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 These corals initially had heat-sensitive algal symbiont communities, endured bleac

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

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

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

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

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

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

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

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

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

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

16 s to heat dissipation, especially for large, heat-sensitive animals.

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

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

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

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

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

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

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

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

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

26 for sensitization of cutaneous mechano- and heat-sensitive C-fibers in CP.

27 ed moving mice through the activation of the heat-sensitive capsaicin receptor (transient receptor po

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

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

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

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

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

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

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

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

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

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

38 on to carboxylation and the abundance of the heat-sensitive chaperone Rubisco activase (Rca) in each

39 up to 65 degrees C, including model enzymes, heat-sensitive clinical diagnostic enzymes (DNA gyrase a

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

41 fect, further complicated by the presence of heat sensitive components, preventing use of high temper

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

43 Notably, heat-sensitive compounds such as lipids and several flav

44 tion (PLE), which is efficient and preserves heat-sensitive compounds.

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

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

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

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

49 ivity to heat, with bud swell being the most heat-sensitive developmental stage with significant redu

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

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

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

53 A heat-sensitive glycoprotein fraction of Melosira EPS acc

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

55 5 degrees C but display pronounced cold- and heat-sensitive growth phenotypes.

56 pening but has no effect on the induction of heat-sensitive guard cell transcripts, supporting the ex

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

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

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

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

61 sensitivity [two heat-tolerant (HT) and two heat-sensitive (HS)] were raised in pots, initially in a

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

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

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

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

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

67 1 receptors have classically been defined as heat-sensitive, ligand-gated, nonselective cation channe

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

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

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

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

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

73 The structure-function relationship is heat sensitive, making thermal processing in its product

74 environment as a driver of behaviour in this heat-sensitive mammal.

75 ected that patterns of habitat use by large, heat-sensitive mammals across multiple scales are critic

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

77 can be used as a promising method for drying heat-sensitive materials such as peroxidase enzyme.

78 n, but the underlying peripheral and central heat-sensitive mechanisms are not fully established.

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

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

81 Blood lactate levels are elevated in both heat-sensitive MHS patients with RYR1 mutations and YS m

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

103 enotypes: the heat-tolerant PI518255 and the heat-sensitive PI598080.

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

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

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

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

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

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

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

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

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

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

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

115 f which Rubisco activation inhibition due to heat sensitive Rubisco activase (RCA) is the most promin

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

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

118 mbrane tyrosine kinase, as a novel marker of heat-sensitive spinal neurons in mice.

119 he amyloplast pentose phosphate pathway is a heat-sensitive step in maize kernel metabolism that cont

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

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

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

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

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

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

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

127 he vanilloid receptor subtype 2 (TRPV2) is a heat-sensitive transient receptor potential (TRP) channe

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

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

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

131 eal TRPM8(+) cold-sensing fibers express the heat-sensitive TRPV1 channel.

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

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

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

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

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

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

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

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

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

141 th at its collection sites compared with the heat-sensitive variant.

142 26.8, and ApHsp26.7b, were isolated from the heat-sensitive variant.

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

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