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Hepcidin regulation of ferroportin 1 expression in the liver and intestine of the rat
10.1152/ajpgi.00246.2003 · doi-reference
Expression of the iron transporter ferroportin in synaptic vesicles and the blood–brain barrier
10.1016/j.brainres.2003.10.066 · doi-reference
Hephaestin, a ceruloplasmin homologue implicated in intestinal iron transport, is defective in the sla mouse
10.1038/5979 · doi-reference
10.1074/jbc.m312807200
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Transferrin receptor 2: a new molecule in iron metabolism
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Combinatorial mRNA regulation: iron regulatory proteins and iso-iron-responsive elements (Iso-IREs)
10.1074/jbc.r000019200 · doi-reference
Expression of the two mRNA isoforms of the iron transporter Nrmap2/DMTI in mice and function of the iron responsive element
10.1042/0264-6021:3630449 · doi-reference
Human NRAMP2/DMT1, which mediates iron transport across endosomal membranes, is localized to late endosomes and lysosomes in HEp-2 cells
10.1074/jbc.m001478200 · doi-reference
Subcellular localization of ferritin and iron taken up by rat hepatocytes
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Effects of iron regulatory protein regulation on iron homeostasis during hypoxia
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Hereditary hemochromatosis
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Characterization of the active site iron in tyrosine hydroxylase. Redox states of the iron
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Targeted drug delivery via the transferrin receptor-mediated endocytosis pathway
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Rethinking the role of ceruloplasmin in brain iron metabolism
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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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Nitric oxide and oxidative stress (H2O2) control mammalian iron metabolism by different pathways
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Ceruloplasmin regulates iron levels in the CNS and prevents free radical injury
10.1523/jneurosci.22-15-06578.2002 · doi-reference
Alternative RNA splicing generates a glycosylphosphatidylinositol-anchored form of ceruloplasmin in mammalian brain
10.1074/jbc.275.6.4305 · doi-reference
A novel glycosylphosphatidylinositol-anchored form of ceruloplasmin is expressed by mammalian astrocytes
10.1074/jbc.272.32.20185 · doi-reference
Association of the transferrin receptor in human placenta with HFE, the protein defective in hereditary hemochromatosis
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The possible significance of the ferrous oxidase activity of ceruloplasmin in normal human serum
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Mobilization of iron from endocytic vesicles. The effects of acidification and reduction
10.1016/s0021-9258(19)39205-1 · doi-reference
Severe iron deficiency anemia in transgenic mice expressing liver hepcidin
10.1073/pnas.072632499 · doi-reference
Lack of hepcidin gene expression and severe tissue iron overload in upstream stimulatory factor 2 (USF2) knockout mice
10.1073/pnas.151179498 · doi-reference
Mechanisms and regulation of intestinal iron absorption
10.1006/bcmd.2002.0578 · doi-reference
Aceruloplasminemia, an iron metabolic disorder
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An iron-regulated ferric reductase associated with the absorption of dietary iron
10.1126/science.1057206 · doi-reference
Increasing striatal iron content associated with normal ageing
10.1002/mds.870130214 · doi-reference
A human mitochondrial ferritin encoded by an intronless gene
10.1074/jbc.c100141200 · doi-reference
Effect of altered thyroid hormone status on rat brain ferritin H and ferritin L mRNA during postnatal development
10.1016/s0165-3806(99)00163-7 · doi-reference
Hepcidin, the recently identified peptide that appears to regulate iron absorption
10.1093/jn/134.1.1 · doi-reference
10.1182/blood-2003-03-0953
10.1182/blood-2003-03-0953 · doi-reference
Expression of the ceruloplasmin gene in the human retina and brain: implications for a pathogenic model in aceruloplasminemia
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Binding of apotransferrin to K562 cells: explanation of the transferrin cycle
10.1073/pnas.80.8.2263 · doi-reference
