Structure, Conformations, and Repair of DNA Adducts from Dibenzo[a,l]pyrene: 32P-Postlabeling and Fluorescence Studies
Author:
Affiliation:
1. Ames Laboratory−USDOE and Department of Chemistry, Iowa State University, Ames, Iowa 50011, Haddow Laboratories, Institute of Cancer Research, Sutton, Surrey SM2 5NG, U.K., and Institute of Toxicology, University of Mainz, D-55131 Mainz, Germany
Publisher
American Chemical Society (ACS)
Subject
Toxicology,General Medicine
Link
https://pubs.acs.org/doi/pdf/10.1021/tx970232k
Reference45 articles.
1. Ralston, S. L., Seidel, A., Luch, A., Platt, K. L., and Baird, W. M. (1995) Stereoselective activation of dibenzo[a,l]pyrene to (−)-anti(11R,12S,13S,14R)- and (+)-syn(11S,12R,13S,14R)-11,12-diol-13,14-epoxides which bind extensively to deoxyadenosine residues of DNA in the human mammary carcinoma cell line MCF-7.Carcinogenesis16, 2899−2907.
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