Mouse models of von Willebrand disease

11Citations
Citations of this article
37Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

von Willebrand disease (VWD), caused by quantitative or qualitative abnormalities in von Willebrand factor (VWF) is considered the most common inherited bleeding disorder in humans. Mild and severe quantitative defects in VWF cause VWD types 1 and 3 respectively, whereas qualitative abnormalities induce VWD type 2. VWD has also been diagnosed in a number of animal species such as dogs, pigs, cats and horses, as a result of naturally occurring mutations. More recently, murine models have drawn a great deal of attention. Their small size along with their well-defined genetic background makes them ideal tools to study the in vivo function of VWF. The most commonly used model is the VWF-deficient mouse engineered through homologous recombination. However, models resulting from changes in modifier genes indirectly affecting VWF have also been described. These various models have proven very useful in elucidating some aspects of VWF biology not easily addressed through in vitro approaches. © 2009 International Society on Thrombosis and Haemostasis.

Cite

CITATION STYLE

APA

Pendu, R., Christophe, O. D., & Denis, C. V. (2009). Mouse models of von Willebrand disease. Journal of Thrombosis and Haemostasis. https://doi.org/10.1111/j.1538-7836.2009.03411.x

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free