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2000
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1992
The Pathogenesis of Cardiomyopathy in Friedreich Ataxia
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1991 Nature
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2000
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Recombinant human hepcidin expressed in Escherichia coli isolates as an iron containing protein
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Relationship between TNF‐α and iron metabolism in differentiating human monocytic THP‐1 cells
2000
The Role of the L-Chain in Ferritin Iron Incorporation
1994
Overexpression of the hereditary hemochromatosis protein, HFE, in HeLa cells induces an iron‐deficient phenotype
1999
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2002
Oxidative stress and cell death in cells expressing L-ferritin variants causing neuroferritinopathy
2009
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2010
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Flow cytometry evaluation of erythroid dysplasia in patients with myelodysplastic syndrome
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Ferroxidase kinetics of human liver apoferritin, recombinant H-chain apoferritin, and site-directed mutants
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Identification of the ferroxidase centre in ferritin
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Neuroferritinopathy: From ferritin structure modification to pathogenetic mechanism
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Defining metal ion inhibitor interactions with recombinant human H- and L-chain ferritins and site-directed variants: an isothermal titration calorimetry study
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Influence of site-directed modifications on the formation of iron cores in ferritin
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The dentate nucleus in Friedreich’s ataxia: the role of iron-responsive proteins
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Functional roles of the ferritin receptors of human liver, hepatoma, lymphoid and erythroid cells
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Microelectronic DNA chip for hereditary hyperferritinemia cataract syndrome, a model for large-scale analysis of disorders of iron metabolism
2006
Structure, function, and evolution of ferritins
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Ferritin, iron homeostasis, and oxidative damage1,2 1Guest Editor: Mario Comporti 2This article is part of a series of reviews on “Iron and Cellular Redox Status.” The full list of papers may be found on the homepage of the journal.
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Expression and structural and functional properties of human ferritin L-chain from Escherichia coli
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The role of iron in mitochondrial function
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A Human Mitochondrial Ferritin Encoded by an Intronless Gene
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Early Embryonic Lethality of H Ferritin Gene Deletion in Mice
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Reconstitution of manganese oxide cores in horse spleen and recombinant ferritins
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Binding and suppressive activity of human recombinant ferritins on erythroid cells
1992
Crystal Structure and Biochemical Properties of the Human Mitochondrial Ferritin and its Mutant Ser144Ala
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Unique Iron Binding and Oxidation Properties of Human Mitochondrial Ferritin: A Comparative Analysis with Human H-chain Ferritin
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Iron detoxifying activity of ferritin
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Genetic hyperferritinaemia and reticuloendothelial iron overload associated with a three base pair deletion in the coding region of the ferroportin gene (SLC11A3)
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Ferritins in malignant and non‐malignant lymphoid cells
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Immunochemical characterization of human liver and heart ferritins with monoclonal antibodies
1986
Construction of a ferroxidase center in human ferritin L-chain.
1994
Effects of modifications near the 2-, 3- and 4-fold symmetry axes on human ferritin renaturation
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Iron incorporation into ferritins: evidence for the transfer of monomeric Fe(III) between ferritin molecules and for the formation of an unusual mineral in the ferritin of Escherichia coli
1994
Defective targeting of hemojuvelin to plasma membrane is a common pathogenetic mechanism in juvenile hemochromatosis
2007
Evidence of H- and L-chains have co-operative roles in the iron-uptake mechanism of human ferritin
1992
Production and characterization of recombinant heteropolymers of human ferritin H and L chains
1993
Analysis of the biologic functions of H- and L-ferritins in HeLa cells by transfection with siRNAs and cDNAs: evidence for a proliferative role of L-ferritin
2003
Mitochondrial ferritin expression in erythroid cells from patients with sideroblastic anemia
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Multiple Pathways for Mineral Core Formation in Mammalian Apoferritin. The Role of Hydrogen Peroxide
2003
Response of Monocyte Iron Regulatory Protein Activity to Inflammation: Abnormal Behavior in Genetic Hemochromatosis
1998
Evidence that residues exposed on the three-fold channels have active roles in the mechanism of ferritin iron incorporation
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Mutated recombinant human heavy-chain ferritins and myelosuppression in vitro and in vivo: a link between ferritin ferroxidase activity and biological function.
1991
Evidence that the specificity of iron incorporation into homopolymers of human ferritin L- and H-chains is conferred by the nucleation and ferroxidase centres
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Human L-ferritin deficiency is characterized by idiopathic generalized seizures and atypical restless leg syndrome
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Suppressive effects in vivo of purified recombinant human H-subunit (acidic) ferritin on murine myelopoiesis
1989
A new mutation (G51C) in the iron‐responsive element (IRE) of l ‐ferritin associated with hyperferritinaemia–cataract syndrome decreases the binding affinity of the mutated IRE for iron‐regulatory proteins
2000
Mechanism of ferritin iron uptake: activity of the H-chain and deletion mapping of the ferro-oxidase site. A study of iron uptake and ferro-oxidase activity of human liver, recombinant H-chain ferritins, and of two H-chain deletion mutants.
1988
Mutational analysis of the channel and loop sequences of human ferritin H-chain
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Specific binding sites for H-ferritin on human lymphocytes: modulation during cellular proliferation and potential implication in cell growth control
1991
Analysis of Ferritins in Lymphoblastoid Cell Lines and in the Lens of Subjects With Hereditary Hyperferritinemia-Cataract Syndrome
1998
Multiple mechanisms of iron-induced ferritin synthesis in HeLa cells
1985
Double-Gradient Denaturing Gradient Gel Electrophoresis Assay for Identification of L-Ferritin Iron-responsive Element Mutations Responsible for Hereditary Hyperferritinemia-Cataract Syndrome: Identification of the New Mutation C14G
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Evidence that a salt bridge in the light chain contributes to the physical stability difference between heavy and light human ferritins.
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Characterization of human ferritin H chain synthetized in Escherichia coli
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The human counterpart of zebrafish shiraz shows sideroblastic-like microcytic anemia and iron overload
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Characteristics of ferritins in human milk secretions: Similarities to serum and tissue isoferritins
1986
Identification of two novel mutations in the 5'-untranslated region of H-ferritin using denaturing high performance liquid chromatography scanning.
2003
Mitochondrial Ferritin Expression in Adult Mouse Tissues
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Characteristics and expression of binding sites specific for ferritin H- chain on human cell lines
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Properties of ferritin from the earthworm Octolasium complanatum
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Human serum ferritin G-peptide is recognized by anti-L ferritin subunit antibodies and concanavalin-A
1987
RNA silencing of the mitochondrial ABCB7 transporter in HeLa cells causes an iron-deficient phenotype with mitochondrial iron overload
2006