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