VWF meets the ADAMTS family

被引:6
作者
Brass, L [1 ]
机构
[1] Univ Penn, Sch Med, Dept Med, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Dept Pharmacol, Philadelphia, PA 19104 USA
[3] Univ Penn, Sch Med, Ctr Expt Therapeut, Philadelphia, PA 19104 USA
关键词
D O I
10.1038/nm1101-1177
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The etiology of thrombotic thrombocytopenic purpura (TTP), a severe blood disorder resulting from increased platelet activation, has been an enigma. The identification of ADAMTS as a protease that cleaves von Willebrand factor and the demonstration of ADAMTS mutations in families with inherited TTP suggest a molecular mechanism for the disease.
引用
收藏
页码:1177 / 1178
页数:2
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