The ferroportin disease
Author:
Affiliation:
1. Division of Internal Medicine 2 and Center for Hemochromatosis; University Hospital of Modena; Modena Italy
Publisher
Wiley
Subject
Hepatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/cld.340/fullpdf
Reference8 articles.
1. Hereditary hemochromatosis in adults without pathogenic mutations in the hemochromatosis gene [see comments];Pietrangelo;N Engl J Med,1999
2. Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLC11A3) gene;Montosi;J Clin Invest,2001
3. The ferroportin disease;Pietrangelo;Blood Cells Mol Dis,2004
4. A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis;Njajou;Nat Genet,2001
5. Non-HFE hepatic iron overload;Pietrangelo;Semin Liver Dis,2011
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1. A small molecule redistributes iron in ferroportin-deficient mice and patient-derived primary macrophages;Proceedings of the National Academy of Sciences;2022-06-22
2. Decreased ferroportin in hepatocytes promotes macrophages polarize towards an M2-like phenotype and liver fibrosis;Scientific Reports;2021-06-28
3. Biology of the iron efflux transporter, ferroportin;Advances in Protein Chemistry and Structural Biology;2021
4. Balance of cardiac and systemic hepcidin and its role in heart physiology and pathology;Laboratory Investigation;2017-10-23
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