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However, controlled human trials have not been published, making evidence quality substantially lower than for Semax or Selank

Perilipin-null mice also display a significant resistance to diet-induced obesity (78, 106, 127) that is explained, at least in part, by increased beta-oxidation of fatty acids, the products of lipolysis (106), following from a compensatory induction of genes involved in lipid and energy metabolism and a downregulation of genes involved in lipid biosynthesis (20)

Data availability statement No large datasets were generated or analyzed during this study

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