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Page 1
Hepcidin in iron metabolism.
Loréal O, Haziza-Pigeon C, Troadec MB, Detivaud L, Turlin B, Courselaud B, Ilyin G, Brissot P. Loréal O, et al. Among authors: detivaud l. Curr Protein Pept Sci. 2005 Jun;6(3):279-91. doi: 10.2174/1389203054065392. Curr Protein Pept Sci. 2005. PMID: 15974953 Review.
Anemia in beta-thalassemia patients targets hepatic hepcidin transcript levels independently of iron metabolism genes controlling hepcidin expression.
Camberlein E, Zanninelli G, Détivaud L, Lizzi AR, Sorrentino F, Vacquer S, Troadec MB, Angelucci E, Abgueguen E, Loréal O, Cianciulli P, Lai ME, Brissot P. Camberlein E, et al. Among authors: detivaud l. Haematologica. 2008 Jan;93(1):111-5. doi: 10.3324/haematol.11656. Haematologica. 2008. PMID: 18166793 Free article.
A novel N491S mutation in the human SLC11A2 gene impairs protein trafficking and in association with the G212V mutation leads to microcytic anemia and liver iron overload.
Bardou-Jacquet E, Island ML, Jouanolle AM, Détivaud L, Fatih N, Ropert M, Brissot E, Mosser A, Maisonneuve H, Brissot P, Loréal O. Bardou-Jacquet E, et al. Among authors: detivaud l. Blood Cells Mol Dis. 2011 Dec 15;47(4):243-8. doi: 10.1016/j.bcmd.2011.07.004. Epub 2011 Aug 26. Blood Cells Mol Dis. 2011. PMID: 21871825
[Normal iron metabolism].
Loréal O, Camberlein E, Troadec MB, Abgueguen E, Detivaud L, Lescoat G, Gaboriau F, Brissot P. Loréal O, et al. Among authors: detivaud l. Nephrol Ther. 2006 Nov;2 Suppl 5:S290-7. Nephrol Ther. 2006. PMID: 17373273 Review. French.
Hepatocyte iron loading capacity is associated with differentiation and repression of motility in the HepaRG cell line.
Troadec MB, Glaise D, Lamirault G, Le Cunff M, Guérin E, Le Meur N, Détivaud L, Zindy P, Leroyer P, Guisle I, Duval H, Gripon P, Théret N, Boudjema K, Guguen-Guillouzo C, Brissot P, Léger JJ, Loréal O. Troadec MB, et al. Among authors: detivaud l. Genomics. 2006 Jan;87(1):93-103. doi: 10.1016/j.ygeno.2005.08.016. Epub 2005 Dec 1. Genomics. 2006. PMID: 16325370 Free article.
Sex and acquired cofactors determine phenotypes of ferroportin disease.
Le Lan C, Mosser A, Ropert M, Detivaud L, Loustaud-Ratti V, Vital-Durand D, Roget L, Bardou-Jacquet E, Turlin B, David V, Loréal O, Deugnier Y, Brissot P, Jouanolle AM. Le Lan C, et al. Among authors: detivaud l. Gastroenterology. 2011 Apr;140(4):1199-1207.e1-2. doi: 10.1053/j.gastro.2010.12.049. Epub 2011 Jan 1. Gastroenterology. 2011. PMID: 21199650
Molecular diagnosis of genetic iron-overload disorders.
Brissot P, Bardou-Jacquet E, Troadec MB, Mosser A, Island ML, Detivaud L, Loréal O, Jouanolle AM. Brissot P, et al. Among authors: detivaud l. Expert Rev Mol Diagn. 2010 Sep;10(6):755-63. doi: 10.1586/erm.10.55. Expert Rev Mol Diagn. 2010. PMID: 20843199 Review.
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