Alary J - Search Results

1

Enzyme immunoassay for a urinary metabolite of 4-hydroxynonenal as a marker of lipid peroxidation.

Guéraud F, Peiro G, Bernard H, Alary J, Créminon C, Debrauwer L, Rathahao E, Drumare MF, Canlet C, Wal JM, Bories G. Guéraud F, et al. Among authors: alary j. Free Radic Biol Med. 2006 Jan 1;40(1):54-62. doi: 10.1016/j.freeradbiomed.2005.08.011. Epub 2005 Sep 2. Free Radic Biol Med. 2006. PMID: 16337879

2

Identification of intermediate pathways of 4-hydroxynonenal metabolism in the rat.

Alary J, Fernandez Y, Debrauwer L, Perdu E, Guéraud F. Alary J, et al. Chem Res Toxicol. 2003 Mar;16(3):320-7. doi: 10.1021/tx025671k. Chem Res Toxicol. 2003. PMID: 12641432

3

Fate of 4-hydroxynonenal in vivo: disposition and metabolic pathways.

Alary J, Guéraud F, Cravedi JP. Alary J, et al. Mol Aspects Med. 2003 Aug-Oct;24(4-5):177-87. doi: 10.1016/s0098-2997(03)00012-8. Mol Aspects Med. 2003. PMID: 12892995 Review.

4

Dihydroxynonene mercapturic acid, a urinary metabolite of 4-hydroxynonenal, as a biomarker of lipid peroxidation.

Peiro G, Alary J, Cravedi JP, Rathahao E, Steghens JP, Guéraud F. Peiro G, et al. Among authors: alary j. Biofactors. 2005;24(1-4):89-96. doi: 10.1002/biof.5520240110. Biofactors. 2005. PMID: 16403967

5

Mercapturic acid conjugates as urinary end metabolites of the lipid peroxidation product 4-hydroxy-2-nonenal in the rat.

Alary J, Bravais F, Cravedi JP, Debrauwer L, Rao D, Bories G. Alary J, et al. Chem Res Toxicol. 1995 Jan-Feb;8(1):34-9. doi: 10.1021/tx00043a004. Chem Res Toxicol. 1995. PMID: 7703364

6

Liquid chromatography-multistage tandem mass spectrometry for the quantification of dihydroxynonene mercapturic acid (DHN-MA), a urinary end-metabolite of 4-hydroxynonenal.

Rathahao E, Peiro G, Martins N, Alary J, Guéraud F, Debrauwer L. Rathahao E, et al. Among authors: alary j. Anal Bioanal Chem. 2005 Apr;381(8):1532-9. doi: 10.1007/s00216-005-3095-6. Epub 2005 Mar 16. Anal Bioanal Chem. 2005. PMID: 15770473

7

Enantioselective metabolism of (R)- and (S)-4-hydroxy-2-nonenal in rat.

Guéraud F, Crouzet F, Alary J, Rao D, Debrauwer L, Laurent F, Cravedi JP. Guéraud F, et al. Among authors: alary j. Biofactors. 2005;24(1-4):97-104. doi: 10.1002/biof.5520240111. Biofactors. 2005. PMID: 16403968

8

Chloramphenicol oxamylethanolamine as an end product of chloramphenicol metabolism in rat and humans: evidence for the formation of a phospholipid adduct.

Cravedi JP, Perdu-Durand E, Baradat M, Alary J, Debrauwer L, Bories G. Cravedi JP, et al. Among authors: alary j. Chem Res Toxicol. 1995 Jul-Aug;8(5):642-8. doi: 10.1021/tx00047a003. Chem Res Toxicol. 1995. PMID: 7548746

9

1,4-Dihydroxynonene mercapturic acid, the major end metabolite of exogenous 4-hydroxy-2-nonenal, is a physiological component of rat and human urine.

Alary J, Debrauwer L, Fernandez Y, Cravedi JP, Rao D, Bories G. Alary J, et al. Chem Res Toxicol. 1998 Feb;11(2):130-5. doi: 10.1021/tx970139w. Chem Res Toxicol. 1998. PMID: 9511904

10

Identification of novel urinary metabolites of the lipid peroxidation product 4-hydroxy-2-nonenal in rats.

Alary J, Debrauwer L, Fernandez Y, Paris A, Cravedi JP, Dolo L, Rao D, Bories G. Alary J, et al. Chem Res Toxicol. 1998 Nov;11(11):1368-76. doi: 10.1021/tx980068g. Chem Res Toxicol. 1998. PMID: 9815199

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