Facioscapulohumeral Muscular Dystrophy is Associated With Altered Myoblast Proteome Dynamics
Author:
Publisher
Elsevier BV
Subject
Molecular Biology,Biochemistry,Analytical Chemistry
Reference76 articles.
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2. A unifying genetic model for facioscapulohumeral muscular dystrophy;Lemmers;Science,2010
3. Endogenous DUX4 expression in FSHD myotubes is sufficient to cause cell death and disrupts RNA splicing and cell migration pathways;Rickard;Hum. Mol. Genet.,2015
4. Expression profiling of FSHD muscle supports a defect in specific stages of myogenic differentiation;Winokur;Hum. Mol. Genet.,2003
5. Facioscapulohumeral muscular dystrophy (FSHD) myoblasts demonstrate increased susceptibility to oxidative stress;Winokur;Neuromuscul. Disord.,2003
Cited by 3 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. A novel family of lncRNAs relate facioscapulohumeral muscular dystrophy to nucleolar architecture and protein synthesis;2024-06-29
2. The DUX4–HIF1α Axis in Murine and Human Muscle Cells: A Link More Complex Than Expected;International Journal of Molecular Sciences;2024-03-15
3. Molecular and Phenotypic Changes in FLExDUX4 Mice;Journal of Personalized Medicine;2023-06-25
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