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Zamami Y, Niimura T, Kawashiri T, Goda M, Naito Y, Fukushima K, et al
Challenges include batch-to-batch variability, absence of standardized extraction protocols, and inconsistent concentrations of bioactive constituents, all of which complicate compliance with Good Manufacturing Practice (GMP) standards and hinder reproducibility in clinical trials
Keap1 is not the only negative regulator of Nrf2
The roles of mitochondrial damage-associated molecular patterns in diseases