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Journal of Thrombosis and Haemostasis : JTH|August 1, 2007
Restoring hemostatic thrombin generation at the time of cutaneous wounding does not normalize healing in hemophilia BA McDonald, M Hoffman, U Hedner, et al.
Thrombosis and Haemostasis|August 31, 1977
Treatment of anti-factor VIII antibodiesP M Blatt, G C White, C W McMillan, et al.
Thrombosis Research|August 1, 1982
Measurement of human factor IXa activity in an isolated factor X activation systemM J Griffith, H M Reisner, R L Lundblad, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1983
Identification of the molecular defect in factor IX Chapel Hill: substitution of histidine for arginine at position 145C M Noyes, M J Griffith, H R Roberts, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|July 2, 1999
Tissue factor de-encryption: ionophore treatment induces changes in tissue factor activity by phosphatidylserine-dependent and -independent mechanismsA S Wolberg, D M Monroe, H R Roberts, et al.
Transfusion Science|May 7, 1998
Mammalian recombinant coagulation proteins: structure and functionG C White, E M Pickens, D K Liles, et al.
American Journal of Hematology|July 1, 1993
Comparison of the behavior of normal factor IX and the factor IX Bm variant Hilo in the prothrombin time test using tissue factors from bovine, human, and rabbit sourcesJ B Lefkowitz, D M Monroe, C K Kasper, et al.
Transfusion|September 1, 1979
Antithrombin III in fresh frozen plasma, cryoprecipitate, and cryoprecipitate-depleted plasmaP D Mintz, P M Blatt, W J Kuhns, et al.
The Journal of Laboratory and Clinical Medicine|March 1, 1986
Granulocyte lysosomal cationic protein alters fibrin assembly: a possible mechanism for granulocyte control of clot structureM E Carr, D A Gabriel, J C Herion, et al.
Biochemistry|February 18, 1992
The endothelial cell binding determinant of human factor IX resides in the gamma-carboxyglutamic acid domainJ R Toomey, K J Smith, H R Roberts, et al.
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