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Hereditary hemochromatosis disrupts uric acid homeostasis and causes hyperuricemia via altered expression/activity of xanthine oxidase and ABCG2
Hereditary hemochromatosis (HH) is mostly caused by mutations in the iron-regulatory gene HFE. The disease is associated with iron overload, resulting in liver cirrhosis/cancer, cardiomegaly, kidney dysfunction, diabetes, and arthritis. Fe(2+)-induced oxidative damage is suspected in the etiology of...
Uloženo v:
| Vydáno v: | Biochem J |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Portland Press Ltd.
2020
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7200644/ https://ncbi.nlm.nih.gov/pubmed/32239172 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/BCJ20190873 |
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