Utrophin-Dystrophin-Deficient Mice as a Model for Duchenne Muscular Dystrophy
Open Access
- 1 August 1997
- Vol. 90 (4), 717-727
- https://doi.org/10.1016/s0092-8674(00)80532-2
Abstract
No abstract availableKeywords
This publication has 43 references indexed in Scilit:
- Genes at the junction—candidates for congenital myasthenic syndromesTrends in Neurosciences, 1997
- The Receptor Tyrosine Kinase MuSK Is Required for Neuromuscular Junction Formation In VivoCell, 1996
- Utrophin: A Structural and Functional Comparison to DystrophinBrain Pathology, 1996
- Site and mechanics of failure in normal and dystrophin‐deficient skeletal muscleMuscle & Nerve, 1995
- Structure and function of the neuromuscular junction in young adultmdx miceJournal of Neurocytology, 1991
- Neuromuscular transmission in the mdx mouseMuscle & Nerve, 1990
- Three myosin heavy chain isoforms in type 2 skeletal muscle fibresJournal of Muscle Research and Cell Motility, 1989
- Ultrastructure of the skeletal muscle in the X chromosome-linked dystrophic (mdx) mouseActa Neuropathologica, 1988
- DUCHENNE DYSTROPHYBrain, 1974
- Neural regulation of enzymes in muscle fibers of red and white muscleExperimental Neurology, 1967