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凝血因子VIII的一种基因变体——因子VIII莱顿的功能缺陷。

The functional defect of factor VIII Leiden, a genetic variant of coagulation factor VIII.

作者信息

Mertens K, van Wijngaarden A, Bertina R M, Veltkamp J J

出版信息

Thromb Haemost. 1985 Oct 30;54(3):650-3.

PMID:3937262
Abstract

Factor VIII Leiden is a genetic variant of coagulation factor VIII which has been detected in the plasma of a patient with mild haemophilia A. In this patient's plasma factor VIII procoagulant antigen was in 5-fold excess over factor VIII procoagulant activity, indicating the presence of an abnormal factor VIII molecule. The variant factor VIII was isolated from the patient's plasma, and its functional properties were studied in a factor X-activating system consisting of purified components. The isolated factor VIII Leiden was normally activated by factor Xa and by thrombin, but the activity of the factor VIIIa was about 3% of normal. The defect of factor VIIIa Leiden was studied by comparison with normal factor VIIIa in kinetic experiments of factor Xa formation. The results support the hypothesis that factor VIIIa Leiden has a reduced affinity for phospholipid-bound factor IXa in the intrinsic factor X-activating complex.

摘要

莱顿因子VIII是凝血因子VIII的一种基因变体,已在一名轻度甲型血友病患者的血浆中检测到。在该患者的血浆中,凝血因子VIII促凝抗原比凝血因子VIII促凝活性高出5倍,表明存在异常的凝血因子VIII分子。从患者血浆中分离出变体凝血因子VIII,并在由纯化成分组成的因子X激活系统中研究其功能特性。分离出的莱顿因子VIII通常被因子Xa和凝血酶激活,但因子VIIIa的活性约为正常活性的3%。在因子Xa形成的动力学实验中,通过与正常因子VIIIa比较研究了莱顿因子VIIIa的缺陷。结果支持以下假设:在内在因子X激活复合物中,莱顿因子VIIIa与磷脂结合的因子IXa的亲和力降低。

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