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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
9                     To this end, we used the tachykinin receptor antagonist Spantide I to eliminate t
10 tamate receptor antagonist; L733,060, an NK1 tachykinin receptor antagonist, and chelerythrine, a pro
11                     The use of the selective tachykinin receptor antagonists SR 140333, SR 48986, and
12                                 By contrast, tachykinin receptor antagonists, which abolished capsaic
13 hykinin peptides and their respective nigral tachykinin receptors are also in position to influence m
14         The present results suggest that the tachykinin receptors are downregulated after subchronic
15           There have been proposals that the tachykinin receptor classification should be extended to
16 hought to be premature to extend the current tachykinin receptor classification.
17 15 and CG7887 by showing these two suspected tachykinin receptor family members respond specifically
18                         The NK(3) subtype of tachykinin receptor is a G protein-coupled receptor that
19            The down-regulation of neurokinin-tachykinin receptors is accomplished by a rapid internal
20 ivities of human and mouse HK-1 on the three tachykinin receptors, neurokinin-1-3 (NK1-3).
21 rpolarization or current was mimicked by the tachykinin receptor NK1 agonist Ac-[Arg6, Sar9, Met(O2)1
22           We demonstrate the presence of the tachykinin receptors NK1 and NK3 in platelets and presen
23 n C3aR, whereas C3a levels were unchanged in tachykinin receptor-null animals.
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
28 lammatory response is altered by alternative tachykinin receptor usage.
29 we have attempted to: (1) define the type of tachykinin receptor which mediates the negative chronotr

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