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Journal Abstract Search
392 related items for PubMed ID: 9843418
1. Multiple conformations of an intercalated (-)-(7S,8R,9S, 10R)-N6-[10-(7,8,9,10-tetrahydrobenzo[a]pyrenyl)]-2'-deoxyadenosyl adduct in the N-ras codon 61 sequence. Zegar IS, Chary P, Jabil RJ, Tamura PJ, Johansen TN, Lloyd RS, Harris CM, Harris TM, Stone MP. Biochemistry; 1998 Nov 24; 37(47):16516-28. PubMed ID: 9843418 [Abstract] [Full Text] [Related]
2. Adduction of the human N-ras codon 61 sequence with (-)-(7S,8R,9R,10S)-7,8-dihydroxy-9,10-epoxy-7,8,9,10-tetrahydrobenzo[a] pyrene: structural refinement of the intercalated SRSR(61,2) (-)-(7S,8R,9S,10R)-N6-[10-(7,8,9,10- tetrahydrobenzo[a]pyrenyl)]-2'-deoxyadenosyl adduct from 1H NMR. Zegar IS, Kim SJ, Johansen TN, Horton PJ, Harris CM, Harris TM, Stone MP. Biochemistry; 1996 May 21; 35(20):6212-24. PubMed ID: 8639561 [Abstract] [Full Text] [Related]
3. Intercalation of the (-)-(1R,2S,3R, 4S)-N6-[1-benz[a]anthracenyl]-2'-deoxyadenosyl adduct in an oligodeoxynucleotide containing the human N-ras codon 61 sequence. Li Z, Mao H, Kim HY, Tamura PJ, Harris CM, Harris TM, Stone MP. Biochemistry; 1999 Mar 09; 38(10):2969-81. PubMed ID: 10074349 [Abstract] [Full Text] [Related]
4. Intercalation of the (1R,2S,3R,4S)-N6-[1-(1,2,3,4-tetrahydro-2,3,4-trihydroxybenz[a]anthracenyl)]-2'-deoxyadenosyl adduct in the N-ras codon 61 sequence: DNA sequence effects. Li Z, Tamura PJ, Wilkinson AS, Harris CM, Harris TM, Stone MP. Biochemistry; 2001 Jun 12; 40(23):6743-55. PubMed ID: 11389588 [Abstract] [Full Text] [Related]
5. Major groove (S)-alpha-(N6-adenyl)styrene oxide adducts in an oligodeoxynucleotide containing the human N-ras codon 61 sequence: conformations of the S(61,2) and S(61,3) sequence isomers from 1H NMR. Feng B, Voehler M, Zhou L, Passarelli M, Harris CM, Harris TM, Stone MP. Biochemistry; 1996 Jun 11; 35(23):7316-29. PubMed ID: 8652508 [Abstract] [Full Text] [Related]
7. Solution conformation of the (-)-cis-anti-benzo[a]pyrenyl-dG adduct opposite dC in a DNA duplex: intercalation of the covalently attached BP ring into the helix with base displacement of the modified deoxyguanosine into the major groove. Cosman M, Hingerty BE, Luneva N, Amin S, Geacintov NE, Broyde S, Patel DJ. Biochemistry; 1996 Jul 30; 35(30):9850-63. PubMed ID: 8703959 [Abstract] [Full Text] [Related]
11. Solution structure of the (+)-cis-anti-benzo[a]pyrene-dA ([BP]dA) adduct opposite dT in a DNA duplex. Mao B, Gu Z, Gorin A, Chen J, Hingerty BE, Amin S, Broyde S, Geacintov NE, Patel DJ. Biochemistry; 1999 Aug 17; 38(33):10831-42. PubMed ID: 10451380 [Abstract] [Full Text] [Related]
13. Structural alignment of the (+)-trans-anti-benzo[a]pyrene-dG adduct positioned opposite dC at a DNA template-primer junction. Feng B, Gorin A, Hingerty BE, Geacintov NE, Broyde S, Patel DJ. Biochemistry; 1997 Nov 11; 36(45):13769-79. PubMed ID: 9374853 [Abstract] [Full Text] [Related]
14. Quantification of (7S,8R)-dihydroxy-(9R,10S)-epoxy-7,8,9,10-tetrahydrobenzo[a]pyrene adducts in human serum albumin by laser-induced fluorescence: implications for the in vivo metabolism of benzo[a]pyrene. Ozbal CC, Skipper PL, Yu MC, London SJ, Dasari RR, Tannenbaum SR. Cancer Epidemiol Biomarkers Prev; 2000 Jul 11; 9(7):733-9. PubMed ID: 10919745 [Abstract] [Full Text] [Related]
15. NMR solution structure of a nonanucleotide duplex with a dG mismatch opposite a 10S adduct derived from trans addition of a deoxyadenosine N6-amino group to (+)-(7R,8S,9S,10R)-7,8-dihydroxy-9,10-epoxy-7,8,9,10- tetrahydrobenzo[a]pyrene: an unusual syn glycosidic torsion angle at the modified dA. Yeh HJ, Sayer JM, Liu X, Altieri AS, Byrd RA, Lakshman MK, Yagi H, Schurter EJ, Gorenstein DG, Jerina DM. Biochemistry; 1995 Oct 17; 34(41):13570-81. PubMed ID: 7577946 [Abstract] [Full Text] [Related]
16. Solution structure of a cis-opened (10R)-N6-deoxyadenosine adduct of (9S,10R)-9,10-epoxy-7,8,9,10-tetrahydrobenzo[a]pyrene in a DNA duplex. Volk DE, Thiviyanathan V, Rice JS, Luxon BA, Shah JH, Yagi H, Sayer JM, Yeh HJ, Jerina DM, Gorenstein DG. Biochemistry; 2003 Feb 18; 42(6):1410-20. PubMed ID: 12578353 [Abstract] [Full Text] [Related]