Hana Hansı́ková

Publications by Year

Research Areas

Mitochondrial Function and Pathology, ATP Synthase and ATPases Research, Metabolism and Genetic Disorders, Photosynthetic Processes and Mechanisms, Genetics and Neurodevelopmental Disorders

Most-Cited Works

• → Retrospective, Multicentric Study of 180 Children with Cytochrome c Oxidase Deficiency(2005)109 cited
• → Altered properties of mitochondrial ATP-synthase in patients with a T → G mutation in the ATPase 6 (subunit a) gene at position 8993 of mtDNA(1995)105 cited
• → Tissue-specific cytochrome c oxidase assembly defects due to mutations in SCO2 and SURF1(2005)100 cited
• → Loss of function of Sco1 and its interaction with cytochrome c oxidase(2009)98 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
• → Functional alteration of cytochrome c oxidase by SURF1 mutations in Leigh syndrome(2003)52 cited
• → Noninvasive diagnostics of mitochondrial disorders in isolated lymphocytes with high resolution respirometry(2014)33 cited
• → Clinical, biochemical and molecular analyses of six patients with isolated cytochrome c oxidase deficiency due to mutations in the SCO2 gene(2004)30 cited
• → A Novel Mutation in SURF1 Causes Skipping of Exon 8 in a Patient with Cytochrome c Oxidase-Deficient Leigh Syndrome and Hypertrichosis(2001)22 cited
• → Segregation pattern and biochemical effect of the G3460A mtDNA mutation in 27 members of LHON family(2004)20 cited