Absence of Dystrophin Disrupts Skeletal Muscle Signaling: Roles of Ca2+, Reactive Oxygen Species, and Nitric Oxide in the Development of Muscular Dystrophy

Peptide-Based Inhibition of NF-κB Rescues Diaphragm Muscle Contractile Dysfunction in a Murine Model of Duchenne Muscular Dystrophy

Peterson, J. M., Kline, W. O., Canan, B. D., Ricca, D. J., Kaspar, B. K., Delfín, D. A., DiRienzo, K., Clemens, P. R., Robbins, P. D., Baldwin, A. S., et al. (2011) · Molecular Medicine · doi:10.2119/molmed.2010.00263 · Cited by 55

The inside and out of dystroglycan post-translational modification

Moore, C. J., & Winder, S. J. (2012) · Neuromuscular Disorders · doi:10.1016/j.nmd.2012.05.016 · Cited by 55

Oxidative modification and aggregation of creatine kinase from aged mouse skeletal muscle

Nuss, J. E., Amaning, J. K., Bailey, C. E., DeFord, J. H., Dimayuga, V. L., Rabek, J. P., & Papaconstantinou, J. (2009) · Aging · doi:10.18632/aging.100055 · Cited by 55

Endogenous Calpain-3 Activation Is Primarily Governed by Small Increases in Resting Cytoplasmic [Ca2+] and Is Not Dependent on Stretch

Murphy, R. M., & Lamb, G. D. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m808655200 · Cited by 55

Contractile properties of skinned muscle fibres from young and adult normal and dystrophic (mdx) mice.

Williams, D. A., Head, S. I., Lynch, G. S., & Stephenson, D. G. (1993) · The Journal of Physiology · doi:10.1113/jphysiol.1993.sp019458 · Cited by 54

Dystrophin and utrophin expression require sarcospan: loss of α7 integrin exacerbates a newly discovered muscle phenotype in sarcospan-null mice

Marshall, J. L., Chou, E., Oh, J., Kwok, A., Burkin, D. J., & Crosbie, R. H. (2012) · Human Molecular Genetics · doi:10.1093/hmg/dds271 · Cited by 54

β2-syntrophin and Par-3 promote an apicobasal Rac activity gradient at cell–cell junctions by differentially regulating Tiam1 activity

Mack, N. A., Porter, A. P., Whalley, H. J., Schwarz, J. P., Jones, R. C., Khaja, A. S. S., Bjartell, A. S., Anderson, K. I., & Malliri, A. (2012) · Nature Cell Biology · doi:10.1038/ncb2608 · Cited by 54

Analysis of Dystrophin Gene Deletions Indicates that the Hinge III Region of the Protein Correlates with Disease Severity

Carsana, A., Frisso, G., Tremolaterra, M. R., Lanzillo, R., Vitale, D. F., Santoro, L., & Salvatore, F. (2005) · Annals of Human Genetics · doi:10.1046/j.1529-8817.2005.00160.x · Cited by 53

Phospholipase A2 activity in dystrophinopathies

Lindahl, M., Backman, E. J., Henriksson, K. G., Gorospe, J. R. M., & Hoffman, E. P. (1995) · Neuromuscular Disorders · doi:10.1016/0960-8966(94)00045-b · Cited by 53

Expression of a NOS transgene in dystrophin-deficient muscle reduces muscle membrane damage without increasing the expression of membrane-associated cytoskeletal proteins

Tidball, J. G., & Wehling‐Henricks, M. (2004) · Molecular Genetics and Metabolism · doi:10.1016/j.ymgme.2004.06.006 · Cited by 53

Identification of New Dystroglycan Complexes in Skeletal Muscle

Johnson, E. K., Li, B., Yoon, J. H., Flanigan, K. M., Martin, P. T., Ervasti, J. M., & Montanaro, F. (2013) · PLoS ONE · doi:10.1371/journal.pone.0073224 · Cited by 52

Molecular Extensibility of Mini-dystrophins and a Dystrophin Rod Construct

Bhasin, N., Law, R., Liao, G. P., Safer, D., Ellmer, J., Discher, B. M., Sweeney, H. L., & Discher, D. E. (2005) · Journal of Molecular Biology · doi:10.1016/j.jmb.2005.07.064 · Cited by 52

α-Syntrophin regulates ARMS localization at the neuromuscular junction and enhances EphA4 signaling in an ARMS-dependent manner

Luo, S., Chen, Y., Lai, K., Arévalo, J. C., Froehner, S. C., Adams, M. E., Chao, M. V., & Ip, N. Y. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200412008 · Cited by 51

Morphological changes and spatial regulation of diacylglycerol kinase‐ζ, syntrophins, and Rac1 during myoblast fusion

Abramovici, H., & Gee, S. (2007) · Cell Motility and the Cytoskeleton · doi:10.1002/cm.20204 · Cited by 50

Cationic channels in normal and dystrophic human myotubes

Vandebrouck, C., Duport, G., Cognard, C., et al. (2001) · Neuromuscular Disorders · doi:10.1016/s0960-8966(00)00153-x · Cited by 48

Ryanodine receptor type-1 (RyR1) expression and protein S-nitrosylation pattern in human soleus myofibres following bed rest and exercise countermeasure

Michele Salanova, A., Schiffl, G., Rittweger, J., Felsenberg, D., & Blottner, D. (2008) · Histochemistry and Cell Biology · doi:10.1007/s00418-008-0399-6 · Cited by 48

Dystrophin glycoprotein complex‐associated Gβγ subunits activate phosphatidylinositol‐3‐kinase/Akt signaling in skeletal muscle in a laminin‐dependent manner

Xiong, Y., Zhou, Y., & Jarrett, H. W. (2008) · Journal of Cellular Physiology · doi:10.1002/jcp.21684 · Cited by 47

β2-Syntrophin Is a Cdk5 Substrate That Restrains the Motility of Insulin Secretory Granules

Schubert, S., Knoch, K.-P., Ouwendijk, J., Mohammed, S., Bodrov, Y., Jäger, M., Altkrüger, A., Wegbrod, C., Adams, M. E., Kim, Y. D., et al. (2010) · PLoS ONE · doi:10.1371/journal.pone.0012929 · Cited by 47

Comparison of the myoplasmic calcium transient elicited by an action potential in intact fibres of mdx and normal mice

Hollingworth, S., Zeiger, U., & Baylor, S. M. (2008) · The Journal of Physiology · doi:10.1113/jphysiol.2008.160507 · Cited by 47

Skeletal Muscle-Specific Calpain, p94, and Connectin/Titin: Their Physiological Functions and Relationship to Limb-Girdle Muscular Dystrophy Type 2A

Sorimachi, H., Ono, Y., & Suzuki, K. (2000) · Advances in experimental medicine and biology · doi:10.1007/978-1-4615-4267-4_23 · Cited by 47

Animal Models of Muscular Dystrophy

Ng, R., Banks, G. B., Hall, J. K., Muir, L. A., Ramos, J. N., Wicki, J., Odom, G. L., Konieczny, P., Seto, J. T., Chamberlain, J. R., et al. (2011) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-394596-9.00004-4 · Cited by 46

Intracellular polarity protein PAR‐1 regulates extracellular laminin assembly by regulating the dystroglycan complex

Masuda‐Hirata, M., Suzuki, A., Amano, Y., Yamashita, K., Ide, M., Yamanaka, T., Sakai, M., Imamura, M., & Ohno, S. (2009) · Genes to Cells · doi:10.1111/j.1365-2443.2009.01315.x · Cited by 46

Zebrafish based small molecule screens for novel DMD drugs

Kawahara, G., & Kunkel, L. M. (2012) · Drug Discovery Today Technologies · doi:10.1016/j.ddtec.2012.03.001 · Cited by 46

Limb-girdle muscular dystrophy

Mathews, K. D., & Moore, S. A. (2003) · Current Neurology and Neuroscience Reports · doi:10.1007/s11910-003-0042-9 · Cited by 46

Convergent regulation of skeletal muscle Ca 2+ channels by dystrophin, the actin cytoskeleton, and cAMP-dependent protein kinase

Johnson, B. D., Scheuer, T., & Catterall, W. A. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0409695102 · Cited by 46

Nitrosative modifications of the Ca2+ release complex and actin underlie arthritis-induced muscle weakness

Yamada, T., Fedotovskaya, O. N., Cheng, A. J., Cornachione, A. S., Minozzo, F. C., Aulin, C., Fridén, C., Turesson, C., Andersson, D. C., Glenmark, B., et al. (2014) · Annals of the Rheumatic Diseases · doi:10.1136/annrheumdis-2013-205007 · Cited by 46

Localization of Phospho-β-dystroglycan (pY892) to an Intracellular Vesicular Compartment in Cultured Cells and Skeletal Muscle Fibers in Vivo

Sotgia, F., Bonuccelli, G., Bedford, M. T., Brancaccio, A., Mayer, U., Wilson, M. T., Campos‐González, R., Brooks, J. W., Sudol, M., & Lisanti, M. P. (2003) · Biochemistry · doi:10.1021/bi0271289 · Cited by 45

Drug Trial of Superoxide Dismutase in Duchenne's Muscular Dystrophy

Stern, L. Z., Ringel, S. P., Ziter, F. A., Menander-Huber, K. B., Ionasescu, V. V., Pellegrino, R. J., & Snyder, R. D. (1982) · Archives of Neurology · doi:10.1001/archneur.1982.00510180020004 · Cited by 45

Running endurance abnormality in mdx mice

Hara, H., Nolan, P. M., Scott, M. O., Bućan, M., Wakayama, Y., & Fischbeck, K. H. (2002) · Muscle & Nerve · doi:10.1002/mus.10023 · Cited by 45

Chemical genetics unveils a key role of mitochondrial dynamics, cytochrome c release and IP3R activity in muscular dystrophy

Giacomotto, J., Brouilly, N., Walter, L., Mariol, M., Berger, J., Ségalat, L., Becker, T. S., Currie, P. D., & Gieseler, K. (2013) · Human Molecular Genetics · doi:10.1093/hmg/ddt302 · Cited by 45

Cavin-1: caveolae-dependent signalling and cardiovascular disease

Williams, J. J. L., & Palmer, T. M. (2014) · Biochemical Society Transactions · doi:10.1042/bst20130270 · Cited by 45

Caveolae Regulation of Mechanosensitive Channel Function in Myotubes

Huang, H., Bae, C., Sachs, F., & Suchyna, T. M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0072894 · Cited by 44

Role of SNTA1 in Rac1 activation, modulation of ROS generation, and migratory potential of human breast cancer cells

Bhat, H. F., Baba, R. A., Adams, M. E., & Khanday, F. A. (2014) · British Journal of Cancer · doi:10.1038/bjc.2013.723 · Cited by 43

The shape of caveolae is omega-like after glutaraldehyde fixation and cup-like after cryofixation

Schlörmann, W., Steiniger, F., Richter, W., Kaufmann, R., Hause, G., Lemke, C., & Westermann, M. (2009) · Histochemistry and Cell Biology · doi:10.1007/s00418-009-0651-8 · Cited by 43

Involvement of calpains in Ca2+-induced disruption of excitation-contraction coupling in mammalian skeletal muscle fibers

Verburg, E., Murphy, R. M., Richard, I., & Lamb, G. D. (2009) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00008.2009 · Cited by 43

AAV-mediated Overexpression of Human α7 Integrin Leads to Histological and Functional Improvement in Dystrophic Mice

Heller, K. N., Montgomery, C. L., Janssen, P. M. L., Clark, K. R., Mendell, J. R., & Rodino‐Klapac, L. R. (2013) · Molecular Therapy · doi:10.1038/mt.2012.281 · Cited by 43

Preventing phosphorylation of dystroglycan ameliorates the dystrophic phenotype in mdx mouse

Miller, G., Moore, C. J., Terry, R. L., Riviere, T. L., Mitchell, A., Piggott, R., Dear, T. N., Wells, D. J., & Winder, S. J. (2012) · Human Molecular Genetics · doi:10.1093/hmg/dds293 · Cited by 43

Caspase-12 ablation preserves muscle function in the mdx mouse

Moorwood, C., & Barton, E. R. (2014) · Human Molecular Genetics · doi:10.1093/hmg/ddu249 · Cited by 43

Myocilin Interacts with Syntrophins and Is Member of Dystrophin-associated Protein Complex

Joe, M. K., Kee, C., & Tomarev, S. I. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.224063 · Cited by 42

Characterization of the tyrosine phosphorylation and distribution of dystrobrevin isoforms

Balasubramanian, S., Fung, E. T., & Huganir, R. L. (1998) · FEBS Letters · doi:10.1016/s0014-5793(98)00804-7 · Cited by 42

Amelioration of Duchenne muscular dystrophy in mdx mice by elimination of matrix-associated fibrin-driven inflammation coupled to the αMβ2 leukocyte integrin receptor

Vidal, B., Ardite, E., Suelves, M., Ruiz‐Bonilla, V., Janué, A., Flick, M. J., Degen, J. L., Serrano, A. L., & Muñoz‐Cánoves, P. (2012) · Human Molecular Genetics · doi:10.1093/hmg/dds012 · Cited by 42

Systemic delivery of NEMO binding domain/IKKγ inhibitory peptide to young mdx mice improves dystrophic skeletal muscle histopathology

Reay, D. P., Yang, M. L., Watchko, J. F., Daood, M., O’Day, T. L., Rehman, K. K., D, D. C. G., Robbins, P. D., & Clemens, P. R. (2011) · Neurobiology of Disease · doi:10.1016/j.nbd.2011.05.008 · Cited by 41

Leupeptin-based inhibitors do not improve the mdx phenotype

Selsby, J. T., Pendrak, K., Zadel, M., Tian, Z., Pham, J., Carver, T., Acosta, P., Barton, E. R., & Sweeney, H. L. (2010) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00586.2009 · Cited by 41

Simultaneous Pathoproteomic Evaluation of the Dystrophin-Glycoprotein Complex and Secondary Changes in the mdx-4cv Mouse Model of Duchenne Muscular Dystrophy

Murphy, S., Henry, M. A., Meleady, P., Zweyer, M., Mundegar, R. R., Swandulla, D., & Ohlendieck, K. (2015) · Biology · doi:10.3390/biology4020397 · Cited by 39

Modulation of Heme/Substrate Binding Cleft of Neuronal Nitric-oxide Synthase (nNOS) Regulates Binding of Hsp90 and Hsp70 Proteins and nNOS Ubiquitination

Peng, H., Morishima, Y., Pratt, W. B., & Osawa, Y. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.323295 · Cited by 39

Golgi Complex Organization in Skeletal Muscle: A Role for Golgi‐Mediated Glycosylation in Muscular Dystrophies?

Percival, J. M., & Froehner, S. C. (2006) · Traffic · doi:10.1111/j.1600-0854.2006.00523.x · Cited by 39

Increased leakage of calcium ion from the sarcoplasmic reticulum of the mdx mouse

Takagi, A., Kojima, S., Ida, M., & Araki, M. (1992) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(92)90023-e · Cited by 39

Dystrophic muscle improvement in zebrafish via increased heme oxygenase signaling

Kawahara, G., Gasperini, M. J., Myers, J. A., Widrick, J. J., Eran, A., Serafini, P. R., Alexander, M. S., Pletcher, M. T., Morris, C. A., & Kunkel, L. M. (2013) · Human Molecular Genetics · doi:10.1093/hmg/ddt579 · Cited by 39

The Syntrophin-Dystrobrevin Subcomplex in Human Neuromuscular Disorders

Compton, A. G., Cooper, S. T., Hill, P. M., et al. (2005) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/64.4.350 · Cited by 39

The membrane hypothesis of duchenne muscular dystrophy: Quest for functional evidence

Hutter, O. F. (1992) · Journal of Inherited Metabolic Disease · doi:10.1007/bf01799615 · Cited by 38

POTENTIAL ROLE OF NITRIC OXIDE IN CONTRACTION‐STIMULATED GLUCOSE UPTAKE AND MITOCHONDRIAL BIOGENESIS IN SKELETAL MUSCLE

McConell, G. K., & Wadley, G. D. (2008) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/j.1440-1681.2008.05038.x · Cited by 38

Muscular dystrophy: The worm turns to genetic disease

Chamberlain, J. S., & Benian, G. M. (2000) · Current Biology · doi:10.1016/s0960-9822(00)00768-5 · Cited by 38

Ascorbic acid protects the diaphragm muscle against myonecrosis in mdx mice

Tonon, É., Ferretti, R., Shiratori, J. H., Neto, H. S., Marques, M. J., & Minatel, E. (2011) · Nutrition · doi:10.1016/j.nut.2011.09.013 · Cited by 38

Neuronal Nitric Oxide Synthase-Rescue of Dystrophin/Utrophin Double Knockout Mice does not Require nNOS Localization to the Cell Membrane

Wehling‐Henricks, M., & Tidball, J. G. (2011) · PLoS ONE · doi:10.1371/journal.pone.0025071 · Cited by 38

Exon-Skipping Therapy: A Roadblock, Detour, or Bump in the Road?

Hoffman, E. P., & McNally, E. M. (2014) · Science Translational Medicine · doi:10.1126/scitranslmed.3008873 · Cited by 37

Poloxamer 188 failed to prevent exercise-induced membrane breakdown in mdx skeletal muscle fibers

Quinlan, J. G., Wong, B. L. Y., Niemeier, R. T., McCullough, A. S., Levin, L. S., & Emanuele, M. (2006) · Neuromuscular Disorders · doi:10.1016/j.nmd.2006.09.016 · Cited by 37

TAPP2 links phosphoinositide 3-kinase signaling to B-cell adhesion through interaction with the cytoskeletal protein utrophin: expression of a novel cell adhesion-promoting complex in B-cell leukemia

Costantini, J. L., Cheung, S., Hou, S., Li, H., Kung, S. K. P., Johnston, J. B., Wilkins, J. A., Gibson, S. B., & Marshall, A. J. (2009) · Blood · doi:10.1182/blood-2009-03-213058 · Cited by 36

Loss of nNOS inhibits compensatory muscle hypertrophy and exacerbates inflammation and eccentric contraction-induced damage in mdx mice

Froehner, S. C., Reed, S. M., Anderson, K. N., Huang, P. L., & Percival, J. M. (2014) · Human Molecular Genetics · doi:10.1093/hmg/ddu469 · Cited by 35

Why short stature is beneficial in duchenne muscular dystrophy

Bodor, M., & McDonald, C. M. (2013) · Muscle & Nerve · doi:10.1002/mus.23793 · Cited by 35

Phosphorylation of dystrophin and α-syntrophin by Ca2+-calmodulin dependent protein kinase II

Madhavan, R., & Jarrett, H. W. (1999) · Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology · doi:10.1016/s0167-4838(99)00193-4 · Cited by 34

Fatigue and Muscle Atrophy in a Mouse Model of Myasthenia Gravis Is Paralleled by Loss of Sarcolemmal nNOS

Meinen, S., Lin, S., Rüegg, M. A., & Punga, A. R. (2012) · PLoS ONE · doi:10.1371/journal.pone.0044148 · Cited by 34

Exploration of Lipid Metabolism in Relation with Plasma Membrane Properties of Duchenne Muscular Dystrophy Cells: Influence of L-Carnitine

Borgne, F. L., Guyot, S., Logerot, M., Beney, L., Gervais, P., & Demarquoy, J. (2012) · PLoS ONE · doi:10.1371/journal.pone.0049346 · Cited by 33

Differential distribution of dystrophin and β-spectrin at the sarcolemma of fast twitch skeletal muscle fibers

Williams, M. W., & Bloch, R. J. (1999) · Journal of Muscle Research and Cell Motility · doi:10.1023/a:1005512217552 · Cited by 33

Isoprostanes in dystrophinopathy: Evidence of increased oxidative stress

Grosso, S., Perrone, S., Longini, M., Bruno, C., Minetti, C., Gazzolo, D., Balestri, P., & Buonocore, G. (2008) · Brain and Development · doi:10.1016/j.braindev.2007.11.005 · Cited by 32

Linking cytoarchitecture to metabolism: sarcolemma-associated plectin affects glucose uptake by destabilizing microtubule networks in mdx myofibers

Raith, M., Valencia, R. G., Fischer, I., Orthofer, M., Penninger, J. M., Spuler, S., Rezniczek, G. A., & Wiche, G. (2013) · Skeletal Muscle · doi:10.1186/2044-5040-3-14 · Cited by 31

Evaluation of the Therapeutic Utility of Phosphodiesterase 5A Inhibition in the mdx Mouse Model of Duchenne Muscular Dystrophy

Percival, J. M., Adamo, C. M., Beavo, J. A., & Froehner, S. C. (2011) · Handbook of experimental pharmacology · doi:10.1007/978-3-642-17969-3_14 · Cited by 30

Modulation of contractile apparatus Ca2+ sensitivity and disruption of excitation–contraction coupling by S‐nitrosoglutathione in rat muscle fibres

Dutka, T. L., Mollica, J. P., Posterino, G. S., & Lamb, G. D. (2010) · The Journal of Physiology · doi:10.1113/jphysiol.2010.200451 · Cited by 30

α-Syntrophin Modulates Myogenin Expression in Differentiating Myoblasts

Kim, M. J., Hwang, S. H., Lim, J. A., Froehner, S. C., Adams, M. E., & Kim, H. S. (2010) · PLoS ONE · doi:10.1371/journal.pone.0015355 · Cited by 29

Evidence That Dystroglycan Is Associated with Dynamin and Regulates Endocytosis

Zhan, Y., Tremblay, M. R., Melian, N. Y., & Carbonetto, S. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m409682200 · Cited by 29

α-Dystrobrevin-1 recruits α-catulin to the α 1D -adrenergic receptor/dystrophin-associated protein complex signalosome

Lyssand, J. S., Whiting, J. L., Lee, K.-S., Kastl, R., Wacker, J. L., Bruchas, M. R., Miyatake, M., Langeberg, L. K., Chavkin, C., Scott, J. D., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1010819107 · Cited by 28

Skeletal Muscle-Specific Ablation of γcyto-Actin Does Not Exacerbate the mdx Phenotype

Prins, K. W., Lowe, D. A., & Ervasti, J. M. (2008) · PLoS ONE · doi:10.1371/journal.pone.0002419 · Cited by 28

Depolarization-induced contraction and SR function in mechanically skinned muscle fibers from dystrophic mdx mice

Plant, D. R., & Lynch, G. S. (2003) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00369.2002 · Cited by 28

iNOS Ablation Does Not Improve Specific Force of the Extensor Digitorum Longus Muscle in Dystrophin-Deficient mdx4cv Mice

Li, D., Shin, J., & Duan, D. (2011) · PLoS ONE · doi:10.1371/journal.pone.0021618 · Cited by 27

Differential targeting of nNOS and AQP4 to dystrophin-deficient sarcolemma by membrane-directed α-dystrobrevin

Adams, M. E., Tesch, Y., Percival, J. M., Albrecht, D. E., Conhaim, J. I., Anderson, K. N. E., & Froehner, S. C. (2007) · Journal of Cell Science · doi:10.1242/jcs.020701 · Cited by 25

A new twist to coiled coil

Rumeur, É. L., Hubert, J., & Winder, S. J. (2012) · FEBS Letters · doi:10.1016/j.febslet.2012.05.004 · Cited by 25

DIAPHRAGM MUSCLE STRIP PREPARATION FOR EVALUATION OF GENE THERAPIES IN mdx MICE

Faulkner, J. A., Ng, R., Davis, C. S., Li, S., & Chamberlain, J. S. (2008) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/j.1440-1681.2007.04865.x · Cited by 25

Chronic Administration of a Leupeptin-Derived Calpain Inhibitor Fails to Ameliorate Severe Muscle Pathology in a Canine Model of Duchenne Muscular Dystrophy

Childers, M. K., Bogan, J. R., Bogan, D. J., Greiner, H. M., Holder, M., Grange, R. W., & Kornegay, J. N. (2012) · Frontiers in Pharmacology · doi:10.3389/fphar.2011.00089 · Cited by 24

Selenium and vitamin E treatment of Duchenne muscular dystrophy: no effect on muscle function

Backman, E. J., Nylander, E., Johansson, I., Henriksson, K. G., & Tagesson, C. (1988) · Acta Neurologica Scandinavica · doi:10.1111/j.1600-0404.1988.tb03681.x · Cited by 24

A quantitative comparison of satellite cell ultrastructure in duchenne muscular dystrophy, polymyositis, and normal controls

Watkins, S. C., & Cullen, M. J. (1986) · Muscle & Nerve · doi:10.1002/mus.880090808 · Cited by 23

Phosphorylation within the cysteine-rich region of dystrophin enhances its association with β-dystroglycan and identifies a potential novel therapeutic target for skeletal muscle wasting

Swiderski, K., Shaffer, S. A., Gallis, B. M., Odom, G. L., Arnett, A. L. H., Edgar, J. S., Baum, D. M., Chee, A., Naim, T., Gregorevic, P., et al. (2014) · Human Molecular Genetics · doi:10.1093/hmg/ddu388 · Cited by 23

Syncoilin upregulation in muscle of patients with neuromuscular disease

Brown, S., Torelli, S., Ugo, I., Biasia, F. D., Howman, E. V., Poon, E. N.-Y., Britton, J. E., Davies, K. E., & Muntoni, F. (2005) · Muscle & Nerve · doi:10.1002/mus.20431 · Cited by 22

Putative roles of Ca2+‐independent phospholipase A2 in respiratory chain‐associated ROS production in brain mitochondria: influence of docosahexaenoic acid and bromoenol lactone

Nordmann, C., Strokin, M., Schönfeld, P., & Reiser, G. (2014) · Journal of Neurochemistry · doi:10.1111/jnc.12789 · Cited by 22

The susceptibility of muscle cells to oxidative stress is independent of nitric oxide synthase expression

Ai, W. Z., Eby, J. C., Cheong, M., Mohapatra, P. K., Bredt, D. S., Disatnik, M., & Rando, T. A. (2001) · Muscle & Nerve · doi:10.1002/mus.1033 · Cited by 21

Biglycan: a promising new therapeutic for neuromuscular and musculoskeletal diseases

Young, M. F., & Fallon, J. R. (2012) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2012.07.008 · Cited by 21

The ABCA1 cholesterol transporter associates with one of two distinct dystrophin‐based scaffolds in Schwann cells

Albrecht, D. E., Sherman, D. L., Brophy, P., & Froehner, S. C. (2008) · Glia · doi:10.1002/glia.20636 · Cited by 21

G.P.75 Variable phenotype of del45–55 Becker patients correlated to nNOSμ mislocalization and RYR1 hypernitrosylation

Gentil, C., Leturcq, F., Yaou, R. B., Jc, K., Laforêt, P., Pénisson-Besnier, I., Espil‐Taris, C., Voït, T., Garcı́a, L., & Piétri‐Rouxel, F. (2012) · Neuromuscular Disorders · doi:10.1016/j.nmd.2012.06.109 · Cited by 20

Syncoilin, an intermediate filament-like protein linked to the dystrophin associated protein complex in skeletal muscle

Moorwood, C. (2008) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-008-8306-9 · Cited by 19

HISTOCHEMICAL FIBRE TYPING AND ULTRASTUCTURE OF THE SMALL FIBRES IN DUCHENNE MUSCULAR DYSTROPHY

Watkins, S. C., & Cullen, M. J. (1985) · Neuropathology and Applied Neurobiology · doi:10.1111/j.1365-2990.1985.tb00039.x · Cited by 19

Lack of the serum- and glucocorticoid-inducible kinase SGK1 improves muscle force characteristics and attenuates fibrosis in dystrophic mdx mouse muscle

Steinberger, M., Föller, M., Vogelgesang, S., Krautwald, M., Landsberger, M., Winkler, C. K., Kasch, J., Füchtbauer, E., Kuhl, D., Voelkl, J. G. J., et al. (2014) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-014-1645-5 · Cited by 18

The Light Chains of Microtubule-Associated Proteins MAP1A and MAP1B Interact with α1-Syntrophin in the Central and Peripheral Nervous System

Fuhrmann‐Stroissnigg, H., Noiges, R., Descovich, L., Fischer, I., Albrecht, D. E., Nothias, F., Froehner, S. C., & Propst, F. (2012) · PLoS ONE · doi:10.1371/journal.pone.0049722 · Cited by 16

Erratum: Autophagy as a new therapeutic target in Duchenne muscular dystrophy

De Palma, C., Morisi, F., Cheli, S., Pambianco, S., Cappello, V, Vezzoli, M., Rovere-Querini, P., Moggio, M., Ripolone, M., Francolini, M., et al. (2014) · Cell Death & Disease · doi:10.1038/cddis.2014.312 · Cited by 16

Syntrophin isoforms play specific functional roles in the α1D-adrenergic receptor/DAPC signalosome

Lyssand, J. S., Lee, K.-S., DeFino, M. C., Adams, M. E., & Hague, C. (2011) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2011.08.004 · Cited by 11

Sast124, a novel splice variant of syntrophin-associated serine/threonine kinase (SAST), is specifically localized in the restricted brain regions

Yano, R., Yap, C. C., Yamazaki, Y., Muto, Y., Kishida, H., Okada, D., & Hashikawa, T. (2003) · Neuroscience · doi:10.1016/s0306-4522(02)00785-6 · Cited by 10

Adiponectin receptor 1 C-terminus interacts with PDZ-domain proteins such as syntrophins

Neumeier, M., Krautbauer, S., Schmidhofer, S., Hader, Y., Eisinger, K., Eggenhofer, E., Froehner, S. C., Adams, M. E., Mages, W., & Buechler, C. (2013) · Experimental and Molecular Pathology · doi:10.1016/j.yexmp.2013.07.002 · Cited by 4

Duchenne muscular dystrophy

Duan, D., Goemans, N., Takeda, S., Mercuri, E., & Aartsma-Rus, A. (2021) · Nature Reviews Disease Primers · doi:10.1038/s41572-021-00248-3 · Cited by 1,312

The Role of Oxidative Stress in Skeletal Muscle Myogenesis and Muscle Disease

Lian, D., Chen, M.-M., Wu, H., Deng, S., & Hu, X. (2022) · Antioxidants · doi:10.3390/antiox11040755 · Cited by 232

Use of capillary Western immunoassay (Wes) for quantification of dystrophin levels in skeletal muscle of healthy controls and individuals with Becker and Duchenne muscular dystrophy

Beekman, C., Janson, A. A., Baghat, A., van Deutekom, J. C., & Datson, N. A. (2018) · PLOS ONE · doi:10.1371/journal.pone.0195850 · Cited by 119

Microalgae Produce Antioxidant Molecules with Potential Preventive Effects on Mitochondrial Functions and Skeletal Muscular Oxidative Stress

Vignaud, J., Loiseau, C., Hérault, J., Mayer, C., Côme, M., Martin, I., & Ulmann, L. (2023) · Antioxidants · doi:10.3390/antiox12051050 · Cited by 72

Myostatin/Activin Receptor Ligands in Muscle and the Development Status of Attenuating Drugs

Rodgers, B. D., & Ward, C. W. (2022) · Endocrine Reviews · doi:10.1210/endrev/bnab030 · Cited by 111