Skoczeń N, et al. (2018) Molecular basis of diseases caused by the mtDNA mutation m.8969G>A in the subunit a of ATP synthase. Biochim Biophys Acta Bioenerg 1859(8):602-611 PMID:29778688
de Taffin de Tilques M, et al. (2018) Decreasing cytosolic translation is beneficial to yeast and human Tafazzin-deficient cells. Microb Cell 5(5):220-232 PMID:29796387
de Taffin de Tilques M, et al. (2017) Overexpression of mitochondrial oxodicarboxylate carrier (ODC1) preserves oxidative phosphorylation in a yeast model of Barth syndrome. Dis Model Mech 10(4):439-450 PMID:28188263
Lasserre JP, et al. (2015) Yeast as a system for modeling mitochondrial disease mechanisms and discovering therapies. Dis Model Mech 8(6):509-26 PMID:26035862
Kabala AM, et al. (2014) Defining the impact on yeast ATP synthase of two pathogenic human mitochondrial DNA mutations, T9185C and T9191C. Biochimie 100:200-6 PMID:24316278
Lasserre JP, et al. (2013) Biochemical, cellular and molecular identification of DNA polymerase α in yeast mitochondria. Biochimie 95(4):759-71 PMID:23160073
Ostojić J, et al. (2013) The energetic state of mitochondria modulates complex III biogenesis through the ATP-dependent activity of Bcs1. Cell Metab 18(4):567-77 PMID:24055101
Lucas P, et al. (2004) Absence of accessory subunit in the DNA polymerase gamma purified from yeast mitochondria. Mitochondrion 4(1):13-20 PMID:16120369