Marek Vrbacký

TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy

Alena Čížková, Viktor Stránecký, Johannes A. Mayr et al. · Nature Genetics · 2008 · 197 citations

Mitochondrial Myopathy, Neonatal Mitochondrial Encephalocardiomyopathy, Mitochondrial Biogenesis +8

Uncoupling protein-1 is not leaky

Irina G. Shabalina, Mario Ost, Nataša Petrovič et al. · Biochimica et Biophysica Acta (BBA) - Bioenergetics · 2010 · 91 citations

Protein Secretion, Biochemistry, Protein Folding +3

Direct linkage of mitochondrial genome variation to risk factors for type 2 diabetes in conplastic strains

Michal Pravenec, Masaya Hyakukoku, J Houštěk et al. · Genome Research · 2007 · 88 citations · Full text

Genetics, Genetic Epidemiology, Molecular Genetics +19

Molecular mechanisms of silybin and 2,3-dehydrosilybin antiradical activity—role of individual hydroxyl groups

Radek Gažák, Petr Sedmera, Marek Vrbacký et al. · Free Radical Biology and Medicine · 2008 · 81 citations

Chemical Biology, Biochemistry, Natural Sciences +5

Comparison of the effect of mitochondrial inhibitors on mitochondrial membrane potential in two different cell lines using flow cytometry and spectrofluorometry

Marie Hubálek Kalbáčová, Marek Vrbacký, Z Drahota et al. · Cytometry Part A · 2003 · 79 citations