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10.1016/j.freeradbiomed.2019.08.002 74 ZhangY.ZhangC.ShuJ.GuoJ.ChangH.LeungP

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Consistent with the effects seen in rat PSCs, high glucose and TGF1 enhanced the proliferation and decreased the apoptosis of hPSCs under low glucose conditions, whereas GSH and SB431542 prevented these effects in the presence of high glucose (Fig

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However, our study demonstrates the efficacy of hCiPSC-NSCs, we recognize that donor sex may influence iPSC reprogramming and differentiation due to potential X chromosome erosion

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