生物
清脆的
基因组编辑
计算生物学
基因组
遗传学
基因
作者
Martin Pacesa,Oana Pelea,Martin Jínek
出处
期刊:Cell
[Cell Press]
日期:2024-02-01
卷期号:187 (5): 1076-1100
被引量:109
标识
DOI:10.1016/j.cell.2024.01.042
摘要
Genome editing has been a transformative force in the life sciences and human medicine, offering unprecedented opportunities to dissect complex biological processes and treat the underlying causes of many genetic diseases. CRISPR-based technologies, with their remarkable efficiency and easy programmability, stand at the forefront of this revolution. In this Review, we discuss the current state of CRISPR gene editing technologies in both research and therapy, highlighting limitations that constrain them and the technological innovations that have been developed in recent years to address them. Additionally, we examine and summarize the current landscape of gene editing applications in the context of human health and therapeutics. Finally, we outline potential future developments that could shape gene editing technologies and their applications in the coming years.
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