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...

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Xehetasun bibliografikoak
Egile Nagusiak: Durland, R H, Rao, T S, Bodepudi, V, Seth, D M, Jayaraman, K, Revankar, G R
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 1995
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC306733/
https://ncbi.nlm.nih.gov/pubmed/7899086
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