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Titlebook: BRAF Targets in Melanoma; Biological Mechanism Ryan J. Sullivan Book 2015 Springer Science+Business Media New York 2015 BRAF-inhibitors.Nex

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发表于 2025-3-21 18:05:47 | 显示全部楼层 |阅读模式
期刊全称BRAF Targets in Melanoma
期刊简称Biological Mechanism
影响因子2023Ryan J. Sullivan
视频video
发行地址Examines BRAF-directed targets in melanoma including molecular biology/signal transduction, molecular diagnostics, immunology, and next-generation analytics.Highlights and summarizes the unique biolog
学科分类Cancer Drug Discovery and Development
图书封面Titlebook: BRAF Targets in Melanoma; Biological Mechanism Ryan J. Sullivan Book 2015 Springer Science+Business Media New York 2015 BRAF-inhibitors.Nex
影响因子​This volume contains a collection of writings from the leaders in the fields of Molecular Biology and Melanoma Research which will begin to tell the ever-expanding story of the most recent findings, discoveries, and potential of BRAF-directed targets in melanoma. Recent research has shown that BRAF inhibitors are effective for a short period of time, but there is little hope that this drugs as single agents will lead to durable benefit in a majority of patients. Among scientists and researchers who work in drug discovery, there is a lot of interest in the development of molecularly targeted cancer agents. Namely, the identification of a molecular target, the selection of molecules which effectively inhibit this target. What is starkly different about the development of this class of compounds, however, is that the mechanism of action of these agents are not as straightforward as was once previously assumed and the mechanisms of resistance that tumor cells employ to evade complete destruction are unlike any that have been described before. These discoveries in addition to utilization of modern molecular biology techniques have led to a series of hypotheses regarding which other typ
Pindex Book 2015
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Targeting the Cell Cycle and p53 in Combination with ,-Directed Therapy,d MDM4. The alterations in these pathways appear to play critical roles in the development of melanoma and may represent potential therapeutic targets. Furthermore, some studies suggest that there is interaction between ., key cell cycle proteins and the p53 pathway and that . inhibitors may synergi
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Telecommunications Network Designion of other pro-survival mediators. These findings are now leading to the development of new combinatorial approaches that involve serial and/or parallel blockade strategies in order to overcome resistance mechanisms, and ultimately to improve outcomes in melanoma patients with activating . mutatio
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Book 2015e previously assumed and the mechanisms of resistance that tumor cells employ to evade complete destruction are unlike any that have been described before. These discoveries in addition to utilization of modern molecular biology techniques have led to a series of hypotheses regarding which other typ
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Springer Optimization and Its Applications the discovery of activating B-raf mutations in melanoma, and concluding with the current immune and targeted based therapies for advanced melanoma. It serves as a segue to the more detailed therapies and advances in the ensuing chapters.
发表于 2025-3-23 08:45:24 | 显示全部楼层
Julio López,Marcos J. Rider,Javier Contrerasys. BRAF is the most commonly affected gene, with BRAF(V600E) mutations found in half of all melanomas. The discovery and characterization of oncogenic mutations in the MAPK, RB, p53, and MITF pathways have set the stage for clinically meaningful progress in the melanoma field.
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