FVIIa as used pharmacologically is not TF dependent in hemophilia B mice
Author:
Affiliation:
1. Department of Biology,
2. Department of Pathology, and
3. Department of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC
Abstract
Publisher
American Society of Hematology
Subject
Cell Biology,Hematology,Immunology,Biochemistry
Link
http://ashpublications.org/blood/article-pdf/123/11/1764/537474/1764.pdf
Reference20 articles.
1. Mechanism of factor VIIa-dependent coagulation in hemophilia blood.;Butenas;Blood,2002
2. Inhibition of thrombin generation by the zymogen factor VII: implications for the treatment of hemophilia A by factor VIIa.;van ’t Veer;Blood,2000
3. High-dose factor VIIa increases initial thrombin generation and mediates faster platelet activation in thrombocytopenia-like conditions in a cell-based model system.;Kjalke;Br J Haematol,2001
4. Further understanding of recombinant activated factor VII mode of action.;Monroe;Semin Hematol,2008
5. The glycoprotein Ib-IX-V complex contributes to tissue factor-independent thrombin generation by recombinant factor VIIa on the activated platelet surface.;Weeterings;Blood,2008
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