These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
143 related items for PubMed ID: 10490495
1. Synthesis and structure determination of the adducts formed by electrochemical oxidation of Dibenzo[a,l]pyrene in the presence of adenine. Li KM, Byun J, Gross ML, Zamzow D, Jankowiak R, Rogan EG, Cavalieri EL. Chem Res Toxicol; 1999 Sep; 12(9):749-57. PubMed ID: 10490495 [Abstract] [Full Text] [Related]
2. Synthesis and structure determination of the adducts formed by electrochemical oxidation of 1,2,3,4-Tetrahydro-7,12-dimethylbenz[a]anthracene in the presence of deoxyribonucleosides or adenine. Mulder PP, Chen L, Sekhar BC, George M, Gross ML, Rogan EG, Cavalieri EL. Chem Res Toxicol; 1996 Dec; 9(8):1264-77. PubMed ID: 8951228 [Abstract] [Full Text] [Related]
3. Synthesis of depurinating DNA adducts formed by one-electron oxidation of 7H-dibenzo[c,g]carbazole and identification of these adducts after activation with rat liver microsomes. Chen L, Devanesan PD, Byun J, Gooden JK, Gross ML, Rogan EG, Cavalieri EL. Chem Res Toxicol; 1997 Feb; 10(2):225-33. PubMed ID: 9049435 [Abstract] [Full Text] [Related]
4. Expanded analysis of benzo[a]pyrene-DNA adducts formed in vitro and in mouse skin: their significance in tumor initiation. Chen L, Devanesan PD, Higginbotham S, Ariese F, Jankowiak R, Small GJ, Rogan EG, Cavalieri EL. Chem Res Toxicol; 1996 Feb; 9(5):897-903. PubMed ID: 8828927 [Abstract] [Full Text] [Related]
8. Identification and quantification of the depurinating DNA adducts formed in mouse skin treated with dibenzo[a,l]pyrene (DB[a,l]P) or its metabolites and in rat mammary gland treated with DB[a,l]P. Cavalieri EL, Rogan EG, Li KM, Todorovic R, Ariese F, Jankowiak R, Grubor N, Small GJ. Chem Res Toxicol; 2005 Jun; 18(6):976-83. PubMed ID: 15962932 [Abstract] [Full Text] [Related]
14. Formation of stable adducts and absence of depurinating DNA adducts in cells and DNA treated with the potent carcinogen dibenzo[a,l]pyrene or its diol epoxides. Melendez-Colon VJ, Smith CA, Seidel A, Luch A, Platt KL, Baird WM. Proc Natl Acad Sci U S A; 1997 Dec 09; 94(25):13542-7. PubMed ID: 9391062 [Abstract] [Full Text] [Related]
20. Spectral and conformational analysis of deoxyadenosine adducts derived from syn- and anti-Dibenzo[a,l]pyrene diol epoxides: fluorescence studies. Jankowiak R, Lin CH, Zamzow D, Roberts KP, Li KM, Small GJ. Chem Res Toxicol; 1999 Sep 09; 12(9):768-77. PubMed ID: 10490497 [Abstract] [Full Text] [Related] Page: [Next] [New Search]