HFE gene: Structure, function, mutations, and associated iron abnormalities
Top Cited Papers
- 1 December 2015
- Vol. 574 (2), 179-192
- https://doi.org/10.1016/j.gene.2015.10.009
Abstract
No abstract availableKeywords
Funding Information
- National Institutes of Health (GM089820)
This publication has 214 references indexed in Scilit:
- Uroporphyria in the Cyp1a2−/− mouseBlood Cells, Molecules, and Diseases, 2011
- Molecular mechanisms of hepcidin regulation in sea bass (Dicentrarchus labrax)Fish & Shellfish Immunology, 2011
- The Transferrin Receptor Modulates Hfe-Dependent Regulation of Hepcidin ExpressionCell Metabolism, 2008
- The origin and spread of the HFE-C282Y haemochromatosis mutationHuman Genetics, 2004
- Constitutive hepcidin expression prevents iron overload in a mouse model of hemochromatosisNature Genetics, 2003
- HFE S65C Variant Is Not Associated with Increased Transferrin Saturation in Voluntary Blood DonorsBlood Cells, Molecules, and Diseases, 1999
- The hemochromatosis protein HFE competes with transferrin for binding to the transferrin receptor 1 1Edited by I. A. WilsonJournal of Molecular Biology, 1999
- The Transferrin Receptor Binding Site on HFE, the Class I MHC-related Protein Mutated in Hereditary HemochromatosisJournal of Molecular Biology, 1999
- Cloning, sequencing and characterization of the rat hereditary hemochromatosis promoter: comparison of the human, mouse and rat HFE promoter regionsGene, 1998
- Genetic mapping of the hemochromatosis locus on chromosome sixHuman Immunology, 1980