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Mutations in genes encoding other components of the PDHc, including the PDHB gene and the DLAT gene, have been shown to be associated with PDH deficiency syndromes
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(I, J) Mitochondrial membrane potential levels in parental and EGR1 knockdown MCF-7 and BT-474 cells treated with or without ferroptosis inducer erastin were detected by TMRE assay
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