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3. Mild hemophilia A caused by increased rate of factor VIII A2 subunit dissociation: evidence for nonproteolytic inactivation of factor VIIIa in vivo. Pipe SW; Eickhorst AN; McKinley SH; Saenko EL; Kaufman RJ Blood; 1999 Jan; 93(1):176-83. PubMed ID: 9864159 [TBL] [Abstract][Full Text] [Related]
4. Slowed release of thrombin-cleaved factor VIII from von Willebrand factor by a monoclonal and a human antibody is a novel mechanism for factor VIII inhibition. Saenko EL; Shima M; Gilbert GE; Scandella D J Biol Chem; 1996 Nov; 271(44):27424-31. PubMed ID: 8910322 [TBL] [Abstract][Full Text] [Related]
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8. Thrombin-activated and factor Xa-activated human factor VIII: differences in cofactor activity and decay rate. Neuenschwander PF; Jesty J Arch Biochem Biophys; 1992 Aug; 296(2):426-34. PubMed ID: 1632634 [TBL] [Abstract][Full Text] [Related]
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10. Structural and functional characterization of platelet receptor-mediated factor VIII binding. Ahmad SS; Scandura JM; Walsh PN J Biol Chem; 2000 Apr; 275(17):13071-81. PubMed ID: 10777612 [TBL] [Abstract][Full Text] [Related]
11. Activation of factor VIII by thrombin increases its affinity for binding to synthetic phospholipid membranes and activated platelets. Saenko EL; Scandella D; Yakhyaev AV; Greco NJ J Biol Chem; 1998 Oct; 273(43):27918-26. PubMed ID: 9774404 [TBL] [Abstract][Full Text] [Related]
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17. Differential proteolytic activation of factor VIII-von Willebrand factor complex by thrombin. Hill-Eubanks DC; Parker CG; Lollar P Proc Natl Acad Sci U S A; 1989 Sep; 86(17):6508-12. PubMed ID: 2505252 [TBL] [Abstract][Full Text] [Related]
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