PAX5基因：人类原发性免疫缺陷候选基因的连锁与突变分析 - Suppr

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The PAX5 gene: a linkage and mutation analysis in candidate human primary immunodeficiencies.

作者信息

Vorechovský I, Koskinen S, Paganelli R, Smith C I, Busslinger M, Hammarström L

机构信息

Karolinska Institute at NOVUM, Center for BioTechnology, Huddinge, Sweden.

出版信息

Immunogenetics. 1995;42(2):149-52. doi: 10.1007/BF00178590.

DOI:10.1007/BF00178590

PMID:7607706

Abstract

摘要

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引用本文的文献

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The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases.与X连锁无丙种球蛋白血症相关的基因是蛋白质酪氨酸激酶src家族的成员。

Nature. 1993 Jan 21;361(6409):226-33. doi: 10.1038/361226a0.

Molecular analysis of IgA deficiency. Evidence for impaired switching to IgA.IgA缺乏症的分子分析。向IgA转换受损的证据。

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Expression of Bruton's agammaglobulinemia tyrosine kinase gene, BTK, is selectively down-regulated in T lymphocytes and plasma cells.布鲁顿无丙种球蛋白血症酪氨酸激酶基因（BTK）在T淋巴细胞和浆细胞中表达选择性下调。

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Long-term persistence of selective IgA deficiency in healthy adults.健康成年人中选择性IgA缺乏的长期持续性。

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