N-(Guanidinoethyl)-2′-deoxy-5-methylisocytidine exhibits selective recognition of a CG interrupting site for the formation of anti-parallel triplexes

Hidenori Okamura, Yosuke Taniguchi, Shigeki Sasaki
  • Organic & Biomolecular Chemistry, January 2013, Royal Society of Chemistry
  • DOI: 10.1039/c3ob40472b
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