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doi: 10.1016/j.bbrc.2019.02.005 143 LernerNAvissarSBeit-YannaiE

ATP-sensitive potassium gain-of-function mutations and mutations in the mitochondrial asparaginyl-tRNA synthetase 2 gene can manifest as developmental delay, epilepsy, and neonatal diabetes syndrome (87, 88)

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They are designed entirely for different classifications of substances

elucidated that sulforaphane restored the downregulation of SLC7A11/GSH, suppressed ferroptosis, and improved cardiac function by activating the AMPK/Nrf2 pathway in the myocardium of type 2 diabetic mice [48]

For example, aromatic rings, the alkyl group and the amino group [3]