Literature DB >> 19630770

Mouse models of von Willebrand disease.

R Pendu1, O D Christophe, C V Denis.   

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.

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Year:  2009        PMID: 19630770     DOI: 10.1111/j.1538-7836.2009.03411.x

Source DB:  PubMed          Journal:  J Thromb Haemost        ISSN: 1538-7836            Impact factor:   5.824


  5 in total

1.  Von Willebrand factor is reversibly decreased during torpor in 13-lined ground squirrels.

Authors:  Scott Cooper; Shawn Sell; Luke Nelson; Jennifer Hawes; Jacob A Benrud; Bridget M Kohlnhofer; Bradley R Burmeister; Veronica H Flood
Journal:  J Comp Physiol B       Date:  2016-01       Impact factor: 2.200

2.  Vwf K1362A resulted in failure of protein synthesis in mice.

Authors:  Naomi Sanda; Nobuaki Suzuki; Atsuo Suzuki; Takeshi Kanematsu; Mayuko Kishimoto; Hidetoshi Hasuwa; Akira Takagi; Tetsuhito Kojima; Tadashi Matsushita; Shigeo Nakamura
Journal:  Int J Hematol       Date:  2018-02-01       Impact factor: 2.490

3.  Utility of a high VWF: FVIII ratio in preventing FVIII accumulation: a study in VWF-deficient mice.

Authors:  Elmar Raquet; Marcus Stockschlaeder; Jochen Mueller-Cohrs; Sabine Zollner; Ingo Pragst; Gerhard Dickneite
Journal:  Blood Coagul Fibrinolysis       Date:  2015-07       Impact factor: 1.276

4.  Von Willebrand Factor Abnormalities Studied in the Mouse Model: What We Learned about VWF Functions.

Authors:  Caterina Casari; Peter J Lenting; Olivier D Christophe; Cécile V Denis
Journal:  Mediterr J Hematol Infect Dis       Date:  2013-07-10       Impact factor: 2.576

Review 5.  Von Willebrand Disease: From In Vivo to In Vitro Disease Models.

Authors:  Suzan de Boer; Jeroen Eikenboom
Journal:  Hemasphere       Date:  2019-09-27
  5 in total

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