Neerman-Arbez M - Search Results

1

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.

2

Activation of multiple cryptic donor splice sites by the common congenital afibrinogenemia mutation, FGA IVS4 + 1 G-->T.

Attanasio C, de Moerloose P, Antonarakis SE, Morris MA, Neerman-Arbez M. Attanasio C, et al. Blood. 2001 Mar 15;97(6):1879-81. doi: 10.1182/blood.v97.6.1879. Blood. 2001. PMID: 11238133 Free article.

3

Outcome of donor splice site mutations accounting for congenital afibrinogenemia reflects order of intron removal in the fibrinogen alpha gene (FGA).

Attanasio C, David A, Neerman-Arbez M. Attanasio C, et al. Blood. 2003 Mar 1;101(5):1851-6. doi: 10.1182/blood-2002-03-0853. Epub 2002 Oct 24. Blood. 2003. PMID: 12406899 Free article.

4

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.

5

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.

6

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.

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

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

9

[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.

10

Molecular basis of fibrinogen deficiency.

Neerman-Arbez M. Neerman-Arbez M. Pathophysiol Haemost Thromb. 2006;35(1-2):187-98. doi: 10.1159/000093566. Pathophysiol Haemost Thromb. 2006. PMID: 16855369 Review.

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