M. Adams, M. Butler, T. Dwyer, M. Peters, A. Murnane et al., Two forms of mouse syntrophin, a 58 kd dystrophin-associated protein, differ in primary structure and tissue distribution, Neuron, vol.11, issue.3, pp.531-540, 1993.
DOI : 10.1016/0896-6273(93)90157-M

E. Apel, D. Glass, L. Moscoso, G. Yancopoulos, and J. Sanes, Rapsyn Is Required for MuSK Signaling and Recruits Synaptic Components to a MuSK-Containing Scaffold, Neuron, vol.18, issue.4, pp.623-635, 1997.
DOI : 10.1016/S0896-6273(00)80303-7

A. Avila, M. Davila-garcia, V. Ascarrunz, Y. Xiao, and K. Kellar, Differential Regulation of Nicotinic Acetylcholine Receptors in PC12 Cells by Nicotine and Nerve Growth Factor, Molecular Pharmacology, vol.64, issue.4, pp.974-986, 2003.
DOI : 10.1124/mol.64.4.974

A. Bardoni, G. Felisari, M. Sironi, G. Comi, M. Lai et al., Loss of Dp140 regulatory sequences is associated with cognitive impairment in dystrophinopathies, Neuromuscular Disorders, vol.10, issue.3, pp.194-199, 2000.
DOI : 10.1016/S0960-8966(99)00108-X

A. Bardoni, N. Sironi, G. Felisar, G. Comi, and N. Bresolin, Absence of brain Dp140 isoform and cognitive impairment in Becker muscular dystrophy, The Lancet, vol.353, issue.9156, pp.897-898, 1999.
DOI : 10.1016/S0140-6736(98)05801-2

D. Blake, J. Schofield, R. Zuellig, D. Gorecki, S. Phelps et al., G-utrophin, the autosomal homologue of dystrophin Dp116, is expressed in sensory ganglia and brain., Proceedings of the National Academy of Sciences, vol.92, issue.9, pp.3697-3701, 1995.
DOI : 10.1073/pnas.92.9.3697

T. Byers, H. Lidov, and L. Kunkel, An alternative dystrophin transcript specific to peripheral nerve, Nature Genetics, vol.239, issue.1, pp.77-81, 1993.
DOI : 10.1083/jcb.116.6.1369

A. Cartaud, L. Strochlic, M. Guerra, B. Blanchard, M. Labergeon et al., MuSK is required for anchoring acetylcholinesterase at the neuromuscular junction, The Journal of Cell Biology, vol.20, issue.4, pp.505-515, 2004.
DOI : 10.1073/pnas.080061997

B. Cisneros, A. Rendon, V. Genty, G. Aranda, F. Marquez et al., Expression of dystrophin Dp71 during PC12 cell differentiation, Neuroscience Letters, vol.213, issue.2, pp.107-110, 1996.
DOI : 10.1016/0304-3940(96)12863-9

J. Connolly, Structure-function relationships in nicotinic acetylcholine receptors, Comparative Biochemistry and Physiology Part A: Physiology, vol.93, issue.1, pp.221-231, 1989.
DOI : 10.1016/0300-9629(89)90210-7

N. Connors and P. Kofuji, Dystrophin Dp71 is critical for the clustered localization of potassium channels in retinal glial cells, J Neurosci, vol.22, pp.4321-4327, 2002.

P. Cote, H. Moukhles, M. Lindenbaum, and S. Carbonetto, Chimaeric mice deficient in dystroglycans develop muscular dystrophy and have disrupted myoneural synapses

C. Dalloz, R. Sarig, P. Fort, D. Yaffe, A. Bordais et al., Targeted inactivation of dystrophin gene product Dp71: phenotypic impact in mouse retina, Human Molecular Genetics, vol.12, issue.13, pp.1543-1554, 2003.
DOI : 10.1093/hmg/ddg170

M. Daniels, B. Lowe, S. Shah, J. Ma, S. Samuelsson et al., Rodent nerve-muscle cell culture system for studies of neuromuscular junction development: Refinements and applications, Microscopy Research and Technique, vol.121, issue.1, pp.26-37, 2000.
DOI : 10.1002/(SICI)1097-0029(20000401)49:1<26::AID-JEMT4>3.0.CO;2-8

R. Defez and P. Brachet, Pheochromocytoma PC12 cells influence the differentiation of co-cultured skeletal myotubes, International Journal of Developmental Neuroscience, vol.4, issue.2, pp.161-168, 1986.
DOI : 10.1016/0736-5748(86)90041-9

K. Deyst, B. Mckechnie, and J. Fallon, The role of alternative splicing in regulating agrin binding to muscle cells, Developmental Brain Research, vol.110, issue.2, pp.185-191, 1998.
DOI : 10.1016/S0165-3806(98)00105-9

M. Durbeej and K. Campbell, Muscular dystrophies involving the dystrophin???glycoprotein complex: an overview of current mouse models, Current Opinion in Genetics & Development, vol.12, issue.3, pp.349-361, 2002.
DOI : 10.1016/S0959-437X(02)00309-X

J. Enriquez-aragon, J. Cerna-cortes, M. Bermudez-de-leon, F. Garcia-sierra, E. Gonzalez et al., Dystrophin Dp71 in PC12 cell adhesion, NeuroReport, vol.16, issue.3, pp.235-238, 2005.
DOI : 10.1097/00001756-200502280-00006
URL : https://hal.archives-ouvertes.fr/inserm-00149909

J. Ervasti, Dystrophin, its interactions with other proteins, and implications for muscular dystrophy, Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, vol.1772, issue.2, pp.108-117, 2007.
DOI : 10.1016/j.bbadis.2006.05.010
URL : https://hal.archives-ouvertes.fr/hal-00562718

J. Ervasti, K. Ohlendieck, S. Kahl, and K. Campbell, Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle, Nature, vol.345, issue.6273, pp.315-319, 1990.
DOI : 10.1038/345315a0

A. Eusebio, F. Oliveri, P. Barzaghi, and M. Ruegg, Expression of mouse agrin in normal, denervated and dystrophic muscle, Neuromuscular Disorders, vol.13, issue.5, pp.408-415, 2003.
DOI : 10.1016/S0960-8966(03)00036-1

E. Fabbrizio, J. Latouche, F. Rivier, G. Hugo, and D. Mornet, Re-evaluation of the distributions of dystrophin and utrophin in sciatic nerve, Biochemical Journal, vol.312, issue.1, pp.309-314, 1995.
DOI : 10.1042/bj3120309

E. Fabbrizio, U. Nudel, G. Hugon, A. Robert, F. Pons et al., Characterization and localization of a 77 kDa protein related to the dystrophin gene family, Biochemical Journal, vol.299, issue.2, pp.359-365, 1994.
DOI : 10.1042/bj2990359

Y. Fraenkel, D. Shalev, J. Gershoni, and G. Navon, Nuclear Magnetic Resonance (NMR) Analysis of Ligand Receptor Interactions: The Cholinergic System ??? A Model, Critical Reviews in Biochemistry and Molecular Biology, vol.101, issue.4, pp.273-301, 1996.
DOI : 10.1038/361088a0

C. Fuhrer, M. Gautam, J. Sugiyama, and Z. Hall, Roles of rapsyn and agrin in interaction of postsynaptic proteins with acetylcholine receptors, J Neurosci, vol.19, pp.6405-6416, 1999.

F. Galvagni, M. Cantini, and S. Oliviero, The Utrophin Gene Is Transcriptionally Up-regulated in Regenerating Muscle, Journal of Biological Chemistry, vol.277, issue.21, pp.19106-19113, 2002.
DOI : 10.1074/jbc.M109642200

A. Gramolini and J. Bj, Expression of the utrophin gene during myogenic differentiation, Nucleic Acids Research, vol.27, issue.17, pp.3603-3609, 1999.
DOI : 10.1093/nar/27.17.3603

Y. Gu, E. Ralston, C. Murphy-erdosh, R. Black, and Z. Hall, Acetylcholine receptor in a C2 muscle cell variant is retained in the endoplasmic reticulum, The Journal of Cell Biology, vol.109, issue.2, pp.729-738, 1989.
DOI : 10.1083/jcb.109.2.729

C. Hanham, F. Zhao, and G. Tignor, Evidence from the anti-idiotypic network that the acetylcholine receptor is a rabies virus receptor, J Virol, vol.67, pp.530-542, 1993.

W. Hoch, Formation of the neuromuscular junction. Agrin and its unusual receptors, European Journal of Biochemistry, vol.21, issue.1, pp.1-10, 1999.
DOI : 10.1016/S0959-4388(98)80062-7

E. Hoffman, R. Brown, . Jr, and L. Kunkel, Dystrophin: The protein product of the duchenne muscular dystrophy locus, Cell, vol.51, issue.6, pp.919-928, 1987.
DOI : 10.1016/0092-8674(87)90579-4

P. Howard, G. Dally, M. Wong, A. Ho, R. Weleber et al., Localization of dystrophin isoform Dp71 to the inner limiting membrane of the retina suggests a unique functional contribution of Dp71 in the retina, Human Molecular Genetics, vol.7, issue.9, pp.1385-1391, 1998.
DOI : 10.1093/hmg/7.9.1385

C. Jacobson, F. Montanaro, M. Lindenbaum, S. Carbonetto, and M. Ferns, ?-dystroglycan functions in acetylcholine receptor aggregation but is not a coreceptor for agrin-MuSK signaling, J Neurosci, vol.18, pp.6340-6348, 1998.

L. Judge, M. Haraguchi, and J. Chamberlain, Dissecting the signaling and mechanical functions of the dystrophin-glycoprotein complex, Journal of Cell Science, vol.119, issue.8, pp.1537-1546, 2006.
DOI : 10.1242/jcs.02857

D. Jung, D. Filliol, M. Metz-boutigue, and A. Rendon, Characterization and subcellular localization of the dystrophin-protein 71 (Dp71) from brain, Neuromuscular Disorders, vol.3, issue.5-6, pp.515-518, 1993.
DOI : 10.1016/0960-8966(93)90107-U

D. Jung, Y. B. Chamberlain, J. Campbell, and K. , Identification and Characterization of the Dystrophin Anchoring Site on ??-Dystroglycan, Journal of Biological Chemistry, vol.270, issue.45, pp.27305-27310, 1995.
DOI : 10.1074/jbc.270.45.27305

J. Kahl and J. Campanelli, A role for the juxtamembrane domain of ?-dystroglycan in agrin-induced acetylcholine receptor clustering, J Neurosci, vol.23, pp.392-402, 2003.

P. Kao, A. Dwork, R. Kaldany, M. Silver, J. Wideman et al., Identification of the ? subunit half-cystine specifically labeled by an affinity reagent for the acetylcholine receptor binding site, J Biol Chem, vol.259, pp.11662-11665, 1984.

N. Kramarcy, A. Vidal, S. Froehner, and R. Sealock, Association of utrophin and multiple dystrophin short forms with the mammalian Mr 58,000 dystophin-associated protein (syntrophin), J Biol Chem, vol.269, pp.2870-2876, 1994.

D. Laska, P. Williams, S. White, C. Thompson, and D. Hoover, In vitro correlation of ultrastructural morphology and creatine phosphokinase release in L6 skeletal muscle cells after exposure to parenteral antibiotics, In Vitro Cellular & Developmental Biology, vol.24, issue.10, pp.393-398, 1990.
DOI : 10.1007/BF02623831

D. Lederfein, Z. Levy, N. Augier, D. Mornet, G. Morris et al., A 71-kilodalton protein is a major product of the Duchenne muscular dystrophy gene in brain and other nonmuscle tissues., Proceedings of the National Academy of Sciences, vol.89, issue.12, pp.5346-5350, 1992.
DOI : 10.1073/pnas.89.12.5346

H. Lidov and L. Kunkel, Dp140: Alternatively Spliced Isoforms in Brain and Kidney, Genomics, vol.45, issue.1, pp.132-139, 1997.
DOI : 10.1006/geno.1997.4905

H. Lidov, S. Selig, and L. Kunkel, Dp140: a novel 140 kDa CNS transcript from the dystrophin locus, Human Molecular Genetics, vol.4, issue.3, pp.329-335, 1995.
DOI : 10.1093/hmg/4.3.329

H. Lidov and L. Kunkel, Dystrophin and Dp140 in the adult rodent kidney, Lab Invest, vol.78, pp.1543-1551, 1998.

C. Lumeng, S. Phelps, J. A. Rafael, G. Cox, T. Hutchinson et al., Characterization of Dystrophin and Utrophin Diversity in the Mouse, Human Molecular Genetics, vol.8, issue.4, pp.593-599, 1999.
DOI : 10.1093/hmg/8.4.593

F. Marquez, B. Cisneros, F. Garcia, V. Ceja, F. Velásquez et al., Differential expression and subcellular distribution of dystrophin Dp71 isoforms during differentiation process, Neuroscience, vol.118, issue.4, pp.957-966, 2003.
DOI : 10.1016/S0306-4522(03)00063-0

K. Matsumura, H. Yamada, T. Shimizu, and K. Campbell, Differential expression of dystrophin, utrophin and dystrophin-associated proteins in peripheral nerve, FEBS Letters, vol.268, issue.3, pp.281-285, 1993.
DOI : 10.1016/0014-5793(93)80695-Q

K. Nagata, C. Huang, J. Song, and T. Narahashi, Lead modulation of the neuronal nicotinic acetylcholine receptor in PC12 cells, Brain Research, vol.754, issue.1-2, pp.21-27, 1997.
DOI : 10.1016/S0006-8993(97)00037-1

K. Nagata, C. Huang, J. Song, and T. Narahashi, Direct actions of anticholinesterases on the neuronal nicotinic acetylcholine receptor channels, Brain Research, vol.769, issue.2, pp.211-218, 1997.
DOI : 10.1016/S0006-8993(97)00707-5

D. Neuman, J. Gershoni, M. Fridkin, and S. Fuchs, Antibodies to synthetic peptides as probes for the binding site on the alpha subunit of the acetylcholine receptor., Proceedings of the National Academy of Sciences, vol.82, issue.10, pp.3490-3493, 1985.
DOI : 10.1073/pnas.82.10.3490

K. Ohlendieck and K. Campbell, Dystrophin-associated proteins are greatly reduced in skeletal muscle from mdx mice, The Journal of Cell Biology, vol.115, issue.6, pp.1685-1694, 1991.
DOI : 10.1083/jcb.115.6.1685

M. Peters, M. Adams, and S. Froehner, Differential Association of Syntrophin Pairs with the Dystrophin Complex, The Journal of Cell Biology, vol.367, issue.1, pp.81-93, 1997.
DOI : 10.1111/j.1432-1033.1994.tb18958.x

B. Petrof, J. Shrager, H. Stedman, A. Kelly, and H. Sweeney, Dystrophin protects the sarcolemma from stresses developed during muscle contraction., Proceedings of the National Academy of Sciences, vol.90, issue.8, pp.3710-3714, 1993.
DOI : 10.1073/pnas.90.8.3710

D. Pillers, R. Weleber, D. Green, S. Rash, G. Dally et al., Effects of Dystrophin Isoforms on Signal Transduction through Neural Retina: Genotype???Phenotype Analysis of Duchenne Muscular Dystrophy Mouse Mutants, Molecular Genetics and Metabolism, vol.66, issue.2, pp.100-110, 1999.
DOI : 10.1006/mgme.1998.2784

J. Prives and D. Bar-sagi, Effect of tunicamycin, and inhibitor of protein glycosylation, on the biological properties of acetylcholine receptor in cultured muscle cells, J Biol Chem, vol.258, pp.1775-1780, 1983.

J. Rafael and S. Brown, Dystrophin and utrophin: Genetic analyses of their role in skeletal muscle, Microscopy Research and Technique, vol.108, issue.3-4, pp.155-166, 2000.
DOI : 10.1002/(SICI)1097-0029(20000201/15)48:3/4<155::AID-JEMT4>3.0.CO;2-0

J. Rafael, J. Tinsley, A. Potter, A. Deconick, and K. Davies, Skeletal muscle-specific expression of a utrophin transgene rescues utrophin-dystrophin deficient mice, Nature Genetics, vol.94, issue.1, pp.79-82, 1998.
DOI : 10.1038/352536a0

D. Rapaport, D. Lederfein, J. Den-dunnen, P. Grootscholten, G. Van-ommen et al., Characterization and cell type distribution of a novel, major transcript of the Duchenne Muscular Dystrophy gene, Differentiation, vol.49, issue.3, pp.187-193, 1992.
DOI : 10.1111/j.1432-0436.1992.tb00666.x

X. Ren, S. Cheng, M. Treuil, J. Mukherjee, J. Rao et al., Structural Determinants of ??4??2 Nicotinic Acetylcholine Receptor Trafficking, Journal of Neuroscience, vol.25, issue.28, pp.6676-6686, 2005.
DOI : 10.1523/JNEUROSCI.1079-05.2005

H. Rosas-vargas, C. Montañez, A. Rendon, D. Mornet, F. Garcia et al., Expression and localization of utrophin in differentiating PC12 cells, NeuroReport, vol.11, issue.10, pp.2253-2257, 2000.
DOI : 10.1097/00001756-200007140-00038

S. Sands and M. Barish, Neuronal nicotinic acetylcholine receptor currents in phaeochromocytoma (PC12) cells: dual mechanisms of rectification., The Journal of Physiology, vol.447, issue.1, pp.467-487, 1992.
DOI : 10.1113/jphysiol.1992.sp019012

T. Scherf, R. Kasher, M. Balass, M. Fridkin, S. Fuchs et al., A ??-hairpin structure in a 13-mer peptide that binds ??-bungarotoxin with high affinity and neutralizes its toxicity, Proceedings of the National Academy of Sciences, vol.98, issue.12, pp.6629-6634, 2001.
DOI : 10.1073/pnas.111164298

E. Schreiber, P. Matthias, M. Müller, and W. Schaffner, Rapid detection of octamer binding proteins with ???mini extracts???, prepared from a small number of cells, Nucleic Acids Research, vol.17, issue.15, p.6419, 1989.
DOI : 10.1093/nar/17.15.6419

D. Schubert, S. Heineman, and Y. Kidokoro, Cholinergic metabolism and synapse formation by a rat nerve cell line., Proceedings of the National Academy of Sciences, vol.74, issue.6, pp.2579-2583, 1977.
DOI : 10.1073/pnas.74.6.2579

J. Tinsley, D. Blake, A. Roche, U. Fairbrother, J. Riss et al., Primary structure of dystrophin-related protein, Nature, vol.360, issue.6404, pp.591-592, 1992.
DOI : 10.1038/360591a0

S. Tokarz, N. Duncan, S. Rash, A. Sadeghi, A. Dewan et al., Redefinition of Dystrophin Isoform Distribution in Mouse Tissue by RT-PCR Implies Role in Nonmuscle Manifestations of Duchenne Muscular Dystrophy, Molecular Genetics and Metabolism, vol.65, issue.4, pp.272-281, 1998.
DOI : 10.1006/mgme.1998.2763

T. Di-vignano, A. , D. Zenzo, G. Sudol, M. Cesareni et al., Contribution of the different modules in the utrophin carboxy-terminal region to the formation and regulation of the DAP complex, FEBS Letters, vol.8, issue.2-3, pp.229-234, 2000.
DOI : 10.1016/S0014-5793(00)01400-9

B. Wiedenmann and W. Franke, Identification and localization of synaptophysin, an integral membrane glycoprotein of Mr 38,000 characteristic of presynaptic vesicles, Cell, vol.41, issue.3, pp.1017-1028, 1985.
DOI : 10.1016/S0092-8674(85)80082-9

B. Wiedenmann, H. Rehm, M. Knierim, and C. Becker, Fractionation of synaptophysin-containing vesicles from rat brain and cultured PC12 pheochromocytoma cells, FEBS Letters, vol.88, issue.1-2, pp.71-77, 1988.
DOI : 10.1016/0014-5793(88)80342-9

J. Wilson, W. Putt, C. Jimenez, and Y. Edwards, Up71 and Up140, two novel transcripts of utrophin that are homologues of short forms of dystrophin, Human Molecular Genetics, vol.8, issue.7, pp.1271-1278, 1999.
DOI : 10.1093/hmg/8.7.1271

M. Yoshida and E. Ozawa, Glycoprotein Complex Anchoring Dystrophin to Sarcolemma1, The Journal of Biochemistry, vol.108, issue.5, pp.748-752, 1990.
DOI : 10.1093/oxfordjournals.jbchem.a123276
URL : http://jb.oxfordjournals.org/cgi/content/short/108/5/748