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Aberrant proteins exceeding the processing ability of mitochondrial chaperones are degraded into peptides by the matrix protease ClpP, transported to the IMS via heat shock factor-1, and then enter the nucleus through the action ATFS-1, thereafter stimulating the transcription of chaperone genes to prevent excessive aggregation of misfolded proteins (Fig

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Glutathione levels and sensitivity to apoptosis are regulated by changes in transaldolase expression

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