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1 d several other salivary proteins, including secretory immunoglobulin A.
2 ame SpsA, the protein has been shown to bind secretory immunoglobulin A.
3             Therefore, a complex enriched in secretory immunoglobulin A and alpha-amylase forms a S.
4 itivity skin reactions, and mucosal defense (secretory immunoglobulin A and dual-sugar permeability).
5 B subunits of cholera toxin induced specific secretory immunoglobulin A and serum immunoglobulin G an
6 c lymphocytes; reduced complement formation, secretory immunoglobulin A, and interferon; and lower T
7 osal secretions containing T. cruzi-specific secretory immunoglobulin A harvested from immune mice we
8       Intestinal M cells bear a receptor for secretory immunoglobulin A (IgA) (sIgA) facing the lumen
9        Fecal extracts were assayed for total secretory immunoglobulin A (IgA) and C. parvum-specific
10 ated significant levels of specific salivary secretory immunoglobulin A (IgA) and serum IgG antibodie
11                                              Secretory immunoglobulin A (IgA) and systemic IgG2a anti
12 immunity for optimal induction of protective secretory immunoglobulin A (IgA) and systemic type 1 imm
13 , respectively, were adherent to immobilized secretory immunoglobulin A (IgA) and two IgA1 myeloma pr
14 y subunit that were recognized by intestinal secretory immunoglobulin A (IgA) antibodies from immune
15 le mucosal immunity to ricin correlates with secretory immunoglobulin A (IgA) antibody levels in vivo
16 r with a mixture of these strains, developed secretory immunoglobulin A (IgA) in tears and serum IgG
17                                              Secretory immunoglobulin A (IgA) protects the mucosal su
18  and cholera holotoxin induced an intestinal secretory immunoglobulin A (IgA) response (P < 0.01 comp
19    Mice infected with C. rodentium develop a secretory immunoglobulin A (IgA) response, but the role
20 time without causing disease while eliciting secretory immunoglobulin A (IgA) responses, as evidenced
21 nterleukin-12 (IL-12) can stimulate elevated secretory immunoglobulin A (IgA) responses.
22 emonstrated significant roles of RV-specific secretory immunoglobulin A (IgA), CD4+ T cells, and CD8+
23 ation was studied using T helper 1 cytokines/secretory immunoglobulin A (IgA), histatins and lysozyme
24  permeability by affecting the production of secretory immunoglobulin A (IgA), the main immune mechan
25 g antibodies in sera and of peptide-specific secretory immunoglobulin A in nasal secretions.
26 zed by enzyme-linked immunosorbent assay for secretory immunoglobulin A, lactoferrin, lysozyme, and i
27 nduced significant increases in LAM-reactive secretory immunoglobulin A (P<.05).
28 ecessary for optimal induction of protective secretory immunoglobulin A responses.
29 rechallenge and, if so, whether antireovirus secretory immunoglobulin A (S-IgA) is a necessary compon
30 use permitted inquiry into the regulation of secretory immunoglobulin A (S-IgA) responses by substanc
31 surface protein C (PspC) binds to both human secretory immunoglobulin A (sIgA) and complement factor
32                                              Secretory immunoglobulin A (SIgA) antibodies directed ag
33                                              Secretory immunoglobulin A (SIgA) antibodies reactive wi
34                                 In addition, secretory immunoglobulin A (sIgA) antibodies were detect
35 s with biochemical approaches to investigate secretory immunoglobulin A (SIgA) as a substrate of BV-a
36                             PspK bound human secretory immunoglobulin A (sIgA) but not the complement
37                                           As secretory immunoglobulin A (SIgA) deficiency in small ai
38                                              Secretory immunoglobulin A (SIgA) enhances host-microbio
39      We investigated the role of whole human secretory immunoglobulin A (sIgA), M6 protein-specific s
40      Furthermore, it expresses receptors for secretory immunoglobulin A (SIgA), the main antibody in
41                         The binding of human secretory immunoglobulin A (SIgA), the primary immunoglo
42 eliac disease and promotes retrotransport of secretory immunoglobulin A (SIgA)-gliadin complexes.

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