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Excision repair reduces doxorubicin-induced genotoxicity

  • Published:1993-10 Issue:3 Volume:294 Page:215-222
  • ISSN:0921-8777
  • Container-title:Mutation Research/DNA Repair
  • language:en
  • Short-container-title:Mutation Research/DNA Repair

Author:

Anderson Russell D.,Veigl Martina L.,Baxter Jeff,David Sedwick W.

Publisher

Elsevier BV

Subject

Genetics,Toxicology,Molecular Biology

Reference27 articles.

1. DNA sequence specificity of doxorubicin-induced mutational damage in uvrB−Escherichia coli;Anderson;Cancer Res.,1991

2. Optimization of double-stranded DNA sequencing for polymerase chain reaction products;Anderson;Coments,1992

3. Optimization of double-stranded DNA sequencing for polymerase chain reaction products;Anderson;Comments,1992

4. Selective displacement of nuclear proteins by antitumor drugs having affinity for nucleic acids;Bartkowiak,1989

5. Genetic and sequence analysis of frameshift mutations induced by ICR-191;Calos;J. Mol. Biol.,1981

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1. Evaluation of chemical mutagenicity using next generation sequencing: A review;Journal of Environmental Science and Health, Part C;2017-06-09

2. CHAPTER 7. Antineoplastic Drugs;Issues in Toxicology;2012

3. Prokaryotic Nucleotide Excision Repair:  The UvrABC System;Chemical Reviews;2006-01-28

4. ‘Close-fitting sleeves’: DNA damage recognition by the UvrABC nuclease system;Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis;2005-09

5. Mismatch repair and drug responses in cancer;Drug Resistance Updates;1999-10
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