ライフサイエンスコーパス: postsynaptic current

1 action potentials and spontaneous excitatory postsynaptic currents.

2 precise interaction of excitatory-inhibitory postsynaptic currents.

3 ease in synaptic AMPA receptors (AMPARs) and postsynaptic currents.

4 ala pyramidal neurons, generating excitatory postsynaptic currents.

5 e is essential for fast, glutamate-activated postsynaptic currents.

6 quency of glutamatergic miniature excitatory postsynaptic currents.

7 increased amplitude of miniature inhibitory postsynaptic currents.

8 and frequency changes in miniature GABAergic postsynaptic currents.

9 , but not frequency, of miniature excitatory postsynaptic currents.

10 s a rapid increase of spontaneous excitatory postsynaptic currents.

11 ase in the amplitude of miniature inhibitory postsynaptic currents.

12 A(A) receptor (GABA(A)R)-mediated inhibitory postsynaptic currents.

13 plitude of alpha3*-nAChR-mediated excitatory postsynaptic currents.

14 requency of GABAergic spontaneous inhibitory postsynaptic currents.

15 ion restricts the potentiation of excitatory postsynaptic currents.

16 AMPA receptor-mediated miniature excitatory postsynaptic currents.

17 e-induced increases in spines and excitatory postsynaptic currents.

18 , accounting for the disappearance of evoked postsynaptic currents.

19 tio (SNR) from its presynaptic arrays to its postsynaptic currents.

20 ncreased frequency of spontaneous inhibitory postsynaptic currents.

21 sue exhibit decreased spontaneous inhibitory postsynaptic currents.

22 robust monosynaptic GABAergic and nicotinic postsynaptic currents.

23 ections to the PVT elicits direct excitatory postsynaptic currents.

24 gnal-to-noise ratio power ratio (SNR) of its postsynaptic currents.

25 t in part, by enhancing miniature inhibitory postsynaptic currents.

26 termined by analysis of miniature excitatory postsynaptic currents.

27 ecording 5-HT1A receptor-mediated inhibitory postsynaptic currents (5-HT1A -IPSCs) generated by the a

28 wer rate of spontaneous miniature inhibitory postsynaptic current activity.

29 xcitatory transmitter release and excitatory postsynaptic currents also were heightened at synapses b

30 uced decay time of AMPAR-mediated excitatory postsynaptic currents (AMPAR-EPSCs), enhanced depression

31 artly by an increase in miniature excitatory postsynaptic current amplitude and partly by a mechanism

32 speptin neurons, estradiol reduced miniature postsynaptic current amplitude independent of time of da

33 affinity, the decrease in arcuate miniature postsynaptic current amplitude was attributed to decreas

34 zepam treatment reduced miniature inhibitory postsynaptic current amplitude, which returned to contro

35 eficits in membrane properties and GABAergic postsynaptic current amplitude.

36 Specifically, spontaneous excitatory postsynaptic current amplitudes measured from individual

37 t frequencies, although miniature excitatory postsynaptic current amplitudes remained similar.

38 type serotonin receptor to reduce excitatory postsynaptic current amplitudes, an effect previously sh

39 hyrin clusters and mean miniature inhibitory postsynaptic current amplitudes, whereas a dominant nega

40 metabolic advantage over quantal excitatory postsynaptic currents--an advantage that may have driven

41 g Na(+)/H(+) exchange activity decreased the postsynaptic current and caused failures in postsynaptic

42 notypes, decreased excitatory and inhibitory postsynaptic current and reduced c-Fos immunoreactivity

43 They contribute to the excitatory postsynaptic current and to the detection of painful aci

44 eptors in MSNs, consisting of an increase in postsynaptic currents and a decrease of presynaptic inhi

45 KO of NL1 impaired NMDAR-mediated excitatory postsynaptic currents and abolished NMDAR-dependent LTP.

46 ed AMPA receptor (AMPAR)-mediated excitatory postsynaptic currents and AMPAR surface expression in pr

47 causes a decrease in NMDA-receptor-mediated postsynaptic currents and an increase in presynaptic glu

48 the amplitude of the spontaneous excitatory postsynaptic currents and decreased the frequency of spo

49 potentiation, altered amplitude of miniature postsynaptic currents and elevated dopamine in basal for

50 n of these channels reduces PF-PC excitatory postsynaptic currents and excitatory postsynaptic potent

51 Measurements of spontaneous glycinergic postsynaptic currents and GlyR immunolabeling revealed t

52 lectrophysiological recordings of excitatory postsynaptic currents and hippocampal long-term potentia

53 nock out (KO) mice display larger excitatory postsynaptic currents and increased spontaneous activity

54 lectrophysiological recordings of excitatory postsynaptic currents and long-term potentiation in brai

55 ic component was absent in evoked inhibitory postsynaptic currents and miniature events.

56 nd modeled using intracellular recordings of postsynaptic currents and potentials, inferring synaptic

57 KO mice, AMPAR-mediated miniature excitatory postsynaptic currents and synaptic levels of AMPAR subun

58 en in the frequency of spontaneous miniature postsynaptic currents and the size of the readily releas

59 in-2 elicited both inhibitory and excitatory postsynaptic currents and triggered network bursting in

60 ese ASIC-1as contribute to the generation of postsynaptic currents and, more relevant, to calcium inf

61 Spontaneous postsynaptic currents are lower in amplitude and have fa

62 ynamins, dynamin 1 and 3, smaller excitatory postsynaptic currents are observed due to an impairment

63 increase in dendritic spines and excitatory postsynaptic currents at 3 days post-exercise, indicativ

64 gnificant decrease in spontaneous excitatory postsynaptic currents at both two and twenty four hours,

65 We found larger excitatory postsynaptic currents at the synapses between the extra-

66 in the frequency and amplitude of GABAergic postsynaptic currents beginning approximately 14 d post-

67 te that hESC-derived neurons receive unitary postsynaptic currents both in vitro and in vivo and adop

68 tion and charge transfer rate of spontaneous postsynaptic current bursts at the neuromuscular junctio

69 The persistent current of cholinergic postsynaptic current bursts is mostly mediated by levami

70 that motoneurons control muscle by producing postsynaptic current bursts.

71 trol animals, IL-6 did not affect excitatory postsynaptic currents but selectively and reversibly red

72 localized ASICs contribute to the excitatory postsynaptic current by responding to the transient acid

73 the depression of AMPAR-mediated excitatory postsynaptic currents by SNRIs required p38 kinase activ

74 The reversal potential of the compound postsynaptic currents (combined simultaneous EPSCs and I

75 litude and frequency of miniature inhibitory postsynaptic currents compared with those in wild-type s

76 Our estimates indicate that APs and postsynaptic currents contribute similar proportions of

77 ower kinetics in vitro and slower excitatory postsynaptic current decays in neurons.

78 The IL-6-induced inhibitory postsynaptic currents decrease was inhibited by drugs in

79 inhibited by tetrodotoxin (TTX), inhibitory postsynaptic currents decreased and currents were no lon

80 The frequency of miniature excitatory postsynaptic currents decreased, accompanied by dendriti

81 efects, long-term potentiation and miniature postsynaptic current defects.

82 This steady-state postsynaptic current does not increase overall synaptic

83 chanisms, we identified a previously unknown postsynaptic current during neurotransmission that was m

84 ty, but induces a steady-state, asynchronous postsynaptic current during stimulus trains.

85 /kainate receptor-mediated evoked excitatory postsynaptic currents (eEPSCs), by 94% and 72%, respecti

86 amplitude of evoked NMDA-mediated excitatory postsynaptic currents (eEPSCs), without affecting AMPA-m

87 mplitude of GABAA-mediated evoked inhibitory postsynaptic currents (eIPSCs).

88 increased amplitudes of miniature excitatory postsynaptic currents, enhancement of LTP, and eliminati

89 itional properties, Q and average excitatory postsynaptic current (EPSC) amplitude, were unaffected b

90 n of these failures leads to mean excitatory postsynaptic current (EPSC) amplitudes that are independ

91 steady-state NMDA currents, NMDAR excitatory postsynaptic current (EPSC) decay kinetics, progressive

92 o reverse ion influxes generating excitatory postsynaptic currents (EPSCs) and action potentials.

93 l fiber synapses, mGluR1-mediated excitatory postsynaptic currents (EPSCs) and associated calcium tra

94 MS patients on glutamate-mediated excitatory postsynaptic currents (EPSCs) and excitotoxic damage in

95 NMDAR-mediated excitatory postsynaptic currents (EPSCs) and puff NMDA-elicited cur

96 ic gene Bax in stem cells reduced excitatory postsynaptic currents (EPSCs) and spine density in matur

97 ls (BCs), we found that classical excitatory postsynaptic currents (EPSCs) are followed by GABA(A) re

98 increased duration of spontaneous excitatory postsynaptic currents (EPSCs) during the symptomatic pha

99 ced the amplitude of monosynaptic excitatory postsynaptic currents (EPSCs) evoked from the dorsal roo

100 aviors and associated deficits in excitatory postsynaptic currents (EPSCs) generated in apical dendri

101 -dependent inhibition of autaptic excitatory postsynaptic currents (EPSCs) in cultured hippocampal ne

102 elrhodopsin-2-assisted mapping of excitatory postsynaptic currents (EPSCs) in L2/3 shows that the rel

103 rease in frequency of spontaneous excitatory postsynaptic currents (EPSCs) in layer V pyramidal neuro

104 Excitatory postsynaptic currents (EPSCs) in monosynaptic nTS neuron

105 induced a transient inhibition of excitatory postsynaptic currents (EPSCs) in NAcSh principal medium

106 ST stimulation elicits excitatory postsynaptic currents (EPSCs) in NTS neurons mediated by

107 Here we examined excitatory postsynaptic currents (EPSCs) of dorsal horn neurons evo

108 n the amplitude of NMDAR-mediated excitatory postsynaptic currents (EPSCs) of dorsal horn neurons evo

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

110 partate receptor (NMDAR)-mediated excitatory postsynaptic currents (EPSCs) onto VTA dopamine neurons.

111 The excitatory postsynaptic currents (EPSCs) recorded in laminae III-V

112 Evaluation of excitatory postsynaptic currents (EPSCs) revealed that rCASP6 rapid

113 been shown to arise from complex excitatory postsynaptic currents (EPSCs) that are evoked in SNR neu

114 -cell voltage clamp recordings of excitatory postsynaptic currents (EPSCs) were performed on dorsal h

115 Excitatory postsynaptic currents (EPSCs) were recorded from superfi

116 he time course of Purkinje neuron excitatory postsynaptic currents (EPSCs).

117 reased the frequency of miniature excitatory postsynaptic currents (EPSCs).

118 iniature excitatory transmission (excitatory postsynaptic currents, EPSCs).

119 nd increased frequency and mean amplitude of postsynaptic current events.

120 uction of synchronous spontaneous inhibitory-postsynaptic-current events in mutants, which was revers

121 o evidence that NMDA receptors contribute to postsynaptic currents evoked in either amacrine.

122 We find that postsynaptic currents exhibit a decreasing ability to ge

123 of an initial fast glutamatergic excitatory postsynaptic current followed by a slow-rising cholinerg

124 inputs, we recorded light-evoked excitatory postsynaptic currents following viral-mediated expressio

125 , together with reduced miniature excitatory postsynaptic current frequencies and behavioral defects.

126 ntly, by a reduction of miniature excitatory postsynaptic current frequencies, although miniature exc

127 sociated with increased miniature excitatory postsynaptic current frequency and amplitude, suggesting

128 h ASD exhibited reduced miniature excitatory postsynaptic current frequency and N-methyl-D-aspartate

129 imulation of astrocytes increased excitatory postsynaptic current frequency through a metabotropic gl

130 Inhibitory postsynaptic current frequency, measured on pyramidal ne

131 ecapitulated diminished miniature excitatory postsynaptic current frequency, supporting a role for th

132 t with an increase in spontaneous excitatory postsynaptic current frequency.

133 Here we show that postsynaptic currents frequently occur in bursts at the

134 ic glutamate receptors is decreased, but the postsynaptic current from activation of NMDA-specific gl

135 ity of only one motoneuron and recordings of postsynaptic currents from inputs formed by the differen

136 ed by these synapses, we recorded excitatory postsynaptic currents from mammalian retinal ganglion ce

137 ity by inferring the magnitude of excitatory postsynaptic currents from the N20 component of the soma

138 bition of GABAA receptor-mediated inhibitory postsynaptic currents (GABAAR IPSCs) is associated with

139 However, unitary postsynaptic currents generated by individual, GAD67-exp

140 In mature neurons, PVs evoke GABA(A) postsynaptic currents (GPSCs) with fast rise and decay p

141 al examples of proton-evoked ASIC excitatory postsynaptic currents have emerged.

142 reduced frequencies of miniature excitatory postsynaptic currents, i.e., to defects in synaptic tran

143 revealed a concomitant nonquantal excitatory postsynaptic current in the calyx terminal that was caus

144 tion of electrically evoked local excitatory postsynaptic current in the saline and ShA groups.

145 However, the average postsynaptic current in the VNLL fails to elicit APs in

146 We find that postsynaptic currents in bipolar MSO neuron models gener

147 that the frequency of spontaneous excitatory postsynaptic currents in dentate gyrus granule cells is

148 n pyramidal neurons and supported inhibitory postsynaptic currents in distal dendrites better than GI

149 d dopamine release in the DMS and excitatory postsynaptic currents in DMS MSNs.

150 t not the amplitude, of miniature excitatory postsynaptic currents in dorsal horn neurons that could

151 n terminals, which was detected by recording postsynaptic currents in downstream neurons.

152 lisecond flashes of blue light produced fast postsynaptic currents in HA neurons, with a high connect

153 m influx, and increased miniature excitatory postsynaptic currents in hippocampal neurons.

154 d to the hippocampus of adult mice triggered postsynaptic currents in host pyramidal neurons in acute

155 d decrements in apically targeted excitatory postsynaptic currents in layer V pyramidal cells of PFC.

156 axons resulting in characteristic "doublet" postsynaptic currents in LSO neurons.

157 lc7a10-null mice and spontaneous glycinergic postsynaptic currents in motor neurons show substantiall

158 glutamatergic interneuron-evoked inhibitory postsynaptic currents in motor neurons.

159 spine density/diameter, increased excitatory postsynaptic currents in mPFC layer V pyramidal neurons,

160 ally for receptors containing GluK5, as were postsynaptic currents in neurons expressing recombinant

161 rate of spontaneous and miniature excitatory postsynaptic currents in pyramidal neurons and hippocamp

162 cacy of spontaneous and miniature inhibitory postsynaptic currents in pyramidal neurons.

163 SACs dampened spontaneous, wave-associated, postsynaptic currents in RGCs and decreased the SAC rele

164 on also increased the frequency of GABAergic postsynaptic currents in rod bipolar cells, suggesting t

165 ncreased frequency of spontaneous excitatory postsynaptic currents in spinal cord nociceptive neurons

166 ly block NMDAR-mediated miniature excitatory postsynaptic currents in the absence of Mg(2+).

167 uced the frequency of spontaneous excitatory postsynaptic currents in the direct pathway MSNs, wherea

168 ased the frequency of spontaneous inhibitory postsynaptic currents in the indirect pathway MSNs.

169 ty and the frequency of miniature excitatory postsynaptic currents in the mPFC were prevented by PKMz

170 Examination of the light-evoked postsynaptic currents in these ON-type orientation-selec

171 tor (GABAAR)-mediated spontaneous inhibitory postsynaptic currents in WT mice, indicating that astroc

172 creased amplitudes of spontaneous excitatory postsynaptic currents in young neonates (-34.4%).

173 ynaptic transmission (spontaneous excitatory postsynaptic currents) in spinal lamina IIo nociceptive

174 ency of excitatory miniature and spontaneous postsynaptic currents increased.

175 t in nanodomains stabilizes the amplitude of postsynaptic currents, indicating that, in addition to t

176 Specifically, miniature excitatory postsynaptic currents, input resistance, hippocampal lon

177 potential (LFP), thought to be dominated by postsynaptic currents integrated over a larger volume of

178 a GABA(A) receptor-mediated slow inhibitory postsynaptic current (IPSC) in a PN and an autaptic IPSC

179 oduced a 5-HT1A receptor-mediated inhibitory postsynaptic current (IPSC) that resulted in only a tran

180 tes action potential duration and inhibitory postsynaptic current (IPSC).

181 OF increased depression of inhibitory postsynaptic currents (IPSCs) along IPSC trains evoked b

182 sure in vivo caused a decrease in inhibitory postsynaptic currents (IPSCs) and an increase in the AMP

183 ll mutations prolong the decay of inhibitory postsynaptic currents (IPSCs) and induce spontaneous Gly

184 pronounced initial depression of inhibitory postsynaptic currents (IPSCs) followed by modest long-te

185 rminals evoked robust D2-receptor inhibitory postsynaptic currents (IPSCs) in GIRK2-expressing MSNs t

186 induces rhythmic, theta-frequency inhibitory postsynaptic currents (IPSCs) in pyramidal cells, even w

187 entiated GABAA and GABAB-mediated inhibitory postsynaptic currents (IPSCs) in VTA dopamine neurons, a

188 ked I-LTD and acute depression of inhibitory postsynaptic currents (IPSCs) induced by D(2) dopamine r

189 ong-lasting enhancement of evoked inhibitory postsynaptic currents (IPSCs) mediated by D1-type recept

190 inergic spontaneous and miniature inhibitory postsynaptic currents (IPSCs) of lamina II neurons.

191 hibition by morphine of GABAergic inhibitory postsynaptic currents (IPSCs) recorded from neurons in t

192 dulator (PAM) AZD7325 potentiates inhibitory postsynaptic currents (IPSCs) specifically in perisomati

193 ntaneous inhibitory transmission (inhibitory postsynaptic currents, IPSCs) in the DR.

194 ces, NMDAR-dependent LTD of AMPAR excitatory postsynaptic currents is abolished in neurons expressing

195 ndeed, the amplitude of miniature excitatory postsynaptic currents is enhanced in both Vac14(-/-) and

196 ors (NMDARs), which generate relatively slow postsynaptic currents, is unclear.

197 atios ( approximately 40:1), fast inhibitory postsynaptic current kinetics (tau(decay) = 2.5 ms) and

198 the light-evoked and spontaneous excitatory postsynaptic currents (light-evoked EPSCs and sEPSCs) fr

199 viously shown that the physiological size of postsynaptic currents maximises energy efficiency rather

200 clustering at synapses, miniature excitatory postsynaptic currents mediated by TARPless AMPARs were r

201 y describes spontaneous miniature inhibitory postsynaptic currents mediated by vesicular dopamine rel

202 ceptor (AMPAR)-mediated miniature excitatory postsynaptic current (mEPSC) amplitudes due to postsynap

203 ry synapses assessed by miniature excitatory postsynaptic current (mEPSC) and electron microscopy.

204 educes the frequency of miniature excitatory postsynaptic current (mEPSC), and reduces AMPA-induced m

205 uency of AMPAR-mediated miniature excitatory postsynaptic current (mEPSC), while expressing wild-type

206 s, (iii) NMDAR-mediated miniature excitatory postsynaptic currents (mEPSCs) and NMDA-evoked currents

207 up of the amplitude of miniature excitatory postsynaptic currents (mEPSCs) and of synaptic levels of

208 uency of NMDAR-mediated miniature excitatory postsynaptic currents (mEPSCs) and the amplitude of puff

209 scaling, all of a cell's AMPAergic miniature postsynaptic currents (mEPSCs) are increased or decrease

210 led higher frequency of miniature excitatory postsynaptic currents (mEPSCs) immediately after 2-h imm

211 the NMDAR component of miniature excitatory postsynaptic currents (mEPSCs) in CA1 interneurons but n

212 mplitude of spontaneous miniature excitatory postsynaptic currents (mEPSCs) in cultured mouse hippoca

213 potentials (fEPSPs) and miniature excitatory postsynaptic currents (mEPSCs) in rat hippocampal slices

214 tch clamp recordings of miniature excitatory postsynaptic currents (mEPSCs) revealed that these behav

215 Miniature excitatory postsynaptic currents (mEPSCs) were recorded from CA1 py

216 and charge transfer of miniature excitatory postsynaptic currents (mEPSCs) were significantly reduce

217 d the amplitude of AMPA miniature excitatory postsynaptic currents (mEPSCs), and shRNA-mediated GRIP1

218 Excitatory miniature postsynaptic currents (mEPSCs), but not miniature inhibi

219 reduction in evoked and miniature excitatory postsynaptic currents (mEPSCs).

220 mplitude of spontaneous miniature excitatory postsynaptic currents (mEPSCs); however, synaptic facili

221 In contrast, spontaneous postsynaptic currents ("minis") resulting from stochasti

222 1 significantly reduced miniature inhibitory postsynaptic current (mIPSC) amplitudes and GABA levels

223 exhibit increased basal miniature inhibitory postsynaptic current (mIPSC) frequency but showed a decr

224 ltered sIPSC amplitude, miniature inhibitory postsynaptic current (mIPSC) frequency, and mIPSC amplit

225 s and decreased frequency of mini inhibitory postsynaptic currents (mIPSC) in the NAc of susceptible

226 uency of miniature inhibitory and excitatory postsynaptic currents (mIPSCs and mEPSCs, respectively)

227 creased EtOH sensitivity of GABAAR miniature postsynaptic currents (mIPSCs) correlated with EtOH depe

228 lopment the duration of miniature inhibitory postsynaptic currents (mIPSCs) mediated by GABAA recepto

229 lopment the duration of miniature inhibitory postsynaptic currents (mIPSCs) mediated by GABAA recepto

230 n potential independent miniature inhibitory postsynaptic currents (mIPSCs) was significantly increas

231 and charge transfer of miniature inhibitory postsynaptic currents (mIPSCs) were significantly increa

232 rents (mEPSCs), but not miniature inhibitory postsynaptic currents (mIPSCs), increase in amplitude af

233 s) and the frequency of miniature inhibitory postsynaptic currents (mIPSCs).

234 ids act tonically to regulate AMPA miniature postsynaptic current (mPSC) frequency in embryonic motor

235 uration of GABAA receptor (GABAAR) miniature postsynaptic currents (mPSCs) was substantially blunted

236 the shortening of NMDAR-mediated excitatory postsynaptic currents (NMDAR-EPSCs) during early life, w

237 neurons in heterozygous mice evoked biphasic postsynaptic currents not significantly different from t

238 generated primarily by the summation of the postsynaptic currents of cortical principal cells.

239 and the amplitude of monosynaptic excitatory postsynaptic currents of dorsal horn neurons in SNL rats

240 the frequency and the amplitude of GABAergic postsynaptic currents of SF-1 GFP-positive neurons.

241 mall DRG neurons and monosynaptic excitatory postsynaptic currents of spinal dorsal horn neurons evok

242 us or endogenous IL-6 on electrically evoked postsynaptic currents on a cortical rat slice preparatio

243 n the CA1 hippocampus to increase inhibitory postsynaptic currents on CA1 pyramidal cells.

244 ferences that are associated with excitatory postsynaptic currents on mPFC principle neurons.

245 sociate with changes in miniature excitatory postsynaptic currents or paired-pulse facilitation, sugg

246 ortical neurons exhibited reduced inhibitory postsynaptic current peak amplitudes, prolonged current

247 Spontaneous postsynaptic currents (PSCs) provide key information abo

248 e exhibit a decrease in NMDA/AMPA excitatory postsynaptic current ratio in area CA1 of the hippocampu

249 d more actively with an increased excitatory postsynaptic current response upon the application of ni

250 mbrane excitability and divergent inhibitory postsynaptic current responses to CRF application.

251 ency of spontaneous and miniature excitatory postsynaptic currents (s/mEPSCs).

252 cs of sound-evoked excitatory and inhibitory postsynaptic currents (seEPSCs and seIPSCs, respectively

253 PVN, the frequency of spontaneous excitatory postsynaptic currents (sEPSC) was elevated in abstinent

254 cing the frequency of spontaneous excitatory postsynaptic current (sEPSCs).

255 affected, we examined spontaneous excitatory postsynaptic currents (sEPSCs) and dopamine (DA) modulat

256 requency of spontaneous glutamate excitatory postsynaptic currents (sEPSCs) in >90% of NTS-TH-EGFP ne

257 ased the frequency of spontaneous excitatory postsynaptic currents (sEPSCs) only in Ndufs4(KO) CA1 ne

258 currents (sIPSCs) and spontaneous excitatory postsynaptic currents (sEPSCs) three- and two-fold highe

259 ased the frequency of spontaneous excitatory postsynaptic currents (sEPSCs) without affecting their a

260 The observation of spontaneous excitatory postsynaptic currents (sEPSCs), spontaneous inhibitory p

261 ch clamp recordings of spontaneous miniature postsynaptic currents show that patient antibodies decre

262 -1 increased both the spontaneous inhibitory postsynaptic current (sIPSC) amplitudes and frequency by

263 ad no clear effect on spontaneous inhibitory postsynaptic current (sIPSC) frequency at IN-PC synapses

264 an elevated baseline spontaneous inhibitory postsynaptic current (sIPSC) frequency compared with con

265 d large reductions in spontaneous inhibitory postsynaptic current (sIPSC) frequency in both granule c

266 ssion (versus N40) of spontaneous inhibitory postsynaptic currents (sIPSCs) across multiple subjects.

267 sented frequencies of spontaneous inhibitory postsynaptic currents (sIPSCs) and spontaneous excitator

268 uced the frequency of spontaneous inhibitory postsynaptic currents (sIPSCs) but did not alter sIPSC a

269 es and frequencies of spontaneous inhibitory postsynaptic currents (sIPSCs) in CA1 pyramidal neurons.

270 on the properties of spontaneous inhibitory postsynaptic currents (sIPSCs) in cultured rat hippocamp

271 xpression and reduced spontaneous inhibitory postsynaptic currents (sIPSCs) in D1-type, but not D2-ty

272 (A) receptor-mediated spontaneous inhibitory postsynaptic currents (sIPSCs) in dlBnST target neurons,

273 ased the frequency of spontaneous inhibitory postsynaptic currents (sIPSCs) in downstream hippocampal

274 sant-induced burst of spontaneous inhibitory postsynaptic currents (sIPSCs) on CA1 pyramidal neurons

275 et charge transfer of spontaneous inhibitory postsynaptic currents (sIPSCs) recorded from CA1 pyramid

276 Spontaneous inhibitory postsynaptic currents (sIPSCs) were not differentially a

277 ic currents (sEPSCs), spontaneous inhibitory postsynaptic currents (sIPSCs), and bidirectional electr

278 ant increases in both spontaneous excitatory postsynaptic current (spEPSC) amplitude and RRP size (es

279 tude and frequency of spontaneous excitatory postsynaptic currents (spEPSCs) increased during PTP in

280 me of NMDAR-dependent spontaneous excitatory postsynaptic currents suggesting a prolonged open time o

281 lled the amplitude and variance of simulated postsynaptic currents, suggesting several ways in which

282 Analysis of miniature postsynaptic currents support that M2 and M3 receptors m

283 re located on tumour microtubes, and produce postsynaptic currents that are mediated by glutamate rec

284 d, nociceptin, and GABA(B) receptors induced postsynaptic currents that desensitized within minutes,

285 ed by depression accompanied by asynchronous postsynaptic currents that increase steadily during the

286 g steps to the hair cell were used to elicit postsynaptic currents that occurred at constant phase fo

287 , trains of depolarizations evoke excitatory postsynaptic currents that show facilitation followed by

288 First, two distinct excitatory postsynaptic currents transmit signals on different time

289 rom PVs and PNs show that unitary inhibitory postsynaptic currents (uIPSCs) are larger in interpatche

290 and a reduction of spontaneous glutamatergic postsynaptic currents, underscoring the relevance of aff

291 We also recorded postsynaptic currents using in vitro whole cell recordin

292 ame visual stimulus is presented repeatedly, postsynaptic currents vary in amplitude.

293 tle consequences for nerve-evoked excitatory postsynaptic currents: vesicle heterogeneity, refractori

294 quency of GABAA receptor-mediated inhibitory postsynaptic currents was depressed in medium spiny neur

295 mice, the frequency of GABAergic spontaneous postsynaptic currents was increased in the PM; this incr

296 because alpha(2)-AR-mediated slow inhibitory postsynaptic currents were depressed in wt but not betaa

297 uced, whereas the amplitude and frequency of postsynaptic currents were enhanced compared with contro

298 le-cell patch clamp recordings of inhibitory postsynaptic currents were performed from ventral tegmen

299 versibly reduced the amplitude of inhibitory postsynaptic currents with a postsynaptic effect.

300 reases the frequency of miniature inhibitory postsynaptic currents with no effect on amplitude, which