Straub, V., Ettinger, A. J., Durbeej, M., Venzke, D.P., Cutshall, S., Sanes, J. and Campbell, K.P. e-Sarcoglycan Replaces a-Sarcoglycan in Smooth Muscle to Form a Unique Dystrophin-Glycoprotein Complex. J. Biol. Chem. 274, 27989-28002, 1999. PDF icon [PDF]

Durbeej, M. and Campbell, K.P. Biochemical Characterization of the Epithelial Dystroglycan Complex. J. Biol. Chem. 274, 26609-26616, 1999. PDF icon [PDF]

Coral, V.R., Cohn, R.D., Moore, S.A., Hill, J.A., Weiss, R.M., Davisson, R., Straub, V., Bansal, D., Hrstka, R.F., Sudig, P., Faulkner, J.A., Williamson, R. and Campbell, K.P. Disruption of the Sarcoglycan-Sarcospan Complex in Vascular Smooth Muscle: A Novel Mechanism in the Pathogenesis of Cardiomyopathy and Muscular Dystrophy. Cell 98, 465-474, 1999. PDF icon [PDF]

Dinsmore, A.J., Rees-Blanchard, W., Bentley, P., Lewis, T., Kahl, S.D., Mullinnix, M.J., Campbell, K.P., and Earley, F.G.P. Characterization of Antibody Models of the Ryanodine Receptor for use in High Throughput Screening and Ligand Design. Pestic. Sci. 54, 345-52, 1998. PDF icon [PDF]

Johnston, J.C., Gasmi, M., Lim, L.E., Elder, J.H., Yee, J.K., Jolly, D.J., Campbell, K.P., Davidson, B.L. and Sauter, S.L. Minimum Requirements for Efficient Transduction of Dividing and Nondividing Cells by Feline Immunodefiency Virus Vectors. J. Virol. 73, 2491-2498, 1999. PDF icon [PDF]

Burgess, D.L., Biddlecome, G.H., McDonough, S.I., Diaz, M.E., Zilinski, C.A., Bean, B.P., Campbell, K.P., and Noebels, J.L. b Subunit Reshuffling Modifies N- and P/Q-type Ca2+ Channel Subunit Compostitions in Lethargic Mouse Brain. Mol. and Cell. Neuro. 13, 293-311, 1999. PDF icon [PDF]

Badorff, C., Lee, G-H., Lamphear, B.J., Martone, M.E., Campbell, K.P., Rhoads, R.E., Knowlton, K.U. Enteroviral Protease 2A Cleaves Dystrophin: Evidence of Cytoskeletal Disruption in an Acquired Cardiomyopathy. Nat. Med. 5, 320-326, 1999. PDF icon [PDF]

Crosbie, R.H., Lebakken, C.S., Holt, K.H., Venzke, D.P., Straub, V., Lee, J.C., Grady, R.M., Chamberlain, J.S., Sanes, J.R., and Campbell, K.P. Membrane Targeting and Stabilization of Sarcospan is Mediated by the Sarcoglycan Subcomplex. J. Cell Biol. 145, 153-165, 1999. PDF icon [PDF]

Brown, S.C., Fassati, A., Popplewell, L., Page, A.M., Henry, M.D., Campbell, K.P. and Dickson, G. Dystrophic phenotype induced in vitro by antibody blockade of muscle a-dystroglycan-laminin interaction. J. Cell Sci. 112, 209-216, 1999. PDF icon [PDF]

Salih, M.A.M., Rayess, M. Al, Cutshall, S., Urtizberea, J.A., Al-Turaiki, M.H.S., Ozo, C.O., Straub, V., Akbar, M., Abid, M., Andeejani, A., and Campbell, K.P. A Novel Form of Familial Congenital Muscular Dystrophy in Two Adolescents. Neuroped. 29, 289-93, 1998. PDF icon [PDF]

Holt, K.H. and Campbell, K.P. Assembly of the sarcoglycan complex: insights for muscular dystrophy. J. Biol. Chem. 273, 34667-34670, 1998. PDF icon [PDF]

Henry, M.D. and Campbell, K.P. A role for dystroglycan in basement membrane assembly. Cell. 95, 859-870, 1998. PDF icon [PDF]

Cao, W., Henry, M.D., Borrow, P., Yamada, H., Elder, J.H., Ravkov, E.V., Nichol, S.T., Compans, R.W., Campbell, K.P. and Oldstone, M.B.A. Identification of a–dystroglycan as a Receptor for Lymphocytic Choriomeningitis Virus and Lassa Fever Virus. Science. 282, 2079-2081, 1998. PDF icon [PDF]

Rambukkana, A., Yamada, H., Salzer, J.L., Zanazi, G., Yurchenco, P.D., Campbell, K.P., and Fischetti, V.A. Role of a-dystroglycan as a Schwann cell receptor for Mycobacterium leprae. Science. 282, 2076-2079, 1998. PDF icon [PDF]

Straub, V., Duclos, F., Venzke, D.P., Lee, J.C., Cutshall, S., Leveille, C.J., and Campbell, K.P. Molecular Pathogenesis of Muscle Degeneration in the d–Sarcoglycan-Deficient Hamster. Amer. J. Path. 153, 1623-1630,1998. PDF icon [PDF]

Duclos, F., Straub, V., Moore, S.A., Venzke, D.P., Hrstka, R.F., Crosbie, R.H., Durbeej, M., Lebakken, C. S., Ettinger, A. J., Meulen, J.V.D., Holt, K. H., Lim, L. E, Sanes, J. R. Davidson, B. L., Faulkner, J. A., Williamson, R., and Campbell, K.P. Progressive Muscular Dystrophy in a-Sarcoglycan Deficient Mice. J. Cell Biol. 142, 1461-1471, 1998. PDF icon [PDF]

Letts, V.A., Felix, R., Biddlecome, G.H., Arikkath, J., Mahaffey, C.L., Valenzuela, A., Bartlett II, F.S., Mori, Y., Campbell, K.P., and Frankel, W.N. The Mouse Stargazer Gene Encodes a Neuronal Ca2+ Channel g Subunit. Nat. Genet. 19, 340-347, 1998. PDF icon [PDF]

Ding, J.M., Buchanan, G.F., Faiman, L., Tischkau, S.A., McPherson, P., Campbell, K.P., and Gillette, M.U. A Neuronal Ryanodine Receptor Mediates Light-Induced Phase Delays of the Circadian Clock. Nature. 394, 381-384, 1998. PDF icon [PDF]

Durbeej, M., Henry, M.D., Ferletta, M., Campbell, K.P., and Ekblom, P. Distribution of Dystroglycan in Normal Adult Mouse Tissues. J. of Histochem. and Cytochem. 46, 449-457, 1998. PDF icon [PDF]

Holt, K.H., Lim, L.E., Straub, V., Venzke, D.P., Duclos, F., Anderson, R.D., Davidson, B.L., and Campbell, K.P. Functional Rescue of the Sarcoglycan Complex in the BIO 14.6 Hamster using d-Sarcoglycan Gene Transfer. Mol. Cell. 1, 841-848, 1998. PDF icon [PDF]

Crosbie, R.H., Yamada, H., Venzke, D.P., Lisanti, M.P., and Campbell, K.P. Caveolin-3 is Not an Integral Component of the Dystrophin-Glycoprotein Complex. FEBS Letters. 427, 279-282, 1998. PDF icon [PDF]

Crosbie, R.H., Straub, V., Yun, H.Y., Lee, J.C., Rafael, J.A., Chamberlain, J.S., Dawson, V.L., Dawson, T.M., and Campbell, K.P. mdx Muscle Pathology is Independent of nNOS Perturbation. Human Mol. Genet. 7, 823-829, 1998. PDF icon [PDF]

Duclos, F., Broux, O., Bourg, N., Straub, V., Feldman, G., Sunada, Y., Lim. L.E., Piccolo, F., Cutshall, S., Gary, F., Quetier, F., Kaplan, J.-C., Jackson, C.E., Beckmann, J.S., and Campbell, K.P. b-Sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish Isolate. Neuromuscul. Disord. 8, 30-38, 1998. PDF icon [PDF]

Bahls, F.H., Lartius, R., Trudeau, L.-E., Doyle, R.T., Fang, Y., Witcher, D., Campbell, K.P., and Haydon, P.G. Contact-Dependent Regulation of N-type Calcium Channel Subunits During Synaptogenesis. J. Neurobio. 35, 198-208, 1998. PDF icon [PDF]

Scott, V.E.S., Felix, R., Arikkath, J., and Campbell, K.P. Evidence for a 95 kDa Short Form of the a1A Subunit Associated with the w-Conotoxin MVIIC Receptor of the P/Q-type Ca2+ Channels. J. Neurosci. 18, 641-647, 1998. PDF icon [PDF]

Walker, D., Bichet, D., Campbell, K.P., and De Waard, M. A b4 Isoform-specific Interaction Site in the Carboxyl-terminal Region of the Voltage-dependent Ca2+ Channel a1A Subunit. J. Biol. Chem. 273, 2361-2367, 1998. PDF icon [PDF]

Bies, R.D., Maeda, M., Roberds, S.L., Holder, E., Bohlmeyer, T., Young, J.B., and Campbell, K.P. A 5' Dystrophin Duplication Mutation Causes Membrane Deficiency of a-Dystroglycan in a Family with X-linked Cardiomyopathy. J. Mol. Cell Card. 29, 3175-3188, 1997. PDF icon [PDF]

Crosbie, R.H., Heighway, J., Venzke, D.P., Lee, J.C., and Campbell, K.P. Sarcospan, the 25-kDa Transmembrane Component of the Dystrophin-Glycoprotein Complex. J. Biol. Chem. 272, 31221-31224, 1997. PDF icon [PDF]

Dinçer, P., Leturcq, F., Richard, I., Piccolo, F., Yalnizoglu, D., de Toma, C., Akçören, Z., Broux, O., Deburgrave, N., Brenguier, L., Roudaut, C., Urtizberea, J.A., Jung, D., Tan, E., Jeanpierre, M., Campbell, K.P., Kaplan, J.-C., Beckmann, J.S., and Topaloglu, H. A Biochemical, Genetic, and Clinical Survey of Autosomal Recessive Limb Girdle Muscular Dystrophies in Turkey. Ann. Neurol. 42, 222-229, 1997. PDF icon [PDF]

Straub, V., Rafael, J.A., Chamberlain, J.S., and Campbell, K.P. Animal Models for Muscular Dystrophy Show Different Patterns of Sarcolemmal Disruption. J. Cell Biol. 139, 375-385, 1997. PDF icon [PDF]

Felix, R., Gurnett, C.A., De Waard, M., and Campbell, K.P. Dissection of Functional Domains Of the Voltage-Dependent Ca2+Channel a2d Subunit. J. Neurosci. 17, 6884-6891, 1997. PDF icon [PDF]

Gurnett, C.A., Felix, R., and Campbell, K.P. Extracellular Interaction of the Voltage-dependent Ca2+ Channel a2d and a1Subunits. J. Biol. Chem. 272, 18508-18512, 1997. PDF icon [PDF]

Eymard, B., Romero, N.B., Leturcq, F., Piccolo, F., Carrié, A., Jeanpierre, M., Collin, H., Deburgrave, N., Azibi, K., Chaouch, M., Merlini, L., Thémar-Noël, C., Penisson, I., Mayer, M., Tanguy, O., Campbell, K.P., Kaplan, J.-C., Tomé, F.M.S., and Fardeau, M. Primary Adhalinopathy (a-Sarcoglycanopathy): Clinical, Pathologic, and Genetic Correlation in 20 Patients With Autosomal Recessive Muscular Dystrophy. Neurol. 48, 1227-1234, 1997. PDF icon [PDF]

Williamson, R.A., Henry, M.D., Daniels, K.J., Hrstka, R.F., Lee, J.C., Sunada, Y., Ibraghimov-Beskrovnaya, O., and Campbell, K.P. Dystroglycan is Essential for Early Embryonic Development: Disruption of Reichert’s membrane in Dag1-Null Mice. Hum. Mol. Gen. 6, 831-841, 1997. PDF icon [PDF]

Matsumura, K., Chiba, A., Yamada, H., Fukuta-Ohi, H., Fujita, S., Endo, T., Kobata, A., Anderson, L.V.B., Kanazawa, I., Campbell, K.P., and Shimizu, T. A Role of Dystroglycan in Schwannoma Cell Adhesion to Laminin. J. Biol. Chem. 272, 13904-13910, 1997. PDF icon [PDF]

Carrié, A., Piccolo, F., Leturcq, F., de Toma, C., Azibi, K., Beldjord, C., Vallat, J-M, Merlini, L., Voit, T., Sewry, C., Urtizberea, J.A., Romero, N., Tomé, F.M.S., Fardeau, M., Sunada, Y., Campbell, K.P., Kaplan, J.-C., and Jeanpierre, M. Mutational Diversity and Hot Spots in the a-Sarcoglycan Gene in Autosomal Recessive Muscular Dystrophy (LGMD2D). J. Med. Genet. 34, 470-475, 1997. PDF icon [PDF]

Allamand, V., Sunada, Y., Salih, M.A.M., Straub, V., Ozo, C.O., Al-Turaiki, M.H.S., Akbar, M., Kolo, T., Colognato, H., Zhang, X., Sorokin, L.M., Yurchenco, P.D., Tryggvason, K., and Campbell, K.P. Mild Congenital Muscular Dystrophy in Two Patients With An Internally Deleted Laminin a2-Chain. Hum. Mol. Gen. 6, 747-752, 1997. PDF icon [PDF]

Durbeej, M., Jung, D., Hjalt, T., Campbell, K.P., and Ekblom, P. Transient Expression of Dp140, a Product of the Duchenne Muscular Dystrophy Locus, During Kidney Tubulogenesis. Develop. Biol. 181, 156-167, 1997. PDF icon [PDF]

De Waard, M., Liu, H., Walker, D., Scott, V.E.S., Gurnett, C.A., and Campbell, K.P. Direct Binding of G-Protein bg Complex to Voltage-Dependent Calcium Channels. Nature 385, 446-450, 1997. PDF icon [PDF]

Fahlke, C., Knittle, T., Gurnett, C.A., Campbell, K.P., and George, A.L., Jr. Subunit Stoichiometry of Human Muscle Chloride Channels. J. Gen. Physiol. 109, 93-104, 1997. PDF icon [PDF]

Seidahmed, M.Z., Sunada, Y., Ozo, C.O., Hamid, F., Campbell, K.P., and Salih, M.A.M. Lethal Congenital Muscular Dystrophy in Two Sibs with Arthrogryposis Multiplex: New Entity or Variant of Cobblestone Lissencephaly Syndrome? Neuropediatrics 27, 305-310, 1996. PDF icon [PDF]

Salih, M.A.M., Sunada, Y., Al-Nasser, M., Ozo, C.O., Al-Turaiki, M.H.S., Akbar, M., and Campbell, K.P. Muscular Dystrophy Associated with b-Dystroglycan Deficiency. Annals of Neurol. 40, 925-928, 1996. PDF icon [PDF]

Piccolo, F., Jeanpierre, M., Leturcq, F., Dodé, C., Azibi, K., Toutain, A., Merlini, L., Jarre, L., Navarro, C., Krishnamoorthy, R., Tomé, F.M.S., Urtizberea, J.A., Beckmann, J.S., Campbell, K.P., and Kaplan, J.-C. A Founder Mutation in the g-Sarcoglycan Gene of Gypsies Possibly Predating Their Migration Out of India. Hum. Mol. Gen. 5, 2019-2022, 1996. PDF icon [PDF]

Clemens, P.R., Kochanek, S., Sunada, Y., Chan, S., Chen, H.-H., Campbell, K.P., and Caskey, C.T. In Vivo Muscle Gene Transfer of Full-Length Dystrophin with an Adenoviral Vector that Lacks All Viral Genes. Gene Ther. 3, 965-972, 1996. PDF icon [PDF]

Cartaud, A., Ludosky, M.A., Haasemann, M., Jung, D., Campbell, K., and Cartaud, J. Non-Neural Agrin Codistributes with Acetylcholine Receptors During Early Differentiation of Torpedo Electrocytes. J. Cell Sci. 109, 1837-1846, 1996. PDF icon [PDF]

Tian, M., Jacobson, C., Gee, S.H., Campbell, K.P., Carbonetto, S., and Jucker, M. Dystroglycan in the Cerebellum is a Laminin-a2-chain Binding Protein at the Glial-Vascular Interface and is Expressed in Purkinje Cells. Eur. J. Neurosci. 8, 2739-2747, 1996. PDF icon [PDF]

Liu, H., Felix, R., Gurnett, C.A., De Waard, M., Witcher, D.R., and Campbell, K.P. Expression and Subunit Interaction of Voltage-Dependent Ca2+ Channels in PC12 Cells. J. of Neurosci. 23, 7557-7565, 1996. PDF icon [PDF]

Jung, D., Duclos, F., Apostol, B., Straub, V., Lee, J.C., Allamand, V., Venzke, D.P., Sunada, Y., Moomaw, C.R., Leveille, C.J., Slaughter, C.A., Crawford, T.O., McPherson, J.D., and Campbell, K.P. Characterization of d-Sarcoglycan, a Novel Component of the Oligomeric Sarcoglycan Complex Involved in Limb-Girdle Muscular Dystrophy. J. Biol. Chem. 271, 32321-32329, 1996. PDF icon [PDF]

Rafael, J.A., Cox, G.A., Corrado, K., Jung, D., Campbell, K.P., and Chamberlain, J.S. Forced Expression of Dystrophin Deletion Constructs Reveals Structure-Function Correlations. J. Cell Biol. 134, 93-102, 1996. PDF icon [PDF]

Liu, H., De Waard, M., Scott, V.E.S., Gurnett, C.A., Lennon, V.A., and Campbell, K.P. Identification of Three Subunits of the High Affinity w-Conotoxin MVIIC-Sensitive Ca2+ Channel. J. Biol. Chem. 271, 13804-13810, 1996. PDF icon [PDF]

Salih, M.A.M., Mahdi, A.H., Al-Rikabi, A.C., Al-Bunyan, M., Roberds, S.L., Anderson, R.D., and Campbell, K.P. Clinical and Molecular Pathological Features of Severe Childhood Autosomal Recessive Muscular Dystrophy in Saudi Arabia. Develop. Med. & Child Neurol. 38, 262-271, 1996. PDF icon [PDF]

Cullen, M.J., Walsh, J., Roberds, S.L. and Campbell, K.P. Immunogold Localization of Adhalin, a-Dystroglycan and Laminin in Normal and Dystrophic Skeletal Muscle. Biochem. Soc. Trans. 24, 274S, 1996. PDF icon [PDF]

Yamada, H., Chiba, A., Endo, T., Kobata, A., Anderson, L.V.B., Hori, H., Fukuta-Ohi, H., Kanazawa, I., Campbell, K.P., Shimizu, T., and Matsumura, K. Characterization of Dystroglycan-Laminin Interaction in Peripheral Nerve. J. Neurochem. 66, 1518-1524, 1996. PDF icon [PDF]

Morandi, L., Barresi, R., Di Blasi, C., Jung, D., Sunada, Y., Confalonieri, V., Dworzak, F., Mantegazza, R., Antozzi, C., Jarre, L.A., Pini, A., Gobbi, G., Bianchi, C., Cornelio, F., Campbell, K.P., and Mora M. Clinical Heterogeneity of Adhalin Deficiency. Annals of Neurol. 39, 196-202, 1996. PDF icon [PDF]

Jung, D., Leturcq, F., Sunada, Y., Duclos, F., Tomé, F.M.S., Moomaw, C., Merlini, L., Azibi, K., Chaouch, M., Slaughter, C., Fardeau, M., Kaplan, J.-C., and Campbell, K.P. Absence of g-Sarcoglycan (35 DAG) in Autosomal Recessive Muscular Dystrophy Linked to Chromosome 13q12. FEBS Lett. 381, 15-20, 1996. PDF icon [PDF]

Gurnett, C.A., De Waard, M., and Campbell, K.P. Dual Function of the Voltage-Dependent Ca2+ Channel a2d Subunit in Current Stimulation and Subunit Interaction. Neuron 16, 431-440, 1996. PDF icon [PDF]

Cullen, M.J., Walsh, J.H., Roberds, S.L., and Campbell, K.P. Ultrastructural Localization of Adhalin, a-Dystroglycan and Merosin in Normal and Dystrophic Muscle. Neuropath. and Applied Neurobiol. 22, 30-37, 1996. PDF icon [PDF]

De Waard, M., Scott, V.E.S., Pragnell, M.,and Campbell, K.P. Identification of Critical Amino Acids Involved in a1-b Interaction in Voltage-Dependent Ca2+ Channels. FEBS Lett. 380, 272-276, 1996. PDF icon [PDF]

Scott, V.E.S., De Waard, M., Liu, H., Gurnett, C.A., Venzke, D.P., Lennon, V.A., and Campbell, K.P. b Subunit Heterogeneity in N-Type Ca2+ Channels. J. Biol. Chem. 271, 3207-3212, 1996. PDF icon [PDF]

Fadic, R., Sunada, Y., Waclawik, A.J., Buck, S., Lewandoski, P.J., Campbell, K.P., and Lotz, B.P. Brief Report: Deficiency of a Dystrophin-Associated Glycoprotein (Adhalin) in a Patient with Muscular Dystrophy and Cardiomyopathy. New Engl. J. of Med. 334, 362-366, 1996. PDF icon [PDF]

Guo, W., Jorgensen, A.O., Jones, L.R., and Campbell, K.P. Biochemical Characterization and Molecular Cloning of Cardiac Triadin. J. Biol. Chem. 271, 458-465, 1996. PDF icon [PDF]

Oexle, K., Herrmann, R., Dodé, C., Leturcq, F., Hübner, Ch., Kaplan, J.-C., Mizuno, Y., Ozawa, E., Campbell, K.P., and Voit, T. Neurosensory Hearing Loss in Secondary Adhalinopathy. Neuropediatrics 27, 32-36, 1996. PDF icon [PDF]

Duclos, F., Lim, L.E., Sunada, Y., Meyer, J., Campbell, K.P., Broux, O., Bourg, N., Allamand, V., Richard, I., Beckmann, J.S., Moomaw, C., Slaughter, C., Tomé, F.M.S., Fardeau, M., and Jackson, C.E. b-sarcoglycane: Une Protéine Du Complexe Dystrophine-Glycoprotéines Est Responsable D’Une Forme Récessive De Dystrophie Musculaire. Médecine Sciences 11, 1732-1738, 1995. PDF icon [PDF]

Sunada, Y., Edgar, T.S., Lotz, B.P., Rust, R.S., and Campbell, K.P. Merosin-Negative Congenital Muscular Dystrophy Associated with Extensive Brain Abnormalities. Neurol. 45, 2084-2089, 1995. PDF icon [PDF]

Jung, D., Yang, B., Meyer, J., Chamberlain, J.S., and Campbell, K.P. Identification and Characterization of the Dystrophin Anchoring Site on b-Dystroglycan. J. Biol. Chem. 270, 27305-27310, 1995. PDF icon [PDF]

Lim, L.E., Duclos, F., Broux, O., Bourg, N., Sunada, Y., Allamand, V., Meyer, J., Richard, I., Moomaw, C., Slaughter, C., Tomé, F.M.S., Fardeau, M., Jackson, C.E., Beckman, J.S., and Campbell, K.P. b-sarcoglycan: Characterization and Role in Limb-Girdle Muscular Dystrophy Linked to 4q12. Nature Genet. 11, 257-265, 1995. PDF icon [PDF]

Kawai, H., Akaike, M., Endo, T., Adachi, K., Inui, T., Mitsui, T., Kashiwagi, S., Fujiwara, T., Okuno, S., Shin, S., Miyoshi, K., Campbell, K.P., Yamada, H., Shimizu, T., Matsumura, K., and Saito, S. Adhalin Gene Mutations in Patients With Autosomal Recessive Childhood Onset Muscular Dystrophy With Adhalin Deficiency. J. Clin. Invest. 96, 1202-1207, 1995. PDF icon [PDF]

Mills, K.A., Sunada, Y., Campbell, K.P., and Mathews, K.D. A Syntrophin Gene Maps to Mouse Chromosome 8 and Is Not the Myodystrophy Gene. Mammalian Genome 6, 664-665, 1995. PDF icon [PDF]

Apel, E.D., Roberds, S.L., Campbell, K.P., and Merlie, J.P. Rapsyn May Function as a Link between the Acetylcholine Receptor and the Agrin-Binding Dystrophin-associated Glycoprotein Complex. Neuron 15, 115-126, 1995. PDF icon [PDF]

Witcher, D.R., De Waard, M., Liu, H., Pragnell, M., and Campbell, K.P. Association of Native Ca2+ Channel b Subunits with the a1 Subunit Interaction Domain. J. Biol. Chem. 270, 18088-18093, 1995. PDF icon [PDF]

Vater, R., Harris, J.B., Anderson, L.V.B., Roberds, S.L., Campbell, K.P., and Cullen, M.J. The Expression of Dystrophin-Associated Glycoproteins During Skeletal Muscle Degeneration and Regeneration. An Immunofluorescence Study. J. Neuropath. & Exper. Neurol. 54, 557-569, 1995. PDF icon [PDF]

Durbeej, M., Larsson, E., Ibraghimov-Beskrovnaya, O., Roberds, S.L., Campbell, K.P., and Ekblom, P. Non-Muscle a-Dystroglycan Is Involved In Epithelial Development. J. Cell Biol. 130, 79-91, 1995. PDF icon [PDF]

Wells, D.J., Wells, K.E., Asante, E.A., Turner, G., Sunada, Y., Campbell, K.P., Walsh, F.S., and Dickson, G. Expression of Human Full-Length and Minidystrophin in Transgenic mdx Mice, Implications for Gene Therapy of Duchenne Muscular Dystrophy. Hum. Mol. Gen. 4, 1245-1250, 1995. PDF icon [PDF]

Passos-Bueno, M.R., Moreira, E.S., Vainzof, M., Chamberlain, J., Marie, S.K., Pereira, L., Akiyama, J., Roberds, S.L., Campbell, K.P., and Zatz, M. A Common Missense Mutation in the Adhalin Gene in Three Unrelated Brazilian Families with a Relatively Mild Form of Autosomal Recessive Limb-Girdle Muscular Dystrophy. Hum. Mol. Gen. 4, 1163-1168, 1995. PDF icon [PDF]

Yamada, H., Tomé, F.M.S., Higuchi, I., Kawai, H., Azibi, K., Chaouch, M., Roberds, S.L., Tanaka, T., Fugita, S., Mitsui, T., Fukunaga, H., Miyoshi, K., Osame, M., Fardeau, M., Kaplan, J.-C., Shimizu, T., Campbell, K.P., and Matsumura, K. Laminin Abnormality in Severe Childhood Autosomal Recessive Muscular Dystrophy. Lab. Invest. 72, 715-722, 1995. PDF icon [PDF]

Fritz, J.D., Danko, I., Roberds, S.L., Campbell, K.P., Latendresse, J.S., and Wolff, J.A. Expression of Deletion-Containing Dystrophins in mdx Muscle, Implications for Gene Therapy and Dystrophin Function. Pediatr. Res. 37, 693-700, 1995. PDF icon [PDF]

Kawai, H., Inui, T., Mitsul, T., Campbell, K.P., Shimizu, M., and Matsumura, K. Complete Deficiency of Adhalin (50kDa DAG) in Skeletal Muscle of Malignant Limb-girdle Muscular Dystrophy. Clin. Neurol. 35, 184-189, 1995. PDF icon [PDF]

Roberds, S.L. and Campbell, K.P. Adhalin mRNA and cDNA Sequence Are Normal in the Cardiomyopathic Hamster. FEBS Lett. 364, 245-249, 1995. PDF icon [PDF]

Sunada, Y., Bernier, S.M., Utani, A., Yamada, Y., and Campbell, K.P. Identification of a Novel Mutant Transcript of Laminin a2 Chain Gene Responsible for Muscular Dystrophy and Dysmyelination in dy2J mice. Hum. Mol. Gen. 4, 1055-1061, 1995. PDF icon [PDF]

Piccolo, F., Roberds, S.L., Jeanpierre, M., Leturcq, F., Azibi, K., Beldjord, C., Carrié, A., Récan, D., Chaouch, M., Reghis, A., El Kerch, F., Sefiani, A., Voit, T., Merlini, L., Collin, H., Eymard, B., Beckmann, J.S., Romero, N.B., Tomé, F.M.S., Fardeau, M., Campbell, K.P., and Kaplan, J.-C. Primary Adhalinopathy: A Common Cause of Autosomal Recessive Muscular Dystrophy of Variable Severity. Nature Genet. 10, 243-245, 1995. PDF icon [PDF]

De Waard, M. and Campbell, K.P. Subunit Regulation of the Neuronal a1A Ca2+ Channel Expressed in Xenopus Oocytes. J. Physiol. 485.3, 619-634, 1995. PDF icon [PDF]

De Waard, M., Witcher, D.R., Pragnell, M., Liu, H., and Campbell, K.P. Properties of the a1-b Anchoring Site in Voltage-dependent Ca2+ Channels. J. Biol. Chem. 270, 12056-12064, 1995. PDF icon [PDF]

Yang, B., Jung, D., Motto, D., Meyer, J., Koretzky, G., and Campbell, K.P. SH3 Domain-mediated Interaction of Dystroglycan and Grb2. J. Biol. Chem. 270, 11711-11714, 1995. PDF icon [PDF]

Cohen, M.W., Jacobson, C., Godfrey, E.W., Campbell, K.P., and Carbonetto, S. Distribution of a-Dystroglycan During Embryonic Nerve-Muscle Synaptogenesis. J. Cell Biol. 129, 1093-1101, 1995. PDF icon [PDF]

Gurnett, C.A., Kahl, S.D., Anderson, R.D., and Campbell, K.P. Absence of the Skeletal Muscle Sarcolemma Chloride Channel ClC-1 in Myotonic Mice. J. Biol. Chem. 270, 9035-9038, 1995. PDF icon [PDF]

Guo, W. and Campbell, K.P. Association of Triadin with the Ryanodine Receptor and Calsequestrin in the Lumen of the Sarcoplasmic Reticulum. J. Biol. Chem. 270, 9027-9030, 1995. PDF icon [PDF]

Yang, B., Jung, D., Rafael, J.A., Chamberlain, J.S., and Campbell, K.P. Identification of a-Syntrophin Binding to Syntrophin Triplet, Dystrophin, and Utrophin. J. Biol. Chem. 270, 4975-4978, 1995. PDF icon [PDF]