ライフサイエンスコーパス: cation channel

1 th accessory subunit surrounding the central cation channel.

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

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

4 tor that forms a nonselective homotetrameric cation channel.

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

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

7 on binding and transport of this promiscuous cation channel.

8 s TRPM2, a Ca(2+), Na(+), and K(+) permeable cation channel.

9 conformational changes to the gating of the cation channel.

10 construct forms an essentially non-selective cation channel.

11 ed them with dTrpA1, a temperature-sensitive cation channel.

12 eurons using a nonnative genetically encoded cation channel.

13 glutamate to the opening of a transmembrane cation channel.

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

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

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

17 or blockade of transient receptor potential cation channels.

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

19 tivity within this superfamily of tetrameric cation channels.

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

21 sensitive transient receptor potential (TRP) cation channels.

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

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

24 long to the TRP superfamily of non-selective cation channels.

25 rent was mediated mainly by sodium-permeable cation channels.

26 are relatives of classical voltage-activated cation channels.

27 ntity and form Ca(2+)-permeable nonselective cation channels.

28 represent Ca(2+) influx through single TRPV4 cation channels.

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

30 ed to transient receptor potential canonical cation channels.

31 -dependent excitation involving non-specific cation channels.

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

33 2X7R) belongs to the P2X family of ATP-gated cation channels.

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

35 -dependent excitation involving non-specific cation channels.

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

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

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

39 osophila TRPA1 (transient receptor potential cation channel A1) was necessary for normal activity pat

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

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

42 atin 8 (TRPM8) channel is a Ca(2+)-permeable cation channel activated by cold, voltage, phosphatidyli

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

44 ential vanilloid 1 (TRPV1) is a nonselective cation channel activated by multiple stimuli and is impl

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

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

47 Acid-sensing ion channels are cation channels activated by external protons and play r

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

49 his issue of Neuron highlights voltage-gated cation channel activity as a likely link and culprit.

50 The voltage-gated cation channel activity gene set, consisting of genes re

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

52 demonstrating that nonselective sarcolemmal cation channel activity plays a critical role in causing

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

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

55 tivated, but Ca2+ -impermeable, nonselective cation channels and are expressed both in atrial and in

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

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

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

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

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

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

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

63 Nonspecific sarcolemmal cation channels are critical for the pathogenesis of mal

64 ient receptor potential (TRPC3) nonselective cation channels are effectors of G-protein-coupled recep

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

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

69 n channels (ASICs) are neuronal proton-gated cation channels associated with nociception, fear, depre

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

71 The transient receptor potential cation channel C6 (TRPC6) is a slit diaphragm protein ex

72 ich encodes the transient receptor potential cation channel, can cause familial episodic pain syndrom

73 In Lotus japonicus, two symbiotic cation channels, CASTOR and POLLUX, are indispensable fo

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

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

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

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

78 MCH neurons the gene for the light-sensitive cation channel, channelrhodopsin-2, was inserted into th

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

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

81 ENaC, which is not a component of the glioma cation channel complex, had no effect on cyclin-dependen

82 Heteromeric nAChRs are pentameric cation channels, composed of combinations of two or thre

83 rant receptors are heteromeric odorant-gated cation channels comprising a conventional odorant-sensit

84 eceptor potential 1 (TRPC1) Ca(2+)-permeable cation channels contribute to vascular tone and blood ve

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

86 A possible role for this cation channel could be hyperpolarization of the nuclear

87 aC) and nonselective cyclic-nucleotide-gated cation channels creates the major driving force for reab

88 d 1 (TRPV1) is a polymodal, Ca(2+)-permeable cation channel crucial to regulation of nociceptor respo

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

90 a suggested that hyperpolarization-activated cation channel currents and T-type calcium channel curre

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

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

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

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

95 Kenyon cells by expressing a thermosensitive cation channel (dTrpA1) leads to a decrease in sNPF immu

96 cially activated via a temperature-sensitive cation channel (dTRPA1), males followed and extended the

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

98 axonal transport (HSPB1, DYNC1H1, DCTN1) and cation-channel dysfunction (ATP7A and TRPV4) in motor-ne

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

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

101 3 (TRPC3), a calcium-permeable, nonselective cation channel endowed with high constitutive function,

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

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

104 sual disease caused by mutations in TRPM1, a cation channel expressed by both melanocytes and retinal

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

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

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

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

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

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

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

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

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

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

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

116 tor potential ankyrin 1 (TRPA1) nonselective cation channel has a conserved function as a noxious che

117 stand how, we focus on TRPV4, a nonselective cation channel highly expressed in epithelial skin cells

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

119 (trpv1, trpv4) encode temperature-sensitive cation channels hypothesized to mediate thermoresponses

120 an autoantibody profile dominated by neural cation channel immunoglobulin Gs (IgGs).

121 , TRPP2) is a Ca(2+)-permeable, nonselective cation channel implicated in Ca(2+) transport and epithe

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

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

124 TRPC6 is a cation channel in the plasma membrane that plays a role

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

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

127 ated with altered expression and function of cation channels in pulmonary arterial smooth muscle cell

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

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

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

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

132 eptors are commonly known as plasma membrane cation channels involved in a wide variety of cell funct

133 imeric adenosine-5'-triphosphate (ATP)-gated cation channels involved in fast signal transduction in

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

135 ient Receptor Potential Melastatin 4 (TRPM4) cation channel is abundantly expressed in cardiac cells,

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

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

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

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

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

141 7 (TRPM7) and member 6 (TRPM6) are divalent cation channel kinases essential for magnesium (Mg(2+))

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

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

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

145 l mRNAs but not transient receptor potential cation channel M7 (TRPM7) channel mRNA.

146 eraction, claudin-14 blocks the paracellular cation channel made of claudin-16 and -19, critical for

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

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

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

150 ) orthologous to the mammalian endolysosomal cation channel Mucolipin 1.

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

152 ions in acr-23, which encodes a ligand-gated cation channel of the cys-loop family.

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

154 est that P2X4 forms functional ATP-activated cation channels on lysosomal membranes regulated by lumi

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

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

157 channels in the ER/SR and the non-selective cation channels or putative 'Ca2+ leak channels', includ

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

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

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

161 kd2L1 (also called TRPP3) is a non-selective cation channel permeable to Ca(2+), Na(+), and K(+) and

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

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

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

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

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

167 Given that virus-encoded cation channels play a crucial role in the life cycle of

168 The TRPV4 calcium-permeable cation channel plays important physiological roles in os

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

170 otential vanilloid 1 (TRPV1), a nonselective cation channel present on most afferents.

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

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

173 Using the cation channel probe 1-amino-4-guanidobutane agmatine (A

174 anilloid transient receptor potential (TRPV) cation channels, promoted the sADP.

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

176 Light responses are generated when a cation channel, recently identified as Trpm1, opens.

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

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

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

180 oid 1 (TRPV1) is a nonselective ligand-gated cation channel responding to noxious heat, protons, and

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

182 -conductance, Ca(2+)-activated, nonselective cation channel (SCAN), TMEM16F.

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

184 ocal Ca(2+) signal generated by nonselective cation channels stimulates TMEM16A channels to induce my

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

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

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

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

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

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

191 minals, whereas transient receptor potential cation channel subfamily M member 8 immunolabeled (cold

192 xpressed TRPM8 (transient receptor potential cation channel subfamily M member 8).

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

194 ssion of TRPV1; transient receptor potential cation channel subfamily M, receptor 8 (TRPM8); and PGP

195 channel 2a, and transient receptor potential cation channel subfamily member M8 (TRPM8) in sensory ga

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

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

198 The transient receptor potential cation channel subfamily V member 1 (TRPV1) is known as

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

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

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

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

203 channel TRPV1 (transient receptor potential cation channel subfamily V member 1), but the mechanisms

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

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

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

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

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

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

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

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

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

213 to test for association of Thy1 and HCN4, a cation channel subunit, in adult rat retina.

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

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

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

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

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

219 (TRPM3) is a calcium-permeable nonselective cation channel that is expressed in a subset of dorsal r

220 TRPA1 is a nonselective cation channel that is expressed in peptidergic sensory

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

222 n-2 (ChR2) is a light-activated nonselective cation channel that is found in the eyespot of the unice

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

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

225 or potential channel TRPP2 is a nonselective cation channel that is mutated in autosomal dominant pol

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

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

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

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

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

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

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

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

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 alcium channels (SOCs) are calcium-selective cation channels that mediate calcium entry in many diffe

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

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

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

244 P2X receptor channels are ATP-activated cation channels that serve important roles in sensory si

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 tivated anion channels (TMEM16A, TMEM16B), a cation channel (TMEM16F) and proteins with unclear funct

249 l-conductance calcium-activated nonselective cation channel, TMEM16F, linked to Scott syndrome.

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

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

252 The nonselective cation channel transient receptor potential canonical (T

253 The monovalent cation channel transient receptor potential melastatin (

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

255 ly mediated by the activation of nociceptive cation channels transient receptor potential ankyrin 1 a

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

257 ceptors are mediated by two Ca(2+) permeable cation channels, transient receptor potential (TRP) and

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

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

260 t low temperatures activate a cold-sensitive cation channel, TRPA-1, which triggers a complex signali

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

262 Transient receptor potential "canonical" cation channels (TRPC) are involved in many cellular act

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

264 (2+) influx mediated by the mechanosensitive cation channel TRPC6, which activates host calpain that

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

266 ubpopulation expresses the calcium activated cation channel TRPM5 (transient receptor potential chann

267 The nociceptive cation channel TRPV1 (transient receptor potential vanil

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

269 sensors of the transient receptor potential cation channel TRPV1.

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

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

272 In the case of the bare cation channel, two distinct reaction pathways were foun

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

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

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

276 Blocking signaling through mechanosensing cation channels using GsMTx4 negated the ability of neur

277 The transient receptor potential cation channel V1 (TRPV1) is also expressed in primary s

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

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

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

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

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

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

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

285 The transient receptor potential-like (TRPL) cation channel was a direct target for camphor in gustat

286 nts of the non-selective Bacillus cereus NaK cation channel we examine are all selective for K(+) ove

287 sors of phototactic algae act as light-gated cation channels when expressed in animal cells.

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

289 l pathogens for genes encoding homologues of cation channels, which are prominent drug targets.

290 Here, we ask whether non-selective cation channels, which share an overall structure and si

291 yrin 1 (TRPA1) channel is a Ca(2+)-permeable cation channel whose activation results from a complex s

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

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

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

295 TRPM7 encodes a Ca2+-permeable nonselective cation channel with kinase activity.

296 l vanilloid 4 (TRPV4) channels--nonselective cation channels with considerable Ca(2+) conductance--ha

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