Aleš Hnı́zda

Heterozygous Loss-of-Function SEC61A1 Mutations Cause Autosomal-Dominant Tubulo-Interstitial and Glomerulocystic Kidney Disease with Anemia

Nikhita Bolar, Christelle Golzio, Martina Živná et al. · The American Journal of Human Genetics · 2016 · 159 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Dimers of DNA-PK create a stage for DNA double-strand break repair

Amanda K. Chaplin, Steven W. Hardwick, Shikang Liang et al. · Nature Structural & Molecular Biology · 2020 · 124 citations

Life Sciences, Genetics, Molecular Biology +10

Conserved roles of C. elegans and human MANFs in sulfatide binding and cytoprotection

Meirong Bai, Roman Vozdek, Aleš Hnı́zda et al. · Nature Communications · 2018 · 81 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +15

PDGFRB mutation and tyrosine kinase inhibitor resistance in Ph-like acute lymphoblastic leukemia

Yingchi Zhang, Yufeng Gao, Hui Zhang et al. · Blood · 2018 · 76 citations · Full text

Medicine, Cancer Biology, Oncology +16

Biochemical and structural analysis of 14 mutant adsl enzyme complexes and correlation to phenotypic heterogeneity of adenylosuccinate lyase deficiency

Marie Zikánová, Václava Škopová, Aleš Hnı́zda et al. · Human Mutation · 2010 · 54 citations

Life Sciences, Biochemistry, Molecular Biology +14