插入突变
生物
向性
转基因
遗传增强
计算生物学
病毒载体
整合酶
载体(分子生物学)
突变
病毒学
基因靶向
基因
遗传学
突变
重组DNA
病毒
基因组
作者
Marisa Banasik,Paul B. McCray
出处
期刊:Gene Therapy
[Springer Nature]
日期:2009-10-22
卷期号:17 (2): 150-157
被引量:119
摘要
Lentiviral vectors (LVs) offer the advantages of a large packaging capacity, broad cell tropism or specific cell-type targeting through pseudotyping, and long-term expression from integrated gene cassettes. However, transgene integration carries a risk of disrupting gene expression through insertional mutagenesis and may not be required for all applications. A non-integrating LV may be beneficial in cases in which transient gene expression is desired. Several recent publications outline the development and initial biological characterization of such vectors. Here, we discuss the potential applications and new directions for the development of integration-defective LVs.
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