Animal Models for Genetic Neuromuscular Diseases
- 18 January 2008
- journal article
- review article
- Published by Springer Science and Business Media LLC in Journal of Molecular Neuroscience
- Vol. 34 (3), 241-248
- https://doi.org/10.1007/s12031-007-9023-9
Abstract
No abstract availableKeywords
This publication has 37 references indexed in Scilit:
- A Mutation in the Myostatin Gene Increases Muscle Mass and Enhances Racing Performance in Heterozygote DogsPLoS Genetics, 2007
- Pharmacologic and Functional Characterization of Malignant Hyperthermia in the R163C RyR1 Knock-in MouseAnesthesiology, 2006
- A rapid PCR method for genotyping the Largemyd mouse, a model of glycosylation-deficient congenital muscular dystrophyNeuromuscular Disorders, 2005
- Canine and feline models of human inherited muscle diseasesNeuromuscular Disorders, 2005
- Functional improvement of dystrophic muscle by myostatin blockadeNature, 2002
- Dystrophin expression in the mdx mouse restored by stem cell transplantationNature, 1999
- Targeted Disruption of Exon 52 in the Mouse Dystrophin Gene Induced Muscle Degeneration Similar to That Observed in Duchenne Muscular DystrophyBiochemical and Biophysical Research Communications, 1997
- Identification of a novel mutant transcript of laminin α2 chain gene responsible for muscular dystrophy and dysmyelination in dy2J miceHuman Molecular Genetics, 1995
- Canine X‐linked muscular dystrophy as an animal model of Duchenne muscular dystrophy: A reviewAmerican Journal of Medical Genetics, 1992
- Muscle development in mdx mutant miceMuscle & Nerve, 1984