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1 capillary electrophoresis (MD-CE) assays for amino acid neurotransmitters.
2 ther calcium binding proteins and inhibitory amino acid neurotransmitters.
3 y of proteins that mediates the packaging of amino acid neurotransmitters.
4 rations, decreased the release of excitatory amino acid neurotransmitters, and decreased the total fr
5 affold to which diverse moieties from lipid, amino acid, neurotransmitter, and nucleoside metabolism
6 between the apoE4 allele and the recovery of amino acid neurotransmitters (aspartate, glutamate, and
7 dic chip that allows for in vivo sampling of amino acid neurotransmitters by low-flow push-pull perfu
8 the peptides into the brain while monitoring amino acid neurotransmitters by microdialysis sampling c
9 he balance between inhibitory and excitatory amino acid neurotransmitters contributes to the control
10 mals to determine the effects of ketamine on amino acid neurotransmitter cycling and glial metabolism
11 banesthetic doses of ketamine increased mPFC amino acid neurotransmitter cycling, as well as neuronal
12                                          The amino acid neurotransmitter D-Ser is a GluD2 receptor li
13 n of the immunohistochemical localization of amino acid neurotransmitters demonstrated that the riMLF
14 ed to include increased de novo synthesis of amino acid neurotransmitters, especially glutamate and G
15 kines for the immune response and excitatory amino acid neurotransmitters for the hippocampus.
16 elective age-related decrement in inhibitory amino acid neurotransmitter function.
17                      In immature neurons the amino acid neurotransmitter, GABA provides the dominant
18 he lateral hypothalamus (LH), the inhibitory amino acid neurotransmitter, GABA, has had a long-standi
19 ons have suggested a role for the inhibitory amino acid neurotransmitter gamma-aminobutyric acid (GAB
20                               The excitatory amino acid neurotransmitter glutamate participates in th
21 is of NAAG yields the more potent excitatory amino acid neurotransmitter glutamate.
22 ty of small organic molecules, including the amino acid neurotransmitters glutamate, aspartate and ta
23 ied by morphology and immunolabeling for the amino acid neurotransmitters glutamate, aspartate, gamma
24 trastructural localization of the excitatory amino acid neurotransmitters, glutamate and aspartate, u
25 ), which mimics the action of the excitatory amino acid neurotransmitter glutamic acid, releases LH-R
26 ontrast, the distributions of the inhibitory amino acid neurotransmitters glycine and GABA were not a
27 ease in the mPfc but had no effect on either amino acid neurotransmitter in the VTA.
28 the growing weight of evidence for a role of amino acid neurotransmitters in pancreatic islets and in
29 ts of histaminergic agents on the release of amino acid neurotransmitters in slices of the medial ves
30 rs sensory processing, we measured levels of amino acid neurotransmitters in spinal dialysates from a
31 equired for the storage of all classical and amino acid neurotransmitters in synaptic vesicles.
32                                    Here, the amino acid neurotransmitter innervation of SLD from dDpM
33                                       As the amino-acid neurotransmitters interact with receptors tha
34 h-level exposure to glutamate, an excitatory amino acid neurotransmitter, leads to neuronal death.
35 ule cells normally contain two "fast-acting" amino acid neurotransmitters, one excitatory and one inh
36 e addressed the topographic distribution and amino acid neurotransmitter phenotype of endocannabinoid
37  the arcuate nucleus differentiated by their amino acid neurotransmitter phenotype.
38 e, and allopregnanolone, modulate ionotropic amino acid neurotransmitter receptors, and may function
39  cell line, GK-P3, that expresses functional amino acid neurotransmitter receptors.
40 itive glycine receptors as a novel target of amino acid neurotransmitter regulation in islets.
41 can result from excess release of excitatory amino acid neurotransmitters, such as glutamate.
42  involve alterations in the major inhibitory amino acid neurotransmitter system of gamma-aminobutyric
43 lance of the major inhibitory and excitatory amino acid neurotransmitter systems of gamma-aminobutyri
44 ough the differential release of peptide and amino acid neurotransmitters to coordinate reproductive
45   Robust efflux of excitatory and inhibitory amino acid neurotransmitters was detected during ischemi
46   Both markers for inhibitory and excitatory amino acid neurotransmitters were found in varicose axon
47 activation, CNS cytokines, and monoamine and amino acid neurotransmitters were quantified.
48 mate and aspartate are endogenous excitatory amino acid neurotransmitters widely distributed in the m
49 for simultaneous monitoring of all the major amino acid neurotransmitters with 10-s temporal resoluti

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