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The Journal of Biological Chemistry|January 5, 1996
Biochemical characterization and molecular cloning of cardiac triadinW Guo, A O Jorgensen, L R Jones, et al.
Annals of Neurology|December 16, 2000
Intracellular accumulation and reduced sarcolemmal expression of dysferlin in limb--girdle muscular dystrophiesF Piccolo, S A Moore, G C Ford, et al.
FEBS Letters|September 19, 1994
Dystroglycan is a binding protein of laminin and merosin in peripheral nerveH Yamada, T Shimizu, T Tanaka, et al.
The Journal of Cell Biology|December 1, 1988
Structural evidence for direct interaction between the molecular components of the transverse tubule/sarcoplasmic reticulum junction in skeletal muscleB A Block, T Imagawa, K P Campbell, et al.
The Journal of Biological Chemistry|June 15, 1990
Purification, calcium binding properties, and ultrastructural localization of the 53,000- and 160,000 (sarcalumenin)-dalton glycoproteins of the sarcoplasmic reticulumE Leberer, B G Timms, K P Campbell, et al.
The Journal of Cell Biology|January 1, 1991
Dystrophin-glycoprotein complex is highly enriched in isolated skeletal muscle sarcolemmaK Ohlendieck, J M Ervasti, J B Snook, et al.
The Journal of Biological Chemistry|September 5, 1987
Identification and characterization of the dihydropyridine-binding subunit of the skeletal muscle dihydropyridine receptorA H Sharp, T Imagawa, A T Leung, et al.
Neuropathology and Applied Neurobiology|February 1, 1996
Ultrastructural localization of adhalin, alpha-dystroglycan and merosin in normal and dystrophic muscleM J Cullen, J Walsh, S L Roberds, et al.
FEBS Letters|February 19, 1996
Identification of critical amino acids involved in alpha1-beta interaction in voltage-dependent Ca2+ channelsM De Waard, V E Scott, M Pragnell, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 15, 1997
Dissection of functional domains of the voltage-dependent Ca2+ channel alpha2delta subunitR Felix, C A Gurnett, M De Waard, et al.
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