- Case report: A rare variant m.4135T>C in the MT-ND1 gene leads to Leber hereditary optic neuropathy and altered respiratory chain supercomplexes +12023 | Přírodovědecká fakulta, 1. lékařská fakulta
- Capture of somatic mtDNA point mutations with severe effects on oxidative phosphorylation in synaptosome cybrid clones from human brain2014 | 1. lékařská fakulta
- Loss of mitochondrial DNA-encoded protein ND1 results in disruption of complex I biogenesis during early stages of assembly2016 | 1. lékařská fakulta
- Genetic variation in house mice (Mus, muridae, rodentia) from the Czech and Slovak republics2002 | Přírodovědecká fakulta
- Multisystem mitochondrial diseases due to mutations in mtDNA-encoded subunits of complex I2020 | 1. lékařská fakulta