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Human Molecular Genetics|June 1, 1997
Dystroglycan is essential for early embryonic development: disruption of Reichert's membrane in Dag1-null miceR A Williamson, M D Henry, K J Daniels, et al.FEBS Letters|June 3, 1991
Dystrophin constitutes 5% of membrane cytoskeleton in skeletal muscleK Ohlendieck, K P CampbellThe Journal of Biological Chemistry|September 3, 1999
Biochemical characterization of the epithelial dystroglycan complexM Durbeej, K P CampbellThe Journal of Cell Biology|December 1, 1991
Dystrophin-associated proteins are greatly reduced in skeletal muscle from mdx miceK Ohlendieck, K P CampbellThe Journal of Biological Chemistry|April 21, 1995
Association of triadin with the ryanodine receptor and calsequestrin in the lumen of the sarcoplasmic reticulumW Guo, K P CampbellThe Journal of Biological Chemistry|October 5, 1991
A monoclonal antibody to the beta subunit of the skeletal muscle dihydropyridine receptor immunoprecipitates the brain omega-conotoxin GVIA receptorJ Sakamoto, K P CampbellNeuromuscular Disorders : NMD|March 1, 1993
Deficiency of dystrophin-associated proteins: a common mechanism leading to muscle cell necrosis in severe childhood muscular dystrophiesK Matsumura, K P CampbellCurrent Opinion in Neurology|April 1, 1997
Muscular dystrophies and the dystrophin-glycoprotein complexV Straub, K P CampbellBiochemistry|May 30, 1989
Calcium transport by sarcoplasmic reticulum of skeletal muscle is inhibited by antibodies against the 53-kilodalton glycoprotein of the sarcoplasmic reticulum membraneH Kutchai, K P CampbellMuscle & Nerve|January 1, 1994
Dystrophin-glycoprotein complex: its role in the molecular pathogenesis of muscular dystrophiesK Matsumura, K P CampbellPageof 26