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Blood|February 9, 2000
Prevention and treatment of factor VIII inhibitors in murine hemophilia AJ Qian, M Collins, A H Sharpe, et al.Thrombosis Research|March 8, 2000
A rapid method to visualize von willebrand factor multimers by using agarose gel electrophoresis, immunolocalization and luminographic detectionD R Krizek, M E RickThe New England Journal of Medicine|June 9, 1983
Danazol increases factor VIII and factor IX in classic hemophilia and Christmas diseaseH R Gralnick, M E RickBlood|January 1, 1988
Phospholipase abolishes the effect of stimulated platelets on the thrombin activation of factor VIIIM E Rick, D M KrizekAmerican Journal of Hematology|April 1, 1996
Identification of a His54Gln substitution in von Willebrand factor from a patient with defective binding of factor VIIIM E Rick, D M KrizekElectrophoresis|May 3, 2001
Clinical application of a rapid method using agarose gel electrophoresis and Western blotting to evaluate von Willebrand factor protease activityD M Kirzek, M E RickBlood|June 1, 1986
Platelets modulate the proteolysis of factor VIII:C protein by plasminM E Rick, D M KrizekThe Journal of Laboratory and Clinical Medicine|July 1, 1975
Determination of the von Willebrand's disease antigen (factor VIII-related antigen) in plasma by quantitative immunoelectrophoresisT S Zimmerman, L W Hoyer, L Dickson, et al.Biochemistry|December 30, 1986
Localization of binding sites within human von Willebrand factor for monomeric type III collagenG J Roth, K Titani, L W Hoyer, et al.Thrombosis and Haemostasis|June 1, 1992
A soluble recombinant factor VIII fragment containing the A2 domain binds to some human anti-factor VIII antibodies that are not detected by immunoblottingD Scandella, L Timmons, M Mattingly, et al.Pageof 12