遗传增强
疾病
向性
腺相关病毒
计算生物学
基因
基因传递
临床试验
生物信息学
医学
生物
病毒学
遗传学
病毒
载体(分子生物学)
病理
重组DNA
作者
Shaza S. Issa,Alisa A. Shaimardanova,Valeriya V. Solovyeva,Albert A. Rizvanov
出处
期刊:Cells
[MDPI AG]
日期:2023-03-01
卷期号:12 (5): 785-785
被引量:111
标识
DOI:10.3390/cells12050785
摘要
Despite scientific discoveries in the field of gene and cell therapy, some diseases still have no effective treatment. Advances in genetic engineering methods have enabled the development of effective gene therapy methods for various diseases based on adeno-associated viruses (AAVs). Today, many AAV-based gene therapy medications are being investigated in preclinical and clinical trials, and new ones are appearing on the market. In this article, we present a review of AAV discovery, properties, different serotypes, and tropism, and a following detailed explanation of their uses in gene therapy for disease of different organs and systems.
科研通智能强力驱动
Strongly Powered by AbleSci AI