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Moreover, quercetin and its metabolites have been shown in vitro to exert weak to moderate inhibitory effects on key drug-metabolizing enzymes, including cytochrome P450 isoforms CYP3A4 and CYP2C19, as well as several major drug transporters (Mohos et al., 2020)
This makes the fragment a useful reference in studies designed to isolate lipolytic endpoints from GH-axis side effects
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The result does not identify the source or diagnose cardiovascular disease