Repair pathways in response to DNA double-strand breaks
Huang, Min; Miao, Ze-Hong; Ding, Jian
2007-10
卷号38
期号4
页码295-300
英文摘要DNA double-strand breaks (DSBs) are the principal cytotoxic lesions caused by many exogenous and endogenous factors. In response to DSBs, cells have evolved complex and highly conserved systems, which mainly consist of homologous recombination repair (HR) and non-homologous end joining (NHEJ) pathways, to effectively repair the lethal lesions. The two pathways play crucial roles in preserving the genomic integrity. Here, we provide an overview of detailed process, concerned molecules and regulatory factors in these pathways. Accumulated knowledge of DSBs repair may offer opportunities to develop more effective treatments for cancer.
会议录Sheng li ke xue jin zhan [Progress in physiology]
文献子类Meeting Abstract;Article;Review
语种中文
内容类型会议论文
源URL[http://119.78.100.183/handle/2S10ELR8/266887]  
专题药理学第一研究室
作者单位Divisn of Anti-tumor Pharmacology, State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China
推荐引用方式
GB/T 7714
Huang, Min,Miao, Ze-Hong,Ding, Jian. Repair pathways in response to DNA double-strand breaks[C]. 见:.
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