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1 ed by reactive blue 2, an antagonist of some P2 purinoceptors.
2  G protein-coupled receptor with homology to P2 purinoceptors.
3 e cerebral vessels through the activation of P2 purinoceptors.
4 cellular functions through the activation of P2-purinoceptors.
5                                              P2 purinoceptor agonists 2-methylthioATP (2-MeSATP), 2-c
6 microinjection of suramin (50 nl, 0.02 M), a P2 purinoceptor antagonist, into the retrofacial area in
7 nal purinoceptors in nociception, the potent P2-purinoceptor antagonist reactive red 2 was studied in
8 was abolished by apamin (0.3 microM) and the P2-purinoceptor antagonist suramin (100 microM); the oth
9               Pyridoxine is converted into a P2-purinoceptor antagonist.
10 the effects of P2X purinoceptor agonists and P2 purinoceptor antagonists on mesenteric afferent nerve
11 re leading to an active search for selective P2-purinoceptor antagonists to alleviate pain.
12 fected by adenosine, but were reduced by the P2-purinoceptor blocker suramin.
13                                              P2-purinoceptors couple extracellular ATP to the activat
14                           The involvement of P2 purinoceptors in chemosensory function in the ventrol
15                                   A role for P2 purinoceptors in the chemosensory response of respira
16  red 2 exerts antinociception by blockade of P2-purinoceptors in the spinal cord and, hence, support
17 s and fibroblasts and that the activation of P2 purinoceptors is involved in the regulation of DNA sy
18    These results support the hypothesis that P2 purinoceptors may be involved in mediating autoregula
19 ays and molecular mechanisms responsible for P2-purinoceptor-mediated chloride (Cl(-)) currents (I(Cl
20 n sequence identity to the G protein-coupled P2 purinoceptors obtained by DNA cloning.
21               Rat mucosal mast cells express P2 purinoceptors, occupation of which mobilizes cytosoli
22     Recent studies have suggested a role for P2 purinoceptors on vascular smooth muscle cells in the
23 l ATP, via interactions with apical membrane P2-purinoceptors, regulates the balance of active ion se
24  indicated that P2Y3 is a previously unknown P2 purinoceptor subtype with a preference for nucleoside
25 his potency order is atypical for any single P2 purinoceptor subtype.
26                         We conclude that two P2 purinoceptor subtypes are present on follicular Xenop
27 ry efficiency before and after saturation of P2 purinoceptors with acute intra-arterial administratio
28 activates extracellular ATP, and by blocking P2 purinoceptors with pyridoxal phosphate-6-azo(benzene-
29 e abolished following the desensitization of P2-purinoceptors with alpha, beta-methylene ATP (m-ATP;

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