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From soluble uric acid to sodium urate crystal: immune metabolic inflammation driven by uric acid morphological transformation and mechanism-oriented therapy

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DP showed strong binding to various tyrosinase residues, reducing the mRNA expression of MITF, tyrosinase, and MC1R ( Additionally, a peptide T-6(FGFRSP), isolated from TFMH, was studied for its interaction with tyrosinase

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