ライフサイエンスコーパス: excitatory postsynaptic current

1 glia induces a rapid increase of spontaneous excitatory postsynaptic currents.

2 ency and amplitude of alpha3*-nAChR-mediated excitatory postsynaptic currents.

3 hosphorylation restricts the potentiation of excitatory postsynaptic currents.

4 GluR1), and AMPA receptor-mediated miniature excitatory postsynaptic currents.

5 and peak amplitude of spontaneous miniature excitatory postsynaptic currents.

6 ecruit surface AMPA receptors and potentiate excitatory postsynaptic currents.

7 traction did not alter parallel fiber-evoked excitatory postsynaptic currents.

8 entiation and NMDA receptor (NMDAR)-mediated excitatory postsynaptic currents.

9 tory postsynaptic currents with no effect on excitatory postsynaptic currents.

10 ely contribute to the biexponential decay of excitatory postsynaptic currents.

11 the exercise-induced increases in spines and excitatory postsynaptic currents.

12 a(2+) concentration ([Ca(2+)](i) spikes) and excitatory postsynaptic currents.

13 rrents and increased the amplitude of evoked excitatory postsynaptic currents.

14 in the amplitude and frequency of miniature excitatory postsynaptic currents.

15 26E), as determined by analysis of miniature excitatory postsynaptic currents.

16 ng SF1 projections to the PVT elicits direct excitatory postsynaptic currents.

17 pontaneous action potentials and spontaneous excitatory postsynaptic currents.

18 teral amygdala pyramidal neurons, generating excitatory postsynaptic currents.

19 ing the frequency of glutamatergic miniature excitatory postsynaptic currents.

20 e amplitude, but not frequency, of miniature excitatory postsynaptic currents.

21 kable depression of AMPAR-mediated miniature excitatory postsynaptic currents, a significant reductio

22 Evoked excitatory transmitter release and excitatory postsynaptic currents also were heightened at

23 ion and reduced decay time of AMPAR-mediated excitatory postsynaptic currents (AMPAR-EPSCs), enhanced

24 on elicits a long-lasting decrease in evoked excitatory postsynaptic current amplitude and a delayed,

25 rea, as well as an increase in the miniature excitatory postsynaptic current amplitude and frequency.

26 mediated partly by an increase in miniature excitatory postsynaptic current amplitude and partly by

27 Excitatory postsynaptic current amplitude was reduced to

28 Specifically, spontaneous excitatory postsynaptic current amplitudes measured from

29 ptic current frequencies, although miniature excitatory postsynaptic current amplitudes remained simi

30 ed hippocampal neurons showed that miniature excitatory postsynaptic current amplitudes were larger i

31 yptamine1b-type serotonin receptor to reduce excitatory postsynaptic current amplitudes, an effect pr

32 A-type glutamate receptor-mediated miniature excitatory postsynaptic currents, an effect dependent on

33 significant metabolic advantage over quantal excitatory postsynaptic currents--an advantage that may

34 a short-term plasticity model and cumulative excitatory postsynaptic current analysis to quantify the

35 They contribute to the excitatory postsynaptic current and to the detection of

36 botropic glutamate receptor type 1)-mediated excitatory postsynaptic currents and a reduced sensitivi

37 or single cKO of NL1 impaired NMDAR-mediated excitatory postsynaptic currents and abolished NMDAR-dep

38 cally reduced AMPA receptor (AMPAR)-mediated excitatory postsynaptic currents and AMPAR surface expre

39 of vesicle exocytosis accompanied by loss of excitatory postsynaptic currents and commensurately pert

40 t increased the amplitude of the spontaneous excitatory postsynaptic currents and decreased the frequ

41 t inhibition of these channels reduces PF-PC excitatory postsynaptic currents and excitatory postsyna

42 al slices, the compound reversibly increased excitatory postsynaptic currents and field excitatory po

43 sured via electrophysiological recordings of excitatory postsynaptic currents and hippocampal long-te

44 ex of BC1 knock out (KO) mice display larger excitatory postsynaptic currents and increased spontaneo

45 d the amplitude and frequency of spontaneous excitatory postsynaptic currents and increased the ampli

46 red using electrophysiological recordings of excitatory postsynaptic currents and long-term potentiat

47 and NR2B expression but also NMDAR-mediated excitatory postsynaptic currents and potentials, without

48 s of CPT1C KO mice, AMPAR-mediated miniature excitatory postsynaptic currents and synaptic levels of

49 nnelrhodopsin-2 elicited both inhibitory and excitatory postsynaptic currents and triggered network b

50 s demonstrate that kainate-receptor-mediated excitatory postsynaptic currents are decreased by SUMOyl

51 neuronal" dynamins, dynamin 1 and 3, smaller excitatory postsynaptic currents are observed due to an

52 ly coupled myenteric neurons, nicotinic fast excitatory postsynaptic currents are occluded during act

53 t-selective increase in dendritic spines and excitatory postsynaptic currents at 3 days post-exercise

54 causes a significant decrease in spontaneous excitatory postsynaptic currents at both two and twenty

55 f variability in the amplitudes of miniature excitatory postsynaptic currents at single synapses reve

56 We found larger excitatory postsynaptic currents at the synapses between

57 In control animals, IL-6 did not affect excitatory postsynaptic currents but selectively and rev

58 naptically localized ASICs contribute to the excitatory postsynaptic current by responding to the tra

59 Moreover, the depression of AMPAR-mediated excitatory postsynaptic currents by SNRIs required p38 k

60 yielded slower kinetics in vitro and slower excitatory postsynaptic current decays in neurons.

61 The frequency of miniature excitatory postsynaptic currents decreased, accompanied

62 recording techniques, evoked or spontaneous excitatory postsynaptic currents (eEPSCs or sEPSCs) were

63 0-50 nm) also produced an increase of evoked excitatory postsynaptic currents (eEPSCs) at mossy fibre

64 oM) significantly decreased the amplitude of excitatory postsynaptic currents (eEPSCs) evoked by stim

65 but had no significant effect on the evoked excitatory postsynaptic currents (eEPSCs) in 10 of these

66 Excitatory postsynaptic currents (eEPSCs) were evoked by

67 R) and AMPA/kainate receptor-mediated evoked excitatory postsynaptic currents (eEPSCs), by 94% and 72

68 educed the amplitude of evoked NMDA-mediated excitatory postsynaptic currents (eEPSCs), without affec

69 leading to increased amplitudes of miniature excitatory postsynaptic currents, enhancement of LTP, an

70 Two additional properties, Q and average excitatory postsynaptic current (EPSC) amplitude, were u

71 r, exclusion of these failures leads to mean excitatory postsynaptic current (EPSC) amplitudes that a

72 ransmitter release, as measured by miniature excitatory postsynaptic current (EPSC) analysis and FM 1

73 creased in normal mice, a glutamate-mediated excitatory postsynaptic current (EPSC) between mitral ce

74 measures: steady-state NMDA currents, NMDAR excitatory postsynaptic current (EPSC) decay kinetics, p

75 mice, as revealed by a decrease in miniature excitatory postsynaptic current (EPSC) frequency and in

76 tion of trigeminal afferent fibres evoked an excitatory postsynaptic current (EPSC) in trigeminal neu

77 own that long-term potentiation (LTP) of the excitatory postsynaptic current (EPSC) through glutamate

78 he trapezoid body (MNTB) neurones during 1 s excitatory postsynaptic current (EPSC) trains delivered

79 Fast P2X receptor-mediated excitatory postsynaptic current (EPSC) was identified in

80 te (NMDA) receptor-mediated component of the excitatory postsynaptic current (EPSC), but did not affe

81 pontaneous, miniature and stimulation-evoked excitatory postsynaptic current (EPSC).

82 gs confirmed that this aberrant AP evoked an excitatory postsynaptic current (EPSC).

83 but not paired-pulse ratio of NMDAR-mediated excitatory postsynaptic currents (EPSC) in PFC slices.

84 y is used to reverse ion influxes generating excitatory postsynaptic currents (EPSCs) and action pote

85 At parallel fiber synapses, mGluR1-mediated excitatory postsynaptic currents (EPSCs) and associated

86 quiescent MS patients on glutamate-mediated excitatory postsynaptic currents (EPSCs) and excitotoxic

87 that presynaptic depression of glutamatergic excitatory postsynaptic currents (EPSCs) and GABAergic i

88 )-Baclofen depressed the amplitude of evoked excitatory postsynaptic currents (EPSCs) and inhibitory

89 NMDAR-mediated excitatory postsynaptic currents (EPSCs) and puff NMDA-e

90 pro-apoptotic gene Bax in stem cells reduced excitatory postsynaptic currents (EPSCs) and spine densi

91 THC (1 microM) inhibited excitatory postsynaptic currents (EPSCs) and whole-cell

92 basket cells (BCs), we found that classical excitatory postsynaptic currents (EPSCs) are followed by

93 MF-gc) synapses of mature cerebellum, evoked excitatory postsynaptic currents (EPSCs) are multiquanta

94 orsal root evoked non-NMDA receptor-mediated excitatory postsynaptic currents (EPSCs) at -60 mV that

95 AMPA-type glutamate receptors mediate most excitatory postsynaptic currents (EPSCs) at central syna

96 luzole nearly completely depresses glutamate excitatory postsynaptic currents (EPSCs) at concentratio

97 (5-HT) receptor signaling potently inhibits excitatory postsynaptic currents (EPSCs) between lamprey

98 d in a slowing of the decay time constant of excitatory postsynaptic currents (EPSCs) by approximatel

99 ective locus for the generation of increased excitatory postsynaptic currents (EPSCs) by serotonin (5

100 he effects of extracellular zinc on NR1/NR2A excitatory postsynaptic currents (EPSCs) by simulating t

101 rtion of glutamate uncaging sites from which excitatory postsynaptic currents (EPSCs) could be evoked

102 PCs showed increased duration of spontaneous excitatory postsynaptic currents (EPSCs) during the symp

103 sent study aims to explore corticogeniculate excitatory postsynaptic currents (EPSCs) evoked by brief

104 ly identified neurons were patch-clamped and excitatory postsynaptic currents (EPSCs) evoked by elect

105 CRF (30-300 nM) increased the amplitude of excitatory postsynaptic currents (EPSCs) evoked by stimu

106 Excitatory postsynaptic currents (EPSCs) evoked by stimu

107 cantly reduced the amplitude of monosynaptic excitatory postsynaptic currents (EPSCs) evoked from the

108 se in the postnatal rat cochlea by recording excitatory postsynaptic currents (EPSCs) from afferent b

109 es are changed during lactation, we recorded excitatory postsynaptic currents (EPSCs) from identified

110 on-like behaviors and associated deficits in excitatory postsynaptic currents (EPSCs) generated in ap

111 marked increase in glutamatergic spontaneous excitatory postsynaptic currents (EPSCs) in apical dendr

112 apses to sensory representation by recording excitatory postsynaptic currents (EPSCs) in cerebellar g

113 dramatic reduction of AMPA receptor-mediated excitatory postsynaptic currents (EPSCs) in cortical neu

114 ncentration-dependent inhibition of autaptic excitatory postsynaptic currents (EPSCs) in cultured hip

115 ds and cones that in turn produced transient excitatory postsynaptic currents (EPSCs) in horizontal a

116 Channelrhodopsin-2-assisted mapping of excitatory postsynaptic currents (EPSCs) in L2/3 shows t

117 used an increase in frequency of spontaneous excitatory postsynaptic currents (EPSCs) in layer V pyra

118 gnificantly increased the amplitude of basal excitatory postsynaptic currents (EPSCs) in MAGL(-/-) mi

119 Excitatory postsynaptic currents (EPSCs) in monosynaptic

120 projection induced a transient inhibition of excitatory postsynaptic currents (EPSCs) in NAcSh princi

121 ST stimulation elicits excitatory postsynaptic currents (EPSCs) in NTS neurons

122 as addressed here by examining glutamatergic excitatory postsynaptic currents (EPSCs) in rat autaptic

123 armacologically isolate KA receptor-mediated excitatory postsynaptic currents (EPSCs) in rat hippocam

124 ion of the STN evoked complex, long-duration excitatory postsynaptic currents (EPSCs) in SNR neurons.

125 1) receptor-mediated inhibition of glutamate excitatory postsynaptic currents (EPSCs) in the nucleus

126 SCs; retigabine had no significant effect on excitatory postsynaptic currents (EPSCs) mediated by act

127 Here we examined excitatory postsynaptic currents (EPSCs) of dorsal horn

128 increase in the amplitude of NMDAR-mediated excitatory postsynaptic currents (EPSCs) of dorsal horn

129 Here, we found that evoked NMDAR-excitatory postsynaptic currents (EPSCs) of retrogradely

130 aptic stimulation at 1 Hz for 30 s, enhanced excitatory postsynaptic currents (EPSCs) on non-pyramida

131 methyl-D-aspartate receptor (NMDAR)-mediated excitatory postsynaptic currents (EPSCs) onto VTA dopami

132 urkinje cells by measuring the inhibition of excitatory postsynaptic currents (EPSCs) produced by a l

133 The excitatory postsynaptic currents (EPSCs) recorded in lam

134 celeration of AMPA receptor (AMPAR)-mediated excitatory postsynaptic currents (EPSCs) remains elusive

135 Evaluation of excitatory postsynaptic currents (EPSCs) revealed that r

136 In second-order NTS neurones, excitatory postsynaptic currents (EPSCs) synaptically ev

137 firing has been shown to arise from complex excitatory postsynaptic currents (EPSCs) that are evoked

138 Trains with 10 stimuli at 25 Hz evoked excitatory postsynaptic currents (EPSCs) that grew in am

139 y stimulation produced bursts of mossy fibre excitatory postsynaptic currents (EPSCs) that summate to

140 n of nucleus tractus solitarii (NTS) induced excitatory postsynaptic currents (EPSCs) that were reduc

141 of N-methyl-d-aspartate (NMDA) component of excitatory postsynaptic currents (EPSCs) through a posts

142 MDA (N-methyl-d-aspartate) receptor-mediated excitatory postsynaptic currents (EPSCs) was decreased a

143 Whole-cell voltage clamp recordings of excitatory postsynaptic currents (EPSCs) were performed

144 Excitatory postsynaptic currents (EPSCs) were recorded f

145 Whole-cell excitatory postsynaptic currents (EPSCs) were recorded f

146 Evoked glutamatergic excitatory postsynaptic currents (EPSCs) were reversibly

147 Evoked excitatory postsynaptic currents (EPSCs) were reversibly

148 Excitatory postsynaptic currents (EPSCs) were studied in

149 synapses, potentiated AMPA receptor (AMPAR) excitatory postsynaptic currents (EPSCs), and occluded L

150 -methyl-D-aspartate (NMDA) receptor-mediated excitatory postsynaptic currents (EPSCs), but not alpha-

151 on in the perforant path-evoked monosynaptic excitatory postsynaptic currents (EPSCs), or in the intr

152 Evoked excitatory postsynaptic currents (EPSCs), spontaneous EP

153 R1 and beta(2)AR, and AMPA receptor-mediated excitatory postsynaptic currents (EPSCs).

154 ors (NMDARs) and a slowing of NMDAR-mediated excitatory postsynaptic currents (EPSCs).

155 ed into CA1 pyramidal cells while monitoring excitatory postsynaptic currents (EPSCs).

156 sites on the time course of Purkinje neuron excitatory postsynaptic currents (EPSCs).

157 ion and decreased the frequency of miniature excitatory postsynaptic currents (EPSCs).

158 t with this, PrRP increased the amplitude of excitatory postsynaptic currents (EPSCs, 154 +/- 33%, 12

159 neous and miniature excitatory transmission (excitatory postsynaptic currents, EPSCs).

160 At 42 h after ischemia, AMPA excitatory postsynaptic currents exhibited pronounced in

161 b consisted of an initial fast glutamatergic excitatory postsynaptic current followed by a slow-risin

162 ic NAc core inputs, we recorded light-evoked excitatory postsynaptic currents following viral-mediate

163 erentiation, together with reduced miniature excitatory postsynaptic current frequencies and behavior

164 d, consequently, by a reduction of miniature excitatory postsynaptic current frequencies, although mi

165 nsity is associated with increased miniature excitatory postsynaptic current frequency and amplitude,

166 ubjects with ASD exhibited reduced miniature excitatory postsynaptic current frequency and N-methyl-D

167 Second, basal miniature excitatory postsynaptic current frequency in alpha(1A) (

168 ly, P2Y1 stimulation of astrocytes increased excitatory postsynaptic current frequency through a meta

169 AS exon 3 recapitulated diminished miniature excitatory postsynaptic current frequency, supporting a

170 y coincident with an increase in spontaneous excitatory postsynaptic current frequency.

171 nd DG GCs exhibit increased mEPSC (miniature excitatory postsynaptic current) frequency.

172 ise generated by these synapses, we recorded excitatory postsynaptic currents from mammalian retinal

173 l excitability by inferring the magnitude of excitatory postsynaptic currents from the N20 component

174 The decay time course of excitatory postsynaptic currents generated by slow gluta

175 years several examples of proton-evoked ASIC excitatory postsynaptic currents have emerged.

176 ency led to reduced frequencies of miniature excitatory postsynaptic currents, i.e., to defects in sy

177 hospholipase D in the generation of the slow excitatory postsynaptic current in cerebellar Purkinje c

178 recordings revealed a concomitant nonquantal excitatory postsynaptic current in the calyx terminal th

179 0%) attenuation of electrically evoked local excitatory postsynaptic current in the saline and ShA gr

180 ses the frequency of AMPA-mediated miniature excitatory postsynaptic currents in CA1 pyramidal neuron

181 Stimulation of the vagus nerve evoked excitatory postsynaptic currents in CVNs that were rever

182 m, we show that the frequency of spontaneous excitatory postsynaptic currents in dentate gyrus granul

183 nding evoked dopamine release in the DMS and excitatory postsynaptic currents in DMS MSNs.

184 equency, but not the amplitude, of miniature excitatory postsynaptic currents in dorsal horn neurons

185 uced calcium influx, and increased miniature excitatory postsynaptic currents in hippocampal neurons.

186 endrites and decrements in apically targeted excitatory postsynaptic currents in layer V pyramidal ce

187 cleus accumbens measuring glutamate-mediated excitatory postsynaptic currents in medium spiny neurons

188 d synaptic spine density/diameter, increased excitatory postsynaptic currents in mPFC layer V pyramid

189 n hippocampal slices and autaptically evoked excitatory postsynaptic currents in neuronal cultures wi

190 Excitatory postsynaptic currents in post-ischemic CA1 ex

191 ently, the rate of spontaneous and miniature excitatory postsynaptic currents in pyramidal neurons an

192 (2+) responses despite a marked reduction in excitatory postsynaptic currents in response to whisker

193 nd causes increased frequency of spontaneous excitatory postsynaptic currents in spinal cord nocicept

194 e effectively block NMDAR-mediated miniature excitatory postsynaptic currents in the absence of Mg(2+

195 rocytes reduced the frequency of spontaneous excitatory postsynaptic currents in the direct pathway M

196 ritic density and the frequency of miniature excitatory postsynaptic currents in the mPFC were preven

197 s serotonin-induced increases in spontaneous excitatory postsynaptic currents in the mPFC, mimicking

198 as cocaine produced comparable inhibition of excitatory postsynaptic currents in the nucleus accumben

199 ected by decreased amplitudes of spontaneous excitatory postsynaptic currents in young neonates (-34.

200 nist at GABA(A) receptors, strongly enhanced excitatory postsynaptic currents in young rats but had l

201 xcitatory synaptic transmission (spontaneous excitatory postsynaptic currents) in spinal lamina IIo n

202 oid subtype-1 (TRPV1)- and TNF-alpha-induced excitatory postsynaptic current increases and TNF-alpha-

203 Specifically, miniature excitatory postsynaptic currents, input resistance, hipp

204 notypic slices, NMDAR-dependent LTD of AMPAR excitatory postsynaptic currents is abolished in neurons

205 Indeed, the amplitude of miniature excitatory postsynaptic currents is enhanced in both Vac

206 By regulating KAR excitatory postsynaptic current kinetics, Neto1 can cont

207 ipolar cell output by recording light-evoked excitatory postsynaptic currents (L-EPSCs) from postsyna

208 rent study, the light-evoked and spontaneous excitatory postsynaptic currents (light-evoked EPSCs and

209 ptors in the cerebellum also leads to a slow excitatory postsynaptic current mediated by nonselective

210 for AMPAR clustering at synapses, miniature excitatory postsynaptic currents mediated by TARPless AM

211 nic acid receptor (AMPAR)-mediated miniature excitatory postsynaptic current (mEPSC) amplitudes due t

212 he inhibitory synapses assessed by miniature excitatory postsynaptic current (mEPSC) and electron mic

213 subunit, reduces the frequency of miniature excitatory postsynaptic current (mEPSC), and reduces AMP

214 de and frequency of AMPAR-mediated miniature excitatory postsynaptic current (mEPSC), while expressin

215 fects were seen with glutamatergic miniature excitatory postsynaptic currents (mEPSCs) and GABAergic

216 The miniature excitatory postsynaptic currents (mEPSCs) and miniature

217 ampal slices, (iii) NMDAR-mediated miniature excitatory postsynaptic currents (mEPSCs) and NMDA-evoke

218 tic scaling up of the amplitude of miniature excitatory postsynaptic currents (mEPSCs) and of synapti

219 ed the frequency of NMDAR-mediated miniature excitatory postsynaptic currents (mEPSCs) and the amplit

220 uced increases in the frequency of miniature excitatory postsynaptic currents (mEPSCs) and the number

221 ic events were larger than quantal miniature excitatory postsynaptic currents (mEPSCs) but had the sa

222 ic density (PSD) and contribute to miniature excitatory postsynaptic currents (mEPSCs) elicited by si

223 Miniature excitatory postsynaptic currents (mEPSCs) from embryonic

224 ers, octopus and T stellate cells, miniature excitatory postsynaptic currents (mEPSCs) had similar sh

225 rats revealed higher frequency of miniature excitatory postsynaptic currents (mEPSCs) immediately af

226 ad no effect on glutamate-mediated miniature excitatory postsynaptic currents (mEPSCs) in 12 of 15 ne

227 napses, allowing us to record NMDA-miniature excitatory postsynaptic currents (mEPSCs) in addition to

228 mplitude of the NMDAR component of miniature excitatory postsynaptic currents (mEPSCs) in CA1 interne

229 in the frequency of glutamatergic miniature excitatory postsynaptic currents (mEPSCs) in cardiac vag

230 uency and amplitude of spontaneous miniature excitatory postsynaptic currents (mEPSCs) in cultured mo

231 The frequency of miniature excitatory postsynaptic currents (mEPSCs) in principal n

232 stsynaptic potentials (fEPSPs) and miniature excitatory postsynaptic currents (mEPSCs) in rat hippoca

233 sed a decrease in the frequency of miniature excitatory postsynaptic currents (mEPSCs) in SON neurone

234 frequency but not the amplitude of miniature excitatory postsynaptic currents (mEPSCs) mediated by al

235 ole cell patch clamp recordings of miniature excitatory postsynaptic currents (mEPSCs) revealed that

236 Miniature excitatory postsynaptic currents (mEPSCs) were recorded

237 hibition were blocked, spontaneous miniature excitatory postsynaptic currents (mEPSCs) were recorded.

238 e amplitude and charge transfer of miniature excitatory postsynaptic currents (mEPSCs) were significa

239 on increased the amplitude of AMPA miniature excitatory postsynaptic currents (mEPSCs), and shRNA-med

240 ith electron microscopy, and giant miniature excitatory postsynaptic currents (mEPSCs), reflecting mo

241 rfold increase in the frequency of miniature excitatory postsynaptic currents (mEPSCs).

242 in the amplitude and frequency of miniature excitatory postsynaptic currents (mEPSCs).

243 ollowed by reduction in evoked and miniature excitatory postsynaptic currents (mEPSCs).

244 Moreover, analysis of the miniature excitatory postsynaptic currents (mEPSCs)/inhibitory pos

245 quency or amplitude of spontaneous miniature excitatory postsynaptic currents (mEPSCs); however, syna

246 porters and mGluRs by evoking mGluR-mediated excitatory postsynaptic currents (mGluR EPSCs) in slices

247 n addition to reduced frequency of miniature excitatory postsynaptic currents (mini-EPSCs) and smalle

248 ed the frequency of miniature inhibitory and excitatory postsynaptic currents (mIPSCs and mEPSCs, res

249 AA IPSCs) and reduces NMDA receptor-mediated excitatory postsynaptic currents (NMDA EPSCs) in a conce

250 We recorded NMDA and AMPA miniature excitatory postsynaptic currents (NMDA- and AMPA-mESPCs)

251 attenuates the shortening of NMDAR-mediated excitatory postsynaptic currents (NMDAR-EPSCs) during ea

252 RG neurons and the amplitude of monosynaptic excitatory postsynaptic currents of dorsal horn neurons

253 rrents in small DRG neurons and monosynaptic excitatory postsynaptic currents of spinal dorsal horn n

254 pecific differences that are associated with excitatory postsynaptic currents on mPFC principle neuro

255 nt with experimental recordings of miniature excitatory postsynaptic currents only when ectopic trans

256 s do not associate with changes in miniature excitatory postsynaptic currents or paired-pulse facilit

257 ermeability and a change in the amplitude of excitatory postsynaptic currents, owing to the incorpora

258 We found that in leaner PCs, PF-evoked excitatory postsynaptic currents (PF-EPSCs) are approxim

259 AMPARs, generating rapid, lasting changes in excitatory postsynaptic current properties.

260 These mice exhibit a decrease in NMDA/AMPA excitatory postsynaptic current ratio in area CA1 of the

261 Quantal analysis of excitatory postsynaptic currents, recorded at neuromuscu

262 on responded more actively with an increased excitatory postsynaptic current response upon the applic

263 d the frequency of spontaneous and miniature excitatory postsynaptic currents (s/mEPSCs).

264 holding current, but facilitated spontaneous excitatory postsynaptic current (sEPSC) frequency in 41%

265 Spontaneous excitatory postsynaptic currents (sEPSC) recorded in cNT

266 In the PVN, the frequency of spontaneous excitatory postsynaptic currents (sEPSC) was elevated in

267 ion by reducing the frequency of spontaneous excitatory postsynaptic current (sEPSCs).

268 Spontaneous and light-evoked excitatory postsynaptic currents (sEPSCs and leEPSCs) in

269 y of glutamatergic spontaneous and miniature excitatory postsynaptic currents (sEPSCs and mEPSCs, res

270 n frequency but not amplitude of spontaneous excitatory postsynaptic currents (sEPSCs) and an increas

271 nctionally affected, we examined spontaneous excitatory postsynaptic currents (sEPSCs) and dopamine (

272 195 % and amplitude to 118 % of spontaneous excitatory postsynaptic currents (sEPSCs) during expirat

273 We recorded spontaneous excitatory postsynaptic currents (sEPSCs) from lamina II

274 eased the frequency of spontaneous glutamate excitatory postsynaptic currents (sEPSCs) in >90% of NTS

275 crt-2 increased the frequency of spontaneous excitatory postsynaptic currents (sEPSCs) in a few neuro

276 0.6%) decreased the frequency of spontaneous excitatory postsynaptic currents (sEPSCs) only in Ndufs4

277 stsynaptic currents (sIPSCs) and spontaneous excitatory postsynaptic currents (sEPSCs) three- and two

278 in adults where the increase in spontaneous excitatory postsynaptic currents (sEPSCs) was mediated s

279 Spontaneous excitatory postsynaptic currents (sEPSCs) were recorded

280 antly increased the frequency of spontaneous excitatory postsynaptic currents (sEPSCs) without affect

281 The observation of spontaneous excitatory postsynaptic currents (sEPSCs), spontaneous i

282 the frequency of spontaneous inhibitory and excitatory postsynaptic currents (sIPSCs and sEPSCs), wh

283 nd significant increases in both spontaneous excitatory postsynaptic current (spEPSC) amplitude and R

284 , the amplitude and frequency of spontaneous excitatory postsynaptic currents (spEPSCs) increased dur

285 he decay time of NMDAR-dependent spontaneous excitatory postsynaptic currents suggesting a prolonged

286 As NR2a-containing NMDARs mediate shorter excitatory postsynaptic currents than those containing N

287 ed an increase in the frequency of miniature excitatory postsynaptic currents that could be rapidly a

288 pal neurons, trains of depolarizations evoke excitatory postsynaptic currents that show facilitation

289 increasing Dalpha7-nAChRs boosted miniature excitatory postsynaptic currents, the ensuing increase i

290 First, two distinct excitatory postsynaptic currents transmit signals on dif

291 quencies, indicating that the rapid burst of excitatory postsynaptic currents underlying the sensory-

292 ve only subtle consequences for nerve-evoked excitatory postsynaptic currents: vesicle heterogeneity,

293 and the amplitude of AMPA receptor-mediated excitatory postsynaptic currents was also observed.

294 soxazolepropionic acid receptor ratio of the excitatory postsynaptic currents was significantly incre

295 Excitatory postsynaptic currents were dramatically reduc

296 In control hippocampus, AMPA excitatory postsynaptic currents were electrically linea

297 d unitary conductance of channels underlying excitatory postsynaptic currents were matched by those o

298 Both evoked and spontaneous excitatory postsynaptic currents were predominantly glut

299 Excitatory postsynaptic currents were recorded in respon

300 induced action potential firing and enhanced excitatory postsynaptic currents, whereas muscarinic ago