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Muscular dystrophies, the cytoskeleton and cell adhesion

✍ Scribed by Heather J. Spence; Yun-Ju Chen; Steven J. Winder


Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
464 KB
Volume
24
Category
Article
ISSN
0265-9247

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πŸ“œ SIMILAR VOLUMES


Respiratory function in the muscular dys
✍ Dr. Y. Rideau; Dr. L. W. Jankowski; Dr. J. Grellet πŸ“‚ Article πŸ“… 1981 πŸ› John Wiley and Sons 🌐 English βš– 779 KB

## Abstract The purpose of this investigation was to compare the respiratory function of patients with different clinical types of muscular dystrophy (MD). A total of 190 patients representing facioscapulohumeral MD (__n__ = 20), limb‐girdle MD (__n__ = 50), Becker MD (__n__ = 20), Duchenne MD (__n

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## Abstract Duchenne's muscular dystrophy (DMD), which affects 1/3500 live male births, involves a progressive degeneration of skeletal and cardiac muscle, leading to early death. The protein dystrophin is lacking in DMD and present, but defective, in the allelic, less severe, Becker muscular dystr

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## Abstract Previously, we reported the identification of a novel immunoglobulin‐like cell adhesion molecule hepaCAM that promotes cell–extracellular matrix (ECM) interactions including cell adhesion and motility. Cell–ECM interactions are known to be directed by the actin cytoskeleton. In this stu