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Oxidative inactivation of redox sensitive cysteine residues in Keap1, specific phosphorylation of Nrf2, or increased expression of p62, which competes with Nrf2 for Keap 1 binding, disrupts the Keap1/Nrf2 interactions to foster the stabilization and nuclear translocation of Nrf2 where it promotes transcription of a variety of protective antioxidant genes via the antioxidant response element or ARE in their promoter regions

Binding of paracetamol metabolites to mouse liver glutathione S-transferases

Oct 8 2022;23(19)doi:10.3390/ijms231911952

The therapy, which will be manufactured and marketed by Eisai, is intended to slow functional decline in people with the disease

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