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5. Alternative polyadenylation and nonsense-mediated decay coordinately regulate the human HFE mRNA levels. Martins R; Proença D; Silva B; Barbosa C; Silva AL; Faustino P; Romão L PLoS One; 2012; 7(4):e35461. PubMed ID: 22530027 [TBL] [Abstract][Full Text] [Related]
6. Iron overload in HFE C282Y heterozygotes at first genetic testing: a strategy for identifying rare HFE variants. Aguilar-Martinez P; Grandchamp B; Cunat S; Cadet E; Blanc F; Nourrit M; Lassoued K; Schved JF; Rochette J Haematologica; 2011 Apr; 96(4):507-14. PubMed ID: 21228038 [TBL] [Abstract][Full Text] [Related]
7. The Q283P amino-acid change in HFE leads to structural and functional consequences similar to those described for the mutated 282Y HFE protein. Ka C; Le Gac G; Dupradeau FY; Rochette J; Férec C Hum Genet; 2005 Sep; 117(5):467-75. PubMed ID: 15965644 [TBL] [Abstract][Full Text] [Related]
10. Duodenal mucosal reductase in wild-type and Hfe knockout mice on iron adequate, iron deficient, and iron rich feeding. Simpson RJ; Debnam E; Beaumont N; Bahram S; Schümann K; Srai SK Gut; 2003 Apr; 52(4):510-3. PubMed ID: 12631660 [TBL] [Abstract][Full Text] [Related]
11. Heterozygous recipient and donor HFE mutations associated with a hereditary haemochromatosis phenotype after liver transplantation. Wigg AJ; Harley H; Casey G Gut; 2003 Mar; 52(3):433-5. PubMed ID: 12584229 [TBL] [Abstract][Full Text] [Related]
12. Frequencies of the hereditary hemochromatosis allele in different populations. Comparison of previous phenotypic methods and novel genotypic methods. Milman N; Pedersen P; Steig Tá; Melsen GV Int J Hematol; 2003 Jan; 77(1):48-54. PubMed ID: 12568299 [TBL] [Abstract][Full Text] [Related]
13. Molecular pathogenesis of iron overload. Trinder D; Fox C; Vautier G; Olynyk JK Gut; 2002 Aug; 51(2):290-5. PubMed ID: 12117898 [TBL] [Abstract][Full Text] [Related]
14. Two novel nonsense mutations of HFE gene in five unrelated italian patients with hemochromatosis. Piperno A; Arosio C; Fossati L; Viganò M; Trombini P; Vergani A; Mancia G Gastroenterology; 2000 Aug; 119(2):441-5. PubMed ID: 10930379 [TBL] [Abstract][Full Text] [Related]
15. Prevalence of C282Y and E168X HFE mutations in an Italian population of Northern European ancestry. Salvioni A; Mariani R; Oberkanins C; Moritz A; Mauri V; Pelucchi S; Riva A; Arosio C; Cerutti P; Piperno A Haematologica; 2003 Mar; 88(3):250-5. PubMed ID: 12651261 [TBL] [Abstract][Full Text] [Related]
16. Transferrin receptor-2 gene and non-C282Y homozygous patients with hemochromatosis. Aguilar-Martinez P; Esculié-Coste C; Bismuth M; Giansily-Blaizot M; Larrey D; Schved JF Blood Cells Mol Dis; 2001; 27(1):290-3. PubMed ID: 11358390 [TBL] [Abstract][Full Text] [Related]
17. A novel mutation of HFE explains the classical phenotype of genetic hemochromatosis in a C282Y heterozygote. Wallace DF; Dooley JS; Walker AP Gastroenterology; 1999 Jun; 116(6):1409-12. PubMed ID: 10348824 [TBL] [Abstract][Full Text] [Related]
18. Abnormal regulation of HFE mRNA expression does not contribute to primary iron overload. Vercesi E; Cerani P; Rolandi V; Rovati A; Bergamaschi G Haematologica; 2000 Aug; 85(8):787-91. PubMed ID: 10942923 [TBL] [Abstract][Full Text] [Related]
19. Current status in identifying the haemochromatosis gene. Jazwinska EC J Gastroenterol Hepatol; 1996 Nov; 11(11):1041-3. PubMed ID: 8985827 [No Abstract] [Full Text] [Related]