Compounds > dibenzo(a,l)pyrene
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dibenzo(a,l)pyrene and guanine

dibenzo(a,l)pyrene has been researched along with guanine in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's4 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Adams, LD; DeMarini, DM; Hanley, NM; King, LC; Warren, SH1
Amin, S; Broyde, S; Cai, Y; Ding, S; Geacintov, NE; Jerina, DM; Lin, CH; Liu, Z; Rodriguez, FA; Sayer, JM; Tang, Y1
Amin, S; Broyde, S; Cai, Y; Ding, S; Geacintov, NE; Kolbanovskiy, A; Kolbanovskiy, M; Kropachev, K; Liu, Z; Schwaid, AG; Zhang, L1
Amin, S; Broyde, S; Cai, Y; Ding, S; Geacintov, NE; Kolbanovskiy, A; Kolbanovskiy, M; Lin, CH; Liu, Z; Rodríguez, FA1

Other Studies

4 other study(ies) available for dibenzo(a,l)pyrene and guanine

ArticleYear
Association between mutation spectra and stable and unstable DNA adduct profiles in Salmonella for benzo[a]pyrene and dibenzo[a,l]pyrene.
    Mutation research, 2011, Sep-01, Volume: 714, Issue:1-2

    Topics: Adenine; Benzo(a)pyrene; Benzopyrenes; DNA Adducts; Guanine; Mutagenicity Tests; Mutagens; Mutation; Salmonella

2011
Nuclear magnetic resonance solution structure of an N(2)-guanine DNA adduct derived from the potent tumorigen dibenzo[a,l]pyrene: intercalation from the minor groove with ruptured Watson-Crick base pairing.
    Biochemistry, 2012, Dec-04, Volume: 51, Issue:48

    Topics: Base Pairing; Benzopyrenes; DNA Adducts; Guanine; Molecular Dynamics Simulation; Nuclear Magnetic Resonance, Biomolecular; Nucleic Acid Conformation

2012
Adenine-DNA adducts derived from the highly tumorigenic Dibenzo[a,l]pyrene are resistant to nucleotide excision repair while guanine adducts are not.
    Chemical research in toxicology, 2013, May-20, Volume: 26, Issue:5

    Topics: Adenine; Benzopyrenes; DNA Adducts; DNA Repair; Guanine; HeLa Cells; Humans; Models, Molecular; Molecular Dynamics Simulation; Molecular Structure; Structure-Activity Relationship; Temperature

2013
Nuclear magnetic resonance studies of an N2-guanine adduct derived from the tumorigen dibenzo[a,l]pyrene in DNA: impact of adduct stereochemistry, size, and local DNA sequence on solution conformations.
    Biochemistry, 2014, Mar-25, Volume: 53, Issue:11

    Topics: Base Sequence; Benzopyrenes; Carcinogens; Crystallography, X-Ray; DNA Adducts; Guanine; Humans; Magnetic Resonance Spectroscopy; Protein Conformation; Stereoisomerism

2014