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Haemophilia : the Official Journal of the World Federation of Hemophilia|January 3, 2001
Low factor VIII recovery in haemophilia A patients without inhibitor titre is not due to the presence of anti-factor VIII antibodies undetectable by the Bethesda assayW Mondorf, J Klinge, N L Luban, et al.Journal of Chromatography. A|September 10, 1999
Use of surface plasmon resonance for studies of protein-protein and protein-phospholipid membrane interactions. Application to the binding of factor VIII to von Willebrand factor and to phosphatidylserine-containing membranesE Saenko, A Sarafanov, N Greco, et al.Journal of Chromatography. A|July 20, 2001
Comparison of the properties of phospholipid surfaces formed on HPA and L1 biosensor chips for the binding of the coagulation factor VIIIE Saenko, A Sarafanov, N Ananyeva, et al.Thrombosis Research|April 27, 2001
Molecular modifications in factor VIII concentrates produced from different plasma poolsE Saenko, D Josic, M Stadler, et al.Blood|May 29, 2000
Antibodies to the FVIII light chain that neutralize FVIII procoagulant activity are present in plasma of nonresponder patients with severe hemophilia A and in normal polyclonal human IgGA Moreau, S Lacroix-Desmazes, N Stieltjes, et al.Blood|September 1, 1995
Some factor VIII inhibitor antibodies recognize a common epitope corresponding to C2 domain amino acids 2248 through 2312, which overlap a phospholipid-binding siteD Scandella, G E Gilbert, M Shima, et al.Pageof 1