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1 firmed that alpha1,2-fucose-containing H and A antigens of the HBGA family were recognized by CNV.
3 s produced a vigorous memory response to B10.A antigens, suggesting immune activation was not inhibit
7 develop alloantibodies to human glycophorin A antigen, we found reduced in vitro and in vivo Treg-su
16 e immunodominant T cell-defined MART-1/Melan-A antigen and downregulation of the TAP-1 gene in a recu
19 chemical studies demonstrated high levels of A antigen on various glycoproteins (GPs) from high-expre
20 elets contained higher than normal levels of A antigen were subdivided into 2 groups, designated Type
23 Histo-blood group A transferase produces A antigens and transfers GalNAc to the acceptor substrat
24 and VA387 (GII-4), which recognize the same A antigen but differ in that NV is unable to bind to the
28 r of cells expressing alpha-gustducin or the A antigen in regenerated taste buds; in the CTX animals
29 he porcine and bovine mucins, suggesting the A antigen as a possible factor for cross-species transmi
31 bserved a new pattern of binding to the type A antigen which is distinct from that of the P[II] RVs.
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