estradiol-3,4-quinone has been researched along with 4-hydroxyestradiol in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 3 (75.00) | 29.6817 |
2010's | 1 (25.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Cavalieri, E; Kohli, E; Rogan, E; Saeed, M; Zahid, M | 1 |
Cavalieri, E; Fernandez, SV; Rogan, E; Russo, J; Saeed, M; Sheriff, F | 1 |
Cavalieri, EL; Gaikwad, NW; Rogan, EG; Zahid, M | 1 |
Ali, MF; Cavalieri, EL; Rogan, EG; Saeed, M; Zahid, M | 1 |
4 other study(ies) available for estradiol-3,4-quinone and 4-hydroxyestradiol
Article | Year |
---|---|
The greater reactivity of estradiol-3,4-quinone vs estradiol-2,3-quinone with DNA in the formation of depurinating adducts: implications for tumor-initiating activity.
Topics: Adenine; Carcinogens; Deoxyadenosines; DNA; DNA Adducts; Estradiol; Estrogens, Catechol; Guanosine; In Vitro Techniques; Lactoperoxidase; Monophenol Monooxygenase; Mutagens; Oxidation-Reduction; Time Factors | 2006 |
Formation of depurinating N3Adenine and N7Guanine adducts by MCF-10F cells cultured in the presence of 4-hydroxyestradiol.
Topics: Adenine; Breast; Cells, Cultured; Chromatography, High Pressure Liquid; DNA; DNA Adducts; DNA Damage; Estradiol; Estrogens, Catechol; Guanine; Humans; Molecular Structure; Solid Phase Extraction; Tandem Mass Spectrometry | 2007 |
Inhibition of depurinating estrogen-DNA adduct formation by natural compounds.
Topics: Animals; Antioxidants; Biological Products; Cattle; DNA; DNA Adducts; Estradiol; Estrogens, Catechol; Molecular Structure | 2007 |
N-acetylcysteine blocks formation of cancer-initiating estrogen-DNA adducts in cells.
Topics: Acetylcysteine; Animals; Antioxidants; Breast; Breast Neoplasms; Cell Line; DNA Adducts; Estradiol; Estrogens, Catechol; Female; Humans; Mammary Glands, Animal; Mammary Neoplasms, Experimental; Mice | 2010 |