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Publications by S. M. Singh
Missense Mutations in Dystrophin That Trigger Muscular Dystrophy Decrease Protein Stability and Lead to Cross- Aggregates
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Related publications
Severe Muscular Dystrophy in Mice That Lack Dystrophin and 7 Integrin
Journal of Cell Science
Cell Biology
Neuronal Nitric Oxide Synthase and Dystrophin-Deficient Muscular Dystrophy.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Two Novel Missense Mutations in the Myostatin Gene Identified in Japanese Patients With Duchenne Muscular Dystrophy
BMC Medical Genetics
Genetics
Protein Stability and in Vivo Concentration of Missense Mutations in Phenylalanine Hydroxylase
Proteins: Structure, Function and Genetics
Biochemistry
Structural Biology
Molecular Biology
Dual Exon Skipping in Myostatin and Dystrophin for Duchenne Muscular Dystrophy
BMC Medical Genomics
Genetics
Immune Responses to Dystrophin: Implications for Gene Therapy of Duchenne Muscular Dystrophy
Gene Therapy
Molecular Medicine
Genetics
Molecular Biology
Distribution of Dystrophin and Dystrophin-Associated Protein 43DAG (.BETA.-dystroglycan) in the Central Nervous System of Normal Controls and Patients With Duchenne Muscular Dystrophy.
Internal Medicine
Internal Medicine
Medicine
Deficiency of Dystrophin-Associated Proteins in Duchenne Muscular Dystrophy Patients Lacking COOH-terminal Domains of Dystrophin.
Journal of Clinical Investigation
Medicine
Limb-Girdle Muscular Dystrophy Due to Emerin Gene Mutations
Archives of Neurology
