Muscle Gene Therapy

Part 1 Foundations for muscle gene therapy.- Chapter 1. An overview of muscle biology and physiology for muscle gene therapy.- Chapter 2. Molecular basis of muscle disease.- Chapter 3. Animal models for muscle disease and muscle gene therapy.- Chapter 4. Muscle stem cell biology and implication in gene therapy.- Chapter 5. Pluripotent stem cells for gene therapy of hereditary muscle disorders.- Chapter 6. MicroRNAs (miRs) in muscle gene therapy.- Chapter 7. Immune system regulation of muscle injury and disease.- Chapter 8. Design of muscle gene therapy expression cassette.- Chapter 9 Non-viral vector mediated muscle gene therapy.- Chapter 10. Viral vectors for muscle gene therapy.- Chapter 11. Development of next generation muscle gene therapy AAV vectors.- Chapter 12. Histological and biochemical evaluation of muscle gene therapy.- Chapter 13. Optical polarization tractography imaging of structural changes in the skeletal and cardiac muscles of the mdx4cv mice.- Chapter 14. Biomarkers for muscle disease gene therapy.- Chapter 15. Large-scale clinical manufacturing of AAV Vectors for systemic muscle gene therapy.- Chapter 16. Genome-editing for muscle gene therapy.- Part 2 Preclinical muscle gene therapy.- Chapter 17. Considerations on preclinical muscle gene therapy studies.- Chapter 18. Gene replacement therapy for Duchenne muscular dystrophy.- Chapter 19. Recent advances in AON-mediated exon-skipping therapy for Duchenne muscular dystrophy.- Chapter 20. AAV-mediated exon-skipping therapy for Duchenne muscular dystrophy.- Chapter 21. Alternate translational initiation of dystrophin: a novel therapeutic approach.- Chapter 22. Genome editing for Duchenne muscular dystrophy.- Chapter 23. Sarcolipin knockdown therapy for Duchenne muscular dystrophy.- Chapter 24. Gene therapy for central nervous system in Duchenne muscular

Dongsheng Duan, Ph.D., is the Margaret Proctor Mulligan Professor in Medical Research, at the Department of Molecular Microbiology & Immunology, Neurology, Bioengineering, and Biomedical Sciences at the University of Missouri. He received his medical degree from the West China University of Medical Science, Chengdu, China in 1987 and his Ph.D. degree from the University of Pennsylvania, Philadelphia, USA in 1997. His research in last two decades has focused on the development of adeno-associated virus as a gene therapy vector, pathogenic mechanisms of Duchenne muscular dystrophy, dystrophin biology and preclinical gene therapy for Duchenne muscular dystrophy in murine and canine models.





Jerry R Mendell, M.D. is the Curran-Peters Research Chair and Professor of Pediatrics and Neurology. His career has been devoted to translational clinical science, beginning as a post doctoral fellow at the National Institutes of Health. His life-long focus has been to make a difference in lives burdened with untreatable neuromuscular disease. He has contributed significantly to the muscular dystrophies and spinal muscular atrophy, at first using pharmaceutical tools and since 1999, the time of his first gene therapy trial, he has been dedicated to the successful replacement of mutant genes that undermine the lives of innocent victims.