Synthesis of Oligonucleotides Containing the N(2)-Deoxyguanosine Adduct of the Dietary Carcinogen 2-Amino-3-methylimidazo[4,5-f]quinoline

Ítems similars

• Conformational Differences of the C8-Deoxyguanosine Adduct of 2-Amino-3-methylimidazo[4,5-f]quinoline (IQ) within the NarI Recognition Sequence
  per: Elmquist, C. Eric, et al.
  Publicat: (2007)
• Translesion Synthesis Past the C8- and N(2)-Deoxyguanosine Adducts of the Dietary Mutagen 2-Amino-3-methylimidazo[4,5-f]quinoline in the NarI Recognition Sequence by Prokaryotic DNA Polymerases
  per: Stover, James S., et al.
  Publicat: (2006)
• The C8-2′-Deoxyguanosine Adduct of 2-Amino-3-methylimidazo[1,2-d]naphthalene, a Carbocyclic Analogue of the Potent Mutagen 2-Amino-3-methylimidazo[4,5-f]quinoline (IQ), is a Block to Replication in Vitro
  per: Christov, Plamen P., et al.
  Publicat: (2010)
• SYNTHESIS OF OLIGONUCLEOTIDES CONTAINING 2′-DEOXYGUANOSINE ADDUCTS OF NITROPYRENES
  per: Colis, Laureen C., et al.
  Publicat: (2009)
• IQ (2-amino-3-methylimidazo[4,5-f]quinoline).
  Publicat: (1993)