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doi:10.3899/jrheum.120989
Int J Pharmacol 12(3):146153
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
doi: 10.1177/1352458516667568 65
