Muscle & Nerve · 2002 · 43 citations · 27 references
Life SciencesNeurosciencePhysiologyExercise TestingMotor NeurosciencePathophysiologyAge-related Muscle LossLocomotion AnalysisMuscular DystrophyMuscular EnduranceMuscular Endurance TestingNeurodegenerative DiseasesDystrophin DeficiencyEnduranceMuscular Dystrophy PathophysiologyQuantitative Data CollectionRodent Movement DisordersRunning AdaptationsRunning Physiology
The mdx mouse lacks dystrophin and has histological features of Duchenne muscular dystrophy but little weakness in the first year of life. We report here an early deficit in voluntary wheel running, as assayed with a computerized wheel. All mdx mice showed an intermittent running pattern, in contrast to the continuous running seen in controls. The average continuous running time differed significantly between mdx and control mice at all ages tested (5-21 weeks). This assay is noninvasive, has the advantage of unbiased automatic data collection, and should be useful for quantifying the mdx deficit in therapeutic studies.
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X chromosome-linked muscular dystrophy (mdx) in the mouse.
G. Bulfield, W. G. Siller, P.A.L. Wight et al. · Proceedings of the National Academy of Sciences · 1984 · 1.8K citations · Full text
The Molecular Basis of Muscular Dystrophy in the <i>mdx</i> Mouse: a Point Mutation
Piotr Siciński, Yan Geng, Allan S. Ryder-Cook et al. · Science · 1989 · 1.2K citations
The mdx mouse diaphragm reproduces the degenerative changes of Duchenne muscular dystrophy
Hansell H. Stedman, H. Lee Sweeney, Joseph B. Shrager et al. · Nature · 1991 · 916 citations
Medicine, Cell Biology, Neurology +12