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1           H-Y was originally discovered as a transplantation antigen.
2            HLA-DPB1 functions as a classical transplantation antigen.
3  therapy to induce allospecific tolerance to transplantation antigens.
4  experimenting on immunological tolerance to transplantation antigens.
5 ntigens are not known to behave as classical transplantation antigens.
6 ve model for studying the immune response to transplantation antigens.
7 These results show that HLA-C functions as a transplantation antigen and that HLA-A and HLA-B allele
8 ically expressed beta-gal behaves as a minor transplantation antigen and that manipulation of the bet
9  effective suppressors of responses to major transplantation antigens, and these Tregs can be expande
10 er, it seems unlikely that ICAM-1 is a minor transplantation antigen, because there were no differenc
11 is and expression of the male-specific minor transplantation antigen H-Y.
12 xplained by the existence of a male-specific transplantation antigen, H-Y, but the molecular nature o
13 or (MB49), which we show to express the male transplantation antigen (HY), we tested the hypothesis t
14     Immune responses to Y chromosome-encoded transplantation antigens (HY) can have life-threatening
15 nous tolerance to a defined transgenic minor transplantation antigen in mice.
16                             The existence of transplantation antigens, in addition to those encoded b
17 efits, for example, ablation of xenoreactive transplantation antigens, inactivation of genes responsi
18  Treg-mediated long-term tolerance to all HY transplantation antigens, irrespective of whether they w
19                                 Tolerance to transplantation antigens is achieved through intrathymic
20 y of CD8(+) T-cell activation in response to transplantation antigens is novel.
21 ity for veto-based induction of tolerance to transplantation antigens is significantly extended.
22                    By contrast, matching for transplantation antigens might be effective for a long t
23  protein p23, the human homolog of the mouse transplantation antigen P198, interacted with the cytopl
24 epimerase-4-reductase (FX or tissue specific transplantation antigen P35B [TSTA3]).
25 epimerase-4-reductase (FX or tissue specific transplantation antigen P35B [TSTA3]).
26  We conclude that MICA may represent novel a transplantation antigen recognized by human allogeneic T
27 ying these epitopes is that they may be the "transplantation antigens" responsible for antibody-media
28  all T cells are specific for the male minor transplantation antigen, with male heart transplants exp

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