Kobayashi, Y.M. and Campbell, K.P. Skeletal Muscle Dystrophin-Glycoprotein Complex and Muscular Dystrophy. In: Muscle Fundamental Biology and Mechanisms of Disease, Joseph A. Hill and Eric N. Olson, ed., Academic Press, pp. 935-942, 2012.

Glass, D.J., Campbell, K.P. and Rudnicki, M.A. Skeletal Muscle - one year on. Skelet. Muscle 2:1, 2012. [PDF]

Oldstone, M.B.A. and Campbell, K.P. Decoding Arenavirus Pathogenesis: Essential Rose for Alpha-Dystroglycan-Virus Interatctions and the Immune Response. Virology 411: 170-179, 2011. [PDF]

Glass, D.J., Campbell, K.P. and Rudnicki, M.A. Welcome to Skeletal Muscle. Skeletal Muscle 1:1, 2011. [PDF]

Satz, J.S., Campbell, K.P. Unraveling the Ribbon Synapse. Nature Neurosci. 11(8):857-9, 2008. [PDF]

Han, R., Campbell, K.P., Dysferlin and Muscle Membrane Repair. Curr Opin Cell Biol. 19:1-8, 2007.  [PDF]

Kanagawa, M., Toda, T., and Campbell, K.P.  Glycosylation of dystroglycan and congenital muscular dystrophies.  The Lung Perspectives. 14(3): 75-81, 2006.  [PDF]

Michele, D. and Campbell, K.P. Cardiomyopathy in Muscular Dystrophies. In: Molecular Mechanisms for Cardiac Hypertrophy and Failure. (Walsh, Ed.) Taylor & Francis, London, pp. 541-567, 2005. [PDF]

Bansal, D., Campbell, K.P. Dysferlin and Plasma Membrane Repair in Muscular Dystrophy. Trends Cell Biol. 14(4): 206-213, 2004.  [PDF]

Cohn, R.D. and Campbell, K.P. Molecular Pathways for Dilated Cardiomyopathy. In: Molecular Basis of Cardiovascular Disease: A Companion to Braunwald's Heart Disease (2nd ed.) (Kenneth Chien, ed). Saunders, Philadelphia, pp.306-310, 2004.  [PDF]

Barresi, R and Campbell, K.P. Limb-Girdle Muscular Dystrophies. In: The Molecular and Genetic Basis of Neurologic and Psychiatric Disease, 3rd ed. (R. N. Rosenberg, et. al., Eds.). Butterworth Heinemann, 479-486, 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]

Kang, M., and Campbell, K.P. The gamma subunit of voltage-activated calcium channels, Mini Review. J. Biol. Chem. 278(24): 21315-21318, 2003.  [PDF]

Michele, D.E., Campbell, K.P. Dystrophin-Glycoprotein Complex: Post-Translational Processing and Dystroglycan Function. J. Biol. Chem. 278(18): 15457-15460, 2003.  [PDF]

Campbell, K.P., and Stull, J.T. Skeletal Muscle Basement Membrane-Sarcolemma-Cytoskeleton. Interaction Minireview Series. J. Biol. Chem. 278(15): 12599-12600, 2003.  [PDF]

Saito, F., and Campbell, K.P. Molecular Mechanism Underlying Congenital Muscular Dystrophy Caused by Aberrant Glycosylation of Dystroglycan. Zikkenigaku 20(18): 2648-2650, 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]

Piccolo, F., Moore, S.A., Mathews, K.D., Campbell, K.P. Limb Girdle Muscular Dystrophies. In: Advances in Neurology, Neuromuscular Disorders. Lippincott Williams and Wilkins, 88, 273-292, 2002.  [PDF]

Cohn, R.D. and Campbell, K.P. Pathogenetic Role of the Sarcoglycan-Sarcospan Complex in Cardiomyopathies. Acta Myologica. 19, 171-180, 2000.  [PDF]

Allamand,V. and Campbell, K.P. Animal Models for Muscular Dystrophy: Valuable Tools for the Development of Therapies. Human Mol. Genet. 9, 2459-2467, 2000.  [PDF]

Cohn, R.D. and Campbell, K.P. The Molecular Basis of Muscular Dystrophies. Muscle and Nerve. 23, 1456-1471, 2000.  [PDF]

Ertel, E.A., Campbell, K.P., Harpold, M.M., Hofmann, F., Mori, Y., Perez-Reyes, E., Schwartz, A., Snutch, T.P., Tanabe, T., Birnbaumer, L., Tsien, R.W., Catterall, W.A. Nomenclature of Voltage-Gated Calcium Channels. Neuron. 25, 533-535, 2000.  [PDF]

Henry, M.D. and Campbell, K.P. Dystroglycan. In: Guidebook to the Extracellular Matrix, Anchor and Adhesion Proteins, Oxford University Press. July 8, 1999. [PDF]

Cao, W., Henry, M.D., Borrow, P., Yamada, H., Elder, J.H., Campbel, K.P., and Oldstone, M.B.A. Isolation of a cellular receptor for lymphocytic choriomeningitis virus and Lassa fever virus. In: Factors in the Emergence and Control of Rodent-borne Viral Diseases (Hantaviruses and Arenal Diseases), J.F. Saluzzo, B. Dodet, eds., Elsevier Publications, France, pp. 225-231, 1999.  [PDF]

Henry, M.D. and Campbell, K.P. Dystroglycan Inside and Out. Curr. Opin. Cell Biol. 11, 602-607, 1999.  [PDF]

Henry, M.D., Campbell, K.P., Dag1. In: The Gene Knockout Factsbook, Ed. Mak, Penninger, Roder, Rossant and Saunders. Academic Press, November 15, 1998.  [PDF]

Lim, L.E. and Campbell, K.P. The Sarcoglycan Complex in Limb-Girdle Muscular Dystrophy. Curr. Opin. Neurol. 11, 443-452, 1998.  [PDF]

Durbeej, M., Henry, M.D., Campbell, K.P., Dystroglycan in Development and Disease. Curr. Opin. Cell Biol. 10, 594-601, 1998. [PDF]

Henry, M.D., Williamson, R.A., and Campbell, K.P. Analysis of the Role of Dystroglycan in Early Post-Implantation Mouse Development. Annals of New York Acad. of Sci. 857, 256-259, 1998.  [PDF]

Liu, H. and Campbell, K.P. Structural Determinants of Ca2+ Channel b Subunit Function. In: Low-Voltage-Activated T-type Calcium Channels, Proceedings from the International Electrophysiology Meeting. (R.W. Tsien, J-P Clozel, and J. Nargeot, eds.). Montpellier Proceedings, Section 3, pp. 229-243, 1998.  [PDF]

Scott, V.E.S., Gurnett, C.A., and Campbell, K.P. Overlay and Bead Assay: Determination of Calcium Channel Subunit Interaction Domains. Methods in Molecular Biology, Protein Targeting Protocols, Chapter 7, 88, 71-86, 1998.  [PDF]

Matsumura, K., Yamada, H., Fujita, S., Fukuta-Ohi, H., Tanaka, T., Campbell, K.P., and Shimizu, T. Peripheral Nerve Dystroglycan: Its Function and Potential Role in the Molecular Pathogenesis of Neuromuscular Diseases. In: Congential Muscular Dystrophies (Y. Fukuyama, M. Osawa, and K. Saito, eds.). Elsevier Science B.V., Chap. 22, pp. 267-273, 1997.  [PDF]

Straub, V. and Campbell, K.P. Muscular Dystrophies and the Dystrophin-Glycoprotein Complex. Curr. Opin. Neurol. 10, 168-175, 1997.  [PDF]

Jeanpierre, M., Carrié, A., Piccolo, F., Leturcq, F., Azibi, K., De Toma, C., Beldjord, C., Merlini, L., Voit, T., Romero, N., Sunada, Y., Tomé, F.M.S., Fardeau, M., Campbell, K.P., and Kaplan, J.-C. From Adhalinopathies to Alpha-Sarcoglycanopathies: An Overview. Neuromuscul. Disord. 6, 463-465, 1996.  [PDF]

Beckmann, J.S., Richard, I., Broux, O., Fougerousse, F., Allamand, V., Chiannilkulchai, N., Lim, L.E., Duclos, F., Bourg, N., Brenguier, L., Pasturaud, P., Quétier, F., Roudaut, C., Sunada, Y., Meyer, J., Dinçer, P., Lefranc, G., Merlini, L., Topaloglu, H., Tomé, F.M.S., Cohen, D., Jackson, C.E., Campbell, K.P., and Fardeau, M. Identification of Muscle-Specific Calpain and b-Sarcoglycan Genes in Progressive Autosomal Recessive Muscular Dystrophies. Neuromuscul. Disord. 6, 455-462, 1996.  [PDF]

Beckmann, J.S., Richard, I., Broux, O., Fougerousse, F., Allamand, V., Chiannilkulchai, N., Lim, L.E., Duclos, F., Bourg, N., Brenguier, L., Roudaut, C., Sunada, Y., Meyer, J., Tomé, F.M.S., Cohen, D., Jackson, C.E., Campbell, K.P., and Fardeau, M. Identification of Muscle-Specific Calpain and b-Sarcoglycan Genes in Progressive Muscular Dystrophies. Cellul. Pharm. 3, 189-194, 1996.  [PDF]

Henry, M.D. and Campbell, K.P. Dystroglycan: An Extracellular Matrix Receptor Linked to the Cytoskeleton. Curr. Opin. In Cell Biol. 8, 625-631, 1996.  [PDF]

Gurnett, C.A. and Campbell, K.P. Transmembrane Auxiliary Subunits of Voltage-dependent Ion Channels. J. Biol. Chem. 271, 27975-27978, 1996.  [PDF]

Campbell, K.P. and Crosbie, R.H. Utrophin to the Rescue. Nature 384, 308-309, 1996.  [PDF]

Guo, W., Jorgensen, A.O., and Campbell, K.P. Triadin, A Linker for Calsequestrin and the Ryanodine Receptor. J. Gen. Physiol. Series: Organellar Ion Channels and Transporters 51, 19-28, 1996.  [PDF]

Sunada, Y. and Campbell, K.P. Dystroglycan: A Novel Laminin Receptor and Its Involvement in the Pathogenesis of Muscular Dystrophy. In The Laminins. (P. Ekblom ed.) Harwood Academic Publishers GMBH 13.291-316, 1996.  [PDF]

De Waard, M., Gurnett, C.A., and Campbell, K.P. Structural and Functional Diversity of Voltage-Activated Calcium Channels. Ion Channels 4, 41-87, 1996.  [PDF]

Montanaro, F., Carbonetto, S., Campbell, K.P., and Lindenbaum, M. Dystroglycan Expression in the Wild Type and mdx Mouse Neural Retina: Synaptic Colocalization With Dystrophin, Dystrophin-Related Protein But Not Laminin. J. Neurosci. Res. 42, 528-538, 1995.  [PDF]

Sunada, Y. and Campbell, K.P. Dystrophin-Glycoprotein Complex: Molecular Organization and Critical Roles in Skeletal Muscle. Curr. Opin. Neurol. 8, 379-384, 1995.  [PDF]

Campbell, K.P. Adhalin Gene Mutations and Autosomal Recessive Limb-Girdle Muscular Dystrophy. Annals of Neurol. 38, 353-354, 1995.  [PDF]

Campbell, K.P. Three Muscular Dystrophies: Loss of Cytoskeleton-Extracellular Matrix Linkage. Cell 80, 675-679, 1995.  [PDF]

Witcher, D.R., De Waard, M., Kahl, S.D., and Campbell, K.P. Purification and Reconstitution of N-Type Calcium Channel Complex from Rabbit Brain. Methods in Enzymology, Chapter 28, 238,335-348, 1994. [PDF]

Matsumura, K. and Campbell, K.P. Dystrophin-Glycoprotein Complex: Its Role in the Molecular Pathogenesis of Muscular Dystrophies. Muscle and Nerve 17, 2-15, 1994. [PDF]

Matsumura, K., Ohlendieck, K., Ionasescu, V.V., Tomé, F.M.S., Ikuya, N., Burghes, A.H.M., Mora, M., Kaplan, J.-C., Fardeau, M., and Campbell, K.P. The Role of the Dystrophin-Glycoprotein Complex in the Molecular Pathogenesis of Muscular Dystrophies. Neuromuscul. Disord. 3, 533-535, 1993.  [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. and Campbell, K.P. Deficiency of Dystrophin-Associated Proteins: A Common Mechanism Leading to Muscle Cell Necrosis in Severe Childhood Muscular Dystrophies. Neuromuscul. Disord. 3, 109-118, 1993.  [PDF]

Ervasti, J.M. and Campbell, K.P. Dystrophin-Associated Glycoproteins: Their Possible Roles in the Pathogenesis of Duchenne Muscular Dystrophy. In: Molecular and Cell Biology of Muscular Dystrophy (T. Partridge, ed.) Chapman and Hall, London, United Kingdom, pp. 139-166, 1993.  [PDF]

Ervasti, J.M. and Campbell, K.P. Dystrophin and the Membrane Skeleton. Curr. Opin. Cell Biol. 5, 82-87, 1993.  [PDF]

Campbell, K.P., Ervasti, J.M., Ohlendieck, K., and Kahl, S.D. The Dystrophin-Glycoprotein Complex: Identification and Biochemical Characterization. In: Frontiers In Muscle Research. (E. Ozawa, T. Masaki, and Y. Nabeshima, eds.). Proceedings of the Uehara Memorial Foundation Symposium on Frontiers of Muscle Research. Elsevier Science Publishers International Congress Series, pp. 321-340, 1991. [PDF]

Krause, K.-H., Campbell, K.P., Welsh, M.J., and Lew, D.P. The Calcium Signal and Neutrophil Activation. Clin. Biochem. 23, 159-166, 1990.  [PDF]

Campbell, K.P., Sharp, A.H., and Leung, A.T. 32,000-Dalton Subunit of the 1,4-Dihydropyridine Receptor. Ann. N. Y. Acad. Sci. 560, 251-257, 1989.  [PDF]

Fill, M.J., Ma, J., Knudson, C.M., Imagawa, T., Campbell, K.P., and Coronado, R. Role of the Ryanodine Receptor of Skeletal Muscle in Excitation-Contraction Coupling. Ann. N. Y. Acad. Sci. 560, 155-162, 1989.  [PDF]

Campbell, K.P., Leung, A.T., Sharp, A.H., Imagawa, T., and Kahl, S.D. Ca2+ Channel Antibodies: Subunit-Specific Antibodies as Probes for Structure and Function. Proceedings from the Bayer Centenary Symposium. In: The Calcium Channel: Structure, Function and Implications. (M. Morad, W. Nayler, S. Kazda, M. Schramm, eds.). Springer-Verlag Berlin Heidelberg, Germany, pp. 586-600, 1988.  [PDF]

Campbell, K.P., Leung, A.T., and Imagawa, T. Structural Characterization of the Nitrendipine Receptor of the Voltage-Dependent Ca2+ Channel: Evidence for a 52,000 Dalton Subunit. J. Cardiovasc. Pharmacol. 12(Suppl. 4), S86-S90, 1988. [PDF]

Campbell, K.P., Leung, A.T., and Sharp, A.H. The Biochemistry and Molecular Biology of the Dihydropyridine-Sensitive Calcium Channel. Trends Neurosci. 11, 425-430, 1988.  [PDF]

Campbell, K.P. Protein Components and Their Roles in Sarcoplasmic Reticulum Function. In: Sarcoplasmic Reticulum in Muscle Physiology. (M.L. Entman and W.B. Van Winkle, eds.). CRC Press, Boca Raton, Florida, Vol. I, pp. 65-99, 1986.  [PDF]

MacLennan, D.H., Campbell, K.P., Takisawa, H., and Tuana, B.S. A Calmodulin-Dependent Protein Kinase System from Skeletal Muscle Sarcoplasmic Reticulum. In: Advances in Cyclic Nucleotide and Protein Phosphorylation Research. (P. Greengard, G.A. Robison, R. Paoletti, and S. Nicosia, eds.). Raven Press, New York, Vol. XVII, pp. 393-401, 1984.  [PDF]

MacLennan, D.H., Campbell, K.P., and Reithmeier, R.A.F. Calsequestrin. In: Calcium and Cell Function. (W. Cheung, ed.) Academic Press, New York, Vol. IV, pp. 151-173, 1983.  [PDF]

MacLennan, D.H., Klip, A., Reithmeier, R.A.F., Michalak, M., and Campbell, K.P. Possible Sites of Ion Flow in the Sarcoplasmic Reticulum Membrane. In: Membrane Bioenergetics (C.P. Lee, G. Schatz and L. Ernster, eds.). Addison-Wesley Reading, Mass., pp. 255-266, 1979.  [PDF]

MacLennan, D.H. and Campbell, K.P. Structure, Function and Biosynthesis of Sarcoplasmic Reticulum Proteins. Trends Biochem. Sci. 4, 148-151, 1979.  [PDF]

Campbell, K.P. and Shamoo, A.E. Identification of Two Intrinsic Proteins Uniquely Associated with the Terminal Cisternae of the Sarcoplasmic Reticulum. In: Calcium Binding Proteins and Calcium Function. (R.H. Wasserman, R.A. Corradino, E. Carafoli, R.H. Kretsinger, D.H. MacLennan, and F.L. Siegel, eds.). Elsevier North-Holland Press, New York, pp. 185-187, 1977.  [PDF]