Predominance of the 1,N2-propano 2′-deoxyguanosine adduct among 4-hydroxy-2-nonenal-induced DNA lesions
- 1 July 2004
- journal article
- Published by Elsevier in Free Radical Biology & Medicine
- Vol. 37 (1) , 62-70
- https://doi.org/10.1016/j.freeradbiomed.2004.04.013
Abstract
No abstract availableKeywords
This publication has 53 references indexed in Scilit:
- Oxy radicals, lipid peroxidation and DNA damageToxicology, 2002
- Lipid hydroperoxide-mediated DNA damageExperimental Gerontology, 2001
- Formation of 1,N6-Ethenoadenine and 3,N4-Ethenocytosine by Lipid Peroxidation Products and Nucleic Acid BasesChemical Research in Toxicology, 1995
- Identification and characterization of deoxyguanosine adducts of mutagenic .beta.-alkyl-substituted acrolein congenersChemical Research in Toxicology, 1993
- The possible role of α,β-unsaturated carbonyl compounds in mutagenesis and carcinogenesisToxicology Letters, 1993
- Chemistry and biochemistry of 4-hydroxynonenal, malonaldehyde and related aldehydesFree Radical Biology & Medicine, 1991
- Possible mutagens derived from lipids and lipid precursorsMutation Research/Reviews in Genetic Toxicology, 1990
- Structural characterization of adducts formed in the reaction of 2,3-epoxy-4-hydroxynonanal with deoxyguanosineChemical Research in Toxicology, 1989
- Identification of adducts formed by reaction of guanine nucleosides with malondialdehyde and structurally related aldehydesChemical Research in Toxicology, 1988
- STRUCTURE OF A NEW MODIFIED NUCLEOSIDE FORMED BY GUANOSINE-MALONALDEHYDE REACTIONChemistry Letters, 1981