Normal cleavage of von Willebrand factor by ADAMTS-13 in the absence of factor VIII in patients with severe hemophilia A
Author:
Affiliation:
1. Research Institute; Puget Sound Blood Center; Seattle WA USA
2. Department of Biochemistry; University of Washington; Seattle WA USA
3. Department of Medicine; University of Washington; Seattle WA USA
Funder
National Institutes of Health
American Heart Association
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/jth.12299/fullpdf
Reference17 articles.
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2. Partial purification and characterization of a protease from human plasma cleaving von Willebrand factor to fragments produced by in vivo proteolysis;Furlan;Blood,1996
3. Physiologic cleavage of von Willebrand factor by a plasma protease is dependent on its conformation and requires calcium ion;Tsai;Blood,1996
4. Ultralarge multimers of von Willebrand factor form spontaneous high-strength bonds with the platelet glycoprotein Ib-IX complex: studies using optical tweezers;Arya;Blood,2002
5. Unusually large plasma factor VIII:von Willebrand factor multimers in chronic relapsing thrombotic thrombocytopenic purpura;Moake;N Engl J Med,1982
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