Han, R., Frett, E.M., Levy, J.R., Rader, E.P., Lueck, J.D., Bansal, D., Moore, S.A., Ng, R.N., Beltran-Valero de Bernabe, D., Faulkner, J.A., Campbell, K.P. Genetic Ablation of the Complement System Attenuates Dysferlin-Deficient Muscular Dystrophy. J. Clin. Invest. 120: 4366-74, 2010. [PDF]

Lueck, J., Rossi, A.E., Thornton, C.A., Campbell, K.P., Dirksen, R.T. Sarcolemmal Restricted Localization of Functional C1C-1 Channels in Mouse Skeletal Muscle. J. Gen. Physiol. 136: 597-613, 2010. [PDF]

Satz, J.S., Ostendorf, A.P., Hou, S., Turner, A., Kusano, H., Lee, J.C., Turk, R., Nguyen, H., Ross-Barta, S.E., Westra., S., Hoshi, T., Moore, S.A., Campbell, K.P. Distinct Functions of Glial and Neuronal Dystroglycan in the Developing and Adult Mouse Brain. J. Neurosci. 30: 14560-72, 2010. [PDF]

Leonoudakis, D., Singh, M., Mohajer, R., Mohajer, P., Fata, J.E., Campbell, K.P., Muschler, J.L. Dystroglycan controls signaling of multiple hormones through modulation of STAT5 activity. J. Cell Sci. 123: 3683-92, 2010. [PDF]

Vassilopoulos, S., Oddoux, S., Groh, S., Cacheaux, M., Faure, J., Brocard, J., Campbell, K.P., Marty, I. Caveolin-3 is Associated with the Calcium Release Complex and is Modified Under in vivo Triadin Modification. Biochemistry 49: 6130-35, 2010. [PDF]

Weiss, R.M., Kerber, R.E., Jones, J.K., Stephan, C.M., Trout, C.J., Lindower, P.D., Staffey, K.S., Campbell, K.P., Mathews, K.D. Exercise-Induced Left Ventricular Dysfunction in Heterozygous Dystrophinopathy. J. Am. Soc. Echocardiogr. 23: 848-53, 2010. [PDF]

Uriu, Y., Kiyonaka, S., Miku, T., Yagi, M., Akiyama, S., Mori, E., Nakao, A., Beedle, A.M., Campbell, K.P., Wakamori, M., Mori, Y. RAB3-interacting molecule γ isoforms lacking the Rab3-binding domain induce long-lasting currents but block neurotransmitter vesicle anchoring in voltage-dependent P/Q-type CA2+ channels. J. Biol. Chem. 285: 21750-67, 2010. [PDF]

Wang, R.X., Urso, M.L., Zambraski, E.J., Rader, E.P., Campbell, K.P., Liang, B.T. Adenosine A3 Receptor Stimulation Induces Protection of Skeletal Muscle from Eccentric Contraction Meditated-Injury. Am. J. Physiol. Regul. Integr. Comp. Physiol. 299: R259-67, 2010. [PDF]

Liou, L-Y., Walsh, K.B., Vartanian, A.R., Beltran, D., Campbell, K.P., Oldstone, M.B.A., Kunz, S. Functional Glycosylation of Dystroglycan is Crucial for Thymocyte Development in the Mouse. PLoS ONE 5:e9915, 2010. [PDF]

Vogtländer, N.P.J., van der Vlag, J.,  Bakker, M.A.H., Dijkman, H.B., Wevers, R.A., Campbell, K.P., Wetzels, J.F.M., Berden, J.H.M. Expression of sialidase and dystroglycan in human glomerular diseases. Nephrol. Dial. Transplant 25: 478-484, 2010. [PDF]

Watanabe, H., Yamashita, T., Saitoh, N., Kiyonaka, S., Iwamatsu, A., Campbell, K.P., Mori, Y., Takahashi, T. Involvement of Ca2+ Channell Synprint Site in Synaptic Vesicle Endocytosis. J. Neurosci. 30: 655-60, 2010. [PDF]

Yoshida-Moriguchi, T., Yu, L., Stalnaker, S.H., Davis, S., Kunz, S., Madson, M., Oldstone, M.B.A., Schachter, H., Wells, L., Campbell, K.P. O-Mannosyl Phosphorylation of Alpha-Dystorglycan Is Required for Laminin Binding. Science 327:88-92, 2010. [PDF]

Andrade, A., Sandoval, A., Gonzalez-Ramirez, R., Lipscombe, D., Campbell, K.P., and Felix, R. The α2δ Subunit Augments functional Expression and Modifies the Pharmacology of Cav1.3 L-type Channels. Cell Calcium 46: 282-92, 2009. [PDF]

Michele, D.E., Kabaeva, Z., Davis, S., Weiss, R.M., Campbell, K.P. Dystroglycan Matrix Receptor Function in Cardiac Myocytes is Important for Limiting Activity-induced Myocardial Damage. Cir. Res. 105:984-93, 2009. [PDF]

Satz, J.S., Philip, A.R., Nguyen, H., Kuzano, H., Lee, J., Turk, R., Riker, M.J., Hernandez, J., Weiss, R.M., Anderson, M.G., Mullins, R.F., Moore, S.A., Stone, E.M., Campbell, K.P. Visual Impairment in the Absence of Dystroglycan. J. Neurosci. 29:13136-46, 2009. [PDF]

Jimenez-Mallebrera, C., Torelli, S., Feng, L., Kim, J., Godfrey, C., Clement, E., Mein, R., Abbs, S., Brown, S., Campbell, K., Kroger, S., Talim, B., Topaloglu, H., Quinlivan, R., Roper, H., Childs, A., Kinali, M., Sewry, C., Muntoni, F. A Comparative Study of α-Dystroglycan Glycosylation in Dystroglycanopathies Suggests that the Hypoglycosylation of α-Dystroglycan Does Not Consistently Correlate with Clinical Severity. Brain Pathol. 19:596-611, 2009. [PDF]

Han, R., Kanagawa, M., Yoshida-Moriguchi, T., Rader, E., Ng., R.A., Michele, D.E., Muirhead, D.E., Kunz, S., Moore, S.A., Iannaccone, S.T., Miyake, K., McNeil, P.L., Mayer, U., Oldstone, M.B.A., Faulkner, J.A., Campbell, K.P. Basal Lamina Strengthens Cell Membrane Integrity via the Laminin G Domain Binding of α-Dystroglycan. Proc. Natl. Acad. Sci. U.S.A. 31:12573-79, 2009. [PDF]

Groh, S., Haihong, Z., Goddeeris, M.M., Lebakken, C.S., Venzke, D., Pessin, J.E., Campbell, K.P. Sarcoglycan Complex: Implications for Metabolic Defects in Muscular Dystrophies. J. Biol. Chem. 284:19178-82, 2009.[PDF]

Beltran-Valero de Barnabe, D., Inamori, K., Moriguchi, T., Weydert, C.J., Harper, H.A., Willer, T., Henry, M.D., Campbell, K.P. Loss of Alpha-Dystroglycan Laminin Binding in Epithelium-Derived Cancers is Caused by Silencing of Large. J. Biol. Chem. 284:11279-84, 2009.[PDF]

Zong, H., Bastie, C.C., Xu, J., Fassler, R., Campbell, K.P., Kurland, I.J., Pessin, J.E. Insulin Resistance in Striated Muscle Specific Integrin Receptor Beta 1 Deficient Mice. J. Biol. Chem. 284:4679-88, 2009.[PDF]

Puckett, R.L., Moore, S.A., Winder, T.L., Willer, T., Romansky, S.G., King Covalt, K., Campbell, K.P., Abdenur, J.E. Further Evidence of Fukutin Mutations as a Cause of Childhood Onset Limb-Girdle Muscular Dystrophy Without Mental Retardation. Neuromusc. Disord. 19:352-6, 2009. [PDF]

Chiang, C.S., Huang, C.H., Chieng, H., Chang, Y.T., Dory Chang, Chen, J. J., Chen, Y.H., Molkentin, J.D., Campbell, K.P., Chen, C.C. The CaV3.2 T-type Ca2+ Channel is Required for Pressure Overload-Induced Cardiac Hypertrophy in Mice. Circ. Res. 104:522-30, 2009.[PDF]

Murakami, T., Hayashi, Y.K., Ogawa, M., Noguchi, S., Campbell, K.P., Togawa, M., Inoue, T., Oka, A., Ohno, K., Nonaka, I., Nishino, I. A Novel POMT2 Mutation Causes Mild Congenital Muscular Dystrophy with Normal Brain MRI. Brain Dev. 31:465-8, 2008.[PDF]

Kanagawa, M., Nishimoto, A., Chiyonobu, T., Takeda, S., Miyagoe-Suzuki, Y., Wang, F., Fujikake, N., Taniguchi, M., Lu, Z., Tachikawa, M., Nagi, Y., Tashiro, F., Miyazaki, J.I., Tajima, Y., Takeda, S., Endo, T., Kobayashi, K., Campbell, K.P., Toda, T. Residual Laminin-Binding Activity and Enhanced Dystroglycan Glycosylation in Novel Model Mice to Dystroglycanopathy. Hum. Mol. Genet. 18: 621-31, 2008.[PDF]

Kobayashi, Y.M., Rader, E.P., Crawford, R.W., Iyengar, N.K., Thedens, D.R., Faulkner, J.A., Parikh, S.V., Weiss, R.M., Chamberlain, J.S., Moore, S.A., Campbell, K.P. Sarcolemma-Localized nNOS is Required to Maintain Activity After Mild Exercise. Nature 456: 511-5, 2008.[PDF]

Becker, A., Pitsch, J., Sochivko, D., Opitz, T., Staniek, M., Chen, C.C., Campbell, K.P., Schoch, S., Yaari, Y., Beck, H. Transcriptional Upregulation of CaV3.2 Mediates Epileptogenesis in the Pilocarpine Model of Epilepsy. J. Neurosci. 28:13341-53, 2008.[PDF]

Satz, J.S., Barresi, R., Durbeej, M., Willer, T., Turner, A., Moore, S.A., Campbell, K.P. Brain and Eye Malformations Resembling Walker-Warburg Syndrome Are Recapitulated in Mice by Dystroglycan-Deletion in the Epiblast. J. Neurosci. 28:10567-10575, 2008.[PDF]

Dylla, D.C., Michele, D.E., Campbell, K.P., McCray, P.B. Basolateral Entry and Release of New and Old World Arenaviruses. J. Virol. 82:6034-8, 2008. [PDF]

Nodari, A., Previtali, S.C., Dati, G., Occhi, S., Court, F.A., Colombelli, C., Zambroni, D., Dina, G., Del Carro, U., Campbell, K.P., Quattrini, A., Wrabetz, L., Feltri, M.L. α6β4 Integrin and Dystroglycan Cooperate to Stabilize the Myelin Sheath. J. Neurosci. 28:6714-9, 2008. [PDF]

Sandoval, A., Arrikath, J., Monjaraz, E., Campbell, K.P., Felix, R. Gamma 1-Dependent Down-Regulation of Recombinant Voltage-Gated Ca2+ Channels. Cell Mol. Neurobiol. 27: 901-8, 2007. [PDF]

Jethwaney, D., Islam, M.R., Leidel, K.G., de Bernabe, D.B., Campbell, K.P., Nauseef, W.M., Gibson, B.W., Proteomic Analysis of Plasma Membrane and Secretory Vesicles from Human Neutrophils. Proteome Sci. 10: 5-2, 2007. [PDF]

Kabosova, A., Azar, D.T., Bannikov, G.A., Campbell, K.P., Durbeej, M., Ghohestani, R.F., Jones, J.C.R., Kenney, M.C., Koch, M., Ninomiya, Y., Patton, B.L., Paulsson, M., Sado, Y., Sage, E.H., Sasaki, T., Sorokin, L.M., Steiner-Champliaud, M.F., Sun, T.T., Sundarraj, N., Teimpl, R., Virtanen, I., Ljubimov, A.V. Compositional Difference Between Infant and Adult Human Corneal Basement Membranes. Invest. Ophthalmol. Vis Sci. 48: 4989-99, 2007. [PDF]

Rojek, J.M., Campbell, K.P., Oldstone, M.B.A., Kunz, S. Old World Arenavirus Infection Interferes with the Expression of Functional Alpha-Dystroglycan in the Host Cell. Mol. Biol. Cell 18: 4493-4507, 2007. [PDF]

Pacak, C.A., Walter, G.A., Gaidosh, G., Bryant, N., Lewis, M.A., Germain, S., Mah, C.S., Campbell, K.P., Byrne, B.J. Long-Term Skeletal Muscle Protection After Gene Transfer in a Mouse Model of LGMD-2D. Mol. Ther. 15:1775-81, 2007. [PDF]

Kobuke, K., Piccolo, F., Garringer, K.W., Sweezer, E., Yang, B., Campbell, K.P. A Common Disease-Associated Missense Mutation in Alpha-Sarcoglycan Fails to Cause Muscular Dystrophy in Mice. Hum. Mol. Genet. 17:1201-13, 2007. [PDF]

Figueroa, X., Chen, C.C., Campbell, K.P., Damon, D.N., Day, K.H., Ramos, S., Duling, B.R. Are Voltage-Dependent Ion Channels Involved in the Endothelial Cell Control of Vasomotor Tone? Am. J. Physiol. Heart Circ. Physiol. 239: H1371-83, 2007. [PDF]

Miki, T., Kiyonaka, S., Uriu, Y., DeWaard, M., Wakamori, M., Beedle, A.M., Campbell, K.P., Mori, Y. Mutation Associated with an Autosomal Dominant Cone-Rod Dystrophy CORD7 Modifies RIM1-Mediated Modulation of Voltage-Dependent Ca2+ Channels. Channels 1: 144-47, 2007. [PDF]

Carmingnac, V., Salih, M.A., Quijano-Roy, S., Marchand, S., Al Rayess, M.M., Mukhtar, M.M., Urtizberea, J.A., Labeit, S., Guicheney, P., Leturcq, F., Gautel, M., Fardeau, M., Campbell, K.P., Richard, I., Estournet, B., Ferreiro, A. C-Terminal Titin Deletions Cause a Novel Early-Onset Myopathy with Fatal Cardiomyopathy. Ann. Neurol. 61: 340-51, 2007. [PDF]

Kiyonaka, S., Wakamori, M., Miki, T., Uriu, Y., Nonaka, M., Bito, H., Beedle, A., Mori, E., Hara, Y. DeWaard, M., Kanagawa, M., Itakara, M., Takahashi, M., Campbell, K.P., Mori, Y. RIM1 Confers Sustained Activity and Neurotransmitter Vesicle Anchoring to Presynaptic Ca(2+) Channels. Nat. Neurosci. 10: 691-701, 2007. [PDF]

Han, R., Bansal, D., Miyaka, K., Muniz, V.P., Weiss, R.M., McNeil, P.L., Campbell, K.P. Dysferlin-Mediated Membrane Repair Protects the Heart from Stress-Induced Left Ventricular Injury. J. Clin. Invest. 117: 1805-13, 2007. [PDF]

Handschin, C., Kobayashi, Y.M., Chin, S., Seale, P., Campbell, K.P., Spiegelman, B.M., PGC-1alpha Regulates the Neuromuscular Junction Program and Ameliorates Duchenne Muscular Dystrophy. Genes Dev. 21: 770-83, 2007. [PDF]

Beedle, A., Nienaber, P., Campbell, K.P. Fukutin-Related Protein Associates with the Sarcolemmal Dystrophon-Glycoprotein Complex. J. Biol. Chem. 282: 16713-17, 2007. [PDF]

Rojek, J.M., Spiropoulou, C.F., Campbell, K.P., and Kunz, S. Old World and Clade C New World Arenaviruses Mimic the Molecular Mechanism of Receptor Recognition Used by Alpha-Dystroglycan's Host-Dirived Ligands. J. Virol. 81: 5685-95, 2007. [PDF]

Sandoval, A., Andrade, A., Beedle, A.M., Campbell, K.P., and Felix, R. Inhibition of Recombinant N-Type CaV Channels by the gamma2 Subunit Involves Unfolded Protein Response UPR-Dependent and UPR-Independent Mechanisms. J. Neurosci. 27: 3317-27, 2007. [PDF]

Escoffier, J., Boisseau, S., Serres, C., Chen, C-C., Kim, D., Stamboulian, S., Shin, H-S., Campbell, K.P., Waard, M.D., and Arnoult, C. Expression, Localization and Functions in Acrosome Reaction and Sperm Motility of CaV3.1 and CaV3.2 Channels in Spearm Cells: and Evaluation from CaV3.1 and CaV3.2 Deficient Mice. J. Cell Physiol. 212: 753-63, 2007. [PDF]

Joksovic, P., Nelson, M., Jevtovic-Todorovic, V. Patel, M., Perez-Reyes, E., Campbell, K.P., Chen, C-C., Todorovic, S. CaV3.2 is the Major Molecular Substrate for Redox Regulation of T-type Ca2+ Channels in the Rat and Mouse Thalamus. J. Physiol. 15;574(Pt 2): 415-30, 2007. [PDF]

Moore, S.A., Shilling, C.J., Westra, S., Wall, C., Wicklund, M.P., Stolle, C., Brown,   C.A., Michele, D.E., Piccolo, F., Winder, T.L., Stence, A., Barresi, R., King, N., King,   W., Florence, J., Campbell, K.P., Fenichel, G.M., Stedman, H.H., Kissel, J.T., Griggs, R.C., Pandya, S., Matthews, K.D., Pestronk, A., Serrano, C., Darvish, D., Mendell, J.R.  Limb-Girdle Muscular Dystrophy in the United States.  J. Neuropathol. Exp. Neurol. 65: 995-1003, 2006. [PDF]

Weir, M.L., Oppizzi, M.L., Henry, M.D., Onishi, A., Campbell, K.P., Bissell, M.J., Muschler, J.L. Dystroglycan loss disrupts polarity and β-casein induction in mammary epithelial cells by perturbing laminin anchoring. J. Cell Sci.119: 4047-58, 2006. [PDF]

Bhosle, R.C., Michele, D.E., Campbell, K.P., Lic, Z., Robson, R.M. Interactions of intermediate filament protein synemin with dystrophin and utrophin. Biochem. Biophys. Res. Commun. 346: 768-77, 2006. [PDF]

Choi, S., Na, H.S., Kim, J., Lee, J., Lee, S., Kim, D., Park, J., Chen, C.C., Campbell, K.P., and Shin, H-S. Attenuated Pain Responses in Mice Lacking Cav3.2 T-type Channels. Genes Brain Behav. 6: 597-602, 2006. [PDF]

Murakami, T., Hayashi, Y.K., Nonaka, I., Tanabe, Y., Ogino, M., Eriguchi, M., Kotataoka, N., Campbell, K.P., Noguchi, S., Osawa, M., and Nishino, I.  Fukutin Gene Mutations can Dilated Cardiomyopathy with Ninimal Muscle Weakensss.  Ann. Neurol. 60: 597-602, 2006. [PDF]

Vogtlander, N.P., Tamboer, W.P., Bakker, M.A., Campbell, K.P., van der Vlag J., Berden, J.H. Reactive oxygen species deglycosilate glomerular alpha-dystroglycan. Kidney Int. 69: 1526-34, 2006. [PDF]

Mehes, E, Czirok, A, Hegedus, B, Szabo, B, Vicsek, T, Satz, J, Campbell, K, Jancsik, V. Dystroglycan is involved in laminin-1-stimulated motility of Muller glial cells: combined velocity and directionality analysis. Glia 49: 492-500, 2005. [PDF]

Kang, M-G., Chen, C-C., Wakamori, M., Hara, Y., Mori, Y., and Campbell, K.P. A Functional AMPA Receptor-calcium Channel Complex in the Postsynaptic Membrane. Proc. Natl. Acad. Sci. U.S.A 103: 5561-66, 2006. [PDF]

Barresi, Rita and Campbell, Kevin P. Dystroglycan: from biosynthesis to pathogenesis of human disease. J. Cell Sci. 119: 199-207, 2006. [PDF]

Turk R., Sterrenburg E., van der Wees C.G.C., de Meijer E.J., de Menezes R.X., Groh S., Campbell K.P., Noguchi S., van Ommen G.J.B., den Dunnen J.T., and 't Hoen P.A.C. Common Pathological Mechanisms in Mouse Models for Muscular Dystrophies. FASEB J. 20: 127-29, 2006. [PDF]