99 related articles for article (PubMed ID: 10409406)
1. Modification of histidine residues by 4,5-epoxy-2-alkenals.
Zamora R; Alaiz M; Hidalgo FJ
Chem Res Toxicol; 1999 Jul; 12(7):654-60. PubMed ID: 10409406
[TBL] [Abstract][Full Text] [Related]
2. Strecker-type degradation of phenylalanine by methyl 9,10-epoxy-13-oxo-11-octadecenoate and methyl 12,13-epoxy-9-oxo-11-octadecenoate.
Zamora R; Gallardo E; Navarro JL; Hidalgo FJ
J Agric Food Chem; 2005 Jun; 53(11):4583-8. PubMed ID: 15913329
[TBL] [Abstract][Full Text] [Related]
3. Phosphatidylethanolamine modification by oxidative stress product 4,5(E)-epoxy-2(E)-heptenal.
Zamora R; Hidalgo FJ
Chem Res Toxicol; 2003 Dec; 16(12):1632-41. PubMed ID: 14680378
[TBL] [Abstract][Full Text] [Related]
4. Stereoselective formation of in vitro nucleic acid adducts by 2,3-epoxy-4-hydroxynonanal.
Sodum RS; Chung FL
Cancer Res; 1991 Jan; 51(1):137-43. PubMed ID: 1703030
[TBL] [Abstract][Full Text] [Related]
5. Identification of advanced reaction products originating from the initial 4-oxo-2-nonenal-cysteine Michael adducts.
Shimozu Y; Shibata T; Ojika M; Uchida K
Chem Res Toxicol; 2009 May; 22(5):957-64. PubMed ID: 19368367
[TBL] [Abstract][Full Text] [Related]
6. Modification of bovine serum albumin structure following reaction with 4,5(E)-epoxy-2(E)-heptenal.
Hidalgo FJ; Zamora R
Chem Res Toxicol; 2000 Jun; 13(6):501-8. PubMed ID: 10858323
[TBL] [Abstract][Full Text] [Related]
7. Quantitative analysis of acrolein-specific adducts generated during lipid peroxidation-modification of proteins in vitro: identification of N(τ)-(3-propanal)histidine as the major adduct.
Maeshima T; Honda K; Chikazawa M; Shibata T; Kawai Y; Akagawa M; Uchida K
Chem Res Toxicol; 2012 Jul; 25(7):1384-92. PubMed ID: 22716039
[TBL] [Abstract][Full Text] [Related]
8. Structural characterization of diastereoisomeric ethano adducts derived from the reaction of 2'-deoxyguanosine with trans,trans-2,4-decadienal.
Loureiro AP; de Arruda Campos IP; Gomes OF; di Mascio P; Medeiros MH
Chem Res Toxicol; 2004 May; 17(5):641-9. PubMed ID: 15144221
[TBL] [Abstract][Full Text] [Related]
9. A spectrophotometric method for the determination of proteins damaged by oxidized lipids.
Hidalgo FJ; Alaiz M; Zamora R
Anal Biochem; 1998 Sep; 262(2):129-36. PubMed ID: 9750127
[TBL] [Abstract][Full Text] [Related]
10. Strecker-type degradation produced by the lipid oxidation products 4,5-epoxy-2-alkenals.
Hidalgo FJ; Zamora R
J Agric Food Chem; 2004 Nov; 52(23):7126-31. PubMed ID: 15537327
[TBL] [Abstract][Full Text] [Related]
11. Detoxification of cytotoxic alpha,beta-unsaturated aldehydes by carnosine: characterization of conjugated adducts by electrospray ionization tandem mass spectrometry and detection by liquid chromatography/mass spectrometry in rat skeletal muscle.
Aldini G; Granata P; Carini M
J Mass Spectrom; 2002 Dec; 37(12):1219-28. PubMed ID: 12489081
[TBL] [Abstract][Full Text] [Related]
12. 2-Alkylpyrrole formation from 4,5-epoxy-2-alkenals.
Zamora R; Hidalgo FJ
Chem Res Toxicol; 2005 Feb; 18(2):342-8. PubMed ID: 15720141
[TBL] [Abstract][Full Text] [Related]
13. Chemical conversion of alpha-amino acids into alpha-keto acids by 4,5-epoxy-2-decenal.
Zamora R; Navarro JL; Gallardo E; Hidalgo FJ
J Agric Food Chem; 2006 Aug; 54(16):6101-5. PubMed ID: 16881723
[TBL] [Abstract][Full Text] [Related]
14. A new approach for measuring protein adducts from benzo[a]pyrene diolepoxide by high performance liquid chromatography/tandem mass spectrometry.
Helleberg H; Törnqvist M
Rapid Commun Mass Spectrom; 2000; 14(18):1644-53. PubMed ID: 10962485
[TBL] [Abstract][Full Text] [Related]
15. Epoxyalkenal-trapping ability of phenolic compounds.
Zamora R; Aguilar I; Hidalgo FJ
Food Chem; 2017 Dec; 237():444-452. PubMed ID: 28764018
[TBL] [Abstract][Full Text] [Related]
16. Characterization and quantification of cysteinyl adducts of benzene diol epoxide.
Waidyanatha S; Sangaiah R; Rappaport SM
Chem Res Toxicol; 2005 Jul; 18(7):1178-85. PubMed ID: 16022511
[TBL] [Abstract][Full Text] [Related]
17. 2-Alkenal modification of hemoglobin: Identification of a novel hemoglobin-specific alkanoic acid-histidine adduct.
Yoshitake J; Shibata T; Shimayama C; Uchida K
Redox Biol; 2019 May; 23():101115. PubMed ID: 30819615
[TBL] [Abstract][Full Text] [Related]
18. Amine degradation by 4,5-epoxy-2-decenal in model systems.
Zamora R; Gallardo E; Hidalgo FJ
J Agric Food Chem; 2006 Mar; 54(6):2398-404. PubMed ID: 16536625
[TBL] [Abstract][Full Text] [Related]
19. Modification of histidine residues in proteins by reaction with 4-hydroxynonenal.
Uchida K; Stadtman ER
Proc Natl Acad Sci U S A; 1992 May; 89(10):4544-8. PubMed ID: 1584790
[TBL] [Abstract][Full Text] [Related]
20. Synthesis and characterization of styrene oxide adducts with cysteine, histidine, and lysine in human globin.
Jágr M; Mráz J; Linhart I; Stránský V; Pospísil M
Chem Res Toxicol; 2007 Oct; 20(10):1442-52. PubMed ID: 17867648
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]