Publications by authors named "Marylise Hebert"

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A new mutation in the AFP gene responsible for a total absence of alpha feto-protein on second trimester maternal serum screening for Down syndrome.
François M Petit, Marylise Hébert, Olivier Picone, Sophie Brisset, Marie-Laure Maurin

Eur J Hum Genet· March 2009

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Rho-ROCK-dependent ezrin-radixin-moesin phosphorylation regulates Fas-mediated apoptosis in Jurkat cells.
Marylise Hébert, Sophie Potin, Michaël Sebbagh, Jacques Bertoglio, Jacqueline Bréard

J Immunol· November 2008

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Large deletion in UGT1A1 gene encompassing the promoter and the exon 1 responsible for Crigler-Najjar type I syndrome.
François M Petit, Marylise Hébert, Vincent Gajdos, Liliane Capel, Ridha M'Rad

Haematologica· October 2008

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Gene polymorphisms of oxidative stress enzymes: prediction of elderly renutrition.
Emmanuelle E Fabre, Agathe Raynaud-Simon, Jean-Louis Golmard, Marylise Hebert, Xavier Dulcire

Am J Clin Nutr· May 2008

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Comments on seven novel mutations of the UGT1A1 gene in patients with unconjugated hyperbilirubinemia by D'Apolito et al.
François M Petit, Marylise Hébert, Vincent Gajdos, Alix Mollet-Boudjemline, Philippe Labrune

Haematologica· July 2007

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