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 · 76 citations · Full text

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 · 61 citations · Full text

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

Cardiac Muscle, Cardiomyopathy, Heart Failure +9

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 · 36 citations

Mutant Wars2 Gene in Spontaneously Hypertensive Rats Impairs Brown Adipose Tissue Function and Predisposes to Visceral Obesity

Michal Pravenec, V. Landa, Petr Mlejnek et al. · Physiological Research · 2017 · 22 citations · Full text

Metabolic Disorder, Genetics, Metabolic Remodeling +23