基因敲除
基因靶向
锌指核酸酶
基因剔除小鼠
基因敲除
同源重组
条件基因敲除
基因
生物
胚胎干细胞
Cre-Lox重组
清脆的
Cas9
遗传学
细胞生物学
转基因
基因组编辑
转基因小鼠
表型
作者
Chaoxuan Wang,Hang Sun
出处
期刊:PubMed
[National Institutes of Health]
日期:2019-05-25
卷期号:35 (5): 784-794
被引量:5
标识
DOI:10.13345/j.cjb.180417
摘要
The establishment and development of gene knockout mice have provided powerful support for the study of gene function and the treatment of human diseases. Gene targeting and gene trap are two techniques for generating gene knockout mice from embryonic stem cells. Gene targeting replaces endogenous knockout gene by homologous recombination. There are two ways to knock out target genes: promoter trap and polyA trap. In recent years, many new gene knockout techniques have been developed, including Cre/loxP system, CRISP/Cas9 system, latest ZFN technology and TALEN technology. This article focuses on the several new knockout mouse techniques.
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