C. Pigeon, G. Ilyin, B. Courselaud, P. Leroyer, B. Turlin et al., A New Mouse Liver-specific Gene, Encoding a Protein Homologous to Human Antimicrobial Peptide Hepcidin, Is Overexpressed during Iron Overload, Journal of Biological Chemistry, vol.276, issue.11, pp.7811-7820, 2001.
DOI : 10.1074/jbc.M008923200

T. Ganz, Hepcidin, a urinary antimicrobial peptide synthesized in the liver, J Biol Chem, vol.276, pp.7806-7816, 2001.

G. Nicolas, M. Bennoun, I. Devaux, C. Beaumont, B. Grandchamp et al., Lack of hepcidin gene expression and severe tissue iron overload in upstream stimulatory factor 2 (USF2) knockout mice, Proceedings of the National Academy of Sciences, vol.98, issue.15, pp.8780-8785, 2001.
DOI : 10.1073/pnas.151179498
URL : https://hal.archives-ouvertes.fr/inserm-00331349

E. Nemeth, M. Tuttle, J. Powelson, M. Vaughn, A. Donovan et al., Hepcidin Regulates Cellular Iron Efflux by Binding to Ferroportin and Inducing Its Internalization, Science, vol.306, issue.5704, pp.2090-2093, 2004.
DOI : 10.1126/science.1104742

D. Domenico, I. Ward, D. Langelier, C. Vaughn, M. Nemeth et al., The Molecular Mechanism of Hepcidin-mediated Ferroportin Down-Regulation, Molecular Biology of the Cell, vol.18, issue.7, pp.2569-78, 2007.
DOI : 10.1091/mbc.E07-01-0060

P. Brissot, M. Troadec, E. Bardou-jacquet, C. Lan, A. Jouanolle et al., Current approach to hemochromatosis, Blood Reviews, vol.22, issue.4, pp.195-210, 2008.
DOI : 10.1016/j.blre.2008.03.001

S. Gehrke, H. Kulaksiz, T. Herrmann, H. Riedel, K. Bents et al., Expression of hepcidin in hereditary hemochromatosis: evidence for a regulation in response to the serum transferrin saturation and to non-transferrin-bound iron, Blood, vol.102, issue.1, pp.371-377, 2003.
DOI : 10.1182/blood-2002-11-3610

K. Bridle, D. Frazer, S. Wilkins, J. Dixon, D. Purdie et al., Disrupted hepcidin regulation in HFE-associated haemochromatosis and the liver as a regulator of body iron homoeostasis, The Lancet, vol.361, issue.9358, pp.669-73, 2003.
DOI : 10.1016/S0140-6736(03)12602-5

A. Roetto and C. Camaschella, New insights into iron homeostasis through the study of non-HFE hereditary haemochromatosis, Best Practice & Research Clinical Haematology, vol.18, issue.2, pp.235-50, 2005.
DOI : 10.1016/j.beha.2004.09.004

A. Pietrangelo and . Non-hfe-hemochromatosis, Non-HFE hemochromatosis, Hepatology, vol.31, issue.1, pp.21-30, 2004.
DOI : 10.1002/hep.20007

A. Roetto, G. Papanikolaou, M. Politou, F. Alberti, D. Girelli et al., Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosis, Nature Genetics, vol.5, issue.1, pp.21-23, 2003.
DOI : 10.1182/blood-2002-04-1260

T. Matthes, P. Aguilar-martinez, L. Pizzi-bosman, R. Darbellay, L. Rubbia-brandt et al., Severe hemochromatosis in a Portuguese family associated with a new mutation in the 5'-UTR of the HAMP gene, Blood, vol.104, issue.7, pp.2181-2184, 2004.
DOI : 10.1182/blood-2004-01-0332

G. Porto, A. Roetto, F. Daraio, J. Pinto, S. Almeida et al., A Portuguese patient homozygous for the -25G>A mutation of the HAMP promoter shows evidence of steady-state transcription but fails to up-regulate hepcidin levels by iron, Blood, vol.106, issue.8, pp.2922-2925, 2005.
DOI : 10.1182/blood-2005-04-1630

A. Merryweather-clarke, E. Cadet, A. Bomford, D. Capron, V. Viprakasit et al., Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis, Human Molecular Genetics, vol.12, issue.17, pp.2241-2248, 2003.
DOI : 10.1093/hmg/ddg225

L. Gac, G. Scotet, V. Ka, C. Gourlaouen, I. Bryckaert et al., The recently identified type 2A juvenile haemochromatosis gene (HJV), a second candidate modifier of the C282Y homozygous phenotype, Human Molecular Genetics, vol.13, issue.17, pp.1913-1921, 2004.
DOI : 10.1093/hmg/ddh206

S. Jacolot, L. Gac, G. Scotet, V. Quere, I. Mura et al., HAMP as a modifier gene that increases the phenotypic expression of the HFE pC282Y homozygous genotype, Blood, vol.103, issue.7, pp.2835-2875, 2004.
DOI : 10.1182/blood-2003-10-3366

V. Falzacappa, M. Casanovas, G. Hentze, M. Muckenthaler, and M. , A bone morphogenetic protein (BMP)-responsive element in the hepcidin promoter controls HFE2-mediated hepatic hepcidin expression and its response to IL-6 in cultured cells, Journal of Molecular Medicine, vol.36, issue.5, pp.531-571, 2008.
DOI : 10.1007/s00109-008-0313-7

T. Ganz, G. Olbina, D. Girelli, E. Nemeth, and M. Westerman, Immunoassay for human serum hepcidin, Blood, vol.112, issue.10, pp.4292-4299, 2008.
DOI : 10.1182/blood-2008-02-139915

M. Therrien and J. Drouin, Cell-specific helix-loop-helix factor required for pituitary expression of the pro-opiomelanocortin gene., Molecular and Cellular Biology, vol.13, issue.4, pp.2342-53, 1993.
DOI : 10.1128/MCB.13.4.2342

J. Babitt, F. Huang, D. Wrighting, Y. Xia, Y. Sidis et al., Bone morphogenetic protein signaling by hemojuvelin regulates hepcidin expression, Nature Genetics, vol.259, issue.5, pp.531-540, 2006.
DOI : 10.1007/BF02100994

R. Wang, C. Li, X. Xu, Y. Zheng, C. Xiao et al., A role of SMAD4 in iron metabolism through the positive regulation of hepcidin expression, Cell Metabolism, vol.2, issue.6, pp.399-409, 2005.
DOI : 10.1016/j.cmet.2005.10.010

K. Kusanagi, H. Inoue, Y. Ishidou, H. Mishima, M. Kawabata et al., Characterization of a bone morphogenetic proteinresponsive Smad-binding element

K. Olsson, M. Vaisanen, J. Konar, and A. Bruce, The effect of withdrawal of food iron fortification in Sweden as studied with phlebotomy in subjects with genetic hemochromatosis, European Journal of Clinical Nutrition, vol.51, issue.11, pp.782-788, 1997.
DOI : 10.1038/sj.ejcn.1600488