CRISPR-mediated Genome Editing Restores Dystrophin Expression and Function in mdx Mice-Reference-Cited by-同舟云学术

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CRISPR-mediated Genome Editing Restores Dystrophin Expression and Function in mdx Mice

Published:2016-03 Issue:3 Volume:24 Page:564-569
ISSN:1525-0016
Container-title:Molecular Therapy
language:en
Short-container-title:Molecular Therapy

Author:

Xu Li,Park Ki Ho,Zhao Lixia,Xu Jing,El Refaey Mona,Gao Yandi,Zhu Hua,Ma Jianjie,Han Renzhi

Publisher

Elsevier BV

Subject

Drug Discovery,Pharmacology,Genetics,Molecular Biology,Molecular Medicine

Reference30 articles.

1. Molecular basis of muscular dystrophies;Cohn;Muscle Nerve,2000

2. Mechanisms of muscle degeneration, regeneration, and repair in the muscular dystrophies;Wallace;Annu Rev Physiol,2009

3. Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals;Koenig;Cell,1987

4. Population frequencies of inherited neuromuscular diseases–a world survey;Emery;Neuromuscul Disord,1991

5. Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage;Campbell;Cell,1995

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2. Molecular and Biochemical Therapeutic Strategies for Duchenne Muscular Dystrophy;Neurology International;2024-07-05

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5. Viral and nonviral nanocarriers for in vivo CRISPR-based gene editing;Nano Research;2024-06-20

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