Vilma Kaplanová
Czech Academy of Sciences(CZ)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, Photosynthetic Processes and Mechanisms
Most-Cited Works
- → TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy(2008)197 cited
- → Mitochondrial ATP synthase deficiency due to a mutation in the ATP5E gene for the F1 subunit(2010)137 cited
- → 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
- → 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(2004)62 cited
- → Nuclear Genetic Defects of Mitochondrial ATP Synthase(2014)48 cited
- → Knockdown of F1 epsilon subunit decreases mitochondrial content of ATP synthase and leads to accumulation of subunit c(2009)46 cited