ライフサイエンスコーパス: cation channel

1 glutamate to the opening of a transmembrane cation channel.

2 des the two-pore channel 2 (TPC2) protein, a cation channel.

3 ember 6 (TRPC6) gene encoding a nonselective cation channel.

4 th accessory subunit surrounding the central cation channel.

5 LGC-55 anion channel to an excitatory LGC-55 cation channel.

6 rm 4 (TRPV4), a polymodal swelling-sensitive cation channel.

7 ted genetically using a hyperactive vacuolar cation channel.

8 tor that forms a nonselective homotetrameric cation channel.

9 ient receptor potential melastatin 1 (TRPM1) cation channel.

10 t Receptor Potential Melanostatine 2 (TRPM2) cation channel.

11 muli in muscle, we examined the role of this cation channel.

12 the transient receptor potential A1 (TRPA1) cation channel.

13 ed to transient receptor potential canonical cation channels.

14 sensitive transient receptor potential (TRP) cation channels.

15 nges in pH, and three are putative ACh-gated cation channels.

16 -dependent excitation involving non-specific cation channels.

17 Two-pore channels (TPCs) are endolysosomal cation channels.

18 2X7R) belongs to the P2X family of ATP-gated cation channels.

19 ls (CNGCs) are nonspecific, Ca(2+)-permeable cation channels.

20 -dependent excitation involving non-specific cation channels.

21 sed in both animals and plants as organellar cation channels.

22 ctivated cyclic-nucleotide-gated nonspecific-cation channels.

23 cyclic-nucleotide-gated (CNG), nonselective cation channels.

24 Na K-ATPase, and hyperpolarization-activated cation channels.

25 tential (TRP) channel family of nonselective cation channels.

26 1) proteins are heat-activated nonselective cation channels.

27 or blockade of transient receptor potential cation channels.

28 Channelrhodopsins (ChRs) are light-gated cation channels.

29 tivity within this superfamily of tetrameric cation channels.

30 function and expression of Ca(2+)-permeable cation channels.

31 uding voltage, stretch, and ligand-activated cation channels.

32 ay have broad applications for voltage-gated cation channels.

33 ich are mechanically-activated non-selective cation channels.

34 pharmacological modulators for nonselective cation channels.

35 hibition of the transient receptor potential cation channel 6 (TRPC6) reduced platelet activation and

36 ntry though the transient receptor potential cation channel 6 (TRPC6), causing hyperactivation and co

37 TRPV1 is a polymodally activated cation channel acting as key receptor in nociceptive neu

38 TRPM8 is a polymodal, nonselective cation channel activated by cold temperature and cooling

39 TRPM8, a nonselective cation channel activated by cold, voltage, and cooling c

40 The P2X7 receptor is a non-selective cation channel activated by extracellular adenosine trip

41 (TRPM3) is a Ca(2+) permeable non-selective cation channel activated by heat and chemical agonists s

42 P2X receptors are trimeric, non-selective cation channels activated by ATP that have important rol

43 eteromeric P2X2/3 receptors are ligand-gated cation channels activated by ATP.

44 P2X receptors are trimeric, non-selective cation channels activated by extracellular ATP.

45 tial Canonical 4 (TRPC4) forms non-selective cation channels activated downstream from receptors that

46 um ion binding (P = 3.55 x 10(-)(1)(5)), and cation channel activity (P = 2.77 x 10(-)(1)(4)) were si

47 colon cancer cells to noninvasively monitor cation channel activity in real time by the appearance o

48 HD), is targeted to Golgi membranes, and has cation channel activity in vitro The E protein from avia

49 targeted to Golgi complex membranes, and has cation channel activity in vitro.

50 locus-encoded beta-subunit of rod cGMP-gated cation channel and associated glutamic acid rich protein

51 l recordings show that it is a non-selective cation channel and that its activity depends on Ca(2+) c

52 (h)KCNE beta subunits each regulate various cation channels and are linked to inherited cardiac arrh

53 at operates downstream from cyclic GMP-gated cation channels and distal guanylate cyclases.

54 arity to canonical VSDs in voltage-dependent cation channels and enzymes.

55 X purinergic receptor family of ligand-gated cation channels and has recently been shown to regulate

56 Many cells express both P2X cation channels and P2Y G-protein-coupled receptors that

57 among the most highly efficient light-gated cation channels and the most blue-shifted channelrhodops

58 (transient receptor potential, "canonical") cation channels, and powerful regulation of lipid metabo

59 ent and transient receptor channel potential cation channel ankyrin subtype 1 (TRPA1)-deficient mice

60 n mutations in mechanically activated Piezo1 cation channels are associated with the dehydrating RBC

61 The P2X receptor family of ATP-gated cation channels are attractive drug targets for pain and

62 (transient receptor potential, "canonical") cation channels are coupled to neuronal discharge proper

63 hodopsins (ChR)1 and ChR2; these light-gated cation channels are located in the plasma membrane.

64 Transient receptor potential (TRP) cation channels are molecular targets of various natural

65 ansient receptor potential melastatin (TRPM) cation channels are polymodal sensors that are involved

66 hat sensory cilia and polycystin-2 (Pkd2), a cation channel, are required for sensing ciliary motilit

67 encodes TRPM4, a Ca(2+)-activated monovalent cation channel, as a cause of an autosomal dominant form

68 AMPA receptors are glutamate-gated cation channels assembled from GluA1-4 subunits and have

69 ) melastatin 4 (TRPM4) is a widely expressed cation channel associated with a variety of cardiovascul

70 ts could be prevented with the non-selective cation channel blocker Gadolinium (Gd(3+)).

71 was inhibited by tetrodotoxin as well as the cation channel blockers, 9-phenanthrol and clotrimazole.

72 ated by phospholipase C, which activates TRP cation channels by an unknown mechanism.

73 t NaRs can be converted into light-activated cation channels by molecular engineering.

74 s, we show that transient receptor potential cation channel C3 (TRPC3) controls the simple spike acti

75 Therefore, opening of a non-selective cation channel causes cell death and Ucn1 maintains this

76 oendocrine bag cell neurons triggers various cation channels, causing an ~30 min afterdischarge of ac

77 the plasma membrane and formed pH-sensitive cation channels, causing collapse of cellular Na(+) and

78 esumptive transient receptor potential (TRP) cation channel, CED-11, that acts in the dying cell to p

79 A variant of the cation channel channelrhodopsin-2 from Chlamydomonas rei

80 Patch-clamping was used to examine TPC1 cation channel characteristics in the ouf suppressor mut

81 Canonical (TRPC) proteins form nonselective cation channels commonly known to be activated downstrea

82 PC6 and function as diacylglycerol-activated cation channels coordinately, the role of TRPC6 in heart

83 Hence, the mechanism by which voltage-gated cation channels couple conformational changes within the

84 EA induced cation channel current (Icat) in SW982 cells with biophy

85 rpolarization-activated and nucleotide-gated cation channels decreasing the firing rate of MNCs and t

86 by the ionotropic glutamate receptor homolog cation channel, delta glutamate receptor 1 (GluD1).

87 This demonstrates that the nuclear cation channel DMI1 is sufficient to support MVA-induced

88 e Infections 2 (DMI2) as well as the nuclear cation channel DMI1.

89 We found the expression of the chemosensory cation channel dTRPA1 in these cells to be necessary and

90 as largely eliminated during the blockade of cation channels due to the internal dialysis of Cs(+) ,

91 Unlike other cation channels, each subunit of most transient receptor

92 nt stimulator of Ca(2+) influx through TRPA1 cation channels (EC50 ca. 200 nM), thereby explaining it

93 3 (TRPC3), a calcium-permeable, nonselective cation channel endowed with high constitutive function,

94 l Melastatin 2 (TRPM2) is a Ca(2+)-permeable cation channel essential for immunocyte activation, insu

95 de-gated (CNG) ion channels are nonselective cation channels, essential for visual and olfactory sens

96 rformed on mice expressing a light sensitive cation channel exclusively on cholinergic neurons (ChAT-

97 ntial melastatin 8 (TRPM8) is a nonselective cation channel expressed in a subpopulation of sensory n

98 l melastatin 2 (TRPM2) is a Ca(2+)-permeable cation channel expressed in immune cells of phagocytic l

99 vanilloid type 1 (TRPV1) is a non-selective cation channel expressed in sensory neurons of the dorsa

100 TRPM5 is a Ca(2+)-activated cation channel expressed in type II taste receptor cells

101 -permeant Transient Receptor Potential (TRP) cation channel expressed primarily on the endoplasmic re

102 ffect was caused by acid activation of these cation channels expressed in airway sensory nerves.

103 The transient receptor potential cation channel family member ankyrin 1 (TRPA1) is a pote

104 kedly induces the expression of Claudin-2, a cation-channel-forming tight junction protein.

105 s caused by mutations in MCOLN1, a lysosomal cation channel from the transient receptor potential (TR

106 Light-gated rhodopsin cation channels from chlorophyte algae have transformed

107 SHL is a powerful tool for evaluating cation channel function in living cells in real time, wi

108 at DmPiezo, a Ca(2+)-permeable non-selective cation channel, functions as an intrinsic inhibitor for

109 omeostasis, AQP1 also acts as a nonselective cation channel gated by cGMP, a property shown previousl

110 under permissive conditions, a nonselective cation channel gated by cGMP.

111 P2X7 receptors are nonselective cation channels gated by high extracellular ATP, but wit

112 Hence in GtCCR2, cation channel gating is tightly coupled to intramolecul

113 P2X4 is an ATP-gated nonselective cation channel highly permeable to calcium.

114 ecies variant of the human apoptosis-related cation channel hTRPM2, is gated by ADP-ribose (ADPR) ind

115 Receptor Potential Melastatin 2 (TRPM2) is a cation channel important for the immune response, insuli

116 TRPP2 functions as a cation channel in its homomeric complex and in the TRPP2

117 een identified as a crucial mechanosensitive cation channel in multiple solid tumours.

118 f a plant ion channel and identify the first cation channel in plant mitochondria from a molecular po

119 ecycling, suggesting APOL1 forms a cytotoxic cation channel in the parasite plasma membrane.

120 (TRPV4), a Ca(2+)-permeable mechanosensitive cation channel in the transient receptor potential vanil

121 e presence of apically located voltage-gated cation channels in a population of electrosensory hair c

122 function as Ca(2+) conducting, non-selective cation channels in endothelial, smooth muscle, and neuro

123 Here, we demonstrate that PSH and FlaK form cation channels in lipid bilayers.

124 DP- and PI(3,5)P2-sensitive Ca(2+)-permeable cation channels in the endolysosomal system of cells, as

125 anoparticles can gate TRPV1, a non-selective cation channel, in a magnetic field.

126 alanced translocation disruption of TRPC6, a cation channel, in a non-syndromic autistic individual.

127 encoding polycystin-L (PCL), a non-selective cation channel, increases neuronal excitability and the

128 It is postulated that mechanically activated cation channels initiate touch sensation, but the identi

129 el, subfamily M, member 2) is a nonselective cation channel involved in the response to oxidative str

130 Gating of voltage-dependent cation channels involves three general molecular process

131 (TRPC5), a calcium-permeable, non-selective cation channel is expressed in the periphery, but there

132 The engineered cation channel is properly trafficked in the native neur

133 e-shift displayed by hyperpolarization-gated cation channels is likely caused by structural changes a

134 vation of transient receptor potential (TRP) cation channels is one of the most striking examples of

135 Piezo2, a mechanically activated cation channel, is expressed in Merkel cells.

136 r potential canonical genes (TRPC1-7) encode cation channels linked to several human diseases.

137 l 3 (TRPML3), a transient receptor potential cation channel localized to lysosomes.

138 lipin 1) is a Ca(2+)-permeable, nonselective cation channel localized to the membranes of endosomes a

139 is a dual water and cyclic-nucleotide-gated cation channel located in lamellipodia and is essential

140 receptor potential mucolipin 1 (TRPML1) is a cation channel located within endosomal and lysosomal me

141 urea receptor-1-transient receptor potential cation channel M4 is upregulated only after brain injury

142 (TRPC6), a nonselective and Ca(2+)-permeable cation channel, mediates pathophysiological responses wi

143 2) expressed in endothelial cells (ECs) is a cation channel mediating Ca(2+) entry in response to int

144 receptor transient receptor potential (TRP) cation channel member A1 (TRPA1).

145 sistent with either the ER stress or surface cation channel models of APOL1-mediated cytotoxicity.

146 triction point in the bacterial nonselective cation channel, NaK.

147 Cation channels of the transient receptor potential (TRP

148 Plant TPC1 functions as a nonselective cation channel on the vacuole membrane, whereas mammalia

149 nation of the Asp-96 homolog is required for cation channel opening and occurs >10-fold faster than r

150 channels in the ER/SR and the non-selective cation channels or putative 'Ca(2+) leak channels', incl

151 hR-2), a direct light-activated nonselective cation channel originally discovered in Chlamydomonas re

152 d forms a pore complex with the ligand-gated cation channel P2X7, allowing the release of excitatory

153 As a non-selective cation channel permeable to Ca(2+) , it transduces physi

154 et al. show that the mechanically activated cation channel Piezo1 is a molecular sensor of physical

155 shown that the endothelial mechanosensitive cation channel PIEZO1 is required for flow-induced ATP r

156 at platelets and Meg-01 cells express the MS cation channel Piezo1, which may contribute to Ca(2+) en

157 that the mechanically activated nonselective cation channel Piezo2 was expressed in sensory endings o

158 Transient receptor potential (TRP) cation channels play a central role in sensory responses

159 vestigated if TRPV4, a temperature-sensitive cation channel, plays an important role in acute itch in

160 ease where it regulates the calcium-permeant cation channel polycystin-2.

161 d at whether the P2X1 receptor, an ATP-gated cation channel present on platelets, neutrophils, and ma

162 ensing ion channel 1 (ASIC1), a proton-gated cation channel primarily expressed in the nervous system

163 Nonselective cation channels promote persistent spiking in many neuro

164 euromediators and expression of chemosensory cation channels, protein gene product 9.5 (PGP 9.5), and

165 proteins form a superfamily Ca(2+)-permeable cation channels regulated by a range of chemical and phy

166 potential channel (TrpC) family, a family of cation channels regulated by activation of phospholipase

167 sential for proper localization of the TRPM1 cation channel required for ON BC light-evoked depolariz

168 Receptor-operated activation of TRPC4 cation channels requires G(i/o) proteins and phospholipa

169 Here, we report that Trpv6, a cation channel responsible for epithelial Ca(2+) absorpt

170 PA-type glutamate receptors are ligand-gated cation channels responsible for a majority of the fast e

171 n the vacuole, cooperating with the vacuolar cation channel SlTPC1 and the two vacuolar H(+)-pumps, S

172 PGP9.5; TRPV1; transient receptor potential cation channel subfamily A, receptor 1 (TRPA1); TRPV4; t

173 upling with the transient receptor potential cation channel subfamily C 3 (TRPC3).

174 Transient receptor potential cation channel subfamily C member 6 (TRPC6) is a widely

175 Ca(2+) channel, transient receptor potential cation channel subfamily C member 6 (TRPC6), and the pro

176 Transient receptor potential (TRP) cation channel subfamily M member 3 (TRPM3), a member of

177 onjunction with transient receptor potential cation channel subfamily M member 4 (TRPM4), and perhaps

178 TRPM7 (transient receptor potential cation channel subfamily M member 7) regulates gene expr

179 EGFPf) from the transient receptor potential cation channel subfamily M member 8 (TRPM8(EGFPf/+)) loc

180 which acted on transient receptor potential cation channel subfamily M member 8 (TRPM8) channels to

181 n of Piezo2 and transient receptor potential cation channel subfamily M member 8 (TRPM8) transcripts

182 pressing TRPM8 (transient receptor potential cation channel subfamily M member 8).

183 (TRPA1); TRPV4; transient receptor potential cation channel subfamily M, member 8 (TRPM8); and nerve

184 l activation of transient receptor potential cation channel subfamily V member 1 (TRPV1) and CB1Rs.

185 ated afferents [transient receptor potential cation channel subfamily V member 1 (TRPV1) expressing C

186 t activates the transient receptor potential cation channel subfamily V member 1 (TRPV1) on sensory n

187 The transient receptor potential cation channel subfamily V member 1 (TRPV1) or vanilloid

188 smitted via the transient receptor potential cation channel subfamily V member 1 (TRPV1) population b

189 ively as either transient receptor potential cation channel subfamily V member 1 (TRPV1)-sensitive or

190 implication of transient receptor potential cation channel subfamily V member 1 (TRPV1).

191 hibiting TRPV1 (transient receptor potential cation channel subfamily V member 1) immunoreactivity (p

192 influx through transient receptor potential cation channel subfamily V member 2 channels.

193 The transient receptor potential cation channel subfamily V member 3 (TRPV3) channel play

194 higher baseline transient receptor potential cation channel subfamily V, receptor 1 (TRPV1) expressio

195 ablation of the transient receptor potential cation channel subfamily V, receptor 1 (TRPV1)-substance

196 oid type-1, -3; transient receptor potential cation channel, subfamily A, member 1) have been implica

197 utations in the transient receptor potential cation channel, subfamily C, member 6 (TRPC6) gene encod

198 pression of the transient receptor potential cation channel, subfamily C, member 6 (TRPC6), consisten

199 docyte-specific transient receptor potential cation channel, subfamily C, member 6.

200 TRPM2 (transient receptor potential cation channel, subfamily M, member 2) is a nonselective

201 )-dependent and transient receptor potential cation channel, subfamily M, member 7 (TRPM7)-dependent

202 ration, and the transient receptor potential cation channel, subfamily V, member 1 (TRPV1), in intest

203 Transient receptor potential cation channel, subfamily V, member 4 (TRPV4) is widely

204 iezo1 by TRPV4 (transient receptor potential cation channel, subfamily V, member 4) channels.

205 l compartments is mediated via intracellular cation channels, such as two-pore channel (TPC) proteins

206 channels are members of the large tetrameric cation channels superfamily but are considered to be uni

207 te (PtdIns(4,5)P2) -modulated, non-selective cation channel that belongs to the family of melastatin-

208 (TRPC5) is a nonselective, Ca(2+)-permeable cation channel that belongs to the large family of trans

209 (CaChR1) is a low-efficiency light-activated cation channel that exhibits properties useful for optog

210 eceptor (P2X7R) is an ATP-gated nonselective cation channel that induces inflammatory responses in ce

211 ng ion channel-1A (ASIC1A) is a proton-gated cation channel that is activated by extracellular acidos

212 TRPV1 is a ligand-gated cation channel that is expressed on a major subclass of

213 nonical type 5 (TRPC5) is a Ca(2+)-permeable cation channel that is highly expressed in the brain and

214 e envelope protein E, forms a homopentameric cation channel that is important for virus pathogenicity

215 ntial melastatin 3 (TRPM3) is a nonselective cation channel that is inhibited by Gbetagamma subunits

216 1) or vanilloid receptor 1 is a nonselective cation channel that is involved in the detection and tra

217 lipin 1) is a Ca(2+)-permeable, nonselective cation channel that is predominantly localized to the me

218 otential channel 1 (TRPC1) is a nonselective cation channel that is required for Ca(2+) homeostasis n

219 otide-gated (HCN) channel is a voltage-gated cation channel that mediates neuronal and cardiac pacema

220 l mucolipin 1 (TRPML1) is a Ca(2+)-releasing cation channel that mediates the calcium signalling and

221 s a TRP-type, Ca(2+)-permeable non-selective cation channel that plays an important role in Ca(2+) si

222 (TRPC6) is a nonselective receptor-operated cation channel that regulates reactive fibrosis and grow

223 TRP vanilloid 4 (TRPV4) is a non-selective cation channel that responds to mechanical, thermal, and

224 ily A member 1 (TRPA1) is a Ca(2+)-permeable cation channel that serves as one of the primary sensors

225 (TRPM8) is a calcium ion (Ca(2+))-permeable cation channel that serves as the primary cold and menth

226 ) channels are Ca(2+)-permeable nonselective cation channels that are activated by a wide variety of

227 Piezo1 and Piezo2 as mechanically activated cation channels that are expressed in many mechanosensit

228 onstitute an important class of ligand-gated cation channels that are involved in the majority of exc

229 s at acidic pH to form pH-gated nonselective cation channels that are opened upon pH neutralization.

230 P2X4 receptors are ATP-gated cation channels that are widely expressed in the nervous

231 ensing ion channels (ASICs) are proton-gated cation channels that contribute to neurotransmission, as

232 rinatal development, 90-pS stretch-activated cation channels that could be blocked by Ca(2+) and by F

233 channels are highly homologous, nonselective cation channels that form many homo- and heterotetrameri

234 zo1 and Piezo2 encode mechanically activated cation channels that function as mechanotransducers invo

235 Channelrhodopsins are light-gated cation channels that have been widely used for optogenet

236 ceptors (nAChRs) are pentameric ligand-gated cation channels that include at least two alpha3 and two

237 spartate receptors (NMDARs) are ligand-gated cation channels that mediate excitatory synaptic transmi

238 AMPA receptors (AMPARs) are glutamate-gated cation channels that mediate fast excitatory neurotransm

239 acid receptors (AMPARs) are glutamate-gated cation channels that mediate fast excitatory synaptic tr

240 glutamate receptors (iGluRs) are tetrameric cation channels that mediate synaptic transmission and p

241 canonical (TRPC) proteins form nonselective cation channels that play physiological roles in a wide

242 Mammalian TRICs function as K(+)-permeable cation channels that provide counter ions for Ca(2+) han

243 MDA) receptors are heteromeric non-selective cation channels that require the binding of glycine and

244 Two-pore channels (TPCs) are cation channels that reside in endo-lysosomal organelles

245 Unlike other voltage-gated cation channels, the Hv1 channel lacks a centrally locat

246 f residues characteristic of the chlorophyte cation channels, these proteins are cation-conducting ch

247 excitatory synaptic transmission by forming cation channels through the membrane that open upon glut

248 H(2)O(2) may regulate a cation channel to influence long-term changes in activit

249 e activation of transient receptor potential cation channels to attenuate cytosolic Ca2+ influx, impl

250 tudy investigated whether H(2)O(2) regulates cation channels to drive the afterdischarge.

251 erfamily, which functions as glutamate-gated cation channels to mediate the majority of excitatory ne

252 Transient receptor potential (TRP) cation channels transduce a variety of disease-relevant

253 esponding to moderate hypoxia via the sensor cation channel transient receptor potential (TRP) A1 but

254 The cation channel transient receptor potential ankyrin 1 (T

255 Here, we evaluated the nonselective cation channel transient receptor potential melastatin 2

256 d] activation of the intracellularly located cation channel transient receptor potential vanilloid 1

257 The cation channel transient receptor potential vanilloid 4

258 The cation channel transient receptor potential vanilloid 4

259 upled to hyperactivation of the nonselective cation channel, transient receptor potential canonical c

260 ular mechanism by which the mechanosensitive cation channel, transient receptor potential vanilloid 4

261 c oxide activates the nitric oxide-sensitive cation channel, transient receptor potential vanilloid f

262 ABSTRACT: The type A trimeric intracellular cation channel (TRIC-A) is a major component of the nucl

263 The trimeric intracellular cation channels, TRIC-A and TRIC-B, represent two subtyp

264 monstrated that transient receptor potential cation channel (TRP)-A1 was the ion channel downstream o

265 tivation of the transient receptor potential cation channels (TRP) TRPV1, TRPV4, and TRPA1 causes vis

266 The cation channel TRPA1 transduces a myriad of noxious chem

267 We found that the cation channel TRPA1, in addition to playing a conserved

268 he soluble guanylate cyclase Gucy1b2 and the cation channel Trpc2.

269 lts reveal a previously unknown role for the cation channel Trpc5 in prolactin homeostasis of female

270 well as a class of excitatory non-selective cation channels, TRPM2.

271 macological inhibition of the heat-activated cation channel TRPM3 alleviates inflammatory heat hypera

272 The nociceptive cation channel TRPV1 (transient receptor potential vanil

273 and function of the polymodal non-selective cation channel TRPV1 (transient receptor potential vanil

274 sensors of the transient receptor potential cation channel TRPV1.

275 ensitive actuator, "Magneto," comprising the cation channel TRPV4 fused to the paramagnetic protein f

276 yses localized the putative mechanosensitive cation channel TRPV4 to the plasma membrane of primary a

277 (AQP5) and the transient receptor potential cation channel (TRPV4), was investigated.

278 olved transient receptor potential vanilloid cation channels (TRPVs) since TRPV1/TRPV4 antagonism blo

279 mily member 1 (WNT1), trimeric intracellular cation channel type b (TRIC-B), and old astrocyte specif

280 Many cation channels use a S4-S5 linker to transmit stimuli t

281 channelrhodopsin-2 (PsChR2), are light-gated cation channels used as optogenetic tools for photocontr

282 , including the transient receptor potential cation channel V1 expressed in the nociceptive neurons o

283 that coexpress transient receptor potential cation channel vanilloid subtype 1 (TRPV1).

284 In contrast, transient receptor potential cation channel vanilloid subtype 1 channels were dispens

285 Furthermore, transient receptor potential cation channel vanilloid type 1 appears to counter the a

286 the ion channel transient receptor potential cation channel vanilloid type 1.

287 urrents is well documented for voltage-gated cation channels (VGCC), and it is considered a voltage-s

288 n activates a Na(+)-permeable, non-selective cation channel via depolarization-induced rise in [Ca(2+

289 trA, a RCK domain from the B. subtilis KtrAB cation channel, we have found that activation by nucleot

290 tial vanilloid type 4, TRPV4, is a polymodal cation channel which can be activated by diverse stimuli

291 tion-activated cyclic nucleotide-gated (HCN) cation channels, which are concentrated on dendritic spi

292 to ATP induces the opening of a nonselective cation channel; while repeated or prolonged exposure ind

293 resents a novel architecture of a tetrameric cation channel whose ion selectivity mechanism appears t

294 RPM7) is a ubiquitous, constitutively active cation channel with a cytosolic alpha-kinase domain that

295 curvature-sensitive, mechanically activated cation channel with a single channel conductance of ~28.

296 tor potential superfamily, is a nonselective cation channel with Ca(2+) permeability.

297 mucolipins) constitute a family of endosomal cation channels with homology to the transient receptor

298 1-3) of eukaryotic voltage- and ligand-gated cation channels with two non-equivalent tandem pore-form

299 Most viroporins are monovalent selective cation channels, with few showing the ability to conduct

300 rm of a tunable, high-conductance vertebrate cation channel, zTrpa1b, coupled with photo-activated ch