ライフサイエンスコーパス: receptor potential

1 2+)-activated Cl(-) channels, generating the receptor potential.

2 rrent through hair cells to produce auditory receptor potential.

3 ows us to separate neural phase locking from receptor potentials.

4 ynergistic activation of canonical transient receptor potential 1 (TRPC1) and Orai channels.

5 to determine the role of canonical transient receptor potential 3 (TRPC3) channel in allergen-induced

6 or example, the vanilloid receptor transient receptor potential 3 (TRPV3), which has been implicated

7 iotensin II (Ang II) via canonical transient receptor potential 6 (TRPC6) channels caused increased i

8 oline (lysoPC), activate canonical transient receptor potential 6 (TRPC6) channels leading to inhibit

9 Classical or canonical transient receptor potential 6 (TRPC6), a nonselective and Ca(2+)-

10 Transient Receptor Potential A 1 (TRPA1) is a ligand-gated ion cha

11 he phospholipase C-beta encoded by norpA (no receptor potential A).

12 lators of cytosolic Ca(2+) levels, transient receptor potential A1 (TRPA1) and ryanodine receptor (Ry

13 gnificant interest in developing a transient receptor potential A1 (TRPA1) antagonist for the treatme

14 The transient receptor potential A1 (TRPA1) channel is an evolutionari

15 t previous studies have found that transient receptor potential A1 (TRPA1) gene deletion blocks CQ-in

16 rature response of the ion channel transient receptor potential A1 (TRPA1) is intriguing; some orthol

17 internal thermo-sensitive channel transient receptor potential A1 (TrpA1).

18 cate that random noise can push subthreshold receptor potentials across the transfer threshold, causi

19 through synergistic activation of transient receptor potential and Orai channels.

20 l incorporates a feedback loop involving the receptor potential and the mechanical load on OHC, and l

21 It is known that transient receptor potential ankyrin 1 (TRPA1) channels, expressed

22 The transient receptor potential ankyrin 1 (TRPA1) ion channel is expr

23 nel involved in inflammatory pain, transient receptor potential ankyrin 1 (TRPA1), we asked whether t

24 component of the pain pathway, the transient receptor potential ankyrin 1 ion channel (TRPA1).

25 These noxious anesthetics activate transient receptor potential ankyrin repeat 1 (TRPA1), a major noc

26 ct may be due in part to increased transient receptor potential ankyrin-1 (TRPA1) expression by lung

27 potential vanilloid-1 (TRPV1) and transient receptor potential ankyrin-1 (TRPA1), but not TRPV4.

28 vagus, and this was inhibited by a transient receptor potential ankyrin-1 antagonist and the antioxid

29 uction, which is known to activate transient receptor potential ankyrin-1 on nociceptive C-fibers.

30 The transient receptor potential ankyrin-repeat 1 (TRPA1) is an import

31 In the Panx1 deficient mice, EP and auditory receptor potential as measured by cochlear microphonics

32 sed whether and how SOCE involving transient receptor potential canonical (TRPC) and Orai1 channels a

33 Transient receptor potential canonical (TRPC) Ca(2+)-permeant chan

34 n regulates not only CRAC but also transient receptor potential canonical (TRPC) channels, but it has

35 oid cells express several forms of transient receptor potential canonical (TRPC) channels, including

36 selective Orai1 and members of the transient receptor potential canonical (TRPC) channels, which are

37 Transient Receptor Potential Canonical (TRPC) proteins form nonsel

38 e, we show that syndecans regulate transient receptor potential canonical (TRPCs) channels to control

39 We found that an inhibition of transient receptor potential canonical 3 (TRPC3) channel activity

40 bone marrow cells deficient in the Transient Receptor Potential Canonical 3 (TRPC3) channel have redu

41 We previously reported that transient receptor potential canonical 3 (TRPC3) channel mediates

42 We demonstrate that transient receptor potential canonical 3 (TRPC3), a Ca(2+)-permeab

43 s in vitro studies, we showed that Transient Receptor Potential Canonical 3 (TRPC3), a calcium-permea

44 Transient receptor potential canonical 5 (TRPC5), a calcium-permea

45 , and synaptopodin and to enhanced transient receptor potential canonical 6 (TRPC6) channel expressio

46 Ca(2+) mobilization and transient receptor potential canonical 6 (TRPC6) translocation wer

47 Transient receptor potential canonical 6 (TRPC6), a Ca(2+) channel

48 calcium signalling is mediated via transient receptor potential canonical 6 (TRPC6), a subtype of cal

49 mediated by melanopsin coupled to transient receptor potential canonical cation channels.

50 f the nonselective cation channel, transient receptor potential canonical channel 6 (Trpc6), in isola

51 The transient receptor potential canonical channel-1 (TRPC1) is a Ca(2

52 indicate that Ca(2+) influxes via transient receptor potential canonical channels and activated the

53 4,5-bisphosphate (PIP2)-sensitive transient receptor potential canonical channels play a critical ro

54 voltage-gated Ca(2+) channels, and transient receptor potential canonical channels, in axons stimulat

55 revious work, we hypothesized that transient receptor potential canonical type 3 (TRPC3) channels are

56 Transient receptor potential canonical type 5 (TRPC5) is a Ca(2+)-

57 down-regulating calcium-permeable transient receptor potential canonical type isoform 6 (TRPC6) chan

58 tion of the calcium permeant TRPC (Transient Receptor Potential Canonical) channels.

59 Here we show that the transient receptor potential canonical-6 (TRPC6) calcium-permeable

60 The Ca(2+)-permeable transient receptor potential cation (TRPC) channel is predominantl

61 ucolipin TRP channel 3 (TRPML3), a transient receptor potential cation channel localized to lysosomes

62 Sulfonylurea receptor-1-transient receptor potential cation channel M4 is upregulated only

63 mRNA expression of PGP9.5; TRPV1; transient receptor potential cation channel subfamily A, receptor

64 ecretion through coupling with the transient receptor potential cation channel subfamily C 3 (TRPC3).

65 TRPM7 (transient receptor potential cation channel subfamily M member 7)

66 uorescent protein (EGFPf) from the transient receptor potential cation channel subfamily M member 8 (

67 mily A, receptor 1 (TRPA1); TRPV4; transient receptor potential cation channel subfamily M, member 8

68 The transient receptor potential cation channel subfamily V member 1 (

69 activation and the implication of transient receptor potential cation channel subfamily V member 1 (

70 ting by differential activation of transient receptor potential cation channel subfamily V member 1 (

71 tates and itch transmitted via the transient receptor potential cation channel subfamily V member 1 (

72 from only unmyelinated afferents [transient receptor potential cation channel subfamily V member 1 (

73 re organized exclusively as either transient receptor potential cation channel subfamily V member 1 (

74 s (IR) is based on ablation of the transient receptor potential cation channel subfamily V, receptor

75 the charged voltage sensors of the transient receptor potential cation channel TRPV1.

76 o the thermosensors, including the transient receptor potential cation channel V1 expressed in the no

77 In contrast, transient receptor potential cation channel vanilloid subtype 1 ch

78 or potential vanilloid type-1, -3; transient receptor potential cation channel, subfamily A, member 1

79 ve been linked to mutations in the transient receptor potential cation channel, subfamily C, member 6

80 lcium influx via podocyte-specific transient receptor potential cation channel, subfamily C, member 6

81 showed increased expression of the transient receptor potential cation channel, subfamily C, member 6

82 ransporter 1 (MAGT1)-dependent and transient receptor potential cation channel, subfamily M, member 7

83 Transient receptor potential cation channel, subfamily V, member 4

84 In mice, activation of the transient receptor potential cation channels (TRP) TRPV1, TRPV4, a

85 66Shc restricted the activation of transient receptor potential cation channels to attenuate cytosoli

86 tion of calcineurin or blockade of transient receptor potential cation channels.

87 Transient receptor potential channel 1 (TRPC1) is a nonselective c

88 (VSMCs), stimulation of canonical transient receptor potential channel 1 (TRPC1) protein-based store

89 (VSMCs), stimulation of canonical transient receptor potential channel 1 (TRPC1) protein-based store

90 tion of SOCs composed of canonical transient receptor potential channel 1 (TRPC1) proteins requires G

91 (SPHK1) in the mechanism by which transient receptor potential channel 1 (Trpc1)-mediated Ca(2+) ent

92 The canonical transient receptor potential channel 4 (TRPC4) comprises an endoth

93 ABSTRACT: Transient receptor potential channel 4 of the vanilloid subfamily

94 Transient receptor potential channel 5 (TRPC5) is highly expressed

95 The up-regulation of transient receptor potential channel 6 (TRPC6) has been found to c

96 s are unconfirmed, but the classic transient receptor potential channel 6 (TRPC6) interacting with th

97 n-of-function mutations of classic transient receptor potential channel 6 (TRPC6) were identified in

98 calization enhanced suppression of transient receptor potential channel 6 (TRPC6), thereby potentiati

99 Transient receptor potential channel C6 (TRPC6) gain-of-function m

100 mutations in the gene encoding the transient receptor potential channel C6 (TRPC6).

101 n of nephrin, podocin, desmin, and transient receptor potential channel C6 in the podocyte was signif

102 2 (PC2 or TRPPC2), a member of the transient receptor potential channel family, is a nonselective cal

103 es, or TRPP-PKD complexes, made of transient receptor potential channel polycystin (TRPP) and polycys

104 the MCOLN1 gene, which encodes the transient receptor potential channel protein mucolipin-1.

105 ity to the cytoskeletal control of transient receptor potential channel regulation.

106 omotes expression of the canonical transient receptor potential channel subunit TRPC4 in normal and t

107 ctivates the extreme cold receptor transient receptor potential channel, subfamily A, member 1 and ma

108 the cold-sensitive TRPM8 channel (transient receptor potential channel, subfamily M, member 8).

109 Several thermosensitive transient receptor potential channels (transient receptor potentia

110 as in vitro confirmed the role of transient receptor potential channels (TRPA1 and TRPV1) as OxPAPC

111 voltage-gated Ca(2+) channels and transient receptor potential channels in addition to release from

112 ivation mechanism of the classical transient receptor potential channels TRPC4 and -5 via the Gq/11 p

113 owever, CB2 cannabinoid receptors, transient receptor potential channels, and peroxisome proliferator

114 ar Ca(2+) concentration, including transient receptor potential channels, voltage-gated Ca(2+) channe

115 ) as a broad-spectrum inhibitor of transient receptor potential channels.

116 resolve inflammation and modulate transient receptor potential channels.

117 r sustained components of the cell's in vivo receptor potential, crucial for sound localization and u

118 , a group of ion channels from the transient receptor potential family, play important functions in p

119 eport that an ion channel from the transient receptor potential family, TRPM8, commonly known as the

120 roperties of ion channels from the transient receptor potential family.

121 base and submillisecond encoding of membrane receptor potential fluctuations in the apex for precise

122 ease in the cochlea ensuring EP and auditory receptor potential generation and hearing.

123 nerve neurons are responsible for converting receptor potentials into spike rates.

124 The transient receptor potential ion channel of the melastatin subfami

125 Since the amplitude of IHC receptor potentials is invariant during this period, the

126 een the astroglial swelling sensor transient receptor potential isoform 4 (TRPV4) and the aquaporin 4

127 Y POINTS: Endothelial cells employ transient receptor potential isoform 4 (TRPV4) channels to sense a

128 meability assays, we show that the transient receptor potential isoform 4 (TRPV4) plays a major role

129 channel aquaporin 4 (AQP4) and the transient receptor potential isoform 4 (TRPV4), a polymodal swelli

130 nt has two components: a canonical transient receptor potential-like conductance in the low-voltage r

131 unctional epidermal isoform of the transient receptor potential M8 (TRPM8) mild-cold receptor, dubbed

132 Transient receptor potential melastatin (TRPM) cation channels are

133 The transient receptor potential melastatin (TRPM)-3 channel is critic

134 s to activation of Go , closure of transient receptor potential melastatin 1 channels and hyperpolari

135 R-211, which is expressed from the transient receptor potential melastatin 1 intronic region, regulat

136 -mediated Ca(2+) entry through the transient receptor potential melastatin 2 (TRPM2) channel in macro

137 Transient receptor potential melastatin 2 (TRPM2) channel is known

138 Transient receptor potential melastatin 2 (TRPM2) ion channel has

139 Transient Receptor Potential Melastatin 2 (TRPM2) is a Ca(2+)-perm

140 or, mefenamic acid (MFA), that the Transient Receptor Potential Melastatin 3 (TRPM3) channel promotes

141 Transient receptor potential melastatin 3 (TRPM3) channels are act

142 The Mg(2+) and Ca(2+) conducting transient receptor potential melastatin 7 (TRPM7) channel-enzyme (

143 Transient receptor potential melastatin 7 (TRPM7) is a divalent io

144 ABSTRACT: The transient receptor potential melastatin 7 (TRPM7) is a protein tha

145 Transient receptor potential melastatin 7 (TRPM7) is a ubiquitousl

146 ogical and molecular inhibition of transient receptor potential melastatin 7 (TRPM7) reduces store-op

147 ic differentiation of MSCs through Transient receptor potential melastatin 7 (TRPM7)-Osterix axis.

148 The cold- and menthol-activated transient receptor potential melastatin 8 (TRPM8) channels are tho

149 The transient receptor potential melastatin 8 (TRPM8) ion channel is a

150 physiological level, inhibitors of transient receptor potential melastatin subfamily 4 (TRPM4), intra

151 novalent cation current carried by transient receptor potential melastatin subfamily 4 channels via t

152 metabotropic glutamate receptor 6/transient receptor potential melastatin subfamily M member 1-signa

153 The transient receptor potential melastatin type 6 (TRPM6) epithelial

154 activates the renal Mg(2+) channel transient receptor potential melastatin type 6 that determines the

155 Pharmacological modulation of the transient receptor potential melastatin type 8 (TRPM8) is currentl

156 RATIONALE: TRPM2 (transient receptor potential melastatin-2) expressed in endothelia

157 rotein-1 (AP-1) via stimulation of transient receptor potential melastatin-3 (TRPM3) channels.

158 We report that human transient receptor potential melastatin-8 (TRPM8) and an N-termina

159 Transient receptor potential melastatin-like 7 channel (TRPM7) is

160 TRPM7 is a member of the Transient-Receptor-Potential Melastatin ion channel family.

161 The transient receptor potential mucolipin (TRPML) channel family belo

162 e lysosomal Ca(2+) release channel transient receptor potential mucolipin 1 (TRPML1) but not the lyso

163 Transient receptor potential mucolipin 1 (TRPML1) is a Ca(2+)-rele

164 Transient receptor potential mucolipin 1 (TRPML1) is a cation chan

165 e lysosomal Ca(2+) release channel Transient Receptor Potential Mucolipin-1 (TRPML1).

166 buprofen-treated worms and a TRPV (transient receptor potential) mutant, and we show that the percept

167 Mutations in polycystin-1 and transient receptor potential polycystin 2 (TRPP2) account for almo

168 anges in membrane potentials, the so called "receptor potentials." Ribbon synapses between IHCs and a

169 SHANK3 interacts with transient receptor potential subtype V1 (TRPV1) via Proline-rich r

170 in-2 (PC2, TRPP2), a member of the transient receptor potential superfamily, is a nonselective cation

171 tion channels with homology to the transient receptor potential superfamily.

172 This current generates a receptor potential that controls release of glutamate ne

173 effective than elastic load in enhancing the receptor potential that drives the cell.

174 We now show that Transient Receptor Potential (TRP) C3 regulates the expression of

175 f the peripheral irritant receptor transient receptor potential (TRP) cation channel member A1 (TRPA1

176 Transient receptor potential (TRP) cation channel subfamily M memb

177 We identify a presumptive transient receptor potential (TRP) cation channel, CED-11, that ac

178 Thermal activation of transient receptor potential (TRP) cation channels is one of the m

179 Transient receptor potential (TRP) cation channels play a central

180 n of neurons using thermosensitive transient receptor potential (TRP) cation channels.

181 and in vivo electrophysiology that transient receptor potential (TRP) channel dephosphorylation at a

182 trations, a unique feature of this transient receptor potential (TRP) channel family member.

183 his study, we assessed the role of transient receptor potential (TRP) channel family members in media

184 The transient receptor potential (TRP) channel NOMPC is important for

185 Although transient receptor potential (TRP) channel research has vastly inc

186 RPM channels are a subgroup of the transient receptor potential (TRP) channel superfamily whose membe

187 a gain-of-function mutation in the transient receptor potential (TRP) channel TRPC3.

188 ion and received major inputs from transient receptor potential (TRP) channel V1 (TRPV1)-positive dor

189 ramine receptor (Oct-TyrR) and the transient receptor potential (TRP) channel Water witch (Wtrw), and

190 The Transient Receptor Potential (TRP) channels are a family of cation

191 Transient receptor potential (TRP) channels are activated by envir

192 Transient Receptor Potential (TRP) channels are emerging as essent

193 From insects to mammals, transient receptor potential (TRP) channels are known mediators fo

194 Transient receptor potential (TRP) channels are polymodal cell sen

195 The transient receptor potential (TRP) channels are unique cellular se

196 before the origin of bilateria and transient receptor potential (TRP) channels before the origin of a

197 ion channels, each subunit of most transient receptor potential (TRP) channels has an additional TRP-

198 e activation of several functional transient receptor potential (TRP) channels in live cells and in r

199 PAR(2) activates transient receptor potential (TRP) channels of nociceptive neurons

200 3), pannexins, presenilins and the transient receptor potential (TRP) channels that are distributed a

201 exploit these properties by using transient receptor potential (TRP) channels to activate or ablate

202 OINTS: Retinal cells use vanilloid transient receptor potential (TRP) channels to integrate light-evo

203 Genetically, the transient receptor potential (TRP) channels Trpm, NompC, and Polyc

204 The Ca(2+)-selective transient receptor potential (TRP) channels TRPV5 and TRPV6 play v

205 Thermal transient receptor potential (TRP) channels, a group of ion channe

206 alcium permeable channels, such as transient receptor potential (TRP) channels, contribute to changes

207 lso underlines the contribution of transient receptor potential (TRP) channels, notably TRPV4, in vol

208 an important activator of certain transient receptor potential (TRP) channels.

209 Polycystin-2 (PC2) belongs to the transient receptor potential (TRP) family and forms a Ca(2+)-regul

210 ey modulate the expression of some transient receptor potential (TRP) family members, yet their role

211 The NOMPC channel in the transient receptor potential (TRP) family, a mechanotransduction c

212 lysosomal cation channel from the transient receptor potential (TRP) family.

213 phorylation of the light-activated transient receptor potential (TRP) ion channel at S936 is a fast,

214 Signaling via the transient receptor potential (TRP) ion channel C6 plays a pivotal

215 cticides are now shown to target a transient receptor potential (TRP) ion channel complex that is uni

216 Members of the transient receptor potential (TRP) ion channel family act as polym

217 Several members of the transient receptor potential (TRP) ion channel family can regulate

218 he ion permeation mechanism in the transient receptor potential (TRP) ion channel family is currently

219 Temperature-sensitive transient receptor potential (TRP) ion channels are members of the

220 Several transient receptor potential (TRP) ion channels can be directly ac

221 Transient receptor potential (TRP) ion channels constitute a large

222 ted the expression and function of transient receptor potential (TRP) ion channels in enteroendocrine

223 Transient receptor potential (TRP) ion channels in peripheral sens

224 Transient receptor potential (TRP) ion channels of peripheral sens

225 proteins known as thermosensitive transient receptor potential (TRP) ion channels.

226 t stimulates cation influx through transient receptor potential (TRP) melastatin 4 (TRPM4) channels t

227 Transient receptor potential (TRP) melastatin 4 (TRPM4) is a widel

228 Transient receptor potential (TRP) proteins form a superfamily Ca(

229 s that converges on an unpredicted transient receptor potential (TRP)-like allosteric domain.

230 nnels (SOCs) composed of canonical transient receptor potential (TRPC) 1 proteins in vascular smooth

231 hether activation of the canonical transient receptor potential (TRPC) 6 channels and successive [Ca(

232 otentiated member of the canonical transient receptor potential (TRPC) channel family, TRPC4.

233 o the family of melastatin-related transient receptor potential (TRPM) channels.

234 members of the melastatin-related transient receptor potential (TRPM) subfamily of ion channels.

235 The transient receptor potential (TRPs) channels persist scarcely expl

236 The transient receptor potential TRPV1 or vanilloid receptor is a nons

237 purinergic P2X receptor channels, transient receptor potential V1 (TRPV1) channels and acid-sensing

238 we report that two members of the Transient Receptor Potential Vanilloid (TRPV) ion channel family,

239 ed Caco-2 resistance by 20-30% via transient receptor potential vanilloid (TRPV)-1 and peroxisome pro

240 Other approaches targeting the transient receptor potential vanilloid (TRPV1) receptor, glutamate

241 responses to inhaled capsaicin, a transient receptor potential vanilloid 1 (TRPV1) agonist, are char

242 allodynia to determine the role of transient receptor potential vanilloid 1 (TRPV1) and oxidative mec

243 tethered to the cation-conducting transient receptor potential vanilloid 1 (TRPV1) by a camelid anti

244 The transient receptor potential vanilloid 1 (TRPV1) channel is abunda

245 The transient receptor potential vanilloid 1 (TRPV1) channel is an ess

246 Transient receptor potential vanilloid 1 (TRPV1) has been shown to

247 The transient receptor potential vanilloid 1 (TRPV1) ion channel is a

248 The transient receptor potential vanilloid 1 (TRPV1) ion channel is ma

249 Transient receptor potential vanilloid 1 (TRPV1) ion channel was e

250 acterized by the expression of the transient receptor potential vanilloid 1 (TRPV1) ion channel.

251 Transient receptor potential vanilloid 1 (TRPV1) is a polymodal io

252 Transient receptor potential vanilloid 1 (TRPV1) is involved in se

253 Although activation of transient receptor potential vanilloid 1 (TRPV1) of superior laryn

254 Here we report that transient receptor potential vanilloid 1 (TRPV1) on astrocytes med

255 of the heat-activated ion channel transient receptor potential vanilloid 1 (TRPV1) through lipids is

256 roduces burning pain by activating transient receptor potential vanilloid 1 (TRPV1), a Ca(2+)-permeab

257 of a thermoregulatory ion channel, transient receptor potential vanilloid 1 (TRPV1), by dihydrocapsai

258 lipid that potently activates the transient receptor potential vanilloid 1 (TRPV1), which mediates p

259 ocalized in human cells expressing transient receptor potential vanilloid 1 and CGRP.

260 associate with a camelid anti-GFP-transient receptor potential vanilloid 1 fusion protein, alphaGFP-

261 TRPV1 (transient receptor potential vanilloid 1) proteins are heat-activa

262 mal thresholds is dependent on the transient receptor potential vanilloid 1.

263 Here we report that transient receptor potential vanilloid 2 (TRPV2) is an intracellul

264 pyroptosis and were controlled by transient receptor potential vanilloid 2 channel-mediated signalin

265 The transient receptor potential vanilloid 3 (TRPV3) channel is a Ca(2

266 Transient receptor potential vanilloid 3 (TRPV3) is a Ca(2+)- and

267 The transient receptor potential vanilloid 4 (TRPV4) channel translate

268 lular Ca(2+) through activation of transient receptor potential vanilloid 4 (TRPV4) channels in the p

269 re we define the overexpression of transient receptor potential vanilloid 4 (TRPV4) in a subgroup of

270 The transient receptor potential vanilloid 4 (TRPV4) ion channel trans

271 t the mechanosensitive ion channel transient receptor potential vanilloid 4 (TRPV4) regulates tumor a

272 Transient receptor potential vanilloid 4 (TRPV4), a mechanosensiti

273 of a mechanosensitive ion channel, transient receptor potential vanilloid 4 (TRPV4), in integrating t

274 Mechanosensitive transient receptor potential vanilloid 4 regulates Dermatophagoide

275 nse to muscarinic receptor, TRPV4 (transient receptor potential vanilloid 4) channel and IK/SK channe

276 on-selective cation channel TRPV1 (transient receptor potential vanilloid isoform 1) remains elusive.

277 Here, we identify TRPV4 (transient receptor potential vanilloid isoform 4) channels as key

278 Calcium-selective transient receptor potential vanilloid subfamily member 6 (TRPV6)

279 d that HA also modulates polymodal transient receptor potential vanilloid subtype 1 (TRPV1) channels.

280 Transient receptor potential vanilloid subtype 1 (TRPV1) is a heat

281 ts at least in part by sensitizing transient receptor potential vanilloid subtype 1 (TRPV1) through T

282 ctly and sensitizes these cells to transient receptor potential vanilloid subtype 1 (TRPV1)-mediated

283 One such studied receptor is transient receptor potential vanilloid subtype 1 (TRPV1).

284 rieties of ion channels, including Transient Receptor Potential vanilloid subtype 4 (TrpV4).

285 Transient receptor potential vanilloid subtype I (TRPV1) is a ther

286 ABSTRACT: The transient receptor potential vanilloid type 1 (TRPV1) receptor is

287 KEY POINTS: The transient receptor potential vanilloid type 1 (TRPV1) receptor is

288 The transient receptor potential vanilloid type 1 (TRPV1) receptor pla

289 e-5-)-methyltransferase 1 (DNMT1), transient receptor potential vanilloid type 1 (TRPV1), and EP300 w

290 the sensory neuron subpopulations transient receptor potential vanilloid type 1 (TRPV1), neurofilame

291 nociceptive cation channel TRPV1 (transient receptor potential vanilloid type 1) modulates RGC Ca(2+

292 ition, our study revealed that the transient receptor potential vanilloid type 1-dependent increase o

293 Activation of the transient receptor potential vanilloid type 4 (TRPV4) channel is a

294 e gating transformations of TRPV4 (transient receptor potential vanilloid type 4).

295 aicin that may be mediated via the transient receptor potential vanilloid type-1 (TRPV1) channel.

296 sient receptor potential channels (transient receptor potential vanilloid type-1, -3; transient recep

297 In contrast, the role of transient receptor potential vanilloid type-4 (TRPV4) in itch is u

298 , and calcium salts also activated transient receptor potential vanilloid-1 (TRPV1) and transient rec

299 sized that polymorphic variants of transient receptor potential vanilloid-1 (TRPV1) would be uniquely

300 s, under the permissive control of transient receptor potential vanilloid-1 receptors.