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Under basal conditions, NRF2 is kept inactive through binding to its negative regulator KEAP1, which is a redox-regulated substrate adaptor for the Cullin (Cul)3-RING-box protein (Rbx)1 ubiquitin ligase complex that directs NRF2 for degradation [10]

2017a,b), as will be discussed in section 4

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Errors and near misses linked to i.v

To explore this possibility, we first assembled a large-scale resource of human blood metabolomics data
