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1 ller cell-activating receptor NKp44, and the polymeric immunoglobulin receptor.
2 inin, but not of the basolaterally delivered polymeric immunoglobulin receptor.
3 by canine kidney (MDCK) cells expressing the polymeric immunoglobulin receptor.
4 ited transcytosis of immunoglobulin A by the polymeric immunoglobulin receptor.
5 ng polarized epithelial cells expressing the polymeric immunoglobulin receptor and monoclonal antibod
7 ane-bound immunoglobulin A (a ligand for the polymeric immunoglobulin receptor), and fluid-phase dext
9 EA1-positive early endosomes while recycling polymeric immunoglobulin receptor-bound immunoglobulin A
11 rgic diarrhea susceptibility of J chain- and polymeric immunoglobulin receptor-deficient mice, which
12 is, chicken ovalbumin-immunized J chain- and polymeric immunoglobulin receptor-deficient mice, which
13 The results of this work suggest that human polymeric immunoglobulin receptor-dependent enhanced inv
15 basolateral to apical transcytosis of IgA in polymeric immunoglobulin receptor-expressing cells by ap
16 hogenic strains to invade a variety of human polymeric immunoglobulin receptor-expressing epithelial
19 o respiratory airways and lung expression of polymeric immunoglobulin receptor induced following intr
20 between choline-binding protein A and human polymeric immunoglobulin receptor may be a key determina
21 on IgA secretion through the epithelial cell polymeric immunoglobulin receptor-mediated pathway, as W
22 zed by local plasma cells and has a specific polymeric immunoglobulin receptor-mediated transport mec
24 ding protein A (CbpA)/laminin receptor, CbpA/polymeric immunoglobulin receptor, or cell wall phosphor
25 A (CbpA) of S. pneumoniae binds to the human polymeric immunoglobulin receptor (pIgR) and enhances pn
26 lizes to vesicular structures containing the polymeric immunoglobulin receptor (pIgR) and located sub
27 lize with the two BBB endothelial receptors: polymeric immunoglobulin receptor (pIgR) and platelet en
28 ear factor kappa B (NFkB)-regulated proteins polymeric immunoglobulin receptor (pIgR) and platelet-ac
29 anscytosis experiments performed using human polymeric immunoglobulin receptor (pIgR) expressing Madi
30 idney disease mouse models, we show that the polymeric immunoglobulin receptor (pIgR) is highly expre
33 ich they are specifically transported by the polymeric immunoglobulin receptor (pIgR) on mucosal and
36 a first-line vertebrate immune defense, the polymeric immunoglobulin receptor (pIgR) transports poly
37 enously transfected basolateral protein, the polymeric immunoglobulin receptor (pIgR), and a secretor
38 ry component (SC), a cleavage product of the polymeric immunoglobulin receptor (pIgR), is added durin
39 depends on the epithelial transport protein, polymeric immunoglobulin receptor (pIgR), which is reduc
40 I-binding site on IgA1 overlaps the reported polymeric immunoglobulin receptor (pIgR)-binding site, w
48 of immunoglobulin A (IgA) (a ligand for the polymeric immunoglobulin receptor [pIgR]), apical recycl
50 retion of IgA into the intestinal lumen, the polymeric immunoglobulin receptor, was also dependent on
51 otein, interacts specifically with the human polymeric immunoglobulin receptor, which is expressed by
52 hydrolases to lysosomes, transcytosis of the polymeric immunoglobulin receptor, Wnt gradient formatio
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