Delivery of CRISPR/Cas9 system by AAV as vectors for gene therapy-Reference-Cited by-同舟云学术

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Delivery of CRISPR/Cas9 system by AAV as vectors for gene therapy

Published:2024-11 Issue: Volume:927 Page:148733
ISSN:0378-1119
Container-title:Gene
language:en
Short-container-title:Gene

Author:

Wang Yanan,Jiang Haibin,Li Mopu,Xu Zidi,Xu Hang,Chen Yuetong,Chen Kepei,Zheng Weihong^ORCID,Lin Wei,Liu Zhiming,Lin Zhenlang,Zhang Min

Funder

National Natural Science Foundation of China

Publisher

Elsevier BV

Reference81 articles.

1. Adenovirus-associated defective virus particles;Atchison;Science,1965

2. A glance at genome editing with CRISPR–Cas9 technology;Barman;Curr. Genet.,2020

3. Engineering the AAV capsid to evade immune responses;Barnes;Curr. Opin. Biotechnol.,2019

4. Infectious entry pathway of adeno-associated virus and adeno-associated virus vectors;Bartlett;J. Virol.,2000

5. In vivo delivery of CRISPR-Cas9 therapeutics: Progress and challenges;Behr;Acta Pharm. Sin. B,2021

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