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1f,m), together with the recent advances in targeting GO or LDHA for the treatment of primary hyperoxaluria 52,53 , we utilized our recently developed salicylic acid derivative, MDMG-935P (Fig

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Independent of induction via Keap1 modification, a recently identified compound, Ab38, as well as resveratrol were shown to decrease extracellular matrix deposition and lower oxidative stress in a high-fat/STZinduced model of DN