Kateřina Tauchmannová

Acadian variant of Fanconi syndrome is caused by mitochondrial respiratory chain complex I deficiency due to a non-coding mutation in complex I assembly factor NDUFAF6

Hana Hartmannová, Lenka Piherová, Kateřina Tauchmannová et al. · Human Molecular Genetics · 2016 · 80 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Bi-allelic Mutations in NDUFA6 Establish Its Role in Early-Onset Isolated Mitochondrial Complex I Deficiency

Charlotte L. Alston, Juliana Heidler, Marris G. Dibley et al. · The American Journal of Human Genetics · 2018 · 64 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Sex difference in the sensitivity of cardiac mitochondrial permeability transition pore to calcium load

Marie Milerová, Z Drahota, Anna Chytilová et al. · Molecular and Cellular Biochemistry · 2015 · 45 citations

Life Sciences, Cell Biology, Physiology +14

TMEM70 facilitates biogenesis of mammalian ATP synthase by promoting subunit c incorporation into the rotor structure of the enzyme

Jana Kovalčíková, Marek Vrbacký, Petr Pecina et al. · The FASEB Journal · 2019 · 37 citations

Life Sciences, Biochemistry, Molecular Biology +17

Selective replacement of mitochondrial DNA increases the cardioprotective effect of chronic continuous hypoxia in spontaneously hypertensive rats

Jan Neckář, Anna Svatoňová, Romana Weissová et al. · Clinical Science · 2017 · 22 citations

Life Sciences, Cardiology, Physiology +17