Maïlis Bietenhader

The pathogenic m.8993 T > G mutation in mitochondrial ATP6 gene prevents proton release from the subunit c-ring rotor of ATP synthase.

R. Kucharczyk, Nahia Ezkurdia, J. di Rago, 2021, Human molecular genetics.

Mitochondrial ATP synthase disorders: molecular mechanisms and the quest for curative therapeutic approaches.

R. Kucharczyk, E. Couplan, M. Blondel, 2009, Biochimica et biophysica acta.

Experimental Relocation of the Mitochondrial ATP9 Gene to the Nucleus Reveals Forces Underlying Mitochondrial Genome Evolution

L. Steinmetz, B. Salin, Raeka S. Aiyar, 2012, PLoS Genetics.

The Atypical Cadherin Fat Directly Regulates Mitochondrial Function and Metabolic State

Lacramioara Fabian, H. McNeill, A. Jurisicova, 2014, Cell.

A Yeast Model of the Neurogenic Ataxia Retinitis Pigmentosa (NARP) T8993G Mutation in the Mitochondrial ATP Synthase-6 Gene*

S. Duvezin-Caubet, Nahia Ezkurdia, J. di Rago, 2007, Journal of Biological Chemistry.

Two nuclear life cycle-regulated genes encode interchangeable subunits c of mitochondrial ATP synthase in Podospora anserina.

P. Golik, J. di Rago, V. Contamine, 2011, Molecular biology and evolution.