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...

Täydet tiedot

Bibliografiset tiedot

Julkaisussa:	Nucleic Acids Res
Päätekijät:	Durland, R H, Rao, T S, Bodepudi, V, Seth, D M, Jayaraman, K, Revankar, G R
Aineistotyyppi:	Artigo
Kieli:	Inglês
Julkaistu:	Oxford University Press 1995
Linkit:	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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