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Equine estrogen metabolite 4-hydroxyequilenin induces anchorage-independent growth of human mammary epithelial MCF-10A cells: differential gene expression

Mutation research, 2004-06, Vol.550 (1), p.109-121

2004

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Antiestrogenic and DNA Damaging Effects Induced by Tamoxifen and Toremifene Metabolites

Chemical research in toxicology, 2003-07, Vol.16 (7), p.832-837

2003

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Effect of Halogenated Substituents on the Metabolism and Estrogenic Effects of the Equine Estrogen, Equilenin

Chemical research in toxicology, 2003-06, Vol.16 (6), p.741-749

2003

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Inhibition of Cellular Enzymes by Equine Catechol Estrogens in Human Breast Cancer Cells: Specificity for Glutathione S-Transferase P1-1

Chemical research in toxicology, 2002-07, Vol.15 (7), p.935-942

2002

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Oxidative DNA Damage Induced by Equine Estrogen Metabolites: Role of Estrogen Receptor α

Chemical research in toxicology, 2002-04, Vol.15 (4), p.512-519

2002

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Evidence That a Metabolite of Equine Estrogens, 4-Hydroxyequilenin, Induces Cellular Transformation in Vitro

Chemical research in toxicology, 2001-01, Vol.14 (1), p.82-90

2001

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A Metabolite of Equine Estrogens, 4-Hydroxyequilenin, Induces DNA Damage and Apoptosis in Breast Cancer Cell Lines

Chemical research in toxicology, 2000-05, Vol.13 (5), p.342-350

2000

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The Major Metabolite of Equilin, 4-Hydroxyequilin, Autoxidizes to an o-Quinone Which Isomerizes to the Potent Cytotoxin 4-Hydroxyequilenin-o-quinone

Chemical research in toxicology, 1999-02, Vol.12 (2), p.204-213

1999

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Role of Quinoids in Estrogen Carcinogenesis

Chemical research in toxicology, 1998-10, Vol.11 (10), p.1113-1127

1998

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Activity-Guided Isolation of Steroidal Alkaloid Antiestrogen-Binding Site Inhibitors from Pachysandra procumbens

Journal of natural products (Washington, D.C.), 1998-10, Vol.61 (10), p.1257-1262

1998

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Synthesis of betulinic acid derivatives with activity against human melanoma

Bioorganic & medicinal chemistry letters, 1998-07, Vol.8 (13), p.1707-1712

1998

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Discovery and mechanism of betulinic acid and natural product estrogens and antiestrogens

Pisha, Emily

1998

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ProQuest

The reactivity of o-quinones which do not isomerize to quinone methides correlates with alkylcatechol-induced toxicity in human melanoma cells

Chemico-biological interactions, 1997-09, Vol.106 (2), p.133-148

1997

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Bioreductive activation of catechol estrogen-ortho-quinones : Aromatization of the B ring in 4-hydroxyequilenin markedly alters quinoid formation and reactivity

Carcinogenesis (New York), 1997-05, Vol.18 (5), p.1093-1101

1997

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Cell-based assay for the determination of estrogenic and anti-estrogenic activities

Methods in cell science, 1997-03, Vol.19 (1), p.37-43

1997

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Discovery of betulinic acid as a selective inhibitor of human melanoma that functions by induction of apoptosis

Nature medicine, 1995-10, Vol.1 (10), p.1046-1051

1995

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Equine estrogen metabolite 4-hydroxyequilenin induces anchorage-independent growth of human mammary epithelial MCF-10A cells: differential gene expression

Antiestrogenic and DNA Damaging Effects Induced by Tamoxifen and Toremifene Metabolites

Effect of Halogenated Substituents on the Metabolism and Estrogenic Effects of the Equine Estrogen, Equilenin

Inhibition of Cellular Enzymes by Equine Catechol Estrogens in Human Breast Cancer Cells: Specificity for Glutathione S-Transferase P1-1

Oxidative DNA Damage Induced by Equine Estrogen Metabolites: Role of Estrogen Receptor α

Evidence That a Metabolite of Equine Estrogens, 4-Hydroxyequilenin, Induces Cellular Transformation in Vitro

A Metabolite of Equine Estrogens, 4-Hydroxyequilenin, Induces DNA Damage and Apoptosis in Breast Cancer Cell Lines

The Major Metabolite of Equilin, 4-Hydroxyequilin, Autoxidizes to an o-Quinone Which Isomerizes to the Potent Cytotoxin 4-Hydroxyequilenin-o-quinone

Role of Quinoids in Estrogen Carcinogenesis

Activity-Guided Isolation of Steroidal Alkaloid Antiestrogen-Binding Site Inhibitors from Pachysandra procumbens

Synthesis of betulinic acid derivatives with activity against human melanoma

Discovery and mechanism of betulinic acid and natural product estrogens and antiestrogens

The reactivity of o-quinones which do not isomerize to quinone methides correlates with alkylcatechol-induced toxicity in human melanoma cells

Bioreductive activation of catechol estrogen-ortho-quinones : Aromatization of the B ring in 4-hydroxyequilenin markedly alters quinoid formation and reactivity

Cell-based assay for the determination of estrogenic and anti-estrogenic activities

Discovery of betulinic acid as a selective inhibitor of human melanoma that functions by induction of apoptosis

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