Enhanced AAV transduction across preclinical CNS models: A comparative study in human brain organoids with cross-species evaluations-Reference-Cited by-同舟云学术

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Enhanced AAV transduction across preclinical CNS models: A comparative study in human brain organoids with cross-species evaluations

Published:2024-09 Issue:3 Volume:35 Page:102264
ISSN:2162-2531
Container-title:Molecular Therapy - Nucleic Acids
language:en
Short-container-title:Molecular Therapy - Nucleic Acids

Author:

Drouyer Matthieu,Merjane Jessica,Nedelkoska Teodora,Westhaus Adrian,Scott Suzanne,Lee Scott,Burke Peter G.R.,McMullan Simon,Lanciego Jose L.,Vicente Ana F.,Bugallo Ricardo,Unzu Carmen,González-Aseguinolaza Gloria,Gonzalez-Cordero Anai,Lisowski Leszek^ORCID

Publisher

Elsevier BV

Reference62 articles.

1. Capsid Modifications for Targeting and Improving the Efficacy of AAV Vectors;Buning;Mol. Ther. Methods Clin. Dev.,2019

2. Fantastic AAV Gene Therapy Vectors and How to Find Them-Random Diversification, Rational Design and Machine Learning;Becker;Pathogens,2022

3. AAV vectors: The Rubik's cube of human gene therapy;Pupo;Mol. Ther.,2022

4. FDA approves first haemophilia B gene therapy;Mullard;Nat. Rev. Drug Discov.,2023

5. FDA approves first gene therapy for Duchenne muscular dystrophy, despite internal objections;Mullard;Nat. Rev. Drug Discov.,2023

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Cas‐CLOVER‐mediated knockout of STAT1: A novel approach to engineer packaging HEK‐293 cell lines used for rAAV production;Biotechnology Journal;2024-09

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