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To assess whether these trends reflected coordinated biochemical changes rather than isolated metabolite fluctuations, we performed pathway-level analysis comparing shunt responders and non-responders ( Figure 2C )

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Therefore, mitochondrial morphology, the amount of mitochondrial DNA(mtDNA) expression, and the efficiency of adenosine-triphosphate(ATP) synthesis in GCs all influence oocyte developmental potential to some extent (91)

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