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1 olecules retained the ability to bind to the polymeric Ig receptor.
2 mologous to two other IgM-binding receptors (polymeric Ig receptor and Fcalpha/muR) but exhibits an e
3 aralleling the gradient in expression of the polymeric Ig receptor and the transport of its ligand, o
7 by heterosubtypic immunity, indicating that polymeric Ig receptor-mediated transport is not required
9 dney (MDCK) cells transfected with the human polymeric Ig receptor (pIgR) and the cells studied by fl
13 nding of dimeric immunoglobulin (Ig)A to the polymeric Ig receptor (pIgR) stimulates transcytosis of
18 epithelial cells transfected to express the polymeric Ig receptor (pIgR), were transfected with HIV
19 and IgM) across epithelia is mediated by the polymeric Ig receptor (pIgR), which is expressed on the
20 om the basolateral to the apical surface via polymeric Ig receptor (pIgR)-mediated binding and the in
21 s study aimed to address the hypothesis that polymeric Ig receptor (pIgR)-mediated secretory IgA immu
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