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Publications by Samira Jambi
Molecular Characterization of Exonic Rearrangements and Frame Shifts in the Dystrophin Gene in Duchenne Muscular Dystrophy Patients in a Saudi Community
Human Genomics
Molecular Medicine
Drug Discovery
Genetics
Molecular Biology
Related publications
Deficiency of Dystrophin-Associated Proteins in Duchenne Muscular Dystrophy Patients Lacking COOH-terminal Domains of Dystrophin.
Journal of Clinical Investigation
Medicine
Corrigendum: Reading Frame Correction by Targeted Genome Editing Restores Dystrophin Expression in Cells From Duchenne Muscular Dystrophy Patients
Molecular Therapy
Molecular Medicine
Molecular Biology
Pharmacology
Medicine
Genetics
Drug Discovery
Dystrophin Dp116: A Yet to Be Investigated Product of the Duchenne Muscular Dystrophy Gene
Genes
Genetics
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
150. Ex Vivo Gene Therapy of Duchenne Muscular Dystrophy Using iPSCs From Duchenne Muscular Dystrophy Patients
Molecular Therapy
Molecular Medicine
Molecular Biology
Pharmacology
Medicine
Genetics
Drug Discovery
Duchenne Muscular Dystrophy Gene Therapy: Lost in Translation?
Research and Reports in Biology
Localisation and Characterisation of Dystrophin in the Central Nervous System of Controls and Patients With Duchenne Muscular Dystrophy.
Journal of Neurology, Neurosurgery and Psychiatry
Psychiatry
Mental Health
Neurology
Surgery
Becker Muscular Dystrophy in Indian Patients: Analysis of Dystrophin Gene Deletion Patterns
Neurology India
Neurology
