AHNAK, a novel component of the dysferlin protein complex, redistributes to the cytoplasm with dysferlin during skeletal muscle regeneration von Huang, Yanchao, Laval, Steven H, van Remoortere, Alexandra, Baudier, Jacques, Benaud, Chriselle, Anderson, Louise V.B, Straub, Volker, Deelder, Andre, Frants, Rune R, den Dunnen, Johan T, Bushby, Kate, van der Maarel, Silvère M

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Identification of putative in vivo substrates of calpain 3 by comparative proteomics of overexpressing transgenic and nontransgenic mice von Cohen, Niaz, Kudryashova, Elena, Kramerova, Irina, Anderson, Louise V. B., Beckmann, Jacques S., Bushby, Katherine, Spencer, Melissa J.

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Clinical variability in calpainopathy: what makes the difference? von de Paula, Flávia, Vainzof, Mariz, Passos-Bueno, Maria Rita, de Cássia M Pavanello, Rita, Matioli, Sergio Russo, V B Anderson, Louise, Nigro, Vincenzo, Zatz, Mayana

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Characterization of Monoclonal Antibodies to Calpain 3 and Protein Expression in Muscle from Patients with Limb-Girdle Muscular Dystrophy Type 2A von Anderson, Louise V.B., Davison, Keith, Moss, Jennifer A., Richard, Isabelle, Fardeau, Michel, Tomé, Fernando M.S., Hübner, Christoph, Lasa, Adriana, Colomer, Jaume, Beckmann, Jacques S.

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A new evidence for the maintenance of the sarcoglycan complex in muscle sarcolemma in spite of the primary absence of δ-SG protein von GOUVEIA, Telma L. F, KOSSUGUE, Patricia M, PAIM, Julia F, ZATZ, Mayana, ANDERSON, Louise V. B, NIGRO, Vincenzo, VAINZOF, Mariz

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Refined mapping of the Welander distal myopathy region on chromosome 2p13 positions the new candidate region telomeric of the DYSF locus von VON TELL, Désirée, BRUDER, Carl E. G, ANDERSON, Louise V. B, ANVRET, Maria, AHLBERG, Gabrielle

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Cloning of the mouse dysferlin gene and genomic characterization of the SJL-Dysf mutation von Vafiadaki, Elizabeth, Reis, Andre, Keers, Sharon, Harrison, Ruth, Anderson, Louise V. B, Raffelsberger, Thomas, Ivanova, Silva, Hoger, Harald, Bittner, Reginald E, Bushby, Kate, Bashir, Rumaisa

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Multiplex Western Blotting System for the Analysis of Muscular Dystrophy Proteins von Anderson, Louise V.B., Davison, Keith

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Dysferlin is a Plasma Membrane Protein and is Expressed Early in Human Development von Anderson, Louise V. B., Davison, Keith, Moss, Jennifer A., Young, Carol, Cullen, Michael J., Walsh, John, Johnson, Margaret A., Bashir, Rumaisa, Britton, Stephen, Keers, Sharon, Argov, Zohar, Mahjneh, Ibrahim, Fougerousse, Françoise, Beckmann, Jacques S., Bushby, Kate M. D.

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Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the IκBα/NF-κB pathway in limb-girdle muscular dystrophy type 2A von Lefranc, Gérard, Baghdiguian, Stephen, Martin, Marianne, Richard, Isabelle, Pons, Françoise, Astier, Catherine, Bourg, Nathalie, Hay, Ronald T, Chemaly, Raymond, Halaby, Georges, Loiselet, Jacques, Anderson, Louise V. B, Munain, Adolfo Lopez de, Fardeau, Michel, Mangeat, Paul, Beckmann, Jacques S

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Patients with a Non‐dysferlin Miyoshi Myopathy have a Novel Membrane Repair Defect von Jaiswal, Jyoti K., Marlow, Gareth, Summerill, Gillian, Mahjneh, Ibrahim, Mueller, Sebastian, Hill, Maria, Miyake, Katsuya, Haase, Hannelore, Anderson, Louise V. B., Richard, Isabelle, Kiuru‐Enari, Sari, McNeil, Paul L., Simon, Sanford M., Bashir, Rumaisa

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Identical Mutation in Patients with Limb Girdle Muscular Dystrophy Type 2B Or Miyoshi Myopathy Suggests a Role for Modifier Gene(s) von Weiler, Tracey, Bashir, Rumaisa, Anderson, Louise V. B., Davison, Keith, Moss, Jennifer A., Britton, Stephen, Nylen, Edward, Keers, Sharon, Vafiadaki, Elizabeth, Greenberg, Cheryl R., Bushby, Kate M. D., Wrogemann, Klaus

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Protein studies in dysferlinopathy patients using llama-derived antibody fragments selected by phage display von HUANG, Yanchao, VERHEESEN, Peter, DE HAARD, Hans, BUSHBY, Kate, DEN DUNNEN, Johan, VAN DER MAAREL, Silvère M, ROUSSIS, Andreas, FRANKHUIZEN, Wendy, GINJAAR, Ieke, HALDANE, Faye, LAVAL, Steve, ANDERSON, Louise V. B, VERRIPS, Theo, FRANTS, Rune R

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Characterization of Dystroglycan‐Laminin Interaction in Peripheral Nerve von Yamada, Hiroki, Chiba, Atsuro, Endo, Tamao, Kobata, Akira, Anderson, Louise V. B., Hori, Hisae, Fukuta‐Ohi, Hiroko, Kanazawa, Ichiro, Campbell, Kevin P., Shimizu, Teruo, Matsumura, Kiichiro

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Identification of putativein vivo substrates of calpain 3 by comparative proteomics of overexpressing transgenic and nontransgenic mice von Cohen, Niaz, Kudryashova, Elena, Kramerova, Irina, Anderson, Louise V. B., Beckmann, Jacques S., Bushby, Katherine, Spencer, Melissa J.

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Dysferlin protein analysis in limb-girdle muscular dystrophies von Vainzof, M, Anderson, L V, McNally, E M, Davis, D B, Faulkner, G, Valle, G, Moreira, E S, Pavanello, R C, Passos-Bueno, M R, Zatz, M

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Diagnostic Protein Expression in Human Muscle Biopsies von Bornemann, Antje, Anderson, Louise V. B.

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Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2i as a milder allelic variant of congenital muscular dystrophy MDC1C von BROCKINGTON, Martin, YUVA, Yeliz, FALLET, Shari, ROMERO, Norma, FARDEAU, Michel, STRAUB, Volker, STOREY, Gillian, POLLITT, Christine, RICHARD, Isabelle, SEWRY, Caroline A, BUSHBY, Kate, VOIT, Thomas, PRANDINI, Paola, BLAKE, Derek J, MUNTONI, Francesco, BROWN, Susan C, TORELLI, Silvia, BENSON, Matthew A, HERRMANN, Ralf, ANDERSON, Louise V. B, BASHIR, Rumaisa, BURGUNDER, Jean-Marc

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Dystrophin nonsense mutation induces different levels of exon 29 skipping and leads to variable phenotypes within one BMD family von Ginjaar, Ieke B, Kneppers, Alexander LJ, v d Meulen, Jan-Douwe M, Anderson, Louise VB, Bremmer-Bout, Mattie, van Deutekom, Judith CT, Weegenaar, Jitske, den Dunnen, Johan T, Bakker, Egbert

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The Expression of Dystrophin-associated Glycoproteins During Skeletal Muscle Degeneration and Regeneration. An Immunofluorescence Study von VATER, RUTH, HARRIS, JOHN B, ANDERSON, LOUISE V. B, ROBERDS, STEVEN L, CAMPBELL, KEVIN P, CULLEN, MICHAEL J

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