Association of Transferrin Saturation With the Arthropathy of Hereditary Hemochromatosis

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چکیده

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منابع مشابه

Transferrin saturation and screening of genetic hemochromatosis.

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Hereditary hemochromatosis (HH) is a common autosomal recessive disease associated with loss of regulation of dietary iron absorption and excessive iron deposition in major organs of the body. Recently, a candidate gene for HH (also called HFE) was identified that encodes a novel MHC class I-like protein. Most patients with HH are homozygous for the same mutation in the HFE gene, resulting in a...

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Comparison of the interactions of transferrin receptor and transferrin receptor 2 with transferrin and the hereditary hemochromatosis protein HFE.

The transferrin receptor (TfR) interacts with two proteins important for iron metabolism, transferrin (Tf) and HFE, the protein mutated in hereditary hemochromatosis. A second receptor for Tf, TfR2, was recently identified and found to be functional for iron uptake in transfected cells (Kawabata, H., Germain, R. S., Vuong, P. T., Nakamaki, T., Said, J. W., and Koeffler, H. P. (2000) J. Biol. Ch...

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ژورنال

عنوان ژورنال: Clinical Gastroenterology and Hepatology

سال: 2017

ISSN: 1542-3565

DOI: 10.1016/j.cgh.2017.06.018