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1. Networking to Optimize Dmd exon 53 Skipping in the Brain of mdx52 Mouse Model

11. Loss-of-function mutations in SCN4A cause severe foetal hypokinesia or ‘classical’ congenital myopathy

14. Dystrophin involvement in peripheral circadian SRF signalling

17. Stem cell function, self-renewal, and behavioral heterogeneity of cells from the adult muscle satellite cell niche

18. Myf5 expression in satellite cells and spindles in adult muscle is controlled by separate genetic elements

22. Dystrophin quantification and clinical correlations in Becker muscular dystrophy: implications for clinical trials

24. Myostatin inhibition in combination with antisense oligonucleotide therapy improves outcomes in spinal muscular atrophy

27. A novel high-throughput immunofluorescence analysis method for quantifying dystrophin intensity in entire transverse sections of Duchenne muscular dystrophy muscle biopsy samples

28. Selective release of muscle-specific, extracellular microRNAs during myogenic differentiation

29. Histopathological Defects in Intestine in Severe Spinal Muscular Atrophy Mice Are Improved by Systemic Antisense Oligonucleotide Treatment

35. Whole exome sequencing in patients with congenital myopathy

37. Loss-of-function mutations inSCN4Acause severe foetal hypokinesia or ‘classical’ congenital myopathy

42. Dystromirs as Serum Biomarkers for Monitoring the Disease Severity in Duchenne Muscular Dystrophy

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