Kateřina Tauchmannová
Czech Academy of Sciences(CZ)Czech Academy of Sciences, Institute of Physiology(CZ)
Publications by Year
Research Areas
Mitochondrial Function and Pathology, ATP Synthase and ATPases Research, Metabolism and Genetic Disorders, RNA modifications and cancer, Adipose Tissue and Metabolism
Most-Cited Works
- → 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(2016)78 cited
- → Bi-allelic Mutations in NDUFA6 Establish Its Role in Early-Onset Isolated Mitochondrial Complex I Deficiency(2018)61 cited
- → Sex difference in the sensitivity of cardiac mitochondrial permeability transition pore to calcium load(2015)45 cited
- → TMEM70 facilitates biogenesis of mammalian ATP synthase by promoting subunit c incorporation into the rotor structure of the enzyme(2019)37 cited
- → Selective replacement of mitochondrial DNA increases the cardioprotective effect of chronic continuous hypoxia in spontaneously hypertensive rats(2017)22 cited
- → Mutant Wars2 Gene in Spontaneously Hypertensive Rats Impairs Brown Adipose Tissue Function and Predisposes to Visceral Obesity(2017)22 cited
- → Sulforaphane Ameliorates Metabolic Changes Associated With Status Epilepticus in Immature Rats(2022)16 cited
- → Conplastic strains for identification of retrograde effects of mitochondrial dna variation on cardiometabolic traits in the spontaneously hypertensive rat(2021)9 cited
- → Haplotype variability in mitochondrial rRNA predisposes to metabolic syndrome(2024)7 cited
- → Variability of Clinical Phenotypes Caused by Isolated Defects of Mitochondrial ATP Synthase(2024)6 cited