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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  two of its receptors, the FcalphauR and the polymeric Immunoglobulin receptor.
6 by local plasma cells is transported through polymeric immunoglobulin receptors(2) and mediates robus
7 he mucosal epithelium into secretions by the polymeric immunoglobulin receptor allows them to play cr
8 ng polarized epithelial cells expressing the polymeric immunoglobulin receptor and monoclonal antibod
9 r the interaction with the ectodomain of the polymeric immunoglobulin receptor and secretory IgA.
10             However, owing to the paucity of polymeric immunoglobulin receptors and plasma cells, how
11 ane-bound immunoglobulin A (a ligand for the polymeric immunoglobulin receptor), and fluid-phase dext
12  of milk proteins, particularly beta-casein, polymeric immunoglobulin receptor, and alpha-lactalbumin
13          Structural similarity to TREM-1 and polymeric immunoglobulin receptor, and evidence for a na
14 ved in interactions with the J-chain and the Polymeric Immunoglobulin Receptor, and in general as ant
15 EA1-positive early endosomes while recycling polymeric immunoglobulin receptor-bound immunoglobulin A
16                            Here we show that polymeric immunoglobulin receptor-deficient (pIgR(-/-))
17 rgic diarrhea susceptibility of J chain- and polymeric immunoglobulin receptor-deficient mice, which
18 is, chicken ovalbumin-immunized J chain- and polymeric immunoglobulin receptor-deficient mice, which
19  The results of this work suggest that human polymeric immunoglobulin receptor-dependent enhanced inv
20 ades a human pharyngeal cell line in a human polymeric immunoglobulin receptor-dependent manner.
21 basolateral to apical transcytosis of IgA in polymeric immunoglobulin receptor-expressing cells by ap
22 hogenic strains to invade a variety of human polymeric immunoglobulin receptor-expressing epithelial
23                                    The mouse polymeric immunoglobulin receptor gene has a 654 nt exon
24 ing the respiratory epithelium via the human polymeric immunoglobulin receptor (hpIgR).
25 o respiratory airways and lung expression of polymeric immunoglobulin receptor induced following intr
26  between choline-binding protein A and human polymeric immunoglobulin receptor may be a key determina
27 on IgA secretion through the epithelial cell polymeric immunoglobulin receptor-mediated pathway, as W
28 zed by local plasma cells and has a specific polymeric immunoglobulin receptor-mediated transport mec
29                           In addition to the polymeric immunoglobulin receptor on mucosal epithelial
30 ding protein A (CbpA)/laminin receptor, CbpA/polymeric immunoglobulin receptor, or cell wall phosphor
31 A (CbpA) of S. pneumoniae binds to the human polymeric immunoglobulin receptor (pIgR) and enhances pn
32 lizes to vesicular structures containing the polymeric immunoglobulin receptor (pIgR) and located sub
33 lize with the two BBB endothelial receptors: polymeric immunoglobulin receptor (pIgR) and platelet en
34 ear factor kappa B (NFkB)-regulated proteins polymeric immunoglobulin receptor (pIgR) and platelet-ac
35                               Expressions of polymeric immunoglobulin receptor (pIgR) by tumor cells
36 anscytosis experiments performed using human polymeric immunoglobulin receptor (pIgR) expressing Madi
37                                              Polymeric immunoglobulin receptor (PIGR) has a major rol
38                           High expression of polymeric immunoglobulin receptor (PIGR) in breast cance
39 idney disease mouse models, we show that the polymeric immunoglobulin receptor (pIgR) is highly expre
40                                          The polymeric immunoglobulin receptor (pIgR) is important in
41                          Transcytosis of the polymeric immunoglobulin receptor (pIgR) is stimulated b
42 ich they are specifically transported by the polymeric immunoglobulin receptor (pIgR) on mucosal and
43                                          The polymeric immunoglobulin receptor (pIgR) plays a crucial
44                                          The polymeric immunoglobulin receptor (pIgR) transcytoses di
45                                          The polymeric immunoglobulin receptor (pIgR) transports immu
46  a first-line vertebrate immune defense, the polymeric immunoglobulin receptor (pIgR) transports poly
47  scRNA-seq, and qPCR analyses indicated that polymeric immunoglobulin receptor (pIgR) was highly expr
48 enously transfected basolateral protein, the polymeric immunoglobulin receptor (pIgR), and a secretor
49 ry component (SC), a cleavage product of the polymeric immunoglobulin receptor (pIgR), is added durin
50 dIgA) can move through cells via the IgA/IgM polymeric immunoglobulin receptor (PIGR), which is expre
51 depends on the epithelial transport protein, polymeric immunoglobulin receptor (pIgR), which is reduc
52 I-binding site on IgA1 overlaps the reported polymeric immunoglobulin receptor (pIgR)-binding site, w
53  as dimers and higher-order polymers, by the polymeric immunoglobulin receptor (pIgR).
54 nism by which CbpA binds its human receptor, polymeric immunoglobulin receptor (pIgR).
55 targeting the respiratory epithelium via the polymeric immunoglobulin receptor (pIgR).
56 ) across epithelial cells is mediated by the polymeric immunoglobulin receptor (pIgR).
57 ich they are specifically transported by the polymeric immunoglobulin receptor (pIgR).
58 ithelial barriers, which is achieved via the polymeric immunoglobulin receptor (pIgR).
59  cells, otherwise refractory to EBV, via the polymeric immunoglobulin receptor (pIgR).
60  blots demonstrates that this protein is the polymeric immunoglobulin receptor (pIgR).
61  of immunoglobulin A (IgA) (a ligand for the polymeric immunoglobulin receptor [pIgR]), apical recycl
62 equenin, whereas basolateral delivery of the polymeric immunoglobulin receptor was unaffected.
63 retion of IgA into the intestinal lumen, the polymeric immunoglobulin receptor, was also dependent on
64 otein, interacts specifically with the human polymeric immunoglobulin receptor, which is expressed by
65 hydrolases to lysosomes, transcytosis of the polymeric immunoglobulin receptor, Wnt gradient formatio