Correction of human nonsense mutation via adenine base editing for Duchenne muscular dystrophy treatment in mouse-Reference-Cited by-同舟云学术

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Correction of human nonsense mutation via adenine base editing for Duchenne muscular dystrophy treatment in mouse

Published:2024-06 Issue:2 Volume:35 Page:102165
ISSN:2162-2531
Container-title:Molecular Therapy - Nucleic Acids
language:en
Short-container-title:Molecular Therapy - Nucleic Acids

Author:

Jin Ming,Lin Jiajia,Li Haisen,Li Zhifang,Yang Dong,Wang Yin,Yu Yuyang,Shao Zhurui,Chen Long,Wang Zhiqiang,Zhang Yu,Zhang Xiumei,Wang Ning,Xu Chunlong^ORCID,Yang Hui,Chen Wan-Jin,Li Guoling

Publisher

Elsevier BV

Reference51 articles.

1. Dystrophin: the protein product of the Duchenne muscular dystrophy locus;Hoffman;Cell,1987

2. Correction of muscular dystrophies by CRISPR gene editing;Chemello;J. Clin. Invest.,2020

3. Dystrophin complex functions as a scaffold for signalling proteins;Constantin;Biochim. Biophys. Acta,2014

4. Function and genetics of dystrophin and dystrophin-related proteins in muscle;Blake;Physiol. Rev.,2002

5. Muscular dystrophies;Mercuri;Lancet,2013

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. Adenine base editing-mediated exon skipping restores dystrophin in humanized Duchenne mouse model;Nature Communications;2024-07-15

2. Therapeutic Nonsense Suppression Modalities: From Small Molecules to Nucleic Acid-Based Approaches;Biomedicines;2024-06-10

3. Anticodon Engineered Transfer RNAs (ACE-tRNAs) are a Platform Technology for Suppressing Nonsense Mutations;2024-06-06

4. Base editing in humanized dystrophic mice;Molecular Therapy - Nucleic Acids;2024-06

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