Duchenne muscular dystrophy and the neuromuscular junction: The utrophin link
Author:
Publisher
Wiley
Subject
General Biochemistry, Genetics and Molecular Biology
Reference42 articles.
1. Subtle Neuromuscular Defects in Utrophin-deficient Mice
2. Postsynaptic Abnormalities at the Neuromuscular Junctions of Utrophin-deficient Mice
3. Amelioration of the dystrophic phenotype of mdx mice using a truncated utrophin transgene
4. Molecular and Functional Analysis of the Utrophin Promoter
5. Local Transcriptional Control of Utrophin Expression at the Neuromuscular Synapse
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1. Age‐dependent changes in metabolite profile and lipid saturation in dystrophic mice;NMR in Biomedicine;2019-03-08
2. Thermodynamic stability, unfolding kinetics, and aggregation of the N-terminal actin-binding domains of utrophin and dystrophin;Proteins: Structure, Function, and Bioinformatics;2012-02-17
3. Transgene Design;Methods in Molecular Biology;2010-10-04
4. The artificial gene Jazz, a transcriptional regulator of utrophin, corrects the dystrophic pathology in mdx mice;Human Molecular Genetics;2009-12-04
5. New therapies for Duchenne muscular dystrophy: challenges, prospects and clinical trials;Trends in Molecular Medicine;2007-12
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