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Journal of Hepatology|October 27, 2023
Adeno-associated viruses for gene therapy - clinical implications and liver-related complications, a guide for hepatologistsMarcus Maximilian Mücke, Sylvia Fong, Graham R Foster, et al.Blood|September 3, 2016
Life in the shadow of a dominant partner: the FVIII-VWF association and its clinical implications for hemophilia ASteven W Pipe, Robert R Montgomery, Kathleen P Pratt, et al.Plos One|December 21, 2013
A novel cell-sheet technology that achieves durable factor VIII delivery in a mouse model of hemophilia AKohei Tatsumi, Mitsuhiko Sugimoto, David Lillicrap, et al.Thrombosis and Haemostasis|May 15, 2002
Aberrant splicing and premature termination of transcription of the FVIII gene as a cause of severe canine hemophilia A: similarities with the intron 22 inversion mutation in human hemophiliaChristine Hough, Seiki Kamisue, Cherie Cameron, et al.Blood|April 8, 2010
Mutation-specific hemostatic variability in mice expressing common type 2B von Willebrand disease substitutionsMia Golder, Cynthia M Pruss, Carol Hegadorn, et al.Blood|September 27, 2003
Helper-dependent adenoviral vectors mediate therapeutic factor VIII expression for several months with minimal accompanying toxicity in a canine model of severe hemophilia ABrian D Brown, Chang Xin Shi, Sandra Powell, et al.Blood|October 23, 2004
Cell type-specific regulation of von Willebrand factor expression by the E4BP4 transcriptional repressorChristine Hough, Carla D Cuthbert, Colleen Notley, et al.The Lancet. Haematology|November 5, 2025
Von Willebrand factor and von Willebrand disease in ageing: mechanisms, evolving phenotypes, and clinical implicationsOmid Seidizadeh, Ferdows Atiq, Nathan T Connell, et al.British Journal of Haematology|November 7, 2008
ADAMTS13 cleavage efficiency is altered by mutagenic and, to a lesser extent, polymorphic sequence changes in the A1 and A2 domains of von Willebrand factorCynthia M Pruss, Colleen R P Notley, Carol A Hegadorn, et al.Journal of Thrombosis and Haemostasis : JTH|June 21, 2021
Stabilin-2 deficiency increases thrombotic burden and alters the composition of venous thrombi in a mouse modelAlison Michels, Laura L Swystun, Courtney N Dwyer, et al.Pageof 19