V. Kaplanová

发表

Expression and processing of the TMEM70 protein.

K. Hejzlarová, M. Tesařová, Alena Vrbacká-Čížková, 2011, Biochimica et biophysica acta.

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

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

Alteration of structure and function of ATP synthase and cytochrome c oxidase by lack of Fo-a and Cox3 subunits caused by mitochondrial DNA 9205delTA mutation.

S. Seneca, K. Hejzlarová, V. Kaplanová, 2015, The Biochemical journal.

Segregation pattern and biochemical effect of the G3460A mtDNA mutation in 27 members of LHON family

V. Kaplanová, J. Zeman, J. Houštěk, 2004, Journal of the Neurological Sciences.

Role of the mitochondrial ATP synthase central stalk subunits γ and δ in the activity and assembly of the mammalian enzyme.

V. Kaplanová, J. Houštěk, T. Mráček, 2012, Biochimica et biophysica acta. Bioenergetics.

TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy

K. Hejzlarová, M. Tesařová, M. Vrbacký, 2008, Nature Genetics.

Mitochondrial ATP synthase deficiency due to a mutation in the ATP5E gene for the F1 epsilon subunit.

V. Kaplanová, V. Havlíčková, J. Houštěk, 2010, Human molecular 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.

Nuclear genetic defects of mitochondrial ATP synthase.

K. Hejzlarová, M. Vrbacký, V. Kaplanová, 2014, Physiological research.

Diminished synthesis of subunit a (ATP6) and altered function of ATP synthase and cytochrome c oxidase due to the mtDNA 2 bp microdeletion of TA at positions 9205 and 9206.

M. Tesařová, V. Kaplanová, J. Zeman, 2004, The Biochemical journal.

Knockdown of F1 epsilon subunit decreases mitochondrial content of ATP synthase and leads to accumulation of subunit c.

V. Kaplanová, V. Havlíčková, J. Houštěk, 2010, Biochimica et biophysica acta.

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

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

Mitochondrial Membrane Potential and ATP Production in Primary Disorders of ATP Synthase

M. Tesařová, V. Kaplanová, J. Zeman, 2004, Toxicology mechanisms and methods.

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.

Alteration of structure and function of ATP synthase and cytochrome c oxidase by lack of Fo-a and Cox3 subunits caused by mitochondrial DNA 9205delTA mutation. Short (page heading) title: Biochemistry of 9205delTA mutation

V. Kaplanová, P. Ješina, N. Hana, 2015 .

Physiological variability in mitochondrial rRNA predisposes to metabolic syndrome

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

Haplotype variability in mitochondrial rRNA predisposes to metabolic syndrome

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