血管性血友病：一个临床与分子层面的谜团。第十二届保罗·M·阿格勒纪念讲座。 - Suppr

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超能文献

Von Willebrand's disease: a clinical and molecular enigma. Twelfth Annual Paul M. Aggeler Memorial Lecture.

作者信息

Nachman R L

出版信息

West J Med. 1982 Apr;136(4):318-25.

PMID:6806985

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1273714/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdc1/1273714/7b938734cc6c/westjmed00212-0084-a.jpg

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本文引用的文献

Heterogeneity of human factor VIII. III. Transitions between forms of factor VIII present in cryoprecipitate and in cryosupernatant plasma.人凝血因子VIII的异质性。III. 冷沉淀和冷上清血浆中存在的因子VIII形式之间的转变

J Lab Clin Med. 1980 Mar;95(3):323-34.

Multimeric structure of factor VIII/von Willebrand factor in von Willebrand's disease.血管性血友病中因子VIII/血管性血友病因子的多聚体结构

J Lab Clin Med. 1980 Apr;95(4):590-602.

Factor VIII/von Willebrand protein. Modification of its carbohydrate causes reduced binding to platelets.凝血因子VIII/血管性血友病因子。其碳水化合物修饰导致与血小板的结合减少。

J Biol Chem. 1980 Nov 10;255(21):10134-9.

Variant von Willebrand's disease: characterization of two subtypes by analysis of multimeric composition of factor VIII/von Willebrand factor in plasma and platelets.血管性血友病：通过分析血浆和血小板中因子VIII/血管性血友病因子的多聚体组成来鉴定两种亚型

J Clin Invest. 1980 Jun;65(6):1318-25. doi: 10.1172/JCI109795.

Heightened interaction between platelets and factor VIII/von Willebrand factor in a new subtype of von Willebrand's disease.血管性血友病新亚型中血小板与凝血因子VIII/血管性血友病因子之间的相互作用增强。

N Engl J Med. 1980 May 8;302(19):1047-51. doi: 10.1056/NEJM198005083021902.

Inherited variants of factor-VIII-related protein in von Willebrand's disease.血管性血友病中与因子VIII相关蛋白的遗传变异

N Engl J Med. 1974 Jul 18;291(3):113-7. doi: 10.1056/NEJM197407182910301.

Quantitative assay of a plasma factor deficient in von Willebrand's disease that is necessary for platelet aggregation. Relationship to factor VIII procoagulant activity and antigen content.对血管性血友病中缺乏的、血小板聚集所必需的一种血浆因子进行定量测定。与凝血因子VIII促凝活性及抗原含量的关系。

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