ライフサイエンスコーパス: voltage-gated calcium channel

1 acket (stj), an alpha(2)delta subunit of the voltage-gated calcium channel.

2 between the sigma-1 receptor and the L-type voltage-gated calcium channel.

3 g at sites in a transcript encoding a muscle voltage-gated calcium channel.

4 gnal from the RyR1 facilitates gating of the voltage-gated calcium channel.

5 scription of these proteins as regulators of voltage gated calcium channels.

6 This is the case for voltage-gated calcium channels.

7 receptors and subsequently inhibiting CaV2.2 voltage-gated calcium channels.

8 ned, and it was inhibited by blocking L-type voltage-gated calcium channels.

9 ane proteins that includes gamma-subunits of voltage-gated calcium channels.

10 epends on the activation of T- and/or L-type voltage-gated calcium channels.

11 aracterized ICK-motif peptidic antagonist of voltage-gated calcium channels.

12 e proteins that can bind and modulate L-type voltage-gated calcium channels.

13 directly influencing the activity of L-type voltage-gated calcium channels.

14 etinal sensitivity through the modulation of voltage-gated calcium channels.

15 t chloride-mediated depolarization activates voltage-gated calcium channels.

16 , and this could be independent of ASICs and voltage-gated calcium channels.

17 icle fusion, also interacts with presynaptic voltage-gated calcium channels.

18 well known inhibition of Ca2+ entry through voltage-gated calcium channels.

19 (alpha(2)-delta) subunits (Type 1 and 2) of voltage-gated calcium channels.

20 were dependent on activation of postsynaptic voltage-gated calcium channels.

21 encoding the alpha(1)2.1 subunit of Ca(v)2.1 voltage-gated calcium channels.

22 usively by calcium entering through P/Q-type voltage-gated calcium channels.

23 rms of LTP also require activation of L-type voltage-gated calcium channels.

24 protection requires the activation of L-type voltage-gated calcium channels.

25 the functional effects that are mediated by voltage-gated calcium channels.

26 um signal arising from calcium entry through voltage-gated calcium channels.

27 neity, function and subunit association with voltage-gated calcium channels.

28 seases, both genetic and acquired, involving voltage-gated calcium channels.

29 lta2 modulates the abundance and function of voltage-gated calcium channels.

30 s in a calcium-dependent manner and binds to voltage-gated calcium channels.

31 mechanisms of direct G protein inhibition of voltage-gated calcium channels.

32 the transient opening of different types of voltage-gated calcium channels.

33 s, including subunits of GABAA receptors and voltage-gated calcium channels.

34 kisspeptin neurons via a mechanism involving voltage-gated calcium channels.

35 ependent upon apoptotic calcium release from voltage-gated calcium channels.

36 mutated hippocalcin, mostly driven by N-type voltage-gated calcium channels.

37 ta3 modulates the expression and function of voltage-gated calcium channels.

38 become widely used as an inhibitor of Cav2.3 voltage-gated calcium channels.

39 he spinal dorsal horn, via the inhibition of voltage-gated calcium channels.

40 synapse formation, dendritic morphology, and voltage-gated calcium channels.

41 L-type Ca(2+) currents conducted by voltage-gated calcium channel 1.2 (CaV1.2) initiate exci

42 vern this unreliability include a paucity of voltage-gated calcium channels, a low probability of cal

43 e omega-hexatoxin-Hv1a (Hv1a) targets insect voltage-gated calcium channels, acting directly at sites

44 e been demonstrated, including inhibition of voltage-gated calcium channel activity and inhibition of

45 presynaptic action potentials (APs) activate voltage-gated calcium channels, allowing calcium to ente

46 Inborn errors of Cacna1a, the P/Q-type voltage-gated calcium channel alpha subunit gene, expres

47 emperature-sensitive paralytic mutant of the voltage-gated calcium channel alpha1 subunit gene, cacop

48 phila, also known as nightblind A, encodes a voltage-gated calcium-channel alpha1 subunit homologous

49 ss typical presynaptic proteins, including a voltage-gated calcium channel (alpha1A), neural cell adh

50 criptional regulator of photoreceptor L-type voltage-gated calcium channel alpha1C subunit (L-VGCCalp

51 nd 1 altering Ile770) in CACNA1D, encoding a voltage-gated calcium channel, among 43 APAs without mut

52 nce suggests that tir-1 acts downstream of a voltage-gated calcium channel and CaMKII (UNC-43) to reg

53 y involving depolarization activating L-type voltage-gated calcium channels and a Ca-dependent kinase

54 GABAB receptors (GABAB Rs) suppress voltage-gated calcium channels and activate G-protein co

55 covers SERCA-dependent mechanisms regulating voltage-gated calcium channels and calcium-activated pot

56 P/Q-type voltage-gated calcium channels and calcium-activated pot

57 frequencies primarily by the interactions of voltage-gated calcium channels and calcium-activated pot

58 terns are regulated by the interplay between voltage-gated calcium channels and calcium-sensitive pot

59 nje cells express a high density of P/Q-type voltage-gated calcium channels and fire dendritic calciu

60 gh affinity to the alpha(2)-delta subunit of voltage-gated calcium channels and is a substrate of the

61 nter cells via nontraditional routes such as voltage-gated calcium channels and N-methyl-d-aspartate

62 in synaptic function, and it is dependent on voltage-gated calcium channels and presynaptic calcium s

63 gh N-methyl-D-aspartate receptors and L-type voltage-gated calcium channels and requires the activity

64 re mediated by calcium influx through L-type voltage-gated calcium channels and ryanodine receptor-in

65 y was mediated by Ca2+ flux through NMDA and voltage-gated calcium channels and was lost within 48 hr

66 dies (most commonly targeting P/Q- or N-type voltage-gated calcium channels); and 15 patients, for an

67 or temporally patterned electrical activity, voltage-gated calcium channels, and CaMKII in modulating

68 equires activation of NMDA receptors, L-type voltage-gated calcium channels, and dendritic spikes.

69 ve alternative splicing, much like the other voltage-gated calcium channels, and employed the transcr

70 ragile X mental retardation protein complex, voltage-gated calcium channels, and genes implicated in

71 pha2delta proteins are auxiliary subunits of voltage-gated calcium channels, and influence their traf

72 of ionotropic glutamate receptors and L-type voltage-gated calcium channels, and is dependent on down

73 transients are mediated primarily by L-type voltage-gated calcium channels, and silencing them with

74 Purkinje neurons express several classes of voltage-gated calcium channels, and the P/Q- and T-type

75 , which causes the depolarization, activates voltage-gated calcium channels, and ultimately elevates

76 tracochlear infusion of verapamil, an L-type voltage-gated calcium channel antagonist.

77 Voltage-gated calcium channels are activated by depolari

78 CaV1 and CaV2 voltage-gated calcium channels are associated with beta

79 These voltage-gated calcium channels are composed of a primary

80 found that protein kinase A (PKA) and L-type voltage-gated calcium channels are crucial for the expre

81 Voltage-gated calcium channels are essential players in

82 The auxiliary alpha2delta subunits of voltage-gated calcium channels are extracellular membran

83 Voltage-gated calcium channels are important mediators o

84 The alpha2delta subunits of voltage-gated calcium channels are important modulatory

85 The accessory alpha(2)delta subunits of voltage-gated calcium channels are membrane-anchored pro

86 Voltage-gated calcium channels are multiprotein complexe

87 Although several prototypical voltage-gated calcium channels are present in spermatozo

88 P/Q-type voltage-gated calcium channels are regulated, in part, t

89 rminal, voltage-gated potassium channels and voltage-gated calcium channels are subtly altered in gen

90 ults identify an extracellular ligand of the voltage-gated calcium channel as well as a new laminin r

91 ich includes oscillatory calcium signals via voltage-gated calcium channels as a key component.

92 ated almost entirely through Cav2.2 (N-type) voltage-gated calcium channels as blocking these channel

93 enes and their implications, with a focus on voltage-gated calcium channels as part of the disease pr

94 tors for thymoma (as recognized for neuronal voltage-gated calcium channel autoantibodies).

95 c neuronal acetylcholine receptor and N-type voltage-gated calcium channel autoantibodies.

96 Voltage-gated calcium-channel blockade prevents iron ent

97 The voltage-gated calcium channel blocker cadmium chloride d

98 ese GABAergic neurons was not altered by the voltage-gated calcium channel blocker cadmium chloride t

99 in glutamatergic mEPSC was unaltered by the voltage-gated calcium channel blocker cadmium, and was a

100 Although the L-type voltage-gated calcium channel blocker nifedipine did not

101 xtual fear memory reactivation by the L-type voltage-gated calcium channel blocker nimodipine interfe

102 ens were blocked by targeted delivery of the voltage-gated calcium channel blocker omega-conotoxin GV

103 ven when the medium contains nitrendipine, a voltage-gated calcium channel blocker, but fails to occu

104 ch was blocked by SOC inhibitors, but not by voltage-gated calcium channel blockers.

105 This increase was dependent on voltage-gated calcium channels but persisted even after

106 ent binders of the alpha(2)-delta subunit of voltage-gated calcium channels, but did not interact wit

107 Kenyan children, levels of antibodies to the voltage-gated calcium channels, but not to other ion cha

108 desensitized the inhibition of postsynaptic voltage-gated calcium channels by activation of GABA(B)R

109 Inhibition of presynaptic voltage-gated calcium channels by direct G-protein betag

110 Inhibition of voltage-gated calcium channels by postsynaptic A1Rs also

111 (CaM) with the IQ-recognition motif from the voltage-gated calcium channel Ca(v)1.2 (IQ), which adopt

112 The voltage-gated calcium channel Ca(v)2.2 (N-type calcium c

113 We identified the T-type voltage-gated calcium channel Ca(v)3.3 as binding to bot

114 gnals produced by pH-sensitive activation of voltage-gated calcium channels (Ca channels) in photorec

115 Voltage-gated calcium channels (Ca(v)) 2.2 currents are

116 P/Q-type Ca(2+) currents through presynaptic voltage-gated calcium channels (Ca(V)2.1) by binding of

117 P/Q-type voltage-gated calcium channels (Ca(v)2.1) play critical

118 Interactions between voltage-gated calcium channels (Ca(V)s) and calmodulin (

119 Voltage-gated calcium channels (Ca(V)s) govern muscle co

120 Precise regulation of N-type (Ca(V)2.2) voltage-gated calcium channels (Ca-channels) controls ma

121 Leaner mice with a mutation in the P/Q-type voltage-gated calcium channel, Cacna1a, develop cerebell

122 function, we show that reduced levels of the voltage-gated calcium channel, cacophony, mediate some o

123 rsed by restoring the expression levels of a voltage-gated calcium channel, cacophony.

124 , single-channel current amplitude of native voltage-gated calcium channels can be resolved accuratel

125 Voltage-gated calcium channels can coassemble with auxil

126 These findings provide evidence that voltage-gated calcium channels can directly activate tra

127 e pore-forming alpha1A subunit of the CaV2.1 voltage-gated calcium channel, cause a number of human n

128 lease-activated calcium modulator 1 but also voltage-gated calcium channel (Cav) 1 channels.

129 Voltage-gated calcium channel (Cav) beta subunits are au

130 Comparison with mammalian voltage-gated calcium channel (CaV) selectivity filters,

131 The transcripts of L-type voltage-gated calcium channels (CaV) 1.3 undergo extensi

132 In excitable cells, voltage-gated calcium channels (Cav) are the major route

133 hysiological processes, and it is known that voltage-gated calcium channels (Cav) mediate calcium inf

134 FMRP was shown to directly interact with the voltage-gated calcium channel, Cav 2.2, and reduce its t

135 e pore-forming alpha1 subunit of the cardiac voltage-gated calcium channel Cav1.2 at Ser1928, suggest

136 Here we show that the voltage-gated calcium channel CaV1.3 and the big conduct

137 Mutations in the skeletal muscle voltage-gated calcium channel (CaV1.1) have been associa

138 ional and mechanical coupling between L-type voltage-gated calcium channels (CaV1.1) and the ryanodin

139 increases expression and activity of L-type, voltage-gated calcium channels (Cav1.2) in coronary arte

140 encoding the alpha1A subunit of the P/Q-type voltage-gated calcium channel Cav2.1.

141 des the pore-forming subunit of the neuronal voltage-gated calcium channel Cav2.1.

142 CaVbeta subunits interact with the voltage-gated calcium channel CaV2.2 on a site in the in

143 ion in the CACNA1B gene, coding for neuronal voltage-gated calcium channels CaV2.2.

144 The use of N-type voltage-gated calcium channel (CaV2.2) blockers to treat

145 CACNA1H encodes a voltage-gated calcium channel (CaV3.2) expressed in adre

146 thesis that TSP4 activates its receptor, the voltage-gated calcium channel Cavalpha2delta1 subunit (C

147 rted CACNA1C (alpha 1C subunit of the L-type voltage-gated calcium channel; combined P = 7.0 x 10(-8)

148 ese resolutions) into the heteromeric L-type voltage-gated calcium channel complex volume reveals mul

149 Voltage-gated calcium channels conduct Ca(2+) ions in re

150 Until recently we held the simple view that voltage-gated calcium channels consisted of an alpha1 su

151 n favour of a selective inhibitory effect on voltage-gated calcium channels containing the alpha2delt

152 electrical activity--mediated through L-type voltage-gated calcium channels--could suppress axon grow

153 Voltage-gated calcium channels couple changes in membran

154 Here, we recorded the voltage-gated calcium channel current in nucleated patch

155 ay a crucial role in allodynia by modulating voltage-gated calcium channel currents (ICa(V)).

156 synaptic strength was not due to changes in voltage-gated calcium channel currents or activation kin

157 requires a physical interaction between the voltage-gated calcium channel dihydropyridine receptor (

158 al muscle excitation-contraction coupling, a voltage-gated calcium channel directly activates opening

159 that produce delayed inactivation of Cav1.2 voltage-gated calcium channels during cellular action po

160 tion via GABA type A receptor activation and voltage-gated calcium channels during early postnatal de

161 enerin/ENaC sodium channel MEC-4, the L-type voltage-gated calcium channel EGL-19, and the Ca/calmodu

162 H caused a reduction in cacophony, a Type II voltage-gated calcium channel, expression and that genet

163 model takes into account calcium influx via voltage-gated calcium channels, extrusion through the ce

164 f four members of the sperm-specific CATSPER voltage-gated calcium channel family known to be essenti

165 n, for a member of the low voltage-activated voltage-gated calcium channel family, CaV3.1, a T-type c

166 CATSPER1 is a voltage-gated calcium channel found exclusively in the p

167 Calcium entry through voltage-gated calcium channels has widespread cellular e

168 CACNA1C gene (alpha-1C subunit of the L-type voltage-gated calcium channel) has been identified as a

169 L-type voltage gated calcium channels have an important role in

170 ls within astrocytes is controversial, these voltage-gated calcium channels have been linked to calci

171 Neuronal voltage-gated calcium channels have evolved as one of th

172 knowledge, in vivo phosphorylation map of a voltage-gated calcium channel in a mammalian brain.

173 In order to assess the role of L-type voltage-gated calcium channels in electrical stimulation

174 We measured CaV1 voltage-gated calcium channels in ependymal cells, but t

175 pathway stimulated by the MOR that inhibits voltage-gated calcium channels in isolated terminals fro

176 Leptin inhibits voltage-gated calcium channels in LH neurons via the act

177 receptor 2 (mGluR2) signaling, which acts on voltage-gated calcium channels in SACs, selectively rest

178 sential for estimating numbers of functional voltage-gated calcium channels in the membrane and the s

179 ell into the IQ domain portion of the Cav1.2 voltage-gated calcium channel, indicating a potential ro

180 ons in the ryanodine receptor but not in the voltage-gated calcium channel, indicating that these phe

181 dephosphorylation was prevented by blocking voltage-gated calcium channels, indicating that distinct

182 stic view that second messenger signaling to voltage-gated calcium channels involved mainly phosphory

183 nding protein 1 (CaBP1) to the CaV1 (L-type) voltage-gated calcium channel IQ domain endows the chann

184 The voltage-gated calcium channel is composed of a pore-form

185 The Ca(V)1.4 voltage-gated calcium channel is predominantly expressed

186 We found that activation of L-type voltage-gated calcium channels is critical for alpha-cel

187 In summary, each vertebrate gene family for voltage-gated calcium channels is represented by a singl

188 ce that the alpha(2)-delta Type 1 subunit of voltage-gated calcium channels is the major binding prot

189 The alpha2delta-1 subunit of voltage-gated calcium channels is upregulated after sens

190 The L-type voltage-gated calcium channels (L-VGCCs) are activated u

191 To determine whether L-type voltage-gated calcium channels (L-VGCCs) are required fo

192 L-type voltage-gated calcium channels (L-VGCCs) in the basolate

193 onin norepinephrine reuptake inhibitors, and voltage-gated calcium channel ligands in the treatment o

194 N-type voltage-gated calcium channels localize to presynaptic n

195 als across cell junctions and in stimulating voltage-gated calcium channels located in T tubules.

196 a C-terminal fragment of Ca(V)1.2, an L-type voltage-gated calcium channel (LTC), translocates to the

197 An increase in L-type voltage-gated calcium channel (LTCC) current is a promin

198 L-type voltage-gated calcium channels (LTCCs) are implicated in

199 L-type voltage-gated calcium channels (LTCs) may control neuron

200 idence has led to the hypothesis that L-type voltage-gated calcium channels (LVGCCs) play a role in c

201 It is suggested that voltage-gated calcium channels make a significant contri

202 fects and suggest the cAMP pathway or L-type voltage-gated calcium channels may be viable targets for

203 Positioning releasable vesicles near voltage-gated calcium channels may ensure transmitter re

204 which stimulates adenylyl cyclase and L-type voltage-gated calcium channels, may be one intracellular

205 Voltage-gated calcium channels mediate excitationcontrac

206 e eliminated by dihydropyridine block of the voltage-gated calcium channels of the hair cell.

207 Conversely, inhibition of voltage-gated calcium channels or calcium release from i

208 (AHPs) that were insensitive to blockade of voltage-gated calcium channels or chelation of intracell

209 rise in intracellular calcium either through voltage-gated calcium channels or from intracellular sto

210 Tp1a had no effect on human voltage-gated calcium channels or nicotinic acetylcholin

211 were not dependent on calcium influx through voltage-gated calcium channels or on calcium mobilizatio

212 Denatonium had no direct effect on voltage-gated calcium channels or on cyclic AMP levels.

213 GluR5 agonists did not require activation of voltage-gated calcium channels or presynaptic GABA(B) re

214 ium influx but did not require activation of voltage-gated calcium channels or presynaptic NMDA recep

215 Blocking voltage-gated calcium channels or ryanodine receptors (R

216 ngs by reducing Ca(2+) calcium entry through voltage-gated calcium channels or, as is the case at amp

217 mium (100 microM, a nonselective blocker for voltage-gated calcium channels), or a medium containing

218 abolished by blockade of alpha4beta2 nAChRs, voltage-gated calcium channels, or intracellular calcium

219 Voltage-gated calcium channels play a central role in re

220 Voltage-gated calcium channels play a key role in chemic

221 CaV1.2 voltage-gated calcium channels play critical roles in th

222 The Ca(V)2 family of voltage-gated calcium channels, present in presynaptic n

223 as used to quantify postsynaptic density and voltage-gated calcium channel protein expression.

224 Presynaptic voltage-gated calcium channels provide calcium for synap

225 The beta subunits of voltage-gated calcium channels regulate surface expressi

226 The Ca(V)beta subunits of voltage-gated calcium channels regulate the trafficking

227 The CaVbeta subunits of voltage-gated calcium channels regulate these channels i

228 regulatory alpha2delta-subunits of mammalian voltage-gated calcium channels, respectively.

229 h affinity for the alpha(2)-delta subunit of voltage-gated calcium channels, several novel beta-amino

230 Most secretory cells possess voltage-gated calcium channels, share homologues of the

231 ive in G(q) and G(o) signaling, or in N-type voltage-gated calcium channels, showed migration phenoty

232 CaV1.1e is the voltage-gated calcium channel splice variant of embryoni

233 e disorder in animal models suggest that the voltage-gated calcium channel subtype Ca(V)1.3 has a rol

234 The CACNA1A gene, encoding the voltage-gated calcium channel subunit alpha1A, is involv

235 Neuron, Tedeschi et al. (2016) describe the voltage-gated calcium channel subunit alpha2delta2 as a

236 ched comparison subjects as well as aberrant voltage-gated calcium channel subunit protein expression

237 The effect of increased voltage-gated calcium channel subunit protein expression

238 mechanical allodynia by regulating auxiliary voltage-gated calcium channel subunits alpha2delta-1 and

239 es between voltage-gated sodium channels and voltage-gated calcium channels suggest that the structur

240 It has been established that Ca(V)3.2 T-type voltage-gated calcium channels (T-channels) play a key r

241 ng human CaV3.3 alpha1 subunit, a subtype of voltage-gated calcium channel that contributes to T-type

242 g the Ca(v)2.1alpha1 subunit of the P/Q-type voltage-gated calcium channel that result in an overall

243 alpha2delta-1 is an auxiliary subunit of voltage-gated calcium channels that affects calcium-chan

244 he mechanism of dopamine activation requires voltage-gated calcium channels that are also present at

245 e-2 (EA2) is caused by mutations in P/Q-type voltage-gated calcium channels that are expressed at hig

246 n isolated by blockade of NMDA receptors and voltage-gated calcium channels, the absence of both tran

247 For all the subtypes of voltage-gated calcium channel, their gating properties a

248 did treatment with nicardipine, which blocks voltage-gated calcium channels through which zinc enters

249 y fiber terminals leverage distinct types of voltage-gated calcium channels to mediate short-term fac

250 -30 acts with muscle-expressed EGL-19 L-type voltage-gated calcium channels to promote vulva developm

251 veral factors modulate the susceptibility of voltage-gated calcium channels to this form of inactivat

252 les, and reduced fusion triggered by opening voltage-gated calcium channels under voltage clamp, with

253 mal motile cilia is not tightly regulated by voltage-gated calcium channels, unlike that of well-stud

254 depend on NMDA receptors (nmdaLTP) or L-type voltage-gated calcium channels (vdccLTP).

255 tional flat surfaces may exhibit exaggerated voltage gated calcium channel (VGCC) functionality.

256 ptor potential vanilloid (TRPV) 4 and L-type voltage-gated calcium channel (VGCC) and an increase in

257 We evaluated the effect of L-type voltage-gated calcium channel (VGCC) and NMDA receptor (

258 lves two major calcium-binding proteins, the voltage-gated calcium channel (VGCC) and the vesicular p

259 he baldness associated with mutations in the voltage-gated calcium channel (VGCC) Cav1.2 underlying T

260 al for exocytosis, also controls presynaptic voltage-gated calcium channel (VGCC) function dictating

261 ed we report that HFS persistently depresses voltage-gated calcium channel (VGCC) function in Fil ter

262 f cell types has shown that Rem2 can inhibit voltage-gated calcium channel (VGCC) function, while stu

263 he final coding exon (exon 47) of the Cav2.1 voltage-gated calcium channel (VGCC) gene produces two m

264 P/Q-type voltage-gated calcium channel (VGCC) puncta colocalized

265 -dimensional structure of the cardiac L-type voltage-gated calcium channel (VGCC) purified from bovin

266 located in an intronic region of the L-type voltage-gated calcium channel (VGCC) subunit gene CACNA1

267 ac encodes an alpha1 subunit of a Drosophila voltage-gated calcium channel (VGCC) that is required fo

268 emphasized the importance of the T-type low-voltage-gated calcium channels (VGCC) in different cance

269 Calcium influx through voltage-gated calcium channels (VGCC) is a key step in n

270 ddition to Gbetagamma-mediated modulation of voltage-gated calcium channels (VGCC), inhibition can al

271 Voltage gated calcium channels (VGCCs) are essential to

272 : N-methyl-d-aspartic acid (NMDA) receptors, voltage gated calcium channels (VGCCs), neuronal nitric

273 Voltage-gated calcium channels (VGCCs) allow for rapid c

274 allow somatic action potentials to activate voltage-gated calcium channels (VGCCs) along the entire

275 fied their ability to activate L- and N-type voltage-gated calcium channels (VGCCs) and delineated th

276 uced calcium influx through L-, P/Q-, N-type voltage-gated calcium channels (VGCCs) and NMDA receptor

277 ised [Ca(2+)](i), mediated by influx through voltage-gated calcium channels (VGCCs) and release from

278 resynaptic activity, postsynaptic potential, voltage-gated calcium channels (VGCCs) and UNC-43, the C

279 Voltage-gated calcium channels (VGCCs) are key regulator

280 Voltage-gated calcium channels (VGCCs) convert electrica

281 , as observed at all other synapses studied, voltage-gated calcium channels (VGCCs) couple membrane d

282 Voltage-gated calcium channels (VGCCs) play an essential

283 beta subunits of voltage-gated calcium channels (VGCCs) regulate channel

284 Voltage-gated calcium channels (VGCCs) regulate hormone

285 First, a pharmacological screen of voltage-gated calcium channels (VGCCs) showed that AIS r

286 tivity-dependent potentiation of presynaptic voltage-gated calcium channels (VGCCs) underlies 3,4-dia

287 Reducing calcium influx by blocking R-type voltage-gated calcium channels (VGCCs) with Ni(2+), or b

288 ere, we show that chronic blockade of L-type voltage-gated calcium channels (VGCCs) with nifedipine d

289 vity depend critically on proper function of voltage-gated calcium channels (VGCCs), whose activity m

290 synapse is supported by both P/Q- and N-type voltage-gated calcium channels (VGCCs).

291 driven by Ca(2+) influx through active zone voltage-gated calcium channels (VGCCs).

292 taste cells to cause calcium influx through voltage-gated calcium channels (VGCCs).

293 erties, density, and the spatial location of voltage-gated calcium channels (VGCCs).

294 s depend on the presence of certain types of voltage-gated calcium channels (VGCCs).

295 In contrast, whereas CP55,940 inhibited voltage-gated calcium channels via CB(2) receptor activa

296 Voltage gated calcium channels were predominantly of the

297 Although voltage-gated calcium channels were expressed throughout

298 Five voltage-gated calcium channels were identified: alpha1A,

299 thus suggest a selective coupling of N-type voltage-gated calcium channels with calcium-activated po

300 ts the identity and cellular distribution of voltage-gated calcium channels within dopaminergic neuro