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Titlebook: Checkpoint Responses in Cancer Therapy; Wei Dai Book 2008 Humana Press 2008 DNA.apoptosis.biotechnology.cancer.cancer research.cancer ther

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發(fā)表于 2025-3-21 17:04:15 | 只看該作者 |倒序瀏覽 |閱讀模式
書目名稱Checkpoint Responses in Cancer Therapy
編輯Wei Dai
視頻videohttp://file.papertrans.cn/225/224213/224213.mp4
概述First book to summarize recent advances in identifying components of cell-cycle checkpoints and validating the use of checkpoint proteins as targets for the development of anticancer drugs.Distinguish
叢書名稱Cancer Drug Discovery and Development
圖書封面Titlebook: Checkpoint Responses in Cancer Therapy;  Wei Dai Book 2008 Humana Press 2008 DNA.apoptosis.biotechnology.cancer.cancer research.cancer ther
描述.Extensive research has uncovered a set of molecular surveillance mechanisms – commonly called “checkpoints” – which tightly monitor cell-cycle processes. Today’s anticancer drug development has identified many of these cell-cycle checkpoint molecules as effective targets. Research now promises to uncover a new generation of anticancer drugs with improved therapeutic indices based on their ability to target emerging checkpoint components. Checkpoint Responses in Cancer Therapy summarizes the advances made over the past 20 years, identifying components of cell-cycle checkpoints and their molecular regulation during checkpoint activation and validating the use of checkpoint proteins as targets for the development of anticancer drugs. This book’s distinguished panel of authors takes a close look at topics ranging from the major molecular players affecting DNA synthesis and the response to DNA damage to advances made in the identification of chemical compounds capable of inhibiting individual mitotic kinases. Illuminating and authoritative, Checkpoint Responses in Cancer Therapy offers a critical summary of findings for researchers in the pharmaceutical and biotechnology industries and
出版日期Book 2008
關(guān)鍵詞DNA; apoptosis; biotechnology; cancer; cancer research; cancer therapy; cell; cell cycle; checkpoint; chemoth
版次1
doihttps://doi.org/10.1007/978-1-59745-274-8
isbn_softcover978-1-61737-847-8
isbn_ebook978-1-59745-274-8Series ISSN 2196-9906 Series E-ISSN 2196-9914
issn_series 2196-9906
copyrightHumana Press 2008
The information of publication is updating

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Advanced and Alternate MapReduce Techniques,se drugs in eliciting apoptosis in cultured cancer cells. Therefore, quantitative differences in the strength of the spindle checkpoint may influence the efficacy of antimitotic drugs in cancer chemotherapy.
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DNA Topoisomerases as Targets for the Chemotherapeutic Treatment of Cancer,r with many aspects of topoisomerase enzymology and cell biology, their interactions with anticancer drugs, and the cellular consequences of topoisomerase-mediated DNA strand breaks. It also will discuss the checkpoint functions and repair pathways that are triggered in response to topoisomerase-generated DNA damage.
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Targeting the Spindle Checkpoint in Cancer Chemotherapy,se drugs in eliciting apoptosis in cultured cancer cells. Therefore, quantitative differences in the strength of the spindle checkpoint may influence the efficacy of antimitotic drugs in cancer chemotherapy.
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Do Histone Deacetylase Inhibitors Target Cell Cycle Checkpoints that Monitor Heterochromatin StructThe ability of cells to detect and respond to perturbations in heterochromatin structure is likely to be critical in determining cell fate, and its disruption in cancers would permit the silencing and unsilencing of genes often observed in modified transcriptomes of cancer cells as compared to their normal tissue counterparts.
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