ライフサイエンスコーパス: transient receptor potential channel

1 ipids that resolve inflammation and modulate transient receptor potential channels.

2 red (5 mum) as a broad-spectrum inhibitor of transient receptor potential channels.

3 channel that belongs to the large family of transient receptor potential channels.

4 y transduction, a property shared with other transient receptor potential channels.

5 nimal small molecule agonists of nociceptive transient receptor potential channels.

6 diated downstream of phospholipase C by TRP (transient receptor potential) channels.

7 ntaining ER Ca(2)(+) levels, is dependent on transient receptor potential channel 1 (TRPC1) activity.

8 Specific biological roles of the classical transient receptor potential channel 1 (TRPC1) are still

9 Transient receptor potential channel 1 (TRPC1) is a nons

10 own, there is considerable evidence that the transient receptor potential channel 1 (TRPC1) participa

11 scle cells (VSMCs), stimulation of canonical transient receptor potential channel 1 (TRPC1) protein-b

12 scle cells (VSMCs), stimulation of canonical transient receptor potential channel 1 (TRPC1) protein-b

13 ), stimulation of SOCs composed of canonical transient receptor potential channel 1 (TRPC1) proteins

14 Inhibition of SOC by lanthanum or transient receptor potential channel 1 (TRPC1), a SOC co

15 e kinase 1 (SPHK1) in the mechanism by which transient receptor potential channel 1 (Trpc1)-mediated

16 Mucolipin transient receptor potential channel 1 (TRPML1) is the p

17 shams, whereas the store-operated canonical transient receptor potential channels 1, 3, and 4 were d

18 ng domain (CSD) in regulating the SOC [i.e., transient receptor potential channel-1 (TRPC1)] in human

19 n subunits G(ialpha2) and G(oalpha), and the transient receptor potential channel 2 (TRP2), is locali

20 Melastatin-related transient receptor potential channel 2 (TRPM2) is a Ca(2

21 We identify an intact transient receptor potential channel 2beta in the dog ge

22 eptors in striatal cholinergic interneurons: transient receptor potential channel 3/7 (TrpC3/C7) and

23 The canonical transient receptor potential channel 4 (TRPC4) comprises

24 crtr1), kappa opioid receptor 1 (Oprk1), and transient receptor potential channel 4 (Trpc4).

25 ABSTRACT: Transient receptor potential channel 4 of the vanilloid

26 ffs also showed attenuated Ca(2+) influx via transient receptor potential channel 5 (TRPC5) channels

27 Canonical transient receptor potential channel 5 (TRPC5) is a nons

28 Transient receptor potential channel 5 (TRPC5) is highly

29 The transient receptor potential channel 5 (TRPC5) is predom

30 annel targets, namely AT1R, angiotensinogen, transient receptor potential channel 6 (TRPC6) channels,

31 The up-regulation of transient receptor potential channel 6 (TRPC6) has been

32 n podocytes are unconfirmed, but the classic transient receptor potential channel 6 (TRPC6) interacti

33 Gain-of-function mutations of classic transient receptor potential channel 6 (TRPC6) were iden

34 ity and Notch-dependent transcription of the transient receptor potential channel 6 (TRPC6) when comp

35 G1alpha localization enhanced suppression of transient receptor potential channel 6 (TRPC6), thereby

36 alpha-actinin-4, CD2-associated protein, and transient receptor potential channel 6), and the role of

37 that H2S and NO production colocalizes with transient receptor potential channel A1 (TRPA1), and tha

38 s in acid-sensing ion channels 2A and 2B and transient receptor potential channel A1, which are thoug

39 ever, it is unknown whether TRPV4 or related transient receptor potential channels account for warmth

40 Polycystin-2 (PC2) is a Ca(2+)-permeable transient receptor potential channel activated and regul

41 triggered calcium flux in mast cells through transient receptor potential channel activation, along w

42 ese results mirror previous studies with the transient receptor potential channel and suggest that PL

43 including: cyclic nucleotide-gated channels, transient receptor potential channels and gap-junctional

44 hannels with a modest contribution from TRP (transient receptor potential) channels and ryanodine-sen

45 ceptors; however, CB2 cannabinoid receptors, transient receptor potential channels, and peroxisome pr

46 exogenous PI(3,4,5)P3 rapidly activated TRP (transient receptor potential) channels, and asymmetrical

47 Transient receptor potential channels are involved in se

48 These findings describe a novel mode of a transient receptor potential channel behavior and sugges

49 A construct or the addition of a nonspecific transient receptor potential channel blocker lanthanum.

50 also suppressed by SK&F96365, a nonspecific transient receptor potential channel blocker.

51 ard currents were blocked by TRPC (canonical transient receptor potential) channel blockers 2-APB (2-

52 Transient receptor potential channel C6 (TRPC6) gain-of-

53 -function mutations in the gene encoding the transient receptor potential channel C6 (TRPC6).

54 Expression of nephrin, podocin, desmin, and transient receptor potential channel C6 in the podocyte

55 previously to enter cells through activated transient receptor potential channels, can also act as c

56 of inositol 1,4,5-triphosphate receptor and transient receptor potential channels) caused substantia

57 Our results support that thermal transient receptor potential channels contain modular th

58 Thermo-transient receptor potential channels display outstandin

59 asome and caspase-1, which was controlled by transient receptor potential channels during RVD.

60 ly agreed upon that members of the classical transient receptor potential channel family (TRPC) are i

61 olycystin-2 (PC2 or TRPPC2), a member of the transient receptor potential channel family, is a nonsel

62 A novel transient receptor potential channel has the ability to

63 isms involving the cannabinoid receptors and transient receptor potential channels have emerged as ar

64 entry via voltage-gated Ca(2+) channels and transient receptor potential channels in addition to rel

65 speculate that PC2 and the Ca(2+)-dependent transient receptor potential channels in general are reg

66 the role of voltage-gated K(+) channels and transient receptor potential channels in the regulation

67 It is now well known that thermoTRP (transient receptor potential) channels in thermosensory

68 In an unexpected context, the canonical transient-receptor-potential channels in the Drosophila

69 ately after wounding, and down-regulation of transient receptor potential channel M, a stress-activat

70 Olfactory sensory neurons that express transient receptor potential channel M5 (TrpM5) or neuro

71 omponent of the phospholipase C pathway, the transient receptor potential channel M5 (TRPM5), is coex

72 the calcium activated cation channel TRPM5 (transient receptor potential channel M5).

73 - and menthol-sensitive receptor-1 (CMR1) or transient receptor potential channel M8 (TRPM8) receptor

74 ggered rise in Ca(2+) requires the epidermal transient receptor potential channel, melastatin family

75 Here we identify two Drosophila melanogaster transient receptor potential channels needed for sensing

76 in complexes, or TRPP-PKD complexes, made of transient receptor potential channel polycystin (TRPP) a

77 ations in the MCOLN1 gene, which encodes the transient receptor potential channel protein mucolipin-1

78 r-related) is a TRPV (vanilloid subfamily of transient receptor potential channel) protein that regul

79 nal diversity to the cytoskeletal control of transient receptor potential channel regulation.

80 erlies the temperature sensitivity in thermo-transient receptor potential channels remains unknown, b

81 As part of the long transient receptor potential channel subfamily implicate

82 (AITC), activates the extreme cold receptor transient receptor potential channel, subfamily A, membe

83 t receptor potential vanilloid 1 (TRPV1) and transient receptor potential channel, subfamily A, membe

84 expressing the cold-sensitive TRPM8 channel (transient receptor potential channel, subfamily M, membe

85 GPR68) promotes expression of the canonical transient receptor potential channel subunit TRPC4 in no

86 ed to polycystin-1 and voltage-activated and transient receptor potential channel subunits, suggestin

87 nt polycystic kidney disease, belongs to the transient receptor potential channel superfamily and has

88 subunits of Na(+) or Ca(2+) channels and the transient receptor potential channel superfamily, which

89 A group of exquisitely temperature-sensitive transient receptor potential channels, termed thermoTRPs

90 ood-averse behaviors, and painless (pain), a transient receptor potential channel that is responsive

91 hat mediate this influx, to the K+ , Cl- and transient receptor potential channels that set the cell

92 odes a putative variant of the C3-type TRPC (transient receptor potential channel) that differs from

93 mbrane (TM) domains, and, by comparison with transient receptor potential channels, the six carboxyl-

94 Several thermosensitive transient receptor potential channels (transient recepto

95 ospholipase C (PLC) and the Ca(2+)-permeable transient receptor potential channel (TRP), but how the

96 ants lacking both classes of light-sensitive transient receptor potential channels (TRP and TRPL).

97 We found previously that the transient receptor potential channel TRPA1 acts internal

98 ensitizes nociceptors via transactivation of transient receptor potential channels TRPA1 and TRPV1.

99 vo as well as in vitro confirmed the role of transient receptor potential channels (TRPA1 and TRPV1)

100 amma wave, and genetic ablation of canonical transient receptor potential channel (TRPC) 7 significan

101 only recently have the mechanisms governing transient receptor potential channel (TRPC) channel func

102 at permissive SOCE was mediated by canonical transient receptor potential channel (TRPC) due to its s

103 Ca(2+) entry (CCE) channels remains elusive, transient receptor potential channel (TRPC) family membe

104 The canonical transient receptor potential channel (TrpC) family, a fa

105 CE is mediated by the nonselective canonical transient receptor potential channel (TRPC) family, TRPC

106 e kinase inhibitors and activation of C-type transient receptor potential channel (TRPC) isoform 3 (T

107 s in endothelial cells via the expression of transient receptor potential channel (TRPC) isoforms.

108 en PKD2 and various members of the mammalian transient receptor potential channel (TRPC) proteins, th

109 the homologous TRPC6 are two members of the transient receptor potential channel (TRPC) superfamily

110 Transient receptor potential channel (TRPC)-related gene

111 Knockdown of transient receptor potential channel (TRPC)1 and TRPC3 c

112 ian isoforms of calcium-permeable Drosophila transient receptor potential channels (TRPC) are involve

113 concentration mediated by the activation of transient receptor potential channels (TRPC) both contri

114 The members of the canonical subfamily of transient receptor potential channels (TRPC) have been i

115 inositol trisphosphate receptor (IP3R) with transient receptor potential channel (TRPC1), and thereb

116 Ca(2+)](i)) through activation of the murine transient receptor potential channel TRPC2, but TRPC2 is

117 The activation mechanism of the classical transient receptor potential channels TRPC4 and -5 via t

118 The unexpected absence of the transient receptor potential channel, Trpc4, from Lyn(-/

119 The calcium- and sodium-permeable transient receptor potential channel TRPC5 has an inhibi

120 he present study, we provide evidence that a transient receptor potential channel (TRPC6) homologue h

121 coded by the Slo1 gene and various canonical transient receptor potential channels (TRPCs) are coexpr

122 Canonical transient receptor potential channels (TRPCs) are recept

123 Transient receptor potential channels (TRPCs) belong to

124 Here, we characterized the expression of transient receptor potential channels (TRPCs) in primary

125 ionotropic glutamate receptors and canonical transient receptor potential channels (TRPCs) was simila

126 trisphosphate receptors (IP(3)Rs), canonical transient receptor potential channels (TRPCs), STIM1 Ca(

127 Astrocytes express transient receptor potential channels (TRPCs), which hav

128 The melastatin-related transient receptor potential channel TRPM2 is a plasma m

129 The transient receptor potential channels TRPML2 and TRPML3

130 Transient receptor potential channel TRPP2 is a nonselec

131 The transient receptor potential channel TRPV3 is a nonselec

132 The transient receptor potential channel TRPV3 is a nonselec

133 The transient receptor potential channel (TRPV3) is a warm-s

134 ypothesized that activation of the vanilloid transient receptor potential channel TRPV4 disrupts the

135 The transient receptor potential channel TRPV5 constitutes t

136 acellular calcium rise via the activation of transient receptor potential channel type M5 (TRPM5).

137 The vertebrate transient receptor potential channel vanilloid subfamily

138 Blockade of the transient receptor potential channel vanilloid subfamily

139 tic retinoids activate recombinant or native transient receptor potential channel vanilloid subtype 1

140 The transient receptor potential channel vanilloid type 1 (T

141 nce that the vanilloid (capsaicin) receptor; transient receptor potential channel, vanilloid subfamil

142 The transient receptor potential channel, vanilloid subfamil

143 ntracellular Ca(2+) concentration, including transient receptor potential channels, voltage-gated Ca(

144 nt found in the microvilli of mammalian VNO, transient receptor potential channel, was also immunorea

145 thymol, a now recognized potent agonist for transient receptor potential channels, was first describ

146 ces intracellular calcium elevations through transient receptor potential channels, which trigger AQP

147 vacuolar Ca(2+) through the mechanosensitive transient receptor potential channel, Yvc1.