ライフサイエンスコーパス: voltage-sensitive

1 ntravenously administered contrast agent, is voltage-sensitive.

2 Channelrhodopsin2 (ChR2), is both light- and voltage-sensitive.

3 n of an inositol lipid 5-phosphatase or by a voltage-sensitive 5-phosphatase (VSP) suppresses Ca(V)1.

4 age imaging in intact neurohypophysis with a voltage sensitive absorbance dye showed that T-1032 redu

5 VSP, we generated chimeric proteins that are voltage-sensitive and display PTEN-like enzymatic activi

6 probes is a nonlinear optical signal that is voltage-sensitive and the basis of a sensitive method fo

7 Both channels are voltage sensitive, and temperature and ligands modulate

8 holinergic signal transduction itself is not voltage-sensitive, but that depolarization facilitates r

9 2-photon glutamate uncaging, to examine how voltage-sensitive Ca channels (VSCCs) and ionotropic glu

10 in acute mouse hippocampal slices, CaV(2.3) voltage-sensitive Ca channels (VSCCs) are found selectiv

11 usly observed age-related increase in L-type voltage-sensitive Ca(2+) channel (L-VSCC) density in hip

12 Voltage-sensitive Ca(2+) channels (VSCCs) are often hete

13 axonal depolarization sufficient to activate voltage-sensitive Ca(2+) channels (VSCCs).

14 depolarization evoked Ca(2+) influx through voltage-sensitive Ca(2+) channels and facilitated spike-

15 yperpolarization will limit Ca(2+) entry via voltage-sensitive Ca(2+) channels and represents a novel

16 a(2+) influx through glutamate receptors and voltage-sensitive Ca(2+) channels located on spines depe

17 ng axonal potential was insufficient to open voltage-sensitive Ca(2+) channels.

18 ors, additional Ca(2+) influx occurs through voltage-sensitive Ca(2+) channels.

19 DISC is eliminated by a mixture of voltage-sensitive Ca2+ channel blockers and is mimicked

20 The conformational state of the voltage-sensitive Ca2+ channel is altered under these di

21 Voltage-sensitive Ca2+ channels (VSCCs) constitute a maj

22 tes of divalent cation entry, NMDA channels, voltage-sensitive Ca2+ channels (VSCCs), and Ca2+-permea

23 ncreases the open probability of sarcolemmal voltage-sensitive Ca2+ channels and flux of Ca2+ into th

24 Voltage-sensitive Ca2+ channels are a large family of re

25 sequential activation of NMDARs followed by voltage-sensitive Ca2+ channels within dendritic spines.

26 currents (VGKCs) and a possible increase in voltage-sensitive Ca2+ currents (I(Ca)).

27 he sperm tail by an alkalinization-activated voltage-sensitive Ca2+-selective current (ICatSper).

28 s a control experiment, nifedipine, a L-type voltage sensitive calcium channel (L-VSCC) inhibitor was

29 d by ligands to the alpha(2)delta subunit of voltage sensitive calcium channels (PD-0332334 and PD-02

30 lular calcium transients initiated by L-type voltage-sensitive calcium channel (VSCC) activation.

31 ed from activation of NMDA receptors, L-type voltage-sensitive calcium channels (VSCC) and the revers

32 BA(B)Rs directly inhibit several subtypes of voltage-sensitive calcium channels (VSCCs) in both spine

33 that PACAP-27-induced calcium influx through voltage-sensitive calcium channels (VSCCs), together wit

34 dritic growth is attenuated by inhibitors of voltage-sensitive calcium channels and by dominant negat

35 ersisted despite pharmacological blockade of voltage-sensitive calcium channels and depletion of intr

36 (formerly SNX-111) selectively blocks N-type voltage-sensitive calcium channels and may be effective

37 Calcium influx via voltage-sensitive calcium channels and NMDA receptors co

38 te that dynorphin induces calcium influx via voltage-sensitive calcium channels in sensory neurons by

39 Influx of calcium, mediated either by L-type voltage-sensitive calcium channels or glutamate receptor

40 through the presynaptic compartment close to voltage-sensitive calcium channels rather than changes i

41 Ca(2+) influx through NMDA receptor or voltage-sensitive calcium channels resulted in a transie

42 cked by inhibition of calcium influx through voltage-sensitive calcium channels, (3) was calcineurin

43 ; the newly activated mGluRs in turn inhibit voltage-sensitive calcium channels, leading to a decreas

44 cally activated by NMDA receptors and L-type voltage-sensitive calcium channels, presumably by nanodo

45 absence of Na+, to prevent the activation of voltage-sensitive calcium channels, the [Ca2+]i changes

46 KATP channels, with the subsequent gating of voltage-sensitive calcium channels.

47 e balance of two calcium sources, NMDARs and voltage-sensitive calcium channels.

48 on or complete absence of the low-threshold, voltage-sensitive calcium conductance that reduces or el

49 )7) potassium currents and suppressed L-type voltage-sensitive calcium currents in A7r5 rat aortic sm

50 Membrane current through voltage-sensitive calcium ion channels at the postsynapt

51 he protein encoded by PKD2 has similarity to voltage-sensitive cation channels and TRP channels and w

52 oxins that modulate the gating properties of voltage-sensitive cation channels are able to bind to ph

53 field, but must be the result of some other voltage-sensitive change in the channel.

54 g of the FO of the F1FO ATP synthase forms a voltage-sensitive channel, the persistent opening of whi

55 otropic glutamate receptors and calcium from voltage-sensitive channels and IP3 receptor-gated stores

56 Reversible control of voltage-sensitive channels through SUMOylation constitut

57 l membrane and allowing Ca(2+) entry through voltage-sensitive channels.

58 eck) more sensitive to plastic changes since voltage sensitive conductances, such as N-methyl-D-aspar

59 ical framework that incorporates ligand- and voltage-sensitive conductances in the dendrites and soma

60 Dendrites contain voltage-sensitive conductances that, in vivo, can be inf

61 revealed that this substitution results in a voltage-sensitive decrease in glycine transport caused b

62 hodopsin-2 (ChR2) stimulation and wide-scale voltage sensitive dye (VSD) imaging in mice to map alter

63 e to the temporal responses seen with RH1692 voltage sensitive dye (VSD), with similar signal amplitu

64 The voltage sensitive dye di-4-ANEPPS was used to assess fun

65 ted from guinea pig ventricles, stained with voltage sensitive dye di-8-ANEPPS, and stimulated along

66 ically reported APs can be detected with the voltage sensitive dye DiO-DPA in multiple locations with

67 We used Voltage Sensitive Dye Imaging, to investigate at high sp

68 ion potential propagation with a red-shifted voltage sensitive dye in whole mouse hearts.

69 -pig ventricular cells (n = 57) stained with voltage-sensitive dye (di-8-ANEPPS) and stimulated longi

70 Voltage-sensitive dye (VSD) imaging directly assays the

71 ntials and action potentials, we developed a voltage-sensitive dye (VSD) imaging technique based on a

72 nstraints, we performed optical imaging with voltage-sensitive dye (VSD) in an animal experimental se

73 is in the slice produced an orderly shift of voltage-sensitive dye (VSD) signals along the AI tonotop

74 iple sites of perfused rabbit hearts using a voltage-sensitive dye and a photodiode array or a CCD ca

75 Using fluorescent imaging with a voltage-sensitive dye and immunolabeling of Cx43, we map

76 yet intact cerebellum was first immersed in voltage-sensitive dye and its responses while intact wer

77 on was optically mapped from 253 sites using voltage-sensitive dye and was anisotropic within the zig

78 lated OHCs at a low frequency using the fast voltage-sensitive dye ANNINE-6plus.

79 l responses were shown to be mediated by the voltage-sensitive dye because the evoked signals had opp

80 in perfused guinea pig hearts stained with a voltage-sensitive dye by comparing APD gradients to the

81 ingle cell maps made from digital imaging of voltage-sensitive dye changes in hippocampal organotypic

82 pping of cardiac electrical activity using a voltage-sensitive dye confirms that cells identified by

83 Optical mapping with the voltage-sensitive dye di-4 ANEPPS was performed to measu

84 Monolayers were stained with voltage-sensitive dye di-4-ANEPPS and mapped at 253 site

85 The voltage-sensitive dye di-4-ANEPPS was utilized to measur

86 ree wall preparations (n=8) stained with the voltage-sensitive dye di-4-ANEPPS.

87 heep right ventricular wall stained with the voltage-sensitive dye di-4-ANEPPS.

88 cence-activated cell sorting (FACS) with the voltage-sensitive dye DiBAC4(3).

89 rat ventricles were optically mapped using a voltage-sensitive dye during pacing and sustained reentr

90 WT) embryos using high-resolution mapping of voltage-sensitive dye fluorescence.

91 We combined computational modeling, voltage-sensitive dye imaging (VSDI) in behaving monkeys

92 between these partial agonists, we utilized voltage-sensitive dye imaging (VSDi) in ventral hippocam

93 Here we used voltage-sensitive dye imaging (VSDI) to measure V1 popul

94 We performed voltage-sensitive dye imaging (VSDi) with GRIN rod lens

95 Combining voltage-sensitive dye imaging (VSDI) with simultaneous e

96 Using simultaneous voltage-sensitive dye imaging and patch-clamp recordings

97 In the present study, fast multi-site voltage-sensitive dye imaging combined with somatic reco

98 no gamma-band subthreshold oscillation, and voltage-sensitive dye imaging demonstrated an absence of

99 Voltage-sensitive dye imaging experiments in primary vis

100 We used voltage-sensitive dye imaging from V1 of behaving monkey

101 ctivity by in vivo recordings and day-by-day voltage-sensitive dye imaging in an acute brain slice pr

102 analysis of cortical activity measured using voltage-sensitive dye imaging in anesthetized animals wa

103 Using in vivo voltage-sensitive dye imaging in anesthetized guinea pig

104 Using voltage-sensitive dye imaging in awake, fixating monkeys

105 Using voltage-sensitive dye imaging in behaving monkeys, we me

106 y of a large neuronal population in V1 using voltage-sensitive dye imaging in behaving monkeys.

107 We measured V1 population responses with voltage-sensitive dye imaging in fixating monkeys that w

108 improvements in the signal-to-noise ratio of voltage-sensitive dye imaging in mouse brain slices, we

109 Voltage-sensitive dye imaging in rat visual cortex shows

110 Voltage-sensitive dye imaging in sagittal slices confirm

111 on in rats, using patch-clamp recordings and voltage-sensitive dye imaging in slices.

112 Using voltage-sensitive dye imaging in vivo, we determined the

113 Voltage-sensitive dye imaging methods showed that epilep

114 Here, we have used voltage-sensitive dye imaging methods to locate the neur

115 Voltage-sensitive dye imaging of mouse thalamocortical s

116 Here, we used voltage-sensitive dye imaging of primary somatosensory c

117 of activity in DCK neurons obtained by using voltage-sensitive dye imaging showed that activity is no

118 By using a recent improvement in voltage-sensitive dye imaging technique that provided ex

119 we used high temporal and spatial resolution voltage-sensitive dye imaging to assess the characterist

120 Here, we applied voltage-sensitive dye imaging to brain slices from anima

121 We used voltage-sensitive dye imaging to evaluate whisker sensor

122 Using voltage-sensitive dye imaging to interrogate the evoked

123 Here we used voltage-sensitive dye imaging to measure directly popula

124 We used quantitative voltage-sensitive dye imaging to probe hippocampal dynam

125 Gs are dedicated or multifunctional, we used voltage-sensitive dye imaging to record from approximate

126 We used voltage-sensitive dye imaging to visualize neuronal acti

127 We combined voltage-sensitive dye imaging with extracellular multiel

128 Using whole-cell somatic recording and voltage-sensitive dye imaging with simultaneous dendriti

129 m radiatum (SR, which contains the SC) using voltage-sensitive dye imaging, field excitatory postsyna

130 ous and evoked up-states were measured using voltage-sensitive dye imaging, intracellular recordings,

131 Based on voltage-sensitive dye imaging, multipatch single-cell re

132 Here we show using in vivo voltage-sensitive dye imaging, that whisker trimming lea

133 As revealed by voltage-sensitive dye imaging, there is an intriguing si

134 oiting the high spatiotemporal resolution of voltage-sensitive dye imaging, we captured population re

135 oral analysis, intracellular recordings, and voltage-sensitive dye imaging, we compared the effects o

136 Using voltage-sensitive dye imaging, we found that short-term

137 Using voltage-sensitive dye imaging, we found that spiral wave

138 lus are encoded in population activity using voltage-sensitive dye imaging.

139 asured changes in net circuit activity using voltage-sensitive dye imaging.

140 aves in rat neocortical slices visualized by voltage-sensitive dye imaging.

141 studied in brainstem slices using high-speed voltage-sensitive dye imaging.

142 s, which is measured macroscopically by fast voltage-sensitive dye imaging.

143 f the RV-epicardial surface was mapped using voltage-sensitive dye in isolated Langendorff-perfused h

144 We used voltage-sensitive dye optical imaging and somatosensory

145 Voltage-sensitive dye optical imaging verified functiona

146 endrites using either calcium-sensitive dye, voltage-sensitive dye or both.

147 eviously characterized using single-unit and voltage-sensitive dye recording methods.

148 within the range of amplitudes detectable by voltage-sensitive dye recording.

149 closest relative) through the combination of voltage-sensitive dye recordings and brain stimulation,

150 Voltage-sensitive dye recordings revealed that this soma

151 Voltage-sensitive dye recordings were used to follow mem

152 campal slices using field, intracellular and voltage-sensitive dye recordings.

153 Optical mapping using voltage-sensitive dye revealed slower conduction velocit

154 Using voltage-sensitive dye to image electrical activity in ra

155 We used a voltage-sensitive dye to image hair-cell electrical reso

156 To address this question, we have used voltage-sensitive dye to image the propagation of action

157 ne potential, simultaneously measured with a voltage-sensitive dye to investigate the activation of C

158 Here we use an electrochromic voltage-sensitive dye which acts as a transmembrane opti

159 Our research confirms that ICG is a voltage-sensitive dye with a dual-component (fast and sl

160 As an infrared voltage-sensitive dye with a low toxicity profile that c

161 Rhodol VoltageFluor-5 (RVF5) is a voltage-sensitive dye with improved 2P cross-section for

162 evealed by high-speed imaging of fluorescent voltage-sensitive dye) were mapped in chick hearts over

163 optically measure membrane potential using a voltage-sensitive dye, but thus far, none of these dyes

164 The voltage-sensitive dye, di-8-ANEPPS, was used to monitor

165 , in combination with a customly synthesized voltage-sensitive dye, is used to simultaneously measure

166 to diminish the fluorescence of a PeT-based voltage-sensitive dye, or VoltageFluor.

167 tal holography and focal glutamate uncaging, voltage-sensitive dye, two-photon imaging, electrophysio

168 SPOT2.1.Cl features an established voltage-sensitive dye, VoltageFluor2.1.Cl--or VF--capped

169 aged responses in hippocampal slices using a voltage-sensitive dye.

170 ntial) on N1E-115 neuroblastoma cells with a voltage-sensitive dye.

171 mbrane potential (E(m)) were measured with a voltage-sensitive dye.

172 We used voltage-sensitive-dye imaging in fixating macaque monkey

173 We combined voltage-sensitive-dye recordings and Ca(2+) imaging of h

174 Ratiometric measurements of voltage sensitive dyes also allow monitoring of intramem

175 he first member of a class of far-red to NIR voltage sensitive dyes that make use of a photoinduced e

176 However, the available voltage-sensitive dyes (VSDs) are not always spectrally

177 d synchronization of cortical activity using voltage-sensitive dyes (VSDs) in the developing rat in v

178 Neuronal populations were monitored with voltage-sensitive dyes after each stimulus.

179 populations in cat visual cortex (V1) using voltage-sensitive dyes and electrode arrays.

180 Using voltage-sensitive dyes and electrophysiological recordin

181 Using voltage-sensitive dyes and electrophysiology, we determi

182 Using voltage-sensitive dyes and high resolution optical mappi

183 simultaneously at 256 ventricular sites with voltage-sensitive dyes and in whole-cell patch-clamped c

184 dvantage of recently developed near-infrared voltage-sensitive dyes and transillumination optical ima

185 maging in conjunction with the fast response voltage-sensitive dyes ANNINE-6 and ANNINE-6plus to reso

186 Voltage-sensitive dyes are important tools for assessing

187 cal mapping of isolated-perfused hearts with voltage-sensitive dyes demonstrated significant slowing

188 f this activity in space and time by imaging voltage-sensitive dyes in cat area V1.

189 -speed optical imaging was implemented using voltage-sensitive dyes in guinea pig visual and somatose

190 lar members of several different families of voltage-sensitive dyes modulate GABA(A) receptor with ma

191 Therefore, the dual effects of voltage-sensitive dyes on GABAergic inhibition require c

192 Optical mapping with voltage-sensitive dyes provides a high-resolution techni

193 Optical mapping of chimeric hearts by use of voltage-sensitive dyes revealed highly irregular epicard

194 used fluorescence resonance energy transfer voltage-sensitive dyes to identify three neurons that ar

195 ultielectrode array recordings, imaging with voltage-sensitive dyes, and recordings from single hippo

196 n-selective nanospheres can be observed with voltage-sensitive dyes, thereby converting nanoscale ele

197 Using voltage-sensitive dyes, we imaged at high spatial and te

198 lar recordings and fast optical imaging with voltage-sensitive dyes, we show that single thalamic inp

199 vealed by real-time optical imaging based on voltage-sensitive dyes, we studied numerically a very la

200 d genetically encoded calcium indicators and voltage-sensitive dyes.

201 ation, as determined by optical mapping with voltage-sensitive dyes.

202 revealed by in vivo optical imaging based on voltage-sensitive dyes.

203 of previously inaccessible applications for voltage-sensitive dyes.

204 on in tree shrews, using optical imaging and voltage-sensitive dyes.

205 ground while simultaneously imaging V1 using voltage-sensitive dyes.

206 onal behavior of voltage-gated ion channels, voltage sensitive enzymes, and proton channels.

207 eature of this prototype of novel engineered voltage-sensitive enzymes, termed Ci-VSPTEN, is the nove

208 ibrium differ from those responsible for the voltage-sensitive equilibrium between high- and low-affi

209 A voltage-sensitive equilibrium between high- and low-affi

210 ght, SPOT2.1.Cl-loaded cells display bright, voltage-sensitive fluorescence associated with the plasm

211 e use V(F)(*), the fractional level at which voltage-sensitive fluorescence, V(F), has maximal time d

212 neuronal inhibition, has been shown to emit voltage-sensitive fluorescence.

213 wall preparations stained with near-infrared voltage-sensitive fluorescent dye DI-4-ANBDQBS.

214 Voltage-sensitive fluorescent dyes are commonly used to

215 Optical mapping using voltage-sensitive fluorescent dyes has become a major to

216 mapping of cardiac electrical signals using voltage-sensitive fluorescent dyes has only been perform

217 Voltage-sensitive fluorescent dyes have become powerful

218 We present a method to target voltage-sensitive fluorescent dyes to specified cells us

219 ine-induced depolarization is followed using voltage-sensitive fluorescent dyes, the presence of thes

220 sing a ROS-sensitive dye and a mitochondrial voltage-sensitive fluorescent indicator, respectively.

221 nt, we have investigated the response of the voltage-sensitive fluorescent probe RH421 to interaction

222 tracellular electrical field stimulation and voltage-sensitive fluorescent probes.

223 We used genetically encoded voltage-sensitive fluorescent protein 2.3 (VSFP2.3) to m

224 acterial membrane potential, we engineered a voltage-sensitive fluorescent protein based on green-abs

225 tains for organelles, Ca(2+) indicators, and voltage-sensitive fluorescent proteins.

226 f voltage-gated ion channels, as well as the voltage-sensitive fluorescent responses observed from a

227 oadly applicable to other types of PeT-based voltage-sensitive fluorophores.

228 eatly weakening amiloride binding, appends a voltage-sensitive gate within the pore of ENaC at low pH

229 show strong outward rectification because of voltage-sensitive gating of the channels.

230 The discovery that these receptors are voltage-sensitive has changed our understanding of their

231 Nickel block of T-type current was voltage sensitive (IC50 of 118.57+/-68.9 microM at -30 m

232 cells the intrinsic gating property of fast voltage-sensitive inactivation is lost.

233 s leading to activation of K(+) channels and voltage-sensitive inhibition of L-type channel activity.

234 icated assembly of transmitter receptors and voltage-sensitive ion channel molecules.

235 charges in voltage-sensing domains (VSD) of voltage-sensitive ion channels and enzymes are carried o

236 Dendritically placed, voltage-sensitive ion channels are key regulators of neu

237 Voltage-sensitive ion channels open and close in respons

238 f Arg over Lys as a mobile charge carrier in voltage-sensitive ion channels.

239 sting sensors based on hydrophobic anions or voltage-sensitive ion channels.

240 Like many voltage-sensitive ion pumps, cytochrome c oxidase is inh

241 aChBac as a functionally expressed bacterial voltage-sensitive ion-selective channel provides insight

242 Voltage-sensitive ionic currents shape both the firing p

243 Large-conductance, Ca(2+)- and voltage-sensitive K(+) (BK) channels regulate neuronal f

244 The beta-subunit of the voltage-sensitive K(+) (K(v)) channels belongs to the al

245 However, voltage-sensitive K(+) channel blockers inhibiting these

246 Voltage-sensitive K(+) channels (Kv) serve numerous impo

247 In contrast to other voltage-sensitive K(+) channels such as HERG and Shaker,

248 ndamental principle underlying the gating of voltage-sensitive K(+) channels.

249 4-AP blocked voltage-sensitive K(+) currents in astrocytes.

250 obability (P(o)) of large conductance Ca(2+)/voltage-sensitive k(+)(BK) channels is increased by 17be

251 umed to occur only in the "microdomain" near voltage-sensitive L-type Ca(2+)-channels, where [Ca(2+)]

252 ents in CA3 pyramidal neurons, including the voltage-sensitive M-current.

253 gulate channel activation, and, therefore, a voltage-sensitive mechanism is unlikely to represent a f

254 tivity, an effect linked to reduction of the voltage-sensitive Mg(2+) block of GluN2B-containing NMDA

255 mp technique alone or in combination with pH/voltage-sensitive microelectrodes or confocal fluorescen

256 voltage-clamp technique, as well as pH- and voltage-sensitive microelectrodes, to characterize the e

257 above results indicate a functionally active voltage-sensitive NBCe in these species.

258 ed excitatory and disinhibitory currents was voltage sensitive, peaking at membrane potentials near r

259 at the native S4 from the Ciona intestinalis voltage-sensitive phosphatase (Ci-VSP) does not exhibit

260 pendent depletion of PtdIns(4,5)P(2) using a voltage-sensitive phosphatase (ci-VSP) inhibited TRPM8 c

261 The Ciona intestinalis voltage-sensitive phosphatase (Ci-VSP) represents the fi

262 B and -C in whole oocytes by co-expressing a voltage-sensitive phosphatase (VSP) that decreases PIP2

263 , we co-expressed either NBCe1-B or -C and a voltage-sensitive phosphatase (VSP), which depletes PIP2

264 voltage-sensing domain of Ciona intestinalis voltage-sensitive phosphatase and super ecliptic pHluori

265 The voltage-sensitive phosphatase Ci-VSP consists of an intr

266 This indicator is based on the Gallus gallus voltage-sensitive phosphatase with the phosphatase domai

267 the voltage sensor of the Ciona intestinalis voltage-sensitive phosphatase, against experimental data

268 ntly faster than those of Ciona intestinalis voltage-sensitive phosphatase.

269 Voltage-sensitive phosphatases (VSPs) are proteins that

270 The recently discovered voltage-sensitive phosphatases (VSPs) hydrolyze phosphoi

271 Fluorescence changes at two wavelengths near voltage-sensitive portions of the emission spectrum and

272 citation between two wavelengths centered at voltage-sensitive portions of the excitation spectrum an

273 Recordings of activation of the voltage-sensitive potassium channel Kv2.1 in mammalian c

274 Kv1.2 is a member of the Shaker family of voltage-sensitive potassium channels and contributes to

275 neurons is determined in part by the type of voltage-sensitive potassium channels expressed.

276 ing shift in voltage-dependent activation of voltage-sensitive potassium currents (I(K)).

277 nced by 4-aminopyridine (4-AP), a well known voltage-sensitive potassium ion channel (K(v)) blocker.

278 asis of the observed fluorescence changes of voltage-sensitive probes.

279 Because ICG has voltage-sensitive properties in the entire heart, we sug

280 of wild-type and mutant CRMP-2 constructs on voltage-sensitive properties of VGSCs in CAD cells: 1) s

281 influx and somatic motility mediated by the voltage-sensitive protein prestin.

282 ting and shaping the action potential, these voltage-sensitive proteins supply the neuron with crucia

283 Lishko et al. now report that Hv1, the voltage-sensitive proton channel, is present in human sp

284 domain but is sufficient for expression of a voltage-sensitive proton-selective ion channel activity.

285 n that focuses the electric field to a small voltage-sensitive region.

286 lar concentrations of dimeric tubulin induce voltage-sensitive reversible closure of VDAC reconstitut

287 y sea anemone neurotoxin that interacts with voltage-sensitive sodium (Na(V)) channels, causing a del

288 The roles of voltage-sensitive sodium (Na) and calcium (Ca) channels

289 toxic effects through interactions with the voltage-sensitive sodium channel (Vssc).

290 The SCN5A gene encodes a voltage-sensitive sodium channel expressed in cardiac an

291 The voltage-sensitive sodium channel Na(v)1.5 (encoded by SC

292 s a type 1 sea anemone toxin, which binds to voltage-sensitive sodium channels (Na(V)'s), thereby del

293 of [(3)H]-PbTx-3 to its binding site on the voltage-sensitive sodium channels in rat brain synaptoso

294 Voltage-sensitive sodium channels were present in axons

295 dal mPFC neurons and inhibition of transient voltage-sensitive sodium current (INaT) as a measure of

296 llular poly(I:C) markedly augments an inward voltage-sensitive sodium current and inhibits the outwar

297 of approximately +/-90 mV, OmpT is much more voltage-sensitive than OmpU (with a V(c) of approximatel

298 H(v)1 currents are activated at depolarizing voltages, sensitive to the transmembrane pH gradient, H+

299 the modulation of I(M) by histamine was not voltage sensitive, whereas channel gating, particularly

300 ut the time-dependent component was strongly voltage sensitive, with an effective electrical distance