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Blood|June 1, 1997
Genomic sequence and transcription start site for the human gamma-glutamyl carboxylaseS M Wu, D W Stafford, L D Frazier, et al.Journal of Thrombosis and Haemostasis : JTH|November 27, 2007
A viable mouse model of factor X deficiency provides evidence for maternal transfer of factor XS J Tai, R W Herzog, P Margaritis, et al.The Journal of Biological Chemistry|February 16, 1996
Structural integrity of the gamma-carboxyglutamic acid domain of human blood coagulation factor IXa Is required for its binding to cofactor VIIIaP J Larson, S A Stanfield-Oakley, W J VanDusen, et al.Gene Therapy|April 21, 2001
Intravenous administration of an E1/E3-deleted adenoviral vector induces tolerance to factor IX in C57BL/6 miceP A Fields, E Armstrong, J N Hagstrom, et al.Blood|June 15, 1994
Severe factor VII deficiency caused by mutations abolishing the cleavage site for activation and altering binding to tissue factorS Chaing, B Clarke, S Sridhara, et al.Blood|February 7, 2001
Improved muscle-derived expression of human coagulation factor IX from a skeletal actin/CMV hybrid enhancer/promoterJ N Hagstrom, L B Couto, C Scallan, et al.The Journal of Biological Chemistry|July 15, 1990
Molecular defect (Gla+14----Lys) and its functional consequences in a hereditary factor X deficiency (factor X "Vorarlberg")H H Watzke, K Lechner, H R Roberts, et al.Journal of Thrombosis and Haemostasis : JTH|May 25, 2010
Generation of a novel factor IX with augmented clotting activities in vitro and in vivoC N Lin, C Y Kao, C H Miao, et al.Gene Therapy|December 4, 2009
High AAV vector purity results in serotype- and tissue-independent enhancement of transduction efficiencyE Ayuso, F Mingozzi, J Montane, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|July 1, 2010
Prevention of spontaneous bleeding in dogs with haemophilia A and haemophilia BT C Nichols, R A Raymer, H W G Franck, et al.Pageof 7