Hybridization properties of the 5-methyl-isocytidine/isoguanosine base pair in synthetic oligodeoxynucleotides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference12 articles.
1. Enzymatic incorporation of a new base pair into DNA and RNA extends the genetic alphabet
2. Enzymic recognition of the base pair between isocytidine and isoguanosine
3. Site-specific enzymic incorporation of an unnatural base, N6-(6-aminohexyl)isoguanosine, into RNA
4. Theoretical investigations of novel nucleic acid bases
5. Transient protection: efficient one-flask syntheses of protected deoxynucleosides
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1. The Base Pairs of Isoguanine and 8-Aza-7-deazaisoguanine with 5-Methylisocytosine as Targets for DNA Functionalization;Bioconjugate Chemistry;2023-02-03
2. 7,8-Dihydro-8-oxo-1,N6-ethenoadenine: an exclusively Hoogsteen-paired thymine mimic in DNA that induces A→T transversions in Escherichia coli;Nucleic Acids Research;2022-03-02
3. Engineering polymerases for applications in synthetic biology;Quarterly Reviews of Biophysics;2020
4. The development of isoguanosine: from discovery, synthesis, and modification to supramolecular structures and potential applications;RSC Advances;2020
5. Enhanced Stability of DNA Nanostructures by Incorporation of Unnatural Base Pairs;ChemPhysChem;2017-09-22
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