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252 related items for PubMed ID: 15257618
1. Synthesis, characterization, and identification of N7-guanine adducts of isoprene monoepoxides in vitro. Begemann P, Christova-Georgieva NI, Sangaiah R, Koc H, Zhang D, Golding BT, Gold A, Swenberg JA. Chem Res Toxicol; 2004 Jul; 17(7):929-36. PubMed ID: 15257618 [Abstract] [Full Text] [Related]
2. Identification and characterization of 2'-deoxyadenosine adducts formed by isoprene monoepoxides in vitro. Begemann P, Boysen G, Georgieva NI, Sangaiah R, Koshlap KM, Koc H, Zhang D, Golding BT, Gold A, Swenberg JA. Chem Res Toxicol; 2011 Jul 18; 24(7):1048-61. PubMed ID: 21548641 [Abstract] [Full Text] [Related]
3. HPLC-ESI+-MS/MS analysis of N7-guanine-N7-guanine DNA cross-links in tissues of mice exposed to 1,3-butadiene. Goggin M, Loeber R, Park S, Walker V, Wickliffe J, Tretyakova N. Chem Res Toxicol; 2007 May 18; 20(5):839-47. PubMed ID: 17455958 [Abstract] [Full Text] [Related]
4. Molecular dosimetry of N-7 guanine adduct formation in mice and rats exposed to 1,3-butadiene. Koc H, Tretyakova NY, Walker VE, Henderson RF, Swenberg JA. Chem Res Toxicol; 1999 Jul 18; 12(7):566-74. PubMed ID: 10409395 [Abstract] [Full Text] [Related]
5. Adducts of N-terminal valines in hemoglobin with isoprene diepoxide, a metabolite of isoprene. Fred C, Cantillana T, Henderson AP, Golding BT, Törnqvist M. Rapid Commun Mass Spectrom; 2004 Jul 18; 18(18):2177-84. PubMed ID: 15378724 [Abstract] [Full Text] [Related]
6. Stereochemical and kinetic comparisons of mono- and diepoxide formation in the in vitro metabolism of isoprene by liver microsomes from rats, mice, and humans. Golding BT, Cottrell L, Mackay D, Zhang D, Watson WP. Chem Res Toxicol; 2003 Jul 18; 16(7):933-44. PubMed ID: 12870896 [Abstract] [Full Text] [Related]
7. Macromolecular adducts of butadiene. Tretyakova NYu, Lin YP, Upton PB, Sangaiah R, Swenberg JA. Toxicology; 1996 Oct 28; 113(1-3):70-6. PubMed ID: 8901884 [Abstract] [Full Text] [Related]
8. 1,3-butadiene: cancer, mutations, and adducts. Part IV: Molecular dosimetry of 1,3-butadiene. Blair IA, Oe T, Kambouris S, Chaudhary AK. Res Rep Health Eff Inst; 2000 Mar 28; (92):151-90; discussion 211-9. PubMed ID: 10925841 [Abstract] [Full Text] [Related]
9. Butadiene diolepoxide- and diepoxybutane-derived DNA adducts at N7-guanine: a high occurrence of diolepoxide-derived adducts in mouse lung after 1,3-butadiene exposure. Koivisto P, Kilpeläinen I, Rasanen I, Adler ID, Pacchierotti F, Peltonen K. Carcinogenesis; 1999 Jul 28; 20(7):1253-9. PubMed ID: 10383898 [Abstract] [Full Text] [Related]
10. Identification of adducts produced by the reaction of 4-(acetoxymethylnitrosamino)-1-(3-pyridyl)-1-butanol with deoxyguanosine and DNA. Upadhyaya P, Sturla SJ, Tretyakova N, Ziegel R, Villalta PW, Wang M, Hecht SS. Chem Res Toxicol; 2003 Feb 28; 16(2):180-90. PubMed ID: 12588189 [Abstract] [Full Text] [Related]
11. Identification of adducts derived from reactions of (1-chloroethenyl)oxirane with nucleosides and calf thymus DNA. Munter T, Cottrell L, Hill S, Kronberg L, Watson WP, Golding BT. Chem Res Toxicol; 2002 Dec 28; 15(12):1549-60. PubMed ID: 12482237 [Abstract] [Full Text] [Related]
12. Capillary HPLC-accurate mass MS/MS quantitation of N7-(2,3,4-trihydroxybut-1-yl)-guanine adducts of 1,3-butadiene in human leukocyte DNA. Sangaraju D, Villalta P, Goggin M, Agunsoye MO, Campbell C, Tretyakova N. Chem Res Toxicol; 2013 Oct 21; 26(10):1486-97. PubMed ID: 23937706 [Abstract] [Full Text] [Related]
14. Identification and quantitation of DNA adducts from calf thymus DNA exposed to 3,4-epoxy-1-butene. Tretyakova N, Lin Y, Sangaiah R, Upton PB, Swenberg JA. Carcinogenesis; 1997 Jan 21; 18(1):137-47. PubMed ID: 9054600 [Abstract] [Full Text] [Related]
15. Synthesis of DNA oligodeoxynucleotides containing structurally defined N6-(2-hydroxy-3-buten-1-yl)-adenine adducts of 3,4-epoxy-1-butene. Dorr DQ, Murphy K, Tretyakova N. Chem Biol Interact; 2007 Mar 20; 166(1-3):104-11. PubMed ID: 16765925 [Abstract] [Full Text] [Related]
16. Quantitative analysis of 1,3-butadiene-induced DNA adducts in vivo and in vitro using liquid chromatography electrospray ionization tandem mass spectrometry. Tretyakova NYu, Chiang SY, Walker VE, Swenberg JA. J Mass Spectrom; 1998 Apr 20; 33(4):363-76. PubMed ID: 9597770 [Abstract] [Full Text] [Related]
19. Identification of adducts formed by pyridyloxobutylation of deoxyguanosine and DNA by 4-(acetoxymethylnitrosamino)-1-(3-pyridyl)-1-butanone, a chemically activated form of tobacco specific carcinogens. Wang M, Cheng G, Sturla SJ, Shi Y, McIntee EJ, Villalta PW, Upadhyaya P, Hecht SS. Chem Res Toxicol; 2003 May 20; 16(5):616-26. PubMed ID: 12755591 [Abstract] [Full Text] [Related]