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1 immunoglobulin G1 and stronger increases in immunoglobulin G2.
2 elicited to E. canis antigens consisting of immunoglobulin G2 antibodies exclusively in both acute a
4 essing autologous BOECs developed anti-FVIII immunoglobulin G2 antibodies, but in only 2 of the dogs
8 ared somatic modifications demonstrated that immunoglobulin G2 (IgG2) and IgA antibodies arose from t
10 rB9, VirB10, and CTP are recognized by serum immunoglobulin G2 (IgG2) and stimulate memory T-lymphocy
11 of IgBP+ strains bound gold-labelled bovine immunoglobulin G2 (IgG2) anti-DNP, indicating that these
12 vidities of individual adult postvaccination immunoglobulin G2 (IgG2) antibodies to PPS serotypes 6B
13 ulfide-mediated structural variants of human immunoglobulin G2 (IgG2) antibodies was recently the sub
15 as been hypothesized to require induction of immunoglobulin G2 (IgG2) antibody against outer membrane
20 hybridoma technology to produce fully human immunoglobulin G2 (IgG2) MAbs from B cells of an individ
23 ients with LJP have elevated levels of serum immunoglobulin G2 (IgG2), and this is most striking in b
24 Ca/A,D > Sa,Sb/B), its heavy-chain isotype (immunoglobulin G2 [IgG2] > IgG3; IgG1 and IgM negative),
26 lls, increased immunoglobulin M, and reduced immunoglobulin G2 levels in serum and impaired vaccine r
28 te glembatumumab vedotin links a fully human immunoglobulin G2 monoclonal antibody against the melano
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