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1 hereditary immunodeficiency syndrome called bare lymphocyte syndrome.
2 everely affected in the FZA patient with the bare lymphocyte syndrome.
3 ization of CIITA and one form of the type II bare lymphocyte syndrome.
11 ree different HLA-DR allelic proteins in the bare lymphocyte syndrome cell line, BLS-1, revealed that
12 utant B-cell lines, which represent distinct bare lymphocyte syndrome class II genetic complementatio
13 lass II expression and that the mutations in bare lymphocyte syndrome complementation groups B and D
14 independently established B cell lines from bare lymphocyte syndrome complementation groups B and D.
15 ived from class II- plasma B-cells, and from bare lymphocyte syndrome group II cell lines, RJ2.2.5 an
17 mmunodeficiency (CID), also known as type II bare lymphocyte syndrome, is an autosomal recessive gene
18 n groups identified in the class II-negative bare lymphocyte syndrome or corresponding laboratory mut
19 NA-binding defects in the protein RFX5 cause bare lymphocyte syndrome or major histocompatibility ant
21 he study of genetic defects in cell lines of bare lymphocyte syndrome patients, as well as in cell li
22 oblasts derived from two recently identified bare lymphocyte syndrome patients, EBA and FZA, were fou
23 findings offer one explanation of why in the Bare Lymphocyte Syndrome, which is a congenital severe c
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