基因组编辑
遗传增强
时间轴
计算生物学
基因传递
疾病
基因组
基因
生物信息学
医学
生物
计算机科学
遗传学
历史
病理
考古
作者
Natalie J. Holl,Han-Jung Lee,Yue‐Wern Huang
标识
DOI:10.2174/1566523220666201208092517
摘要
There are more than 3,500 genes that are being linked to hereditary diseases or correlated with an elevated risk of certain illnesses. As an alternative to conventional treatments with small molecule drugs, gene therapy has arisen as an effective treatment with the potential to not just alleviate disease conditions but also cure them completely. In order for these treatment regimens to work, genes or editing tools intended to correct diseased genetic material must be efficiently delivered to target sites. There have been many techniques developed to achieve such a goal. In this article, we systematically review a variety of gene delivery and therapy methods that include physical methods, chemical and biochemical methods, viral methods, and genome editing. We discuss their historical discovery, mechanisms, advantages, limitations, safety, and perspectives.
科研通智能强力驱动
Strongly Powered by AbleSci AI