Vendula Havlíčková

Publications by Year

Research Areas

Mitochondrial Function and Pathology, ATP Synthase and ATPases Research, Metabolism and Genetic Disorders, Birth, Development, and Health, Protein Kinase Regulation and GTPase Signaling

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
• → Mitochondrial DNA content and expression of genes involved in mtDNA transcription, regulation and maintenance during human fetal development(2010)68 cited
• → Knockdown of F1 epsilon subunit decreases mitochondrial content of ATP synthase and leads to accumulation of subunit c(2009)46 cited
• → Expression and processing of the TMEM70 protein(2010)35 cited
• → Role of the mitochondrial ATP synthase central stalk subunits γ and δ in the activity and assembly of the mammalian enzyme(2012)3 cited
• → Developmental changes of mitochondrial DNA content and expression of genes involved in mtDNA transcription and maintenance in human fetal liver and muscle tissues(2010)2 cited
• The study of mitochondrial energy metabolism in liver tissue during prenatal development(2007)
• → Down-regulation of F1 ε subunit in HEK293 cells(2010)
• → 45 Mitochondrial energy system in liver and muscle tissue during foetal development(2010)