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IgA 缺陷供体中 IgA 重链恒定区基因的检测:反对基因缺失的证据

Detection of IgA heavy chain constant region genes in IgA deficient donors: evidence against gene deletions.

作者信息

Hammarström L, Carlsson B, Smith C I, Wallin J, Wieslander L

出版信息

Clin Exp Immunol. 1985 Jun;60(3):661-4.

Abstract

Sixty-six donors with selective IgA deficiency and one patient with selective IgA2 deficiency were investigated for immunoglobulin gene defects using restriction enzyme digestions and Southern blot analysis. All patients carried alpha 1 and alpha 2 genes in their genome, suggesting that large deletions are uncommon causes for IgA deficiency. Digestion with Bam HI, Pst I and Pvu II, did not reveal any polymorphism in the studied samples.

摘要

对66例选择性IgA缺乏症供体和1例选择性IgA2缺乏症患者进行了免疫球蛋白基因缺陷研究,采用限制性内切酶消化和Southern印迹分析。所有患者基因组中均携带α1和α2基因,这表明大片段缺失并非IgA缺乏症的常见病因。用Bam HI、Pst I和Pvu II进行消化后,在所研究的样本中未发现任何多态性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b130/1577211/2bee2ed08740/clinexpimmunol00135-0217-a.jpg

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