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Through molecular docking and molecular dynamics simulations, the binding modes of these natural tyrosinase inhibitors with human tyrosinase (hTYR) and mushroom tyrosinase (mTYR) were systematically explored

Both the TBI + saline and TBI + ALCAR groups showed similar escape latency as Sham + NS and Sham + ALCAR groups

This product contains aluminum that may be toxic

The site of administration and the presence or absence of a vasoconstrictor agent are factors that contribute to drug absorption

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