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

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