ライフサイエンスコーパス: gated

1 st sensory encoding in dlPFC is contextually gated.

2 ila melanogaster larvae expressing the light-gated activator CsChrimson and the inhibitor GtACR2 with

3 urrent physiological state with hypothalamus-gated amygdala inputs that signal upcoming ingestion of

4 utionary dynamic networks revealing enhanced gated and cascaded functions.

5 cterium thermoautotrophicum-a purely calcium-gated and inactivating channel-in a lipid environment.

6 o the allosteric gating and regulation of CN-gated and nucleotide-modulated channels and CNG channel-

7 t nanobody (designated Chessbody) for ligand-gated antigen recognition in living cells.

8 three aortic levels on three retrospectively gated axial gradient-echo (GRE) data sets.

9 e, whose necked aperture to the cytoplasm is gated by a 12-fold symmetric, 35-nm diameter "crown" com

10 fficking during homeostatic upscaling can be gated by a single phosphorylation site on the GluA2 subu

11 organic semiconductors as OECTs that can be gated by aqueous solutions.

12 Like upward FRH, downward FRH was gated by arousal state but in the opposite direction: it

13 A study demonstrates that Hrd1 is gated by autoubiquitination and a soluble ERAD substrate

14 ied endolysosomes via connexin 43 (Cx43) and gated by cAMP-EPAC-RAP1-PP2A signaling.

15 Unlike classic HCN channels, HCNL1 is not gated by cyclic nucleotides.

16 MDA) receptors are Ca(2+)-permeable channels gated by glutamate and glycine that are essential for ce

17 S+) after learning, and these responses were gated by internal state and task context.

18 nput at each moment, and this integration is gated by local prediction error.

19 L-1) sets period length and behavioral phase gated by photic signals.

20 the human siesta, is a "hard-wired" property gated by specific neurons of the master clock to favor s

21 tional change indicates Kir channels are not gated by the canonical mechanism.

22 2+) in both the cytosol and chloroplasts are gated by the nuclear circadian oscillator.

23 ic plants, environmental signals are locally gated by the presence of developing fruits initiated in

24 es open a short tunnel to the catalytic site gated by the ValG8/IleE15 pair and LeuE11.

25 s, function by inhibiting the L-type voltage-gated Ca(2+) (Ca(v) ) channels.

26 mation processing units that rely on voltage-gated Ca(2+) (Ca(v)) channels to trigger Ca(2+)-dependen

27 the circadian regulation of distinct voltage-gated Ca(2+) channel (VGCC) components has not been comp

28 sts for the pharmacoresistant R-type voltage-gated Ca(2+) channel (VGCC) to be involved in transretin

29 ly, highlighted roles for the L-type voltage-gated Ca(2+) channel Ca(V)1.2 in nonexcitable cells.

30 n the regulation of the plasmalemmal voltage-gated Ca(2+) channel, Ca(v)1.2.

31 al models had suggested that several voltage-gated Ca(2+) channels (VGCCs) regulated critical signali

32 In previous studies, T-type voltage-gated Ca(2+) channels (VGCCs) were implicated in this pa

33 To determine whether Cav1.2 voltage-gated Ca(2+) channels contribute to astrocyte activation

34 Voltage-gated Ca(2+) channels play a pivotal role in this proces

35 microenvironment of the presynaptic voltage gated Ca(2+) channels revealed that alkalinization also

36 r understanding of the properties of voltage-gated Ca(2+) channels that support their presynaptic fun

37 erall increased expression of L-type voltage-gated Ca(2+) channels that, at presynaptic terminals, ab

38 ion-competent synaptic vesicles near voltage-gated Ca(2+) channels.

39 that regulate SCN firing, including voltage-gated Ca(2+) currents, but the circadian regulation of d

40 ases.SIGNIFICANCE STATEMENT Reducing voltage-gated Ca(2+) influx in astrocytes during brain demyelina

41 ; and that attenuation of astrocytic voltage-gated Ca(2+) influx may be an effective therapy to reduc

42 Voltage-gated Ca(v)1 and Ca(v)2 Ca(2+) channels are comprised of

43 tostella vectensis use a specialized voltage-gated calcium channel (nCa(V)) to distinguish salient se

44 ychiatric risk gene that encodes the voltage-gated calcium channel Ca(V)1.2.

45 gy in bystander neurons, as were the voltage-gated calcium channel Cacophony (Cac) and the mitogen-ac

46 es demonstrated that the anti-L-type voltage-gated calcium channel immunoglobulin G purified from pat

47 hat BsYetJ/TMBIM6 is a pH-dependent, voltage-gated calcium channel.

48 For example, presynaptic voltage-gated calcium channels (VGCCs) and postsynaptic ligand-g

49 armacological manipulation of L-type voltage-gated calcium channels (VGCCs) and purinoceptors induced

50 MDA-type glutamate receptors but not voltage-gated calcium channels (VGCCs), and can also be observed

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

52 deletions in the significant set of voltage-gated calcium channels among CNVs called from both exome

53 AP) waveform controls the opening of voltage-gated calcium channels and contributes to the driving fo

54 econditioning was mediated by L-type voltage-gated calcium channels and is consistent with computatio

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

56 renal autoregulation mechanisms and voltage-gated calcium channels can maintain overall renal blood

57 (2020) demonstrate that Ca(v)2-type voltage-gated calcium channels do not mediate presynaptic assemb

58 und that the alpha2delta2 subunit of voltage-gated calcium channels negatively regulates axon growth

59 y unknown endogenous activator of the ligand-gated calcium channels transient receptor potential V1 a

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

61 n each compartment were dependent on voltage-gated calcium channels, and somatic and nuclear calcium

62 ation including glutamate receptors, voltage-gated calcium channels, the dopamine D2 receptor, and co

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

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

65 ment was only partially dependent on voltage-gated calcium channels.

66 t confers adrenergic modulation upon voltage-gated calcium channels.

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

68 Voltage-gated calcium currents were unchanged between the genoty

69 hysiological relevance in control of voltage-gated calcium influx and calcium-dependent cellular func

70 the P2X purinergic receptor family of ligand-gated cation channels and has recently been shown to reg

71 The P2X receptor family of ATP-gated cation channels are attractive drug targets for pa

72 Acid-sensing ion channels (ASICs) are proton-gated cation channels that contribute to neurotransmissi

73 yperpolarization-activated cyclic nucleotide-gated channel (HCN) conductance in the afferent and crea

74 yperpolarization-activated cyclic nucleotide-gated channel 4) locus of the mouse genome.

75 ralogs differs from the voltage- and calcium-gated channel CALHM1.

76 polarization-activated and cyclic nucleotide-gated channel HCN2 in the family of so-called pacemaker

77 etastable protein possesses superior voltage-gated channel regulation, efficient mitochondrial target

78 Gene expression of KCNA5 (potassium voltage-gated channel subfamily A member 5; encoding Kv1.5) was

79 4 palmitoylates the Shaker-like K(+) voltage-gated channel subunit (Kv1.1), thereby regulating Kv1.1

80 rom the receptor guanylate cyclase to a cGMP-gated channel that serves as a perfect chemo-electrical

81 a plasma membrane CO(2) channel, possibly a gated channel.

82 ution of Na(+)-selective four-domain voltage-gated channels (4D-Na(v)s) in animals allowed rapid Na(+

83 encode single-domain Na(+)-selective voltage-gated channels (BacNa(v)), they typically exhibit much s

84 s 1 represent a unique, large group of light-gated channels (viral channelrhodopsins, VirChR1s).

85 framework for understanding gating in ligand-gated channels and how mutations in the acetylcholine re

86 lification and impulse generation by voltage-gated channels are dispensable.

87 dependent pumping of Ca(2+) entering voltage-gated channels at the synaptic terminal.

88 Recent advances of plant cyclic nucleotide-gated channels give new insight into their molecular fun

89 Besides polycystin channels voltage gated channels like HCN4 and KCNQ1 have been implicated

90 transducin that sensitizes cyclic nucleotide gated channels to cGMP and causes photoreceptor cell dea

91 yperpolarization-activated cyclic nucleotide-gated channels(5), and may represent an unexpected link

92 In S4-based voltage sensors voltage-gated channels, a common feature is shared; the transmem

93 yperpolarization-activated cyclic nucleotide-gated channels, and from ATP-dependent pumping of Ca(2+)

94 In certain ligand-gated channels, such as BK channels and MthK, a Ca(2+)-a

95 ducing the generation potentials and voltage-gated channels, translating the generation potentials in

96 CLC-2 is a voltage-gated chloride channel that is widely expressed in mamma

97 indicate that Hodor is a pH-sensitive, zinc-gated chloride channel that mediates a previously unreco

98 glutamate transporter and also as glutamate-gated chloride channel, the chloride conductance being l

99 e positive allosteric modulator of glutamate-gated chloride channels found in nematodes and insects.

100 sis supports allosteric binding to glutamate-gated chloride channels similar to ivermectin.

101 egalovirus (HCMV) and identified the voltage-gated chloride ion channel inhibitor 4,4'-diisothiocyano

102 both Brugia osm-9 and the cyclic nucleotide-gated (CNG) channel subunit tax-4 in larval chemotaxis t

103 Cyclic nucleotide-gated (CNG) channels convert cyclic nucleotide (CN) bind

104 d by adenylyl cyclase (AC)/cyclic nucleotide-gated (CNG) channels or by protein kinase A (PKA) activi

105 e characterized by high circuity, typical of gated communities.

106 ECG-gated computed tomography scans were acquired at end-exp

107 This voltage-gated conductance increases neuronal gain and selectivit

108 sual stimulation reveal an intrinsic voltage-gated conductance that profoundly alters the integrative

109 in into an allosteric ligand- and counterion-gated conformational molecular switch.

110 d both light- and energetic/oxidative stress-gated control of this interaction.

111 Further, we demonstrate time-gated CPL acquisition, enabling long-lived CPL luminesce

112 eptors are functional and exhibit robust ACh-gated currents blocked by alpha-bungarotoxin and strychn

113 whole-body surveys, quick reconstructions of gated data to select the optimal gate for a given attenu

114 Compared with RPM-gated, DDG-retro gave an average increase in SUV(max) of

115 mplex media using a lifetime-based or a time-gated detection scheme.

116 ure of twisted bilayer graphene using a back-gated device architecture for angle-resolved photoemissi

117 is critical for the operation of electrolyte-gated devices in application-relevant environments.

118 tations in the CLCN5 gene encoding a voltage-gated electrogenic nCl(-)/H(+) exchanger ClC-5.

119 on (PE-ALD) of Al(2)O(3) on graphene for top gated field effect transistors (FETs).

120 it to operate an ultra-sensitive electrolyte-gated field-effect transistor (EGOFET) as a sensor and f

121 selectivity were monitored using liquid-ion gated field-effect transistors (FETs).

122 The results from logic-gated flow cytometry analysis was validated with bioinfo

123 nanopore, which enables fast, selective, and gated flow of water de novo would remain challenging, su

124 Moreover, time-gated FRET imaging with the Ln-dye FRET pairs efficientl

125 Circuits based on these dual-gated Gaussian devices enable a variety of biological sp

126 unprecedented electrostatic control of dual-gated Gaussian heterojunction transistors for simplified

127 Critically, the gated generation of a fluorescent product allows for flu

128 yperpolarization-activated cyclic nucleotide-gated (HCN) and small conductance calcium-activated pota

129 yperpolarization-activated cyclic nucleotide-gated (HCN) channels are essential for rhythmic activity

130 yperpolarization-activated cyclic nucleotide-gated (HCN) channels are major regulators of synaptic pl

131 yperpolarization-activated cyclic nucleotide-gated (HCN) channels.

132 The voltage-gated Hv1 proton channel is a ubiquitous membrane protei

133 tive hot spot was reduced by 24% in the dual gated images compared to non-gated images.

134 24% in the dual gated images compared to non-gated images.

135 Until now, time-gated imaging could not be used to develop LFM on porous

136 been successfully photographed using a time-gated imaging scheme.

137 equivalent, DDG-retro was preferred over RPM-gated in 13% of examinations, whereas the opposite occur

138 G-protein-gated inward rectifier potassium (GIRK) channels are reg

139 activate a shared pool of cardiac G protein-gated inwardly rectifying K(+) (GIRK) channels in SAN ce

140 G-protein-gated inwardly-rectifying K(+) (GIRK) channels are targe

141 tic homolog, the Erwinia chrysanthemi ligand-gated ion channel (ELIC).

142 tion in the membrane protein, Erwinia ligand-gated ion channel (ELIC).

143 on-selective member of the pentameric ligand-gated ion channel (pLGIC) superfamily.

144 discuss our current understanding of ligand-gated ion channel and G protein-coupled receptor complex

145 sitive neurons express the cyclic nucleotide-gated ion channel CNGA3, and that mouse, but not squirre

146 mitochondrial calcium uniporter is a Ca(2+)-gated ion channel complex that controls mitochondrial Ca

147 P2X7 is an important ligand-gated ion channel expressed in multiple immune cell popu

148 Antagonists for the ATP-gated ion channel receptor P2X1 have potential as antith

149 roton channel Hv1 is a member of the voltage-gated ion channel superfamily, which stands out in desig

150 otonin type 3 receptor (5-HT(3)) is a ligand-gated ion channel that converts the binding of the neuro

151 al homolog ELIC (Erwinia chrysanthemi ligand-gated ion channel) has a similar lipid sensitivity.

152 acetylcholine receptor, a pentameric ligand-gated ion channel, converts the free energy of binding o

153 otonin type 3A receptor, a pentameric ligand-gated ion channel, is crucial for regulating conductance

154 One such ligand-gated ion channel, the NMDAR, impacts nearly all forms o

155 Pentameric ligand-gated ion channels (pLGICs) are allosteric receptors tha

156 GlyRs) are anion-permeable pentameric ligand-gated ion channels (pLGICs).

157 e-function relationship of pentameric ligand-gated ion channels (pLGICs).

158 s are affected as well, particularly voltage-gated ion channels (VGICs).

159 Targeting receptor proteins, such as ligand-gated ion channels and G protein-coupled receptors, has

160 The opening and closing of voltage-gated ion channels are regulated by voltage sensors coup

161 Voltage-gated ion channels endow membranes with excitability and

162 1 is an outstanding representative of ligand-gated ion channels in ligand selectivity and sensitivity

163 T Changes in dendritic function, and voltage-gated ion channels in particular, are increasingly the f

164 Glutamate receptors are essential ligand-gated ion channels in the central nervous system that me

165 receptor-like (GLR) channels are amino acid-gated ion channels involved in physiological processes i

166 vary in their selectivity for human voltage-gated ion channels involved in the ventricular action po

167 Voltage-gated ion channels play important roles in physiological

168 nhibitory cell types, genes encoding voltage-gated ion channels responsible for depolarizing and repo

169 ium channels (VGCCs) and postsynaptic ligand-gated ion channels such as AMPA receptors (AMPARs) are o

170 Ionotropic glutamate receptors are ligand-gated ion channels that mediate excitatory synaptic tran

171 NMDA receptors (NMDARs) are glutamate-gated ion channels that mediate fast excitatory synaptic

172 D-aspartate receptors (NMDARs) are glutamate-gated ion channels that play critical roles in neuronal

173 5-HT(3) receptors are pentameric ligand-gated ion channels that regulate synaptic activity in th

174 Channelrhodopsins are light-gated ion channels widely used to control neuronal firin

175 ASICs have become bona fide neurotransmitter-gated ion channels, activated by the smallest neurotrans

176 at function as light-driven ion pumps, light-gated ion channels, and photosensors, with potential uti

177 onship among gating modifier toxins, voltage-gated ion channels, and the lipid membrane surrounding t

178 action potential depends on several voltage-gated ion channels, including Na(V), Ca(V), and K(V) cha

179 receptors to the dynamics shaped by voltage-gated ion channels.

180 LQTS because they are modulators of voltage-gated ion channels.

181 th similarity to those in other mechanically gated ion channels.

182 izing K(+) current (I(K)) carried by voltage gated K(+) (K(v)1.5) channels were reduced.

183 ense variant in KCNA2, which encodes voltage-gated K(+) channel K(V) 1.2.

184 The EAG (ether-a-go-go) family of voltage-gated K(+) channels are important regulators of neuronal

185 Voltage-gated K(+) channels function in macromolecular complexes

186 hat induced autoimmunity against the voltage-gated KCNQ1 K(+) channels accelerates cardiac repolariza

187 The function of the voltage-gated KCNQ1 potassium channel is regulated by co-assembl

188 This gated ketal is further incorporated into the polymer bac

189 Voltage-gated L-type Ca(2+) channel (Ca(v)1.2) blockers (LCCBs)

190 2 (also known as KCNK5) channels generate pH-gated leak-type K(+) currents to control cellular electr

191 y on-target/off-tumor toxicity, we use logic-gated (log) GPC3-synNotch-inducible CD147-CAR to target

192 The assay is based on a time-gated luminescence microscopy technique enabling visuali

193 e IgA1 protease subscribes to an active-site-gated mechanism where a domain undergoes a 10.0 angstrom

194 Acid-sensing ion channels (ASICs) are proton-gated members of the epithelial sodium channel/degenerin

195 P2X7 is an ATP-gated membrane ion channel that is expressed by multiple

196 cumferential ramp, self-organizes around tip-gated microcantilevers to form contracting CaMiRi.

197 ced by the environmental pH, ruling out a pH-gated model and confirming that the chemistry of the His

198 Recently, a pH-gated model has been postulated to regulate the phosphat

199 istration of contrast media, and non-cardiac-gated multidetector CT with and without contrast media t

200 ing its application in high-performance back-gated n-type MoS(2) and p-type WSe(2) transistors with s

201 The voltage-gated Na(+) (Na(v)) channel is the molecular determinant

202 Voltage-gated Na(+) (Na(V)) channels regulate homeostasis in bac

203 with reduced expression of SCN5a and voltage gated Na(+) (Na(V)1.5) channels as well as a shift in I(

204 is mediated by excessive activity of voltage-gated Na(+) and Ca(2+) channels that is initially counte

205 Modification of voltage-gated Na(+) channel (Na(V) ) function by intracellular C

206 luding the NMDA receptor (NMDAR) and voltage-gated Na(+) channels.

207 an influx of sodium (Na(+)) ions via voltage-gated Na(+) channels.

208 minated the onset response by moving voltage-gated Na+ channels (VGSCs) to closed-state inactivation

209 gating (real-time position management (RPM)-gated), no gating but using only the first 3 min of data

210 lanar lipid bilayers at acidic pH to form pH-gated nonselective cation channels that are opened upon

211 cohort and compared with BG using optimally gated (OG) and fully motion-corrected (elastic motion co

212 Thus, locomotion-gated optic flow, combined with the presence of contextu

213 e investigate solution processed Electrolyte Gated Organic Field Effect Transistors (EGOFETs) based o

214 a label-free sensor based on an Electrolyte-Gated Organic Field-Effect Transistor (EGOFET) integrate

215 istor is changed from that of an electrolyte-gated organic field-effect transistor (EGOFET) to that o

216 p device integrating a multigate electrolyte gated organic field-effect transistor (EGOFET) with a 6.

217 y used for cell monitoring while Electrolyte-Gated Organic Field-Effect Transistors (EGOFETs) have ne

218 is tightly linked to the opening of voltage-gated P/Q-type Ca(2+) channels, the activation of which

219 xtracellular ATP, or inactivation of the ATP-gated P2X7R channel also compromised the effects of MerT

220 Here, we identify a family of voltage-gated "pacemaker" channels, HCNL1, that are exquisitely

221 tched; that is, noise was much lower than in gated PET.

222 In voltage-gated potassium (K(V)) channels, the voltage-sensing dom

223 Voltage-gated potassium (Kv) channels display several types of i

224 Voltage-gated potassium (Kv) channels of the Kv4 subfamily assoc

225 trically silent (KvS) members of the voltage-gated potassium (Kv) subfamilies Kv5, Kv6, Kv8, and Kv9

226 Voltage-gated potassium 11.1 (K(v)11.1) channels play a critical

227 sistent with increased expression of voltage-gated potassium channel gene Kcna1 and decreased express

228 The voltage-gated potassium channel Kv1.5 plays important roles in a

229 nsional structure of the human KCNQ1 voltage-gated potassium channel VSD in the intermediate state.

230 emonstrated that microglial Kv1.3, a voltage-gated potassium channel, was transcriptionally upregulat

231 idine (4AP) is a specific blocker of voltage-gated potassium channels (K(V)1 family) clinically appro

232 Neuronal voltage-gated potassium channels (Kv) are critical regulators of

233 e VLS, we analyzed the expression of voltage-gated potassium channels in rodent and primate brains us

234 Kv3 voltage-gated potassium channels mediate action potential (AP) r

235 of action is via blockade of axonal voltage gated potassium channels, thereby enhancing conduction i

236 However, in several voltage-gated potassium channels, using specific S4-S5(L)-mimick

237 e four derivatives are able to block voltage-gated potassium channels.

238 through the activation of associated calcium-gated potassium channels.

239 application of ALD increased outward voltage-gated potassium currents significantly, and simultaneous

240 embranes using the dynamic clamp and voltage-gated potassium ionic channels (Kv1.3) expressed in Xeno

241 ddition, we examined the role of the voltage-gated potassium Kv4.2 subunit, a molecular determinant o

242 d self-inhibitory because of ClC-5's voltage-gated properties, but shunt conductance facilitated furt

243 Here, we report a light- and cellular stress-gated protein switch based on cofilin-actin rod formatio

244 The voltage-gated proton channel Hv1 is a member of the voltage-gate

245 The voltage-gated proton channel Hv1 regulates proton fluxes across

246 Hv1 is a voltage-gated proton channel whose main function is to facilitat

247 Voltage-gated proton channels (H(V)1) are essential for various

248 if acquisition was executed with an inverse-gated pulse sequence.

249 cific binding of neurotransmitters to ligand-gated receptor ion channels.

250 Gated reconstruction using the external device failed in

251 Results indicated that generally the Gated Recurrent Unit (GRU) and Quasi Recurrent Neural Ne

252 boxylate transporter 1, which facilitates pH-gated release.

253 s, in the presence of a primer, P(1), to the gated replication of the scaffolds and to the displaceme

254 staining or abrogating the light- and stress-gated response.

255 nce, Na-activated K channels (Slo2), voltage-gated (SCN) Na(+) and Na(+) leak channels, nonselective

256 anges were sensitive to the specific voltage-gated sodium (Na(V)) channel blocker tetrodotoxin.

257 We tagged the sole voltage-gated sodium (Na(V)) channel in the fly, para, and ident

258 Voltage-gated sodium (Na(V)) channels are a functional hallmark

259 Voltage-gated sodium (Na(V)) channels are pore-forming transmemb

260 osa) use tetrodotoxin (TTX) to block voltage-gated sodium (Na(v)) channels as a chemical defense agai

261 Voltage-gated sodium (Na(V)) channels drive neuronal excitabilit

262 ntracellular proteins which regulate voltage-gated sodium (Na(v)) channels in the brain and other tis

263 n mice by inhibiting inactivation of voltage-gated sodium (Na(V)) channels involved in nociceptive si

264 BFOX2(40)-driven splicing defects in voltage-gated sodium and potassium channels, which alter their e

265 the consequence of the properties of voltage-gated sodium and potassium channels.

266 Voltage-gated sodium channel (VGSC) beta1 subunits are multifunc

267 und alterations in the properties of voltage-gated sodium channel currents in Jedi-1 null neurons.

268 Missense variants in the SCN8A voltage-gated sodium channel gene are linked to early-infantile

269 Nav1.6 is the primary voltage-gated sodium channel isoform expressed in mature axon in

270 The voltage-gated sodium channel isoform Na(V)1.7 is highly expresse

271 Voltage-gated sodium channel Na(v)1.5 generates cardiac action p

272 Voltage-gated sodium channel Na(V)1.7 is a genetically validated

273 estigated the effect of LITAF on the voltage-gated sodium channel Nav1.5, which is critical for cardi

274 Gain-of-function mutations of voltage-gated sodium channel Nav1.7 underlie dorsal root ganglio

275 ffinity and in vitro activity at the voltage-gated sodium channel subtype 1.7 (Na(V)1.7), a channel t

276 teractions between CBD and the NavMs voltage-gated sodium channel, and electrophysiology to show the

277 in (TTX), a neurotoxin that binds to voltage-gated sodium channels (Na(v) proteins), arresting electr

278 Voltage-gated sodium channels (Na(V)) are indispensable for tran

279 ther human SAN excitability requires voltage-gated sodium channels (Nav) remains controversial.

280 We hypothesize that the voltage-gated sodium channels (VGSC) on the dorsal root ganglion

281 Voltage-gated sodium channels are subjected to S-palmitoylation

282 Voltage-gated sodium channels are targets for a range of pharmac

283 Voltage-gated sodium channels comprise an ion-selective alpha-su

284 e in the density of Nav1.5-generated voltage-gated sodium current I (Na) and Nav1.5 surface protein l

285 It displays reversible, multistep gated sorption of CO(2) below 0.33 atm.

286 how that our model reproduces neuromodulator-gated spike-timing-dependent plasticity as observed in t

287 This reduction-potential-gated strategy enables access to residues unavailable wi

288 also demonstrate light- and cellular stress-gated switch function in cultured hippocampal neurons.

289 by magneto-transport measurements in a dual-gated system.

290 Voltage-gated T-type Ca(2+) (Ca(V)3) channels regulate diverse p

291 photoluminescence (PL) lifetime enables time-gated (TG) detection without autofluorescence background

292 of individual HeLa cells using a single cell gated transistor (SCGT).

293 Here, a nanoscale triboelectrification-gated transistor has been studied with contact-mode atom

294 Nonvolatile electrolyte-gated transistors (EGTs) provide prominent analog switch

295 genes, as well as genes specific to voltage-gated transmembrane ion transporters.

296 duced and reduced forms, was investigated by gated-trapped ion mobility spectrometry (G-TIMS).

297 Inwardly rectifying, voltage-gated, two-pore domain, and related K(+) channels are lo

298 rin-like compounds that open the two voltage-gated type 1 potassium (K(V)1) channels K(V)1.5 and Shak

299 regions of interest.Objectives: Respiratory-gated, ultrashort echo time magnetic resonance imaging w

300 ling kinetics during regeneration, showing a gated versus graded response, respectively.