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Journal Articles

Cryo-EM Structure of BIVV001 Reveals Coagulation Factor VIII-Von Willebrand Factor D'D3 Interaction Mode

James Fuller, PhD, Joseph Batchelor, PhD, Kevin Knockenhauer, PhD, Hans-Peter Biemann, PhD, Robert Peters
Journal: Blood
Blood (2019) 134 (Supplement_1): 94.
https://doi.org/10.1182/blood-2019-126645
Published: 2019
Journal Articles

The Ability of Von Willebrand Factor (VWF) to Bind Factor VIII (FVIII) Can Decrease during Pregnancy

Kerry W Lannert, Hilary S Gammill, MD, Barbara A. Konkle, MD, Jill M Johnsen, MD
Journal: Blood
Blood (2014) 124 (21): 4244.
https://doi.org/10.1182/blood.V124.21.4244.4244
Published: 2014
Journal Articles

Characterization of Type 2N Von Willebrand Disease Mutations Using Ιn Vitro and Ιn Vivo Mouse Models

Laura L Swystun, PhD, Ilinca Georgescu, Meghan Deforest, Mia Golder, PhD, Kate Sponagle, Christine Brown, Colleen Notley, David Lillicrap, MD
Journal: Blood
Blood (2014) 124 (21): 471.
https://doi.org/10.1182/blood.V124.21.471.471
Published: 2014
Journal Articles

Solution structure of the major factor VIII binding region on von Willebrand factor

Nuha Shiltagh, John Kirkpatrick, Lisa D. Cabrita, Tom A. J. McKinnon, Konstantinos Thalassinos, Edward G. D. Tuddenham, D. Flemming Hansen
Journal: Blood
Blood (2014) 123 (26): 4143–4151.
https://doi.org/10.1182/blood-2013-07-517086
Published: 2014
Includes: Supplemental data
Journal Articles

von Willebrand Factor-ADAMTS13 Interactions

X. Long Zheng, MD, PhD
Journal: Blood
Blood (2012) 120 (21): SCI-18.
https://doi.org/10.1182/blood.V120.21.SCI-18.SCI-18
Published: 2012
Journal Articles

Fourteen Percent of Healthy African Americans Participating In the Zimmerman Program for the Molecular and Clinical Biology of VWD (ZPMCB VWD) Are Heterozygous for the VWF Gene Mutation H817Q Associated with Type 2N Von Willebrand Disease

Kenneth D Friedman, MD, Daniel B. Bellissimo, PhD, Pamela A. Christopherson, Veronica H Flood, MD, Joan Cox Gill, MD, Robert R. Montgomery, MD, Sandra L Haberichter, PhD, Primary Clinical Center Directors
Journal: Blood
Blood (2010) 116 (21): 239.
https://doi.org/10.1182/blood.V116.21.239.239
Published: 2010
Journal Articles

Unbalanced X-chromosome inactivation with a novel FVIII gene mutation resulting in severe hemophilia A in a female

Brief Report
Rémi Favier, Jean-Maurice Lavergne, Jean-Marc Costa, Claudine Caron, Claudine Mazurier, Michèle Viémont, Marc Delpech, Sophie Valleix
Journal: Blood
Blood (2000) 96 (13): 4373–4375.
https://doi.org/10.1182/blood.V96.13.4373
Published: 2000
Journal Articles

A Patient With Type 2N von Willebrand Disease Is Heterozygous for a New Mutation: Gly22Glu. Demonstration of a Defective Expression of the Second Allele by the Use of Monoclonal Antibodies

J. Gu, S. Jorieux, J.M. Lavergne, C. Ruan, C. Mazurier, D. Meyer
Journal: Blood
Blood (1997) 89 (9): 3263–3269.
https://doi.org/10.1182/blood.V89.9.3263
Published: 1997