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Titlebook: Molecular Basis of Sex Hormone Receptor Function; New Targets for Inte H. Gronemeyer,U. Fuhrmann,K. Parczyk Conference proceedings 1998 Spr

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书目名称Molecular Basis of Sex Hormone Receptor Function
副标题New Targets for Inte
编辑H. Gronemeyer,U. Fuhrmann,K. Parczyk
视频video
丛书名称Ernst Schering Foundation Symposium Proceedings
图书封面Titlebook: Molecular Basis of Sex Hormone Receptor Function; New Targets for Inte H. Gronemeyer,U. Fuhrmann,K. Parczyk Conference proceedings 1998 Spr
描述How sex hormone receptors and all the other members of the nuclear receptor superfamily do such a remarkable job has fascinated scientists for decades. A series of discoveries in the past few years has dramatically enlightened our understanding of the molecular mechanisms that govern nuclear receptor action. The elucidation of the 3D structures of several nuclear receptor ligand binding domains in the presence of agonists or antagonists has provided an allosteric concept of ligand action, and the discovery of a plethora of ligand-dependent protein interactions has linked this transconformation with the ability of nuclear receptors to act as transcriptional activators and repressors and the enzymatic modification of chromatin and factors of the basal transcriptional machinery.
出版日期Conference proceedings 1998
关键词breast cancer; cancer; dopamine; endocrine therapy; endocrinology; glucocorticoids; growth factor; gynecolo
版次1
doihttps://doi.org/10.1007/978-3-662-03689-1
isbn_softcover978-3-662-03691-4
isbn_ebook978-3-662-03689-1Series ISSN 0947-6075
issn_series 0947-6075
copyrightSpringer-Verlag Berlin Heidelberg 1998
The information of publication is updating

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https://doi.org/10.1007/978-3-662-03689-1breast cancer; cancer; dopamine; endocrine therapy; endocrinology; glucocorticoids; growth factor; gynecolo
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0947-6075 or decades. A series of discoveries in the past few years has dramatically enlightened our understanding of the molecular mechanisms that govern nuclear receptor action. The elucidation of the 3D structures of several nuclear receptor ligand binding domains in the presence of agonists or antagonists
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