Publications
- TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy2008 | First Faculty of Medicine
- Tissue-specific cytochrome c oxidase assembly defects due to mutations in SCO2 and SURF12005 | First Faculty of Medicine
- Reduced respiratory control with ADP and changed pattern in respiratory chain enzymes as a result of selective deficiency of mitochondrial ATP synthase2004 | First Faculty of Medicine
- Polarographic Evaluation of Mitochondrial Enzymes Activity in Isolated Mitochondria and in Permeabilized Human Muscle Cells with Inherited Mitochondrial Defects2003 | First Faculty of Medicine
- TMEM70 protein - A novel ancillary factor of mammalian ATP synthase2009 | First Faculty of Medicine
- HIF and reactive oxygen species regulate oxidative phosphorylation in cancer2008 | First Faculty of Medicine
- Development of a human mitochondrial oligonucleotide microarray (h-MitoArray) and gene expression analysis of fibroblast cell lines from 13 patients with isolated FIFo ATP synthase deficiency2008 | First Faculty of Medicine
- Mitochondrial complex I inhibition in cerebral cortex of immature rats following homocysteic acid-induced seizures2007 | First Faculty of Medicine
- Mitochondrial complex I inhibition in cerebral cortex of immature rats following homocysteic acid-induced seizures2007 | Faculty of Physical Education and Sport
- Specific Properties of Heavy Fraction of Mitochondria from Human-term Placenta - Glycerophosphate-dependent Hydrogen Peroxide Production2006 | First Faculty of Medicine
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