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1 z, which is time-locked to the glutamatergic barrages.
2 stematically with the magnitude of the input barrages.
3  may reflect muscle mechanoreceptor afferent barrage and dysregulated sensory processing.
4 king is associated with increased inhibitory barrages and narrower visually evoked synaptic potential
5  activity, independent of ascending afferent barrage, and enlarged receptive fields.
6                               The inhibitory barrages are effectively nullified at low doses of picro
7                       Here, we injected EPSC barrages at the soma and at the proximal, middle, and di
8  4.4 mV for the IPSP and 3.0 mV for the EPSP barrage, because of temporal summation and/or facilitati
9                                 During these barrages, both sets of interneurons show intense burstin
10 isted after interruption of ascending spinal barrage by spinal cord transection above the level of th
11                                         This barrage consisted of postsynaptic responses to spiking a
12 membrane potential (e.g., -65 mV), these PSP barrages could result in the activation of a low-thresho
13  dendritic and somatic EPSPs were identical, barrages delivered to the dendrite generated much higher
14 tal event, the number of preictal inhibitory barrages dropped, and in parallel with this change, the
15                In the distal dendrites, EPSC barrages evoked repetitive bursts of action potentials,
16        Beyond these clues, the mechanisms of barrage firing are unknown.
17 on of one interneuron in some cases triggers barrage firing in a nearby, unstimulated interneuron.
18        Together, these findings suggest that barrage firing is probably triggered by a multicellular
19                                 Induction of barrage firing was blocked by lowering extracellular cal
20                                     Finally, barrage firing was normal in mice with deletion of the p
21              Despite its calcium dependence, barrage firing was not prevented by inhibiting chemical
22 it here as 'retroaxonal barrage firing', or 'barrage firing' for short.
23  firing, we refer to it here as 'retroaxonal barrage firing', or 'barrage firing' for short.
24 ecorded interneuron with BAPTA did not block barrage firing, suggesting that the required calcium ent
25  compete with the noisy spontaneous synaptic barrage for control of postsynaptic SNr neurons, which h
26 nced virus transmission, but did not prevent barrage formation associated with mycelial incompatibili
27 ractions between two tightly linked genes in barrage formation, heterokaryon formation, and asymmetri
28 ons receive a continuous inhibitory synaptic barrage from 1 or 2 presynaptic GPe neurons.
29                         The ongoing synaptic barrage from spontaneous firing, frequency-dependent sho
30                        The enhanced afferent barrage from these neurons sensitizes spinal neurons and
31 oked plateau potentials in SGCs and synaptic barrages in downstream hilar neurons without blocking fa
32      These observations suggest that ectopic barrages in the injured IAN contribute more to the devel
33 nal bursting is time-locked to glutamatergic barrages in the pre-ictal period.
34  are thought to reflect a sustained synaptic barrage, involving the coordination of hundreds of pyram
35  patients) received prophylactic 360 degrees barrage laser 4 weeks after cataract surgery.
36                                 Prophylactic barrage laser might be a useful intervention in eyes wit
37  effects of different components of synaptic barrages (namely, depolarization, increase in membrane c
38  that one or more cometary airbursts/impacts barraged North America approximately 12,900 cal yr B.P.
39      When present, however, these inhibitory barrages occlude an intense excitatory synaptic drive th
40 expressing (CCK+) basket cells, which fire a barrage of action potentials ("BARR") during non-rapid e
41 tens of seconds to minutes produces a sudden barrage of action potentials lasting about a minute beyo
42                                   During the barrage of antidromic spikes, high-frequency firing will
43 ynchronous release component is reduced, the barrage of asynchronous GABA release from CCK interneuro
44 sensory input to the olfactory bulb evokes a barrage of asynchronous synaptic excitation and highly r
45                                          The barrage of comets and asteroids that produced many young
46 120-gp41) with CD4 and coreceptors trigger a barrage of conformational changes in Env that drive the
47 e cellular genome is subjected to a constant barrage of endogenous DNA damage, but surprisingly littl
48 us synaptic bombardment, receiving a complex barrage of excitatory and inhibitory inputs.
49                             By introducing a barrage of excitatory and inhibitory synaptic conductanc
50 nd stereotyped temporal sequence: an initial barrage of excitatory input was rapidly quenched by inhi
51  an olfactory nerve stimulation with a short barrage of excitatory inputs mediated by mitral, tufted,
52 neurons experience a significant spontaneous barrage of fast, amino-acid-mediate synaptic transmissio
53 work both types of neurone received a phasic barrage of gamma frequency excitatory inputs but, due to
54 n-specific firing despite receiving a steady barrage of heterogeneously tuned excitatory inputs that
55                                     (ii) The barrage of impulses that came from the peripheral nocice
56                                    (iii) The barrage of impulses that came from the sensitized second
57 d peptides attributable to an injury-induced barrage of impulses.
58 tion provides a means of selecting among the barrage of information reaching the retina and of enhanc
59 This persistence of firing during a constant barrage of inhibition raises the question of what patter
60 put from many PCs, resulting in a continuous barrage of inhibitory inputs.
61 idal cells resulting from the high frequency barrage of interneurons.
62 rs must separate relevant information from a barrage of irrelevant information.
63 t synaptic conductance input, similar to the barrage of noisy synaptic input that cortical neurons ha
64 Unfortunately, the field is complicated by a barrage of overlapping clinical syndromes and histopatho
65 rrier tissue that is exposed to a continuous barrage of pathogens, many fundamental aspects of the an
66 the integrity of the genome from a continual barrage of potentially detrimental insults.
67 s-a sales pitch, a teaching demonstration, a barrage of questions, and a description of a future rese
68  stimulated with a computer-generated steady barrage of random inputs, mimicking weak synaptic conduc
69                    Fungal pathogens deploy a barrage of secreted effectors to subvert host immunity,
70 nder natural conditions, animals encounter a barrage of sensory information from which they must sele
71 ile animals navigating the real world face a barrage of sensory input, their brains evolved to percep
72                             Transforming the barrage of sensory signals into a coherent multisensory
73                            Transforming this barrage of sensory signals into a coherent percept of th
74                     We hypothesized that the barrage of signals present in the extracellular milieu o
75 ryonic stages, immune cells are faced with a barrage of signals that will not all be directing the ce
76 rimate chromosomes were compared, creating a barrage of speculation.
77 tive must be accomplished despite a constant barrage of spontaneous DNA double strand breaks.
78 h increased production of cytokines led to a barrage of studies and lively debate on the relative con
79 ed by both a tonic and respiratory-modulated barrage of synaptic events that were blocked by intrathe
80 vent underlying the Up state is a maintained barrage of synaptic excitation, but that the membrane po
81 o increasing concentrations of odorants with barrages of action potentials, and their terminals have
82  or tolbutamide (50-200 microM), we recorded barrages of amperometric events.
83 al cells in vivo and in vitro receive strong barrages of both excitatory and inhibitory postsynaptic
84  fast spiking interneurons, receiving robust barrages of both excitatory and inhibitory synaptic pote
85 Consistent with this hypothesis, we observed barrages of electrochemical signals that far exceeded th
86  The firing evoked by injection of simulated barrages of EPSCs into the proximal dendrite of layer 5
87 ing the generation of spindle waves revealed barrages of EPSPs and IPSPs.
88 ed EPSPs was 4.7-fold greater than identical barrages of EPSPs generated from distal (572 +/- 13 micr
89              Sensory axon stimulation evokes barrages of EPSPs in Blanes cells that trigger long epoc
90 y for evoking action potentials, we injected barrages of EPSPs that simulate the inputs generated by
91  precision, can be achieved through balanced barrages of excitatory and inhibitory synaptic activity.
92  state, in which neurons transiently receive barrages of excitatory and inhibitory synaptic inputs th
93 ortical pyramidal cells receive proportional barrages of excitatory and inhibitory synaptic potential
94 ay be driven by rebound depolarization after barrages of GABA(A) receptor (GABA(A)R)-mediated IPSPs a
95                      Pyramidal cells receive barrages of inhibitory inputs in advance of the epilepti
96 on," with the latter resulting from repeated barrages of neural activity from nociceptors.
97  we report that LGN neurons receive periodic barrages of postsynaptic currents from the retina that d
98 on and excitation of interneurons and evoked barrages of postsynaptic GABAergic currents.
99                                 In contrast, barrages of proximal simulated EPSPs enhanced the rate o
100                        Here, the efficacy of barrages of simulated EPSPs generated at known dendritic
101 3 +/- 15 microm from soma; n = 28) dendritic barrages of simulated EPSPs was 4.7-fold greater than id
102 ed patch whole-cell recording, we found that barrages of such events were well coupled in time and gr
103                            We first recorded barrages of synaptic conductances from neurons during ep
104 n rat hippocampal slices evoked long-lasting barrages of synaptic inputs in subpopulations of dentate
105                       We found that synaptic barrages originate from semilunar granule cells (SGCs),
106 due to the ongoing local inhibitory synaptic barrage produced by the spontaneous firing of other GPe
107                              We measured the barrage's effect on the firing rate and regularity of GP
108 ite this level of excitation, the inhibitory barrages suppress firing, thereby limiting further neuro
109 g flow of excitatory and inhibitory synaptic barrages that not only control participation of neurons
110 tic GPe neurons produces inhibitory synaptic barrages that significantly alter the firing regularity
111 g modulated component of the evoked synaptic barrages (the F1 component).
112                                     Synaptic barrages triggered persistent firing in hilar neurons (h
113 -5/6 received inputs that generated rhythmic barrages (up to 25 Hz) of antidromic spikes during BMPs.
114                              To simulate the barrage, we constructed conductance waveforms for dynami
115 llowed by a prolonged (up to 1 sec) synaptic barrage, which fatigued at stimulus repetition rates of
116                          Mammalian cells are barraged with endogenous metabolic byproducts and enviro

 
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