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Haematologica|March 13, 2025
Regulation of immune responses to therapeutic factor VIII by transplacental delivery of Fc-fused immunodominant factor VIII domains or peptidesAlejandra Reyes-Ruiz, Sandrine Delignat, Aurélien Azam, et al.Nature Communications|April 20, 2026
Disruption of the SAGA CORE triggers collateral degradation of KAT2APaul Batty, Hannah Beneder, Caroline Schätz, et al.British Journal of Haematology|February 16, 2017
Treatment burden, haemostatic strategies and real world inhibitor screening practice in non-severe haemophilia APaul Batty, Steve K Austin, Kate Khair, et al.Nature Reviews. Disease Primers|July 25, 2024
von Willebrand diseaseOmid Seidizadeh, Jeroen C J Eikenboom, Cécile V Denis, et al.Biomaterials|September 25, 2010
Hierarchical scaffold design for mesenchymal stem cell-based gene therapy of hemophilia BDaniel L Coutu, Jessica Cuerquis, Rouwayda El Ayoubi, et al.Thrombosis and Haemostasis|February 9, 2011
Frequency of platelet type versus type 2B von Willebrand disease. An international registry-based studyAlexander Hamilton, Margareth Ozelo, Jayne Leggo, et al.Blood|July 28, 2019
Genetic determinants of VWF clearance and FVIII binding modify FVIII pharmacokinetics in pediatric hemophilia A patientsLaura L Swystun, Kenichi Ogiwara, Orla Rawley, et al.Molecular Cell|August 17, 2023
Cohesin mediates DNA loop extrusion and sister chromatid cohesion by distinct mechanismsKota Nagasaka, Iain F Davidson, Roman R Stocsits, et al.Blood|October 31, 2002
Therapeutic factor VIII levels and negligible toxicity in mouse and dog models of hemophilia A following gene therapy with high-capacity adenoviral vectorsMarinee K L Chuah, Gudrun Schiedner, Lieven Thorrez, et al.Journal of Thrombosis and Haemostasis : JTH|April 25, 2022
von Willebrand factor propeptide variants lead to impaired storage and ER retention in patient-derived endothelial colony-forming cellsMackenzie Bowman, Lara Casey, Soundarya N Selvam, et al.Pageof 19