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Nature Neuroscience 11, 251-253CrossRefGoogle ScholarPubMed 132Estvez, A.G., Spear, N., Manuel, S.M

This suggested that the increased activities of PEPCK and G6P could at least partly account for increased CYP2E1-mediated oxidation and sulfation in obese patients

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Mutations in genes encoding other components of the PDHc, including the PDHB gene and the DLAT gene, have been shown to be associated with PDH deficiency syndromes

It is worth emphasizing that RF-1 was isolated and purified by researchers, and the purity of this metabolite was not disclosed in this study

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