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]