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1 ined by sequencing TAP1, in conjunction with HLA class II genes.
2 and Sjogren's syndrome are influenced by the HLA class II genes.
3 ears to be strongly associated with specific HLA class II genes.
4 ajor histocompatibility complex region, near HLA class II genes.
5 ith variation in the IL4RA gene (16p12), the HLA class II genes (6p21), and the interferon-alpha gene
7 es of the highly polymorphic HLA class I and HLA class II genes and the complex structural diversity
8 ssociations between human leukocyte antigen (HLA) class II genes and both rubella-specific immunoglob
9 nt P. aeruginosa infection were enriched for HLA class II genes, and those associated with MI were re
11 rcial sex workers had individual alleles for HLA class II genes determined by using labeled sequence-
14 s mellitus in humans is linked with specific HLA class II genes, e.g., HLA-DQA1*0301/ DQB1*0302 (DQ8)
15 DAC activity can repress IFN-gamma-inducible HLA class II gene expression and also demonstrate that H
18 islet autoantibodies localizing to the same HLA class II genes, HLA-DRB1 and HLA-DQB1, the effects o
19 Tg) mice has helped to elucidate the role of HLA class II genes in chronic inflammatory and demyelina
21 human histocompatibility leukocyte antigen (HLA) class II genes in 54 cases of tuberculoid leprosy (
22 re to inherit putative protective alleles of HLA class II genes is linked to the development of breas
23 ase ( P = 7.5 x 10(-35)), which included the HLA class II genes, known to be the primary determinants
24 human histocompatibility leukocyte antigen (HLA) class II gene most commonly associated with human t
25 of the TAP1 gene to human leukocyte antigen (HLA) class II genes on chromosome 6, we postulated that
27 These mice were generated by introduction of HLA class II genes, various human cytokines, and human B
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