The lipid peroxidation product 4-hydroxynonenal is a potent inducer of the SOS response

This publication has 29 references indexed in Scilit:

• Identification and characterization of deoxyguanosine adducts of methyl vinyl ketone and ethyl vinyl ketone. Genotoxicity of the ketones in the SOS chromotest
  Chemical Research in Toxicology, 1991
• Possible mutagens derived from lipids and lipid precursors
  Mutation Research/Reviews in Genetic Toxicology, 1990
• Comparison of rates of enzymic oxidation of aflatoxin B1, aflatoxin G1, and sterigmatocystin and activities of the epoxides in forming guanyl-N7 adducts and inducing different genetic responses
  Chemical Research in Toxicology, 1989
• Methods for determination of aldehydic lipid peroxidation products
  Free Radical Biology & Medicine, 1989
• Identification of N-(2-propenal)ethanolamine as a urinary metabolite of malondialdehyde
  Free Radical Biology & Medicine, 1989
• Identification of N‐ε‐(2‐propenal)lysine as a major urinary metabolite of malondialdehyde
  Lipids, 1988
• Study of reactions of .alpha.,.beta.-unsaturated carbonyl compounds with deoxyguanosine
  The Journal of Organic Chemistry, 1988
• Identification of adducts formed by reaction of guanine nucleosides with malondialdehyde and structurally related aldehydes
  Chemical Research in Toxicology, 1988
• Fresh tomato aroma volatiles: a quantitative study
  Journal of Agricultural and Food Chemistry, 1987
• Dissociation of malondialdehyde mutagenicity in Salmonella typhimurium from its ability to induce interstrand DNA cross-links
  Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 1984