清脆的
Cas9
生物
回文
核酸酶
基因
基因组编辑
DNA
遗传学
计算生物学
作者
Haibin Jiang,Mengyan Tang,Zidi Xu,Yanan Wang,Mopu Li,Shuyin Zheng,Jianghu Zhu,Zhenlang Lin,Min Zhang
标识
DOI:10.1016/j.gendis.2023.03.017
摘要
The clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) system is an acquired immune system of many bacteria and archaea, comprising CRISPR loci, Cas genes, and its associated proteins. This system can recognize exogenous DNA and utilize the Cas9 protein's nuclease activity to break DNA double-strand and to achieve base insertion or deletion by subsequent DNA repair. In recent years, multiple laboratory and clinical studies have revealed the therapeutic role of the CRISPR/Cas9 system in neurological diseases. This article reviews the CRISPR/Cas9-mediated gene editing technology and its potential for clinical application against neurological diseases.
科研通智能强力驱动
Strongly Powered by AbleSci AI