Muscle stem cells

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

Asymmetric self-renewal and commitment of satellite stem cells in muscle

Kuang, S., Kuroda, K., Le Grand, F., & Rudnicki, M. A. (2007) · Cell · doi:10.1016/j.cell.2007.03.044 · Cited by 1,449 · see citing works

A Pax3/Pax7-dependent population of skeletal muscle progenitor cells

Relaix, F., Rocancourt, D., Mansouri, A., & BUCKINGHAM, M. E. (2005) · Nature · doi:10.1038/nature03594 · Cited by 1,167 · 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

Pax3 and Pax7 have distinct and overlapping functions in adult muscle progenitor cells

Relaix, F., Montarras, D., Zaffran, S., Gayraud-Morel, B., Rocancourt, D., Tajbakhsh, S., Mansouri, A., Cumano, A., & BUCKINGHAM, M. E. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200508044 · Cited by 736 · see citing works

The molecular regulation of myogenesis

Sabourin, L. A., & Rudnicki, M. A. (2000) · Clinical Genetics · doi:10.1034/j.1399-0004.2000.570103.x · Cited by 720 · see citing works

Fate tracing reveals the endothelial origin of hematopoietic stem cells

Zovein, A. C., Hofmann, J. J., Lynch, M., French, W. J., Turlo, K. A., Yang, Y., Becker, M. S., Zanetta, L., Dejana, E., Gasson, J. C., et al. (2008) · Cell Stem Cell · doi:10.1016/j.stem.2008.09.018 · Cited by 691 · 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

A common somitic origin for embryonic muscle progenitors and satellite cells

Gros, J., Manceau, M., Thomé, V., & Marcelle, C. (2005) · Nature · doi:10.1038/nature03572 · Cited by 596 · see citing works

Stem and Progenitor Cells in Skeletal Muscle Development, Maintenance, and Therapy

Péault, B., Rudnicki, M. A., Torrente, Y., Cossu, G., Tremblay, J. P., Partridge, T. A., Gussoni, E., Kunkel, L. M., & Huard, J. (2007) · Molecular Therapy · doi:10.1038/mt.sj.6300145 · Cited by 572 · see citing works

Pax3/Pax7 mark a novel population of primitive myogenic cells during developmentPreprint

Kassar-Duchossoy, L., Giacone, E., Gayraud-Morel, B., Jory, A., Gomès, D., & Tajbakhsh, S. (2005) · Genes & Development · doi:10.1101/gad.345505 · Cited by 556 · see citing works

Wnt7a Activates the Planar Cell Polarity Pathway to Drive the Symmetric Expansion of Satellite Stem Cells

Grand, F. L., Jones, A., Seale, V., Scimè, A., & Rudnicki, M. A. (2009) · Cell stem cell · doi:10.1016/j.stem.2009.03.013 · Cited by 531 · see citing works

Pax7 directs postnatal renewal and propagation of myogenic satellite cells but not their specification

Oustanina, S., Hause, G., & Braun, T. W. (2004) · The EMBO Journal · doi:10.1038/sj.emboj.7600346 · Cited by 531 · see citing works

Molecular Signature of Quiescent Satellite Cells in Adult Skeletal Muscle

Fukada, S.-I., Uezumi, A., Ikemoto, M., Masuda, S., Segawa, M., Tanimura, N., Yamamoto, H., Miyagoe-Suzuki, Y., & Takeda, S. (2007) · Stem Cells · doi:10.1634/stemcells.2007-0019 · Cited by 506 · 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

Distinct roles for Pax7 and Pax3 in adult regenerative myogenesis

Kuang, S., CHARGÉ, S. B. P., Seale, P., Huh, M. S., & Rudnicki, M. A. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.200508001 · Cited by 490 · see citing works

Two distinct endothelial lineages in ontogeny, one of them related to hemopoiesis

Pardanaud, L., Luton, D., Prigent, M., Bourcheix, L.-M., Catala, M., & Dieterlen‐Lièvre, F. (1996) · Development · doi:10.1242/dev.122.5.1363 · Cited by 417 · see citing works

Distinct Regulatory Cascades Govern Extraocular and Pharyngeal Arch Muscle Progenitor Cell Fates

Sambasivan, R., Gayraud-Morel, B., Dumas, G., Cimper, C., Paisant, S., Kelly, R. G., & Tajbakhsh, S. (2009) · Developmental Cell · doi:10.1016/j.devcel.2009.05.008 · Cited by 400 · see citing works

The differentiation and morphogenesis of craniofacial muscles

Noden, D. M., & Francis‐West, P. H. (2006) · Developmental Dynamics · doi:10.1002/dvdy.20697 · Cited by 393 · see citing works

Pax7 activates myogenic genes by recruitment of a histone methyltransferase complex

McKinnell, I. W., Ishibashi, J., Le Grand, F., Punch, V. G. J., Addicks, G. C., Greenblatt, J. F., Dilworth, F. J., & Rudnicki, M. A. (2008) · Nature Cell Biology · doi:10.1038/ncb1671 · Cited by 380 · see citing works

Divergent functions of murine Pax3 and Pax7 in limb muscle developmentPreprint

Relaix, F., Rocancourt, D., Mansouri, A., & BUCKINGHAM, M. E. (2004) · Genes & Development · doi:10.1101/gad.301004 · Cited by 313 · see citing works

Embryonic and fetal limb myogenic cells are derived from developmentally distinct progenitors and have different requirements for β-cateninPreprint

Hutcheson, D. A., Zhao, J., Merrell, A. J., Haldar, M., & Kardon, G. (2009) · Genes & Development · doi:10.1101/gad.1769009 · Cited by 301 · 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 · see citing works

The genetics of vertebrate myogenesis

Bryson‐Richardson, R. J., & Currie, P. D. (2008) · Nature Reviews Genetics · doi:10.1038/nrg2369 · Cited by 285 · see citing works

Premature myogenic differentiation and depletion of progenitor cells cause severe muscle hypotrophy in Delta1 mutants

Schuster-Gossler, K., Cordes, R., & Gossler, A. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0608281104 · Cited by 262 · see citing works

Distinct Origins and Genetic Programs of Head Muscle Satellite Cells

Harel, I., Nathan, E., Tirosh-Finkel, L., Zigdon, H., Guimarães‐Camboa, N., Evans, S. Μ., & Tzahor, E. (2009) · Developmental Cell · doi:10.1016/j.devcel.2009.05.007 · Cited by 244 · see citing works

RBP-J ( Rbpsuh ) is essential to maintain muscle progenitor cells and to generate satellite cells

Vasyutina, E. L., Lenhard, D. C., Wende, H., Erdmann, B., Epstein, J. A., & Birchmeier, C. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0610647104 · Cited by 238 · see citing works

A Two-Step Mechanism for Myotome Formation in Chick

Gros, J., Scaal, M., & Marcelle, C. (2004) · Developmental Cell · doi:10.1016/j.devcel.2004.05.006 · Cited by 225 · see citing works

Somitic origin of limb muscle satellite and side population cells

Schienda, J., Engleka, K. A., Jun, S. J., Hansen, M. S. T., Epstein, J. A., Tabin, C. J., Kunkel, L. M., & Kardon, G. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0510164103 · Cited by 216 · 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

Progenitors of skeletal muscle satellite cells express the muscle determination gene, MyoD

Kanisicak, O., Mendez, J. J., Yamamoto, S., Yamamoto, M., & Goldhamer, D. J. (2009) · Developmental Biology · doi:10.1016/j.ydbio.2009.05.554 · Cited by 192 · see citing works

Lineage analysis of the avian dermomyotome sheet reveals the existence of single cells with both dermal and muscle progenitor fates

Ben-Yair, R., & Kalcheim, C. (2005) · Development · doi:10.1242/dev.01617 · Cited by 187 · see citing works

Local Extrinsic Signals Determine Muscle and Endothelial Cell Fate and Patterning in the Vertebrate Limb

Kardon, G., Campbell, J. K., & Tabin, C. J. (2002) · Developmental Cell · doi:10.1016/s1534-5807(02)00291-5 · Cited by 178 · see citing works

Delta 1-activated Notch inhibits muscle differentiation without affecting Myf5 and Pax3 expression in chick limb myogenesis

Delfini, M.-C., Hirsinger, E., Pourquié, O., & Duprez, D. (2000) · Development · doi:10.1242/dev.127.23.5213 · Cited by 175 · see citing works

Myostatin promotes the terminal differentiation of embryonic muscle progenitorsPreprint

Manceau, M., Gros, J., Savage, K., Thomé, V., McPherron, A. C., Paterson, B., & Marcelle, C. (2008) · Genes & Development · doi:10.1101/gad.454408 · Cited by 161 · see citing works

Satellite cells, myoblasts and other occasional myogenic progenitors: Possible origin, phenotypic features and role in muscle regeneration

Cossu, G., & Biressi, S. (2005) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2005.07.003 · Cited by 156 · see citing works

FGFR4 signaling is a necessary step in limb muscle differentiation

Marics, I., Padilla, F., Guillemot, J.-F., Scaal, M., & Marcelle, C. (2002) · Development · doi:10.1242/dev.129.19.4559 · Cited by 151 · see citing works

The Transcriptional Activity of Sox9 in Chondrocytes Is Regulated by RhoA Signaling and Actin Polymerization

Kumar, D. V., & Lassar, A. B. (2009) · Molecular and Cellular Biology · doi:10.1128/mcb.01779-08 · Cited by 147 · see citing works

Pax3 regulation of FGF signaling affects the progression of embryonic progenitor cells into the myogenic programPreprint

Lagha, M., Kormish, J. D., Rocancourt, D., Manceau, M., Epstein, J. A., Zaret, K. S., Relaix, F., & BUCKINGHAM, M. E. (2008) · Genes & Development · doi:10.1101/gad.477908 · Cited by 143 · see citing works

Origin of satellite cells in avian skeletal muscles.

Armand, O., Boutineau, A. M., Mauger, A., Pautou, M.-P., & Kieny, M. (1983) · PubMed · Cited by 138 · see citing works

Integrated Functions of Pax3 and Pax7 in the Regulation of Proliferation, Cell Size and Myogenic Differentiation

Collins, C. A., Gnocchi, V. F., White, R. B., Boldrin, L., Ruiz, A. P., Relaix, F., Morgan, J. E., & Zammit, P. S. (2009) · PLoS ONE · doi:10.1371/journal.pone.0004475 · Cited by 127 · see citing works

Id3 Is a Direct Transcriptional Target of Pax7 in Quiescent Satellite Cells

Kumar, D. V., Shadrach, J. L., Wagers, A. J., & Lassar, A. B. (2009) · Molecular Biology of the Cell · doi:10.1091/mbc.e08-12-1185 · Cited by 113 · see citing works

Mediolateral somitic origin of ribs and dermis determined by quail-chick chimeras

Olivera-Martínez, I., Coltey, M., Dhouailly, D., & Pourquié, O. (2000) · Development · doi:10.1242/dev.127.21.4611 · Cited by 106 · see citing works

Thein VivoExpression of the FGF Receptor FREK mRNA in Avian Myoblasts Suggests a Role in Muscle Growth and Differentiation

Marcelle, C., Wolf, J. J., & Bronner-Fraser, M. E. (1995) · Developmental Biology · doi:10.1006/dbio.1995.0008 · Cited by 100 · see citing works

β-Catenin Interacts with MyoD and Regulates Its Transcription Activity

Kim, C., Neiswender, H., Baik, E. J., Xiong, W., & Mei, L. (2008) · Molecular and Cellular Biology · doi:10.1128/mcb.01682-07 · Cited by 93 · see citing works

Stra13 regulates satellite cell activation by antagonizing Notch signaling

Sun, H., Li, L., Vercherat, C., Gülbağcı, N. T., Acharjee, S., Li, J., Chung, T., Thin, T. H., & Taneja, R. (2007) · The Journal of Cell Biology · doi:10.1083/jcb.200609007 · Cited by 76 · see citing works

Myf5 expression in satellite cells and spindles in adult muscle is controlled by separate genetic elements

Zammit, P. S., Carvajal, J. J., Golding, J. P., Morgan, J. E., Summerbell, D., Zolnerciks, J. K., Partridge, T. A., Rigby, P. W. J., & Beauchamp, J. R. (2004) · Developmental Biology · doi:10.1016/j.ydbio.2004.05.038 · Cited by 71 · see citing works

Differential effects of N-cadherin-mediated adhesion on the development of myotomal waves

Cinnamon, Y., Ben-Yair, R., & Kalcheim, C. (2006) · Development · doi:10.1242/dev.02291 · Cited by 60 · see citing works

Three different fates of cells migrating from somites into the limb bud

He, L., Papoutsi, M., Huang, R., Tomarev, S. I., Christ, B., Kurz, H., & Wilting, J. (2003) · Anatomy and Embryology · doi:10.1007/s00429-003-0327-4 · Cited by 43 · see citing works

Heparin-binding EGF-like growth factor shows transient left–right asymmetrical expression in mouse myotome pairs

Golding, J. P., Tsoni, S. V., Dixon, M., Yee, K. T., Partridge, T. A., Beauchamp, J. R., Gassmann, M., & Zammit, P. S. (2004) · Gene Expression Patterns · doi:10.1016/j.modgep.2004.08.004 · Cited by 20 · see citing works

Mesenchymal Stem Cells Isolated from Adipose and Other Tissues: Basic Biological Properties and Clinical Applications

Orbay, H., Tobita, M., & Mizuno, H. (2012) · Stem Cells International · doi:10.1155/2012/461718 · Cited by 250 · see citing works

Colonization of the Satellite Cell Niche by Skeletal Muscle Progenitor Cells Depends on Notch Signals

Bröhl, D., Vasyutina, E. L., Czajkowski, M. T., Griger, J., Raßek, C., Rahn, H.-P., Purfürst, B., Wende, H., & Birchmeier, C. (2012) · Developmental Cell · doi:10.1016/j.devcel.2012.07.014 · Cited by 214 · see citing works

Molecular and Cellular Regulation of Skeletal Myogenesis

Comai, G., & Tajbakhsh, S. (2014) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/b978-0-12-405943-6.00001-4 · Cited by 205 · see citing works

Combination of inflammation-related cytokines promotes long-term muscle stem cell expansion

Fu, X., Xiao, J., Wei, Y., Li, S., Liu, Y., Yin, J., Sun, K., Sun, H., Wang, H., Zhang, Z., et al. (2015) · Cell Research · doi:10.1038/cr.2015.58 · Cited by 196 · see citing works

Biological properties of mesenchymal Stem Cells from different sources.

Via, A. G., Frizziero, A., & Oliva, F. (2012) · Europe PMC (PubMed Central) · Cited by 188 · see citing works

Stem cell activation in skeletal muscle regeneration

Fu, X., Wang, H., & Hu, P. (2015) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-014-1819-5 · Cited by 189 · see citing works

The Skeletal Muscle Satellite Cell

Yablonka‐Reuveni, Z. (2011) · Journal of Histochemistry & Cytochemistry · doi:10.1369/0022155411426780 · Cited by 164 · see citing works

NUMB-ing down cancer by more than just a NOTCH

Pece, S., Confalonieri, S., Romano, P. R., & Fiore, P. P. D. (2010) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2010.10.001 · Cited by 147 · see citing works

Origin of Vertebrate Limb Muscle

Murphy, M. M., & Kardon, G. (2011) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/b978-0-12-385940-2.00001-2 · Cited by 118 · see citing works

Nitric Oxide Sustains Long-Term Skeletal Muscle Regeneration by Regulating Fate of Satellite Cells Via Signaling Pathways Requiring Vangl2 and Cyclic GMP

Buono, R., Vantaggiato, C., Pisa, V., Azzoni, E., Bassi, M. T., Brunelli, S., Sciorati, C., & Clementi, E. (2011) · Stem Cells · doi:10.1002/stem.783 · Cited by 113 · see citing works

Potential Roles of n-3 PUFAs during Skeletal Muscle Growth and Regeneration

Tachtsis, B., Camera, D., & Lacham-Kaplan, O. (2018) · Nutrients · doi:10.3390/nu10030309 · Cited by 104 · see citing works

Advantages of mesenchymal stem cell over the other stem cells

Janani, G., Nair, A. P., Iyer, M., Vellingiri, B., & Subramaniam, M. D. (2023) · Acta Histochemica · doi:10.1016/j.acthis.2023.152041 · Cited by 92 · see citing works

Muscle stem cells in developmental and regenerative myogenesis

Kang, J.-S., & Krauss, R. S. (2010) · Current Opinion in Clinical Nutrition and Metabolic Care · doi:10.1097/mco.0b013e328336ea98 · Cited by 90 · see citing works

Advances in research on the prenatal development of skeletal muscle in animals in relation to the quality of muscle-based food. I. Regulation of myogenesis and environmental impact

Rehfeldt, C., PAS, M. F. W. T., Wimmers, K., Brameld, J. M., Nissen, P. M., Berri, C., Valente, L. M. P., Power, D. M., Picard, B. B., Stickland, N. C., et al. (2010) · animal · doi:10.1017/s1751731110002089 · Cited by 88 · see citing works

TRAF6 regulates satellite stem cell self-renewal and function during regenerative myogenesis

Hindi, S. M., & Kumar, A. (2015) · Journal of Clinical Investigation · doi:10.1172/jci81655 · Cited by 77 · see citing works

Changes in mitochondrial reactive oxygen species synthesis during differentiation of skeletal muscle cells

Malińska, D., Kudin, A. P., Bejtka, M., & Kunz, W. S. (2011) · Mitochondrion · doi:10.1016/j.mito.2011.06.015 · Cited by 73 · see citing works

Notch and Wnt Signaling, Physiological Stimuli and Postnatal Myogenesis

Tsivitse, S. K. (2010) · International Journal of Biological Sciences · doi:10.7150/ijbs.6.268 · Cited by 72 · see citing works

BMP signaling regulates satellite cell-dependent postnatal muscle growth

Stantzou, A., Schirwis, E., Swist, S., Alonso‐Martín, S., Polydorou, I., Zarrouki, F., Mouisel, É., Beley, C., Julien, A., Grand, F. L., et al. (2017) · Development · doi:10.1242/dev.144089 · Cited by 66 · see citing works

Nitric Oxide in Myogenesis and Therapeutic Muscle Repair

Palma, C. D., & Clementi, E. (2012) · Molecular Neurobiology · doi:10.1007/s12035-012-8311-8 · Cited by 66 · see citing works

Common Pathogenic Mechanisms in Centronuclear and Myotubular Myopathies and Latest Treatment Advances

Gómez, R., Cowling, B. S., & Laporte, J. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222111377 · Cited by 61 · see citing works

Genetic Ablation of TWEAK Augments Regeneration and Post-Injury Growth of Skeletal Muscle in Mice

Mittal, A., Bhatnagar, S., Kumar, A., Paul, P. K., Kuang, S., & Kumar, A. (2010) · American Journal Of Pathology · doi:10.2353/ajpath.2010.100335 · Cited by 61 · see citing works

Gene Expression Profiling of Muscle Stem Cells Identifies Novel Regulators of Postnatal Myogenesis

Alonso‐Martín, S., Rochat, A., Mademtzoglou, D., Morais, J., de Reyniès, A., Aurade, F., Chang, T. H., Zammit, P. S., & Relaix, F. (2016) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2016.00058 · Cited by 62 · see citing works

Neural Crest Cell Lineage Restricts Skeletal Muscle Progenitor Cell Differentiation through Neuregulin1-ErbB3 Signaling

Ho, A. T. V., Hayashi, S., Bröhl, D., Aurade, F., Rattenbach, R., & Relaix, F. (2011) · Developmental Cell · doi:10.1016/j.devcel.2011.06.019 · Cited by 53 · see citing works

A global downregulation of microRNAs occurs in human quiescent satellite cells during myogenesis

Koning, M., Werker, P. M. N., van Luyn, M. J. A., Krenning, G., & Harmsen, M. C. (2012) · Differentiation · doi:10.1016/j.diff.2012.08.002 · Cited by 47 · see citing works

Proinflammatory Cytokine Tumor Necrosis Factor (TNF)-like Weak Inducer of Apoptosis (TWEAK) Suppresses Satellite Cell Self-renewal through Inversely Modulating Notch and NF-κB Signaling Pathways

Ogura, Y., Mishra, V. K., Hindi, S. M., Kuang, S., & Kumar, A. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.517300 · Cited by 43 · see citing works

Notch and Stem Cells

Bigas, A., & Porcheri, C. (2018) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-89512-3_12 · Cited by 36 · see citing works

MicroRNA-1 and MicroRNA-206 Improve Differentiation Potential of Human Satellite Cells: A Novel Approach for Tissue Engineering of Skeletal Muscle

Koning, M., Werker, P. M. N., van der Schaft, D. W. J., Bank, R. A., & Harmsen, M. C. (2011) · Tissue Engineering Part A · doi:10.1089/ten.tea.2011.0191 · Cited by 35 · see citing works

Regulation of Skeletal Muscle Satellite Cell Differentiation by Omega-3 Polyunsaturated Fatty Acids: A Critical Review

Isesele, P., & Mazurak, V. C. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.682091 · Cited by 33 · see citing works

Purification of Progenitors from Skeletal Muscle

Yi, L., & Rossi, F. M. V. (2011) · Journal of Visualized Experiments · doi:10.3791/2476 · Cited by 30 · see citing works

Extensive morphological and immunohistochemical characterization in myotubular myopathy

Shichiji, M., Biancalana, V., Fardeau, M., Hogrel, J., Ōsawa, M., Laporte, J., & Romero, N. B. (2013) · Brain and Behavior · doi:10.1002/brb3.147 · Cited by 29 · see citing works

Implanted Muscle-Derived Stem Cells Ameliorate Erectile Dysfunction in a Rat Model of Type 2 Diabetes, but Their Repair Capacity Is Impaired by Their Prior Exposure to the Diabetic Milieu

Kovanecz, I., Vernet, D. A., Masouminia, M., Gelfand, R., Loni, L., Aboagye, J., Tsao, J., Rajfer, J., & González-Cadavid, N. F. (2016) · The Journal of Sexual Medicine · doi:10.1016/j.jsxm.2016.02.168 · Cited by 28 · see citing works

Myostatin genetic inactivation inhibits myogenesis by muscle-derived stem cells in vitro but not when implanted in the mdx mouse muscle

Tsao, J., Vernet, D. A., Gelfand, R., Kovanecz, I., Nolazco, G., Bruhn, K. W., & González-Cadavid, N. F. (2013) · Stem Cell Research & Therapy · doi:10.1186/scrt152 · Cited by 27 · see citing works

Muscle Satellite Cell Heterogeneity: Does Embryonic Origin Matter?

Rodríguez-Outeiriño, L., Hernández‐Torres, F., Acuña, F. R.-D., Matías-Valiente, L., Sánchez–Fernández, C., Franco, D., & Aránega, A. E. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.750534 · Cited by 26 · see citing works

In Vitro Development and Characterization of a Tissue-Engineered Conduit Resembling Esophageal Wall Using Human and Pig Skeletal Myoblast, Oral Epithelial Cells, and Biologic Scaffolds

Poghosyan, T., Gaujoux, S., Vanneaux, V., Bruneval, P., Domet, T., Lecourt, S., Jarraya, M., Sfeir, R., Larghero, J., & Cattan, P. (2013) · Tissue Engineering Part A · doi:10.1089/ten.tea.2012.0565 · Cited by 26 · see citing works

New Insights into Mechanisms of Stem Cell Daughter Fate Determination in Regenerative Tissues

Sada, A., & Tumbar, T. (2012) · International review of cytology · doi:10.1016/b978-0-12-405210-9.00001-1 · Cited by 24 · see citing works

Myocyte-derived Tnfsf14 is a survival factor necessary for myoblast differentiation and skeletal muscle regeneration

Waldemer, R. J., & Chen, J. (2015) · Cell Death and Disease · doi:10.1038/cddis.2015.375 · Cited by 23 · see citing works

PUFA Treatment Affects C2C12 Myocyte Differentiation, Myogenesis Related Genes and Energy Metabolism

Risha, M. A., Siengdee, P., Dannenberger, D., Wimmers, K., & Ponsuksili, S. (2021) · Genes · doi:10.3390/genes12020192 · Cited by 20 · see citing works

Skeletal Muscle Stem Cells in the Spotlight: The Satellite Cell

Yablonka‐Reuveni, Z., & Day, K. R. (2011) · Humana Press eBooks · doi:10.1007/978-1-61779-021-8_11 · Cited by 19 · see citing works

Meat Industries: Characteristics and Manufacturing Processes

Hui, Y. H. (2012) · CRC Press eBooks · doi:10.1201/b11479-5 · Cited by 18 · see citing works

Influence of DUX4 Expression in Facioscapulohumeral Muscular Dystrophy and Possible Treatments

Duranti, E., & Villa, C. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24119503 · Cited by 17 · see citing works

Eupalinilide E Inhibits Erythropoiesis and Promotes the Expansion of Hematopoietic Progenitor Cells

de Lichtervelde, L., Boitano, A. E., Wang, Y., Krastel, P., Petersen, F., Cooke, M. P., & Schultz, P. G. (2013) · ACS Chemical Biology · doi:10.1021/cb4000234 · Cited by 15 · see citing works

Developing laryngeal muscle of Xenopus laevis as a model system: Androgen‐driven myogenesis controls fiber type transformation

Nasipak, B. T., & Kelley, D. B. (2011) · Developmental Neurobiology · doi:10.1002/dneu.20983 · Cited by 12 · see citing works

M-Cadherin Is a PAX3 Target During Myotome Patterning

de Lima, J. E., Akar, R. B., Mansour, M., Rocancourt, D., BUCKINGHAM, M. E., & Relaix, F. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.652652 · Cited by 11 · see citing works

Efficient Single Muscle Fiber Isolation from Alcohol-Fixed Adult Muscle following β-Galactosidase Staining for Satellite Cell Detection

Verma, M., & Asakura, A. (2010) · Journal of Histochemistry & Cytochemistry · doi:10.1369/jhc.2010.956730 · Cited by 10 · see citing works

Waking up muscle stem cells: PI3K signalling is ringing

Relaix, F., & Machado, L. (2018) · The EMBO Journal · doi:10.15252/embj.201899297 · Cited by 9 · see citing works

Epigenetics of Genes Preferentially Expressed in Dissimilar Cell Populations: Myoblasts and Cerebellum

Ehrlich, M., Ehrlich, K. C., Lacey, M. R., Baribault, C., Sen, S., Estève, P., & Pradhan, S. (2024) · Epigenomes · doi:10.3390/epigenomes8010004 · Cited by 8 · see citing works

The Satellite Cell Builds Its Nest under Notch’s Guidance

Lepper, C., Low, S., & Partridge, T. A. (2012) · Cell stem cell · doi:10.1016/j.stem.2012.09.010 · Cited by 4 · see citing works

GREM1 is epigenetically reprogrammed in muscle cells after exercise training and controls myogenesis and metabolismPreprint

Fabre, O., Giordani, L., Parisi, A., Pattamaprapanont, P., Ahwazi, D., Brun, C. E., Chakroun, I., Taleb, A., Blais, A., Andersen, E., et al. (2020) · bioRxiv · doi:10.1101/2020.02.20.956300 · Cited by 5 · see citing works

Skeletal Muscle Development: From Stem Cells to Body Movement

Deries, M., Gonçalves, A. B., & Þorsteinsdóttir, S. (2020) · Learning materials in biosciences · doi:10.1007/978-3-030-43939-2_9 · Cited by 3 · see citing works

Hippo pathway inhibition promotes metabolic adaptability and antioxidant response in myoblasts

Liu, Q., Pan, S., Li, P., & Dixon, R. A. F. (2023) · Scientific Reports · doi:10.1038/s41598-023-29372-8 · Cited by 3 · see citing works

Methods to Mimic In Vivo Muscle Cell Biology in Primary Human Myoblasts Using Quiescence as a Guidepost in Regenerative Medicine Research

Gudagudi, K. B., & Myburgh, K. H. (2021) · OMICS A Journal of Integrative Biology · doi:10.1089/omi.2020.0211 · Cited by 1 · see citing works

Skeletal Muscle Stem Cell Niche from Birth to Old Age

Barbu, M. G., Boboc, A. E., Filip, L., Bugnar, O. L., Crețoiu, D., Suciu, N., Toader, O. D., Creţoiu, S. M., & Voinea, S.-C. (2020) · IntechOpen eBooks · doi:10.5772/intechopen.93502 · Cited by 1 · see citing works

Myogenic Differentiation of ES Cells for Therapies in Neuromuscular Diseases: Progress to Date

Camila, F., Ayub-Guerrieri, D., & Vainzof, M. (2011) · InTech eBooks · doi:10.5772/25047

MODELLING OF INSULIN SIGNALLING: EFFECTS ON GLUCOSE METABOLISM IN SKELETAL MUSCLE

Sögård, P. (2010)

Characterization and Function of the ~70kDa Immunoreactive Species of Pannexin3 in Rhabdomyosarcomas

Gill, K. (2015) · uO Research (University of Ottawa) · doi:10.20381/ruor-2832

Stem cell activation in skeletal muscle regeneration

FuHuating, X., & Hu, W. (2015)

Modélisation pathologique des maladies monogéniques par l'utilisation des cellules souches embryonnaires humaines : preuve de concept appliquée à la dystrophie myotonique de type 1

Denis, J. A. (2010) · doi:10.70675/99903e3ezfc77z4fe6z870ez3fd60335eafa

Skeletal muscle growth and maintenance depend on BMP signaling

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

Conditions de survie des cellules souches du muscle squelettique à des conditions extrêmes d'hypoxie : caractérisation phénotypique et fonctionnelle des sous populations de cellules pour optimiser la régénération tissulaire et les thérapies cellulaires

Latil, M. (2013) · doi:10.70675/05468b01z26d3z4497za6b2z8a8bc4d00e4f

Identification and characterisation of new genes associated to multiminicore disease

Davignon, L. (2015) · theses.fr (ABES) · doi:10.70675/faa2747az5fc3z460fzb9adz5411c56ffe66

The influence of Notch over-stimulation on muscle stem cell quiescence versus proliferation, and on muscle regeneration

Ding, C. (2015) · theses.fr (ABES) · doi:10.70675/e39ac2a3zc169z42fez8503zaab6a215936e

BMP signaling controls postnatal muscle development

Stantzou, A. (2015) · doi:10.70675/5f5055dezcb3dz4bdbz84e8zb743b6f0172d

Thérapie par l’exercice et dystrophie facio-scapulo-humérale : étude contrôlée randomisée de 6 mois d’entraînement à domicile : précédée d’une étude histologique du potentiel régénératif musculaire dans deux modèles distincts de myopathies

Bankolé, S. L. C. (2014) · doi:10.70675/0d4d5dd2z8b73z4599zbeb1zf674fd67620b

Influence of hypoxia and reoxygenation on muscle stem cell fate and myogenesis during skeletal muscle repair

Quétin, M. (2019) · doi:10.70675/b9963449z4ba2z4f62z9991z66974e549c9c

Effets combinés de stratégies thérapeutiques et d'un entraînement en endurance sur la fonction musculaire et le métabolisme énergétique chez le modèle murin Townes de la drépanocytose

Michel, C. P. (2022) · doi:10.70675/a23402d9z6576z4a4ez84eczba2d94df994d

Caractérisation des mécanismes impliqués dans le développement des lésions musculaires après exposition aux rayonnements ionisants et mise en place de contre-mesures thérapeutiques sur modèles rongeurs

Graziosi, E. R. (2023) · doi:10.70675/dcd86f4bz9715z436fza2c3z2bedaebaede6

Muscle Stem Cells and Regenerative Myogenesis

McKinnell, I. W., Parise, G., & Rudnicki, M. A. (2005) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(05)71004-8 · Cited by 31 · see citing works

Adult Skeletal Muscle Stem Cells

Sambasivan, R., & Tajbakhsh, S. (2014) · Results and problems in cell differentiation · doi:10.1007/978-3-662-44608-9_9 · Cited by 68 · see citing works

Adult skeletal muscle growth and regeneration: The development and differentiation of myogenic stem cells

Seale, P., & Rudnicki, M. A. (2002) · Advances in cell aging and gerontology · doi:10.1016/s1566-3124(02)09048-x · Cited by 2 · see citing works

A New Look at the Origin, Function, and “Stem-Cell” Status of Muscle Satellite Cells

Seale, P., & Rudnicki, M. A. (2000) · Developmental Biology · doi:10.1006/dbio.1999.9565 · Cited by 590 · see citing works

Adult stem cells derived from skeletal muscle — biology and potential

Danišovič, Ľ., Polák, Š., & Vojtaššák, J. (2013) · Open Life Sciences · doi:10.2478/s11535-013-0137-x · Cited by 1 · see citing works