| 标题 |
Adeno-Associated Virus Vectors: Principles, Practicesand Prospects in Gene Therapy
腺相关病毒载体：基因治疗的原理、实践与展望
|
| 网址 |
求助人暂未提供
|
| DOI |
暂未提供，该求助的时间将会延长，查看原因？
|
| 其它 |
Abstract Gene therapy offers promising potential as an efficacious and long-lasting therapeutic option for genetic conditions, by correcting defective mutations using engineered vectors to deliver genetic material to host cells. Among these vectors, adeno-associated viruses (AAVs) stand out for their efficiency, versatility, and safety, making them one of the leading platforms in gene therapy. The enormous potential of AAVs has been demonstrated through their use in over 225 clinical trials and the FDA’s approval of six AAV-based gene therapy products, positioning these vectors at the forefront of the field. This review highlights the evolution and current applications of AAVs in gene therapy, focusing on their clinical successes, ongoing developments, and the manufacturing processes required for the rapid commercial growth anticipated in the AAV therapy market. |
| 求助人 | |
| 下载 |
PDF的下载单位、IP信息已删除
(2025-6-4)
菜菜菜
cdercder
GingerF
Nole
Criminology34
馨馨的科科
无极微光
潇洒的惋清
平淡的梦菲
乐空思
heekkll
活雷锋
你嵙这个期刊没买
cherry
伶俐书芹
mafukairi
怡然的凌兰
XX
轻松骁
初景
皖公网安备34019202002308
