Allamand, V., Leturcq, F., Piccolo, F., Jeanpierre, M., Azibi, K., Roberds, S.L., Lim, L.E., Campbell, K.P., Beckmann, J.S., and Kaplan, J.C. Adhalin Gene Polymorphism. Hum. Mol. Gen. 3, 2269, 1994.  [PDF]

Greenberg, D.S., Sunada, Y., Campbell, K.P., Yaffe, D., and Nudel, U. Exogenous Dp71 Restores the Levels of Dystrophin Associated Proteins But Does Not Alleviate Muscle Damage in mdx Mice. Nature Genet. 8, 340-344, 1994.  [PDF]

Cox, G.A., Sunada, Y., Campbell, K.P., and Chamberlain, J.S. Dp71 Can Restore the Dystrophin-Associated Glycoprotein Complex in Muscle But Fails to Prevent Dystrophy. Nature Genet. 8, 333-339, 1994.  [PDF]

Guo, W., Jorgensen, A.O., and Campbell, K.P. Characterization and Ultrastructural Localization of a Novel 90 kDa Protein Unique to Skeletal Muscle Junctional Sarcoplasmic Reticulum. J. Biol. Chem. 269, 28359-28365, 1994.  [PDF]

Yamada, H., Shimizu, T., Tanaka, T., Campbell, K.P., and Matsumura, K. Dystroglycan is a Binding Protein of Laminin and Merosin in Peripheral Nerve. FEBS Lett. 352, 49-53, 1994.  [PDF]

Birnbaumer, L., Campbell, K.P., Catterall, W.A., Harpold, M.M., Hofmann, F., Horne, W.A., Mori, Y., Schwartz, A., Snutch, T.P., Tanabe, T. and Tsien, R.W. The Naming of Voltage Gated Calcium Channels. Neuron. 13, 505-506, 1994.  [PDF]

Sewry, C.A., Matsumura, K., Campbell, K.P., and Dubowitz, V. Expression of Dystrophin-Associated Glycoproteins and Utrophin in Carriers of Duchenne Muscular Dystrophy. Neuromuscul. Disord. 4, 401-409, 1994.  [PDF]

Rafael, J.A., Sunada, Y., Cole, N.M., Campbell, K.P., Faulkner, J.A., and Chamberlain, J.S. Prevention of Dystrophic Pathology in mdx Mice by a Truncated Dystrophin Isoform. Hum. Mol. Gen. 3, 1725-1733, 1994.  [PDF]

De Waard, M., Pragnell, M., and Campbell, K.P. Ca2+ Channel Regulation by a Conserved b Subunit Domain. Neuron 13, 495-503, 1994.  [PDF]

Roberds, S.L., Leturcq, F., Allamand, V., Piccolo, F., Jeanpierre, M., Anderson, R.D., Lim, L.E., Lee, J.C., Tomé, F.M.S., Romero, N.B., Fardeau, M., Beckmann, J.S., Kaplan, J.-C., and Campbell, K.P. Missense Mutations in the Adhalin Gene Linked to Autosomal Recessive Muscular Dystrophy. Cell 78, 625-633, 1994.  [PDF]

Tomé, F.M.S., Matsumura, K., Chevallay, M., Campbell, K.P., and Fardeau, M. Expression of Dystrophin-Associated Glycoproteins During Human Fetal Muscle Development: A Preliminary Immunocytochemical Study. Neuromuscul. Disord. 4, 343-348, 1994.  [PDF]

Ervasti, J.M., Roberds, S.L., Anderson, R.D., Sharp, N.J.H., Kornegay, J.N., and Campbell, K.P. a-Dystroglycan Deficiency Correlates with Elevated Serum Creatine Kinase and Decreased Muscle Contraction Tension in Golden Retriever Muscular Dystrophy. FEBS Lett. 350, 173-176, 1994.  [PDF]

Campanelli, J.T., Roberds, S.L., Campbell, K.P., and Scheller, R.H. A Role for Dystrophin-Associated Glycoproteins and Utrophin in Agrin-Induced AChR Clustering. Cell 77, 663-674, 1994.  [PDF]

Higuchi, I., Yamada, H., Fukunaga, H., Iwaki, H., Okubo, R., Nakagawa, M., Osame, M., Roberds, S.L., Shimizu, T., Campbell, K.P., and Matsumura, K. Abnormal Expression of Laminin Suggests Disturbance of Sarcolemma-Extracellular Matrix Interaction in Japanese Patients with Autosomal Recessive Muscular Dystrophy Deficient in Adhalin. J. Clin. Invest. 94, 601-606, 1994.  [PDF]

Mickelson, J.R., Ervasti, J.M., Litterer, L.A., Campbell, K.P., and Louis, C.F. Skeletal Muscle Junctional Membrane Protein Content in Pigs with Different Ryanodine Receptor Genotypes. Amer. J. Physiol. Cell Physiol. 267, C282-C292, 1994.  [PDF]

Zatz, M., Matsumura, K., Vainzof, M., Passos-Bueno, M.R., Pavanello, R.C.M., Marie, S.K., and Campbell K.P. Assessment of the 50-kDa Dystrophin-Associated Glycoprotein in Brazilian Patients with Severe Childhood Autosomal Recessive Muscular Dystrophy. J. Neurol. Sci. 123, 122-128, 1994.  [PDF]

Sunada, Y., Bernier, S.M., Kozak, C.A., Yamada, Y., and Campbell, K.P. Deficiency of Merosin in Dystrophic dy Mice and Genetic Linkage of the Laminin M Chain Gene to the dy Locus. J. Biol. Chem. 269, 13729-13732, 1994.  [PDF]

El Kerch, F., Sefiani, A., Azibi, K., Boutaleb, N., Yahyaoui, M., Bentahila, A., Vinet, M.-C., Leturcq, F., Bachner, L., Beckmann, J., Campbell, K.P., Tomé, F.M.S., Fardeau, M., and Kaplan, J.-C. Linkage Analysis of Families With Severe Childhood Autosomal Recessive Muscular Dystrophy in Morocco Indicates Genetic Homogeneity of the Disease in North Africa. J. Med. Genet. 31, 342-343, 1994.  [PDF]

Sewry, C.A., Sansome, A., Matsumura, K., Campbell, K.P., and Dubowitz, V. Deficiency of the 50 kDa Dystrophin-Associated Glycoprotein and Abnormal Expression of Utrophin in Two South Asian Cousins with Variable Expression of Severe Childhood Autosomal Recessive Muscular Dystrophy. Neuromuscul. Disord. 4, 121-129, 1994.  [PDF]

Tomé, F.M.S., Evangelista, T., Leclerc, A., Sunada, Y., Manole, E., Estournet, B., Barois, A., Campbell, K.P., and Fardeau, M. Congenital Muscular Dystrophy with Merosin Deficiency. C.R. Acad. Sci. Paris, Sciences de la vie/Life Sciences 317, 351-357, 1994.  [PDF]

Witcher, D.R., McPherson, P.S., Kahl, S.D., Lewis, T., Bentley, P., Mullinnix, M.J., Windass, J.D., and Campbell, K.P. Photoaffinity Labeling of the Ryanodine Receptor/Ca2+ Release Channel with an Azido Derivative of Ryanodine. J. Biol. Chem. 269, 13076-13079, 1994.  [PDF]

Kahl, S.D., McPherson, P.S., Lewis, T., Bentley, P., Mullinnix, M.J., Windass, J.D., and Campbell, K.P. Radioimmunoassay for the Calcium Release Channel Agonist Ryanodine. Analytical Biochem. 218, 55-62, 1994.  [PDF]

Parys, J.B., McPherson, S.M., Mathews, L., Campbell, K.P., and Longo, F.J. Presence of Inositol 1,4,5-Trisphosphate Receptor, Calreticulin, and Calsequestrin in Eggs of Sea Urchins and Xenopus Laevis. Development. Biol. 161, 466-476, 1994.  [PDF]

Yang, B., Ibraghimov-Beskrovnaya, O., Moomaw, C.R., Slaughter, C.A., and Campbell, K.P. Heterogeneity of the 59-kDa Dystrophin-Associated Protein Revealed by cDNA Cloning and Expression. J. Biol. Chem. 269, 6040-6044, 1994.  [PDF]

Pragnell, M., De Waard, M., Mori, Y., Tanabe, T., Snutch, T.P.,and Campbell, K.P. Calcium Channel b-Subunit Binds to a Conserved Motif in the I-II Cytoplasmic Linker of the a1-Subunit. Nature 368, 67-70, 1994.  [PDF]

Romero, N.B., Tomé, F.M.S., Leturcq, F., El Kerch, F., Kemal, A., Bachner, L., Anderson, R.D., Roberds, S.L., Campbell, K.P., Fardeau, M.M., and Kaplan, J.-C. Genetic Heterogeneity of Severe Autosomal Recessive Muscular Dystrophy with Adhalin (50 kDa Dystrophin-Associated Glycoprotein) Deficiency. C.R. Acad. Sci. Paris, Sciences de la Vie/Life Sciences 317, 70-76, 1994.  [PDF]

Matsumura, K., Tomé, F.M.S., Collin, H., Leturcq, F., Jeanpierre, M., Kaplan, J.-C., Fardeau, M., and Campbell, K.P. Expression of Dystrophin-Associated Proteins in Dystrophin-Positive Muscle Fibers (Revertants) in Duchenne Muscular Dystrophy. Neuromuscul. Disord. 4, 115-120, 1994.  [PDF]

De Waard, M., Witcher, D.R., and Campbell, K.P. Functional Properties of the Purified N-type Ca2+ Channel From Rabbit Brain. J. Biol. Chem. 269, 6716-6724, 1994.  [PDF]

Matsumura, K., Burghes, A.H.M., Mora, M., Tomé, F.M.S., Morandi, L., Cornello, F., Leturcq, F., Jeanpierre, M., Kaplan, J.-C., Reinert, P., Fardeau, M., Mendell, J.R., and Campbell, K.P. Immunohistochemical Analysis of Dystrophin-Associated Proteins in Becker/Duchenne Muscular Dystrophy with Huge In-Frame Deletions in the NH2-Terminal and Rod Domains of Dystrophin. J. Clin. Invest. 93, 99-105, 1994.  [PDF]

McPherson, P.S. and Campbell, K.P.  Characterization of the Major Brain Form of the Ryanodine Receptor/ Ca2+ Release Channel.  J. Biol. Chem. 268:19785-19790, 1993.  [PDF]

Matsumura, K., Yamada, H., Shimizu, T., and Campbell, K.P. Differential Expression of Dystrophin, Utrophin and Dystrophin-Associated Proteins in Peripheral Nerve. FEBS Lett. 334, 281-285, 1993.  [PDF]

Phillips, W.D., Noakes, P.G., Roberds, S.L., Campbell, K.P., and Merlie, J.P. Clustering and Immobilization of Acetylcholine Receptors by the 43-kD Protein: A Role For Dystrophin-Related Protein (DRP). J. Cell Biol. 123, 729-740, 1993.  [PDF]

Ibraghimov-Beskrovnaya, O., Sheffield, V.C., and Campbell, K.P. Single Base Polymorphism in the DAG1 Gene Detected by DGGE and Mismatch PCR. Hum. Mol. Gen. 2, 1983, 1993.  [PDF]

Passos-Bueno, M.R., Oliveira, J.R., Bakker, E., Anderson, R.D., Marie, S.K., Vainzof, M., Roberds, S., Campbell, K.P., and Zatz, M. Genetic Heterogeneity for Duchenne-like Muscular Dystrophy (DLMD) Based on Linkage and 50 DAG Analysis. Hum. Mol. Gen.2, 1945-1947, 1993.  [PDF]

Roberds, S.L., Anderson, R.D., Ibraghimov-Beskrovnaya, O., and Campbell, K.P. Primary Structure and Muscle-Specific Expression of the 50-kDa Dystrophin-Associated Glycoprotein (Adhalin). J. Biol. Chem. 268, 23739-23742, 1993.  [PDF]

Witcher, D.R., De Waard, M., and Campbell, K.P. Characterization of the Purified N-Type Ca2+ Channel and the Cation Sensitivity of w-Conotoxin GVIA Binding. Neuropharmacology 32, 1127-1139, 1993.  [PDF]

Stea, A., Dubel, S.J., Pragnell, M., Leonard, J.P., Campbell, K.P., and Snutch, T.P. A b-Subunit Normalizes the Electrophysiological Properties of a Cloned N-Type Ca2+ Channel a1-Subunit. Neuropharmacology 32, 1103-1116, 1993.  [PDF]

Ibraghimov-Beskrovnaya, O., Milatovich, A., Ozcelik, T., Yang, B., Koepnick, K., Francke, U., and Campbell, K.P. Human Dystroglycan: Skeletal Muscle cDNA, Genomic Structure, Origin of Tissue Specific Isoforms and Chromosomal Localization. Hum. Mol. Gen. 2, 1651-1657, 1993.  [PDF]

Fardeau, M., Matsumura, K., Tomé, F.M.S., Collin, H., Leturcq, F., Kaplan, J.C., and Campbell K.P. Deficiency of the 50 kDa Dystrophin Associated Glycoprotein (Adhalin) in Severe Autosomal Recessive Muscular Dystrophies in Children Native from European Countries. C.R. Acad. Sci. Paris 316, 799-804, 1993.  [PDF]

Azibi, K., Bachner, L., Beckmann, J.S., Matsumura, K., Hamouda, E., Chaouch, M., Chaouch, A., Ait-Ouarab, R., Vignal, A., Weissenbach, J., Vinet, M.-C., Leturcq, F., Collin, H., Tomé, F.M.S., Reghis, A., Fardeau, M., Campbell, K.P., and Kaplan, J.-C., Severe Childhood Autosomal Recessive Muscular Dystrophy With the Deficiency of the 50 kDa Dystrophin-Associated Glycoprotein Maps to Chromosome 13q12. Hum. Mol. Gen. 2, 1423-1428, 1993.  [PDF]

Matsumura, K., Tomé, F.M.S., Ionasescu, V., Ervasti, J.M., Anderson, R.D., Romero, N.B., Simon, D., Récan, D., Kaplan, J.-C., Fardeau, M., and Campbell, K.P. Deficiency of Dystrophin-Associated Proteins in Duchenne Muscular Dystrophy Patients Lacking COOH-Terminal Domains of Dystrophin. J. of Clinical Investigation 92, 866-871, 1993.  [PDF]

Cox, G.A., Cole, N.M. Matsumura, K., Phelps, S.F., Hauschka, S.D., Campbell, K.P., Faulkner, J.A., and Chamberlain, J.S. Overexpression of Dystrophin in Transgenic mdx Mice Eliminates Dystrophic Symptoms Without Toxicity. Nature 364, 725-729, 1993.  [PDF]

Ervasti, J.M. and Campbell, K.P. A Role for the Dystrophin-Glycoprotein Complex as a Transmembrane Linker Between Laminin and Actin. J. Cell Biol. 122, 809-823, 1993.  [PDF]

Matsumura, K., Shasby, M., and Campbell, K.P. Purification of Dystrophin-Related Protein (Utrophin) From Lung and Its Identification in Pulmonary Artery Endothelial Cells. FEBS Lett. 326, 289-293, 1993.  [PDF]

Matsumura, K., Nonaka, I., Tomé, F.M.S., Arahata, K., Collin, H., Leturcq, F., Recan, D., Kaplan, J.-C., Fardeau, M., and Campbell, K.P. Mild Deficiency of Dystrophin-Associated Proteins in Becker Muscular Dystrophy Patients Having In-Frame Deletions in the Rod Domain of Dystrophin. Amer. J. Hum. Genet. 53, 409-416, 1993.  [PDF]

Witcher, D.R., De Waard, M., Sakamoto, J., Franzini-Armstrong, C., Pragnell, M., Kahl, S.D., and Campbell, K.P. Subunit Identification and Reconstitution of the N-Type Ca2+ Channel Complex Purified From Brain. Science 261, 486-489, 1993.  [PDF]

McPherson, P.S. and Campbell, K.P. The Ryanodine Receptor/Ca2+ Release Channel. J. Biol. Chem. 268, 13765-13768, 1993.  [PDF]

Sharp, A.H., McPherson, P.S., Dawson, T.M., Aoki, C., Campbell, K.P., and Snyder, S.H. Differential Immunohistochemical Localization of Inositol 1,4,5-Trisphosphate- and Ryanodine-Sensitive Ca2+ Release Channels in Rat Brain. J. Neurosci. 13, 3051-3063, 1993.  [PDF]

Knudson, C. M., Stang, K.K., Moomaw, C.R., Slaughter, C.A., and Campbell, K.P. Primary Structure and Topological Analysis of a Skeletal Muscle-Specific Junctional Sarcoplasmic Reticulum Glycoprotein (Triadin). J. Biol. Chem. 268, 12646-12654, 1993.  [PDF]

Knudson, C. M., Stang, K.K., Jorgensen, A.O., and Campbell, K.P. Biochemical Characterization and Ultrastructural Localization of a Major Junctional Sarcoplasmic Reticulum Glycoprotein (Triadin). J. Biol. Chem. 268, 12637-12645, 1993.  [PDF]

Matsumura, K., Nonaka, I., Arahata, K., and Campbell, K.P. Partial Deficiency of Dystrophin-Associated Proteins in a Young Girl with Sporadic Myopathy and Normal Karyotype. Neurol. 43, 1267-1268, 1993.  [PDF]

Roberds, S.L., Ervasti, J.M., Anderson, R.D., Ohlendieck, K., Kahl, S.D., Zoloto, D., and Campbell, K.P. Disruption of the Dystrophin-Glycoprotein Complex in the Cardiomyopathic Hamster. J. Biol. Chem. 268, 11496-11499, 1993.  [PDF]

Ohlendieck, K., Matsumura, K., Ionasescu, V.V., Towbin, J.A., Bosch, E.P., Weinstein, S.L., Sernett, S.W., and Campbell, K.P. Duchenne Muscular Dystrophy: Deficiency of Dystrophin-Associated Proteins in the Sarcolemma. Neurol. 43, 795-800, 1993.  [PDF]

Matsumura, K., Lee, C.C., Caskey, C.T., and Campbell, K.P. Restoration of Dystrophin-Associated Proteins in Skeletal Muscle of mdx Mice Transgenic for Dystrophin Gene. FEBS Lett. 320, 276-280, 1993.  [PDF]

Jorgensen, A.O., Shen, A.C.Y., Arnold, W., McPherson, P.S., and Campbell, K.P. The Ca2+ Release Channel/Ryanodine Receptor is Localized in Junctional and Corbular Sarcoplasmic Reticulum in Cardiac Muscle. J. Cell Biol. 120, 969-980, 1993.  [PDF]

Matsumura, K., Nonaka, I. and Campbell, K.P., Abnormal Expression of Dystrophin-Associated Proteins in Fukuyama-type Congenital Muscular Dystrophy. Lancet 341, 521-522, 1993.  [PDF]

Kleitsch, R., Ervasti, J.M., Arnold, W., Campbell, K.P., and Jorgensen, A.O. Dystrophin-Glycoprotein Complex and Laminin Colocalize to the Sarcolemma and Transverse Tubules of Cardiac Muscle. Circ. Res. 72, 349-360, 1993.  [PDF]

Matsumura, K., Ervasti, J.M., Ohlendieck, K., Kahl, S.D., and Campbell, K.P. Association of Dystrophin-Related Protein With Dystrophin-Associated Proteins in mdx Mouse Muscle. Nature 360, 588-591, 1992.  [PDF]

Matsumura, K., Tomé, F.M.S., Collin, H., Azibi, K., Chaouch, M., Kaplan, J.-C., Fardeau, M., and Campbell, K.P. Deficiency of the 50K Dystrophin-Associated Glycoprotein in Severe Childhood Autosomal Recessive Muscular Dystrophy. Nature 359, 320-322, 1992.  [PDF]

Parys, J.B., Sernett, S.W., DeLisle, S., Snyder, P.M., Welsh, M.J., and Campbell, K.P. Isolation, Characterization, and Localization of the Inositol 1,4,5-Trisphosphate Receptor Protein in Xenopus laevis Oocytes. J. Biol. Chem. 267, 18776-18782, 1992.  [PDF]

Mickelson, J.R., Knudson, C.M., Kennedy, C.F.H., Yang, D.-I., Litterer, L.A., Rempel, W.E., Campbell, K.P., and Louis, C.F. Structural and Functional Correlates of a Mutation in the Malignant Hyperthermia-Susceptible Pig Ryanodine Receptor. FEBS Lett.301, 49-52, 1992.  [PDF]

Ibraghimov-Beskrovnaya, O., Ervasti, J.M., Leveille, C.J., Slaughter, C.A., Sernett, S.W., and Campbell, K.P. Primary Structure of Dystrophin-Associated Glycoproteins Linking Dystrophin to the Extracellular Matrix. Nature 355, 696-702, 1992.  [PDF]

McPherson, S.M., McPherson, P.S., Mathews, L., Campbell, K.P., and Longo, F.J. Cortical Localization of a Calcium Release Channel in Sea Urchin Eggs. J. Cell Biol. 116, 1111-1121, 1992.  [PDF]

Ohlendieck, K. and Campbell, K.P. Dystrophin-Associated Proteins are Greatly Reduced in Skeletal Muscle from mdx Mice. J. Cell Biol. 115, 1685-1694, 1991.  [PDF]

Pragnell, M., Sakamoto, J., Jay, S.D., and Campbell, K.P. Cloning and Tissue Specific Expression of the Brain Calcium Channel b-Subunit. FEBS Lett. 291, 253-258, 1991.  [PDF]

Ervasti, J.M. and Campbell, K.P. Membrane Organization of the Dystrophin-Glycoprotein Complex. Cell 66, 1121-1131, 1991.  [PDF]

Sakamoto, J. and Campbell, K.P. A Monoclonal Antibody to the b Subunit of the Skeletal Muscle Dihydropyridine Receptor Immunoprecipitates the Brain w-Conotoxin GVIA Receptor. J. Biol. Chem. 266, 18914-18919, 1991.  [PDF]

Ohlendieck, K., Briggs, F.N., Lee, K.F., Wechsler, A.W., and Campbell, K.P. Analysis of Excitation-Contraction-Coupling Components in Chronically Stimulated Canine Skeletal Muscle. Eur. J. Biochem. 202, 739-747, 1991.  [PDF]

Ohlendieck, K., Ervasti, J.M., Matsumura, K., Kahl, S.D., Leveille, C.J., and Campbell, K.P. Dystrophin-Related Protein Is Localized to Neuromuscular Junctions of Adult Skeletal Muscle. Neuron 7, 499-508, 1991.  [PDF]

Ohlendieck, K. and Campbell, K.P. Dystrophin Constitutes 5% of Membrane Cytoskeleton in Skeletal Muscle. FEBS Lett. 283, 230-234, 1991.  [PDF]

McLeod, A.G., Shen, A.C.-Y., Campbell, K.P., Michalak, M., and Jorgensen, A.O. Frog Cardiac Calsequestrin. Identification, Characterization and Subcellular Distribution in Two Structurally Distinct Regions of Peripheral Sarcoplasmic Reticulum in Frog Ventricular Myocardium. Circ. Res. 69, 344-359, 1991.  [PDF]

McPherson, P.S., Kim, Y.-K., Valdivia, H., Knudson, C.M., Takekura, H., Franzini-Armstrong, C., Caronado, R., and Campbell, K.P. The Brain Ryanodine Receptor: A Caffeine-Sensitive Calcium Release Channel. Neuron 7, 17-25, 1991.  [PDF]

Ervasti, J.M., Kahl, S.D., and Campbell, K.P. Purification of Dystrophin from Skeletal Muscle. J. Biol. Chem. 266, 9161-9165, 1991.  [PDF]

Ohlendieck, K., Ervasti, J.M., Snook, J.B., and Campbell, K.P. Dystrophin-Glycoprotein Complex Is Highly Enriched in Isolated Skeletal Muscle Sarcolemma. J. Cell Biol. 112, 135-148, 1991.  [PDF]

Jay, S.D., Sharp, A.H., Kahl, S.D., Vedvick, T.S., Harpold, M.M., and Campbell, K.P. Structural Characterization of the Dihydropyridine-Sensitive Calcium Channel a2-Subunit and the Associated d Peptides. J. Biol. Chem. 266, 3287-3293, 1991.  [PDF]

Movsesian, M.A., Leveille, C., Krall, J., Colyer, J., Wang, J.H., and Campbell, K.P. Identification and Characterization of Proteins in Sarcoplasmic Reticulum from Normal and Failing Human Left Ventricles. J. Mol. Cell. Cardiol. 22, 1477-1485, 1990.  [PDF]

McPherson, P.S. and Campbell, K.P. Solubilization and Biochemical Characterization of the High Affinity [3H]Ryanodine Receptor from Rabbit Brain Membranes. J. Biol. Chem. 265, 18454-18460, 1990.  [PDF]

Chu, A., Sumbilla, C. Inesi, G., Jay, S.D., and Campbell, K.P. Specific Association of Calmodulin-Dependent Protein Kinase and Related Substrates with the Junctional Sarcoplasmic Reticulum of Skeletal Muscle. Biochemistry 29, 5899-5905, 1990.  [PDF]

Krause, K.-H., Simmerman, H.K.B., Jones, L.R., and Campbell, K.P. Sequence Similarity of Calreticulin with a Ca2+-Binding Protein That Co-Purifies with an Ins(1,4,5)P3-Sensitive Ca2+ Store in HL-60 Cells. Biochem. J. 270, 545-548, 1990.  [PDF]

Leberer, E., Timms, B.G., Campbell, K.P., and MacLennan, D.H. Purification, Calcium Binding Properties, and Ultrastructural Localization of the 53,000- and 160,000 (Sarcalumenin)-Dalton Glycoproteins of the Sarcoplasmic Reticulum. J. Biol. Chem. 265, 10118-10124, 1990.  [PDF]

Jay, S.D., Ellis, S.B., McCue, A.F., Williams, M.E., Vedvick, T.S., Harpold, M.M., and Campbell, K.P. Primary Structure of the g Subunit of the DHP-Sensitive Calcium Channel from Skeletal Muscle. Science 248, 490-492, 1990.  [PDF]

Ervasti, J.M., Ohlendieck, K., Kahl, S.D., Gaver, M.G., and Campbell, K.P. Deficiency of a Glycoprotein Component of the Dystrophin Complex in Dystrophic Muscle. Nature 345, 315-319, 1990.  [PDF]

Jorgensen, A.O., Arnold, W., Shen, A.C.-Y., Yuan, S., Gaver, M., and Campbell, K.P. Identification of Novel Proteins Unique to Either Transverse Tubules (TS28) or the Sarcolemma (SL50) in Rabbit Skeletal Muscle. J. Cell. Biol. 110, 1173-1185, 1990.  [PDF]

Knudson, C.M., Mickelson, J.R., Louis, C.F., and Campbell, K.P. Distinct Immunopeptide Maps of the Sarcoplasmic Reticulum Ca2+ Release Channel in Malignant Hyperthermia. J. Biol. Chem. 265, 2421-2424, 1990.  [PDF]

Briggs, F.N., Lee, K.F., Feher, J.J., Wechsler, A.S., Ohlendieck, K., and Campbell, K.P. Ca-ATPase Isozyme Expression in Sarcoplasmic Reticulum Is Altered by Chronic Stimulation of Skeletal Muscle. FEBS Lett. 259, 269-272, 1990.  [PDF]