Immunohistochemistry of the Hfe Protein in Patients with Hereditary Hemochromatosis, Iron Deficiency Anemia, and Normal Controls

This publication has 16 references indexed in Scilit:

• Transferrin receptor is negatively modulated by the hemochromatosis protein HFE: Implications for cellular iron homeostasis
  Proceedings of the National Academy of Sciences, 1999
• Hemochromatosis in Ireland and HFE
  Blood Cells, Molecules, and Diseases, 1998
• Hereditary hemochromatosis: Effects of C282Y and H63D mutations on association with β ₂ -microglobulin, intracellular processing, and cell surface expression of the HFE protein in COS-7 cells
  Proceedings of the National Academy of Sciences, 1997
• The Significance of the 187G (H63D) Mutation in Hemochromatosis
  American Journal of Human Genetics, 1997
• Immunohistochemistry of HLA-H, the protein defective in patients with hereditary hemochromatosis, reveals unique pattern of expression in gastrointestinal tract
  Proceedings of the National Academy of Sciences, 1997
• Haemochromatosis and HLA–H
  Nature Genetics, 1996
• Haemochromatosis and HLA–H
  Nature Genetics, 1996
• Mutation Analysis in Hereditary Hemochromatosis
  Blood Cells, Molecules, and Diseases, 1996
• A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosis
  Nature Genetics, 1996
• Hemochromatosis: The genetic disorder of the twenty–first century
  Nature Medicine, 1996