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Blood|October 1, 1989
Molecular characterization of human factor XSan AntonioS V Reddy, Z Q Zhou, K J Rao, et al.Biochemistry|May 16, 1998
Structure/function analyses of recombinant variants of human factor Xa: factor Xa incorporation into prothrombinase on the thrombin-activated platelet surface is not mimicked by synthetic phospholipid vesiclesP J Larson, R M Camire, D Wong, et al.Human Gene Therapy|March 1, 1994
Efficient transfection of primary cells in a canine hemophilia B model using adenovirus-polylysine-DNA complexesJ N Lozier, A R Thompson, P C Hu, et al.Blood|February 3, 1998
Human factor IX corrects the bleeding diathesis of mice with hemophilia BS H Kung, J N Hagstrom, D Cass, et al.Proceedings of the National Academy of Sciences of the United States of America|May 27, 1997
Stable gene transfer and expression of human blood coagulation factor IX after intramuscular injection of recombinant adeno-associated virusR W Herzog, J N Hagstrom, S H Kung, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|September 8, 2001
Risk and prevention of anti-factor IX formation in AAV-mediated gene transfer in the context of a large deletion of F9P A Fields, V R Arruda, E Armstrong, et al.Blood|May 1, 1989
Functional consequences of an arginine180 to glutamine mutation in factor IX HiloD M Monroe, D M McCord, M N Huang, et al.Gene Therapy|July 13, 2012
Prevalence and pharmacological modulation of humoral immunity to AAV vectors in gene transfer to synovial tissueF Mingozzi, Y Chen, S C Edmonson, et al.Blood|March 1, 1990
Factor IX New London: substitution of proline for glutamine at position 50 causes severe hemophilia BJ N Lozier, D M Monroe, S Stanfield-Oakley, et al.Journal of Thrombosis and Haemostasis : JTH|September 12, 2006
A novel missense mutation responsible for factor VII deficiency in research Beagle coloniesM B Callan, M N Aljamali, P Margaritis, et al.Pageof 7