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This is in contrast to our earlier results in the absence of salicylamine (Figures 3d and e), suggesting that the ability to form -KA-DAT adducts is necessary for AA to impair DAT function

Furthermore, Dox inhibits ketone body metabolism by suppressing -hydroxybutyrate dehydrogenase and other ketolytic enzymes, diminishing the hearts ability to utilize -hydroxybutyrate as an alternative energy source

Epidemic history of hepatitis C virus genotypes and subtypes in Portugal

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