Publications
- Expression of human BRCA1 Delta 17-19 alternative splicing variant with a truncated BRCT domain in MCF-7 cells results in impaired assembly of DNA repair complexes and aberrant DNA damage response2013 | First Faculty of Medicine, Third Faculty of Medicine
- The PALB2 Gene Is a Strong Candidate for Clinical Testing in BRCA1- and BRCA2-Negative Hereditary Breast Cancer2013 | First Faculty of Medicine
- Gain-of-function mutations of PPM1D/Wip1 impair the p53-dependent G1 checkpoint2013 | First Faculty of Medicine
- The clinical importance of a genetic analysis of moderate-risk cancer susceptibility genes in breast and other cancer patients from the Czech Republic2012 | First Faculty of Medicine
- Contribution of the Beta-ureidopropionase (UPB1) gene alterations to the development of fluoropyrimidine-related toxicity2012 | First Faculty of Medicine
- Alterations of CHEK2 forkhead-associated domain increase the risk of Hodgkin lymphoma2011 | First Faculty of Medicine, Second Faculty of Medicine, Third Faculty of Medicine
- The AIB1 gene polyglutamine repeat length polymorphism and the risk of breast cancer development2011 | First Faculty of Medicine
- Screening for genomic rearrangements in BRCA1 and BRCA2 genes in Czech high-risk breast/ovarian cancer patients: high proportion of population specific alterations in BRCA1 gene2010 | First Faculty of Medicine
- Contribution of dihydropyrimidinase gene alterations to the development of serious toxicity in fluoropyrimidine-treated cancer patients.2010 | First Faculty of Medicine
- Prerequisites for preimplantation genetic diagnosis (PGD in carriers of mutations responsible for hereditary cancers2009 | First Faculty of Medicine, Third Faculty of Medicine
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