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1 h either epidermal growth factor receptor or bradykinin B2 receptor.
2 prototypical G protein-coupled receptor, the bradykinin B2 receptor.
3 tory interactions with the G protein-coupled bradykinin B2 receptor.
4 hose with caveolin-1 but also occur with the bradykinin B2 receptor.
5 2 nM as cells transfected with the wild type bradykinin B2 receptor.
6 n of bradykinin and subsequent activation of bradykinin B2 receptors.
7 iggered by activation of adenosine A1/A3 and bradykinin B2 receptors.
8 (I(M)) suppression by muscarinic M1, but not bradykinin B2, receptors.
9 inhibitors are partly mediated by increased bradykinin B2 receptor activation, this study aimed to d
10 g effects of bradykinin are mediated through bradykinin B2 receptors, and that differences in distrib
12 e Pro2-Pro3-Gly4-Phe5 section of the peptide bradykinin B2 receptor antagonist [Pro3, Phe5]HOE 140 (D
14 in December 2009) and icatibant (a selective bradykinin B2 receptor antagonist approved for use in th
15 adykinin (1 microM) and was abolished by the bradykinin B2 receptor antagonist HOE 140 (1 microM).
17 ty response to bradykinin was blocked by the bradykinin B2 receptor antagonist HOE 140, by inhibition
19 tudy does not support clinical efficacy of a bradykinin B2 receptor antagonist in ACE inhibitor-assoc
21 in tumors was significantly inhibited by the bradykinin B2 receptor antagonist, d-Arg, [Hyp3, Thi5,8,
23 30 mg of subcutaneous icatibant, a selective bradykinin B2 receptor antagonist, or to the current off
25 ted rats was abolished by application of the bradykinin B2-receptor antagonist, icatibant (0.5 mg/kg)
26 dykinin with HOE-140 (0.3 mg/kg), a specific bradykinin B2-receptor antagonist, produced no significa
28 ted by NPC 17647 and Hoe 140 (p < 0.05), two bradykinin B2 receptor antagonists, but not by desArg9,[
30 differential dynamic regulation of endosomal bradykinin B2 receptor (B2R) complexes with either beta-
31 targeting of the C5a receptor (C5aR) or the bradykinin B2 receptor (B2R) inhibited plasma leakage in
35 ein, high-molecular-weight kininogen, or the bradykinin B2 receptor, but not the B1 receptor, largely
38 trating that Akita diabetic mice lacking the bradykinin B2 receptor develop overt albuminuria, excret
39 late Ras, we examined whether PDGF regulates bradykinin B2 receptor expression in cultured arterial s
41 and P2 may be important in the regulation of bradykinin B2 receptor gene expression in response to in
42 protein revealed that virtually 100% of the bradykinin B2 receptor-immunoreactive positive cells wer
44 or to establish the cellular distribution of bradykinin B2 receptor immunoreactivity in the rat brain
49 -converting enzyme levels, or absence of the bradykinin B2 receptor, increase kidney damage in diabet
51 ental studies suggest that activation of the bradykinin B2 receptor is an important trigger of ischem
52 of the amino acid motif(s) participating in bradykinin B2 receptor-mediated signal transduction proc
54 ever, chronic ACE inhibition caused a marked bradykinin/B2 receptor-mediated increase in LV ISF chyma
55 rast to S1P, activation of G protein-coupled bradykinin B2 receptors neither activates kinase Akt nor
58 ion of NHE-1 is blocked by inhibitors of the bradykinin B2 receptor, phospholipase C, Ca2+/calmodulin
61 using a scanning format, we have chosen the bradykinin B2 receptor system in the NG108-15 cell line,
62 -acid portion of the C-terminal of the human bradykinin B2 receptor to establish the cellular distrib
63 pendent depolarization through activation of bradykinin B2 receptors, to which eNOS is physically com
64 internalization, and resensitization of the bradykinin B2 receptor, we identified two critical motif
65 Rat-1 cells, which do not contain detectable bradykinin B2 receptor, were transfected with wild type
66 Double-labeling experiments colocalizing the bradykinin B2 receptor with the neuronal marker NeuN or
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