Skeletal Muscle Degenerative Diseases and Strategies for Therapeutic Muscle Repair

Induction of Pluripotent Stem Cells from Adult Human Fibroblasts by Defined Factors

Takahashi, K., Tanabe, K., Ohnuki, M., Narita, M., Ichisaka, T., Tomoda, K., & Yamanaka, S. (2007) · Cell · doi:10.1016/j.cell.2007.11.019 · Cited by 20,221 · see citing works

Induced Pluripotent Stem Cell Lines Derived from Human Somatic Cells

Yu, J., Vodyanik, M. A., Smuga-Otto, K., Antosiewicz-Bourget, J., Frane, J. L., Tian, S., Nie, J., Jonsdottir, G. A., Ruotti, V., Stewart, R., et al. (2007) · Science · doi:10.1126/science.1151526 · Cited by 10,310 · see citing works

Regulation of skeletal muscle mass in mice by a new TGF-p superfamily member

McPherron, A. C., Lawler, A. M., & Lee, S.-J. (1997) · Nature · doi:10.1038/387083a0 · Cited by 4,013 · see citing works

SATELLITE CELL OF SKELETAL MUSCLE FIBERS

Mauro, A. (1961) · The Journal of Cell Biology · doi:10.1083/jcb.9.2.493 · Cited by 3,683 · see citing works

Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member

Brook, J. D., McCurrach, M. E., Harley, H. G., Buckler, A., Church, D. M., Aburatani, H., Hunter, K. W., Stanton, V. P., Thirion, J., Hudson, T. J., et al. (1992) · Cell · doi:10.1016/0092-8674(92)90154-5 · Cited by 2,754 · see citing works

Pax7 Is Required for the Specification of Myogenic Satellite Cells

Seale, P., Sabourin, L. A., Girgis-Gabardo, A., Mansouri, A., Gruß, P., & Rudnicki, M. A. (2000) · Cell · doi:10.1016/s0092-8674(00)00066-0 · Cited by 2,345 · see citing works

Rejuvenation of aged progenitor cells by exposure to a young systemic environment

Conboy, I. M., Conboy, M. J., Wagers, A. J., Girma, E. R., Weissman, I. L., & Rando, T. A. (2005) · Nature · doi:10.1038/nature03260 · Cited by 2,287 · see citing works

Dystrophin expression in the mdx mouse restored by stem cell transplantation

Gussoni, E., Soneoka, Y., Strickland, C. D., Buzney, E. A., Khan, M. K., Flint, A., Kunkel, L. M., & Mulligan, R. C. (1999) · Nature · doi:10.1038/43919 · Cited by 1,800 · see citing works

Muscle injury activates resident fibro/adipogenic progenitors that facilitate myogenesis

Joe, A. W. B., Yi, L., Natarajan, A., Le Grand, F., So, L., Wang, J., Rudnicki, M. A., & Rossi, F. M. V. (2010) · Nature Cell Biology · doi:10.1038/ncb2015 · Cited by 1,690 · see citing works

Myotonic Dystrophy Mutation: an Unstable CTG Repeat in the 3′ Untranslated region of the Gene

Mahadevan, M. S., Tsilfidis, C., Sabourin, L. A., Shutler, G., Amemiya, C. T., Jansen, G., Neville, C., Narang, M. A., Barceló, J. M., O'Hoy, K., et al. (1992) · Science · doi:10.1126/science.1546325 · Cited by 1,656 · see citing works

Interaction of Nitric Oxide Synthase with the Postsynaptic Density Protein PSD-95 and α1-Syntrophin Mediated by PDZ Domains

Brenman, J. E., Chao, D. S., Gee, S., McGee, A. W., Craven, S. E., Santillano, D. R., Wu, Z., Huang, F., Xia, H., Peters, M. F., et al. (1996) · Cell · doi:10.1016/s0092-8674(00)81053-3 · Cited by 1,596 · see citing works

Bee and Wasp Venoms

Habermann, E. (1972) · Science · doi:10.1126/science.177.4046.314 · Cited by 1,570 · see citing works

Increased Wnt signaling during aging alters muscle stem cell fate and increases fibrosis

Brack, A. S., Conboy, M. J., Roy, S., Lee, M., Kuo, C. J., Keller, C., & Rando, T. A. (2007) · Science · doi:10.1126/science.1144090 · Cited by 1,564 · see citing works

A deletion in the bovine myostatin gene causes the double–muscled phenotype in cattle

Grobet, L., Royo Martin, L. J., Poncelet, D., Pirottin, D., Brouwers, B., Riquet, J., Schoeberlein, A., Dunner, S., Ménissier, F., Massabanda, J., et al. (1997) · Nature Genetics · doi:10.1038/ng0997-71 · Cited by 1,556 · see citing works

An Unstable Triplet Repeat in a Gene Related to Myotonic Muscular Dystrophy

Fu, Y., Pizzuti, A., Fenwick, R. G., King, J., Rajnarayan, S., Dunne, P. W., Dubel, J., Nasser, G. A., Ashizawa, T., de Jong, P., et al. (1992) · Science · doi:10.1126/science.1546326 · Cited by 1,453 · see citing works

Annexins: linking Ca2+ signalling to membrane dynamics

Gerke, V., Creutz, C. E., & Moss, S. E. (2005) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1661 · Cited by 1,412 · see citing works

Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix

Ibraghimov‐Beskrovnaya, O., Ervasti, J. M., Leveille, C. J., Slaughter, C. A., Sernett, S. W., & Campbell, K. P. (1992) · Nature · doi:10.1038/355696a0 · Cited by 1,411 · see citing works

Myostatin Mutation Associated with Gross Muscle Hypertrophy in a Child

Schuelke, M., Wagner, K. R., Stolz, L. E., Hübner, C., Riebel, T., Kömen, W., Braun, T., Tobin, J. F., & Lee, S.-J. (2004) · New England Journal of Medicine · doi:10.1056/nejmoa040933 · Cited by 1,399 · see citing works

Inflammatory processes in muscle injury and repair.

Tidball, J. (2005) · American Journal of Physiology. Regulatory Integrative and Comparative Physiology · doi:10.1152/ajpregu.00454.2004 · Cited by 1,392 · see citing works

A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin

Ervasti, J. M., & Campbell, K. P. (1993) · The Journal of Cell Biology · doi:10.1083/jcb.122.4.809 · Cited by 1,388 · see citing works

Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy

Bonne, G., di Barletta, M. R., Varnous, S., Bécane, H. M., Hammouda, E.-H., Merlini, L., Francesco Muntoni, A., Greenberg, C. R., Gary, F., Urtizberea, J. A., et al. (1999) · Nature Genetics · doi:10.1038/6799 · Cited by 1,353 · see citing works

Membrane organization of the dystrophin-glycoprotein complex

Ervasti, J. M., & Campbell, K. P. (1991) · Cell · doi:10.1016/0092-8674(91)90035-w · Cited by 1,332 · see citing works

Mesenchymal progenitors distinct from satellite cells contribute to ectopic fat cell formation in skeletal muscle

Uezumi, A., Fukada, S., Yamamoto, N., Takeda, S., & Tsuchida, K. (2010) · Nature Cell Biology · doi:10.1038/ncb2014 · Cited by 1,315 · see citing works

Macrophage Polarization Comes of Age

Mantovani, Sica, & Locati, M. (2005) · Immunity · doi:10.1016/j.immuni.2005.10.001 · Cited by 1,259 · cited 1× · see citing works

Myotonic Dystrophy Type 2 Caused by a CCTG Expansion in Intron 1 of ZNF9

Liquori, C. L., Ricker, K., Moseley, M. L., Jacobsen, J. F., Kreß, W., Naylor, S. L., Day, J., & Ranum, L. P. W. (2001) · Science · doi:10.1126/science.1062125 · Cited by 1,230 · see citing works

PTC124 targets genetic disorders caused by nonsense mutations

Welch, E. M., Barton, E. R., Zhuo, J., Tomizawa, Y., Friesen, W. J., Trifillis, P., Paushkin, S. V., Patel, M., Trotta, C. R., Hwang, S., et al. (2007) · Nature · doi:10.1038/nature05756 · Cited by 1,138 · see citing works

Notch-Mediated Restoration of Regenerative Potential to Aged Muscle

Conboy, I. M., Conboy, M. J., Smythe, G. M., & Rando, T. A. (2003) · Science · doi:10.1126/science.1087573 · Cited by 1,121 · see citing works

Defective membrane repair in dysferlin-deficient muscular dystrophy

Bansal, D., Miyake, K., Vogel, S. S., Groh, S., Chen, C.-C., Williamson, R., McNeil, P. L., & Campbell, K. P. (2003) · Nature · doi:10.1038/nature01573 · Cited by 1,022 · see citing works

Pericytes of human skeletal muscle are myogenic precursors distinct from satellite cells

Dellavalle, A., Sampaolesi, M., Tonlorenzi, R., Tagliafico, E., Sacchetti, B., Perani, L., Innocenzi, A., Gálvez, B. G., Messina, G., Roberta Morosetti, A., et al. (2007) · Nature Cell Biology · doi:10.1038/ncb1542 · Cited by 1,001 · see citing works

Polymyositis, Dermatomyositis, and Inclusion-Body Myositis

Dalakas, M. C. (1991) · New England Journal of Medicine · doi:10.1056/nejm199111213252107 · Cited by 944 · see citing works

Recruitment of human muscleblind proteins to (CUG)n expansions associated with myotonic dystrophy

Miller, J. W., Urbinati, C. R., Teng‐umnuay, P., Stenberg, M. G., Byrne, B. J., Thornton, C. A., & Swanson, M. S. (2000) · The EMBO Journal · doi:10.1093/emboj/19.17.4439 · Cited by 937 · see citing works

Muscle satellite cells adopt divergent fates

Zammit, P. S., Golding, J. P., Nagata, Y., Hudon, V., Partridge, T. A., & Beauchamp, J. R. (2004) · The Journal of Cell Biology · doi:10.1083/jcb.200312007 · Cited by 924 · see citing works

Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy

Liu, J., Aoki, M., Illa, I., Wu, C., Fardeau, M., Angelini, C. I., Serrano, C., Urtizberea, J. A., Hentati, F., Hamida, M. B., et al. (1998) · Nature Genetics · doi:10.1038/1682 · Cited by 919 · see citing works

Expression of Cd34 and Myf5 Defines the Majority of Quiescent Adult Skeletal Muscle Satellite Cells

Beauchamp, J. R., Heslop, L., Yu, D. S., Tajbakhsh, S., Kelly, R. G., Wernig, A., BUCKINGHAM, M. E., Partridge, T. A., & Zammit, P. S. (2000) · The Journal of Cell Biology · doi:10.1083/jcb.151.6.1221 · Cited by 917 · see citing works

Growth factors in the extracellular matrix

Taipale, J., & Keski‐Oja, J. (1997) · The FASEB Journal · doi:10.1096/fasebj.11.1.9034166 · Cited by 916 · see citing works

The Regulation of Notch Signaling Controls Satellite Cell Activation and Cell Fate Determination in Postnatal Myogenesis

Conboy, I. M., & Rando, T. A. (2002) · Developmental Cell · doi:10.1016/s1534-5807(02)00254-x · Cited by 905 · see citing works

Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy

Bione, S., Maestrini, E., Rivella, S., Mancini, M., Regis, S., Romeo, G., & Toniolo, D. (1994) · Nature Genetics · doi:10.1038/ng1294-323 · Cited by 886 · see citing works

Functional improvement of dystrophic muscle by myostatin blockade

Bogdanovich, S., Krag, T. O. B., Barton, E. R., Morris, L. D., Whittemore, L.-A., Ahima, R. S., & Khurana, T. S. (2002) · Nature · doi:10.1038/nature01154 · Cited by 831 · see citing works

Disruption of Splicing Regulated by a CUG-Binding Protein in Myotonic Dystrophy

Philips, A. V., Timchenko, L., & Cooper, T. A. (1998) · Science · doi:10.1126/science.280.5364.737 · Cited by 818 · see citing works

Biological Progression from Adult Bone Marrow to Mononucleate Muscle Stem Cell to Multinucleate Muscle Fiber in Response to Injury

LaBarge, M. A., & Blau, H. M. (2002) · Cell · doi:10.1016/s0092-8674(02)01078-4 · Cited by 798 · see citing works

Aberrant regulation of insulin receptor alternative splicing is associated with insulin resistance in myotonic dystrophy

Savkur, R. S., Philips, A. V., & Cooper, T. A. (2001) · Nature Genetics · doi:10.1038/ng704 · Cited by 795 · see citing works

A Unifying Genetic Model for Facioscapulohumeral Muscular Dystrophy

Lemmers, R. J. L. F., van der Vliet, P. J., Klooster, R., Sacconi, S., Camaño, P., Dauwerse, J. G., Snider, L. D., Straasheijm, K. R., van Ommen, G. J., Padberg, G. W., et al. (2010) · Science · doi:10.1126/science.1189044 · Cited by 789 · see citing works

Myostatin negatively regulates satellite cell activation and self-renewal

McCroskery, S., Thomas, M., Maxwell, L., Sharma, M., & Kambadur, R. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200207056 · Cited by 784 · see citing works

Local Dystrophin Restoration with Antisense Oligonucleotide PRO051

van Deutekom, J. C., Janson, A. A. M., Ginjaar, I. B., Frankhuizen, W. S., Aartsma-Rus, A. M., Bremmer-Bout, M., den Dunnen, J. T., Koop, K., van der Kooi, A. J., Goemans, N., et al. (2007) · New England Journal of Medicine · doi:10.1056/nejmoa073108 · Cited by 780 · see citing works

Post-translational disruption of dystroglycan–ligand interactions in congenital muscular dystrophies

Michele, D. E., Barresi, R., Kanagawa, M., Saito, F., Cohn, R. D., Satz, J. S., Dollar, J., Nishino, I., Kelley, R. I., Somer, H., et al. (2002) · Nature · doi:10.1038/nature00837 · Cited by 779 · see citing works

Mesoangioblast stem cells ameliorate muscle function in dystrophic dogs

Sampaolesi, M., Blot, S., D’Antona, G., Granger, N. P., Tonlorenzi, R., Innocenzi, A., Mognol, P., Thibaud, J. L., Gálvez, B. G., Barthélémy, I., et al. (2006) · Nature · doi:10.1038/nature05282 · Cited by 768 · see citing works

Polymyositis, Dermatomyositis, and Inclusion Body Myositis

Holton, J., Wedderburn, L. R., & Hanna, M. G. (2013) · UCL Discovery (University College London) · Cited by 764 · see citing works

A Muscleblind Knockout Model for Myotonic Dystrophy

Kanadia, R. N., Johnstone, K. A., Mankodi, A., Lungu, C., Thornton, C. A., Esson, D., Timmers, A. M., Hauswirth, W. W., & Swanson, M. S. (2003) · Science · doi:10.1126/science.1088583 · Cited by 743 · see citing works

Entries in the Leiden Duchenne muscular dystrophy mutation database: An overview of mutation types and paradoxical cases that confirm the reading‐frame rule

Aartsma-Rus, A. M., van Deutekom, J. C. T., Fokkema, I. F. A. C., van Ommen, G. B., & den Dunnen, J. T. (2006) · Muscle & Nerve · doi:10.1002/mus.20586 · Cited by 742 · see citing works

Molecular Cloning of Caveolin-3, a Novel Member of the Caveolin Gene Family Expressed Predominantly in Muscle

Tang, Z., Scherer, P. E., Okamoto, T., Song, K. S., Chu, C., Kohtz, D. S., Nishimoto, I., Lodish, H. F., & Lisanti, M. P. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.4.2255 · Cited by 738 · see citing works

Myotonic Dystrophy in Transgenic Mice Expressing an Expanded CUG Repeat

Mankodi, A. K., Logigian, E. L., Callahan, L. M., McClain, C., White, R. J., Henderson, D., Krym, M., & Thornton, C. A. (2000) · Science · doi:10.1126/science.289.5485.1769 · Cited by 738 · see citing works

Association of dystrophin and an integral membrane glycoprotein

Campbell, K. P., & Kahl, S. D. (1989) · Nature · doi:10.1038/338259a0 · Cited by 732 · see citing works

Muscle Satellite Cells and Endothelial Cells: Close Neighbors and Privileged Partners

Christov, C., Chrétien, F. C., Abou-Khalil, R., Bassez, G., Vallet, G., Authier, F., Bassaglia, Y., Shinin, V., Tajbakhsh, S., Chazaud, B., et al. (2007) · Molecular Biology of the Cell · doi:10.1091/mbc.e06-08-0693 · Cited by 702 · see citing works

Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy

Wijmenga, C., Hewitt, J., Sandkuijl, L. A., Clark, L. N., Wright, T. J., Dauwerse, H. G., Gruter, A.-M., Hofker, M. H., Moerer, P., Williamson, R., et al. (1992) · Nature Genetics · doi:10.1038/ng0992-26 · Cited by 689 · see citing works

A Temporal Switch from Notch to Wnt Signaling in Muscle Stem Cells Is Necessary for Normal Adult Myogenesis

Brack, A. S., Conboy, I. M., Conboy, M. J., Shen, J., & Rando, T. A. (2008) · Cell Stem Cell · doi:10.1016/j.stem.2007.10.006 · Cited by 682 · see citing works

Local restoration of dystrophin expression with the morpholino oligomer AVI-4658 in Duchenne muscular dystrophy: a single-blind, placebo-controlled, dose-escalation, proof-of-concept study

Kinali, M., Arechavala‐Gomeza, V., Feng, L., Çırak, S., Hunt, D. M., Adkin, C. F., Guglieri, M., Ashton, E., Abbs, S. J., Nihoyannopoulos, P., et al. (2009) · The Lancet Neurology · doi:10.1016/s1474-4422(09)70211-x · Cited by 653 · see citing works

Cell Therapy of α-Sarcoglycan Null Dystrophic Mice Through Intra-Arterial Delivery of Mesoangioblasts

Sampaolesi, M., Torrente, Y., Innocenzi, A., Tonlorenzi, R., D’Antona, G., Pellegrino, M. A., Barresi, R., Bresolin, N., Angelis, M. G. C. D., Campbell, K. P., et al. (2003) · Science · doi:10.1126/science.1082254 · Cited by 639 · see citing works

Monoclonal antibody analysis of mononuclear cells in myopathies. I: Quantitation of subsets according to diagnosis and sites of accumulation and demonstration and counts of muscle fibers invaded by T cells

Arahata, K., & Engel, A. G. (1984) · Annals of Neurology · doi:10.1002/ana.410160206 · Cited by 631 · see citing works

Interferon‐α/β–mediated innate immune mechanisms in dermatomyositis

Greenberg, S. A., Pinkus, J. L., Pinkus, G. S., Burleson, T., Sanoudou, D., Tawil, R., Barohn, R. J., Saperstein, D., Briemberg, H., Ericsson, M., et al. (2005) · Annals of Neurology · doi:10.1002/ana.20464 · Cited by 623 · see citing works

Loss of the Muscle-Specific Chloride Channel in Type 1 Myotonic Dystrophy Due to Misregulated Alternative Splicing

Charlet‐Berguerand, N., Savkur, R. S., Singh, G., Philips, A. V., Grice, E. A., & Cooper, T. A. (2002) · Molecular Cell · doi:10.1016/s1097-2765(02)00572-5 · Cited by 619 · see citing works

Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B)

Muchir, A. (2000) · Human Molecular Genetics · doi:10.1093/hmg/9.9.1453 · Cited by 615 · see citing works

Foci of trinucleotide repeat transcripts in nuclei of myotonic dystrophy cells and tissues.

Taneja, K. L., McCurrach, M. E., Schalling, M., Housman, D. E., & Singer, R. H. (1995) · The Journal of Cell Biology · doi:10.1083/jcb.128.6.995 · Cited by 599 · see citing works

Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy

Minetti, C., Sotgia, F., Bruno, C., Scartezzini, P., Broda, P., Bado, M., Masetti, E., Mazzocco, M., Egeo, A., Donati, M. A., et al. (1998) · Nature Genetics · doi:10.1038/ng0498-365 · Cited by 597 · see citing works

Aminoglycoside antibiotics restore dystrophin function to skeletal muscles of mdx mice

Barton-Davis, E. R., Cordier, L., Shoturma, D. I., Leland, S. E., & Sweeney, H. L. (1999) · Journal of Clinical Investigation · doi:10.1172/jci7866 · Cited by 579 · see citing works

Glucocorticoid corticosteroids for Duchenne muscular dystrophy

Manzur, A. Y., Küntzer, T., Pike, M. G., & Swan, A. V. (2004) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd003725.pub2 · Cited by 539 · see citing works

Nesprin-1 and -2 are involved in the pathogenesis of Emery–Dreifuss muscular dystrophy and are critical for nuclear envelope integrity

Zhang, Q., Bethmann, C., Worth, N. F., Davies, J. D., Wasner, C., Feuer, A., Ragnauth, C. D., Yi, Q., Mellad, J. A., Warren, D. T., et al. (2007) · Human Molecular Genetics · doi:10.1093/hmg/ddm238 · Cited by 539 · see citing works

Microvascular Deposition of Complement Membrane Attack Complex in Dermatomyositis

Kissel, J. T., Mendell, J. R., & Rammohan, K. W. (1986) · New England Journal of Medicine · doi:10.1056/nejm198602063140601 · Cited by 527 · see citing works

Inflammatory cell response to acute muscle injury

Tidball, J. G. (1995) · Medicine & Science in Sports & Exercise · doi:10.1249/00005768-199507000-00011 · Cited by 522 · see citing works

Short Telomeres and Stem Cell Exhaustion Model Duchenne Muscular Dystrophy in mdx/mTR Mice

Sacco, A., Mourkioti, F., Tran, R., Choi, J., Llewellyn, M., Kraft, P., Shkreli, M., Delp, S., Pomerantz, J. H., Artandi, S. E., et al. (2010) · Cell · doi:10.1016/j.cell.2010.11.039 · Cited by 512 · see citing works

A Subpopulation of Adult Skeletal Muscle Stem Cells Retains All Template DNA Strands after Cell Division

Rocheteau, P., Gayraud-Morel, B., Siegl-Cachedenier, I., Blasco, M. A., & Tajbakhsh, S. (2012) · Cell · doi:10.1016/j.cell.2011.11.049 · Cited by 510 · see citing works

Asymmetric division and cosegregation of template DNA strands in adult muscle satellite cells

Shinin, V., Gayraud-Morel, B., Gomès, D., & Tajbakhsh, S. (2006) · Nature Cell Biology · doi:10.1038/ncb1425 · Cited by 504 · see citing works

SUN1 Interacts with Nuclear Lamin A and Cytoplasmic Nesprins To Provide a Physical Connection between the Nuclear Lamina and the Cytoskeleton

Haque, F., Lloyd, D. J., Smallwood, D. T., Dent, C. L., Shanahan, C. M., Fry, A. M., Trembath, R. C., & Shackleton, S. (2006) · Molecular and Cellular Biology · doi:10.1128/mcb.26.10.3738-3751.2006 · Cited by 504 · see citing works

Cyclic nucleotide phosphodiesterases

Essayan, D. M. (2001) · Journal of Allergy and Clinical Immunology · doi:10.1067/mai.2001.119555 · Cited by 503 · see citing works

Systemic delivery of morpholino oligonucleotide restores dystrophin expression bodywide and improves dystrophic pathology

Alter, J., Lou, F., Rabinowitz, A. H., Yin, H., Rosenfeld, J., Wilton, S. D., Partridge, T. A., & Lu, Q. L. (2006) · Nature Medicine · doi:10.1038/nm1345 · Cited by 494 · see citing works

Isolation of Adult Mouse Myogenic Progenitors

Sherwood, R. I., Christensen, J. L., Conboy, I. M., Conboy, M. J., Rando, T. A., Weissman, I. L., & Wagers, A. J. (2004) · Cell · doi:10.1016/j.cell.2004.10.021 · Cited by 491 · see citing works

Imbalance between pSmad3 and Notch induces CDK inhibitors in old muscle stem cells

Carlson, M. E., Hsu, M., & Conboy, I. M. (2008) · Nature · doi:10.1038/nature07034 · Cited by 483 · see citing works

Pericytes resident in postnatal skeletal muscle differentiate into muscle fibres and generate satellite cells

Dellavalle, A., Maroli, G., Covarello, D., Azzoni, E., Innocenzi, A., Perani, L., Antonini, S., Sambasivan, R., Brunelli, S., Tajbakhsh, S., et al. (2011) · Nature Communications · doi:10.1038/ncomms1508 · Cited by 474 · see citing works

Highly Efficient, Functional Engraftment of Skeletal Muscle Stem Cells in Dystrophic Muscles

Cerletti, M., Jurga, S., Witczak, C. A., Hirshman, M. F., Shadrach, J. L., Goodyear, L. J., & Wagers, A. J. (2008) · Cell · doi:10.1016/j.cell.2008.05.049 · Cited by 472 · see citing works

MG53 nucleates assembly of cell membrane repair machinery

Cai, C., Masumiya, H., Weisleder, N. L., Matsuda, N., Nishi, M., Hwang, M., Ko, J., Lin, P., Thornton, A., Zhao, X., et al. (2008) · Nature Cell Biology · doi:10.1038/ncb1812 · Cited by 472 · see citing works

The Basement Membrane/Basal Lamina of Skeletal Muscle

Sanes, J. R. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.r200027200 · Cited by 471 · see citing works

Expansion of a CUG trinucleotide repeat in the 3′ untranslated region of myotonic dystrophy protein kinase transcripts results in nuclear retention of transcripts

Davis, B. M., McCurrach, M. E., Taneja, K. L., Singer, R. H., & Housman, D. E. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.14.7388 · Cited by 468 · see citing works

Stem cells in postnatal myogenesis: molecular mechanisms of satellite cell quiescence, activation and replenishment

Dhawan, J., & Rando, T. A. (2005) · Trends in Cell Biology · doi:10.1016/j.tcb.2005.10.007 · Cited by 466 · see citing works

Identification of a (CUG)n Triplet Repeat RNA-Binding Protein and Its Expression in Myotonic Dystrophy

Timchenko, L., Miller, J. W., Timchenko, N. A., DeVore, D. R., Datar, K. V., Lin, L., Roberts, R., Caskey, C. T., & Swanson, M. S. (1996) · Nucleic Acids Research · doi:10.1093/nar/24.22.4407 · Cited by 465 · see citing works

Identification of inducible brown adipocyte progenitors residing in skeletal muscle and white fat

Schulz, T. J., Huang, T. L., Tran, T. T., Zhang, H., Townsend, K. L., Shadrach, J. L., Cerletti, M., McDougall, L. E., Giorgadze, N., Tchkonia, T., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1010929108 · Cited by 459 · see citing works

DUX4 Activates Germline Genes, Retroelements, and Immune Mediators: Implications for Facioscapulohumeral Dystrophy

Geng, L. N., Yao, Z., Snider, L. D., Fong, A. P., Cech, J. N., Young, J. M., van der Maarel, S. M., Ruzzo, W. L., Gentleman, R. C., Tawil, R., et al. (2011) · Developmental Cell · doi:10.1016/j.devcel.2011.11.013 · Cited by 459 · see citing works

Functional muscle ischemia in neuronal nitric oxide synthase-deficient skeletal muscle of children with Duchenne muscular dystrophy

Sander, M., Chavoshan, B., Harris, S. A., Iannaccone, S. T., Stull, J. T., Thomas, G. D., & Victor, R. G. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.250379497 · Cited by 446 · see citing works

Increased Steady-State Levels of CUGBP1 in Myotonic Dystrophy 1 Are Due to PKC-Mediated Hyperphosphorylation

Kuyumcu-Martinez, N. M., Wang, G., & Cooper, T. A. (2007) · Molecular Cell · doi:10.1016/j.molcel.2007.07.027 · Cited by 445 · see citing works

A vinculin-containing cortical lattice in skeletal muscle: transverse lattice elements ("costameres") mark sites of attachment between myofibrils and sarcolemma.

Pardo, J. V., Siliciano, J. D., & Craig, S. W. (1983) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.80.4.1008 · Cited by 443 · see citing works

Skeletal muscle degeneration induced by venom phospholipases A2: insights into the mechanisms of local and systemic myotoxicity

Gutiérrez, J. M., & Ownby, C. L. (2003) · Toxicon · doi:10.1016/j.toxicon.2003.11.005 · Cited by 443 · see citing works

Facioscapulohumeral muscular dystrophy

Tawil, R., & Van Der Maarel, S. M. (2006) · Muscle & Nerve · doi:10.1002/mus.20522 · Cited by 441 · see citing works

Glucocorticoid corticosteroids for Duchenne muscular dystrophy

Manzur, A. Y., Küntzer, T., Pike, M., & Swan, A. V. (2008) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd003725.pub3 · Cited by 434 · see citing works

Disruptions of muscle fiber plasma membranes. Role in exercise-induced damage.

McNeil, P. L., & Khakee, R. (1992) · PubMed Central · Cited by 427 · see citing works

Acute phase response in exercise. III. Neutrophil and IL-1 beta accumulation in skeletal muscle

Fielding, R. A., Manfredi, T., Ding, W., FIATARONE, M. A., Evans, W. J., & Cannon, J. G. (1993) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1993.265.1.r166 · Cited by 415 · see citing works

Hydrogen peroxide stimulates the synthesis of platelet-activating factor by endothelium and induces endothelial cell-dependent neutrophil adhesion.

Lewis, M. S., Whatley, R. E., Cain, P., McIntyre, T. M., Prescott, S. M., & Zimmerman, G. A. (1988) · Journal of Clinical Investigation · doi:10.1172/jci113825 · Cited by 415 · see citing works

Different Mutations in the LMNA Gene Cause Autosomal Dominant and Autosomal Recessive Emery-Dreifuss Muscular Dystrophy

di Barletta, M. R., Ricci, E., Galluzzi, G., Tonali, P. A., Mora, M., Morandi, L. O., Romorini, A., Voït, T., Ørstavik, K. H., Merlini, L., et al. (2000) · The American Journal of Human Genetics · doi:10.1086/302869 · Cited by 415 · see citing works

Dysferlin Interacts with Annexins A1 and A2 and Mediates Sarcolemmal Wound-healing

Lennon, N. J., Kho, A. T., Bacskai, B. J., Perlmutter, S. L., Hyman, B. T., & Brown, R. H. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m307247200 · Cited by 407 · see citing works

Aminoglycoside antibiotics mediate context-dependent suppression of termination codons in a mammalian translation system

Manuvakhova, M., Keeling, K. M., & Bedwell, D. M. (2000) · RNA · doi:10.1017/s1355838200000716 · Cited by 404 · see citing works

Detailed analysis of the repeat domain of dystrophin reveals four potential hinge segments that may confer flexibility.

Koenig, M., & Kunkel, L. M. (1990) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)39599-7 · Cited by 403 · see citing works

Systemic delivery of antisense oligoribonucleotide restores dystrophin expression in body-wide skeletal muscles

Lu, Q. L., Rabinowitz, A. H., Chen, Y. C., Yokota, T., Yin, H., Alter, J., Jadoon, A., Bou–Gharios, G., & Partridge, T. A. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0406700102 · Cited by 402 · see citing works

Syndecan-3 and Syndecan-4 Specifically Mark Skeletal Muscle Satellite Cells and Are Implicated in Satellite Cell Maintenance and Muscle Regeneration

Cornelison, D., Filla, M. S., Stanley, H. M., Rapraeger, A. C., & Olwin, B. B. (2001) · Developmental Biology · doi:10.1006/dbio.2001.0416 · Cited by 399 · see citing works

Functional amounts of dystrophin produced by skipping the mutated exon in the mdx dystrophic mouse

Lu, Q. L., Mann, C. J., Lou, F., Bou–Gharios, G., Morris, G. E., Xue, S., Fletcher, S., Partridge, T. A., & Wilton, S. D. (2003) · Nature Medicine · doi:10.1038/nm897 · Cited by 398 · see citing works

Primary structure of dystrophin-related protein

Tinsley, J. M., Blake, D. J., Roche, A., Fairbrother, U. L., Riss, J., Byth, B. C., Knight, A. E., Kendrick‐Jones, J., Suthers, G. K., Love, D. R., et al. (1992) · Nature · doi:10.1038/360591a0 · Cited by 392 · see citing works

Reversal of RNA Dominance by Displacement of Protein Sequestered on Triplet Repeat RNA

Wheeler, T. M., Sobczak, K., Lueck, J. D., Osborne, R. J., Lin, X., Dirksen, R. T., & Thornton, C. A. (2009) · Science · doi:10.1126/science.1173110 · Cited by 387 · see citing works

The Emery-Dreifuss muscular dystrophy protein, emerin, is a nuclear membrane protein

Manilal, S. (1996) · Human Molecular Genetics · doi:10.1093/hmg/5.6.801 · Cited by 380 · see citing works

Reversal of RNA missplicing and myotonia after muscleblind overexpression in a mouse poly(CUG) model for myotonic dystrophy

Kanadia, R., Shin, J., Yuan, Y., Beattie, S. G., Wheeler, T. M., Thornton, C. A., & Swanson, M. S. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0604970103 · Cited by 372 · see citing works

Functional skeletal muscle regeneration from differentiating embryonic stem cells

Darabi, R., Gehlbach, K., Bachoo, R. M., Kamath, S., Osawa, M., Kamm, K. E., Kyba, M., & Perlingeiro, R. C. R. (2008) · Nature Medicine · doi:10.1038/nm1705 · Cited by 358 · see citing works

Mice lacking the myotonic dystrophy protein kinase develop a late onset progressive myopathy

Reddy, S., Smith, D. B. J., Rich, M. M., Leferovich, J. M., Reilly, P., Davis, B. M., Tran, K., Rayburn, H., Bronson, R. T., Cros, D. P., et al. (1996) · Nature Genetics · doi:10.1038/ng0796-325 · Cited by 352 · see citing works

Major histocompatibility complex class I antigen expression, immunolocalization of interferon subtypes, and T cell-mediated cytotoxicity in myopathies

Emslie‐Smith, A. M., Arahata, K., & Engel, A. G. (1989) · Human Pathology · doi:10.1016/0046-8177(89)90128-7 · Cited by 349 · see citing works

Mechanisms of Muscle Degeneration, Regeneration, and Repair in the Muscular Dystrophies

Wallace, G. Q., & McNally, E. M. (2008) · Annual Review of Physiology · doi:10.1146/annurev.physiol.010908.163216 · Cited by 343 · see citing works

Misregulated alternative splicing of BIN1 is associated with T tubule alterations and muscle weakness in myotonic dystrophy

Fugier, C., Klein, A. F., Hammer, C., Vassilopoulos, S., Ivarsson, Y., Toussaint, A., Tosch, V., Vignaud, A., Ferry, A., Messaddeq, N., et al. (2011) · Nature Medicine · doi:10.1038/nm.2374 · Cited by 335 · see citing works

Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin

Moreira, E. S., Wiltshire, T., Faulkner, G., Nilforoushan, A., Vainzof, M., Suzuki, O., Valle, G., Reeves, R. H., Zatz, M., Passos‐Bueno, M. R., et al. (2000) · Nature Genetics · doi:10.1038/72822 · Cited by 335 · see citing works

Aberrant alternative splicing and extracellular matrix gene expression in mouse models of myotonic dystrophy

Du, H., Cline, M. S., Osborne, R. J., Tuttle, D. L., Clark, T. A., Donohue, J. P., Hall, M. P., Shiue, L., Swanson, M. S., Thornton, C. A., et al. (2010) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.1720 · Cited by 332 · see citing works

Muscle assembly: a titanic achievement?

Gregorio, C. C., Granzier, H., Sorimachi, H., & Labeit, S. (1999) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(99)80003-9 · Cited by 327 · see citing works

Early events in stretch-induced muscle damage

Morgan, D. L., & Allen, D. G. (1999) · Journal of Applied Physiology · doi:10.1152/jappl.1999.87.6.2007 · Cited by 315 · see citing works

De novo LMNA mutations cause a new form of congenital muscular dystrophy

Quijano-Roy, S., Mbieleu, B., Bönnemann, C. G., Jeannet, P., Colomer, J., Clarke, N. F., Cuisset, J., Roper, H., Meırleır, L. D., D’Amico, A., et al. (2008) · Annals of Neurology · doi:10.1002/ana.21417 · Cited by 298 · see citing works

Location of facioscapulohumeral muscular dystrophy gene on chromosome 4

Wijmenga, C., Brouwer, O. F., Moerer, P., Padberg, G. W., Wijmenga, C., Frants, R. R., Moerer, P., & Weber, J. L. (1990) · The Lancet · doi:10.1016/0140-6736(90)92148-b · Cited by 295 · see citing works

Myotilin is mutated in limb girdle muscular dystrophy 1A

Hauser, M. A. (2000) · Human Molecular Genetics · doi:10.1093/hmg/9.14.2141 · Cited by 291 · see citing works

High Incidence of Non-Random Template Strand Segregation and Asymmetric Fate Determination In Dividing Stem Cells and their Progeny

Conboy, M. J., Karasov, A. O., & Rando, T. A. (2007) · PLoS Biology · doi:10.1371/journal.pbio.0050102 · Cited by 287 · cited 1× · see citing works

Recessive Mutations in the Putative Calcium-Activated Chloride Channel Anoctamin 5 Cause Proximal LGMD2L and Distal MMD3 Muscular Dystrophies

Bolduc, V., Marlow, G., Boycott, K. M., Saleki, K., Inoue, H., Kroon, J., Itakura, M., Robitaille, Y., Parent, L., Baas, F., et al. (2010) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2009.12.013 · Cited by 286 · see citing works

Calcium-regulated exocytosis is required for cell membrane resealing.

Bi, G., Alderton, J. M., & Steinhardt, R. A. (1995) · The Journal of Cell Biology · doi:10.1083/jcb.131.6.1747 · Cited by 285 · see citing works

The primary localization of free radical generation after anoxia/reoxygenation in isolated endothelial cells.

Ratych, R. E., Chuknyiska, R. S., & Bulkley, G. B. (1987) · PubMed · Cited by 283 · see citing works

An adult tissue-specific stem cell in its niche: A gene profiling analysis of in vivo quiescent and activated muscle satellite cells

Pallafacchina, G., François, S., Regnault, B., Czarny, B., Dive, V., Cumano, A., Montarras, D., & BUCKINGHAM, M. E. (2009) · Stem Cell Research · doi:10.1016/j.scr.2009.10.003 · Cited by 278 · see citing works

Dysferlin and muscle membrane repair

Han, R., & Campbell, K. P. (2007) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2007.07.001 · Cited by 275 · see citing works

Pentamidine reverses the splicing defects associated with myotonic dystrophy

Warf, M. B., Nakamori, M., Matthys, C. M., Thornton, C. A., & Berglund, J. A. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0903234106 · Cited by 265 · see citing works

Complete Genetic Correction of iPS Cells From Duchenne Muscular Dystrophy

Kazuki, Y., Hiratsuka, M., Takiguchi, M., Osaki, M., Kajitani, N., Hoshiya, H., Hiramatsu, K., Yoshino, T., Kazuki, K., Ishihara, C., et al. (2009) · Molecular Therapy · doi:10.1038/mt.2009.274 · Cited by 263 · see citing works

Ischemia reperfusion injury: A review

Kerrigan, C. L., & Stotland, M. A. (1993) · Microsurgery · doi:10.1002/micr.1920140307 · Cited by 262 · see citing works

A cDNA clone from the Duchenne/Becker muscular dystrophy gene

Burghes, A. H. M., Logan, C., Hu, X., Belfall, B., Worton, R. G., & Ray, P. N. (1987) · Nature · doi:10.1038/328434a0 · Cited by 260 · see citing works

Triplet-repeat oligonucleotide-mediated reversal of RNA toxicity in myotonic dystrophy

Mulders, S. A. M., van den Broek, W. J. A. A., Wheeler, T. M., Croes, H. J. E., van Kuik‐Romeijn, P., de Kimpe, S. J., Furling, D., Platenburg, G. J., Gourdon, G., Thornton, C. A., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0905780106 · Cited by 257 · see citing works

Correction of ClC-1 splicing eliminates chloride channelopathy and myotonia in mouse models of myotonic dystrophy

Wheeler, T. M., Lueck, J. D., Swanson, M. S., Dirksen, R. T., & Thornton, C. A. (2007) · Journal of Clinical Investigation · doi:10.1172/jci33355 · Cited by 256 · see citing works

The sarcolemmal proteins dysferlin and caveolin-3 interact in skeletal muscle

Matsuda, C. (2001) · Human Molecular Genetics · doi:10.1093/hmg/10.17.1761 · Cited by 254 · see citing works

Differential expression of perforin in muscle-infiltrating T cells in polymyositis and dermatomyositis.

Goebels, N., Michaelis, D., Engelhardt, M., Huber, S., Bender, A., Pongratz, D. E., Johnson, M. A., Wekerle, H., Tschopp, J., Jenne, D. E., et al. (1996) · Journal of Clinical Investigation · doi:10.1172/jci118749 · Cited by 252 · see citing works

Mesoangioblasts — vascular progenitors for extravascular mesodermal tissues

Cossu, G., & Bianco, P. (2003) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2003.08.001 · Cited by 246 · see citing works

What does chronic electrical stimulation teach us about muscle plasticity?

Pette, D., & Vrbov�, G. (1999) · Muscle & Nerve · doi:10.1002/(sici)1097-4598(199906)22:6 · Cited by 246 · see citing works

The impact of sarcopenia and exercise training on skeletal muscle satellite cells

Snijders, T., Verdijk, L. B., & van Loon, L. J. C. (2009) · Ageing Research Reviews · doi:10.1016/j.arr.2009.05.003 · Cited by 245 · see citing works

The Muscleblind family of proteins: an emerging class of regulators of developmentally programmed alternative splicing

Pascual, M., Vicente-Crespo, M., Monferrer, L., & Artero, R. D. (2006) · Differentiation · doi:10.1111/j.1432-0436.2006.00060.x · Cited by 243 · see citing works

Transgenic mice expressing CUG-BP1 reproduce splicing mis-regulation observed in myotonic dystrophy

Ho, T. H., Bundman, D. S., Armstrong, D. L., & Cooper, T. A. (2005) · Human Molecular Genetics · doi:10.1093/hmg/ddi162 · Cited by 242 · see citing works

Myostatin propeptide‐mediated amelioration of dystrophic pathophysiology

Bogdanovich, S., Perkins, K. J., Krag, T. O. B., Whittemore, L.-A., & Khurana, T. S. (2005) · The FASEB Journal · doi:10.1096/fj.04-2796com · Cited by 240 · see citing works

The role of free radicals in the pathophysiology of muscular dystrophy

Tidball, J. G., & Wehling‐Henricks, M. (2006) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01145.2006 · Cited by 232 · see citing works

Requirement for Annexin A1 in Plasma Membrane Repair

McNeil, A. K., Rescher, U., Gerke, V., & McNeil, P. L. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m606406200 · Cited by 232 · see citing works

Exercise-induced muscle injury: A calpain hypothesis

BELCASTRO, A. N., Shewchuk, L. D., & Raj, D. A. (1998) · Molecular and Cellular Biochemistry · doi:10.1023/a:1006816123601 · Cited by 229 · see citing works

A simple ligand that selectively targets CUG trinucleotide repeats and inhibits MBNL protein binding

Arambula, J. F., Ramisetty, S. R., Baranger, A. M., & Zimmerman, S. C. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0901824106 · Cited by 223 · see citing works

Inflammation in dysferlin myopathy: Immunohistochemical characterization of 13 patients

Gallardo, E., Rojas‐García, R., de Luna, N., Serradell, A. P., Brown, R. H., & Illa, I. (2001) · Neurology · doi:10.1212/wnl.57.11.2136 · Cited by 223 · see citing works

Specific removal of the nonsense mutation from the mdx dystrophin mRNA using antisense oligonucleotides

Wilton, S. D., Lloyd, F., Carville, K. S., Fletcher, S., Honeyman, K., Agrawal, S., & Kole, R. (1999) · Neuromuscular Disorders · doi:10.1016/s0960-8966(99)00010-3 · Cited by 214 · see citing works

Myotilin, a novel sarcomeric protein with two Ig-like domains, is encoded by a candidate gene for limb-girdle muscular dystrophy

Salmikangas, P. (1999) · Human Molecular Genetics · doi:10.1093/hmg/8.7.1329 · Cited by 211 · see citing works

Trim32 is a Ubiquitin Ligase Mutated in Limb Girdle Muscular Dystrophy Type 2H that Binds to Skeletal Muscle Myosin and Ubiquitinates Actin

Kudryashova, E., Kudryashov, D. S., Kramerova, I. A., & Spencer, M. J. (2005) · Journal of Molecular Biology · doi:10.1016/j.jmb.2005.09.068 · Cited by 207 · see citing works

Mexiletine is an effective antimyotonia treatment in myotonic dystrophy type 1

Logigian, E. L., Martens, W. B., Moxley, R. T., McDermott, M., Dilek, N., Wiegner, A. W., Pearson, A. T., Barbieri, C. A., Annis, C., Thornton, C. A., et al. (2010) · Neurology · doi:10.1212/wnl.0b013e3181dc1a3a · Cited by 203 · see citing works

Myoblast implantation in Duchenne muscular dystrophy: The San Francisco study

Miller, R. G., Sharma, K. R., Pavlath, G. K., Gussoni, E., Mynhier, M. A., Yu, P. L., Lanctot, A. M., Greco, C. M., Steinman, L., & Blau, H. M. (1997) · Muscle & Nerve · doi:10.1002/(sici)1097-4598(199704)20:4 · Cited by 202 · see citing works

Eccentric exercise‐induced morphological changes in the membrane systems involved in excitation—contraction coupling in rat skeletal muscle

Takekura, H., Fujinami, N., Nishizawa, T., Ogasawara, H., & Kasuga, N. (2001) · The Journal of Physiology · doi:10.1111/j.1469-7793.2001.0571a.x · Cited by 201 · see citing works

Long-term persistence of donor nuclei in a Duchenne muscular dystrophy patient receiving bone marrow transplantation

Gussoni, E., Bennett, R. R., Muskiewicz, K. R., Meyerrose, T. E., Nolta, J. A., Gilgoff, I. S., Stein, J. H., Chan, Y.-M. M., Lidov, H. G. W., Bönnemann, C. G., et al. (2002) · Journal of Clinical Investigation · doi:10.1172/jci16098 · Cited by 198 · see citing works

Blood borne macrophages are essential for the triggering of muscle regeneration following muscle transplant

Lescaudron, L., Peltékian, E., Fontaine-Pérus, J., Paulin, D., Zampieri, M., Garcı́a, L., & Parrish, E. (1999) · Neuromuscular Disorders · doi:10.1016/s0960-8966(98)00111-4 · Cited by 197 · see citing works

Review: An update on inflammatory and autoimmune myopathies

Dalakas, M. C. (2010) · Neuropathology and Applied Neurobiology · doi:10.1111/j.1365-2990.2010.01153.x · Cited by 195 · see citing works

Muscle hypertrophy driven by myostatin blockade does not require stem/precursor-cell activity

Amthor, H., Otto, A., Vulin, A., Rochat, A., Dumonceaux, J., Garcı́a, L., Mouisel, É., Hourdé, C., Macharia, R., Friedrichs, M., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0811129106 · Cited by 195 · see citing works

Differential requirement for individual sarcoglycans and dystrophin in the assembly and function of the dystrophin-glycoprotein complex

Hack, A. A., Lam, M.-Y., Cordier, L., Shoturma, D. I., Ly, C. T., Hadhazy, M. A., Hadhazy, M., Sweeney, H. L., & McNally, E. M. (2000) · Journal of Cell Science · doi:10.1242/jcs.113.14.2535 · Cited by 195 · see citing works

Morpholino antisense oligonucleotide induced dystrophin exon 23 skipping in mdx mouse muscle

Gebski, B. L., Mann, C. J., Fletcher, S., & Wilton, S. D. (2003) · Human Molecular Genetics · doi:10.1093/hmg/ddg196 · Cited by 194 · see citing works

Drug screening in a zebrafish model of Duchenne muscular dystrophy

Kawahara, G., Karpf, J. A., Myers, J. A., Alexander, M. S., Guyon, J. R., & Kunkel, L. M. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1102116108 · Cited by 191 · see citing works

Somatic instability of CTG repeat in myotonic dystrophy

Ashizawa, T., Dubel, J., & Harati, Y. (1993) · Neurology · doi:10.1212/wnl.43.12.2674 · Cited by 190 · see citing works

The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies

Vainzof, M. (1996) · Human Molecular Genetics · doi:10.1093/hmg/5.12.1963 · Cited by 189 · see citing works

Dynamic Combinatorial Selection of Molecules Capable of Inhibiting the (CUG) Repeat RNA−MBNL1 Interaction In Vitro: Discovery of Lead Compounds Targeting Myotonic Dystrophy (DM1)

Gareiss, P. C., Sobczak, K., McNaughton, B. R., Palde, P. B., Thornton, C. A., & Miller, B. L. (2008) · Journal of the American Chemical Society · doi:10.1021/ja804398y · Cited by 187 · see citing works

Daily Treatment with SMTC1100, a Novel Small Molecule Utrophin Upregulator, Dramatically Reduces the Dystrophic Symptoms in the mdx Mouse

Tinsley, J. M., Fairclough, R. J., Storer, R., Wilkes, F. J., Potter, A. C., Squire, S. E., Powell, D., Cozzoli, A., Capogrosso, R. F., Lambert, A. G., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0019189 · Cited by 186 · see citing works

Rational Design of Ligands Targeting Triplet Repeating Transcripts That Cause RNA Dominant Disease: Application to Myotonic Muscular Dystrophy Type 1 and Spinocerebellar Ataxia Type 3

Pushechnikov, A. O., Lee, M. M., Childs‐Disney, J. L., Sobczak, K., French, J. M., Thornton, C. A., & Disney, M. D. (2009) · Journal of the American Chemical Society · doi:10.1021/ja9020149 · Cited by 184 · see citing works

Muscle weakness in myotonic dystrophy associated with misregulated splicing and altered gating of CaV1.1 calcium channel

Tang, Z. Z., Yarotskyy, V., Wei, L., Sobczak, K., Nakamori, M., Eichinger, K. J., Moxley, R. T., Dirksen, R. T., & Thornton, C. A. (2011) · Human Molecular Genetics · doi:10.1093/hmg/ddr568 · Cited by 181 · see citing works

Identical Mutation in Patients with Limb Girdle Muscular Dystrophy Type 2B Or Miyoshi Myopathy Suggests a Role for Modifier Gene(s)

Weiler, T., Bashir, R., Anderson, L. V. B., Davison, K., Moss, J. A., Britton, S., Nylen, E. G., Keers, S. M., Vafiadaki, E., Greenberg, C. R., et al. (1999) · Human Molecular Genetics · doi:10.1093/hmg/8.5.871 · Cited by 180 · see citing works

The earliest pathologic alterations in dysferlinopathy

Selcen, D., Stilling, G. A., & Engel, A. G. (2001) · Neurology · doi:10.1212/wnl.56.11.1472 · Cited by 176 · see citing works

BAF: roles in chromatin, nuclear structure and retrovirus integration

Segura‐Totten, M., & Wilson, K. L. (2004) · Trends in Cell Biology · doi:10.1016/j.tcb.2004.03.004 · Cited by 176 · see citing works

Dysferlin in Membrane Trafficking and Patch Repair

Glover, L. E., & Brown, R. H. (2007) · Traffic · doi:10.1111/j.1600-0854.2007.00573.x · Cited by 170 · see citing works

Do immune cells promote the pathology of dystrophin-deficient myopathies?

Spencer, M. J., & Tidball, J. G. (2001) · Neuromuscular Disorders · doi:10.1016/s0960-8966(01)00198-5 · Cited by 168 · see citing works

Prevention of pathology in mdx mice by expression of utrophin: analysis using an inducible transgenic expression system

Squire, S. E. (2002) · Human Molecular Genetics · doi:10.1093/hmg/11.26.3333 · Cited by 167 · see citing works

Generation of skeletal muscle stem/progenitor cells from murine induced pluripotent stem cells

Mizuno, Y., Chang, H., Umeda, K., Niwa, A., Iwasa, T., Awaya, T., Fukada, S.-I., Yamamoto, H., Yamanaka, S., Nakahata, T., et al. (2010) · The FASEB Journal · doi:10.1096/fj.09-137174 · Cited by 166 · see citing works

Immunopathogenesis of inflammatory myopathies

Dalakas, M. C. (1995) · Annals of Neurology · doi:10.1002/ana.410370709 · Cited by 163 · see citing works

ED2+ macrophages increase selectively myoblast proliferation in muscle cultures.

Massimino, M., Rapizzi, E., Cantini, M., Libera, L., Mazzoleni, F., Arslan, P., & Carraro, U. (1997) · Biochemical and Biophysical Research Communications - BBRC · doi:10.1006/bbrc.1997.6823 · Cited by 162 · see citing works

Sildenafil reverses cardiac dysfunction in the mdx mouse model of Duchenne muscular dystrophy

Adamo, C. M., Dai, D., Percival, J. M., Minami, E., Willis, M. S., Patrucco, E., Froehner, S. C., & Beavo, J. A. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1013077107 · Cited by 162 · see citing works

Read-Through Strategies for Suppression of Nonsense Mutations in Duchenne/ Becker Muscular Dystrophy: Aminoglycosides and Ataluren (PTC124)

Finkel, R. S. (2010) · Journal of Child Neurology · doi:10.1177/0883073810371129 · Cited by 161 · see citing works

Oxidative stress in SEPN1‐related myopathy: From pathophysiology to treatment

Arbogast, S., Beuvin, M., Fraysse, B., Zhou, H., Francesco Muntoni, A., & Ferreiro, A. (2009) · Annals of Neurology · doi:10.1002/ana.21644 · Cited by 161 · see citing works

RNase H-mediated degradation of toxic RNA in myotonic dystrophy type 1

Lee, J. E., Bennett, C. F., & Cooper, T. A. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1117019109 · Cited by 159 · see citing works

muscleblind , a gene required for photoreceptor differentiation in Drosophila , encodes novel nuclear Cys3His-type zinc-finger-containing proteins

Begemann, G., Paricio, N., Artero, R. D., Kiss, I., Pérez‐Alonso, M., & Mlodzik, M. (1997) · Development · doi:10.1242/dev.124.21.4321 · Cited by 159 · see citing works

The endomembrane requirement for cell surface repair

McNeil, P. L., Miyake, K., & Vogel, S. S. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0736739100 · Cited by 157 · see citing works

Evaluation of cardiac and respiratory involvement in sarcoglycanopathies

Politano, L., Nigro, V., Passamano, L., Petretta, V. R., Comi, L. I., Papparella, S., G.E., N., Rambaldi, P. F., Raia, P., Pini, A., et al. (2001) · Neuromuscular Disorders · doi:10.1016/s0960-8966(00)00174-7 · Cited by 156 · see citing works

Calpain 3 Is Activated through Autolysis within the Active Site and Lyses Sarcomeric and Sarcolemmal Components

Taveau, M., Bourg, N., Sillon, G., Roudaut, C., Bartoli, M., & Richard, I. (2003) · Molecular and Cellular Biology · doi:10.1128/mcb.23.24.9127-9135.2003 · Cited by 155 · see citing works

Muscle Diseases: The Muscular Dystrophies

McNally, E. M., & Pytel, P. (2007) · Annual Review of Pathology Mechanisms of Disease · doi:10.1146/annurev.pathol.2.010506.091936 · Cited by 154 · see citing works

Long-term persistence of donor nuclei in a Duchenne muscular dystrophy patient receiving bone marrow transplantation

Gussoni, E., Bennett, R. R., Muskiewicz, K. R., Meyerrose, T. E., Nolta, J. A., Gilgoff, I. S., Stein, J. H., Chan, Y.-M. M., Lidov, H. G. W., Bönnemann, C. G., et al. (2002) · Journal of Clinical Investigation · doi:10.1172/jci0216098 · Cited by 153 · see citing works

Monoclonal antibody analysis of mononuclear cells in myopathies. IV: Cell‐mediated cytotoxicity and muscle fiber necrosis

Arahata, K., & Engel, A. G. (1988) · Annals of Neurology · doi:10.1002/ana.410230210 · Cited by 152 · see citing works

Myotoxic phospholipases A2 and the regeneration of skeletal muscles

Harris, J. B. (2003) · Toxicon · doi:10.1016/j.toxicon.2003.11.011 · Cited by 150 · see citing works

Initiation and duration of muscle precursor replication after mild and severe injury to skeletal muscle of mice

McGeachie, J. K., & Grounds, M. D. (1987) · Cell and Tissue Research · doi:10.1007/bf01239972 · Cited by 146 · see citing works

In Vivo Myogenic Potential of Human CD133+ Muscle-derived Stem Cells: A Quantitative Study

Négroni, E., Riederer, I., Chaouch, S., Belicchi, M., Razini, P., Santo, J. P. D., Torrente, Y., Butler-Browne, G. S., & Mouly, V. (2009) · Molecular Therapy · doi:10.1038/mt.2009.167 · Cited by 145 · see citing works

Biglycan recruits utrophin to the sarcolemma and counters dystrophic pathology in mdx mice

Amenta, A. R., Yilmaz, A., Bogdanovich, S., McKechnie, B. A., Abedi, M., Khurana, T. S., & Fallon, J. R. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1013067108 · Cited by 144 · see citing works

Design of a Bioactive Small Molecule That Targets the Myotonic Dystrophy Type 1 RNA via an RNA Motif–Ligand Database and Chemical Similarity Searching

Parkesh, R., Childs‐Disney, J. L., Nakamori, M., Kumar, A., Wang, E. T., Wang, T., Hoskins, J. W., Tran, T. A., Housman, D. E., Thornton, C. A., et al. (2012) · Journal of the American Chemical Society · doi:10.1021/ja210088v · Cited by 144 · see citing works

Clinical characteristics of patients with myositis and autoantibodies to different fragments of the Mi-2β antigen

Hengstman, G. J. D., Egberts, W. T. M. V., Seelig, H. P., Lundberg, I. E., Moutsopoulos, H. Μ., Doria, A., Mosca, M., Vencovský, J., VENROOIJ, W. J. V., & van Engelen, B. G. M. (2006) · Annals of the Rheumatic Diseases · doi:10.1136/ard.2005.040717 · Cited by 140 · see citing works

Direct visualization of the dystrophin network on skeletal muscle fiber membrane.

Straub, V. W., Bittner, R. E., Leger, J. J., & Voït, T. (1992) · The Journal of Cell Biology · doi:10.1083/jcb.119.5.1183 · Cited by 140 · see citing works

Macrophages Regulate Proliferation and Differentiation of Satellite Cells

Cantini, M., Massimino, M. L., Bruson, A., Catani, C., Dallalibera, L., & Carraro, U. (1994) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1994.2129 · Cited by 139 · see citing works

Inclusion Body Myositis: A Degenerative Muscle Disease Associated with Intra‐Muscle Fiber Multi‐Protein Aggregates, Proteasome Inhibition, Endoplasmic Reticulum Stress and Decreased Lysosomal Degradation

Askanas, V., Engel, W. K., & Nogalska, A. (2009) · Brain Pathology · doi:10.1111/j.1750-3639.2009.00290.x · Cited by 138 · see citing works

Calpain 3: a key regulator of the sarcomere?

Duguez, S., Bartoli, M., & Richard, I. (2006) · FEBS Journal · doi:10.1111/j.1742-4658.2006.05351.x · Cited by 137 · see citing works

How do mutations in lamins A and C cause disease?

Worman, H. J., & Courvalin, J. (2004) · Journal of Clinical Investigation · doi:10.1172/jci20832 · Cited by 136 · see citing works

Anticipation in myotonic dystrophy

Ashizawa, T., Dubel, J., Dunne, P. W., Dunne, C. J., Fu, Y., Pizzuti, A., Caskey, C. T., Boerwinkle, E., Perryman, M. B., Epstein, H. F., et al. (1992) · Neurology · doi:10.1212/wnl.42.10.1877 · Cited by 131 · see citing works

Calpain Is Required for the Rapid, Calcium-dependent Repair of Wounded Plasma Membrane

Mellgren, R. L., Zhang, W., Miyake, K., & McNeil, P. L. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m604560200 · Cited by 130 · see citing works

Sarcoglycanopathies: molecular pathogenesis and therapeutic prospects

Sandonà, D., & Betto, R. (2009) · Expert Reviews in Molecular Medicine · doi:10.1017/s1462399409001203 · Cited by 128 · see citing works

Laminin-111 protein therapy prevents muscle disease in the mdx mouse model for Duchenne muscular dystrophy

Rooney, J. E., Gurpur, P. B., & Burkin, D. J. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0811599106 · Cited by 128 · see citing works

Primary Role of Functional Ischemia, Quantitative Evidence for the Two-Hit Mechanism, and Phosphodiesterase-5 Inhibitor Therapy in Mouse Muscular Dystrophy

Asai, A., Sahani, N., Kaneki, M., Ouchi, Y., Martyn, J. A. J., & Yasuhara, S. (2007) · PLoS ONE · doi:10.1371/journal.pone.0000806 · Cited by 127 · see citing works

Skeletal Muscle Stem Cells: Effects of Aging and Metabolism on Muscle Regenerative FunctionPreprint

Jang, Y. C., Sinha, M., Cerletti, M., Dall’Osso, C., & Wagers, A. J. (2011) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2011.76.010652 · Cited by 127 · see citing works

Assessment of the Myogenic Stem Cell Compartment Following Transplantation of Pax3/Pax7-Induced Embryonic Stem Cell-Derived Progenitors

Darabi, R., Santos, F. N. C., Filareto, A., Pan, W., Koene, R. J., Rudnicki, M. A., Kyba, M., & Perlingeiro, R. C. R. (2011) · Stem Cells · doi:10.1002/stem.625 · Cited by 126 · see citing works

A Special Population of Regulatory T Cells Potentiates Muscle Repair

Burzyn, D., Kuswanto, W., Kolodin, D., Shadrach, J. L., Cerletti, M., Jang, Y., Sefik, E., Tan, T. G., Wagers, A. J., Benoist, C., et al. (2013) · Cell · doi:10.1016/j.cell.2013.10.054 · Cited by 1,234 · see citing works

NAD ⁺ repletion improves mitochondrial and stem cell function and enhances life span in mice

Zhang, H., Ryu, D., Wu, Y., Gariani, K., Wang, X., Luan, P., D’Amico, D., Ropelle, E. R., Lutolf, M. P., Aebersold, R., et al. (2016) · Science · doi:10.1126/science.aaf2693 · Cited by 1,255 · see citing works

In vivo gene editing in dystrophic mouse muscle and muscle stem cells

Tabebordbar, M., Zhu, K., Cheng, J. K. W., Chew, W. L., Widrick, J. J., Yan, W. X., Maesner, C., Wu, E. Y., Xiao, R., Ran, F. A., et al. (2016) · Science · doi:10.1126/science.aad5177 · Cited by 1,046 · see citing works

Stem cell aging: mechanisms, regulators and therapeutic opportunities

Oh, J., Lee, Y. D., & Wagers, A. J. (2014) · Nature Medicine · doi:10.1038/nm.3651 · Cited by 796 · see citing works

Tissue Tregs

Panduro, M., Benoist, C., & Mathis, D. (2016) · Annual Review of Immunology · doi:10.1146/annurev-immunol-032712-095948 · Cited by 536 · see citing works

Exosomes from differentiating human skeletal muscle cells trigger myogenesis of stem cells and provide biochemical cues for skeletal muscle regeneration

Choi, J. S., Yoon, H. I., Lee, K. S., Choi, Y. C., Yang, S. H., Kim, I.-S., & Cho, Y. W. (2015) · Journal of Controlled Release · doi:10.1016/j.jconrel.2015.12.018 · Cited by 197 · see citing works

Muscle Expression of Mutant Androgen Receptor Accounts for Systemic and Motor Neuron Disease Phenotypes in Spinal and Bulbar Muscular Atrophy

Cortés, C. J., Ling, S., Guo, L. T., Hung, G., Tsunemi, T., Ly, L. T., Tokunaga, S., Lopez, E., Sopher, B. L., Bennett, C. F., et al. (2014) · Neuron · doi:10.1016/j.neuron.2014.03.001 · Cited by 167 · see citing works

Physiopathology of the Permeability Transition Pore: Molecular Mechanisms in Human Pathology

Bonora, M., Patergnani, S., Ramaccini, D., Morciano, G., Pedriali, G., Kahsay, A., Bouhamida, E., Giorgi, C., Wieckowski, M., & Pinton, P. (2020) · Biomolecules · doi:10.3390/biom10070998 · Cited by 135 · see citing works

Adiponectin promotes muscle regeneration through binding to T-cadherin

Tanaka, Y., Kita, S., Nishizawa, H., Fukuda, S., Fujishima, Y., Obata, Y., Nagao, H., Masuda, S., Nakamura, Y., Shimizu, Y., et al. (2019) · Scientific Reports · doi:10.1038/s41598-018-37115-3 · Cited by 103 · see citing works

A Novel Microplate 3D Bioprinting Platform for the Engineering of Muscle and Tendon Tissues

Laternser, S., Keller, H., Leupin, O., Rausch, M., Graf‐Hausner, U., & Rimann, M. (2018) · SLAS TECHNOLOGY · doi:10.1177/2472630318776594 · Cited by 102 · see citing works

Barium chloride injures myofibers through calcium-induced proteolysis with fragmentation of motor nerves and microvessels

Morton, A. B., Norton, C. E., Jacobsen, N. L., Fernando, C. A., Cornelison, D., & Segal, S. S. (2019) · Skeletal Muscle · doi:10.1186/s13395-019-0213-2 · Cited by 90 · see citing works

Functions and Regulatory Mechanisms of lncRNAs in Skeletal Myogenesis, Muscle Disease and Meat Production

Wang, S., Jin, J., Xu, Z., & Zuo, B. (2019) · Cells · doi:10.3390/cells8091107 · Cited by 88 · see citing works

Magnetically Activated Electroactive Microenvironments for Skeletal Muscle Tissue Regeneration

Ribeiro, S., Ribeiro, C., Carvalho, E. O., Tubio, C. R., Castro, N., Pereira, N. M., Correia, V. M. G., Gomes, A. C., & Lanceros-Méndez, S. (2020) · ACS Applied Bio Materials · doi:10.1021/acsabm.0c00315 · Cited by 78 · see citing works

iPSC s: A powerful tool for skeletal muscle tissue engineering

Ortuño‐Costela, M. D. C., García‐López, M., Cerrada, V., & Gallardo, M. E. (2019) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.14292 · Cited by 59 · see citing works

Platelet-Derived Growth Factor BB Influences Muscle Regeneration in Duchenne Muscle Dystrophy

Piñol‐Jurado, P., Gallardo, E., de Luna, N., Suárez‐Calvet, X., Riera, C. S., Fernández‐Simón, E., Gomis, C., Illa, I., & Díaz‐Manera, J. (2017) · American Journal Of Pathology · doi:10.1016/j.ajpath.2017.04.011 · Cited by 46 · see citing works

3D biofabrication for soft tissue and cartilage engineering

Turnbull, G. S., Clarke, J., Picard, F., Zhang, W., Riches, P. E., Li, B., & Shu, W. (2020) · Medical Engineering & Physics · doi:10.1016/j.medengphy.2020.06.003 · Cited by 46 · see citing works

MicroRNA-432 targeting E2F3 and P55PIK inhibits myogenesis through PI3K/AKT/mTOR signaling pathway

Ma, M., Wang, X., Chen, X., Cai, R., Chen, F., Dong, W., Yang, G., & Pang, W. (2017) · RNA Biology · doi:10.1080/15476286.2017.1279786 · Cited by 44 · see citing works

An emerging role of regulatory T-cells in cardiovascular repair and regeneration

Fung, T. H. W., Yang, Y., & Lui, K. O. (2020) · Theranostics · doi:10.7150/thno.47118 · Cited by 43 · see citing works

Preparation of decellularized biphasic hierarchical myotendinous junction extracellular matrix for muscle regeneration

Zhao, C., Wang, S., Wang, G., Su, M., Song, L., Chen, J., Fan, S., & Lin, X. (2017) · Acta Biomaterialia · doi:10.1016/j.actbio.2017.12.035 · Cited by 38 · see citing works

The extraocular muscle stem cell niche is resistant to ageing and disease

Formicola, L., Marazzi, G., & Sassoon, D. A. (2014) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2014.00328 · Cited by 36 · see citing works

The effect of hypoxia on myogenic differentiation and multipotency of the skeletal muscle-derived stem cells in mice

Elashry, M. I., Kinde, M. Z., Klymiuk, M. C., Eldaey, A., Wenisch, S., & Arnhold, S. (2022) · Stem Cell Research & Therapy · doi:10.1186/s13287-022-02730-5 · Cited by 34 · see citing works

Skeletal muscle dedifferentiation during salamander limb regeneration

Wang, H., & Simon, A. (2016) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2016.06.013 · Cited by 32 · see citing works

Cytoskeleton and Adhesion in Myogenesis

Costa, M. L. (2014) · ISRN Developmental Biology · doi:10.1155/2014/713631 · Cited by 32 · see citing works

New roles for Smad signaling and phosphatidic acid in the regulation of skeletal muscle mass

Goodman, C. A., & Hornberger, T. A. (2014) · F1000Prime Reports · doi:10.12703/p6-20 · Cited by 30 · see citing works

Cell fusion is differentially regulated in zebrafish post-embryonic slow and fast muscle

Hromowyk, K. J., Talbot, J. C., Martin, B. L., Janssen, P. M. L., & Amacher, S. L. (2020) · Developmental Biology · doi:10.1016/j.ydbio.2020.03.005 · Cited by 29 · see citing works

Investigating the passive mechanical behaviour of skeletal muscle fibres: Micromechanical experiments and Bayesian hierarchical modelling

Böl, M., Kumar, R. I., Dittmann, J., Garcés-Schröder, M., & Dietzel, A. H. (2019) · Acta Biomaterialia · doi:10.1016/j.actbio.2019.05.015 · Cited by 28 · see citing works

Development and application of human skeletal muscle microphysiological systems

Truskey, G. A. (2018) · Lab on a Chip · doi:10.1039/c8lc00553b · Cited by 27 · see citing works

Hypoglycosylation of dystroglycan due to T192M mutation: A molecular insight behind the fact

Bhattacharya, S., Das, A., Ghosh, S., Dasgupta, R., & Bagchi, A. (2013) · Gene · doi:10.1016/j.gene.2013.11.071 · Cited by 25 · see citing works

Nanomaterial‐Mediated Reprogramming of Macrophages to Inhibit Refractory Muscle Fibrosis

Cheng, X., Sui, H., Chen, F., Li, C., Du, M., Zhang, S., Chen, J., Dou, J., Huang, Y., Xie, X., et al. (2024) · Advanced Materials · doi:10.1002/adma.202410368 · Cited by 24 · see citing works

Genome Editing in Neurosciences

Jaenisch, R., Gage, F. H., & Zhang, F. (2017) · Research and perspectives in neurosciences · doi:10.1007/978-3-319-60192-2 · Cited by 23 · see citing works

Regulatory T cells were recruited by CCL3 to promote cryo-injured muscle repair.

Zhang, C.-Q., Qiao, Y., Huang, L., Li, F., Zhang, Z., Ping, Y., Shen, Z.-B., Lian, J., Zhao, L., & Zhang, Y. (2018) · Immunology Letters · doi:10.1016/j.imlet.2018.10.004 · Cited by 22 · see citing works

Insights into the Notch signaling pathway in degenerative musculoskeletal disorders: Mechanisms and perspectives

Liu, G., Wei, J., Xiao, W., Xie, W., Ru, Q., Chen, L., Wu, Y., Mobasheri, A., & Li, Y. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.115884 · Cited by 23 · see citing works

Direct measurement of the direction-dependent mechanical behaviour of skeletal muscle extracellular matrix

Kohn, S., Leichsenring, K., Kuravi, R., Ehret, A. E., & Böl, M. (2021) · Acta Biomaterialia · doi:10.1016/j.actbio.2020.12.050 · Cited by 21 · see citing works

Novel Insights Into the Multifaceted Functions of RNA n6-Methyladenosine Modification in Degenerative Musculoskeletal Diseases

Li, H., Xiao, W., He, Y., Wen, Z., Cheng, S., Zhang, Y., & Li, Y. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.766020 · Cited by 20 · see citing works

Effects of physical exercise on neuromuscular junction degeneration during ageing: A systematic review

Wang, Q., Cui, C., Zhang, N., Lin, W., Chai, S., Chow, S. K., Wong, R. M. Y., Hu, Y. S., Law, S. W., & Cheung, W. (2024) · Journal of Orthopaedic Translation · doi:10.1016/j.jot.2024.03.007 · Cited by 20 · see citing works

Myofiber-specific TEAD1 overexpression drives satellite cell hyperplasia and counters pathological effects of dystrophin deficiency

Southard, S. M., Kim, J.-R., Low, S., Tsika, R. W., & Lepper, C. (2016) · eLife · doi:10.7554/elife.15461 · Cited by 20 · see citing works

Targeting of miR-432 to myozenin1 to regulate myoblast proliferation and differentiation

Ren, R. M., Liu, H., Zhao, S. H., & Cao, J. H. (2016) · Genetics and Molecular Research · doi:10.4238/gmr15049313 · Cited by 19 · see citing works

Novel insights of EZH2-mediated epigenetic modifications in degenerative musculoskeletal diseases

Ma, Z., Chen, L., Wang, Y., Zhang, S., Zheng, J., Luo, Y., Wang, C., Zeng, H., Xue, L., Tan, Z. W., et al. (2023) · Ageing Research Reviews · doi:10.1016/j.arr.2023.102034 · Cited by 19 · see citing works

LncRNAs as a new regulator of chronic musculoskeletal disorder

Huang, H., Xing, D., Zhang, Q., Li, H., Lin, J., He, Z., & Lin, J. (2021) · Cell Proliferation · doi:10.1111/cpr.13113 · Cited by 18 · see citing works

Two Enhancers Control Transcription of Drosophila muscleblind in the Embryonic Somatic Musculature and in the Central Nervous System

Bargiela, A., Llamusí, B., Cerro-Herreros, E., & Artero, R. D. (2014) · PLoS ONE · doi:10.1371/journal.pone.0093125 · Cited by 18 · see citing works

Role and molecular mechanism of ghrelin in degenerative musculoskeletal disorders

Sun, J.-F., Tan, Y., Su, J.-Y., Mikhail, H., Pavel, V., Deng, Z., & Li, Y.-S. (2023) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.17944 · Cited by 11 · see citing works

Inhibition of the Activin Receptor Type-2B Pathway Restores Regenerative Capacity in Satellite Cell-Depleted Skeletal Muscle

Formicola, L., Pannérec, A., Correra, R. M., Gayraud-Morel, B., Ollitrault, D., Besson, V., Tajbakhsh, S., Lachey, J. L., Seehra, J. S., Marazzi, G., et al. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.00515 · Cited by 15 · see citing works

Growth and Differentiation of Circulating Stem Cells After Extensive Ex Vivo Expansion

Barbon, S., Rajendran, S., Bertalot, T., Piccione, M., Gasparella, M., Parnigotto, P. P., Liddo, R. D., & Conconi, M. T. (2021) · Tissue Engineering and Regenerative Medicine · doi:10.1007/s13770-021-00330-7 · Cited by 15 · see citing works

Wnt7a induces satellite cell expansion, myofiber hyperplasia and hypertrophy in rat craniofacial muscle

Cheng, X., Huang, H., Luo, X., Shi, B., & Li, J. (2018) · Scientific Reports · doi:10.1038/s41598-018-28917-6 · Cited by 13 · see citing works

Cryoinjury Model for Tissue Injury and Repair in Bioengineered Human Striated Muscle

Mills, R. J., Voges, H. K., Porrello, E. R., & Hudson, J. E. (2017) · Methods in molecular biology · doi:10.1007/978-1-4939-7283-8_15 · Cited by 10 · see citing works

The dual guardians of cellular stability: exploring nesprin and lamin in senescence

Zhou, Z., Qin, Q., Dong, C., Liu, Y., Cao, C., & Teng, L. (2025) · Cell Death and Disease · doi:10.1038/s41419-025-08087-w · Cited by 10 · see citing works

Fatty acids impact sarcomere integrity through myristoylation and ER homeostasis

Tang, H., Cui, M., & Han, M. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109539 · Cited by 9 · see citing works

Metabolic adaptation orchestrates tissue context‐dependent behavior in regulatory T cells

Wang, H., Lu, C., & Ho, P. (2020) · Immunological Reviews · doi:10.1111/imr.12844 · Cited by 9 · see citing works

Human MuStem cells repress T-cell proliferation and cytotoxicity through both paracrine and contact-dependent pathways

Charrier, M., Lorant, J., Contreras-López, R. A., Téjédor, G., Blanquart, C., Lieubeau, B., Schleder, C., Leroux, I., Deshayes, S., Fonteneau, J., et al. (2022) · Stem Cell Research & Therapy · doi:10.1186/s13287-021-02681-3 · Cited by 9 · see citing works

Transplantation of Muscle Stem Cell Mitochondria Rejuvenates the Bioenergetic Function of Dystrophic MusclePreprint

Mohiuddin, M., Choi, J. J., Lee, N. H., Jeong, H., Anderson, S. E., Han, W. M., Aliya, B., Peykova, T. Z., Verma, S., Garcı́a, A. J., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.04.17.017822 · Cited by 8 · see citing works

Polymer-based stimuli-responsive biomaterials featuring self-generated electric fields for tissue repair

Li, X., Zhang, Y., Deng, Z., Zhao, X., Zhang, S., Shan, Y., Guo, B., & Han, Y. (2026) · Progress in Materials Science · doi:10.1016/j.pmatsci.2026.101660 · Cited by 8 · see citing works

Bioengineered human pre-vascularized microtissues reconstruct vascular niche and regenerative microenvironment to enhance functional skeletal muscle regeneration.

Liang, C., Gao, Y., Li, J., Liang, Q.-Q., Li, M.-J., Yang, J., Su, X.-X., Zhang, J.-Y., Tian, W.-D., & Liao, L. (2025) · Biomaterials · doi:10.1016/j.biomaterials.2025.123645 · Cited by 9 · see citing works

Biomaterial-based strategies for cell-free nucleic acids scavenging and macrophage modulation in oral diseases: Mechanisms and therapeutic potential

Chen, J., Xu, C., Zhang, S., Sui, H., Fang, K., Li, S. L., Yang, R., Yang, C., Shao, D., Zheng, Q., et al. (2025) · Biomaterials · doi:10.1016/j.biomaterials.2025.123773 · Cited by 6 · see citing works

5-Azacytidine incorporated skeletal muscle-derived hydrogel promotes rat skeletal muscle regeneration

Ahmadi, B. M., Noori, A., Ashtiani, M. K., Rajabi, S., & Talkhabi, M. (2023) · Cells and Development · doi:10.1016/j.cdev.2023.203826 · Cited by 6 · see citing works

Combinations of Kinase Inhibitors Protecting Myoblasts against Hypoxia

Kang, Y., Tierney, M. T., Ong, E., Zhang, L., Piermarocchi, C., Sacco, A., & Paternostro, G. (2015) · PLoS ONE · doi:10.1371/journal.pone.0126718 · Cited by 6 · see citing works

Elemental Composition of Skeletal Muscle Fibres Studied with Synchrotron Radiation X-ray Fluorescence (SR-XRF)

Kasprzyk, P., Wróbel, P., Dudała, J., Geraki, K., Szczerbowska‐Boruchowska, M., Radwańska, E., Krzyżewski, R. M., Adamek, D., & Lankosz, M. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23147931 · Cited by 5 · see citing works

Transplantation-based screen identifies inducers of muscle progenitor cell engraftment across vertebrate species

Tavakoli, S., Garcia, V., Gähwiler, E. K. N., Adatto, I., Rangan, A., Messemer, K. A., Kakhki, S. A., Yang, S. P., Chan, V., Manning, M. E., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112365 · Cited by 4 · see citing works

Muscle Stem Cell Immunostaining

Wang, S., Zhang, B., Addicks, G. C., Zhang, H., Menzies, K. J., & Zhang, H. (2018) · Current Protocols in Mouse Biology · doi:10.1002/cpmo.47 · Cited by 4 · see citing works

Therapeutic Gene Editing in Muscles and Muscle Stem Cells

Tabebordbar, M., Cheng, J. K. W., & Wagers, A. J. (2017) · Research and perspectives in neurosciences · doi:10.1007/978-3-319-60192-2_10 · Cited by 3 · see citing works

A novel intraoral injection technique for rat levator veli palatini muscle regeneration

Cheng, X., Huang, H., Shi, B., & Li, J. (2019) · Annals of Anatomy - Anatomischer Anzeiger · doi:10.1016/j.aanat.2019.01.012 · Cited by 3 · see citing works

Effects of the purified dry extract of fermented ginseng BST204 on muscle fiber regeneration

Jo, S. I., Park, Y. S., Chang, Y., Moon, J.-H., Lee, S. B., Lee, H., Kim, M., Kim, D. Y., Bae, S., Park, S. Y., et al. (2023) · Biochemistry and Biophysics Reports · doi:10.1016/j.bbrep.2023.101525 · Cited by 2 · see citing works

XLOC_015548 Mitigates Skeletal Muscle Atrophy via the Gadd45g/MEK/ERK Pathway and Redox Regulation

Qi, T., Qin, H., Yu, F., Zhou, Z., Chen, Y., Liu, P., Zeng, H., & Weng, J. (2025) · Frontiers in Bioscience-Landmark · doi:10.31083/fbl36233 · Cited by 2 · see citing works

Non-canonical muscle stem cells and other lessons from regenerative vertebrates

Jamwal, V. S., Masselink, W., Crawford, K., & Murawala, P. (2026) · npj Regenerative Medicine · doi:10.1038/s41536-026-00468-9 · Cited by 1 · see citing works

Enhancing Skeletal Muscle Fiber Type Transition Through Substrate Coating Alteration in Myoblast Cell Culture

Riskawati, Y. K., Lin, C., Niwa, A., & Chang, H. C. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26125637 · Cited by 2 · see citing works

Prospects of 3D Bioprinting as a Possible Treatment for Cancer Cachexia

Galib, M., Araf, Y., Naser, I. B., & Promon, S. K. (2021) · Journal of Clinical and Experimental Investigations · doi:10.29333/jcei/11289 · Cited by 1 · see citing works

Influência do tempo de irradiação da terapia por ultrassom sobre o tecido conjuntivo no processo de reparação muscular de ratos

Baldan, C. S. (2013) · doi:10.11606/t.5.2013.tde-26032013-151130

T CELL SUBSETS AND DISEASE MECHANISMS IN INFLAMMATORY MYOPATHIES

Pandya, J. M. (2014) · Figshare

Plastyczność mięśni szkieletowych: Od miogenezy po regenerację

Rędowicz, M. J., & Wojton, D. (2021) · Kosmos · doi:10.36921/kos.2020_2708

Skeletal muscle weakness and mitochondrial dysfunction in the osteogenesis imperfecta murine (oim) model

Gremminger, V. L. (2021) · doi:10.32469/10355/85774

Sub-cellular elemental imaging of human muscle tissues affected by neuromuscular diseases

Śliż-Szpytma, P., Lankosz, M., Dudała, J., Adamek, D., Radwańska, E., Kwinta, B. M., Jakšić, M., Mihalić, I. B., & Provatas, G. (2021) · Nukleonika · doi:10.2478/nuka-2021-0024

Transplantation-based screen uncovers inducers of muscle progenitor cell engraftment across vertebrate speciesPreprint

Tavakoli, S., Adatto, I., Kakhki, S. A., Chan, V., Fotowat, H., Gähwiler, E. K. N., Manning, M. E., Messemer, K. A., Rangan, A., Yang, S. P., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.01.13.523942

Defining Threshold values of Paraspinal Sarcopenia in Patients with Degenerative Lumbar DiseasesPreprint

Kiram, A., Wang, M., Li, J., Xu, Y., Hu, J., Liu, Q., Hu, Z., Qiu, Y., Zhu, Z., & Liu, Z. (2025) · Research Square · doi:10.21203/rs.3.rs-7085436/v1

Study of the biomolecular composition of skeletal muscle fibres affected by different types of pathology using by FTIR microspectroscopy

Kasprzyk, P., Dudała, J., Lankosz, M., Adamek, D., Kwinta, B. M., Radwańska, E., Lekkas, J., Cinque, G., & Szczerbowska‐Boruchowska, M. (2025) · Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy · doi:10.1016/j.saa.2025.126727

Additional file 1 of The effect of hypoxia on myogenic differentiation and multipotency of the skeletal muscle-derived stem cells in mice

Elashry, M. I., Kinde, M., Klymiuk, M. C., Eldaey, A., Wenisch, S., & Arnhold, S. (2022) · Figshare · doi:10.6084/m9.figshare.19128863

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Sahu, R., Thapa, A., Ashraf, G. J., Das, P., Maiti, P. P., Paul, P., Dua, T. K., & Nandi, G. (2026) · BENTHAM SCIENCE PUBLISHERS eBooks · doi:10.2174/9798898813369126010009

Skeletal muscle growth and maintenance depend on BMP signaling

Schirwis, E. (2014) · theses.fr (ABES) · doi:10.70675/7234357bz1f9dz4a42za02cz799ec1dedf12

Deficiency of G9a boosts muscle regeneration through IL13/Musclin-mediated crosstalk between macrophage and myofiber

Jin, Y., Zhou, K., Hao, S., Hu, Y., Wang, H., Liu, Z., Zhou, Y., Xie, Y., Liu, X., Chen, H., et al. (2026) · Cell Death and Disease · doi:10.1038/s41419-026-08944-2

Beyond immune suppression: regenerative programs in regulatory T cells

You, Y., Hu, X., Xue, Y., & Liu, Z. (2026) · Cell Insight · doi:10.1016/j.cellin.2026.100355

Mechanisms of Muscle Degeneration, Regeneration, and Repair in the Muscular Dystrophies

Wallace, G. Q., & McNally, E. M. (2008) · Annual Review of Physiology · doi:10.1146/annurev.physiol.010908.163216 · Cited by 343 · see citing works

Stem Cells in Skeletal Muscle

Polesskaya, A., & Rudnicki, M. A. (2004) · Humana Press eBooks · doi:10.1007/978-1-59259-732-1_3

Regenerative Therapy

Morgan, J. E., Brimah, K., & Collins, C. A. (2006) · CRC Press eBooks · doi:10.3109/9780849374456-16

Downstream Pathways of Dystrophin Deficiency in Duchenne Muscular Dystrophy: Implications for Muscle Degeneration and Regeneration

Epis, R., Rovetta, G., Ferrari, G., Bonfanti, C., Careccia, G., & Messina, G. (2026) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.70333 · Cited by 1 · see citing works

Attenuating Muscle Wasting: Cell and Gene Therapy Approaches

Musarò, A., & Rosenthal, N. (2003) · Current Genomics · doi:10.2174/1389202033490222 · Cited by 5 · see citing works