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1  leukemia)-2H3 mast cells (a tumor analog of mucosal mast cells).
2 pus of mice appear to be bone marrow-derived mucosal mast cells.
3 philic esophagitis have increased numbers of mucosal mast cells.
4  antibody dissociation from its receptors on mucosal mast cells.
5  are not essential for exocytosis in RBL-2H3 mucosal mast cells.
6  blood eosinophils, and increased intestinal mucosal mast cells.
7 uft cell hyperplasia along with expansion of mucosal mast cells.
8  involved in colonic goblet cell release and mucosal mast cell activation after immobilization stress
9                                              Mucosal mast cell and neutrophil activity were measured
10 expulsion is correlated with high numbers of mucosal mast cells and an increase in IL-13 and IL-10 se
11 er levels of PNA-specific IgE and intestinal mucosal mast cells and eosinophils over sham treatments.
12  accompanied by accelerated degranulation of mucosal mast cells and increased Ag-specific production
13                            Using the RBL-2H3 mucosal mast cell as a model, we have studied the tempor
14 nhibited elevations in blood eosinophils and mucosal mast cells at day 14 after inoculation.
15 vity reflects the permanent sensitization of mucosal mast cells by allergen-specific IgE antibodies b
16                                              Mucosal mast cells contribute to expulsion of a number o
17 even though they developed marked intestinal mucosal mast cell degranulation.
18          Nausea is associated with increased mucosal mast cell density, non-gastrointestinal somatic
19                           Porcine intestinal mucosal (mast cell-derived) heparin (PIM-heparin) shows
20 nstrate a critical role for IL-10 in driving mucosal mast cell expansion and activation, suggesting t
21                                          Rat mucosal mast cells express P2 purinoceptors, occupation
22 ifferentiation of intraepithelial intestinal mucosal mast cells expressing mouse mast cell protease 1
23 r (SCF), whereas helminth-induced intestinal mucosal mast cell hyperplasia also requires T cell-deriv
24                                   Intestinal mucosal mast cells (IMMC) express granule neutral protea
25 r results reveal a potential function of gut mucosal mast cells in HIV-1 dissemination in tissues.
26 d beta(6)(-/-) mice, we show accumulation of mucosal mast cells in the lamina propria of the small in
27                 The secretion process of the mucosal mast cell line RBL-2H3 was imaged using infrared
28 xtracts of intact and permeabilized RBL-2H3 (mucosal mast cell line) cells.
29                                 Cells of the mucosal mast cell line, RBL-2H3, are normally stimulated
30 finity receptor for IgE (FcepsilonRI) on the mucosal mast cell line, RBL-2H3, results in the rapid an
31 the same receptors on the widely studied rat mucosal mast cell line, RBL-2H3.
32 leukemia cells (RBL-2H3 m1), an immortalized mucosal mast cell line, was studied at the single-channe
33 ranulation in permeabilized RBL-2H3 cells, a mucosal mast cell line.
34                                              Mucosal mast cells lining the stomach and small intestin
35  These results provide the mechanism whereby mucosal mast cells mediate parasite expulsion from the i
36 inal nematodes is associated with pronounced mucosal mast cell (MMC) hyperplasia, differentiation, an
37                              Peak intestinal mucosal mast cell (MMC) recruitment coincides with expul
38                                              Mucosal mast cells (MMC) or their precursors migrate thr
39 oup has previously identified IL-9-producing mucosal mast cell (MMC9) as the primary source of IL-9 t
40 tification of multifunctional IL-9-producing mucosal mast cells (MMC9s) that can secrete prodigious a
41              In hybridoma-transplanted mice, mucosal mast cell numbers correlate with serum IgE level
42                              Postirradiation mucosal mast cell numbers were partially restored by rhI
43 toplasm of rat basophilic leukemia (RBL-2H3) mucosal mast cells or anchored (via LynB protein) to the
44 lation but not with allergen-specific IgE or mucosal mast cell protease 1 levels, indicating systemic
45 ntributing factor to the observed changes in mucosal mast cell protease and epithelial cytokine expre
46 tocytosis was absent, the protease unique to mucosal mast cells, rat mast cell protease II (RMCPII),
47 1 and -2) is consistent with intraepithelial mucosal mast cell recruitment.
48 usly compromised in their ability to mount a mucosal mast cell response after infection, and there is
49 t cell protease-1 and down-regulation of the mucosal mast cell response.
50 APs channel food allergens to lamina propria mucosal mast cells through an IL-13-CD38-cyclic adenosin
51                          Adhesion of RBL-2H3 mucosal mast cells to fibronectin-coated surfaces has be
52 th trypsin in patients with IBS-D stimulates mucosal mast cells to release PGE2, which downregulates
53 Our aim was to elucidate the contribution of mucosal mast cells to the effector phase of a secondary
54                                     Abundant mucosal mast cells were observed in the gastric tissues