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When chromatography and mass spectrometry are integrated, the chromatography system segregates metabolites into a gradient series of substances, subsequently analyzed and identified by the mass spectrometer
Glutathione- and cysteine-mediated cytotoxicity of allyl and benzyl isothiocyanate
Rogers JT
NRF2 can directly activate G6PD, PGD, TKT, and TALDO1 by binding to the well-conserved AREs in their promoters, thereby directing carbon flux towards the PPP [35]
