- Mutations in tumor suppressor gene NBS1 in adult patients with malignancies2006 | Second Faculty of Medicine
- Tumor suppressor genes1997 | Second Faculty of Medicine
- Mutations in Tumor Suppressor Gene NBS1 in Adult Patients with Malignancies2006 | First Faculty of Medicine
- Methylation analysis of tumor suppressor genes in endometroid carcinoma of endometrium using MS-MLPA2013 | Faculty of Medicine in Hradec Králové
- A method for detection of germinal mutations in the p53 tumor suppressor gene1996 | Second Faculty of Medicine
- Germline variants of the promyelocytic leukemia tumor suppressor gene in patients with familial cancer2009 | Second Faculty of Medicine
- Evaluation of pathology of tumor suppressor gene TP53 in urotelial tumors of the urinary bladderPublication without faculty affiliation
- Evaluation of tumor suppressor gene expressions and aberrant methylation in the colon of cancer-induced rats: a pilot study2013 | First Faculty of Medicine
- Intracellular localisation of the Wilm´s tumor suppressor gene (WT-1) in relation to the proliferation of in vitro differentiating podocytesPublication without faculty affiliation
- Molecular mechanisms and signaling pathways in pancreatic carcinoma2018 | First Faculty of Medicine, Third Faculty of Medicine
- DNA Methylation and Neoplasia2000 | Second Faculty of Medicine
- Methylation analysis in NSCLC. Frequency of gene-specific hypermethylation depending on the histological type of carcinoma and smoking status2010 | Central Library of Charles University
- Methylation analysis in NSCLC. Frequency of gene-specific hypermethylation depending on the histological type of carcinoma and smoking status2010 | Faculty of Medicine in Pilsen
- Genetic Causes of the Thyroid Carcinomas2004 | Second Faculty of Medicine
- Cytoskeletal proteins regulate chromatin access of BR-C transcription factor and Rpd3-Sin3A histone deacetylase complex in Drosophila salivary glands2011 | First Faculty of Medicine
- The Molecular Biology of Cancer: the Basics for Clinical Practice2017 | First Faculty of Medicine
- Genetic causes of papillary thyroid carcinoma +12007 | Faculty of Medicine in Hradec Králové
- Genetic causes of papillary thyroid carcinoma2007 | First Faculty of Medicine
- Molecular monitoring of residual disease in chronic lymphocytic leukemiaPublication without faculty affiliation
- TP53, EGFR, and KRAS mutations in relation to VHL inactivation and lifestyle risk factors in renal-cell carcinoma from central and eastern Europe2010 | First Faculty of Medicine
- Diagnostic and Prognostic Value of microRNA-21 in Colorectal Cancer: An Original Study and Individual Participant Data Meta-analysis2014 | Faculty of Medicine in Pilsen
- The significance of the fusion partner gene genomic neighborhood analysis in translocation-defined tumors2022 | Faculty of Medicine in Pilsen
- Prognostic Impact of Specific Chromosomal Aberrations in a Large Group of Pediatric Patients With Acute Myeloid Leukemia Treated Uniformly According to Trial AML-BFM 982010 | First Faculty of Medicine
- Prognostic Impact of Specific Chromosomal Aberrations in a Large Group of Pediatric Patients With Acute Myeloid Leukemia Treated Uniformly According to Trial AML-BFM 982010 | Second Faculty of Medicine
- Discordant expression of a new WT1 gene mutation in a family with monozygotic twins presenting with congenital nephrotic syndrome2012 | Second Faculty of Medicine
- Genotype/Phenotype Correlation in Nephrotic Syndrome Caused by WT1 Mutations2010 | Second Faculty of Medicine
- Mutations in the Wilms' tumor 1 gene cause isolated steroid resistant nephrotic syndrome and occur in exons 8 and 92006 | Second Faculty of Medicine
- Ovarian cancer: Origin and factors involved in carcinogenesis with potential use in diagnosis, treatment and prognosis of the disease2011 | First Faculty of Medicine
- Real-time PCR quantification of major Wilms' tumor gene 1 (WT1) isoforms in acute myeloid leukemia, their characteristic expression patterns and possible functional consequences2012 | Second Faculty of Medicine