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Titlebook: Emerging Therapeutic Targets in Ovarian Cancer; Stan Kaye,Robert Brown,Martin Gore Book 2011 Springer Science+Business Media, LLC 2011

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發(fā)表于 2025-3-21 19:37:58 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書(shū)目名稱(chēng)Emerging Therapeutic Targets in Ovarian Cancer
編輯Stan Kaye,Robert Brown,Martin Gore
視頻videohttp://file.papertrans.cn/309/308470/308470.mp4
概述Discusses the progress in linking the biology of ovarian cancer with novel targets and innovative therapies entering clinical trials..Provides an up-to-date perspective on successful therapeutic devel
圖書(shū)封面Titlebook: Emerging Therapeutic Targets in Ovarian Cancer;  Stan Kaye,Robert Brown,Martin Gore Book 2011 Springer Science+Business Media, LLC 2011
描述.
出版日期Book 2011
版次1
doihttps://doi.org/10.1007/978-1-4419-7216-3
isbn_softcover978-1-4899-8233-9
isbn_ebook978-1-4419-7216-3
copyrightSpringer Science+Business Media, LLC 2011
The information of publication is updating

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Epigenetic Therapies,d the achievement of a clear therapeutic index. In addition, the development of robust predictive biomarkers linked to an understanding of the underlying biology will be key to improved epigenetic therapy approaches. Defining the epigenetic alongside the genetic landscape of individual ovarian cance
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French Nuclear Command and Control,e in ovarian cancer and summarise the current progress in developing clinically applicable inhibitors of AKT pathway components for potential use in the ovarian cancer setting either alone or in combination with conventional cytotoxic agents such as the platinum drugs.
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Specific Measurements, Units, and Termss have been implicated in T-cell suppression mediated by a number of cell surface molecules such as B7-H1 or enzymes such as arginase. Inflammation may be important in mediating suppression or defective response to treatment. Novel immune therapies have endeavoured to address immune suppression alon
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https://doi.org/10.1007/978-90-481-3411-3appears to reverse platinum-resistance, in part, by upregulation of caspase-3-mediated apoptosis. Src is an attractive target in ovarian cancers, and current trials using various Src inhibitors are underway.
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