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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
11 olished by pretreatment of the animal with a bradykinin B2 receptor antagonist (HOE 140).
12 e Pro2-Pro3-Gly4-Phe5 section of the peptide bradykinin B2 receptor antagonist [Pro3, Phe5]HOE 140 (D
13 methacin, l-NG-nitroarginine methyl ester, a bradykinin B2 receptor antagonist and tetrodotoxin.
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).
16                                          The bradykinin B2 receptor antagonist HOE 140 abolished the
17 ty response to bradykinin was blocked by the bradykinin B2 receptor antagonist HOE 140, by inhibition
18 hibitor l-N(6)-nitroarginine methyl ester or bradykinin B2 receptor antagonist icatibant.
19 tudy does not support clinical efficacy of a bradykinin B2 receptor antagonist in ACE inhibitor-assoc
20      We sought to test the hypothesis that a bradykinin B2 receptor antagonist would shorten time-to-
21 in tumors was significantly inhibited by the bradykinin B2 receptor antagonist, d-Arg, [Hyp3, Thi5,8,
22                                 Icatibant, a bradykinin B2 receptor antagonist, is an established tre
23 30 mg of subcutaneous icatibant, a selective bradykinin B2 receptor antagonist, or to the current off
24                                   Hoe 140, a bradykinin B2-receptor antagonist, had no effect on the
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
27                                         Both bradykinin B2 receptor antagonists had no significant ef
28 ted by NPC 17647 and Hoe 140 (p < 0.05), two bradykinin B2 receptor antagonists, but not by desArg9,[
29                             We conclude that bradykinin B2 receptors are expressed in skeletal muscle
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
32                     TAp73 also activated the bradykinin B2 receptor (B2R) promoter, a developmentally
33                                              Bradykinin-B2-receptor (B2R) blockade by icatibant subst
34 llular loop (IC1) in the function of the rat bradykinin B2 receptor (BKB2R) was probed.
35 ein, high-molecular-weight kininogen, or the bradykinin B2 receptor, but not the B1 receptor, largely
36                                              Bradykinin B2 receptor-deleted mice (Bdkrb2(-/-)) have d
37 ated terminals of dental pulp fibers via the bradykinin B2 receptor-dependent mechanism.
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
40                 It was demonstrated that the bradykinin B2 receptor gene (BdkrB2) is a direct transcr
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
43               The widespread distribution of bradykinin B2 receptor immunoreactivity in neuronal comp
44 or to establish the cellular distribution of bradykinin B2 receptor immunoreactivity in the rat brain
45                                              Bradykinin B2 receptor immunoreactivity was also present
46                                              Bradykinin B2 receptor immunoreactivity was ubiquitously
47 tumor permeability specifically involves the bradykinin B2 receptor in brain tumor tissue.
48                            Activation of the bradykinin B2 receptor in endothelial cells initiates a
49 -converting enzyme levels, or absence of the bradykinin B2 receptor, increase kidney damage in diabet
50                         Thus, absence of the bradykinin B2 receptor increases the oxidative stress, m
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
53             These data suggest that a strong bradykinin B2-receptor-mediated upregulation of osteopon
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
56           By contrast, expression of neither bradykinin B2 receptors nor the scaffolding protein cave
57  stimulation of diverse receptors, including bradykinin B2 receptors on endothelial cells.
58 ion of NHE-1 is blocked by inhibitors of the bradykinin B2 receptor, phospholipase C, Ca2+/calmodulin
59              These data demonstrate that the bradykinin B2 receptor physically associates with eNOS i
60 tions -70 and -707, respectively, in the rat bradykinin B2 receptor promoter.
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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