Optimized lentiviral vector to restore full-length dystrophin via a cell-mediated approach in a mouse model of Duchenne muscular dystrophy-Reference-Cited by-同舟云学术

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Optimized lentiviral vector to restore full-length dystrophin via a cell-mediated approach in a mouse model of Duchenne muscular dystrophy

Published:2022-06 Issue: Volume:25 Page:491-507
ISSN:2329-0501
Container-title:Molecular Therapy - Methods & Clinical Development
language:en
Short-container-title:Molecular Therapy - Methods & Clinical Development

Author:

Meng Jinhong^ORCID,Moore Marc^ORCID,Counsell John,Muntoni Francesco,Popplewell Linda,Morgan Jennifer^ORCID

Funder

NIHR Great Ormond Street Hospital Biomedical Research Centre

Wellcome Trust

Muscular Dystrophy UK

Great Ormond Street Hospital Charity

Publisher

Elsevier BV

Subject

Genetics,Molecular Biology,Molecular Medicine

Reference112 articles.

1. Genetic analysis of Duchenne dystrophy;Kunkel;Adv. Exp. Med. Biol.,1985

2. Duchenne muscular dystrophy;Duan;Nat. Rev. Dis. Prim.,2021

3. Systemic AAV micro-dystrophin gene therapy for duchenne muscular dystrophy;Duan;Mol. Ther.,2018

4. Adeno-associated virus (AAV) mediated dystrophin gene transfer studies and exon skipping strategies for duchenne muscular dystrophy (DMD);Kawecka;Curr. Gene Ther.,2015

5. Full-length dystrophin reconstitution with adeno-associated viral vectors;Lostal;Hum. Gene Ther.,2014

Cited by 4 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. Cell therapy for duchenne muscular dystrophy using induced pluripotent stem cell-derived muscle stem cells and the potential of regenerative rehabilitation;Current Opinion in Biomedical Engineering;2024-06

2. Designing molecules: directing stem cell differentiation;Frontiers in Bioengineering and Biotechnology;2024-05-10

3. Duchenne muscular dystrophy treatment with lentiviral vector containing mini‐dystrophin gene in vivo;MedComm;2024-01

4. Modified mRNA as a Treatment for Myocardial Infarction;International Journal of Molecular Sciences;2023-03-01

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