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Human Molecular Genetics|September 27, 2000
Animal models for muscular dystrophy: valuable tools for the development of therapiesV Allamand, K P CampbellCurrent Opinion in Neurology|October 1, 1995
Dystrophin-glycoprotein complex: molecular organization and critical roles in skeletal muscleY Sunada, K P CampbellCell|September 20, 1991
Membrane organization of the dystrophin-glycoprotein complexJ M Ervasti, K P CampbellCirculation Research|October 1, 1987
Affinity purification of antibodies specific for 1,4-dihydropyridine Ca2+ channel blockersA H Sharp, K P CampbellThe Journal of Biological Chemistry|September 15, 1993
Characterization of the major brain form of the ryanodine receptor/Ca2+ release channelP S McPherson, K P CampbellThe Journal of Cell Biology|August 1, 1993
A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actinJ M Ervasti, K P CampbellThe Journal of Physiology|June 15, 1995
Subunit regulation of the neuronal alpha 1A Ca2+ channel expressed in Xenopus oocytesM De Waard, K P CampbellThe Journal of Biological Chemistry|February 10, 1982
A calmodulin-dependent protein kinase system from skeletal muscle sarcoplasmic reticulum. Phosphorylation of a 60,000-dalton proteinK P Campbell, D H MacLennanCurrent Opinion in Neurology|December 16, 1998
The sarcoglycan complex in limb-girdle muscular dystrophyL E Lim, K P CampbellPageof 26