- The spectrum of mitochondrial DNA (mtDNA) mutations in pediatric CNS tumors2021 | Second Faculty of Medicine
- The most frequent manifestation of mitochondrial DNA( mtDNA) mutation 8344 G Is MERRF.1999 | Faculty of Physical Education and Sport
- Near Eastern Neolithic Genetic Input in a Small Oasis of the Egyptian Western Desert2009 | Faculty of Science, Faculty of Physical Education and Sport, Faculty of Mathematics and Physics, First Faculty of Medicine
- 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
- Linking the sub-Saharan and West Eurasian gene pools: maternal and paternal heritage of the Tuareg nomads from the African Sahel2010 | Faculty of Science, Faculty of Physical Education and Sport, Faculty of Mathematics and Physics, Faculty of Arts
- Busting the myths: DNA typeability after 48 hours of boil2019 | Second Faculty of Medicine
- Fluorescent in situ hybridization of mitochondrial DNA and RNA2010 | Central Library of Charles University
- A Novel MTTK Gene Variant m.8315A>C as a Cause of MERRF Syndrome2022 | First Faculty of Medicine
- Characterization of microsatellite markers in the genera Anguis and Pseudopus (Reptilia: Anguidae)2018 | Faculty of Science
- Base excision repair in mitochondria, mitochondrial DNA copy number and telomere length and link to colorectal cancer outcomePublication without faculty affiliation
- Mitochondrial DNA content and expression of genes involved in mtDNA transcription, regulation and maintenance during human fetal development2010 | First Faculty of Medicine
- Psychiatric disturbances in five patients with MELAS syndrome2014 | First Faculty of Medicine
- Mitochondrial genome acquisition restores respiratory function and tumorigenic potential of cancer cells without mitochondrial DNA2015 | Central Library of Charles University
- Large copy number variations in combination with point mutations in the TYMP and SCO2 genes found in two patients with mitochondrial disorders2014 | First Faculty of Medicine
- 60,000 years of interactions between Central and Eastern Africa documented by major African mitochondrial haplogroup L22015 | Faculty of Science
- Reactivation of Dihydroorotate Dehydrogenase-Driven Pyrimidine Biosynthesis Restores Tumor Growth of Respiration-Deficient Cancer Cells2019 | Faculty of Science, Third Faculty of Medicine
- Mitochondria - from origin to current therapies2021 | Third Faculty of Medicine
- Circum-Saharan Prehistory through the Lens of mtDNA Diversity2022 | Faculty of Science
- POLRMT mutations impair mitochondrial transcription causing neurological disease2021 | Faculty of Physical Education and Sport, First Faculty of Medicine
- A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis2021 | Second Faculty of Medicine
- Diverse origin of mitochondrial lineages in Iron Age Black Sea Scythians2017 | Faculty of Education
- Capture of somatic mtDNA point mutations with severe effects on oxidative phosphorylation in synaptosome cybrid clones from human brain2014 | First Faculty of Medicine
- Loss of mitochondrial DNA-encoded protein ND1 results in disruption of complex I biogenesis during early stages of assembly2016 | First Faculty of Medicine
- Detection of mitochondrial DNA variants at low level heteroplasmy in pediatric CNS and extra-CNS solid tumors with three different enrichment methods2020 | Second Faculty of Medicine
- Non-bioenergetic roles of mitochondrial GPD2 promote tumor progression2023 | Faculty of Science
- Phenotypic spectrum associated with mutations of the mitochondrial polymerase gamma gene2006 | First Faculty of Medicine
- The Expansion of mtDNA Haplogroup L3 within and out of Africa2012 | Faculty of Science
- Mitochondrially Targeted Vitamin E Succinate Modulates Expression of Mitochondrial DNA Transcripts and Mitochondrial Biogenesis2015 | Central Library of Charles University
- Unique presentation of LHON/MELAS overlap syndrome caused by m.13046T > C in MTND52016 | First Faculty of Medicine, Second Faculty of Medicine
- A transgenic minipig model of Huntington's disease shows early signs of behavioral and molecular pathologies2018 | Faculty of Science, First Faculty of Medicine, Central Library of Charles University