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1 A1 inhibitory postsynaptic potential into an excitatory postsynaptic potential.
2 currents sum effectively and produce a large excitatory postsynaptic potential.
3 eceptors mediate the slower component of the excitatory postsynaptic potential.
4 ng spatial and temporal summation of smaller excitatory postsynaptic potentials.
5 ersibly increased the slope and amplitude of excitatory postsynaptic potentials.
6 inhibitory effect of ethanol on NMDAR field excitatory postsynaptic potentials.
7 ices during extracellular recording of field excitatory postsynaptic potentials.
8 tentials from basket interneurons (BAS) into excitatory postsynaptic potentials.
9 erm potentiation and long-term depression of excitatory postsynaptic potentials.
10 equency but not the amplitude of spontaneous excitatory postsynaptic potentials.
11 RIIA) level and the frequency of spontaneous excitatory postsynaptic potentials.
12 mplitude and frequency of glutamate-mediated excitatory postsynaptic potentials.
13 cted by a concomitant decrease in the evoked excitatory postsynaptic potentials.
14 spike, but not those that exhibit only fast excitatory postsynaptic potentials.
15 ion of ventral CA1 fibers, and this broadens excitatory postsynaptic potentials.
16 ilm oxide leading to responses that resemble excitatory postsynaptic potentials.
17 n net synaptic efficacy as measured by field excitatory postsynaptic potentials.
18 temporal summation of their thalamocortical excitatory postsynaptic potentials.
19 AC-induced depression of inhibitory, but not excitatory, postsynaptic potentials.
21 ime-dependent manner, significantly reducing excitatory postsynaptic potentials after a >/=30-min app
23 pines compartmentalize voltage, specifically excitatory postsynaptic potentials, albeit critical, rem
26 ression of the simultaneously recorded field excitatory postsynaptic potential and was greatly reduce
28 pagating action potentials, the amplitude of excitatory postsynaptic potentials and dendritic excitab
29 erm potentiation (LTP) of both intracellular excitatory postsynaptic potentials and evoked field pote
30 by tetrodotoxin, and all display spontaneous excitatory postsynaptic potentials and IPSPs that remain
31 simultaneously recording the uncaging-evoked excitatory postsynaptic potentials and local Ca2+ signal
32 on in FB-m1KO hippocampal slices resulted in excitatory postsynaptic potentials and long-term synapti
35 ) using voltage-sensitive dye imaging, field excitatory postsynaptic potentials and whole cell patch
36 shape and duration of the vestibular-evoked excitatory postsynaptic potential, and the time of onset
37 y depends on the magnitude and timing of the excitatory postsynaptic potentials, and that blockade of
38 action potentials fully invade spines, that excitatory postsynaptic potentials are large in the spin
39 enhancement of the monosynaptic sensorimotor excitatory postsynaptic potential, as compared with the
40 owever, the initial increase in the slope of excitatory postsynaptic potentials, as well as the eleva
42 Consistent with that idea, PTP of evoked excitatory postsynaptic potentials at Aplysia sensory-mo
43 ow dynamic range (1 log unit intensity), and excitatory postsynaptic potentials at light on and light
44 ment of mGlu II-mediated depression of field excitatory postsynaptic potentials at mossy fiber-CA3 sy
45 oes the low input resistance make individual excitatory postsynaptic potentials brief so that they mu
47 measured as the change in layer II/III field excitatory postsynaptic potentials by a multielectrode a
48 he amplitude and sharpens the time course of excitatory postsynaptic potentials by reducing current s
49 ow that reliably timed action potentials (or excitatory postsynaptic potentials) can be observed up t
50 nterneurons to the extent that even a single excitatory postsynaptic potential could initiate spiking
51 other neurons in the ARC and that all evoked excitatory postsynaptic potentials could be blocked by t
52 ion to neurotransmitter release, feedforward excitatory postsynaptic potentials could spread through
53 uency sensitivity of NMDA receptor-dependent excitatory postsynaptic potentials differed significantl
54 quency voltage fluctuations (presumed "field excitatory postsynaptic potentials") during 89% of chron
55 CA1 are associated with an increase in both excitatory postsynaptic potential (EPSP) amplitude and a
56 an excitatory action while also reducing the excitatory postsynaptic potential (EPSP) amplitude throu
57 extracellular stimulation experiments to map excitatory postsynaptic potential (EPSP) amplitudes and
58 llaterals depressed the initial slope of the excitatory postsynaptic potential (EPSP) in aged but not
60 cal pyramidal neurons, we observed an evoked excitatory postsynaptic potential (EPSP) or current (EPS
61 c population spike (PS) and minor effects on excitatory postsynaptic potential (EPSP) slope amplitude
62 mplitude was by 72+/-17% of control, and the excitatory postsynaptic potential (EPSP) slope was decre
63 IPSP, the amplitude of the cholinergic fast excitatory postsynaptic potential (EPSP) was partially i
64 tic potential (IPSP) is abolished before the excitatory postsynaptic potential (EPSP) when the extrac
65 postsynaptic potential (IPSP) followed by an excitatory postsynaptic potential (EPSP) whereas CSS onl
66 increase in stimulus intensity evoked a slow excitatory postsynaptic potential (EPSP) which was assoc
67 rimary afferent fibers-mediated monosynaptic excitatory postsynaptic potential (EPSP), and long-lasti
68 edback loop within the spine head; during an excitatory postsynaptic potential (EPSP), Ca(2+) influx
69 eta more potently blocks the potentiation of excitatory postsynaptic potential (EPSP)-spike coupling
73 ribute to hippocampal CA(1) stratum radiatum excitatory postsynaptic potentials (EPSP) is a matter of
74 -methyl-D-aspartate (NMDA) receptor-mediated excitatory postsynaptic potentials (EPSPAs and EPSPNs, r
76 at activation of K(v)1 channels by dendritic excitatory postsynaptic potentials (EPSPs) accelerated m
77 As a result, subthreshold parallel fiber excitatory postsynaptic potentials (EPSPs) activate Cav3
78 fects Ca(2+) elevations evoked by coincident excitatory postsynaptic potentials (EPSPs) and back-prop
79 s the integration time window of concomitant excitatory postsynaptic potentials (EPSPs) and dampens t
80 h that their activity modulates the shape of excitatory postsynaptic potentials (EPSPs) and increases
81 d temperature-insensitive neurones displayed excitatory postsynaptic potentials (EPSPs) and inhibitor
82 0 nM) increased the frequency of spontaneous excitatory postsynaptic potentials (EPSPs) and spontaneo
83 ked compound glutamatergic receptor-mediated excitatory postsynaptic potentials (EPSPs) and spontaneo
84 nd rat axons, but the forward propagation of excitatory postsynaptic potentials (EPSPs) and the backw
85 unisensory and multisensory stimulation with excitatory postsynaptic potentials (EPSPs) and/or action
86 uch a model: it is reversible, anti-hebbian (excitatory postsynaptic potentials (EPSPs) are depressed
88 ification (increase in duration and area) of excitatory postsynaptic potentials (EPSPs) at depolarize
91 N-methyl-D-aspartate (NMDA) and compared the excitatory postsynaptic potentials (EPSPs) elicited by N
92 the observed EPSC changes, we also compared excitatory postsynaptic potentials (EPSPs) elicited by P
94 cally connected cells were used to study the excitatory postsynaptic potentials (EPSPs) elicited in b
95 tion of oxytocin (1 and 10 microM) inhibited excitatory postsynaptic potentials (EPSPs) evoked by dor
96 upling determined the degree of summation of excitatory postsynaptic potentials (EPSPs) evoked by eac
97 ave performed a detailed quantal analysis of excitatory postsynaptic potentials (EPSPs) evoked by min
99 Specifically, we sought to determine whether excitatory postsynaptic potentials (EPSPs) evoked by sti
101 ibly decreased the amplitude of monosynaptic excitatory postsynaptic potentials (EPSPs) evoked in BA1
102 ne, but resembled asynchronous glutamatergic excitatory postsynaptic potentials (EPSPs) evoked in the
103 of the L-MAN and the HVc fiber tracts evoked excitatory postsynaptic potentials (EPSPs) from >70% of
105 vin-binding protein ApVAP33 inhibited evoked excitatory postsynaptic potentials (EPSPs) in cultured c
106 ulated VPM or POm axons, and recorded evoked excitatory postsynaptic potentials (EPSPs) in different
107 ge-gated A-type Kv4 channels shape dendritic excitatory postsynaptic potentials (EPSPs) in hippocampa
108 nels on dendritic processing of subthreshold excitatory postsynaptic potentials (EPSPs) in mouse CA1
109 on evoked faster rising and shorter duration excitatory postsynaptic potentials (EPSPs) in MSNs (n =
110 channels) modulate excitability and curtail excitatory postsynaptic potentials (EPSPs) in neuronal d
111 evoked abrupt increases in the frequency of excitatory postsynaptic potentials (EPSPs) in two thirds
113 lls, spikes evoked 5 ms after parallel-fiber excitatory postsynaptic potentials (EPSPs) led to long-t
115 te or pyramidal cells) (n = 6) produce large excitatory postsynaptic potentials (EPSPs) of up to 4 mV
116 ormed to investigate the interaction between excitatory postsynaptic potentials (EPSPs) or currents (
117 th the mean peak amplitudes of the resulting excitatory postsynaptic potentials (EPSPs) ranging betwe
118 es the amplitude of two-photon (2P) uncaging excitatory postsynaptic potentials (EPSPs) recorded at t
121 rm manner; 85% of these cells responded with excitatory postsynaptic potentials (EPSPs) that maintain
122 rong stimulus by increasing the frequency of excitatory postsynaptic potentials (EPSPs) to TC cells,
123 In CA3 neurons, the amplitude and slope of excitatory postsynaptic potentials (EPSPs) transiently d
129 4) rats, TBS failed to induce LTP unless the excitatory postsynaptic potentials (EPSPs) were of suffi
132 d excitatory postsynaptic currents and field excitatory postsynaptic potentials (EPSPs) with threshol
133 es (paired-pulse facilitation, small initial excitatory postsynaptic potentials (EPSPs), a graded act
134 the endogenous release of glutamate, mediate excitatory postsynaptic potentials (EPSPs), alter presyn
135 hose temporal periods, and time constants of excitatory postsynaptic potentials (EPSPs), both increas
136 ential discharges to previously subthreshold excitatory postsynaptic potentials (EPSPs), even though
137 ulation of forward input evoked monosynaptic excitatory postsynaptic potentials (EPSPs), followed by
150 rate at which each source was bombarded with excitatory postsynaptic potentials (EPSPs); and (3) the
151 ort-term depression, where successive evoked excitatory postsynaptic potentials (EPSPs; >5 Hz) usuall
152 anism depends on a passively conducted giant excitatory postsynaptic potential evoked by a mossy fibe
153 indle afferent population was estimated from excitatory postsynaptic potentials evoked by muscle stre
155 tocol altered both the [Zn2+]t and the field excitatory postsynaptic potential (fEPSP) coordinately,
156 mined the cornu ammonis region 1 (CA1) field excitatory postsynaptic potential (fEPSP) response to co
158 tion had different actions on both the field excitatory postsynaptic potentials (fEPSPS) and LTP in t
159 (2R,6R)-HNK were examined by recording field excitatory postsynaptic potentials (fEPSPs) and miniatur
160 s of isoflurane were similar on evoked field excitatory postsynaptic potentials (fEPSPs) and paired p
161 P) acting at P2 receptors mediates some fast excitatory postsynaptic potentials (fEPSPs) in myenteric
162 Intracellular recordings of evoked fast excitatory postsynaptic potentials (fEPSPs) in myenteric
163 acts at P2X receptors to contribute to fast excitatory postsynaptic potentials (fEPSPs) in myenteric
164 lethality in mice, (ii) NMDAR-mediated field excitatory postsynaptic potentials (fEPSPs) in the CA1 f
165 ically isolated NMDA-receptor-mediated field excitatory postsynaptic potentials (fEPSPs) in the CA1 r
168 red oxygen and the amplitude of evoked field excitatory postsynaptic potentials (fEPSPs) recorded fro
169 ted one or two populations of nicotinic fast excitatory postsynaptic potentials (fEPSPs) that were gr
173 while in one AH-cell, some spontaneous fast excitatory postsynaptic potentials (FEPSPs) were recorde
175 oved the recovery of Schaffer collateral-CA1 excitatory postsynaptic potentials following a 15 min hy
176 potential, as compared with the sensorimotor excitatory postsynaptic potential in preparations that r
177 gulation of a prominent thalamocortical NMDA excitatory postsynaptic potential in stellate cells regu
179 n fact, both NMDAR- and AMPAR-mediated field excitatory postsynaptic potentials in CA1 decrease with
180 rlier reversal to polarizing currents of ATD excitatory postsynaptic potentials in comparison to thos
181 y correlated with both the onset of compound excitatory postsynaptic potentials in fast-spiking inter
182 d the size (amplitude and duration) of field excitatory postsynaptic potentials in hippocampal slices
184 Excitatory stimuli drove trains of single excitatory postsynaptic potentials in relay cells, but g
187 optic tract stimulation routinely evoked an excitatory postsynaptic potential/inhibitory postsynapti
190 cytosolic glutamate and decreased miniature excitatory postsynaptic potential (mEPSC) frequency.
192 rkinje cell TRPC3 channels underlie the slow excitatory postsynaptic potential observed after paralle
193 uced a similar biphasic modulatory action on excitatory postsynaptic potentials or currents (EPSPs/EP
194 rated predominantly by synchronised cortical excitatory postsynaptic potentials oscillating at freque
196 pecific dissociation of synaptic [population excitatory postsynaptic potential (pEPSP)] and cellular
197 omega-conotoxin GVIA (CTX) on the population excitatory postsynaptic potentials (pEPSP) in stratum ra
200 reduces the amplitude of two-photon uncaging excitatory postsynaptic potentials recorded at the soma.
202 contributions are reduced because the early excitatory postsynaptic potential retards the opening of
206 nule cells NMDA receptors are increased, and excitatory postsynaptic potentials should be strongly NM
207 onstrated that ethanol inhibited NMDAR field excitatory postsynaptic potential slope and amplitude to
208 from control mice and (ii) the plot of field excitatory postsynaptic potential slope versus the popul
209 l recording was used to study a type of slow excitatory postsynaptic potential (slow EPSP) that was m
210 hippocampal area CA3 sum distal and proximal excitatory postsynaptic potentials sublinearly and activ
211 aused a NMDA receptor-dependent, supralinear excitatory postsynaptic potential summation, indicating
212 oping nicotine-induced potentiation of field excitatory postsynaptic potential that appeared to be de
213 r and nonlinear mechanisms were caused by an excitatory postsynaptic potential that reversed near 0 m
214 to excitatory neurons, heterogeneity in the excitatory postsynaptic potentials that impinge on PV ne
215 lectrical stimulation generated monosynaptic excitatory postsynaptic potentials that were indistingui
217 , and slow-wave sleep, produce a large field excitatory postsynaptic potential throughout stratum rad
222 dual spines while monitoring uncaging-evoked excitatory postsynaptic potentials (uEPSPs) and Ca trans
224 nstant for STP of the AMPA receptor-mediated excitatory postsynaptic potential was approximately 6 mi
225 and ethanol's inhibition of the NMDAR field excitatory postsynaptic potential was attenuated by a br
227 at this time, indicating that the underlying excitatory postsynaptic potential was more probable, but
230 High-frequency summation of AMPA-mediated excitatory postsynaptic potentials was smaller in OT neu
233 lateral pathway was stimulated and the field excitatory postsynaptic potentials were recorded in the
234 in post-tetanization the slopes of the field excitatory postsynaptic potentials were significantly di
235 red synaptic inputs as the amplitude of fast excitatory postsynaptic potentials were significantly la
236 ion that increase the size of NMDAR-mediated excitatory postsynaptic potentials, whereas at high conc
237 acellular spike-triggered averaging revealed excitatory postsynaptic potentials, which confirmed thes
238 m-CPP enhances the occurrence of spontaneous excitatory postsynaptic potentials with no alteration in