Publications

1994-1990

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]