Page last updated: 2024-08-17

estrone and 8-hydroxy-2'-deoxyguanosine

estrone has been researched along with 8-hydroxy-2'-deoxyguanosine in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	2 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Bolton, JL; Chandrasena, ER; Peng, KW; Thatcher, GR; van Breemen, RB; Wang, Z; Yuan, Y	1
Fleck, SC; Hildebrand, AA; Metzler, M; Müller, E; Pfeiffer, E	1

Other Studies

2 other study(ies) available for estrone and 8-hydroxy-2'-deoxyguanosine

Article	Year
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

Article

Year

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