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Journal ArticleDOI

Disorders of iron metabolism.

Nancy C. Andrews
- 23 Dec 1999 - 
- Vol. 341, Iss: 26, pp 1986-1995
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TLDR
Iron has the capacity to accept and donate electrons readily, interconverting between ferric (Fe2+) and ferrous (Fe3+) forms, which makes it a useful component of cytochromes, oxygen-binding molecules, and many enzymes.
Abstract
Iron has the capacity to accept and donate electrons readily, interconverting between ferric (Fe2+) and ferrous (Fe3+) forms. This capability makes it a useful component of cytochromes, oxygen-bind...

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Journal ArticleDOI

IL-6 mediates hypoferremia of inflammation by inducing the synthesis of the iron regulatory hormone hepcidin

TL;DR: These studies in human liver cell cultures, mice, and human volunteers indicate that IL-6 is the necessary and sufficient cytokine for the induction of hepcidin during inflammation and that the IL- 6-hepcid in axis is responsible for the hypoferremia of inflammation.
Journal ArticleDOI

Hepcidin, a key regulator of iron metabolism and mediator of anemia of inflammation.

TL;DR: Human hepcidin, a 25-amino acid peptide made by hepatocytes, may be a new mediator of innate immunity and the long-sought iron-regulatory hormone and its role in iron metabolism could lead to new therapies for hemochromatosis and anemia of inflammation.
Journal ArticleDOI

Targeted Drug Delivery via the Transferrin Receptor-Mediated Endocytosis Pathway

TL;DR: The OX26 monoclonal antibody against the rat transferrin receptor offers great promise in the delivery of therapeutic agents across the blood-brain barrier to the brain and serves as a potential alternative to viral vector for gene therapy.
Journal ArticleDOI

Hepcidin and iron homeostasis.

TL;DR: Hepcidin, ferroportin and their regulators represent potential targets for the diagnosis and treatment of iron disorders and anemias.
References
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Journal ArticleDOI

Juvenile Hemochromatosis Locus Maps to Chromosome 1q

TL;DR: The JH locus does not correspond to the chromosomal localization of any known gene involved in iron metabolism and provides a means to recognize patients in affected families and provide a starting point for the identification of the affected gene by positional cloning.
Journal ArticleDOI

Association of HFE protein with transferrin receptor in crypt enterocytes of human duodenum

TL;DR: It is proposed that the HFE protein modulates the uptake of transferrin-bound iron from plasma by crypt enterocyte and participates in the mechanism by which the crypt enterocytes sense the level of body iron stores.
Journal ArticleDOI

Reticulocyte Hemoglobin Content to Diagnose Iron Deficiency in Children

TL;DR: Reticulocyte Hb content level was the strongest predictor of iron deficiency and iron deficiency anemia in children and holds promise as an alternative to biochemical iron studies in diagnosis.
Journal ArticleDOI

Management of hemochromatosis

TL;DR: Although iron overload often develops in patients with hemochromatosis, the demonstration of hepatic or systemic iron overload and associated complications is not needed to confirm the diagnosis and the quantity of iron removed by therapeutic phlebotomy is a valuable retrospective indicator of the severity of iron overload.
Journal ArticleDOI

HFE Genotype in Patients with Hemochromatosis and Other Liver Diseases

TL;DR: The contribution of HFE genotyping to the diagnosis of hemochromatosis was evaluated and the prevalence of H FE mutations in a group of patients with liver disease was determined.
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