In Vivo Genome Engineering for the Treatment of Muscular Dystrophies-Reference-Cited by-同舟云学术

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In Vivo Genome Engineering for the Treatment of Muscular Dystrophies

Published:2020-06-19 Issue:3 Volume:6 Page:52-66
ISSN:2198-7866
Container-title:Current Stem Cell Reports
language:en
Short-container-title:Curr Stem Cell Rep

Author:

Kustermann Monika,Rok Matthew J.,Cohn Ronald D.,Ivakine Evgueni A.

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Developmental Biology,Genetics,Molecular Biology

Link

https://link.springer.com/content/pdf/10.1007/s40778-020-00173-3.pdf

Reference106 articles.

1. Dowling JJ, Gonorazky HD, Cohn RD, Campbell C. Treating pediatric neuromuscular disorders: the future is now. Am J Med Genet A. 2018;176(4):804–41. https://doi.org/10.1002/ajmg.a.38418.

2. Shieh PB. Muscular dystrophies and other genetic myopathies. Neurol Clin. 2013;31(4):1009–29. https://doi.org/10.1016/j.ncl.2013.04.004.

3. Crispi V, Matsakas A. Duchenne muscular dystrophy: genome editing gives new hope for treatment. Postgrad Med J. 2018;94(1111):296–304. https://doi.org/10.1136/postgradmedj-2017-135377.

4. Bladen CL, Salgado D, Monges S, Foncuberta ME, Kekou K, Kosma K, et al. The TREAT-NMD DMD global database: analysis of more than 7,000 Duchenne muscular dystrophy mutations. Hum Mutat. 2015;36(4):395–402. https://doi.org/10.1002/humu.22758.

5. Wong TWY, Cohn RD. Therapeutic applications of CRISPR/Cas for Duchenne muscular dystrophy. Curr Gene Ther. 2017;17(4):301–8. https://doi.org/10.2174/1566523217666171121165046.

Cited by 2 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. Prevention of early-onset cardiomyopathy in Dmd exon 52–54 deletion mice by CRISPR-Cas9-mediated exon skipping;Molecular Therapy - Methods & Clinical Development;2023-09

2. Advances in CRISPR/Cas9 Genome Editing for the Treatment of Muscular Dystrophies;Human Gene Therapy;2023-05-01

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