- Genome editing using the CRISPR/Cas9 system and its application in haematology2019 | Second Faculty of Medicine
- CRISPR/Cas9 in Leishmania mexicana: A case study of LmxBTN12018 | Faculty of Science
- DNA methylation can alter CRISPR/Cas9 editing frequency and DNA repair outcome in a target-specific manner2022 | Faculty of Science
- Agroinfiltration Mediated Scalable Transient Gene Expression in Genome Edited Crop Plants2021 | Publication without faculty affiliation
- CRISPR/Cas9-Mediated Correction of the FANCD1 Gene in Primary Patient Cells2017 | Second Faculty of Medicine
- Missense mutation in RPS7 causes Diamond-Blackfan anemia via alteration of erythrocyte metabolism, protein translation and induction of ribosomal stress2022 | Central Library of Charles University
- Manipulation of spermatogonial stem cells in livestock species2019 | First Faculty of Medicine
- Efficient CRISPR Mutagenesis in Sturgeon Demonstrates Its Utility in Large, Slow-Maturing Vertebrates2022 | Faculty of Science
- Efficient CRISPR/Cas9-mediated gene disruption in the tetraploid protist Giardia intestinalis2022 | Faculty of Science, First Faculty of Medicine
- Knock-Out of Retrovirus Receptor Gene Tva in the Chicken Confers Resistance to Avian Leukosis Virus Subgroups A and K and Affects Cobalamin (Vitamin B-12)-Dependent Level of Methylmalonic Acid2021 | First Faculty of Medicine
- Můžeme to, co umíme? : kontroverzní témata mezi současnou medicínou a etikou2018 | First Faculty of Medicine
- Characterization of RACK1-depleted mammalian cells by a palette of microscopy approaches reveals defects in cell cycle progression and polarity establishment2023 | Faculty of Science, Second Faculty of Medicine
- CRISPR-Cas9 Arabidopsis mutants of genes for ARPC1 and ARPC3 subunits of ARP2/3 complex reveal differential roles of complex subunits2022 | Faculty of Science
- Germline CHEK2 Gene Mutations in Hereditary Breast Cancer Predisposition - Mutation Types and their Biological and Clinical Relevance2019 | First Faculty of Medicine
- The role of invariant surface glycoprotein 75 in xenobiotic acquisition by African trypanosomes2023 | Faculty of Science, Central Library of Charles University
- Generation and characterization of human U-2 OS cell lines with the CRISPR/Cas9-edited protoporphyrinogen oxidase IX gene2022 | Faculty of Science, Central Library of Charles University, Faculty of Physical Education and Sport
- Abrogation of IFN-gamma Signaling May not Worsen Sensitivity to PD-1/PD-L1 Blockade2020 | Faculty of Science
- Abrogation of IFN-γ Signaling May not Worsen Sensitivity to PD-1/PD-L1 Blockade2020 | Faculty of Science
- CRISPR/Cas9-targeted enrichment and long-read sequencing of the Fuchs endothelial corneal dystrophy-associated TCF4 triplet repeat2019 | First Faculty of Medicine
- Semi-Lethal Primary Ciliary Dyskinesia in Rats Lacking the Nme7 Gene2021 | First Faculty of Medicine
- Cadmium Phytotoxicity, Tolerance, and Advanced Remediation Approaches in Agricultural Soils; A Comprehensive Review2022 | Faculty of Science
- Adaptation of the late ISC pathway in the anaerobic mitochondrial organelles of Giardia intestinalis2023 | Faculty of Science
- Aspartate β-hydroxylase Regulates Expression of Ly6 Genes2024 | Faculty of Science
- Proteomic Interactome of C. elegans Mediator Complex Subunit 28 (MDT-28) Reveals Predominant Association with a Restricted Set of Core Mediator Subunits and an Affinity to Additional Structural and Enzymatic Proteins2019 | First Faculty of Medicine, Central Library of Charles University, Third Faculty of Medicine
- Changes in cellular prion protein expression, processing and localisation during differentiation of the neuronal cell line CAD 52020 | Faculty of Science, First Faculty of Medicine
- Searching for Wip1 targets on chromatin2019 | Faculty of Science
- Identification of inhibitors for the transmembrane Trypanosoma cruzi eIF2α kinase relevant for parasite proliferation2023 | Faculty of Science
- Chimeric Antigen Receptor Based Cellular Therapy for Treatment Of T-Cell Malignancies2022 | First Faculty of Medicine
- Aagenaes syndrome/lymphedema cholestasis syndrome 1 is caused by a founder variant in the 5'-untranslated region of UNC45A2023 | Faculty of Medicine in Hradec Králové
- Epilepsy and sudden unexpected death in epilepsy in a mouse model of human SCN1B-linked developmental and epileptic encephalopathy2023 | Second Faculty of Medicine