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Adults receiving an SGLT2 inhibitor also had a lower risk for an adverse safety outcome than the GLP-1 receptor agonist group (HR = 0.91

The fact that nrc2 , a mutant affected in GSH2, also exhibited greater sensitivity in its response to AITC confirmed that the root length phenotype was due to the impairment in the glutathione biosynthetic pathway, irrespective of whether GSH1 or GSH2 carried the mutation