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3. Severe respiratory complex III defect prevents liver adaptation to prolonged fasting

4. iPSC-derived neural progenitors carrying a MT-ATP6 mutation exhibit mitochondrial hyperpolarization and calcium-related defects

5. Tissue- and Cell-Specific Mitochondrial Defect in Parkin-Deficient Mice

6. Effect of Lon protease knockdown on mitochondrial function in HeLa cells

7. Defective mitochondrial fusion, altered respiratory function, and distorted cristae structure in skin fibroblasts with heterozygous OPA1 mutations

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