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1 s receptors, the FcalphauR and the polymeric Immunoglobulin receptor.
2 activating receptor NKp44, and the polymeric immunoglobulin receptor.
3 ng that Lmsp1 is a putative Trypanosomatidae immunoglobulin receptor.
4 not of the basolaterally delivered polymeric immunoglobulin receptor.
5 kidney (MDCK) cells expressing the polymeric immunoglobulin receptor.
6 cytosis of immunoglobulin A by the polymeric immunoglobulin receptor.
7 of clonally related B cells with diversified immunoglobulin receptors.
8 st cells as well as their activation through immunoglobulin receptors.
9 on is dependent on antigen interactions with immunoglobulin receptors.
10 iated with CLL cells that express nonmutated immunoglobulin receptors.
11 roteins mediate cell activation for multiple immunoglobulin receptors.
12 eta-1,4-galactosyl transferase, and poly-Ig (immunoglobulin) receptor.
13 lasma cells is transported through polymeric immunoglobulin receptors(2) and mediates robust protecti
14 epithelium into secretions by the polymeric immunoglobulin receptor allows them to play critical rol
15 ng in the draining LN after WNV infection is immunoglobulin receptor and macrophage independent but r
16 ed epithelial cells expressing the polymeric immunoglobulin receptor and monoclonal antibodies agains
18 e foreign antigens by virtue of cell surface immunoglobulin receptors and are most effectively activa
19 However, owing to the paucity of polymeric immunoglobulin receptors and plasma cells, how and wheth
20 immunoglobulin A (a ligand for the polymeric immunoglobulin receptor), and fluid-phase dextran are co
21 roteins, particularly beta-casein, polymeric immunoglobulin receptor, and alpha-lactalbumin, is pH-de
22 tructural similarity to TREM-1 and polymeric immunoglobulin receptor, and evidence for a naturally oc
23 eractions with the J-chain and the Polymeric Immunoglobulin Receptor, and in general as antibody glyc
28 like receptor type B2 (LilrB2)/murine Paired immunoglobulin receptor B (PirB) receptors expressed in
29 lonal antibody specific for the coinhibitory immunoglobulin receptor, B and T lymphocyte associated (
30 ve early endosomes while recycling polymeric immunoglobulin receptor-bound immunoglobulin A is delive
32 ich encodes the cytidine deaminase AID), the immunoglobulin receptor CD23 and the costimulatory molec
33 ocompatibility complex, complement proteins, immunoglobulin receptors, cytokines, and other as yet un
35 hea susceptibility of J chain- and polymeric immunoglobulin receptor-deficient mice, which are unable
36 n ovalbumin-immunized J chain- and polymeric immunoglobulin receptor-deficient mice, which have high
37 ts of this work suggest that human polymeric immunoglobulin receptor-dependent enhanced invasion of e
39 l to apical transcytosis of IgA in polymeric immunoglobulin receptor-expressing cells by approximatel
40 rains to invade a variety of human polymeric immunoglobulin receptor-expressing epithelial cell lines
41 highly variable glycoprotein related to the immunoglobulin receptor family that maps at the extreme
42 adhesion molecule (ESAM) is a member of the immunoglobulin receptor family that mediates homophilic
43 r inhibitory NK cell receptors, they contain immunoglobulin receptor family tyrosine-based inhibitory
46 he relationships between the affinity of the immunoglobulin receptor for antigen, the ability of B ce
49 uble-stranded breaks (DSBs) generated during immunoglobulin receptor gene (Ig) recombination and by i
50 tive colitis (P < 5 x 10(-8)), including the immunoglobulin receptor gene FCGR2A, 5p15, 2p16 and ORMD
54 4 silencing increased levels of cell-surface immunoglobulin receptors (i.e. Fcgamma receptors (Fcgamm
55 cells (TREM) family of single extracellular immunoglobulin receptors includes both activating and in
56 ory airways and lung expression of polymeric immunoglobulin receptor induced following intranasal vac
57 cyRI, with ID(50) values of <0.1 ug/ml; this immunoglobulin receptor is expressed on macrophages and
58 cytosis were identified: Type I, used by the immunoglobulin receptor, is mediated by Cdc42 and Rac, a
61 Here, we investigated the role of killer immunoglobulin receptors (KIR), which are expressed on N
62 ctionally tuned by education via killer cell immunoglobulin receptors (KIRs) interacting with HLA cla
63 hat recognition of these molecules by killer immunoglobulin receptors (KIRs) on maternal decidual NK
64 T cells express a repertoire of killer cell immunoglobulin receptors (KIRs) that recognize major his
65 ince most NK cells express inhibitory killer-immunoglobulin receptors (KIRs), we hypothesized that th
66 We examined the clinical impact of killer-immunoglobulin receptor-ligand (KIR-L) mismatch in 257 r
67 holine-binding protein A and human polymeric immunoglobulin receptor may be a key determinant of S. p
68 retion through the epithelial cell polymeric immunoglobulin receptor-mediated pathway, as Western blo
69 al plasma cells and has a specific polymeric immunoglobulin receptor-mediated transport mechanism for
71 yed by specialized antigen-presenting cells, immunoglobulin receptors of B lymphocytes primarily reco
74 iatic arthritis with mutations in the killer immunoglobulin receptors on natural killer cells is part
76 in A (CbpA)/laminin receptor, CbpA/polymeric immunoglobulin receptor, or cell wall phosphorylcholine/
77 f S. pneumoniae binds to the human polymeric immunoglobulin receptor (pIgR) and enhances pneumococcal
78 esicular structures containing the polymeric immunoglobulin receptor (pIgR) and located subjacent to
79 the two BBB endothelial receptors: polymeric immunoglobulin receptor (pIgR) and platelet endothelial
80 kappa B (NFkB)-regulated proteins polymeric immunoglobulin receptor (pIgR) and platelet-activating f
82 experiments performed using human polymeric immunoglobulin receptor (pIgR) expressing Madine-Darby c
85 ase mouse models, we show that the polymeric immunoglobulin receptor (pIgR) is highly expressed by re
88 re specifically transported by the polymeric immunoglobulin receptor (pIgR) on mucosal and glandular
92 ine vertebrate immune defense, the polymeric immunoglobulin receptor (pIgR) transports polymeric IgA
93 , and qPCR analyses indicated that polymeric immunoglobulin receptor (pIgR) was highly expressed in D
94 ansfected basolateral protein, the polymeric immunoglobulin receptor (pIgR), and a secretory protein,
95 nt (SC), a cleavage product of the polymeric immunoglobulin receptor (pIgR), is added during the tran
96 move through cells via the IgA/IgM polymeric immunoglobulin receptor (PIGR), which is expressed mainl
97 the epithelial transport protein, polymeric immunoglobulin receptor (pIgR), which is reduced during
98 site on IgA1 overlaps the reported polymeric immunoglobulin receptor (pIgR)-binding site, which might
107 globulin A (IgA) (a ligand for the polymeric immunoglobulin receptor [pIgR]), apical recycling of pIg
108 The dependence of tumor cells on surface immunoglobulin receptor signaling, survival pathways, an
109 nases, and is inhibited by G6b-B, a platelet immunoglobulin receptor that has two immunoreceptor tyro
110 motif-containing 21 (TRIM21) is a cytosolic immunoglobulin receptor that mediates antibody-dependent
112 IgA into the intestinal lumen, the polymeric immunoglobulin receptor, was also dependent on IL-17RA s
113 eracts specifically with the human polymeric immunoglobulin receptor, which is expressed by cells in
114 to lysosomes, transcytosis of the polymeric immunoglobulin receptor, Wnt gradient formation, iron tr