Neerman-Arbez M - Search Results

1

[Congenital afibrinogenemia: focusing on molecular mechanisms controlling fibrinogen secretion].

Vu D, Neerman-Arbez M. Vu D, et al. Med Sci (Paris). 2006 Feb;22(2):117-20. doi: 10.1051/medsci/2006222117. Med Sci (Paris). 2006. PMID: 16457748 Free article. French. No abstract available.

2

Congenital afibrinogenemia: identification and expression of a missense mutation in FGB impairing fibrinogen secretion.

Vu D, Bolton-Maggs PH, Parr JR, Morris MA, de Moerloose P, Neerman-Arbez M. Vu D, et al. Blood. 2003 Dec 15;102(13):4413-5. doi: 10.1182/blood-2003-06-2141. Epub 2003 Jul 31. Blood. 2003. PMID: 12893758 Free article.

3

Quality control of fibrinogen secretion in the molecular pathogenesis of congenital afibrinogenemia.

Vu D, Di Sanza C, Caille D, de Moerloose P, Scheib H, Meda P, Neerman-Arbez M. Vu D, et al. Hum Mol Genet. 2005 Nov 1;14(21):3271-80. doi: 10.1093/hmg/ddi360. Epub 2005 Sep 29. Hum Mol Genet. 2005. PMID: 16195396

4

Molecular mechanisms accounting for fibrinogen deficiency: from large deletions to intracellular retention of misfolded proteins.

Vu D, Neerman-Arbez M. Vu D, et al. J Thromb Haemost. 2007 Jul;5 Suppl 1:125-31. doi: 10.1111/j.1538-7836.2007.02465.x. J Thromb Haemost. 2007. PMID: 17635718 Free article. Review.

5

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 Free article.

6

Manipulating the quality control pathway in transfected cells: low temperature allows rescue of secretion-defective fibrinogen mutants.

Vu D, Di Sanza C, Neerman-Arbez M. Vu D, et al. Haematologica. 2008 Feb;93(2):224-31. doi: 10.3324/haematol.11868. Epub 2008 Jan 26. Haematologica. 2008. PMID: 18223281 Free article.

7

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.

8

Prenatal diagnosis for congenital afibrinogenemia caused by a novel nonsense mutation in the FGB gene in a Palestinian family.

Neerman-Arbez M, Vu D, Abu-Libdeh B, Bouchardy I, Morris MA. Neerman-Arbez M, et al. Blood. 2003 May 1;101(9):3492-4. doi: 10.1182/blood-2002-10-3116. Epub 2003 Jan 2. Blood. 2003. PMID: 12511408 Free article.

9

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 Free article.

10

Clinical Consequences and Molecular Bases of Low Fibrinogen Levels.

Neerman-Arbez M, Casini A. Neerman-Arbez M, et al. Int J Mol Sci. 2018 Jan 8;19(1):192. doi: 10.3390/ijms19010192. Int J Mol Sci. 2018. PMID: 29316703 Free PMC article. Review.

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