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1

Angerer, Erwin von. The estrogen receptor as a target for rational drug design. Springer, 1995.

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2

Angerer, Erwin von. The estrogen receptor as a target for rational drug design. Springer, 1995.

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3

Elke, Dopp, Stopper Helga, Alink Gerrit Mannes, and Research Signpost (Trivandrum India), eds. Natural and synthetic estrogens: Aspects of the cellular and molecular activity. Research Signpost, 2002.

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4

Parker, Philip M. The 2007-2012 World Outlook for Estrogen Hormones and Synthetic Substitute Pharmaceuticals. ICON Group International, Inc., 2006.

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5

The 2006-2011 World Outlook for Estrogen Hormones and Synthetic Substitute Pharmaceuticals. Icon Group International, Inc., 2005.

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6

Parker, Philip M. The 2007-2012 Outlook for Estrogen Hormones and Synthetic Substitute Pharmaceuticals in Japan. ICON Group International, Inc., 2006.

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Parker, Philip M. The 2007-2012 Outlook for Estrogen Hormones and Synthetic Substitute Pharmaceuticals in India. ICON Group International, Inc., 2006.

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8

Parker, Philip M. The 2007-2012 Outlook for Estrogen Hormones and Synthetic Substitute Pharmaceuticals in Greater China. ICON Group International, Inc., 2006.

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9

Castellanos, Madeleine M. Female Sexual Biochemistry (DRAFT). Edited by Madeleine M. Castellanos. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190225889.003.0001.

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“Female Sexual Biochemistry” reviews the key hormones and neurotransmitters that have a major role in female sexuality. Estrogens—estradiol, estrone, and estriol—as well as major androgens, such as testosterone and dihydrotestosterone (DHT), are presented with a discussion of their role in the support of the reproductive organs and genitals as well as their actions on the central nervous system to affect sexual desire, arousal, and responsiveness. The interaction and regulation of estrogen by progesterone and thyroid hormone is included. A review of the dual-control model of sexual responsiven
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10

Parker, Philip M. The 2007-2012 Outlook for Estrogen Hormones and Synthetic Substitute Pharmaceuticals in the United States. ICON Group International, Inc., 2006.

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11

Atta-ur-Rahman and Khurshid Zaman, eds. Topics in Anti-Cancer Research: Volume 8. BENTHAM SCIENCE PUBLISHERS, 2019. http://dx.doi.org/10.2174/97898114043821190801.

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Topics in Anti-Cancer Research covers new developments in the field of cancer. Novel drugs as anticancer agents include natural and synthetic phenazines and other anti-cancer compounds. It also encompasses the role of estrogen as endocrine disruptors and strategies targeting cancer stem cells for the treatment of different types of cancers, including myeloma and renal cell cancer. The diversity of researches and topics published in this eBook Series will be valuable to cancer researchers, clinicians, and cancer professionals aiming to develop novel anti-cancer targets for the treatment of vari
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12

National Cancer Institute (U.S.). Office of Cancer Communications, ed. Recently reported health effects of exposure before birth and during pregnancy to the synthetic estrogen diethylstilbestrol (DES). National Cancer Institute/Office of Cancer Communications, 1985.

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13

Henderson, Lindsey. Estradiol: Synthesis, Functions and Effectiveness. Nova Science Publishers, Incorporated, 2017.

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14

Palmeri, Ricco, and Sal Grimaudo. Estradiol: Synthesis, Health Effects and Drug Interactions. Nova Science Publishers, Incorporated, 2013.

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15

Dopp, Helga Stopper and Gerrit M. Alink Elke. Natural and Synthetic Estrogens: Cellular and Molecular Mechanisms. Research Signpost, 2002.

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16

Kuznetsov, Yuriy, Inna Levina, and Igor Zavarzin. Estrogens and antiestrogens. Modern synthetic approaches to directed modification of estra-1,3,5(10)-triene steroids: goals, reactions, and methods. LCC MAKS Press, 2021. http://dx.doi.org/10.29003/m2020.978-5-317-06626-0.

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The monograph summarizes the information over the past 20 years on the currently widely used and promising methods for the synthesis of estra-1,3,5(10)-triene derivatives by modifying natural estrogens - estrone and estradiol. The main practical goals of modifying this class of steroids and achievements in the chemistry of steroidal antiestrogens, which are promising drugs for hormonal therapy, are considered. Special attention is paid to the stereochemical features of the reactions and the specific problems of modification of the steroid nucleus of estratrienes associated with the presence of
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