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In its acetylated form this residue is associated with active transcription (Wang et al., 2008)
5-oxoprolinase deficiency due to OPLAH gene mutation on chromosome 8q24.3 is a benign biochemical disorder of the gamma-glutamyl cycle that is transmitted as an autosomal recessive trait (04
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The findings of the aforementioned studies suggest that exploring the link between the MAPK signaling pathway and ferroptosis may reveal intervention targets for ferroptosis-related diseases
