Voluntary wheel running improves molecular and functional deficits in a murine model of facioscapulohumeral muscular dystrophy
Author:
Funder
NIAMS
American Physical Therapy Association
Muscular Dystrophy Association
NICHD
Publisher
Elsevier BV
Subject
Multidisciplinary
Reference101 articles.
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2. Loss of epigenetic silencing of the DUX4 transcription factor gene in facioscapulohumeral muscular dystrophy: Figure 1;Hewitt;Hum Mol Gen,2015
3. Facioscapulohumeral Muscular Dystrophy;Statland;Continuum,2016
4. DUX4, a candidate gene of facioscapulohumeral muscular dystrophy, encodes a transcriptional activator of PITX1;Dixit;Proc. Natl. Acad. Sci. USA,2007
5. Facioscapulohumeral muscular dystrophy is uniquely associated with one of the two variants of the 4q subtelomere;Lemmers;Nat. Genet.,2002
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1. Muscle strength, quantity and quality and muscle fat quantity and their association with oxidative stress in patients with facioscapulohumeral muscular dystrophy: Effect of antioxidant supplementation;Free Radical Biology and Medicine;2024-07
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