Basic aspects of the biochemical reactivity of 4-hydroxynonenal
- 27 June 2003
- journal article
- review article
- Published by Elsevier in Molecular Aspects of Medicine
- Vol. 24 (4-5) , 149-159
- https://doi.org/10.1016/s0098-2997(03)00009-8
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Antioxidative Function and Substrate Specificity of NAD(P)H- dependent Alkenal/one OxidoreductaseJournal of Biological Chemistry, 2001
- Detection of 1,N2-propanodeoxyguanosine adducts of trans-4-hydroxy-2-nonenal after gavage of trans-4-hydroxy-2-nonenal or induction of lipid peroxidation with carbon tetrachloride in F344 ratsChemico-Biological Interactions, 2001
- Effect of 4‐hydroxy‐2(E)‐nonenal on soybean lipoxygenase‐1Lipids, 2001
- Two Distinct Pathways of Formation of 4-HydroxynonenalJournal of Biological Chemistry, 2001
- Protection by thiols of the mitochondrial complexes from 4-hydroxy-2-nonenalFree Radical Biology & Medicine, 2001
- Selective protection by stably transfected human ALDH3A1 (but not human ALDH1A1) against toxicity of aliphatic aldehydes in V79 cellsChemico-Biological Interactions, 2001
- Oxidative Stress Induces Increase in Intracellular Amyloid β-Protein Production and Selective Activation of βI and βII PKCs in NT2 CellsBiochemical and Biophysical Research Communications, 2000
- Independent Synthesis, Solution Behavior, and Studies on the Mechanism of Formation of a Primary Amine-Derived Fluorophore Representing Cross-linking of Proteins by (E)-4-Hydroxy-2-nonenalThe Journal of Organic Chemistry, 1999
- Regulation of Rat Hepatocyte Protein Kinase C β Isoenzymes by the Lipid Peroxidation Product 4–Hydroxy–2,3–Nonenal: A Signaling Pathway to Modulate Vesicular Transport of GlycoproteinsHepatology, 1999
- 2,3-epoxy-4-hydroxynonanal, a potential lipid peroxidation product for etheno adduct formation, is not a substrate of human epoxide hydrolaseCarcinogenesis: Integrative Cancer Research, 1998