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9. [Hereditary hemochromatosis--new developments after discovery of the HFE gene]. Erhardt A, Niederau C, Osman Y, Häussinger D. Z Gastroenterol; 1999 Dec; 37(12):1179-85. PubMed ID: 10666843 [Abstract] [Full Text] [Related]
10. Mutations of the HFE gene among Turkish hereditary hemochromatosis patients. Simsek H, Balaban YH, Yilmaz E, Sumer H, Buyukasik Y, Cengiz C, Ozcebe O, Hascelik G, Tatar G. Ann Hematol; 2005 Oct; 84(10):646-9. PubMed ID: 15871018 [Abstract] [Full Text] [Related]
13. HFE gene knockout produces mouse model of hereditary hemochromatosis. Zhou XY, Tomatsu S, Fleming RE, Parkkila S, Waheed A, Jiang J, Fei Y, Brunt EM, Ruddy DA, Prass CE, Schatzman RC, O'Neill R, Britton RS, Bacon BR, Sly WS. Proc Natl Acad Sci U S A; 1998 Mar 03; 95(5):2492-7. PubMed ID: 9482913 [Abstract] [Full Text] [Related]
14. Association of the transferrin receptor in human placenta with HFE, the protein defective in hereditary hemochromatosis. Parkkila S, Waheed A, Britton RS, Bacon BR, Zhou XY, Tomatsu S, Fleming RE, Sly WS. Proc Natl Acad Sci U S A; 1997 Nov 25; 94(24):13198-202. PubMed ID: 9371823 [Abstract] [Full Text] [Related]
15. Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis. de Tayrac M, Roth MP, Jouanolle AM, Coppin H, le Gac G, Piperno A, Férec C, Pelucchi S, Scotet V, Bardou-Jacquet E, Ropert M, Bouvet R, Génin E, Mosser J, Deugnier Y. J Hepatol; 2015 Mar 25; 62(3):664-72. PubMed ID: 25457201 [Abstract] [Full Text] [Related]
16. Increased capacity of lymphocytes from hereditary hemochromatosis patients homozygous for the C282Y HFE mutation to respond to the genotoxic effect of diepoxybutane. Porto B, Vieira R, Porto G. Mutat Res; 2009 Feb 19; 673(1):37-42. PubMed ID: 19146986 [Abstract] [Full Text] [Related]
19. Hepatic iron overload: direct HFE (HLA-H) mutation analysis vs quantitative iron assays for the diagnosis of hereditary hemochromatosis. Press RD, Flora K, Gross C, Rabkin JM, Corless CL. Am J Clin Pathol; 1998 May 19; 109(5):577-84. PubMed ID: 9576576 [Abstract] [Full Text] [Related]