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The bioactive natural product T1 , bis(4-hydroxybenzyl)sulfide, with the most striking inhibitory potency against tyrosinase, was chosen as the target compound to characterize its biological effects in tyrosinase inhibition, cell viability, in vitro and in vivo melanin biosynthesis and acute oral toxicity in mice

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Cadmium-induced hematological, renal, and hepatic toxicity: the amelioration by: spirulina platensis

Anemia from A to zinc: Hypocupremia in the setting of gastric bypass and zinc excess