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1 iated with both mast cell- and IgE-dependent passive cutaneous anaphylaxis (except at sites engrafted
4 n of MC functions in vivo was studied in the passive cutaneous anaphylaxis (PCA) MC-dependent model.
5 endent responses using a mast cell-dependent passive cutaneous anaphylaxis (PCA) model, as well as in
7 mast cell biology and a preclinical model of passive cutaneous anaphylaxis and passive systemic anaph
8 rgic actions of artesunate were evaluated in passive cutaneous anaphylaxis and passive systemic anaph
9 antly increased sensitivity to IgE-dependent passive cutaneous anaphylaxis as assessed by greater tis
10 T(1)R-deficient mice undergoing IgE-mediated passive cutaneous anaphylaxis as compared with the wild-
11 pression of IgE-mediated mast cell-dependent passive cutaneous anaphylaxis but can enhance the tissue
13 e WPE-induced, peanut-specific, IgE-mediated passive cutaneous anaphylaxis in hFcepsilonRIalpha trans
14 lity to respond to Ag in vivo as measured by passive cutaneous anaphylaxis in mice after irradiation.
15 isruptive IgE inhibitors efficiently prevent passive cutaneous anaphylaxis in mice expressing the hum
17 y and the absence of IgE/mast cell-dependent passive cutaneous anaphylaxis in the ear and joint as we
18 ation of plasma protein and the IgE-mediated passive cutaneous anaphylaxis in the ear were significan
19 rophenylacetyl) and anti-dansyl IgE-mediated passive cutaneous anaphylaxis in transgenic mice express
20 when tested for IgE- and mast cell-dependent passive cutaneous anaphylaxis in vivo or IgE-dependent m
21 gene deletion prevents vascular leakage and passive cutaneous anaphylaxis in vivo, and ROCK inhibito
23 oral HMO treatment were also measured in the passive cutaneous anaphylaxis model, and direct effects
24 basophilic leukemia mast cell model, in the passive cutaneous anaphylaxis mouse model of allergy, an
25 ant animal conferred an abnormally decreased passive cutaneous anaphylaxis reaction on mast cell-defi
26 n complexes in their secretory granules, the passive cutaneous anaphylaxis reaction was induced in th
27 In addition, we found significantly reduced passive cutaneous anaphylaxis reactions in gal3(-/-) mic
28 osyllactose and 6'-sialyllactose reduced the passive cutaneous anaphylaxis response, but only 6'-sial
32 nous LTC4 and to endogenous CysLTs evoked by passive cutaneous anaphylaxis was augmented in TG mice.
34 r permeability associated with IgE-dependent passive cutaneous anaphylaxis was significantly reduced
35 in inflammation (histamine- and IgE-mediated passive cutaneous anaphylaxis) we topically applied fing
36 s, impaired gastric acid secretion, impaired passive cutaneous anaphylaxis, and decreased mast cell d
37 to be responsible for FcgammaRIIA-dependent passive cutaneous anaphylaxis, and monocytes/macrophages
39 em were contrasted with data generated using passive cutaneous anaphylaxis, ovalbumin-induced asthma
44 nut-, cat-, and dansyl-specific IgE-mediated passive cutaneous anaphylaxis; and attenuate dansyl IgE-
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