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Journal of Thrombosis and Haemostasis : JTH|February 4, 2009
Non-classical anti-factor VIII C2 domain antibodies are pathogenic in a murine in vivo bleeding modelS L Meeks, J F Healey, E T Parker, et al.Journal of Thrombosis and Haemostasis : JTH|December 22, 2006
The humoral response to human factor VIII in hemophilia A miceJ F Healey, E T Parker, R T Barrow, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|April 23, 2014
Lack of recombinant factor VIII B-domain induces phospholipid vesicle aggregation: implications for the immunogenicity of factor VIIIK Grushin, J Miller, D Dalm, et al.The Journal of Clinical Investigation|June 1, 1994
Inhibition of human factor VIIIa by anti-A2 subunit antibodiesP Lollar, E T Parker, J E Curtis, et al.Journal of Thrombosis and Haemostasis : JTH|July 8, 2018
Anti-C1 domain antibodies that accelerate factor VIII clearance contribute to antibody pathogenicity in a murine hemophilia A modelG Batsuli, J Ito, R Mercer, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|November 19, 2016
Anti-factor VIII antibodies in brothers with haemophilia A share similar characteristicsJ Kahle, A Orlowski, D Stichel, et al.Journal of Thrombosis and Haemostasis : JTH|November 21, 2015
Characterization of a genetically engineered mouse model of hemophilia A with complete deletion of the F8 geneB N Chao, W H Baldwin, J F Healey, et al.Pageof 2