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乙型血友病莱顿中假定的凝血因子IX基因启动子。

The putative factor IX gene promoter in hemophilia B Leyden.

作者信息

Reitsma P H, Bertina R M, Ploos van Amstel J K, Riemens A, Briët E

机构信息

Department of Hematology, Leiden University Hospital, The Netherlands.

出版信息

Blood. 1988 Sep;72(3):1074-6.

PMID:3416069
Abstract

Hemophilia B Leyden is characterized by low levels of factor IX antigen and activity before the age of 15, whereas after puberty factor IX levels rise at a rate of about 5% per year. A single base substitution (-A----T) at position -20 was identified in the putative promoter of the gene cloned from a patient with hemophilia B Leyden. This nucleotide change was confirmed in a second patient from the same pedigree and was also found in a patient from a second Dutch pedigree with the same hemophilic phenotype. The results indicate that the two Dutch kindreds are related and point to the functional significance of the -20 position for the expression of the human factor IX gene.

摘要

莱顿B型血友病的特征是15岁之前IX因子抗原和活性水平较低,而青春期后IX因子水平以每年约5%的速度上升。在从一名莱顿B型血友病患者克隆的基因的假定启动子中,在-20位置鉴定出一个单碱基替换(-A----T)。在来自同一谱系的另一名患者中证实了这种核苷酸变化,并且在具有相同血友病表型的另一个荷兰谱系的一名患者中也发现了这种变化。结果表明,这两个荷兰家族有亲缘关系,并指出-20位置对人IX因子基因表达的功能意义。

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