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Journal ArticleDOI

Disorders of iron metabolism.

Nancy C. Andrews
- 23 Dec 1999 - 
- Vol. 341, Iss: 26, pp 1986-1995
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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Citations
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Journal ArticleDOI

Relationship between Serum Ferritin Levels and Dyslipidemia in Korean Adolescents.

TL;DR: Serum ferritin levels were significantly associated with major dyslipidemia parameters, more prominently in boys than in girls, and this association represents a cardiometabolic risk factor.
Journal ArticleDOI

A Case–Control Study Examining the Effects of Active Versus Sedentary Lifestyles on Measures of Body Iron Burden and Oxidative Stress in Postmenopausal Women

TL;DR: It is suggested that aerobic forms of exercise may mitigate the risk of developing CVD in postmenopausal women by improving antioxidant capacity and decreasing body iron burden.
Journal ArticleDOI

A novel dehydroabietic acid-based fluorescent probe for detection of Fe3+ and Hg2+ ions and its application in live-cell imaging

TL;DR: In this article, a novel dehydroabietic acid-based fluorescent probe (DBH) containing 2,4-diarylbenzimidazole moiety was designed and synthesized, and the compound was characterized by its UV-Vis, FT-IR, 1H NMR, 13C NMR and ESI-MS spectra.
Journal ArticleDOI

Ceruloplasmin and hephaestin jointly protect the exocrine pancreas against oxidative damage by facilitating iron efflux.

TL;DR: Data indicate that HEPH and CP play mutually compensatory roles in facilitating iron efflux from the exocrine pancreas, and show that multicopper ferroxidases are able to protect the Pancreas against iron-induced oxidative damage.
References
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Journal Article

A novel MHC class-I-like gene is mutated in patients with hereditary haemochromatosis

John N. Feder
- 01 Jan 1996 - 
TL;DR: Using linkage–disequilibrium and full haplotype analysis, a region more than 3 megabases telomeric of the major histocompatibility complex (MHC) that is identical–by–descent in 85% of patient chromosomes is identified, containing a gene related to the MHC class I family, termed HLA–H, containing two missense alterations.
Journal ArticleDOI

Cloning and characterization of a mammalian proton-coupled metal-ion transporter

TL;DR: A new metal-ion transporter in the rat, DCT1, which has an unusually broad substrate range that includes Fe2+, Zn2+, Mn2+, Co2+, Cd2+, Cu2+, Ni2+ and Pb2+.
Journal ArticleDOI

Prevalence of Iron Deficiency in the United States

TL;DR: Iron deficiency and iron deficiency anemia are still relatively common in toddlers, adolescent girls, and women of childbearing age and were more likely in those who are minority, low income, and multiparous.
Journal ArticleDOI

Microcytic anaemia mice have a mutation in Nramp2, a candidate iron transporter gene.

TL;DR: A positional cloning strategy is undertaken to identify the causative mutation in mice with microcytic anaemia, and it is suggested that the phenotype is a consequence of a missense mutation in Nramp2 (ref. 5), a previously identified gene of unknown function.
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