N 4-acyl-2′-deoxycytidine-5′-triphosphates for the enzymatic synthesis of modified DNA
Author:
Affiliation:
1. Department of Molecular Microbiology and Biotechnology, Institute of Biochemistry, Life Sciences Center, Vilnius University, Sauletekio al. 7, LT-10257 Vilnius, Lithuania
Funder
Horizon 2020 Research and Innovation Program
Publisher
Oxford University Press (OUP)
Subject
Genetics
Link
http://academic.oup.com/nar/article-pdf/46/12/5911/25844730/gky435.pdf
Reference76 articles.
1. Fluorescent nucleobases as tools for studying DNA and RNA;Xu;Nat. Chem.,2017
2. Synthesis of base-modified 2′-deoxyribonucleoside triphosphates and their use in enzymatic synthesis of modified DNA for applications in bioanalysis and chemical biology;Hocek;J. Org. Chem.,2014
3. Synthesis of pyridone-based nucleoside analogues as substrates or inhibitors of DNA polymerases;Tauraitė;Nucleosides Nucleotides Nucleic Acids,2016
4. The toolbox for modified aptamers;Lapa;Mol. Biotechnol.,2016
5. Molecular evolution of functional nucleic acids with chemical modifications;Kuwahara;Molecules,2010
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1. Oligonucleotide‐Based Photoaffinity Probes: Chemical Tools and Applications for Protein Labeling;ChemBioChem;2024-07-02
2. Facilitated Synthetic Access to Boronic Acid-Modified Nucleoside Triphosphates and Compatibility with Enzymatic DNA Synthesis;Synlett;2023-11-16
3. Photochemical and Single Electron Transfer Generation of 2′-Deoxycytidin-N4-yl Radical from Oxime Esters;The Journal of Organic Chemistry;2023-05-23
4. Cytidine deaminases catalyze the conversion of N ( S , O ) 4 -substituted pyrimidine nucleosides;Science Advances;2023-02-03
5. Enzymatic Synthesis of Base-Modified Nucleic Acids;Handbook of Chemical Biology of Nucleic Acids;2023
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