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1  EOMs provides mechanistic insight for their allotypic and layer-specific viscoelastic properties.
2 , 20 to 50% of serum Igs and B cells bear a2 allotypic determinants.
3           Together, these data indicate that allotypic differences in peptide repertoire impact KIR r
4                                 Furthermore, allotypic differences of MHC-I with regard to the editin
5                                          The allotypic diversity of rabbit immunoglobulins prompted u
6 a mediate intraspecific competition, support allotypic diversity, control the level at which selectio
7 mpact on HLA-I results in multiple geno- and allotypic effects in a so far unparalleled and multimoda
8  and IgA2, and IgA2 is found in at least two allotypic forms, IgA2m(1) or IgA2m(2).
9                                              Allotypic KIR3DL1 variants, defined by neighboring resid
10 ed peritoneal exudate cells differing in IgA allotypic markers also demonstrated that B2 cells (B1-ce
11                       Using mice bearing Igk allotypic markers and a wild-type Ig repertoire, we demo
12 ave shown by mixed bone marrow chimeras with allotypic markers that Sle1 is expressed in B cells.
13  host T cells could be distinguished by Thy1 allotypic markers, adoptive transfer of LCMV-immune T ce
14 the antigen-binding site of the DPbeta1*0201 allotypic protein, suggesting that susceptibility to chi
15 m infectious agents, by DPbeta1*0201-related allotypic proteins, leading to the activation of helper
16 estricted CD8(+) T cell able to recognize an allotypic variant of the UL40 peptide with a modificatio
17                                              Allotypic variants of a key complement fluid-phase regul
18 inding characteristics of the most prevalent allotypic variants of M. mulatta FcgammaR for binding to
19                                              Allotypic variation in IgG3 resulted in widely different
20 hat targets the regulatory site suggest that allotypic variation influences the communication between