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Sections were mounted with Canada Balsam and imaged using a Leica SP8 confocal microscope

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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

This dual anti-inflammatory and anti-angiogenic action helps to diminish inflammation-associated angiogenesis [86]

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