- TMEM70 protein - A novel ancillary factor of mammalian ATP synthase2009 | First Faculty of Medicine
- Mitochondrial membrane potential and ATP production in primary disorders of ATP synthase2004 | Publication without faculty affiliation
- Genetic Complementation of ATP Synthase Deficiency Due to Dysfunction of TMEM70 Assembly Factor in Rat2022 | First Faculty of Medicine, Faculty of Science
- Mitochondrial Membrane Potential and ATP Production in Primary Disorders of ATP Synthase2004 | First Faculty of Medicine
- Compensatory upregulation of respiratory chain complexes III and IV in isolated deficiency of ATP synthase due to TMEM70 mutation2012 | First Faculty of Medicine
- TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy2008 | First Faculty of Medicine
- Altered properties of mitochondrial ATP-synthase in patients with a T --> G mutation in the ATPase 6 (subunit a) gene at position 8993 of mtDNA1995 | First Faculty of Medicine
- Knockdown of human OXA1L impairs the biogenes of F(1)F(0)- ATP synthase and NADH2007 | First Faculty of Medicine
- Follow-up study of subunit c of mitochondrial ATP synthase (SCMAS) in Batten disease and in unrelated lysosomal disorders1997 | First Faculty of Medicine
- Mitochondrial diseases and genetic defects of ATP synthase2006 | First Faculty of Medicine
- Mitochondrial diseases and genetic defects of ATP synthase2006 | Faculty of Physical Education and Sport
- Deficiency of mitochondrial ATP synthase of nuclear genetic origin2006 | First Faculty of Medicine
- Deficiency of mitochondrial ATP synthase of nuclear genetic origin2006 | Faculty of Physical Education and Sport
- Isolated defects of mitochondrial ATP synthase : overview of 15 casesPublication without faculty affiliation
- Biochemical and molecular genetic consequences in patient with ATP synthase defect caused by mtDNA mutation 9205delTAPublication without faculty affiliation
- Isolated deficiency of mitochondrial ATP synthase caused by nuclear genetic defectsPublication without faculty affiliation
- Mitochondrial membrane potential and ATP production in primary disorders of ATP synthase2004 | First Faculty of Medicine, Faculty of Mathematics and Physics
- TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy2008 | Publication without faculty affiliation
- Diminished synthesis of subunit a (ATP6) and altered function of ATP synthase and cytochrome c oxidase due to the mtDNA 2bp microdeletion of TA at positions 9205 and 92062004 | First Faculty of Medicine
- Inherited disorders of mitochondrial ATP synthase2004 | First Faculty of Medicine
- Hereditary disorders of mitochondrial ATP synthase2004 | First Faculty of Medicine
- Hereditary disorders of mitochondrial ATP synthase2004 | Faculty of Physical Education and Sport
- Inherited disorders of mitochondrial ATP synthase2004 | Faculty of Physical Education and Sport
- The impact of mitochondrial tRNA mutations on the amount of ATP synthase differs in the brain compared to other tissues2008 | First Faculty of Medicine
- Knockout of Tmem70 alters biogenesis of ATP synthase and leads to embryonal lethality in mice2016 | First Faculty of Medicine, Faculty of Physical Education and Sport
- Two components in pathogenic mechanism of mitochondrial ATP synthase deficiency: energy deprivation and ROS productionPublication without faculty affiliation
- Variants in Mitochondrial ATP Synthase Cause Variable Neurologic Phenotypes2022 | First Faculty of Medicine
- Two Photon-Induced Electron Injection From a Nanotrigger in Native Endothelial NO-Synthase2008 | First Faculty of Medicine
- Hyperammonemic crisis in a child with ATP synthase deficiency caused by mtDNA mutation m.8851T>C2015 | First Faculty of Medicine
- Isoflavonoids are present in Arabidopsis thaliana despite the absence of any homologue to known isoflavonoid synthases2006 | Faculty of Science