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1 antigen challenge appears to unmask an NK-2 tachykinin receptor.
2 reference to the existence of a novel human tachykinin receptor.
3 salt appetite was due to a downregulation of tachykinin receptors.
4 mmation were mediated by neurokinin-2 (NK-2) tachykinin receptors.
5 d analysis of sialyltransferase 4A (SIAT4A), tachykinin receptor 1 (TACR1), and gamma-aminobutyric ac
6 rotein-coupled receptor, previously known as tachykinin receptor 86C (also known as the neurokinin K
7 human ileum, we examined a possible role of tachykinin receptors and neurokinin (NK) A in neurally i
8 ulphonic acid (PPADS; 10 microM) or an NK(3) tachykinin receptor antagonist (Neurokinin A 4-10; 100 n
10 tamate receptor antagonist; L733,060, an NK1 tachykinin receptor antagonist, and chelerythrine, a pro
13 hykinin peptides and their respective nigral tachykinin receptors are also in position to influence m
17 15 and CG7887 by showing these two suspected tachykinin receptor family members respond specifically
21 rpolarization or current was mimicked by the tachykinin receptor NK1 agonist Ac-[Arg6, Sar9, Met(O2)1
24 been implicated in RSV pathophysiology, and tachykinin receptor-null mice were similarly protected f
25 GIR shares 31-34% amino acid identity to the tachykinin receptors (substance P receptor, neurokinin A
26 ith DOCA once daily for 11 days and analyzed tachykinin receptor subtype, neurokinin 3 (NK3r)-immunor
27 ent studies determined to what extent nigral tachykinin receptor subtypes contribute to striatal D1-m
29 we have attempted to: (1) define the type of tachykinin receptor which mediates the negative chronotr
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