Overexpression of hemochromatosis protein, HFE, alters transferrin recycling process in human hepatoma cells
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology
Reference26 articles.
1. A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis;Feder;Nat. Genet.,1996
2. HFE gene knockout produces mouse model of hereditary hemochromatosis;Zhou;Proc. Natl. Acad. Sci. USA,1998
3. The hemochromatosis founder mutation in HLA-H disrupts β2-microglobulin interaction and cell surface expression;Feder;J. Biol. Chem.,1997
4. Hereditary hemochromatosis: effects of C282Y and H63D mutations on association with β2-microglobulin, intracellular processing, and cell surface expression of the HFE protein in COS-7 cells;Waheed;Proc. Natl. Acad. Sci. USA,1997
5. Association of the transferrin receptor in human placenta with HFE, the protein defective in hereditary hemochromatosis;Parkkila;Proc. Natl. Acad. Sci. USA,1997
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