Hana Hansı́ková

Retrospective, Multicentric Study of 180 Children with Cytochrome c Oxidase Deficiency

Marek Böhm, Ewa Pronicka, Elżbieta Karczmarewicz et al. · Pediatric Research · 2005 · 109 citations · Full text

Multicentric Study, Pediatric Hematology, Inherited Metabolic Disease +7

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

J Houštěk, Petr Klement, Jana Heřmanská et al. · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · 1995 · 105 citations

Mitochondrial Biogenesis, Mitochondrial Function, Biochemistry +11

Tissue-specific cytochrome <i>c</i> oxidase assembly defects due to mutations in <i>SCO2</i> and <i>SURF1</i>

Lukáš Stibůrek, Kateřina Veselá, Hana Hansı́ková et al. · Biochemical Journal · 2005 · 100 citations · Full text

Loss of function of Sco1 and its interaction with cytochrome <i>c</i> oxidase

Lukáš Stibůrek, Kateřina Veselá, Hana Hansı́ková et al. · American Journal of Physiology-Cell Physiology · 2009 · 98 citations

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

Pavel Ješina, Markéta Tesařová, Daniela Fornůsková et al. · Biochemical Journal · 2004 · 60 citations · Full text