K. Tauchmannová

发表

Genetic Complementation of ATP Synthase Deficiency Due to Dysfunction of TMEM70 Assembly Factor in Rat

M. Pravenec, P. Mlejnek, V. Kaplanová, 2022, Biomedicines.

Mutant Wars2 gene in spontaneously hypertensive rats impairs brown adipose tissue function and predisposes to visceral obesity.

V. Zídek, M. Pravenec, P. Mlejnek, 2017, Physiological research.

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

J. Novotný, M. Pravenec, O. Novakova, 2017, Clinical science.

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

J. Houštěk, Z. Drahota, B. Ošt̕ádal, 2015, Molecular and Cellular Biochemistry.

Sulforaphane Ameliorates Metabolic Changes Associated With Status Epilepticus in Immature Rats

J. Svoboda, J. Danek, T. Mráček, 2022, Frontiers in Cellular Neuroscience.

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

Robert W. Taylor, Courtney E. French, A. Pagnamenta, 2018, American Journal of Human Genetics.

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.

K. Hodaňová, M. Vrbacký, H. Hartmannová, 2016, Human molecular genetics.

Conplastic strains for identification of retrograde effects of mitochondrial dna variation on cardiometabolic traits in the spontaneously hypertensive rat.

M. Pravenec, P. Mlejnek, J. Houštěk, 2021, Physiological research.

MLQ is responsible for stabilisation of subunit a in the holoenzyme of mammalian ATP synthase

M. Vrbacký, V. Kaplanová, J. Houštěk, 2020, bioRxiv.

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

J. Houštěk, Z. Drahota, B. Ošt̕ádal, 2015, Molecular and Cellular Biochemistry.

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

M. Vrbacký, V. Kaplanová, J. Houštěk, 2019, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

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

J. Novotný, M. Pravenec, O. Novakova, 2017, Clinical science.

Physiological variability in mitochondrial rRNA predisposes to metabolic syndrome

M. Pravenec, M. Vrbacký, V. Kaplanová, 2023, bioRxiv.

Variability of Clinical Phenotypes Caused by Isolated Defects of Mitochondrial ATP Synthase (Review).

K. Tauchmannová, J. Houštěk, A. Pecinová, 2024, Physiological research.

Haplotype variability in mitochondrial rRNA predisposes to metabolic syndrome

M. Vrbacký, V. Kaplanová, T. Mráček, 2024, Communications biology.