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Consistent with their important roles in maintaining health, mutations in ATP7A and ATP7B cause inherited disorders of Cu metabolism, which have been recognized as Menkes disease (MD) and Wilsons disease (WD), respectively

[DOI] [PMC free article] [PubMed] [Google Scholar] [32].Thomas G, Skrinska VA, Lucas FV

Specifically, germ-free mouse models or FMT can be adopted to confirm a causal chain that iron overload mediates a reduction of gut Lactobacillus , which in turn aggravates the development of OA

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Barrett thinks people that live to be 100 are genetically blessed from an insulin resistance standpoint as well