Overexpression of γ-Sarcoglycan Induces Severe Muscular Dystrophy
Open Access
- 1 June 2001
- journal article
- Published by Elsevier
- Vol. 276 (24) , 21785-21790
- https://doi.org/10.1074/jbc.m101877200
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- Clinical Protocol: Phase I Clinical Trial Utilizing Gene Therapy for Limb Girdle Muscular Dystrophy: alpha-, beta-, gamma-, or delta-Sarcoglycan Gene Delivered with Intramuscular Instillations of Adeno-Associated VectorsHuman Gene Therapy, 2000
- Rescue of Skeletal Muscles of γ-Sarcoglycan- Deficient Mice with Adeno-Associated Virus-Mediated Gene TransferMolecular Therapy, 2000
- Functional Rescue of the Sarcoglycan Complex in the BIO 14.6 Hamster Using δ-Sarcoglycan Gene TransferMolecular Cell, 1998
- Transcriptional targeting of replication-defective adenovirus transgene expression to smooth muscle cells in vivo.Journal of Clinical Investigation, 1997
- Efficient muscle-specific transgene expression after adenovirus-mediated gene transfer in mice using a 1.35 kb muscle creatine kinase promoter/enhancerGene Therapy, 1997
- β–sarcoglycan: characterization and role in limb–girdle muscular dystrophy linked to 4q12Nature Genetics, 1995
- β–sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complexNature Genetics, 1995
- Deficiency of dystrophin-associated proteins in Duchenne muscular dystrophy patients lacking COOH-terminal domains of dystrophin.Journal of Clinical Investigation, 1993
- MdxTransgenic Mouse: Restoration of Recombinant Dystrophin to the Dystrophic MuscleHuman Gene Therapy, 1993
- Fast muscle fibers are preferentially affected in Duchenne muscular dystrophyCell, 1988