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Iron uptake from plasma transferrin by the duodenum is impaired in the Hfe knockout mouse.
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Regulation of transferrin-mediated iron uptake by HFE, the protein defective in hereditary hemochromatosis.
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Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLC11A3) gene.
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Lack of hepcidin gene expression and severe tissue iron overload in upstream stimulatory factor 2 (USF2) knockout mice.
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A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis.
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Expression of the duodenal iron transporters divalent-metal transporter 1 and ferroportin 1 in iron deficiency and iron overload.
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An iron-regulated ferric reductase associated with the absorption of dietary iron.
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A new mouse liver-specific gene, encoding a protein homologous to human antimicrobial peptide hepcidin, is overexpressed during iron overload.
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