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