Alena Čížková

TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy

Alena Čížková, Viktor Stránecký, Johannes A. Mayr et al. · Nature Genetics · 2008 · 200 citations

Life Sciences, Genetics, Neuroscience +16

HIF and reactive oxygen species regulate oxidative phosphorylation in cancer

Éric Hervouet, Alena Čížková, Jocelyne Demont et al. · Carcinogenesis · 2008 · 99 citations

Medicine, Cancer Biology, Oncology +17

Mutations in TMEM76 Cause Mucopolysaccharidosis IIIC (Sanfilippo C Syndrome)

Martin Hřebı́ček, Lenka Mrázová, Volkan Seyrantepe et al. · The American Journal of Human Genetics · 2006 · 96 citations · Full text

Life Sciences, Genetics, Molecular Genetics +5

Development of a human mitochondrial oligonucleotide microarray (h-MitoArray) and gene expression analysis of fibroblast cell lines from 13 patients with isolated F1Fo ATP synthase deficiency

Alena Čížková, Viktor Stránecký, Robert Ivánek et al. · BMC Genomics · 2008 · 27 citations · Full text

Life Sciences, Genetics, Molecular Biology +16