Frameshift mutagenesis by 9-aminoacridine, ICR191, AMSA and related experimental antitumour acridines in recA+ and recA1 strains of Salmonella typhimurium

This publication has 7 references indexed in Scilit:

• The relationship between frameshift mutagenicity and DNA-binding affinity in a series of acridine-substituted derivatives of the experimental antitumour drug 4′-(9-acridinylamino)methanesulphonanilide (AMSA)
  Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 1981
• Inhibition of T4 bacteriophage yield by 9-anilinoacridines; comparison with in vivo antitumour activity
  Published by Elsevier ,1980
• 4′-(9-Acridinylamino) Methanesulfon-m-Anisidide (AMSA): A New Drug Effective in the Treatment of Adult Acute Leukemia
  Annals of Internal Medicine, 1980
• Segregation of the mutator property of plasmid R46 from its ultraviolet-protecting property
  Molecular Genetics and Genomics, 1979
• Methods for detecting carcinogens and mutagens with the salmonella/mammalian-microsome mutagenicity test
  Mutation Research/Environmental Mutagenesis and Related Subjects, 1975
• Antitumor and mutagenic properties of a variety of heterocyclic nitrogen and sulfur mustards
  Journal of Medicinal Chemistry, 1972