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Titlebook: Death Receptors in Cancer Therapy; Wafik S. El-Deiry Book 2005 Humana Press 2005 TNF.apoptosis.carcinoma.cell.cell death.gene therapy.inte

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發(fā)表于 2025-3-21 17:58:02 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Death Receptors in Cancer Therapy
編輯Wafik S. El-Deiry
視頻videohttp://file.papertrans.cn/264/263995/263995.mp4
概述Includes supplementary material:
叢書名稱Cancer Drug Discovery and Development
圖書封面Titlebook: Death Receptors in Cancer Therapy;  Wafik S. El-Deiry Book 2005 Humana Press 2005 TNF.apoptosis.carcinoma.cell.cell death.gene therapy.inte
描述An in depth review of our latest understanding of the molecular events that regulate cell death and those molecules that provide targets for developing agonists or antagonists to modulate death signaling for therapeutic purposes. The authors focus on the extrinsic system of death receptors, their regulation and function, and their abnormalities in cancer. Topics of particular interest include resistance to apoptosis, TRAIL signaling, death receptors in embryonic development, mechanisms of caspase activation, and death receptor mutations in cancer. Additional chapters address death signaling in melanoma, synthetic retinoids and death receptors, the role of p53 in death receptor regulation, immune suppression of cancer, and combination therapy with death ligands.
出版日期Book 2005
關(guān)鍵詞TNF; apoptosis; carcinoma; cell; cell death; gene therapy; interferon; melanoma; prostate cancer; tumor
版次1
doihttps://doi.org/10.1385/159259851X
isbn_softcover978-1-61737-401-2
isbn_ebook978-1-59259-851-9Series ISSN 2196-9906 Series E-ISSN 2196-9914
issn_series 2196-9906
copyrightHumana Press 2005
The information of publication is updating

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發(fā)表于 2025-3-22 00:05:02 | 只看該作者
https://doi.org/10.1007/978-3-030-22094-5 None of the other members of the TNFR family identified to date contain recognizable intracellular domains, and instead present binding sites for interactions with TNF receptor-associated factors (TRAFs) and other adaptor proteins.
板凳
發(fā)表于 2025-3-22 01:00:30 | 只看該作者
地板
發(fā)表于 2025-3-22 07:04:33 | 只看該作者
Mammalian Cell Death Pathways,immune surveillance/suppression of cancer. Caspase activation is highly regulated and defects at virtually all levels of death regulation are observed in cancer. This chapter focuses on the cell biology, biochemistry, and genetics of programmed cell death.
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發(fā)表于 2025-3-22 11:41:58 | 只看該作者
Death Signaling and Therapeutic Applications of TRAIL,ecules, ligand-type cytokine molecules including the tumor necrosis factor (TNF) family members have been best characterized. The TNF family members most extensively characterized for death signaling and structure include TNF-α, Fas ligand (FasL), and TNF-related apoptosis-inducing ligand (TRAIL).
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發(fā)表于 2025-3-22 13:41:57 | 只看該作者
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發(fā)表于 2025-3-22 18:52:00 | 只看該作者
Regulation of Death Receptors by Synthetic Retinoids,s such as acne and psoriasis, and in the prevention or treatment of certain types of cancer, such as the treatment of acute promyelocytic leukemia (APL) and cutaneous T-cell lymphoma, reversal of premalignant lesions, and inhibition of the development of second primary tumors (.,.).
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發(fā)表于 2025-3-23 00:15:33 | 只看該作者
Proapoptotic Gene Silencing Via Methylation in Human Tumors,eath, disassembly of various cellular components, and eventual engulfment of the resulting cellular debris (.,.). Inappropriate apoptosis has been associated with a variety of pathological conditions, such as neurodegenerative disorders, autoimmune phenomena, mitochondrial disorders, ischemic damage and cancer (.,.).
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發(fā)表于 2025-3-23 02:14:34 | 只看該作者
Book 2005ors in embryonic development, mechanisms of caspase activation, and death receptor mutations in cancer. Additional chapters address death signaling in melanoma, synthetic retinoids and death receptors, the role of p53 in death receptor regulation, immune suppression of cancer, and combination therapy with death ligands.
10#
發(fā)表于 2025-3-23 08:15:24 | 只看該作者
Book 2005g agonists or antagonists to modulate death signaling for therapeutic purposes. The authors focus on the extrinsic system of death receptors, their regulation and function, and their abnormalities in cancer. Topics of particular interest include resistance to apoptosis, TRAIL signaling, death recept
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