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 , including land plants and fungi, have lost voltage-sensitive 4D-Ca(v)/Na(v)s [5-7].

4 otein, decreasing PI(4,5)P(2) levels using a voltage-sensitive 5'-phosphatase induced a stronger inhi

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

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

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

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

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

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

11 2-photon glutamate uncaging, to examine how voltage-sensitive Ca channels (VSCCs) and ionotropic glu

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

51 potential of nerve and muscle is produced by voltage-sensitive channels that include a specialized de

52 Reversible control of voltage-sensitive channels through SUMOylation constitut

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

68 al prostatectomy using near-infrared cyanine voltage-sensitive dye (VSD) imaging, which visualizes me

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

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

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

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

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

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

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

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

77 essment of membrane potential using the slow voltage-sensitive dye bis-(1,3-diethylthiobarbituric aci

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

93 Functional voltage-sensitive dye imaging confirmed GABA circuit fun

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

95 Voltage-sensitive dye imaging experiments in primary vis

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

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

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

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

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

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

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

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

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

105 alled "correspondence problem." Here, we use voltage-sensitive dye imaging in primary visual cortex (

106 Voltage-sensitive dye imaging in rat visual cortex shows

107 Voltage-sensitive dye imaging in sagittal slices confirm

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

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

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

111 Voltage-sensitive dye imaging of mouse thalamocortical s

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

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

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

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

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

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

118 Using voltage-sensitive dye imaging to interrogate the evoked

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

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

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

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

123 We combined voltage-sensitive dye imaging with extracellular multiel

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

140 We used voltage-sensitive dye optical imaging and somatosensory

141 Voltage-sensitive dye optical imaging verified functiona

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

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

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

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

146 Voltage-sensitive dye recordings revealed that this soma

147 Voltage-sensitive dye recordings were used to follow mem

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

165 Using a fast voltage-sensitive dye, we have imaged the AP waveform fr

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

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

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

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

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

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

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

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

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

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

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

177 Using voltage-sensitive dyes and electrophysiological recordin

178 Using voltage-sensitive dyes and electrophysiology, we determi

179 Using voltage-sensitive dyes and high resolution optical mappi

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

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

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

183 Voltage-sensitive dyes are important tools for assessing

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

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

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

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

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

189 Chemically synthesized voltage-sensitive dyes that use photoinduced electron tr

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

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

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

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

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

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

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

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

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

199 of previously inaccessible applications for voltage-sensitive dyes.

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

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

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

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

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

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

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

207 s) based on microbial rhodopsins utilize the voltage-sensitive fluorescence of all-trans retinal (ATR

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

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

210 Voltage sensitive fluorescent dyes (VSDs) are important

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

212 readily functionalizable, fluorescein-based voltage-sensitive fluorescent dyes (sarcosine-VoltageFlu

213 Voltage-sensitive fluorescent dyes are commonly used to

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

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

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

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

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

219 ynthesis, and applications of a new class of voltage-sensitive fluorescent indicators built on a modi

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

221 Optical recording using voltage-sensitive fluorescent probes has provided unprec

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 Voltair consists of a voltage-sensitive fluorophore and a reference fluorophor

228 onalize them to access 13 new, BODIPY-based, voltage-sensitive fluorophores (VF).

229 Voltage-sensitive fluorophores enable the direct visuali

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

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

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

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

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

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

236 otoinduced electron transfer triggered RhoVR voltage-sensitive indicator coupled to a chloroalkane Ha

237 , a red fluorescent GEVI that fuses Ace2N, a voltage-sensitive inhibitory rhodopsin, with mScarlet, a

238 ethods can be found in the literature to fit voltage-sensitive ion channel models to whole-cell curre

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

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

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

242 Voltage-sensitive ion channels open and close in respons

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

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

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

246 Voltage-sensitive ionic currents shape both the firing p

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

268 Voltage-sensitive phosphatases (VSPs) are proteins that

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

270 elated S1-S4 domains have been identified in voltage-sensitive phosphatases and voltage-activated pro

271 n non-small-cell lung cancer in vivo using a voltage-sensitive, positron emission tomography (PET) ra

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

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

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

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

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

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

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

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

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

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

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

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

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

285 neral approach to GEVIs containing different voltage sensitive rhodopsin domains and various fluoresc

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

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

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

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

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

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

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

293 Voltage-sensitive sodium channels were present in axons

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

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

296 The studied systems thus behave like voltage-sensitive switching molecular diodes, which is r

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