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Importantly, despite the enhanced formation of hydrogen peroxide in the dismutation reaction, LPO is very limited

345,346 FOXO4-DRI, a cell-permeable peptide, disrupted the FOXO4-p53 interaction, thereby reducing senescence-induced FOXO4 activity and selectively targeting SnCs for p53-dependent apoptosis (Table 1)

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Hyperglycaemia-induced OS is crucial for diabetes development and progression, leading to the exploration of antioxidative strategies []