- Chromosome-wide characterization of meiotic noncrossovers (gene conversions) in mouse hybrids2021 | Faculty of Science
- Playing hide-and-seek in beta-globin genes: gene conversion transferring a beneficial mutation between differentially expressed gene duplicates2018 | Faculty of Science
- Diversity of cystathionine beta-synthase haplotypes bearing the most common homocystinuria mutation c.833T>C: a possible role for gene conversion2007 | First Faculty of Medicine
- MHC Class IIB Exon 2 Polymorphism in the Grey Partridge (Perdix perdix) Is Shaped by Selection, Recombination and Gene Conversion2013 | Faculty of Science
- Diversity of Cystathionine beta-Synthase Haplotypes Bearing the Most Common Homocystinuria Mutation c.833>C:A Possible Role for Gene Conversion2007 | First Faculty of Medicine
- Diversity of Cystathionine beta-Synthase Haplotypes Bearing the Most Common Homacystinutia Mutation c.833>C:A Posssible Role for Gene Conversion2007 | First Faculty of Medicine
- Genome Fractionation and Loss of Heterozygosity in Hybrids and Polyploids: Mechanisms, Consequences for Selection, and Link to Gene Function2021 | Faculty of Science, Central Library of Charles University
- Purification and characterization of a nitrilase from Fusarium solani O12008 | Faculty of Science
- Genome Compositional Organization in Gars Shows More Similarities to Mammals than to Other Ray-Finned Fish2017 | Faculty of Science
- Crizotinib - a novel multikinase inhibitor of signalling pathways for treatment in selected patients with non-small cell lung cancwer2013 | Faculty of Medicine in Pilsen
- Absence of SBDS mutations in sporadic paediatric acute myeloid leukaemia2013 | Second Faculty of Medicine
- Substitution in the promoter region ofthe CYP21 affects a phenotype ofthe disease in patients with 21-hydroxylase deficiency2009 | Third Faculty of Medicine
- Identification of CYP21A2 mutant alleles in Czech patients with 21-hydroxylase deficiency2010 | Second Faculty of Medicine, Third Faculty of Medicine
- Molecular etiopathogenesis of spinal muscular atrophy2002 | Second Faculty of Medicine
- Frequency of CYP21 gene mutations in Czech patients with steroid 21-hydroxylase deficiency and statistical comparison with other populations2003 | Second Faculty of Medicine
- The evolution of the green-light-sensitive visual opsin genes (RH2) in teleost fishes2023 | Faculty of Science