 TRPV1(-/-) mice had more heat-sensitive neurons, and these neurons had normal tem

70 naling depends on NGF and is mediated by the heat-sensitive nociceptive channel TRPV1.

71 and that TRPV1 immunoreactivity is absent in heat-sensitive nociceptors.

72 decreased the response of acid- and noxious heat-sensitive nociceptors.

73 hibition of autophagy by spautin-1 generated heat-sensitive, noninfectious dengue virus particles, re

74 the suppressor mutation was the cause of the heat-sensitive phenotype of the SLC strain 7R4.

75 n base auxotrophy (SLC, strain 7R4) showed a heat-sensitive phenotype that was corrected by transform

76 The ability of sphingolipids to rescue the heat-sensitive phenotype was examined, and two endogenou

77 y but, in combination with sua7-1, created a heat-sensitive phenotype.

78 and that a bZIP28 null mutant has a striking heat-sensitive phenotype.

79 onase (EC 3.2.1.15) activity, resulting in a heat-sensitive phenotype.

80 in which mutations within pcaH or -G cause a heat-sensitive phenotype.

81 mutation conferred recessive slow-growth and heat-sensitive phenotypes in yeast, but quantitative eff

82 Mutants with null, leaky, and heat-sensitive phenotypes were isolated.

83 the knockout mutants of these genes display heat-sensitive phenotypes.

84 groups structurally related to well-studied heat-sensitive phosphate/thiophosphate protecting groups

85 suppression through asymmetric effects, e.g. heat-sensitive predator vs. heat-tolerant prey.

86 enhanced at higher temperatures, revealing a heat-sensitive process that is normally masked by the pr

87 We describe the identification of a heat-sensitive protein complex whose integrity is requir

88 perfusion system, contained LPS-independent, heat-sensitive protein molecules that activated macropha

89 s to prevent the irreversible aggregation of heat-sensitive proteins.

90 tage for solid-state and solution studies of heat-sensitive proteins.

91 Genetic interactions between CUS2 and a heat-sensitive prp5 allele parallel those observed betwe

92 use infrared warning signals in response to heat-sensitive rattlesnakes.

93 We show that tableting stabilizes heat-sensitive reagents and simplifies a broad range of

94 skilled technicians, and facilities to store heat-sensitive reagents.

95 rons expressed the vanilloid receptor VR1, a heat-sensitive receptor expressed by many IB4-positive n

96 The heat-sensitive SOAF component, SOAF-I(m), becomes solubi

97 lly in a manner that mimics the new mutant's heat-sensitive song anomaly.

98 The heat-sensitive strain had greater infection success at 2

99 varying infectiousness among differentially heat-sensitive Symbiodinium strains could provide a mech

100 was reduced, but readily detectable, in the heat-sensitive tfa1 mutant at the non-permissive tempera

101 In particular, we find proficient TCR in a heat-sensitive tfa1 mutant at the non-permissive tempera

102 eptive field, nociceptors were classified as heat-sensitive (threshold, </=53 degrees C, 1 sec) or he

103 eptide 3 expression and editing function was heat sensitive to a certain degree, partly explaining th

104 eat shock proteins (HSP genes) is reduced in heat-sensitive transgenic plants expressing miR398-resis

105 eceptor potential (TRP) channel superfamily: heat-sensitive TRP vanilloid subtype 1 (TRPV1) and cold-

106 ounds capsaicin and menthol activate noxious heat-sensitive TRPV1 and cold-sensitive TRPM8, respectiv

107 ative QX-314 through the pore of the noxious-heat-sensitive TRPV1 channel.

108 C-fibers expressing heat-sensitive TRPV1 channels are proposed, for example,

109 ergic activation increases expression of the heat-sensitive TRPV1 ion channel and reduces expression

110 The heat-sensitive TRPV1 ion channel responds to various nox

111 vampire bats tune a channel that is already heat-sensitive, TRPV1, by lowering its thermal activatio

112 r NA might also interact with the homologous heat-sensitive TRPV2-4 channels, particularly given that

113 r of a TFIIB (sua7-1) defect, resulting in a heat-sensitive (Ts(-)) phenotype and a dramatic downstre

114 Expression of the heat-sensitive vanilloid receptor 1 (VR1) and sensitivit

115 The sequence of ApHsp26.2m from the heat-sensitive variant was identical to ApHsp26.2, excep

116 tional CP-sHSP isoforms not expressed in the heat-sensitive variant, that accumulation of the additio

117 26.8, and ApHsp26.7b, were isolated from the heat-sensitive variant.

118 akes (vipers, pythons and boas) are the most heat-sensitive vertebrate ion channels thus far identifi

119 Sts repressor mutants are heat sensitive when in supE or supF hosts and heat resis