ライフサイエンスコーパス: depolarize

1 e than the relative time that the channel is depolarized.

2 when resting membrane potential was slightly depolarized.

3 ion curve of somatic A-type K(+) current was depolarized.

4 ective foci, and in 54.5% the foci were also depolarizing.

5 in [Ca(2+) ]i in cells that were moderately depolarized (11-20 mV) by elevation of [KCl]o (12-20 mm)

6 ells held at hyperpolarized (-40 mV) but not depolarized (-20 mV) voltages.

7 old, the membrane voltage will automatically depolarize above the INa threshold due to the large nega

8 polarized below -40 mV and decreased as V(m) depolarized above -40 mV.

9 data suggest that GABA acquires a transient depolarizing action during recovery from UVN, which pote

10 ly suggesting that GABA acquires a transient depolarizing action in the VN during the recovery period

11 During development, GABA exerts depolarizing action on immature neurons and, acting in s

12 During development GABA exerts a depolarizing action on immature neurons.

13 s importantly contribute to GDPs, due to the depolarizing actions of GABA early in development.

14 sting induction and suppression of prolonged depolarizing afterpotential.

15 locked the ability of GLP-1 agonists and the depolarizing agent KCl to potentiate this.

16 The loss of Cdc42 resulted in a shift to depolarized AML cells that is associated with a decrease

17 (BL) photoactivation of CRY is sufficient to depolarize and activate Drosophila neurons.

18 ia in C452F mouse embryonic fibroblasts were depolarized and had reduced calcium uptake with impaired

19 ss, the inner mitochondrial membrane becomes depolarized and permeable to osmolytes, proposedly due t

20 At sleep onset RIS depolarizes and releases FLP-11 to induce a systemic sle

21 ree cycles), occurred when PVs and PYRs were depolarizing and entrained their membrane potential dyna

22 s channels of interest, including dephasing, depolarizing and erasure channels.

23 At these synapses, GABA is depolarizing and exerts a bimodal control on excitabilit

24 ionally control the membrane potential using depolarizing and hyperpolarizing opsins; the ability to

25 ctance increased stepwise and gradually with depolarizing and hyperpolarizing pulses, respectively.

26 expressing G77R and G83V were significantly depolarized as compared with WTKir4.1, whereas cells exp

27 nhanced ENaC current contributed to the more depolarized basal membrane potential observed in VP neur

28 elease by closing ATP-sensitive K+ channels, depolarizing beta cells, and opening voltage-dependent C

29 ues molecular pathology at the photoreceptor-depolarizing bipolar cell (photoreceptor-DBC) synapse an

30 For normal function, ON or depolarizing bipolar cells (DBCs) require the G-protein-

31 ARC glial activation non-specifically depolarizes both AgRP/NPY and POMC neurons but a strong

32 GABAergic current was depolarizing but inhibitory in 8.5 mM K(+), suggesting a

33 n C-neurons 7 d after axotomy, and their Ems depolarized by approximately 10 mV.

34 BK/Kv became basally active when cells were depolarized by elevated [KCl]o (>12 mm).

35 Surprisingly, dentate PV interneurons are depolarized by GABA signaling, which is in sharp contras

36 nts are insensitive to sound and only weakly depolarized by glutamate release from OHCs.

37 perisomatic regions (basket cells, BCs) were depolarized by muscarinic receptors.

38 ls only activate in spines that are strongly depolarized by their synaptic input, a process requiring

39 ochondrial membrane potential (Deltapsimito) depolarized; Ca(2+) was released from the endoplasmic re

40 endered them responsive to C12: Deltapsimito depolarized, Cacyto increased, and caspase 3/7 activated

41 , released from efferent terminals, directly depolarizes calyceal endings by activating nicotinic ACh

42 faced particle photothermally induces a cell-depolarizing capacitive current, and predicts that deliv

43 coded by the SCN5A gene, conducts the inward depolarizing cardiac Na(+) current (INa) and is vital fo

44 iomyocyte gap junctional coupling, TGF-beta1 depolarized cardiomyocytes coupled to myofibroblasts by

45 ffect mediated by the emergence of a rapidly depolarizing cell population, and the expression of hERG

46 ce, inhibition of Sty1 converts non-growing, depolarized cells into growing, polarized cells.

47 d CaMKII had enhanced persistent current and depolarized channel inactivation resembling the properti

48 ur voltage-clamp analysis showed that R1279P depolarizes channel activation, a change that was suppor

49 be searched, when decoherence is modelled by depolarizing channels' deleterious effects imposed on th

50 internal reflectivity, presence of internal depolarizing characteristics, and presence of overlying

51 leotide-gated (CNG) channel and stimulates a depolarizing chloride current by opening the olfactory C

52 Here we show that, in mice, 5-HT depolarizes cholinergic interneurons (ChIs) of the dSt w

53 er direct control, we used densely-expressed depolarizing (ChR2) or hyperpolarizing (eArch3.0, eNpHR3

54 The voltage sensor adopts a depolarized conformation, and the pore is closed.

55 this structure, the voltage sensors adopt a depolarized conformation, and the pore is open.

56 ogeneous medium internal reflectivity and no depolarizing contents (55.3% of drusen).

57 holds that optimal states exhibit tonically depolarized cortical neurons with enhanced spiking activ

58 e-type releaser at DAT that evoked an inward depolarizing current and calcium influx, whereas other a

59 ts due to a severe reduction of a muscarinic depolarizing current and M1 receptor internalization.

60 activation might cause a sharp escalation in depolarizing current and underlie the steep initial rise

61 the number of action potentials evoked by a depolarizing current at 2X rheobase in neurons from CCD

62 s can fire single action potentials (APs) to depolarizing current commands, but are unable to dischar

63 es the action potential waveform by reducing depolarizing current during the plateau phase of the act

64 e sodium current (INa) that provides a rapid depolarizing current during the upstroke of the action p

65 re quiescent or made to fire at low rates by depolarizing current injection, light-induced activation

66 the voltage-response to hyperpolarizing and depolarizing current injection.

67 The magnitude of [Ca(2+)]i reduction during depolarizing current injections correlated with the ampl

68 The maximum spike frequency evoked by depolarizing current injections in Scn8a(N1768D/+) CA1,

69 e majority of cells preset at -80 mV, 500 ms depolarizing current injections to cells led to a brief

70 y quantifying the impact of an infinitesimal depolarizing current pulse on the time of occurrence of

71 l Pv interneuron activation by intracellular depolarizing current pulses.

72 When driven by various forms of depolarizing current stimulus, Re neurons display consid

73 esponse increased indefinitely with injected depolarizing current, but reached saturation with chemic

74 tion of an M1-coupled, pirenzepine-sensitive depolarizing current, which appeared to be, at least in

75 A receptor activation initiated a secondary, depolarizing current.

76 sponses to hyperpolarizing (P < 0.00007) and depolarizing currents (P < 0.001) in threshold electroto

77 edictions and experimental results: net soma depolarizing currents increased choice hysteresis, while

78 In contrast, with stronger depolarizing currents, eliciting firing above approximat

79 exhibit no K(+) conductance, have a markedly depolarized DeltaPsi and little sensitivity to changes i

80 s, PAG shifted the transwall gradient in the depolarizing direction.

81 The SIAs depolarize during flipping and their optogenetic activat

82 nels only becomes important when the cell is depolarized (e.g. by a high external K(+) concentration)

83 patch-clamp recordings demonstrated that the depolarizing effect of 5-HT on PVINs was mediated by 5-H

84 The depolarizing effect of GLP-1 on electrical activity was

85 no such effect was observed when placing the depolarizing electrode over lateral PFC.

86 We placed the soma depolarizing electrode over medial frontal PFC.

87 ommon spectroscopic characteristics, such as depolarized emission, viscosity-dependent radiationless

88 ells equilibrated with FMP-Red-Dye exhibited depolarized equilibrium membrane potentials compared wit

89 de bifurcation, the system can automatically depolarize even in the absence of INa to voltages higher

90 ic ventral posterior medial neurons and with depolarizing events in the posterior nucleus neurons.

91 1632G mutation hyperpolarizes activation and depolarizes fast-inactivation, both gain-of-function att

92 ernal depolarizing structures and associated depolarizing foci.

93 These include the depolarizing 'funny current' (If ) and the sodium-calciu

94 ur findings show that early post-SE abnormal depolarizing GABA and p75(NTR) signaling fosters a long-

95 s of the K(+)/Cl(-) cotransporter KCC2 and a depolarizing GABAA receptor-mediated synaptic component

96 We found that depolarizing GABAergic and glutamatergic currents act in

97 A similar depolarizing GABAergic plexus exists in the developing h

98 increase in glutamatergic input and requires depolarizing GABAergic transmission and NMDA receptor ac

99 fuse intracerebrally a specific inhibitor of depolarizing GABAergic transmission as well as a functio

100 vivo also change the type of excitability: a depolarized gamma-Aminobutyric acid receptor (GABAR) rev

101 rewiring of excitatory circuits, an abnormal depolarizing gamma-aminobutyric acidergic (GABAergic) dr

102 ent individual principal cells from strongly depolarizing granule cells, which likely discharge in re

103 ation (EDH) characteristic of arteries, LECs depolarized (>15 mV) to either ACh or TRPV4 channel acti

104 13R expression is uniquely associated with a depolarizing, HCO3(-) independent, Cl(-) -conductance in

105 expressed ligand-gated Na(+) channel, which depolarizes horizontal cells, causes synaptic acidificat

106 h release depolarized VIP BCs whereas PV BCs depolarized, hyperpolarized or produced biphasic respons

107 abilization could also be elicited by single depolarizing/hyperpolarizing pulses of very high field s

108 Search-inducing sensory input depolarizes I4.

109 how that BK/Kv are activated as glomus cells depolarize in response to hypoxia, which then limits the

110 ve a negative resting membrane potential and depolarize in synchrony with cardiomyocytes.

111 To maintain CICR as rods remain depolarized in darkness, we hypothesized that Ca(2+) rel

112 be sustained indefinitely while rods remain depolarized in darkness.

113 that the reversal potential for GABA is more depolarized in mutant mice, but is restored by applicati

114 Resting membrane potential was more depolarized in Pitx2c(+/-) atria, and TWIK-related acid-

115 and miR-34c, which subsequently targeted key depolarizing (INa) and repolarizing (Ito) currents alter

116 ed with larger persistent sodium current and depolarized inactivation in neurons from F1.Q54 animals.

117 easing activity during behavior and directly depolarizing inhibitory cells.

118 ounted for largely by granule cells, receive depolarizing input from M/T dendrites and in turn inhibi

119 A depolarizing 'leak' current supports this firing pattern

120 rt in brain slices that activation of nAChRs depolarizes LHb cells and robustly increases firing, and

121 Depolarized light images were computed using a polarizat

122 atrial cardiomyocyte monolayers expressing a depolarizing light-gated ion channel (Ca(2+)-translocati

123 erences between the behavior of polarized vs depolarized mammalian mitochondria.

124 citatory and inhibitory synaptic inputs that depolarize many neurons to spike threshold before return

125 al of 30.5% of the drusen exhibited internal depolarizing material; 0.3% presented overlying hyperref

126 Finally, an ERalpha agonist depolarized MeA SIM1 neurons and increased their firing

127 leads to reduced Kv7.4 membrane abundance, a depolarized membrane potential and an augmented response

128 leads to reduced Kv7.4 membrane abundance, a depolarized membrane potential and an augmented response

129 flufenamic acid, an agent that restores the depolarized membrane potential of SCA1 Purkinje neurons

130 lular calcium ([Ca(2+)]i) and recovered with depolarized membrane potentials or elevated [Ca(2+)]i Co

131 ing K(+) channels conduct greater current at depolarized membrane potentials, whereas inward rectifie

132 us Ca release activates inward current which depolarizes membrane potential (Vm) and can trigger acti

133 rrent clamp, block of BKCa current increased depolarizing membrane potential excursions, raising the

134 amped horizontal cells, BKCa channels subdue depolarizing membrane potential excursions, reduce the a

135 Morpholino-induced knockdown of KCNE4 depolarized mesenteric artery smooth muscle cells and re

136 nction pharmacologically or by gene knockout depolarizes microglia, which decreases microglial ramifi

137 , we found that it was also able to directly depolarize mitochondria.

138 and 2-deoxyglucose, a glycolytic inhibitor, depolarized mitochondria after respiratory inhibition, w

139 PINK1 is stabilized on the outside of depolarized mitochondria and phosphorylates polyubiquiti

140 insufficient vesicle induction, accumulating depolarized mitochondria and PINK1.

141 not its E3 ligase-deficient mutants, reduces depolarized mitochondria and rescues cell death in neona

142 and Parkin E3 ubiquitin ligase in targeting depolarized mitochondria for degradation.

143 was shown to bind, ubiquitinate, and target depolarized mitochondria for destruction by autophagy.

144 ubiquitin ligase and mitophagy effector, on depolarized mitochondria in neonatal rat cardiac myocyte

145 l shRNA transduction induces accumulation of depolarized mitochondria in resting neonatal rat cardiac

146 The removal of damaged or depolarized mitochondria occurs via mitophagy, in which

147 intracellular oxidative stress by targeting depolarized mitochondria to the plasma membrane via arre

148 activation by PINK1, parkin is recruited to depolarized mitochondria where it ubiquitinates outer mi

149 e find that TBK1 is corecruited with OPTN to depolarized mitochondria.

150 increased recruitment of cytosolic Parkin to depolarized mitochondria.

151 and activation of TFEB, enhancing removal of depolarized mitochondria.

152 bilization of PINK1 on the outer membrane of depolarized mitochondria.

153 bioenergetics in MTC cells, as indicated by depolarized mitochondrial membrane, decreased oxygen con

154 by potent inhalation anesthetics and/or the depolarizing muscle relaxant succinylcholine in malignan

155 Basolateral membranes of DCT cells were depolarized, nearly devoid of conductive potassium trans

156 se of intracellular potassium, which in turn depolarizes neighbouring cells.

157 dullary respiratory networks that is able to depolarize neurons of the parafacial respiratory group d

158 d extracellular nTS glutamate concentration, depolarized neurons and enhanced spontaneous EPSCs.

159 Although GABA depolarizes neurons at rest and at the onset of populati

160 Reduction in temperature depolarizes neurons by a partial closure of potassium ch

161 The trapped mitochondria were depolarized on chip using an ionophore with results show

162 bative: e.g., by intentionally polarizing or depolarizing one spin species while detecting the respon

163 ience research through their use as membrane-depolarizing optogenetic tools for targeted photoactivat

164 oporation) that occurs while the membrane is depolarized or hyperpolarized to voltages beyond so-call

165 inguish whether a sympathetic nerve fibre is depolarized or not.

166 manipulated the activity of CI1 by injecting depolarizing or hyperpolarizing current or killing the c

167 post-trial activity decay through simulated depolarizing or hyperpolarizing network stimulation.

168 With mildly depolarizing or hyperpolarizing pulses just above thresh

169 e potassium in the synaptic cleft, and would depolarize other hair cells enveloped by the same neurit

170 Moreover, LPI depolarizes PAG neurons and upon intra-PAG microinjectio

171 Depolarizing PCs initiated a long-lasting increase in GA

172 Depolarizing pFL neurons produced active expiration at r

173 odium (Nav) channels are responsible for the depolarizing phase of the action potential in most nerve

174 on of cytosolic Ca(2+) concentration and the depolarized PM drive the efflux of K(+) from the cell, r

175 may hold even greater potential as tools for depolarizing political debates and resolving policy disp

176 l neurons between two SLEs correlated with a depolarizing potential.

177 polarized resting membrane potentials; these depolarized potentials cause cardiac arrhythmia; however

178 At depolarized potentials, the input-output function for sy

179 A735V shifted DII-VSD voltage dependence to depolarized potentials, whereas G752R significantly slow

180 rectifying K(+) channels are reduced at more depolarized potentials.

181 activation gating was slowed and shifted to depolarized potentials.

182 the threshold for channel activation to more depolarized potentials.

183 ft in their voltage activation curve to more depolarized potentials.

184 ssing a catalytically dead VSP mutant at all depolarized potentials.

185 this activity is observed in vitro as giant depolarizing potentials (GDPs) during the first postnata

186 ting in synergy with glutamate, drives giant depolarizing potentials (GDPs) in the hippocampal networ

187 taneous network events, referred to as giant depolarizing potentials (GDPs) in the hippocampus.

188 ated nicotinic ACh receptor (nAChR)-mediated depolarizing potentials and muscarinic ACh receptor (mAC

189 Our analysis reveals that these giant depolarizing potentials are mediated by the activation o

190 rticocallosal neurons lacking mAChR-mediated depolarizing potentials did not show persistent firing.

191 These prolonged depolarizing potentials generated persistent firing in c

192 rons, ACh generated prolonged mAChR-mediated depolarizing potentials in corticocollicular neurons.

193 re hyperexcitable and generated long-lasting depolarizing potentials with bursts of action potentials

194 ous activities appeared in the form of giant depolarizing potentials.

195 s, ACh release also generated nAChR-mediated depolarizing potentials.

196 olonged critical period permissive for giant depolarizing potentials.

197 When UV was applied at progressively more depolarized preopen holding potentials, cross-linking of

198 and slowing of deactivation in response to a depolarizing prepulse.

199 inhibition was voltage-dependent, and strong depolarizing prepulses attenuated Hm-3 activity.

200 time course of recovery from short and long depolarizing prepulses, which, under drug-free condition

201 on was voltage-independent and unaffected by depolarizing prepulses.

202 oltage-dependent and transiently relieved by depolarizing prepulses.

203 entries using Grover's QSA at an aggressive depolarizing probability of 10(-3), the success probabil

204 Using long (20 s) depolarizing pulses both gating modes were activated, an

205 e receptor agonist (4-chloro-meta-cresol) or depolarizing pulses were used.

206 -VSD deactivation kinetics were modulated by depolarizing pulses with durations in the intermediate t

207 parated signals, i.e., the polarized and the depolarized Raman signal.

208 ptical Kerr-effect spectroscopy to study the depolarized Raman spectra of lysozyme and its complex wi

209 Tonic firing was seen in depolarized regimes and bursting at hyperpolarized membr

210 Depolarizing responses in VIP or PV BCs resulted in incr

211 allenged mice displayed a significantly more depolarized resting membrane potential, decreased rheoba

212 er hyperpolarization-activated current (Ih), depolarized resting membrane potential, faster action po

213 gs showed significantly decreased amplitude, depolarized resting membrane potential, increased durati

214 ent-clamp experiments small neurons had more depolarized resting membrane potentials, and required sm

215 rbil IHCs (~0.3 kHz) have significantly more depolarized resting membrane potentials, faster kinetics

216 cardiomyocytes show both hyperpolarized and depolarized resting membrane potentials; these depolariz

217 d Go-opsin1 coexpressed with two r-opsins in depolarizing rhabdomeric photoreceptor cells in the pigm

218 rebound or post-stimulation recovery, and no depolarizing sag.

219 l mutations (W1775R and L1831X) exhibiting a depolarizing shift in channel activation.

220 Application of VU0463271 caused a reversible depolarizing shift in E(GABA) values and increased spiki

221 According to computational modeling, a depolarizing shift in GABA reversal potential (EGABA) an

222 uced membrane hyperpolarization and caused a depolarizing shift in GABA reversal potential of dorsal

223 physically distinct K(+) currents revealed a depolarizing shift in the activation of a rapidly inacti

224 SNAP caused a depolarizing shift in voltage-dependent N-type channel a

225 fter spinal cord injury (SCI) resulting in a depolarizing shift of the chloride equilibrium potential

226 d with loss-of-function effects, including a depolarizing shift of voltage-dependent activation or a

227 isolated from ST3Gal4(-/-) mice demonstrated depolarizing shifts in activation gating of the transien

228 Non-depolarizing shunts of 3-10 nS converted cells from clas

229 lts in inward transient cation currents that depolarize smooth muscle cells, leading to vasoconstrict

230 out preventing further prolongation by brief depolarizing somatic prepulses.

231 hat glucose-stimulated beta cells spent in a depolarized state with high cytosolic Ca(2+) concentrati

232 ty, in the form of recurring self-maintained depolarized states (Up states), which allows us to exami

233 cells demonstrated that R1279P significantly depolarizes steady-state fast-, slow-, and closed-state

234 ulse potentiation," in which activation by a depolarizing step facilitates activation in a subsequent

235 reported that the K current in response to a depolarizing step to ENa was delayed if the step was pre

236 age-dependence of channel activation so that depolarizing steps evoke larger sodium currents.

237 ion, rather than to the timing of subsequent depolarizing steps, suggesting that cholinergic signal t

238 CO2/H+ changes), in the absence of external depolarizing stimulation, showed no signs of postinhibit

239 unced slowing of current inactivation during depolarizing stimuli (p.G407R).

240 ormally governs cortical neuron responses to depolarizing stimuli by opposing prolonged discharges an

241 porting persistent firing modes triggered by depolarizing stimuli following cholinergic receptor acti

242 T-channels switched burst firing with lower depolarizing stimuli to regular spiking, and fully aboli

243 entate granule neurons in response to strong depolarizing stimuli was also observed.

244 ted modest transient electrical responses to depolarizing stimuli, revealing the potential for circad

245 ted modest transient electrical responses to depolarizing stimuli.

246 rotein densin and CaMKII and that outlasts a depolarizing stimulus by seconds.

247 il current of up to 8 s duration following a depolarizing stimulus in both tsA-201 cells and male rat

248 enings that can last for seconds following a depolarizing stimulus train.

249 litation of channel activity that outlasts a depolarizing stimulus.

250 utward tail current of up to 8 s following a depolarizing stimulus.

251 n scheme, including the presence of internal depolarizing structures and associated depolarizing foci

252 of Parkin, VCP/p97, p62/Ref(2)P and Atg8a to depolarized swollen mitochondria.

253 peak spike rates, and were more sensitive to depolarizing synaptic input.

254 n contrast, PID ripples were associated with depolarizing synaptic inputs frequently reaching the thr

255 lexiform layers after glutamatergic synapses depolarize TH cell dendrites in the inner plexiform laye

256 harge transfer, allows presynaptic AMPARs to depolarize the bouton membrane sufficiently to modulate

257 glucose metabolism alone is insufficient to depolarize the cell and evoke GLP-1 secretion in the mod

258 vating non-selective cationic channels which depolarize the membrane potential.

259 single motoneuron inputs were sufficient to depolarize the Renshaw cell beyond threshold for firing.

260 Local CRFR2 activation by urocortin 3 depolarized the cells, increased the neuronal input resi

261 Mechanistically, GABA depolarized the majority of sensory neuron somata, yet p

262 sed the GluN1/GluN3A equilibrium current and depolarized the membrane in a glycine concentration-depe

263 The elevated potassium concentration also depolarized the postsynaptic neuron by altering ion perm

264 CXCL12 depolarized the resting membrane potential, decreased th

265 Blocking SK channels with apamin depolarized the resting membrane potential, reduced rest

266 f quanta released, elevates [K(+) ]cleft and depolarizes the afferent to potentials at which smaller

267 tores activates inward membrane currents and depolarizes the beta cell to the threshold for VDCC acti

268 Blocking K(ATP) channels pharmacologically depolarizes the beta-cell plasma membrane and terminates

269 ducing a flux of Na(+) and/or K(+) ions that depolarizes the cell, thus modulating cellular Ca(2+) en

270 This current depolarizes the hair cell and triggers the calcium-induc

271 tials in response to a current stimulus that depolarizes the membrane above an excitation threshold.

272 In addition, we also found that shizukaol F depolarizes the mitochondrial membrane and inhibits resp

273 Elevated potassium depolarizes the postsynaptic afferent by altering ion pe

274 ide-gated (HCN) channels, and contributes to depolarizing the afferent to potentials where a single E

275 y of ENaCs, which augments synaptic drive by depolarizing the basal membrane potential close to the a

276 to heat, which changes membrane capacitance, depolarizing the cell and eliciting action potentials.

277 ctivity of sarcolemmal Na(+)-Ca(2+) exchange depolarizing the cell membrane.

278 on potential firing to current injection and depolarizing the membrane potential.

279 oss-linked 300 kDa increased excitability by depolarizing the resting membrane potential, and decreas

280 l enhancement is accomplished by selectively depolarizing the xenon within a cage molecule which, upo

281 here transduction currents are sufficient to depolarize them to voltages necessary for calcium influx

282 ium conductance via the NA/NALCN ion channel depolarizes these neurons.

283 cted selectively to increase their activity, depolarizing these neurons and increasing their firing r

284 An accompanying increase in depolarizing threshold electrotonus at 90 to 100 millise

285 ts transiently switched their direction from depolarizing to hyperpolarizing as a result of neuronal

286 e that PIN-PMN-PT crystals became completely depolarized under 3.9 GPa compression.

287 ons display synchronized transitions between depolarized Up states and hyperpolarized Down states.

288 ia and 4 unaffected control individuals were depolarized using potassium chloride.

289 lf-maximal Kv11.3 channel activation to more depolarized values and reduced its voltage sensitivity.

290 ACh release depolarized VIP BCs whereas PV BCs depolarized, hyperpol

291 sponses in V1 to a stationary scene, 2) that depolarized VIP cells enhance V1 responses to moving obj

292 ength to overcome a weakened current sink to depolarize Vm and trigger action potentials.

293 Local Ca waves depolarized Vm in HF but not CTL hearts, suggesting weak

294 y describes one physiological form of KCNQ1, depolarized voltage sensors with a closed pore in the ab

295 ed that strong hyperpolarization preceding a depolarizing voltage-clamp pulse delayed the rise of the

296 s study observed residual STOC production at depolarized voltages that was independent of CaV 1.2 and

297 (IKur) inactivates slowly but completely at depolarized voltages.

298 Being activated by depolarizing voltages and increases in cytoplasmic Ca(2+

299 JZTx-27 was more efficacious at weaker depolarizing voltages and significantly slowed the activ

300 is not dependent on the level of maturation (depolarizing vs. hyperpolarizing) of postsynaptic GABAA