220 related articles for article (PubMed ID: 20397229)
1. Identification of adducts formed in the reactions of malonaldehyde-glyoxal and malonaldehyde-methylglyoxal with adenosine and calf thymus DNA.
Pluskota-Karwatka D; Pawłowicz AJ; Bruszyńska M; Greszkiewicz A; Latajka R; Kronberg L
Chem Biodivers; 2010 Apr; 7(4):959-74. PubMed ID: 20397229
[TBL] [Abstract][Full Text] [Related]
2. Formation of adducts in the reaction of glyoxal with 2'-deoxyguanosine and with calf thymus DNA.
Pluskota-Karwatka D; Pawłowicz AJ; Tomas M; Kronberg L
Bioorg Chem; 2008 Apr; 36(2):57-64. PubMed ID: 18078668
[TBL] [Abstract][Full Text] [Related]
3. Identification of a novel fluorescent adduct formed in the reaction of malonaldehyde with adenosine.
Backman J; Kronberg L
Chemosphere; 2005 Feb; 58(5):637-43. PubMed ID: 15620757
[TBL] [Abstract][Full Text] [Related]
4. Formation of conjugate adducts in the reactions of malonaldehyde-acetaldehyde and malonaldehyde-formaldehyde with guanosine.
Pluskota-Karwatka D; Le Curieux F; Munter T; Sjöholm R; Kronberg L
Chem Res Toxicol; 2005 Feb; 18(2):300-7. PubMed ID: 15720136
[TBL] [Abstract][Full Text] [Related]
5. Reaction of glyoxal with 2'-deoxyguanosine, 2'-deoxyadenosine, 2'-deoxycytidine, cytidine, thymidine, and calf thymus DNA: identification of DNA adducts.
Olsen R; Molander P; Øvrebø S; Ellingsen DG; Thorud S; Thomassen Y; Lundanes E; Greibrokk T; Backman J; Sjöholm R; Kronberg L
Chem Res Toxicol; 2005 Apr; 18(4):730-9. PubMed ID: 15833033
[TBL] [Abstract][Full Text] [Related]
6. Formation of malonaldehyde-acetaldehyde conjugate adducts in calf thymus DNA.
Pluskota-Karwatka D; Pawłowicz AJ; Kronberg L
Chem Res Toxicol; 2006 Jul; 19(7):921-6. PubMed ID: 16841960
[TBL] [Abstract][Full Text] [Related]
7. Reactions of malonaldehyde and acetaldehyde with calf thymus DNA: formation of conjugate adducts.
Pluskota-Karwatka D; Pawlowicz AJ; Kronberg L
Nucleosides Nucleotides Nucleic Acids; 2007; 26(6-7):567-71. PubMed ID: 18066857
[TBL] [Abstract][Full Text] [Related]
8. Identification of an ethenoformyl adduct formed in the reaction of the potent bacterial mutagen 3-chloro-4-(dichloromethyl)-5-hydroxy-2(5H)-furanone with guanosine.
Munter T; Le Curieux F; Sjöholm R; Kronberg L
Chem Res Toxicol; 1999 Jan; 12(1):46-52. PubMed ID: 9894017
[TBL] [Abstract][Full Text] [Related]
9. Reactions of 9-substituted guanines with bromomalondialdehyde in aqueous solution predominantly yield glyoxal-derived adducts.
Ruohola AM; Koissi N; Andersson S; Lepistö I; Neuvonen K; Mikkola S; Lönnberg H
Org Biomol Chem; 2004 Jul; 2(13):1943-50. PubMed ID: 15227548
[TBL] [Abstract][Full Text] [Related]
10. Reaction of epichlorohydrin with adenosine, 2'-deoxyadenosine and calf thymus DNA: identification of adducts.
Sund P; Kronberg L
Bioorg Chem; 2006 Jun; 34(3):115-30. PubMed ID: 16549090
[TBL] [Abstract][Full Text] [Related]
11. Formation of acrolein adducts with 2'-deoxyadenosine in calf thymus DNA.
Pawłowicz AJ; Munter T; Zhao Y; Kronberg L
Chem Res Toxicol; 2006 Apr; 19(4):571-6. PubMed ID: 16608169
[TBL] [Abstract][Full Text] [Related]
12. Formation of a fluorescent adduct in the reaction of 2'-deoxyadenosine with a malonaldehyde-acetaldehyde condensation product.
Le Curieux F; Pluskota D; Munter T; Sjöholm R; Kronberg L
Chem Res Toxicol; 1998 Sep; 11(9):989-94. PubMed ID: 9760272
[TBL] [Abstract][Full Text] [Related]
13. Mechanisms of formation of adducts from reactions of glycidaldehyde with 2'-deoxyguanosine and/or guanosine.
Golding BT; Slaich PK; Kennedy G; Bleasdale C; Watson WP
Chem Res Toxicol; 1996; 9(1):147-57. PubMed ID: 8924584
[TBL] [Abstract][Full Text] [Related]
14. Analysis of glyoxal-induced DNA cross-links by capillary liquid chromatography nanospray ionization tandem mass spectrometry.
Chen HJ; Chen YC
Chem Res Toxicol; 2009 Jul; 22(7):1334-41. PubMed ID: 19527002
[TBL] [Abstract][Full Text] [Related]
15. Reactions of formaldehyde plus acetaldehyde with deoxyguanosine and DNA: formation of cyclic deoxyguanosine adducts and formaldehyde cross-links.
Cheng G; Shi Y; Sturla SJ; Jalas JR; McIntee EJ; Villalta PW; Wang M; Hecht SS
Chem Res Toxicol; 2003 Feb; 16(2):145-52. PubMed ID: 12588185
[TBL] [Abstract][Full Text] [Related]
16. Identification of fluorescent 2'-deoxyadenosine adducts formed in reactions of conjugates of malonaldehyde and acetaldehyde, and of malonaldehyde and formaldehyde.
Le Curieux F; Pluskota D; Munter T; Sjöholm R; Kronberg L
Chem Res Toxicol; 2000 Dec; 13(12):1228-34. PubMed ID: 11123963
[TBL] [Abstract][Full Text] [Related]
17. Identification of conjugate adducts formed in the reactions of malonaldehyde-acetaldehyde and malonaldehyde-formaldehyde with cytidine.
Pluskota-Karwatka D; Le Curieux F; Munter T; Sjöholm R; Kronberg L
Chem Res Toxicol; 2002 Feb; 15(2):110-7. PubMed ID: 11849036
[TBL] [Abstract][Full Text] [Related]
18. Coupling products of nucleosides with the glyoxal adduct of deoxyguanosine.
Brock AK; Kozekov ID; Rizzo CJ; Harris TM
Chem Res Toxicol; 2004 Aug; 17(8):1047-56. PubMed ID: 15310236
[TBL] [Abstract][Full Text] [Related]
19. Formation of cyclic 1,N2-propanodeoxyguanosine adducts in DNA upon reaction with acrolein or crotonaldehyde.
Chung FL; Young R; Hecht SS
Cancer Res; 1984 Mar; 44(3):990-5. PubMed ID: 6318992
[TBL] [Abstract][Full Text] [Related]
20. High-performance liquid chromatographic determination of glyoxal and methylglyoxal in urine by prederivatization to lumazinic rings using in serial fast scan fluorimetric and diode array detectors.
Espinosa-Mansilla A; Durán-Merás I; Cañada FC; Márquez MP
Anal Biochem; 2007 Dec; 371(1):82-91. PubMed ID: 17884007
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
