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Nutrients|February 13, 2026
Sex Disparities in the Processes Underlying Aging: Mitochondrial DNA Copy Number Associations with Dynapenia, 25-Hydroxyvitamin D<sub>3</sub> Levels and Quality of Life in Older AdultsZoraida Verde, Sara Martins, Isabel Erenas-Ondategui, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|August 2, 2024
Homozygosity for a Rare FASTKD2 Variant Resulting in an Adult Onset Autosomal Recessive Mitochondrial PodocytopathyFrancisco Pereira Gonçalves, Isabel Tavares, Roberto Silva, et al.
Experimental Neurology|January 19, 2010
Mitochondrial-dependent apoptosis in Huntington's disease human cybridsIldete L Ferreira, Maria V Nascimento, Márcio Ribeiro, et al.
Clinical Pharmacology and Therapeutics|August 4, 2019
Genomic Ancestry, CYP2D6, CYP2C9, and CYP2C19 Among Latin AmericansFernanda Rodrigues-Soares, Eva M Peñas-Lledó, Eduardo Tarazona-Santos, et al.
Neuromuscular Disorders : NMD|February 6, 2018
Disclosing the functional changes of two genetic alterations in a patient with Chronic Progressive External Ophthalmoplegia: Report of the novel mtDNA m.7486G>A variantMafalda Bacalhau, Marta Simões, Mariana C Rocha, et al.
Omics : a Journal of Integrative Biology|September 6, 2018
Interethnic Variability in CYP2D6, CYP2C9, and CYP2C19 Genes and Predicted Drug Metabolism Phenotypes Among 6060 Ibero- and Native Americans: RIBEF-CEIBA Consortium Report on Population PharmacogenomicsMaría-Eugenia G Naranjo, Fernanda Rodrigues-Soares, Eva M Peñas-Lledó, et al.
Mitochondrion|July 5, 2016
Secondary coenzyme Q10 deficiencies in oxidative phosphorylation (OXPHOS) and non-OXPHOS disordersDelia Yubero, Raquel Montero, Miguel A Martín, et al.
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