Factor VIII inhibitors: von Willebrand factor makes a differencein vitroandin vivo
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1538-7836.2012.04902.x/fullpdf
Reference27 articles.
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2. Cell biology of von Willebrand factor;Wagner;Annu Rev Cell Biol,1990
3. Factor VIII binds to von Willebrand factor via its Mr-80 000 light chain;Hamer;Eur J Biochem,1987
4. Factor VIII: structure and function in blood clotting;Chavin;Am J Hematol,1984
5. How we choose factor VIII to treat hemophilia;Mannucci;Blood,2012
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1. Binding Promiscuity of Therapeutic Factor VIII;Thrombosis and Haemostasis;2024-07-01
2. Development of a rapid and fully automated factor VIII inhibitor assay, insensitive to emicizumab, and a lowest level of quantification of 0.2 BU/mL;Journal of Thrombosis and Haemostasis;2024-07
3. Hematopoietic Stem Cell-Based Platelet-Targeted Gene Therapy for Hemophilia;Comprehensive Hematology and Stem Cell Research;2024
4. Factor VIII antibody immune complexes modulate the humoral response to factor VIII in an epitope-dependent manner;Frontiers in Immunology;2023-08-31
5. Polyphosphate Activates von Willebrand Factor Interaction with Glycoprotein Ib in the Absence of Factor VIII In Vitro;International Journal of Molecular Sciences;2022-11-15
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