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4. Metabolic switch from fatty acid oxidation to glycolysis in knock‐in mouse model of Barth syndrome

9. Interferon-driven brain phenotype in a mouse model of RNaseT2 deficient leukoencephalopathy

10. An in vitro system to silence mitochondrial gene expression

12. Global kinome profiling reveals DYRK1A as critical activator of the human mitochondrial import machinery

13. ALANET

16. COA6 Facilitates Cytochrome c Oxidase Biogenesis as Thiol-reductase for Copper Metallochaperones in Mitochondria

19. Defective Mitochondrial Cardiolipin Remodeling Dampens HIF-1α Expression in Hypoxia

20. Mutations of the mitochondrial carrier translocase channel subunit TIM22 cause early-onset mitochondrial myopathy

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