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通过血凝抑制检测因子VIII:甲型血友病和血管性血友病。

Factor 8 detection by hemagglutination inhibition: hemophilia A and von Willebrand's disease.

作者信息

Stites D P, Hershgold E J, Perlman J D, Fudenberg H H

出版信息

Science. 1971 Jan 15;171(3967):196-7. doi: 10.1126/science.171.3967.196.

Abstract

Factor VIII activity was detected immunologically in both the serums and plasmas of 14 normal individuals and 14 patients with hemophilia A. A hemagglutination-inhibition test with rabbit antibody to highly purified (10,000-fold) factor VIII from humans was used. Serums and plasmas from eight patients with von Willebrand's disease showed little or no factor VIII activity in this test, an indication that the test may serve as a specific assay for differentiation between von Willebrand's disease and hemophilia A.

摘要

在14名正常个体和14名甲型血友病患者的血清和血浆中,通过免疫学方法检测到了凝血因子VIII活性。采用了用兔抗人高度纯化(10000倍)凝血因子VIII抗体进行的血凝抑制试验。在该试验中,8名血管性血友病患者的血清和血浆显示出很少或没有凝血因子VIII活性,这表明该试验可作为区分血管性血友病和甲型血友病的特异性检测方法。

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