Azole substituted oligonucleotides promote antiparallel triplex formation at non-homopurine duplex targets.
The ability of certain azole substituted oligodeoxy-ribonucleotides to promote antiparallel triple helix formation with duplex targets having CG or TA interruptions in the otherwise homopurine sequence was examined. 2'-Deoxyribonucleosides of the azoles, which include pyrazole, imidazole, 1,2,4-tria...
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| Vydáno v: | Nucleic Acids Res |
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| Hlavní autoři: | , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Oxford University Press
1995
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| On-line přístup: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC306733/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7899086/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/23.4.647 |
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