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1 amined for antigen specificity, isotype, and crossreactivity.
2 o distinguish true double sensitization from crossreactivity.
3 es it encounters is based on T cell receptor crossreactivity.
4 more, we conclude that MOR1(C)-ir represents crossreactivity.
5 eneous Tregs is not due to alloreactivity or crossreactivity.
6 of genotypes 2a, 3a, 4a, 5a, and 6a to study crossreactivity.
7 emonstrated their specificity and absence of crossreactivity.
8 y insensitive to ligand structure, to enable crossreactivity.
9 a "rigid adaptation" mechanism governs such crossreactivity.
11 a cooperative fashion such that specificity, crossreactivity and MHC restriction are inextricably lin
14 t work from our laboratory identified T cell crossreactivity between epitopes of OspA and lymphocyte
15 olecular-mimicry theory proposes that immune crossreactivity between microbial and self-antigen is th
16 ow how binding by a self-reactive TCR favors crossreactivity between self and microbial antigens.
17 mechanisms, indicating that receptor-ligand crossreactivity can occur in the absence of molecular mi
20 ot retained on heparin agarose showed strong crossreactivity in immunoblot assays with anti-rat liver
24 terminally adjacent to the LBD increased the crossreactivity of monobodies to the apo-ER alpha-LBD, s
26 report results of experiments examining the crossreactivity of TCRs recognizing the myelin basic pro
27 of these proteins which participate in their crossreactivity or in their direct interaction, represen
28 gnition either through T cell receptor (TCR) crossreactivity or independently from TCR recognition.
31 e analyzed T-cell activation in the GALT and crossreactivity to the same antigen in the liver as well
32 s both sequence similarity and immunological crossreactivity to yeast Rrn3 and is capable of rescuing
33 gatively selected TCRs exhibited promiscuous crossreactivity toward multiple other major histocompati
34 eterologous CIDR1; however, a broad range of crossreactivity was detected in mice that were immunized
35 GlyRbeta (mAb-GlyRbeta) and does not exhibit crossreactivity with any of the GlyRalpha1-4 subunits.
37 me selectivity of the TCR and its remarkable crossreactivity with different MHC-peptide complexes.
39 es that in vitro demonstrate strong cellular crossreactivity with DR molecules expressed by the previ
40 s process through an unprecedented degree of crossreactivity with myelin-associated inhibitory ligand
41 6D2 bound tumor melanin and demonstrated no crossreactivity with normal melanized tissues in black m
44 re we report the structural mechanism of TCR crossreactivity with two distinct peptides from human pa
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