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Journal Abstract Search

176 related items for PubMed ID: 3016288

  • 1. Covalent carcinogenic O6-methylguanosine lesions in DNA. Structural studies of the O6 meG X A and O6meG X G interactions in dodecanucleotide duplexes.
    Patel DJ, Shapiro L, Kozlowski SA, Gaffney BL, Jones RA.
    J Mol Biol; 1986 Apr 20; 188(4):677-92. PubMed ID: 3016288
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  • 2. Covalent carcinogenic lesions in DNA: NMR studies of O6-methylguanosine containing oligonucleotide duplexes.
    Patel DJ, Shapiro L, Kozlowski SA, Gaffney BL, Kuzmich S, Jones RA.
    Biochimie; 1985 Apr 20; 67(7-8):861-86. PubMed ID: 4084607
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  • 3. Structural studies of the O6meG.C interaction in the d(C-G-C-G-A-A-T-T-C-O6meG-C-G) duplex.
    Patel DJ, Shapiro L, Kozlowski SA, Gaffney BL, Jones RA.
    Biochemistry; 1986 Mar 11; 25(5):1027-36. PubMed ID: 3964658
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  • 8. NMR structural studies of the ionizing radiation adduct 7-hydro-8-oxodeoxyguanosine (8-oxo-7H-dG) opposite deoxyadenosine in a DNA duplex. 8-Oxo-7H-dG(syn).dA(anti) alignment at lesion site.
    Kouchakdjian M, Bodepudi V, Shibutani S, Eisenberg M, Johnson F, Grollman AP, Patel DJ.
    Biochemistry; 1991 Feb 05; 30(5):1403-12. PubMed ID: 1991121
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  • 9. Deoxyguanosine-deoxyadenosine pairing in the d(C-G-A-G-A-A-T-T-C-G-C-G) duplex: conformation and dynamics at and adjacent to the dG X dA mismatch site.
    Patel DJ, Kozlowski SA, Ikuta S, Itakura K.
    Biochemistry; 1984 Jul 03; 23(14):3207-17. PubMed ID: 6466638
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  • 13. NMR studies of an exocyclic 1,N2-propanodeoxyguanosine adduct (X) located opposite deoxyadenosine (A) in DNA duplexes at basic pH: simultaneous partial intercalation of X and A between stacked bases.
    Kouchakdjian M, Eisenberg M, Live D, Marinelli E, Grollman AP, Patel DJ.
    Biochemistry; 1990 May 08; 29(18):4456-65. PubMed ID: 2161685
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  • 14. Base pair mismatches and carcinogen-modified bases in DNA: an NMR study of G.T and G.O4meT pairing in dodecanucleotide duplexes.
    Kalnik MW, Kouchakdjian M, Li BF, Swann PF, Patel DJ.
    Biochemistry; 1988 Jan 12; 27(1):108-15. PubMed ID: 3349021
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  • 16. Base pair mismatches and carcinogen-modified bases in DNA: an NMR study of A.C and A.O4meT pairing in dodecanucleotide duplexes.
    Kalnik MW, Kouchakdjian M, Li BF, Swann PF, Patel DJ.
    Biochemistry; 1988 Jan 12; 27(1):100-8. PubMed ID: 2831951
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  • 20. 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
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