Long-term maintenance of dystrophin expression and resistance to injury of skeletal muscle in gene edited DMD mice
Author:
Publisher
Elsevier BV
Subject
Drug Discovery,Molecular Medicine
Reference46 articles.
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2. Therapy for Duchenne muscular dystrophy: renewed optimism from genetic approaches;Fairclough;Nat. Rev. Genet.,2013
3. Absence of Dystrophin disrupts skeletal muscle signaling: roles of Ca2+, reactive oxygen species, and nitric oxide in the development of muscular dystrophy;Allen;Physiol. Rev.,2016
4. Single-cut genome editing restores dystrophin expression in a new mouse model of muscular dystrophy;Amoasii;Sci. Transl Med.,2017
5. Gene editing restores dystrophin expression in a canine model of Duchenne muscular dystrophy;Amoasii;Science,2018
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