- The cause of death of neural cells in ataxia telangiectasia2014 | First Faculty of Medicine
- Ataxia-telangiectasia mutated kinase (ATM) as a central regulator of radiation-induced DNA damage response2010 | Faculty of Medicine in Hradec Králové
- Characterisation of ATM mutations in Slavic Ataxia telangiectasia patients2011 | First Faculty of Medicine, Second Faculty of Medicine
- Characterisation of ATM Mutations in Slavic Ataxia Telangiectasia Patients2011 | Second Faculty of Medicine
- Ataxia Telangiectasia Gene Mutation in Isolated Segmental Dystonia Without Ataxia and Telangiectasia2018 | First Faculty of Medicine
- The development of ataxia telangiectasia mutated kinase inhibitors2014 | Publication without faculty affiliation
- Small Molecules Targeting Ataxia Telangiectasia and Rad3-Related (ATR) Kinase: An Emerging way to Enhance Existing Cancer Therapy2016 | Publication without faculty affiliation
- Louis-Bar Syndrome of Ataxia Telangiectasia in Consanguinous Family2006 | Second Faculty of Medicine
- The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q211997 | Second Faculty of Medicine
- The Ataxia telangiectasia variant genes 1 and 2 show no linkage to the AT candidate region on chromosome 11q22-23 +11995 | Second Faculty of Medicine
- In silico library screening to find novel anticancer agent with chemosensitizing properties: focus on targeting ataxia telangiectasia and Rad3 related kinase2024 | Faculty of Medicine in Hradec Králové
- Progressive choreodystonia in X-linked hyper-IgM immunodeficiency: a rare but recurrent presentation2022 | First Faculty of Medicine
- Nibrin, a novel DNA double-strand break repair protein, is mutated in nijmegen breakage syndrome1998 | Second Faculty of Medicine
- Antibody -Like Phosphorylation Sites in Focus of Statistically Based Bilingual Approach2016 | Faculty of Science, Central Library of Charles University
- Homozygous pathogenic variant in BRAT1 associated with nonprogressive cerebellar ataxia2019 | Faculty of Science
- Contribution of mutations in ATM to breast cancer development in the Czech population2008 | First Faculty of Medicine
- Non-Hodgkin lymphoma and pre-existing conditions: spectrum, clinical characteristics and outcome in 213 children and adolescents2016 | Second Faculty of Medicine
- Caffeine-suppressed ATM pathway leads to decreased p53 phosphorylation and increased programmed cell death in gamma-irradiated leukaemic molt-4 cells2011 | Faculty of Medicine in Hradec Králové
- Rescue of a telomere length defect of Nijmegen breakage syndrome cells requires NBS and telomerase catalytic subunit2001 | Second Faculty of Medicine
- Novel caffeine derivatives with antiproliferative activity2016 | Faculty of Medicine in Hradec Králové
- Cancer risk of heterozygotes with the NBN founder mutation2007 | Second Faculty of Medicine
- Nijmegen breakage syndrome (NBS) with neurological abnormalities and without chromosomal instability2006 | Second Faculty of Medicine
- Modulation of ionizing radiation-induced effects by NU7441, KU55933 and VE821 in peripheral blood lymphocytes2016 | Publication without faculty affiliation
- Analysis of D1853N ATM polymorphism in radiosensitive patients with cervical carcinoma2011 | Faculty of Medicine in Hradec Králové
- A novel assay for screening WIP1 phosphatase substrates in nuclear extracts2021 | Faculty of Science
- Gamma-Radiation-Induced Phosphorylation of p53 on Serine 15 Is Dose-Dependent in MOLT-4 Leukaemia Cells +12009 | Faculty of Medicine in Hradec Králové
- ATM-Dependent Phosphorylation of Hepatitis B Core Protein in Response to Genotoxic Stress2021 | Faculty of Science, Central Library of Charles University
- Quantitative Oculomotor Assessment in Hereditary Ataxia: Discriminatory Power, Correlation with Severity Measures, and Recommended Parameters for Specific Genotypes2024 | Second Faculty of Medicine