Kunz, S., Rojek, J.M., Kanagawa, M., Spiropoulou, C.F., Barresi, R., Campbell, K.P., Oldstone, M.B. Posttranslational modification of alpha-dystroglycan, the cellular receptor for arenaviruses, by the glycosyltransferase LARGE is critical for virus binding. J Virol.79: 14282-96, 2005.  [PDF]

Occhi, S., Zambroni, D., Del Carro, U., Amadio, S., Sirkowski, E.E., Scherer, S.S., Campbell, K.P., Moore, S.A., Chen, Z.-L., Strickland, S., Di Muzio, A., Uncini, A., Wrabetz, L., and Feltri, M.L. Both Laminin and Schwann Cell Dystroglycan are Necessary for Proper Clustering of Sodium Channels at Nodes of Ranvier. J. Neurosci. 25: 9418-9427, 2005.  [PDF]

Kanagawa, M., Michele, D.E., Satz, J. S., Barresi, R., Kusano, H., Sasaki, T., Timpl, R., Henry, M.D., and Campbell, K.P. Disruption of Perlecan Binding and Matrix Assembly by Post-Translational or Genetic Disruption of Dystroglycan Function. FEBS Lett. 579: 4792-4796, 2005.  [PDF]

Nakagawa, O., Arnold M., Nakagawa M., Hamada H., Shelton J.M., Kusano H., Harris T.M., Childs G., Campbell K.P., Richardson J.A., Nishino I., and Olson E.N. Centronuclear myopathy in mice lacking a novel muscle-specific protein kinase transcriptionally regulated by MEF2. Genes Dev. 19: 2066-2077, 2005.  [PDF]

Matsumoto, H., Hayashi, Y.K., Kim, D., Ogawa, M., Murakami, T., Noguchi, S., Nonaka, I., Nakazawa, T., Matsuo, T., Futagami, S., Campbell, K.P., Nishino, I. Congenital muscular dystrophy with glycosylation defects of a-dystroglycan in Japan. Neuromuscul Disord. 15: 342-348, 2005.  [PDF]

Consolino, C.M., Duclos, F., Lee, J., Williamson, R.A., Campbell, K.P., and Brooks, S.V. Muscles of mice deficient in a-sarcoglycan maintain large masses and near control force values throughout the life span. Physiol Genomics. 22: 244-256, 2005.  [PDF]

Vogtlander, N.P.J., Dijkman, H., Bakker, M.A.H., Campbell, K.P., and van der Vlag, J., Berden, J.H.M. Localization of alpha-dystroglycan on the podocyte: from top to toe. J Histochem Cytochem, 205, 2005.  [PDF]

Jones, J.C.R., Lane, K., Hopkinson, S.B., Lecuona, E., Geiger, R.C., Dean, D.A., Correa-Meyer, E., Gonzales, M., Campbell, K.P., Sznajder, J.I., and Budinger, S. Laminin-6 assembles into multimolecular fibrillar complexes with perlecan and participates in mechanical-signal transduction via a dystroglycan-dependent, Integrin-independent mechanism. J. Cell Sci., 118(2): 2557-2566.  [PDF]

Saito, F., Blank, M., Schroder, J., Manya, H., Shimizu, T., Campbell, K.P., Endo, T., Mizutani, M., Kroger, S., and Matsumura. Aberrant glycosylation of a-dystroglycan causes defective binding of laminin in the muscle of chicken muscular dystrophy. FEBS Letters, 579: 2359-2363, 2005.  [PDF]

Huang, H., Sylvan, J., Jonas, M., Barresi, R., So, P.T.C., Campbell, K.P. and Lee, R.T. Cell Stiffness and Receptors: Evidence for Cytoskeletal Subnetworks. Am J Physiol Cell Physiol, 288: C72-C80, 2005.  [PDF]

Saito, F., Matsumura, K., Campbell, K.P. Function of dystroglycan in the nervous system. Tanpakushitsu Kakusan Koso 49(15): 2437-2444, 2004.  [PDF]

Kanagawa, M., and Campbell, K.P. a-dystroglycanopathy and LARGE. Medical Science Digest 30(12): 491-494, 2004.  [PDF]

Kanagawa, M. and Campbell, K.P. Dystroglycan Posttranslational Modification by LARGE and Congenital Muscular Dystrophy. Zikkenigaku 22(15): 2171-2173, 2004.  [PDF]

Kikkawa, Y., Yu, H., Genersch, E., Sanzen, N., Sekiguchi, K., Fassler, R., Campbell, K.P., Talts, J.F. and Ekblom, P. Laminin Isoforms Differentially Regulate Adhesion, Spreading, Proliferation and ERK Activation of ß1 Integrin-null Cells. Exp Cell Res 300: 94-108, 2004.  [PDF]

Singh, J., Itahana, Y., Knight-Krajewski, S., Kanagawa, M., Campbell, K.P., Bissell, M.J. and Muschler, J. Proteolytic Enzymes and Altered Glycosylation Modulate Dystroglycan Function in Carcinoma Cells. Cancer Res 64(17): 6152-6159, 2004.  [PDF]

Barresi, R., Michele, D.E., Kanagawa, M., Harper, H.A., Dovico, S.A., Satz, J.S., Moore, S.A., Dumanski, J.P., Schachter, H., Cohn, R.D., Nishino, I. Campbell, K.P. LARGE Can Functionally Bypass a-Dystroglycan Glycosylation Defects in Distinct Congenital Muscular Dystrophies. Nat Med. 10(7): 696-703, 2004.  [PDF]

Kanagawa, M., Saito, F., Kunz, S., Yoshida-Moriguchi, T., Barresi, R., Kobayashi, Y.M., Muschler, J., Dumanski, J.P., Michele, D.E., Oldstone, M.B.A., and Campbell, K.P. Molecular recognition by LARGE is essential for expression of functional dystroglycan. Cell117(7): 953-964, 2004.  [PDF]

Opatowsky, Y., Chen, C-C., Campbell, K.P and Hirsch, J.A. Structural Analysis of the Voltage-dependent Calcium Channel b Subunit Functional Core and its Complex with the a1 Interaction Domain. Neuron 42(3): 387-399, 2004.  [PDF]

Kim, D.-S., Hayashi, Y.K., Matsumoto, H., Ogawa, M., Noguchi, S., Murakami, N., Sakuta, R., Mochizuki, M., Michele, D.E., Campbell, K.P., Nonaka, I., and Nishino, I. POMT1 mutation results indefective glycosylation and loss of laminin-binding activity in a-dystroglycan. Neurology 62(6): 1009-1011, 2004.  [PDF]

Yurchenco, P.D., Cheng, Y.-S., Campbell, K., and Li, S. Loss of Basement Membrane, Receptor and Cytoskeletal Lattices in a Laminin-deficient Muscular Dystrophy. J. Cell. Sci. 117(5): 735-742, 2004.  [PDF]

Kunz, S., Campbell, K.P., and Oldstone, M.B. Alpha-Dystroglycan Can Mediate Arenavirus Infection in the Absence of Beta-Dystroglycan. Virology 316(2): 213-30, 2003.  [PDF]

Opatowsky, Y., Chomsky-Hecht, O., Kang, M.G., Campbell, K.P., And Hirsch, J.A. The Voltage-Dependent Calcium Channel b Subunit Contains Two Stable Interacting Domains. J Biol. Chem. 278: 52323-52332, 2003.  [PDF]

Rambukkana, A., Kunz, S., Min, J., Campbell, K.P., and.Oldstone, M.B.A.  Targeting schwann cells by Nonlytic Arenaviral Infection Selectively Inhibits Myelination.  Proc Natl Acad Sci 100: 16071-16076, 2003.  [PDF]

Murakami, M., Yamamura, H., Suzuki, T., Kang, M., Murakami, A., Miyoshi, I., Muraki, K., Hano, T., Kasai, N., Campbell, K.P., Flockerzi, V., Imaizumi, Y., and Yanagisawa, T.  Modified Cardiovascular L-Type Channels in the Mice Lacking the b3 Subunit of the Voltage-Dependent Ca2+ Channel.  Journal of Biological Chemistry 278(44): 43261-43267, 2003.  [PDF]

Chen, C.C., Lamping, K.G., Nuno, D.B., Barresi, R., Prouty, S.J., Lavoie, J.L., Cribbs, L.L., England, S.K., Sigmund, C.D., Weiss, R.M., Williamson, R.A., Hill, J.A., and Campbell, K.P. Abnormal coronary function in mice deficient in a1H T-type Ca2+ Channels. Science 302(5649): 1416-1418, 2003.  [PDF]

Letts, V.A., Kang, M., Mahaffey, C.L., Beyer, B., Tenbrink, H., Campbell, K.P., Frankel, W.N. Phenotypic Heterogeneity in the Stargazing Allelic Series. Mammalian Genome 14:506-513, 2003.  [PDF]

Muntoni, F., Valero de Bernabe, B., Bittner, R., Blake, D., van Bokhoven, H., Brrockington, M., Brown, S., Bushby, K., Campbell, K.P., Fiszman, M., Grunewald, S., Merlini, L., Quijano-Roy, S., Romero, N., Sabatelli, P., Sewry, C.A., Straub, V., Talim, H., Topaloglu, H., Voit, T., Yurchenco, P.D., Urtizeberea, A., Wewer, U., Guicheney, P. Report of the 114th ENMC International Workshop on Congenital Muscular Dystrophy. Neuromuscular Disorders. 13(7-8): 579-588, 2003.  [PDF]

Sampaolesi, M., Torrente, I., Innocenzi, A., Tonlorenzi, R., D’Antona, G., Pellegrino, M.A., Barresi, R., Bresolin, N., Cusella de Angelis, M.G., Campbell, K.P., Bottinelli, R. and Cossu, G. Cell therapy of alpha sarcoglycan null dystrophic mice through intra-arterial delivery of mesoangioblasts. Science. 301(5632): 487-492, 2003.  [PDF]

Durbeej, M., Sawatzki, S.M., Barresi, R., Schmainda, K.M., Allamand, V., Michele, D.E., and Campbell, K.P. Gene transfer establishes primacy of striated versus smooth muscle sarcoglycan complex in limb-girdle muscular dystrophy. Proc. Natl. Acad. Sci. 100(15): 8910-8915, 2003.  [PDF]

Arikkath, J. and Campbell, K.P. Auxillary Subunits: Essential Components of the Voltage-Gated Calcium Channel Complex. Curr. Opin. in Neurobiol. 13: 298-307, 2003.   [PDF]

Saito, F., Moore, S.A., Barresi, R., Henry, M.D., Messing, A., Ross-Barta, S.E., Cohn, R.D., Williamson, R.A., Sluka, K.A., Sherman, D.L., Brophy, P.J., Schmelzer, J.D., Low, P.A., Wrabetz, L., Fletri, M.L., Campbell, K.P. Unique Role of Dystroglycan in Peripheral Nerve Myelination, Nodal Structure and Sodium Channel Stabilization. Neuron. 38(5): 747-758, 2003.  [PDF]

Ferletta, M., Kikkawa, Y., Yu, H.., Talts, J.F., Durbeej, M., Sonnenberg, A. Timpl, R., Campbell, K.P., Ekblom, P., and Genersch, E. Opposing Roles of Integrin a6Ab1 and Dystroglycan in Laminin-mediated Extracellular Signal-regulated Kinase Activation. Mol. Biol. of the Cell. 14(5): 2088-2103, 2003.  [PDF]

Bansal, D., Miyake, K., Vogel, S.S., Groh, S., Chen, C.C., Williamson, R., McNeil, P.L., Campbell, K.P. Defective Membrane Repair in Dysferlin-Deficient Muscular Dystrophy. Nature. 423(6936): 168-172, 2003.  [PDF]

Arikkath, J. , Chen, C.C., Ahern, C., Allamand, V., Flanagan, J.D., Coronado, R.G., Campbell, K.P. g1 Subunit Interactions Within the Skeletal Muscle L-Type Voltage Gated Calcium Channels. J. Biol. Chem. 278: 1212-1219, 2003.  [PDF]

Arikkath, J., Felix, R., Ahern, C., Chen, C.C., Song, I., Shin, H., Coronado, R., Campbell, K.P. Molecular Characterization of a Two-Domain Form of the Neuronal Voltage-Gated P/Q Type Calcium Channel a12.1 Subunit. FEBS Letters 532: 3, 261-468, 2002.  [PDF]

Muschler, J., Levy, D., Boudreau, R., Henry, M., Campbell, K.P., Bissel, M.J. A Role for Dystroglycan in Epilthelial Polarization: Loss of Function in Breast Tumor Cells. Cancer Research 62: 7102-7109, 2002.  [PDF]

Crosbie, R.H., Barresi, R. and Campbell, K.P. Loss of Sarcolemma nNOS in Sarcoglycan-Deficient Muscle. FASEB 16: 1786-1791, 2002.  [PDF]

Kang, M., Felix, R., Campbell, K.P. Long-term Regulation of Voltage-Gated Calcium Channels by Gabapentin. FEBS Letters 528: 177-182, 2002.  [PDF]

Cohn, R.D., Henry, M.D., Michele, D.E., Barresi, R., Saito, F., Moore, S.A., Flanagan, J.D., Skwarchuk, M.W., Robbins, M.E., Mendell, J.R., Williamson, R., Campbell, K.P. Disruption of Dag1 in Differentiated Skeletal Muscle Reveals a Role for Dystroglycan in Muscle Regeneration. Cell. 110: 639-648, 2002.  [PDF]

Michele, D.E., Barresi, R., Kanagawa, M., Saito, F., Cohn, R.D., Satz, J.S., Dollar, H., Nishino, I., Kelley, R.I., Somer, H., Straub, V., Mathews, K.D., Moore, S.A. and Campbell, K.P. Posttranslational Disruption of Dystroglycan-Ligand Interactions in Congenital Muscular Dystrophies. Nature 418(6896): 417-422, 2002.  [PDF]

Moore, S.A., Saito, F., Chen, J., Michele, D.E., Henry, M., Messing, A., Cohn, R.D., Barta, S.R., Westra, S., Williamson, R., Hoshi, T., Campbell, K.P. Deletion of Brain Dystroglycan Recapitulates Aspects of Congenital Muscular Dystrophy. Nature 418: 422-425, 2002.  [PDF]

Crosbie, R.H., Dovico, S.A., Flangan, J., Chamberlain, J.S., Ownby, C.L., Campbell, K.P. Characterization of Aquaporin-4 in Muscle and Muscular Dystrophy. FASEB 16: 943-949, 2002.  [PDF]

Levi, S., Grady, R.M., Campbell, K.P., Sanes, J.R., Craig, A.M. Dystroglycan Is Selectively Associated with Inhibitory Garbaergic Synapses but Dispensable for Their Differentiation. J. Neurosci. 22: 4274-4285, 2002.  [PDF]

Durbeej, M. and Campbell, K.P. Muscular Dystrophies Involving the Dystrophin-Glycoprotein Complex: and overview of Current Mouse Models. Current Opinion in Genetics & Development 12:3:349-361, 2002.  [PDF]

Spiropoulou, C.F., Kunz, S., Rollin, P.E., Campbell, K.P. and Oldstone, M.B.A. New World Arenavirus Clade C, but not Clade A and B viruses, Utilize a-Dystroglycan as Its Major Receptor. J Virol. 15: 5140-5146, 2002.  [PDF]

Durbeej, M., Talts, J., Henry, M., Yurchenco, P., Campbell, K.P., Ekbolm, P. Dystroglycan Binding to Laminin a1LG4 Module Influences Epthelial Morphogenisis of Salavary Gland and Lung In Vitro. Differentiation. 69: 121-134, 2001.  [PDF]

Kunz, S., Sevilla, N., Campbell, K.P., Oldstone, M.B.A Molecular Analysis of the Interaction of LCMV with its Cellular Receptor a-Dystroglycan. J. Cell Biol. 155: 301-310, 2001.  [PDF]

Henry, M., Cohen, M.B., Campbell, K.P. Reduced Expression of Dystroglycan in Breast and Prostate Cancer. Hum. Path. 32(8), 791-795, 2001.  [PDF]

Kang, M.G., Chen, C.C., Felix, R., Letts, V.A., Frankel, W.N., Mori, Y., Campbell, K.P. Biochemical and Biophysical Evidence for g2 Subunit Association with Neuronal Voltage-Gated Ca2+ Channels. J. Biol. Chem. 276(35), 32917-32924, 2001.  [PDF]

Ahern, C.A., Powers P.A., Biddlecome, G.H., Roethe, L.,Vallejo, P., Mortenson, L., Strube, C., Campbell, K.P., Coronado, R., Gregg R.G. Modulation of L-Type Ca2+ Current but not Activation of Ca2+ release by the g1 Subunit of the Dihydropyridine Receptor of Skeletal Muscle. BMC Physiol 1:8, 2001.  [PDF]

Sugita, S., Saito, F., Tang, J., Satz, J., Campbell, K.P., and Sudhof, T.C. A Stoichiometric Complex of Neurexins and Dystroglycan in Brain. J. Cell Biol. 154: 435-446, 2001.  [PDF]

Ahern, C., Arikkath, J., Vallejo, P., Gurnett, C.A., Powers, P., Campbell, K.P., Coronado, R. Intramembrane Charge Movements and Excitation-Contraction Coupling Expressed by Two-Domain Fragments of the Ca2+ Channel. Proc. Natl. Acad. Sci. 5;98(12), 6935-6940, 2001.  [PDF]

Henry, M.D., Satz, J.S., Brakebush, C., Costell, M., Gustaffson, E., Fassler, R., Campbell, K.P. Distinct Roles for Dystroglycan, b-1 Integrin and Perlecan in Cell Surface Laminin Organization. J. Cell Science 114, 1137-1144, 2001.  [PDF]

Cohn, R.D., Durbeej, M., Moore, S.A., Coral-Vazquez, R., Prouty, S., Campbell, K.P. Prevention of Cardiomyopathy in Mouse Models Lacking the Smooth Muscle Sarcoglycan-Sarcospan Complex. J. Clin. Invest. 107, R1-R7, 2001.  [PDF]

Smelt, S.C., Borrow, P., Kunz, S., Cao, W., Tishon, A., Lewicki, H., Campbell, K.P. and Oldstone, M.B.A. Differences in Affinity of Binding of Lymphocytic Choriomeningitis Virus Strains to the Cellular Receptor a-Dystroglycan Correlate with Viral Tropism and Disease Kinetics. J. Virol. 75, 448-457, 2000.  [PDF]

Piccolo, F., Moore, S.A., Ford, G.C., Campbell, K.P. Intracellular Accumulation and Reduced Sarcolemmal Expression of Dysferlin in Limb-Girdle Muscular Dystrophies. Ann Neurol. 48, 902-912, 2000.  [PDF]

Sevilla, N., Kunz, S. Holz, A., Lewicki, H., Homman, D., Yamada, H., Campbell, K.P., de la Torre, J.C., Oldstone, M.B.A. Immunosppression and Resultant Viral Persistence by Specific Viral Targeting of Dendritic Cells. J. Exper. Med. 192, 1249-1260, 2000.  [PDF]

Heathcote, D.R., Ekman, J.M., Campbell, K.P., Godfrey, E.W. Dystroglycan Overexpression In Vivo Alters Acetylcholine Receptor Aggregation at the Neuromuscular Junction. Devel. Biol. 227, 595-605, 2000.  [PDF]

Straub, V., Donahue, K.M., Allamand, V., Davisson, R.L., Kim, Y.R. and Campbell, K.P. Contrast Agent-Enhanced Magnetic Resonance Imaging of Skeletal Muscle Damage in Animal Models of Muscular Dystrophy. Mag. Resonance in Med. 44, 655-659, 2000.  [PDF]

Barresi, R., Moore, S.A., Stolle, C.A., Mendell, J., Campbell, K.P. Expression of g-Sarcoglycan in Smooth Muscle and Its Interaction with the Smooth Muscle Sarcoglycan-Sarcospan Complex. J. Biol. Chem. 275, 38554-38560, 2000.  [PDF]

Crawford, G.E., Faulkner, J.A., Crosbie, R.H., Campbell, K.P., Froehner, S.C., Chamberlain, J.S. Assembly of the Dystrophin-Associated Protein Complex Does Not Require the Dystrophin COOH-Terminal Domain. J. Cell Biol. 18, 1399-1410, 2000.  [PDF]

Allamand, V., Donahue, K.M., Straub, V., Davisson, R.L., Davidson, B.L., Campbell, K.P. Early Adenovirus-Mediated Gene Transfer Effectively Prevents Muscular Dystrophy in a-Sarcoglycan-Deficient Mice. Gene Therapy. 7, 1385-1391, 2000.  [PDF]

Crosbie, R.H., Lim, L.E., Moore, S.A., Hirano, M., Hays, A.P., Maybaum, S.W., Collin, H., Dovico, S.A., Stolle, C.A., Fardeau, M., Tomé, F.M.S., Campbell, K.P. Molecular and Genetic Characterization of Sarcospan: Insights into Sarcoglycan-Sarcospan Domains. Human Mol. Genet. 9, 2019-2027, 2000.  [PDF]

Grady, R.M., Zhou, H., Cunningham, J.M., Henry, M.D., Campbell, K.P. and Sanes, J.R. Maturation and Maintenance of the Neuromuscular Synapse: Genetic Evidence for Roles of the Dystrophin-Glycoprotein Complex. Neuron. 25, 279-293, 2000.  [PDF]

Holt, K.H., Crosbie, R.H., Venzke, D.P. and Campbell, K.P. Biosynthesis of Dystroglycan: Processing of a Precursor Propeptide. FEBS Letters. 468, 79-83, 2000.  [PDF]

Flanigan, K.M., Kerr, L., Bromberg, M.B., Leonard, C., Tsuruda, J., Zhang, P.,Gonzalez-Gomez, I., Cohn, R., Campbell, K.P. and Leppert, M. Congenital Muscular Dystrophy with Rigid Spine Syndrome: A Clinical, Pathological, Radiological, and Genetic Study. Annals of Neurol. 47, 152-161, 2000.  [PDF]

Lebakken, C.S., Venzke, D.P., Hrstka, R.F., Consolino, C., Faulkner, J.A., Williamson, R.A., Campbell, K.P. Sarcospan-Deficient Mice Maintain Normal Muscle Function. Mol. and Cell. Biol. 20, 1669-1677, 2000.  [PDF]

Durbeej, M., Cohn, R.D., Hrstka, R.F., Moore, S.A., Allamand, V., Davidson, B.L. Williamson, R.A. and Campbell, K.P. Disruption of the b-Sarcoglycan Gene Reveals Pathogenetic Complexity of Limb-Girdle Muscular Dystrophy Type 2E. Mol. Cell 5, 141-151, 2000.  [PDF]

Leschiziner, A., Moukhles, H., Lindenbaum, M., Gee, S.H., Butterworth, J., Campbell, K.P. and Carbonetto, S. Neural Regulation of a-dystroglycan biosynthesis and glycosylation in skeletal muscle. J. Neurochem. 74, 70-80, 2000.  [PDF]