Publications
- Telomere length and telomerase complex mutations in pediatric acute myeloid leukemia2013 | Second Faculty of Medicine
- Evaluation of WT1 expression in bone marrow vs peripheral blood samples of children with acute myeloid leukemia-impact on minimal residual disease detection2013 | Second 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 consequences +12012 | Second Faculty of Medicine
- No Prognostic Impact of the WT1 Gene Single Nucleotide Polymorphism rs16754 in Pediatric Acute Myeloid Leukemia2010 | Second Faculty of Medicine
- Real-time quantitative PCR detection of WT1 gene expression in children with AML: prognostic significance, correlation with disease status and residual disease detection by flow cytometry2002 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- RQ-PCR detection of WT1 gene expression in children with AML: excellent correlation with disease status and residual disease detection by flow cytometry2001 | Second Faculty of Medicine, Central Library of Charles University
- RQ-PCR detection of WT1 gene expression in transplanted and non-transplanted children with AML: correlation with disease status and residual disease detection by flow cytometry2001 | Second Faculty of Medicine, Central Library of Charles University
- RQ-PCR detection of WT1 gene expression in children with AML: prognostic significance and excellent correlation with disease status and residual disease detection by flow cytometry2001 | Second Faculty of Medicine, Central Library of Charles University
- Genomic DNA-based measurable residual disease monitoring in pediatric acute myeloid leukemia: unselected consecutive cohort study2024 | Second Faculty of Medicine
- Restored biosynthetic pathways induced by MSCs serve as rescue mechanism in leukemia cells after L-asparaginase therapy2023 | Faculty of Science, Second Faculty of Medicine
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