Duodenal metal-transporter (DMT-1, NRAMP-2) expression in patients with hereditary haemochromatosis

This publication has 19 references indexed in Scilit:

• Crystal Structure of the Hemochromatosis Protein HFE and Characterization of Its Interaction with Transferrin Receptor
  Cell, 1998
• HFE gene knockout produces mouse model of hereditary hemochromatosis
  Proceedings of the National Academy of Sciences, 1998
• The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding
  Proceedings of the National Academy of Sciences, 1998
• Association of the transferrin receptor in human placenta with HFE, the protein defective in hereditary hemochromatosis
  Proceedings of the National Academy of Sciences, 1997
• Cloning and characterization of a mammalian proton-coupled metal-ion transporter
  Nature, 1997
• Haemochromatosis and HLA–H
  Nature Genetics, 1996
• Haemochromatosis and HLA–H
  Nature Genetics, 1996
• Defective iron homeostasis in beta 2-microglobulin knockout mice recapitulates hereditary hemochromatosis in man.
  The Journal of Experimental Medicine, 1996
• A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosis
  Nature Genetics, 1996
• beta2 knockout mice develop parenchymal iron overload: A putative role for class I genes of the major histocompatibility complex in iron metabolism.
  Proceedings of the National Academy of Sciences, 1996