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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 heart rate variability, salivary cortisol or secretory Immunoglobulin A.
5 itivity skin reactions, and mucosal defense (secretory immunoglobulin A and dual-sugar permeability).
6 B subunits of cholera toxin induced specific secretory immunoglobulin A and serum immunoglobulin G an
7 c lymphocytes; reduced complement formation, secretory immunoglobulin A, and interferon; and lower T
9 osal secretions containing T. cruzi-specific secretory immunoglobulin A harvested from immune mice we
12 ated significant levels of specific salivary secretory immunoglobulin A (IgA) and serum IgG antibodie
14 immunity for optimal induction of protective secretory immunoglobulin A (IgA) and systemic type 1 imm
15 , respectively, were adherent to immobilized secretory immunoglobulin A (IgA) and two IgA1 myeloma pr
16 y subunit that were recognized by intestinal secretory immunoglobulin A (IgA) antibodies from immune
17 le mucosal immunity to ricin correlates with secretory immunoglobulin A (IgA) antibody levels in vivo
18 r with a mixture of these strains, developed secretory immunoglobulin A (IgA) in tears and serum IgG
20 and cholera holotoxin induced an intestinal secretory immunoglobulin A (IgA) response (P < 0.01 comp
21 Mice infected with C. rodentium develop a secretory immunoglobulin A (IgA) response, but the role
22 time without causing disease while eliciting secretory immunoglobulin A (IgA) responses, as evidenced
24 emonstrated significant roles of RV-specific secretory immunoglobulin A (IgA), CD4+ T cells, and CD8+
25 ation was studied using T helper 1 cytokines/secretory immunoglobulin A (IgA), histatins and lysozyme
26 permeability by affecting the production of secretory immunoglobulin A (IgA), the main immune mechan
28 zed by enzyme-linked immunosorbent assay for secretory immunoglobulin A, lactoferrin, lysozyme, and i
31 rechallenge and, if so, whether antireovirus secretory immunoglobulin A (S-IgA) is a necessary compon
33 use permitted inquiry into the regulation of secretory immunoglobulin A (S-IgA) responses by substanc
34 surface protein C (PspC) binds to both human secretory immunoglobulin A (sIgA) and complement factor
38 s with biochemical approaches to investigate secretory immunoglobulin A (SIgA) as a substrate of BV-a
40 s to explore the association between natural secretory immunoglobulin A (sIgA) capsular antibodies in
41 ject of this study was to determine if stool secretory immunoglobulin A (sIgA) concentrations in chil
44 otein and amino acids, fat, lactoferrin, and secretory immunoglobulin A (sIgA) in human milk of a sub
45 stinal permeability and elevated circulating secretory immunoglobulin A (sIgA) in KD patients, as wel
48 ites, the mucus, antimicrobial peptides, and secretory immunoglobulin A (sIgA) protect the intestinal
50 ents of HM: lysozyme (LZ), lactoferrin (LF), secretory immunoglobulin A (sIgA), basal lipase (BL), cy
51 ents of HM: lysozyme (LZ), lactoferrin (LF), secretory immunoglobulin A (sIgA), basal lipase (BL), cy
55 eliac disease and promotes retrotransport of secretory immunoglobulin A (SIgA)-gliadin complexes.