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

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

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

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

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

5 cooperation with the orthologue of an R-type voltage-gated calcium channel.

6 ggests that BsYetJ/TMBIM6 is a pH-dependent, voltage-gated calcium channel.

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

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

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

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

11 changes that led to abnormal inactivation of voltage-gated calcium channels.

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

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

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

15 r Ca(2+) levels due to Ca(2+) influx through voltage-gated calcium channels.

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

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

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

19 tial segment was only partially dependent on voltage-gated calcium channels.

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

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

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

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

24 nism that confers adrenergic modulation upon voltage-gated calcium channels.

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

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

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

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

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

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

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

32 by which beta-adrenergic agonists stimulate voltage-gated calcium channels.

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

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

35 utoregulatory mechanism in Ca(V)1 and Ca(V)2 voltage-gated calcium channels.

36 hanisms and enter the cytosol mostly through voltage-gated calcium channels.

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

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

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

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

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

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

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

44 study the effect of LITAF on Cav1.2 (L-type voltage-gated calcium channel 1.2) channel expression, s

45 by beta-adrenergic augmentation of Ca(V)1.2 voltage-gated calcium channels(1-4).

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

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

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

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

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

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

52 n of all deletions in the significant set of voltage-gated calcium channels among CNVs called from bo

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

54 e distribution of trajectories recorded from voltage gated calcium channels and phospholipid anchored

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

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

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

58 ential (AP) waveform controls the opening of voltage-gated calcium channels and contributes to the dr

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

60 Deconditioning was mediated by L-type voltage-gated calcium channels and is consistent with co

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

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

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

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

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

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

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

72 ponses in each compartment were dependent on voltage-gated calcium channels, and somatic and nuclear

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

74 ies in the serum (21.30 nmol/L) and P/Q-type voltage-gated calcium channel antibodies (220 pmol/L).

75 Voltage-gated calcium channels are activated by depolari

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

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

78 Voltage-gated calcium channels are essential players in

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

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

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

82 Voltage-gated calcium channels are multiprotein complexe

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

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

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

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

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

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

89 The alpha(2)delta-1 subunit of voltage-gated calcium channels binds to gabapentin and p

90 Voltage-gated calcium-channel blockade prevents iron ent

91 The voltage-gated calcium channel blocker cadmium chloride d

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

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

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

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

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

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

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

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

100 We have studied the regulation of voltage-gated calcium channels by MDIMP, which disrupts

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

102 is a psychiatric risk gene that encodes the voltage-gated calcium channel Ca(V)1.2.

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

104 forming subunit of the pre-synaptic neuronal voltage-gated calcium channel Ca(v)2.2/N-type, crucial f

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

106 report the presence of a splice isoform of a voltage-gated calcium channel (Ca(V)1.3) in the pigeon i

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

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

109 tors juxtaposed with presynaptic ribbons and voltage-gated calcium channels (Ca(V)1.3).

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

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

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

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

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

115 ll biology in bystander neurons, as were the voltage-gated calcium channel Cacophony (Cac) and the mi

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

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

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

119 Voltage-gated calcium channels can coassemble with auxil

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

121 Mutations in pre-synaptic voltage-gated calcium channels can lead to familial hemi

122 of known renal autoregulation mechanisms and voltage-gated calcium channels can maintain overall rena

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

138 show that FMRP binds the mRNA of the R-type voltage-gated calcium channel Cav2.3 in mouse brain syna

139 rves as a key translational regulator of the voltage-gated calcium channel Cav2.3 under basal conditi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

154 (2020) demonstrate that Ca(v)2-type voltage-gated calcium channels do not mediate presynapti

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

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

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

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

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

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

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

162 The dominant role of Ca(V)2 voltage-gated calcium channels for driving neurotransmit

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

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

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

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

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

168 iomyocytes demonstrated that the anti-L-type voltage-gated calcium channel immunoglobulin G purified

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

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

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

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

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

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

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

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

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

178 , there is a dose-dependent effect of L-type voltage gated calcium channel inhibitors on synchronous

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

196 y, we found that BIN1 interacted with L-type voltage-gated calcium channels (LVGCCs) and that BIN1-LV

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

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

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

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

201 rom Nematostella vectensis use a specialized voltage-gated calcium channel (nCa(V)) to distinguish sa

202 e, we found that the alpha2delta2 subunit of voltage-gated calcium channels negatively regulates axon

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

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

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

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

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

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

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

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

211 synapses), the glutamate transporter, and a voltage-gated calcium channel, or if ASP cells lacked Sy

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

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

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

215 In contrast, blocking the T-type or L-type voltage-gated calcium channel promoted the spontaneous c

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

217 Presynaptic voltage-gated calcium channels provide calcium for synap

218 Presynaptic alpha(2)delta subunits of voltage-gated calcium channels regulate channel abundanc

219 psychiatric disorders.SIGNIFICANCE STATEMENT Voltage-gated calcium channels regulate important neuron

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

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

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

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

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

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

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

227 Gene mutations in L-type voltage gated calcium channel subunit genes are strongly

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

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

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

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

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

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

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

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

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

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

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

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

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

241 glycosylation including glutamate receptors, voltage-gated calcium channels, the dopamine D2 receptor

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

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

244 hibition: first, the action of Gbetagamma on voltage-gated calcium channels to inhibit calcium influx

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

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

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

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

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

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

251 tracellular Ca(2+) levels through the T-type voltage-gated calcium channel (VGCC) and mobilization of

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

253 Genetic polymorphisms of the L-type voltage-gated calcium channel (VGCC) are associated with

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

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

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

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

258 bicistronic expression may be common to the voltage-gated calcium channel (VGCC) gene family and may

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

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

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

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

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

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

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

266 ar calcium involves purinergic receptors and voltage-gated calcium channels (VGCC).

267 Voltage gated calcium channels (VGCCs) are essential to

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

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

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

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

272 ACh release is supported by P/Q- and N-type voltage-gated calcium channels (VGCCs) and negatively re

273 For example, presynaptic voltage-gated calcium channels (VGCCs) and postsynaptic

274 that pharmacological manipulation of L-type voltage-gated calcium channels (VGCCs) and purinoceptors

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

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

277 Here, we show that voltage-gated calcium channels (VGCCs) are critical for

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

279 Voltage-gated calcium channels (VGCCs) convert electrica

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

281 Voltage-gated calcium channels (VGCCs) regulate hormone

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

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

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

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

286 sfer depend on the molecular organization of voltage-gated calcium channels (VGCCs) within the presyn

287 ade of NMDA-type glutamate receptors but not voltage-gated calcium channels (VGCCs), and can also be

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

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

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

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

292 te calcium current (I (Ca)) through neuronal voltage-gated calcium channels (VGCCs).

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

294 ulation were mediated, in part, by dendritic voltage-gated calcium channels (VGCCs): pharmacological

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

296 tibody against the pore domain of the L-type voltage-gated calcium channel was consistently identifie

297 Voltage gated calcium channels were predominantly of the

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