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Targeting pyrimidine single strands by triplex formation: structural optimization of binding.

Recent reports describe a new strategy for the binding of single-stranded pyrimidine sequences by triple helix formation. In this approach, a double-length purine-rich oligonucleotide binds a target strand, folding back to form an antiparallel pur.pur.pyr triple helix. We now describe a series of st...

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Bibliográfalaš dieđut
Publikašuvnnas:Nucleic Acids Res
Váldodahkkit: Vo, T, Wang, S, Kool, E T
Materiálatiipa: Artigo
Giella:Inglês
Almmustuhtton: Oxford University Press 1995
Liŋkkat:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC307133/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7544889/
https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/23.15.2937
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