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Titlebook: Melanoma; Biologically Targete Ernest C. Borden (Director) Book 2002 Springer Science+Business Media New York 2002 Staging.angiogenesis.met

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发表于 2025-3-21 16:13:23 | 显示全部楼层 |阅读模式
书目名称Melanoma
副标题Biologically Targete
编辑Ernest C. Borden (Director)
视频video
概述Includes supplementary material:
丛书名称Current Clinical Oncology
图书封面Titlebook: Melanoma; Biologically Targete Ernest C. Borden (Director) Book 2002 Springer Science+Business Media New York 2002 Staging.angiogenesis.met
描述Strategies of treatment involving therapeutic proteins, irnrnune immune cells, or cel­ lular protein targets are those of greatest potential for further reducing mortality from melanoma. Therapeutic proteins or cells may inhibit melanoma cell growth either by augmentation of immune cell function or by inhibition of angiogenesis. Cytokines and melanoma antigens may be used either in vivo as a vaccine to stimulate irnrnune immune cell cell function or ex vivo to stimulate or proliferate cells for infusion. Alternatively, alteration in melanoma cell growth can occur through inhibition of protein signal transduction pathways within melanoma cells or in the endothelial cells constituting the necessary angiogenic support for tumor growth. The great promise of these therapies and their cellular targets constitutes the basis for Melanoma: Biologically Targeted Therapeutics. THE CLINlCAL PROBLEM More than four million people will be diagnosed with melanoma in the first decade of the 21st century. Half of those who will die will be individuals who would otherwise have had a life expectancy of another 25 years or more. These individuals will die of systemic systernic metastases, which are pre
出版日期Book 2002
关键词Staging; angiogenesis; metastatic disease; surgery; tumor growth
版次1
doihttps://doi.org/10.1007/978-1-59259-159-6
isbn_softcover978-1-4684-9668-0
isbn_ebook978-1-59259-159-6Series ISSN 2364-1134 Series E-ISSN 2364-1142
issn_series 2364-1134
copyrightSpringer Science+Business Media New York 2002
The information of publication is updating

书目名称Melanoma影响因子(影响力)




书目名称Melanoma影响因子(影响力)学科排名




书目名称Melanoma网络公开度




书目名称Melanoma网络公开度学科排名




书目名称Melanoma被引频次




书目名称Melanoma被引频次学科排名




书目名称Melanoma年度引用




书目名称Melanoma年度引用学科排名




书目名称Melanoma读者反馈




书目名称Melanoma读者反馈学科排名




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A Pathologist’s Perspective on Prognostic Features of Malignant Melanomaw of pigment lesion pathology. It consists of benign nevus, including dysplastic nevus, . melanoma, and invasive melanoma. These are regarded as discrete entities with only minimal reference to a sequence of change from dysplasia to melanoma. Once invasive melanoma is diagnosed, the only additional
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Immunotherapy of Advanced Melanoma Directed at Specific Antigens with melanoma. Several lines of evidence may support this hypothesis: (.) in documented cases of children with spontaneous regression of cancer, melanoma has been found to be the cancer second in incidence to neuroblastoma .; (.) approximately 5% of patients with metastatic melanoma have an unknown
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Melanoma Antigensost simple approach seemed to be to inject subjects with crude tumor material, and there have been well over a hundred reports from 1902 through 1990 of patients being injected with tumor extracts . .Few of these reports are interpretable, however. Early studies in the 1950s using inbred strains of
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Interleukin-12uration factor .,.. It was identified as a factor secreted by Epstein Barr virus-transformed B cell lines. Its production can be induced by bacteria, intracellular parasites, viruses, or their products in T cell-dependent and -independent pathways. IL-12 has proinflammatory and immunoregulatory acti
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Interferonsntial role of biological strategies for melanoma. IFN-α2 is now licensed in more than 50 countries for more than a dozen clinical indications including melanoma. The clinical effectiveness of IFN-α2 has been established both in the adjuvant and metastatic clinical settings. IFNs were the first previ
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