Selectivity of DNA polymerases toward α and β nucleotide substrates ofdandlseries

This publication has 15 references indexed in Scilit:

• Synthesis of the four possible stereoisomeric 5′-nor carbocyclic nucleosides from one common enantiomerically pure starting material
  Tetrahedron Letters, 1994
• Modified nucleoside 5'-triphosphates containing 2',3'-fused threemembered rings as substrates for different DNA polymerases
  FEBS Letters, 1993
• Formation of phosphonester bonds catalyzed by DNA polymerase
  Nucleic Acids Research, 1992
• The potential of carbocyclic nucleosides for the treatment of AIDS: synthesis of some diphosphorylphosphonates possessing potent activity against HIV-coded reverse transcriptase
  Journal of the Chemical Society, Perkin Transactions 1, 1992
• Deoxyribonucleotide analogs as inhibitors and substrates of DNA polymerases
  Pharmacology & Therapeutics, 1990
• Comparison of the effect of Carbovir, AZT, and dideoxynucleoside triphosphates on the activity of human immunodeficiency virus reverse transcriptase and selected human polymerases
  Biochemical and Biophysical Research Communications, 1989
• Selective Inhibition of DNA Chain Elongation Catalyzed by DNA Polymerases
  Nucleosides and Nucleotides, 1988
• Biochemical and physical characterization of an unmodified yeast phenylalanine transfer RNA transcribed in vitro.
  Proceedings of the National Academy of Sciences, 1988
• Inhibition of HIV-associated reverse transcriptase by sugar-modified derivatives of thymidine 5′-triphosphate in comparison to cellular DNA polymerases α and β
  Biochemical and Biophysical Research Communications, 1987
• Properties of 2′,3′‐dideoxy‐2′,3′‐dehydrothymidine 5′‐triphosphate in terminating DNA synthesis catalyzed by several different DNA polymerases
  FEBS Letters, 1987