Publications
- Tissue-specific cytochrome c oxidase assembly defects due to mutations in SCO2 and SURF12005 | First Faculty of Medicine
- Functional alteration of cytochrome c oxidase by SURF1 mutations in Leigh syndrome2003 | First Faculty of Medicine
- Functional alteration of cytochrome c oxidase by SURF1 mutations in Leigh syndromePublication without faculty affiliation
- Structural and functional consequences of mutation in subunit a of mitochondrial F F-ATP synthasePublication without faculty affiliation
- Structural and functional changes of mitochondrial ATP synthase caused by mtDNA 9205delTA mutation in ATP genePublication without faculty affiliation
- 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
- TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy2008 | First Faculty of Medicine
- Mitochondrial complex I inhibition in cerebral cortex of immature rats following homocysteic acid-induced seizures2007 | First Faculty of Medicine
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