Publication | Open Access

Identification of mitochondrial dysfunction in Hutchinson–Gilford progeria syndrome through use of stable isotope labeling with amino acids in cell culture

Mitochondrial DiseaseAmino AcidsMitochondrial FunctionBiochemistryMitochondrial DysfunctionMitochondrial DynamicMitochondrial DynamicsMitochondrial BiologyMitochondrial BioenergeticsMetabolismMedicineCell BiologyStable IsotopeOxidative Stress