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Expression and analysis of a split premature termination codon in FGG responsible for congenital afibrinogenemia: escape from RNA surveillance mechanisms in transfected cells.
Neerman-Arbez M, Germanos-Haddad M, Tzanidakis K, Vu D, Deutsch S, David A, Morris MA, de Moerloose P. Neerman-Arbez M, et al. Blood. 2004 Dec 1;104(12):3618-23. doi: 10.1182/blood-2004-06-2312. Epub 2004 Jul 29. Blood. 2004. PMID: 15284111
Hypofibrinogenaemia caused by a novel FGG missense mutation (W253C) in the gamma chain globular domain impairing fibrinogen secretion.
Vu D, de Moerloose P, Batorova A, Lazur J, Palumbo L, Neerman-Arbez M. Vu D, et al. J Med Genet. 2005 Sep;42(9):e57. doi: 10.1136/jmg.2005.033530. J Med Genet. 2005. PMID: 16141000 Free PMC article.
In vitro rescue of FGA deletion by lentiviral transduction of an afibrinogenemic patient's hepatocytes.
Stroka D, Keogh A, Vu D, Fort A, Stoffel MH, Kühni-Boghenbor K, Furer C, Banz V, Demarmels Biasiutti F, Lämmle B, Candinas D, Neerman-Arbez M. Stroka D, et al. J Thromb Haemost. 2014 Nov;12(11):1874-9. doi: 10.1111/jth.12714. Epub 2014 Oct 1. J Thromb Haemost. 2014. PMID: 25163824
Transcription regulator LMO4 interferes with neuritogenesis in human SH-SY5Y neuroblastoma cells.
Vu D, Marin P, Walzer C, Cathieni MM, Bianchi EN, Saïdji F, Leuba G, Bouras C, Savioz A. Vu D, et al. Brain Res Mol Brain Res. 2003 Jul 23;115(2):93-103. doi: 10.1016/s0169-328x(03)00119-0. Brain Res Mol Brain Res. 2003. PMID: 12877980
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