- Methylation changes in promoter and enhancer regions of the WT1 gene in Wilms'tumours2001 | Second Faculty of Medicine
- Minimal residual disease detectable by quantitative assessment of WT1 gene before allogeneic stem cell transplantation in patients in first remission of acute myeloid leukemia has an impact on their future prognosis2013 | First 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
- Standardization of WT1 mRNA quantitation for minimal residual disease monitoring in childhood AML and implications of WT1 gene mutations: a European multicenter study2009 | Second Faculty of Medicine
- Is WT1 gene hyperexpression a malignant cells marker?2006 | Second Faculty of Medicine
- Regulatory element methylation of WT1 gene in patients with Wilms tumor2000 | Second Faculty of Medicine
- 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 children with AML: Prognostic significance and Excellent correlation with disease status and residual disease detection by flow cytometryPublication without faculty affiliation
- 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
- No Prognostic Impact of the WT1 Gene Single Nucleotide Polymorphism rs16754 in Pediatric Acute Myeloid Leukemia2010 | Second Faculty of Medicine
- Molecular Genetics of the Wilms' Tumor2001 | Second Faculty of Medicine
- WT1 Gene Expression in Peripheral Blood Before and After Allogeneic Stem Cell Transplantation is a Clinically Relevant Prognostic Marker in AML - A Single-center 14-year Experience2021 | First 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 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Clinical relevance of Wilms tumor 1 gene mutations in childhood acute myeloid leukemia2009 | 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
- Alteration in DNA-binding affinity of Wilms tumor 1 protein due to WT1 genetic variants associated with steroid - resistant nephrotic syndrome in children2022 | Second Faculty of Medicine
- Desmoplastic Small Round Cell Tumor of the Uterus: A Report of Molecularly Confirmed Case with EWSR1-WT1 Fusion2022 | First Faculty of Medicine, Third Faculty of Medicine
- Genotype-phenotype associations in WT1 glomerulopathy2014 | Second Faculty of Medicine
- Genetic diagnosis of steroid-resistant nephrotic syndrome in a longitudinal collection of Czech and Slovak patients: a high proportion of causative variants in NUP932018 | Second Faculty of Medicine
- WT1 Expression in Peripheral Blood at Diagnosis and During the Course of Early Consolidation Treatment Correlates With Survival in Patients With Intermediate and Poor-Risk Acute Myeloid Leukemia2020 | First Faculty of Medicine