Ferroportin disease: A systematic meta-analysis of clinical and molecular findings
Open Access
- 19 July 2010
- journal article
- research article
- Published by Elsevier in Journal of Hepatology
- Vol. 53 (5), 941-949
- https://doi.org/10.1016/j.jhep.2010.05.016
Abstract
No abstract availableKeywords
This publication has 76 references indexed in Scilit:
- Human mutation D157G in ferroportin leads to hepcidin-independent binding of Jak2 and ferroportin down-regulationBlood, 2010
- ER Stress Controls Iron Metabolism Through Induction of HepcidinScience, 2009
- The molecular basis of hepcidin-resistant hereditary hemochromatosisBlood, 2009
- Hereditary hemochromatosis due to resistance to hepcidin: high hepcidin concentrations in a family with C326S ferroportin mutationBlood, 2009
- Identification and in silico analysis of 14 novel GJB1, MPZ and PMP22 gene mutationsEuropean Journal of Human Genetics, 2009
- Investigation of the Biophysical and Cell Biological Properties of Ferroportin, a Multipass Integral Membrane Protein Iron ExporterJournal of Molecular Biology, 2009
- Clinical, pathological, and molecular correlates in ferroportin disease: A study of two novel mutationsJournal of Hepatology, 2008
- RETRACTED: The Hepcidin-Binding Site on Ferroportin Is Evolutionarily ConservedCell Metabolism, 2008
- A Systematic Genetic Assessment of 1,433 Sequence Variants of Unknown Clinical Significance in the BRCA1 and BRCA2 Breast Cancer–Predisposition GenesAmerican Journal of Human Genetics, 2007
- Disease progression and liver cancer in the ferroportin diseaseGut, 2007