Dystrophin and disease
Author:
Publisher
Elsevier BV
Subject
Clinical Biochemistry,Molecular Biology,Molecular Medicine,General Medicine,Biochemistry
Reference72 articles.
1. Immunostaining of skeletal and cardiac muscle surface membrane with antibody against Duchenne muscular dystrophy peptide;Arahata;Nature,1988
2. Mosaic expression of dystrophin in symptomatic carriers of Duchenne's muscular dystrophy;Arahata;New Eng J Med,1989
3. Dystrophin Diagnosis: Comparison of Dystrophin Abnormalities by Immunofluorescent and Immunoblot Analyses;Arahata,1989
4. Preservation of the C-terminus of dystrophin molecule in the skeletal muscle from Becker muscular dystrophy;Arahata;J. Neurol. Sci.,1991
5. The frequency of patients having dystrophin abnormalities in a limb-girdle patient population;Arikawa;Neurology,1991
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1. Increase in cathepsin K gene expression in Duchenne muscular dystrophy skeletal muscle;Neuropathology;2024-07-16
2. The potential and benefits of repurposing existing drugs to treat rare muscular dystrophies;Expert Opinion on Orphan Drugs;2018-03-20
3. Ryanodine channel complex stabilizer compound S48168/ARM210 as a disease modifier in dystrophin‐deficient mdx mice: proof‐of‐concept study and independent validation of efficacy;The FASEB Journal;2018-01-03
4. Elusive sources of variability of dystrophin rescue by exon skipping;Skeletal Muscle;2015-12
5. Long-term treatment with naproxcinod significantly improves skeletal and cardiac disease phenotype in the mdx mouse model of dystrophy;Human Molecular Genetics;2014-01-23
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