Standout Papers

A potent specific pure antiestrogen with clinical potential. 1991 2026 2002 2014 950
  1. A potent specific pure antiestrogen with clinical potential. (1991)
    A. E. Wakeling, Michael Dukes et al. PubMed

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Works of A. E. Wakeling being referenced

Modulation of Epidermal Growth Factor Receptor in Endocrine‐Resistant, Estrogen‐Receptor‐Positive Breast Cancer
2002
Modulation of epidermal growth factor receptor in endocrine-resistant, oestrogen receptor-positive breast cancer.
2001
Circumvention of tamoxifen resistance by the pure anti‐estrogen ICI 182, 780
1993
A comparative study of the interaction of oestradiol and the steroidal pure antioestrogen, ICI 164,384, with the molybdate-stabilized oestrogen receptor
1990
Pure Antiestrogens The Most Important Advance in the Endocrine Therapy of Breast Cancer since 1896?a
1996
Novel antioestrogens without partial agonist activity
1988
Responses to Pure Antiestrogens (ICI 164384, ICI182780) in Estrogen‐Sensitive and‐Resistant Experimental and Clinical Breast Cancera
1995
Fulvestrant ('Faslodex')--a new treatment option for patients progressing on prior endocrine therapy.
2002
Short-term effects of pure anti-oestrogen ICI 182780 treatment on oestrogen receptor, epidermal growth factor receptor and transforming growth factor-alpha protein expression in human breast cancer
1996
Biology and mode of action of pure antioestrogens
1988
Effects of a non-steroidal pure antioestrogen, ZM 189,154, on oestrogen target organs of the rat including bones
1994
Comparison of the Effects of a Pure Steroidal antiestrogen With Those of Tamoxifen in a Model of Human Breast Cancer
1995
Novel Pure Antiestrogens. Mode of Action and Therapeutic Prospects
1990
Mechanisms of Tamoxifen Resistance: Increased Estrogen Receptor-HER2/neu Cross-Talk in ER/HER2-Positive Breast Cancer
2004
Similarities and distinctions in the mode of action of different classes of antioestrogens.
2000
Epidermal growth factor receptor tyrosine kinase inhibitors
2002
Fulvestrant: an oestrogen receptor antagonist with a novel mechanism of action
2004
Insulin-like growth factor-I receptor signalling and acquired resistance to gefitinib (ZD1839; Iressa) in human breast and prostate cancer cells
2004
Specific inhibition of epidermal growth factor receptor tyrosine kinase by 4-anilinoquinazolines
1996
Oestrogen receptor expression in human breast cancer during long-term fulvestrant treatment
2004
Prostaglandin specific binding in the rabbit oviduct
1973
A potent specific pure antiestrogen with clinical potential.
1991 Standout
The Antiepidermal Growth Factor Receptor Agent Gefitinib (ZD1839/Iressa) Improves Antihormone Response and Prevents Development of Resistance in Breast Cancer in Vitro
2003
Biology and mode of action of pure antioestrogens.
1988
Apoptotic death in epithelial cells: cleavage of DNA to 300 and/or 50 kb fragments prior to or in the absence of internucleosomal fragmentation.
1993
New targets for therapeutic attack
1997
Prospects for combining hormonal and nonhormonal growth factor inhibition.
2001
Comparison of the short-term biological effects of 7alpha-[9-(4,4,5,5,5-pentafluoropentylsulfinyl)-nonyl]estra-1,3,5, (10)-triene-3,17beta-diol (Faslodex) versus tamoxifen in postmenopausal women with primary breast cancer.
2001
Non-steroidal antioestrogens—Receptor binding and biological response in rat uterus, rat mammary carcinoma and human breast cancer cells
1984
Oestrogen receptor expression in human breast cancer during long-term fulvestrant treatment
2004
Points of action of estrogen antagonists and a calmodulin antagonist within the MCF-7 human breast cancer cell cycle.
1989
ZD1839, AN EPIDERMAL GROWTH FACTOR TYROSINE KINASE INHIBITOR SELECTED FOR CLINICAL DEVELOPMENT
1997
Rankless by CCL
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