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Macrophage LRP1 contributes to the clearance of von Willebrand factor.
Rastegarlari G, Pegon JN, Casari C, Odouard S, Navarrete AM, Saint-Lu N, van Vlijmen BJ, Legendre P, Christophe OD, Denis CV, Lenting PJ. Rastegarlari G, et al. Blood. 2012 Mar 1;119(9):2126-34. doi: 10.1182/blood-2011-08-373605. Epub 2012 Jan 10. Blood. 2012. PMID: 22234691 Free article.
ADAMTS-13: double trouble for von Willebrand factor.
Lenting PJ, Rastegarlari G. Lenting PJ, et al. J Thromb Haemost. 2010 Dec;8(12):2775-7. doi: 10.1111/j.1538-7836.2010.04124.x. J Thromb Haemost. 2010. PMID: 21188794 Free article. No abstract available.
A novel alanine or threonine 789 to proline mutation causing type 2N von Willebrand's disease when inherited homozygously or heterozygously with arginine 854 to glutamine mutation.
Enayat MS, Guilliatt AM, Short PE, Rastegar-Lari G, Jazebi M, Ravonbod S, Ala F, Chapman OG, Hill FG. Enayat MS, et al. Among authors: rastegar lari g. Haemophilia. 2010 Nov;16(6):966-9. doi: 10.1111/j.1365-2516.2010.02271.x. Haemophilia. 2010. PMID: 20491956 No abstract available.
11 results