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To exclude any effects associated with the procedure used for generation of a new monoclonal sub-clone, wild-type HepG2 cells were treated with varying concentrations of NFT or DEM for 24 h, fixed, and subjected to immunocytochemistry to visualize Nrf2 localization (Fig
With the increasing demand for wound healing management and frequent dressing changes, the development of biologically active and cost-effective wound dressings with high healing capacity is urgently required
2c and Supplementary Data 1)
Chi et al., S -thiolations in the pathogenic bacteria S
