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1 ity to co-release both a fast excitatory and inhibitory transmitter.
2 scent brain, when GABA is mainly known as an inhibitory transmitter.
3 that GABA may not function exclusively as an inhibitory transmitter.
4 ely by the brief (0.5-10 sec) application of inhibitory transmitter.
5 tic) responses to uncaging of excitatory and inhibitory transmitters.
6 ogical activity or release of other, largely inhibitory transmitters.
7 lasses of interneurons may release different inhibitory transmitters.
8 ce a long-term increase in the release of an inhibitory transmitter and thus modify the activity of a
9 y transmitter can increase the release of an inhibitory transmitter and thus paradoxically produces a
10 ivity of its neurons for these two important inhibitory transmitters and may provide novel inputs to
11 he symmetric-type (83/187) characteristic of inhibitory transmitters, and were equally prevalent on d
12                         Local application of inhibitory transmitter antagonists disabled the short in
13                            GABA is the major inhibitory transmitter at CNS synapses.
14                                   GABA is an inhibitory transmitter but can sometimes produce paradox
15 se of or increased receptors for one or more inhibitory transmitters, e.g., dopamine, serotonin, and
16 nsmitter 5-HT at one set of synapses and the inhibitory transmitter FMRFamide at another, long-term f
17 ion neurons through vesicular release of the inhibitory transmitter GABA (gamma-aminobutyric acid).
18                                     The fast inhibitory transmitter GABA is robustly expressed in the
19 he excitatory transmitter glutamate, and the inhibitory transmitter GABA onto target cells in the str
20 posure to the antiepileptic phenytoin or the inhibitory transmitter GABA.
21 ctance is activated by ambient levels of the inhibitory transmitter GABA.
22 ischofberger, and Sandkuhler showed that the inhibitory transmitters GABA and glycine can be coreleas
23 indicate that NO modulates the levels of the inhibitory transmitters GABA and glycine through several
24           In the lobster, application of the inhibitory transmitters GABA or histamine suppressed act
25 e excitatory transmitter, glutamate, and the inhibitory transmitter, GABA, in the two layers, the rol
26 ls" can be synchronized to each other by the inhibitory transmitter gamma-aminobutyric acid (GABA).
27 unopositive to antibodies raised against the inhibitory transmitter gamma-aminobutyric acid.
28                   Brain levels of glutamate, inhibitory transmitters gamma-aminobutyric acid (GABA) a
29 by their immunoreactivities for the putative inhibitory transmitters, gamma-aminobutyric acid (GABA)
30 uced by pressure application of the putative inhibitory transmitter glycine in the same cells.
31 n the brain, modulation of GABA, the primary inhibitory transmitter, has not been detected with elect
32  and immunostaining, we show that GABA is an inhibitory transmitter in mouse taste buds, acting on GA
33    GABA (gamma-aminobutyric acid), the major inhibitory transmitter in the brain, goes through a tran
34  gamma-Aminobutyric acid (GABA) is the major inhibitory transmitter in the mature brain but is excita
35  (gamma-aminobutyrate) is the most prevalent inhibitory transmitter in the mature hypothalamus.
36         However, glycine is a more prevalent inhibitory transmitter in the mature superior olivary co
37 ory and inhibitory ascending inputs, and the inhibitory transmitters include both gamma-aminobutyric
38 al lobe epilepsy, mossy fibers coexpress the inhibitory transmitter neuropeptide Y (NPY) with glutama
39  (GABA) has been identified as the potential inhibitory transmitter of spiking type I local interneur
40 smitters and, if so, what function might the inhibitory transmitter play in a particular circuit?
41 the transient increase in the probability of inhibitory transmitter release associated with posttetan
42                  We conclude that GABA is an inhibitory transmitter released during taste stimulation
43 strogen availability modulates expression of inhibitory transmitters, resulting in increased BDNF exp
44          Thus, the existence of two parallel inhibitory transmitter systems may increase the range an
45 gs are consistent with a role for CGRP as an inhibitory transmitter that shapes peripheral taste sign
46               GABA and glycine are the major inhibitory transmitters that attune neuronal activity in
47 and a decreased number of neurons expressing inhibitory transmitters; the reverse occurs when activit
48 t as autaptic and heterosynaptic presynaptic inhibitory transmitters through metabotropic glutamate r
49 K-A receptor myenteric neurons contained the inhibitory transmitter vasoactive intestinal polypeptide
50 S, gamma-aminobutyric acid (GABA) acts as an inhibitory transmitter via ligand-gated GABA(A) receptor

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