- 7-Aryl-7-deazaadenine 2'-Deoxyribonucleoside Triphosphates (dNTPs): Better Substrates for DNA Polymerases than dATP in Competitive Incorporations2014 | Faculty of Science
- Protected 2'-deoxyribonucleoside triphosphate building blocks for the photocaging of epigenetic 5-(hydroxymethyl)cytosine in DNA2018 | Faculty of Science
- Synthesis of Base-Modified 2'-Deoxyribonucleoside Triphosphates and Their Use in Enzymatic Synthesis of Modified DNA for Applications in Bioanalysis and Chemical Biology2014 | Faculty of Science
- Phenothiazine-linked nucleosides and nucleotides for redox labelling of DNA2017 | Faculty of Science, Central Library of Charles University
- 6-Aryl-4-amino-pyrimido[4,5-b]indole 2 '-deoxyribonucleoside triphosphates (benzo-fused 7-deaza-dATP analogues): Synthesis, fluorescent properties, enzymatic incorporation into DNA and DNA-protein binding study2016 | Faculty of Science
- Brightly Fluorescent 2'-Deoxyribonucleoside Triphosphates Bearing Methylated Bodipy Fluorophore for in Cellulo Incorporation to DNA, Imaging, and Flow Cytometry2018 | Faculty of Science
- 5-Substituted Pyrimidine and 7-Substituted 7-Deazapurine dNTPs as Substrates for DNA Polymerases in Competitive Primer Extension in the Presence of Natural dNTPs2016 | Faculty of Science
- 2-Substituted 2'-deoxyinosine 5'-triphosphates as substrates for polymerase synthesis of minor-groove-modified DNA and effects on restriction endonuclease cleavage2020 | Faculty of Science
- Trifluoroacetophenone-Linked Nucleotides and DNA for Studying of DNA-Protein Interactions by F-19 NMR Spectroscopy2017 | Faculty of Science
- Enzymatic Synthesis of Base-Functionalized Nucleic Acids for Sensing, Cross-linking, and Modulation of Protein-DNA Binding and Transcription2019 | Faculty of Science
- Synthesis of Dihydroxyalkynyl and Dihydroxyalkyl Nucleotides as Building Blocks or Precursors for Introduction of Diol or Aldehyde Groups to DNA for Bioconjugations2018 | Faculty of Science
- Chloroacetamide-Linked Nucleotides and DNA for Cross-Linking with Peptides and Proteins2016 | Faculty of Science
- Nucleotides Bearing Red Viscosity-Sensitive Dimethoxy-Bodipy Fluorophore for Enzymatic Incorporation and DNA Labeling2023 | Faculty of Science
- Polymerase Synthesis of DNA Containing Iodinated Pyrimidine or 7-Deazapurine Nucleobases and Their Post-synthetic Modifications through the Suzuki-Miyaura Cross-Coupling Reactions2022 | Faculty of Science
- Synthesis of Polycyclic Hetero-Fused 7-Deazapurine Heterocycles and Nucleosides through C-H Dibenzothiophenation and Negishi Coupling2022 | Faculty of Science, Central Library of Charles University
- Influence of major-groove chemical modifications of DNA on transcription by bacterial RNA polymerases2016 | Faculty of Science, Faculty of Mathematics and Physics
- Protected 5-(hydroxymethyl) uracil nucleotides bearing visible-light photocleavable groups as building blocks for polymerase synthesis of photocaged DNA2018 | Faculty of Science
- Epigenetic Pyrimidine Nucleotides in Competition with Natural dNTPs as Substrates for Diverse DNA Polymerases2022 | Faculty of Science, Central Library of Charles University
- Lipid-linked nucleoside triphosphates for enzymatic synthesis of hydrophobic oligonucleotides with enhanced membrane anchoring efficiency2023 | Faculty of Science
- Enzymatic synthesis of hypermodified DNA polymers for sequence-specific display of four different hydrophobic groups2020 | Faculty of Science
- Vicinal Diol-Tethered Nucleobases as Targets for DNA Redox Labeling with Osmate Complexes2020 | Faculty of Science
- Carborane- or Metallacarborane-Linked Nucleotides for Redox Labeling. Orthogonal Multipotential Coding of all Four DNA Bases for Electrochemical Analysis and Sequencing2021 | Faculty of Science
- trans-Cyclooctene- and Bicyclononyne-Linked Nucleotides for Click Modification of DNA with Fluorogenic Tetrazines and Live Cell Metabolic Labeling and Imaging2023 | Faculty of Science
- Electrochemical Detection of Single-Nucleotide Polymorphism Associated with Rifampicin Resistance in Mycobacterium tuberculosis Using Solid-Phase Primer Elongation with Ferrocene-Linked Redox-Labeled Nucleotides2021 | Faculty of Science