Article
Duchenne-like myopathy in double-mutant mdx mice expressing exaggerated mast cell activity.
Journal of the neurological sciences - 1 Jul 1995
Granchelli J A, Pollina C, Hudecki M S
Abstract excerpt
Dystrophin-deficient female mdx mice were bred with male Tsk+/+ pa mice to examine the role played by mast cells in the pathophysiology of dystrophin deficiency. Resultant mdx/Tsk double-mutant mice were then examined functionally, biochemically, and histologically. While mdx mice remained as strong as their normal counterparts, mdx/Tsk double-mutant mice became progressively weak with age. Serum creatine kinase...
Topics
- Animals
- Chymases
- Creatine Kinase
- Dystrophin
- Female
- Male
- Mast Cells
- Mice
- Mice, Mutant Strains
- Muscle, Skeletal
- Muscular Dystrophy, Animal
- Mutation
