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Original Articles

Cg Base Pair Recognition Within Dna Triple Helices Using N-Methyl-3H-Pyrrolo[2,3-d]Pyrimidin-2(7H)-One Nucleoside Analogues

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Pages 1363-1367 | Published online: 05 Dec 2007

REFERENCES

  • Praseuth , D. , Guieysse , A. L. and Helene , C. 1999 . Triple helix formation and the antigene strategy for sequence-specific control of gene expression . Biochimica et Biophysica Acta , 1489 : 181 – 206 .
  • Karympalis , V. , Kalopita , K. , Zarros , A. and Carageorgiou , H. 2004 . Regulation of gene expression via triple helical formations . Biochemistry (Moscow) , 69 : 855 – 860 .
  • Moser , H. E. and Dervan , P. B. 1987 . Sequence-specific cleavage of double helical DNA by triple helix formation . Science , 238 : 645 – 650 .
  • Seidman , M. M. and Glazer , P. M. 2003 . The potential for gene repair via triple helix formation . J. Clin. Invest. , 112 : 487 – 494 .
  • Gowers , D. M. and Fox , K. R. 1999 . Towards mixed sequence recognition by triple helix formation . Nucleic Acids Res. , 27 : 1569 – 1577 .
  • Fox , K. R. 2000 . Targeting DNA with triplexes . Curr. Med. Chem. , 7 : 17 – 37 .
  • Prevót-Halter , I. and Leumann , C. J. 1999 . Selective recognition of a C-G base pair in the Parallel DNA triple-helical binding motif . Ang. Chem. Int. Ed. , 43 : 2657 – 2660 .
  • Ranasinghe , R. T. , Rusling , D. A. , Powers , V. E.C. , Fox , K. R. and Brown , T. 2005 . Recognition of CG inversions in DNA triple helices by methylated 3H-pyrrolo[2,3-d]pyrimidin-2(7H)-one nucleoside analogues . Chem. Comm. , : 2555 – 2557 .
  • Hobbs , F. W. Jr. 1989 . Palladium-catalyzed synthesis of alkynylamino nucleoside. A universal linker for nucleic acids . J. Org. Chem. , 54 : 3420 – 3422 .
  • McGuigan , C. , Barucki , H. , Blewett , S. , Carangio , A. , Erichsen , J. T. , Andrei , G. , Snck , R. , De Clercq , E. and Balzarini , J. 2000 . Highly potent and selective inhibition of varicella-zoster virus by bicyclic furopyrimidine nucleosides bearing an aryl side chain . J. Med. Chem. , 43 : 4993 – 4997 .

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