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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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| Hlavní autoři: | , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
1995
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| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC306733/ https://ncbi.nlm.nih.gov/pubmed/7899086 |
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