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918 Inhibition of FOXO3a or oxidative stress reverses iron overload-induced muscle atrophy by reactivating the AKT-FOXO3a pathway

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Future studies are also warranted to investigate the impact of AOX on LBR, MR, and SDF since only few well-designed studies have analyzed these outcomes in infertile patients following AOX therapy

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These properties have made it a focal point in peptide therapy research, especially for musculoskeletal injuries and acute injuries where rapid tissue regeneration is desired