Disrupted hepcidin regulation in HFE -associated haemochromatosis and the liver as a regulator of body iron homoeostasis
Top Cited Papers
- 1 February 2003
- journal article
- Published by Elsevier in The Lancet
- Vol. 361 (9358) , 669-673
- https://doi.org/10.1016/s0140-6736(03)12602-5
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- Increased hepatic iron in mice lacking classical MHC class I moleculesBlood, 2002
- Inappropriate expression of hepcidin is associated with iron refractory anemia: implications for the anemia of chronic diseaseBlood, 2002
- Autosomal-dominant hemochrom-atosis is associated with a mutation in the ferroportin (SLC11A3) geneJournal of Clinical Investigation, 2001
- A New Mouse Liver-specific Gene, Encoding a Protein Homologous to Human Antimicrobial Peptide Hepcidin, Is Overexpressed during Iron OverloadJournal of Biological Chemistry, 2001
- Hepcidin, a Urinary Antimicrobial Peptide Synthesized in the LiverJournal of Biological Chemistry, 2001
- Mouse strain differences determine severity of iron accumulation in Hfe knockout model of hereditary hemochromatosisProceedings of the National Academy of Sciences, 2001
- A Novel Mammalian Iron-regulated Protein Involved in Intracellular Iron MetabolismJournal of Biological Chemistry, 2000
- Immunohistochemistry of HLA-H, the protein defective in patients with hereditary hemochromatosis, reveals unique pattern of expression in gastrointestinal tractProceedings of the National Academy of Sciences, 1997
- A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosisNature Genetics, 1996
- Genetic HemochromatosisSeminars in Liver Disease, 1984