Mutagenicity of benzo[a]pyrene–deoxyadenosine adducts in a sequence context derived from the p53 gene

This publication has 18 references indexed in Scilit:

• Sequence Context Effects on Mutational Properties of cis-Opened Benzo[c]phenanthrene Diol Epoxide−Deoxyadenosine Adducts in Site-Specific Mutation Studies
  Biochemistry, 1998
• Sequence Context Profoundly Influences the Mutagenic Potency of Trans-Opened Benzo[a]pyrene 7,8-Diol 9,10-Epoxide−Purine Nucleoside Adducts in Site-Specific Mutation Studies
  Biochemistry, 1998
• How Stereochemistry Affects Mutagenesis by N²-Deoxyguanosine Adducts of 7,8-Dihydroxy-9,10-epoxy-7,8,9,10-tetrahydrobenzo[a]pyrene: Configuration of the Adduct Bond Is More Important Than Those of the Hydroxyl Groups
  Biochemistry, 1997
• Sequence Specific Mutagenesis of the Major (+)-anti-Benzo[a]pyrene Diol Epoxide−DNA Adduct at a Mutational Hot Spot in Vitro and in Escherichia coli Cells
  Chemical Research in Toxicology, 1997
• Preferential Formation of Benzo[ a ]pyrene Adducts at Lung Cancer Mutational Hotspots in P53
  Science, 1996
• Fidelity of Translesional Synthesis past Benzo[a]pyrene Diol Epoxide−2‘-Deoxyguanosine DNA Adducts: Marked Effects of Host Cell, Sequence Context, and Chirality
  Biochemistry, 1996
• The Major, N2-Gua Adduct of the (+)-anti-Benzo[a]pyrene Diol Epoxide Is Capable of Inducing G.fwdarw.A and G.fwdarw.C, in Addition to G.fwdarw.T, Mutations
  Biochemistry, 1995
• Synthesis of Oligonucleotide Adducts of the Bay Region Diol Epoxide Metabolites of Carcinogenic Polycyclic Aromatic Hydrocarbons
  The Journal of Organic Chemistry, 1995
• Mutagenesis by (+)-anti-B[α]P-N²-Gua, the major adduct of activated benzo[α]pyrene, when studied in an Escherichia coli plasmid using site-directed methods
  Carcinogenesis: Integrative Cancer Research, 1992
• DNA adducts from carcinogenic and noncarcinogenic enantiomers of benzo[a]pyrenedihydrodiol epoxide
  Chemical Research in Toxicology, 1989