Gene Editing for Duchenne Muscular Dystrophy Using the CRISPR/Cas9 Technology: The Importance of Fine-tuning the Approach
Author:
Publisher
Elsevier BV
Subject
Drug Discovery,Pharmacology,Genetics,Molecular Biology,Molecular Medicine
Reference15 articles.
1. In vivo genome editing improves muscle function in a mouse model of Duchenne muscular dystrophy;Nelson;Science,2016
2. In vivo gene editing in dystrophic mouse muscle and muscle stem cells;Tabebordbar;Science,2016
3. Postnatal genome editing partially restores dystrophin expression in a mouse model of muscular dystrophy;Long;Science,2016
4. CRISPR-mediated genome editing restores dystrophin expression and function in mdx mice;Xu;Mol Ther,2016
5. Current understanding of molecular pathology and treatment of cardiomyopathy in Duchenne muscular dystrophy;van Westering;Molecules,2015
Cited by 6 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. GENOME EDITING TECHNOLOGIES: CRISPR, LEAPER, RESTORE, ARCUT, SATI, AND RESCUE;EXCLI J;2021
2. In vivo non-invasive monitoring of dystrophin correction in a new Duchenne muscular dystrophy reporter mouse;Nature Communications;2019-10-04
3. AAV9 Edits Muscle Stem Cells in Normal and Dystrophic Adult Mice;Molecular Therapy;2019-09
4. Canada's Assisted Human Reproduction Act: Pragmatic Reforms in Support of Research;Frontiers in Medicine;2019-07-10
5. Gene editing restores dystrophin expression in a canine model of Duchenne muscular dystrophy;Science;2018-10-05
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