Marguerite Neerman-Arbez Selected Research

Afibrinogenemia (Fibrinogen Deficiency)

06/2007	Mutations in the fibrinogen gene cluster accounting for congenital afibrinogenemia: an update and report of 10 novel mutations.
02/2006	[Congenital afibrinogenemia: focusing on molecular mechanisms controlling fibrinogen secretion]
11/2005	Quality control of fibrinogen secretion in the molecular pathogenesis of congenital afibrinogenemia.
12/2004	Expression and analysis of a split premature termination codon in FGG responsible for congenital afibrinogenemia: escape from RNA surveillance mechanisms in transfected cells.
12/2003	Congenital afibrinogenemia: identification and expression of a missense mutation in FGB impairing fibrinogen secretion.
05/2003	Prenatal diagnosis for congenital afibrinogenemia caused by a novel nonsense mutation in the FGB gene in a Palestinian family.
03/2003	Outcome of donor splice site mutations accounting for congenital afibrinogenemia reflects order of intron removal in the fibrinogen alpha gene (FGA).

7	Afibrinogenemia (Fibrinogen Deficiency) 06/2007 - 03/2003
2	Hemophilia A (Haemophilia) 02/2008 - 05/2006
1	Thrombosis (Thrombus) 10/2008
1	Fibrosis (Cirrhosis) 07/2006

7	Fibrinogen (Factor I)IBA 10/2008 - 03/2003
2	Factor V (Coagulation Factor V)IBA 02/2008 - 05/2006
2	Nonsense Codon (Nonsense Mutation)IBA 12/2004 - 05/2003
1	fibrinopeptides gammaIBA 10/2008
1	RNA (Ribonucleic Acid)IBA 12/2004