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The American Journal of Clinical Nutrition|February 4, 2012
Iron metabolism in patients with anorexia nervosa: elevated serum hepcidin concentrations in the absence of inflammationSolesne Papillard-Marechal, Marc Sznajder, Margarita Hurtado-Nedelec, et al.
Plos One|October 18, 2011
Iron insufficiency compromises motor neurons and their mitochondrial function in Irp2-null miceSuh Young Jeong, Daniel R Crooks, Hayden Wilson-Ollivierre, et al.
Haematologica|January 30, 2009
A new missense mutation in the L ferritin coding sequence associated with elevated levels of glycosylated ferritin in serum and absence of iron overloadCaroline Kannengiesser, Anne-Marie Jouanolle, Gilles Hetet, et al.
Gastroenterology|January 30, 2007
Genetic study of variation in normal mouse iron homeostasis reveals ceruloplasmin as an HFE-hemochromatosis modifier geneLaurent Gouya, Francoise Muzeau, Anne-Marie Robreau, et al.
Blood|September 28, 2006
Increased plasma transferrin, altered body iron distribution, and microcytic hypochromic anemia in ferrochelatase-deficient miceSaïd Lyoumi, Marie Abitbol, Valérie Andrieu, et al.
Human Mutation|May 15, 2012
Inactive matriptase-2 mutants found in IRIDA patients still repress hepcidin in a transfection assay despite having lost their serine protease activityFlavia Guillem, Caroline Kannengiesser, Claire Oudin, et al.
American Journal of Human Genetics|December 31, 2005
Contribution of a common single-nucleotide polymorphism to the genetic predisposition for erythropoietic protoporphyriaLaurent Gouya, Caroline Martin-Schmitt, Anne-Marie Robreau, et al.
The American Journal of Pathology|September 8, 2015
Serum pantetheinase/vanin levels regulate erythrocyte homeostasis and severity of malariaSamuel Rommelaere, Virginie Millet, Pascal Rihet, et al.
Cell|November 13, 2004
Ferritin heavy chain upregulation by NF-kappaB inhibits TNFalpha-induced apoptosis by suppressing reactive oxygen speciesCan G Pham, Concetta Bubici, Francesca Zazzeroni, et al.
Human Molecular Genetics|September 15, 2005
Mutations in human CPO gene predict clinical expression of either hepatic hereditary coproporphyria or erythropoietic harderoporphyriaCaroline Schmitt, Laurent Gouya, Eva Malonova, et al.
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