Conversely, mutations in genes involved in methionine metabolism, dysregulated methionine metabolism, and abnormal hydrogen-sulfide and glutathione levels have all been implicated in neurodegenerative disease and in aging more generally (Paul, 2021
Over time, repeated exposure can impair cognitive function, slow metabolism, and heighten inflammation
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To address copper-dependent toxicity in WD in human liver cells, we reanalysed the RNA sequencing data (GSE107323) [2], validated gene expression signatures and functionally addressed our findings in the HepG2 ATP7B knockout (ATP7B-KO) model [7]
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