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MAGT1 deficiency in XMEN disease is associated with severe platelet dysfunction and impaired platelet glycoprotein N-glycosylation.
Kauskot A, Mallebranche C, Bruneel A, Fenaille F, Solarz J, Viellard T, Feng M, Repérant C, Bordet JC, Cholet S, Denis CV, McCluskey G, Latour S, Martin E, Pellier I, Lasne D, Borgel D, Kracker S, Ziegler A, Tuffigo M, Fournier B, Miot C, Adam F. Kauskot A, et al. Among authors: denis cv. J Thromb Haemost. 2023 Nov;21(11):3268-3278. doi: 10.1016/j.jtha.2023.05.007. Epub 2023 May 18. J Thromb Haemost. 2023. PMID: 37207862
Mouse models of von Willebrand disease.
Pendu R, Christophe OD, Denis CV. Pendu R, et al. Among authors: denis cv. J Thromb Haemost. 2009 Jul;7 Suppl 1:61-4. doi: 10.1111/j.1538-7836.2009.03411.x. J Thromb Haemost. 2009. PMID: 19630770 Free article. Review.
von Willebrand factor: the old, the new and the unknown.
Lenting PJ, Casari C, Christophe OD, Denis CV. Lenting PJ, et al. Among authors: denis cv. J Thromb Haemost. 2012 Dec;10(12):2428-37. doi: 10.1111/jth.12008. J Thromb Haemost. 2012. PMID: 23020315 Free article. Review.
Clearance of von Willebrand factor.
Casari C, Lenting PJ, Wohner N, Christophe OD, Denis CV. Casari C, et al. Among authors: denis cv. J Thromb Haemost. 2013 Jun;11 Suppl 1:202-11. doi: 10.1111/jth.12226. J Thromb Haemost. 2013. PMID: 23809124 Free article. Review.
LIM kinase/cofilin dysregulation promotes macrothrombocytopenia in severe von Willebrand disease-type 2B.
Kauskot A, Poirault-Chassac S, Adam F, Muczynski V, Aymé G, Casari C, Bordet JC, Soukaseum C, Rothschild C, Proulle V, Pietrzyk-Nivau A, Berrou E, Christophe OD, Rosa JP, Lenting PJ, Bryckaert M, Denis CV, Baruch D. Kauskot A, et al. Among authors: denis cv. JCI Insight. 2016 Oct 6;1(16):e88643. doi: 10.1172/jci.insight.88643. JCI Insight. 2016. PMID: 27734030 Free PMC article.
169 results