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Biochemistry|August 25, 1999
Engineered recombinant factor VII Q217 variants with altered inhibitor specificitiesY J Chang, N Hamaguchi, S C Chang, et al.Biochemistry|September 12, 2001
The distinct roles that Gln-192 and Glu-217 of factor IX play in selectivity for macromolecular substrates and inhibitorsY C Hsu, N Hamaguchi, Y J Chang, et al.Blood|September 15, 1994
Characterization of a factor IX variant with a glycine207 to glutamic acid mutationS W Lin, C N Lin, N Hamaguchi, et al.Thrombosis and Haemostasis|November 1, 2000
Hemophilia B with mutations at glycine-48 of factor IX exhibited delayed activation by the factor VIIa-tissue factor complexP C Wu, N Hamaguchi, Y S Yu, et al.British Journal of Haematology|November 1, 1995
Genetic diagnosis of haemophilia A of Chinese originS R Lin, S C Chang, C C Lee, et al.Thrombosis and Haemostasis|October 1, 1991
Characterization of genetic defects of hemophilia B of Chinese originS W Lin, M C ShenThrombosis and Haemostasis|March 1, 1993
Genetic basis and carrier detection of hemophilia B of Chinese originS W Lin, M C ShenGenomics|December 1, 1993
Characterization of genetic defects of hemophilia A in patients of Chinese originS W Lin, S R Lin, M C ShenBlood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|November 18, 1998
The interaction of activated factor VII with tissue factor: insight into the mechanism of cofactor-mediated activation of activated factor VIIW RufBiochemistry|September 27, 1994
Factor VIIa residue Arg290 is required for efficient activation of the macromolecular substrate factor XW RufPageof 99