Compounds > estrone
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estrone and deoxyguanosine

estrone has been researched along with deoxyguanosine in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (25.00)18.2507
2000's1 (25.00)29.6817
2010's2 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Dasaradhi, L; Downey, KM; Shibutani, S; Suzuki, N; Tan, CK; Terashima, I1
Broyde, S; Hingerty, BE; Shapiro, R; Wang, L1
Bolton, JL; Chandrasena, ER; Peng, KW; Thatcher, GR; van Breemen, RB; Wang, Z; Yuan, Y1
Fleck, SC; Hildebrand, AA; Metzler, M; Müller, E; Pfeiffer, E1

Other Studies

4 other study(ies) available for estrone and deoxyguanosine

ArticleYear
Translesional synthesis on DNA templates containing an estrogen quinone-derived adduct: N2-(2-hydroxyestron-6-yl)-2'-deoxyguanosine and N6-(2-hydroxyestron-6-yl)-2'-deoxyadenosine.
    Biochemistry, 1998, Sep-29, Volume: 37, Issue:39

    Topics: Animals; Catalysis; Deoxyadenosines; Deoxyguanosine; DNA Adducts; DNA Polymerase beta; DNA Polymerase III; DNA Primers; DNA Replication; Estrone; Humans; Hydroxyestrones; Kinetics; Oligodeoxyribonucleotides; Templates, Genetic

1998
Structural and stereoisomer effects of model estrogen quinone-derived DNA adducts: N6-(2-hydroxyestron-6(alpha,beta)-yl)-2'-deoxyadenosine and N2-(2-hydroxyestron-6(alpha,beta)-yl)-2'-deoxyguanosine.
    Chemical research in toxicology, 2004, Volume: 17, Issue:3

    Topics: Deoxyadenosines; Deoxyguanosine; DNA Adducts; Hydroxyestrones; Models, Chemical; Molecular Structure; Protein Conformation; Stereoisomerism

2004
Redox cycling of catechol estrogens generating apurinic/apyrimidinic sites and 8-oxo-deoxyguanosine via reactive oxygen species differentiates equine and human estrogens.
    Chemical research in toxicology, 2010, Aug-16, Volume: 23, Issue:8

    Topics: 8-Hydroxy-2'-Deoxyguanosine; Animals; Cattle; Cell Line, Tumor; Chelating Agents; Copper; Deoxyguanosine; DNA; DNA Damage; DNA, Neoplasm; Equilenin; Estrogens, Catechol; Free Radical Scavengers; Horses; Humans; Hydrogen Peroxide; Hydroxyestrones; Molecular Structure; NADP; Oxidation-Reduction; Reactive Oxygen Species; Structure-Activity Relationship

2010
Genotoxicity and inactivation of catechol metabolites of the mycotoxin zearalenone.
    Mycotoxin research, 2012, Volume: 28, Issue:4

    Topics: 8-Hydroxy-2'-Deoxyguanosine; Animals; Catechol O-Methyltransferase; Cattle; Cell-Free System; Chromatography, Liquid; Deoxyguanosine; DNA; DNA Damage; Estradiol; Estrone; Humans; Inactivation, Metabolic; Liver; Methylation; Mice; Microsomes, Liver; Oxidation-Reduction; Rats; Tandem Mass Spectrometry; Zearalenone; Zeranol

2012