Self-renewal and expansion of single transplanted muscle stem cells

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

Cellular and Molecular Regulation of Muscle Regeneration

CHARGÉ, S. B. P., & Rudnicki, M. A. (2004) · Physiological Reviews · doi:10.1152/physrev.00019.2003 · Cited by 2,691

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

Long-Term Lymphohematopoietic Reconstitution by a Single CD34-Low/Negative Hematopoietic Stem Cell

Osawa, M., Hanada, K., Hamada, H., & Nakauchi, H. (1996) · Science · doi:10.1126/science.273.5272.242 · Cited by 2,141

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

Stem Cell Function, Self-Renewal, and Behavioral Heterogeneity of Cells from the Adult Muscle Satellite Cell Niche

Collins, C. A., Olsen, I., Zammit, P. S., Heslop, L., Petrie, A., Partridge, T. A., & Morgan, J. E. (2005) · Cell · doi:10.1016/j.cell.2005.05.010 · Cited by 1,445

Direct Isolation of Satellite Cells for Skeletal Muscle Regeneration

Montarras, D., Morgan, J., Collins, C., Relaix, F., Zaffran, S., Cumano, A., Partridge, T., & Buckingham, M. (2005) · Science · doi:10.1126/science.1114758 · Cited by 1,100

Primary mouse myoblast purification, characterization, and transplantation for cell-mediated gene therapy.

Rando, T. A., & Blau, H. M. (1994) · The Journal of Cell Biology · doi:10.1083/jcb.125.6.1275 · Cited by 944

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

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

Isolation of satellite cells and transplantation into mice for lineage tracing in muscle

Feige, P., & Rudnicki, M. A. (2020) · Nature Protocols · doi:10.1038/s41596-019-0278-8 · Cited by 27

Regenerative Strategies for Craniofacial Disorders

Garland, C. B., & Pomerantz, J. H. (2012) · Frontiers in Physiology · doi:10.3389/fphys.2012.00453 · Cited by 28

A discrete ‘early-responder’ stromal-cell subtype orchestrates immunocyte recruitment to injured tissue

Yaghi, O., Hanna, B. S., Langston, P. K., Michelson, D. A., Jayewickreme, T., Marin-Rodero, M., Benoist, C. O., & Mathis, D. J. (2023) · Nature Immunology · doi:10.1038/s41590-023-01669-w · Cited by 25

The satellite cell in skeletal muscle: A story of heterogeneity

Guilhot, C., Catenacci, M., Lofaro, S., & Rudnicki, M. A. (2024) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2024.01.018 · Cited by 27

Single cell dynamics of embryonic muscle progenitor cells in zebrafish

Sharma, P., Ruel, T. D., Kocha, K. M., Liao, S., & Huang, P. (2019) · Development · doi:10.1242/dev.178400 · Cited by 25

Poised Regeneration of Zebrafish Melanocytes Involves Direct Differentiation and Concurrent Replenishment of Tissue-Resident Progenitor Cells

Iyengar, S., Kasheta, M., & Ceol, C. J. (2015) · Developmental Cell · doi:10.1016/j.devcel.2015.04.025 · Cited by 26

Forkhead Box M1 Transcriptionally Regulates the Expression of Long Noncoding RNAs Snhg8 and Gm26917 to Promote Proliferation and Survival of Muscle Satellite Cells

Chen, Z., Bu, N., Qiao, X., Zuo, Z., Shu, Y.-H., Liu, Z., Qian, Z., Chen, J., & Hou, Y. (2018) · Stem Cells · doi:10.1002/stem.2824 · Cited by 27

Communicating breast cancer risk: patient perceptions of provider discussions.

Royak-Schaler, R., Klabunde, C. N., Greene, W. F., Lannin, D. R., DeVellis, B. M., Wilson, K. R., & Cheuvront, B. (2002) · PubMed · Cited by 26

Regulation of Cell Cycle Entry and Exit: A Single Cell Perspective

Coller, H. A. (2019) · Comprehensive physiology · doi:10.1002/cphy.c190014 · Cited by 33

Harnessing Sphingosine-1-Phosphate Signaling and Nanotopographical Cues To Regulate Skeletal Muscle Maturation and Vascularization

Tsui, J. H., Janebodin, K., Ieronimakis, N. M., Yama, D. M. P., Yang, H. S., Chavanachat, R., Hays, A. L., Lee, H., Reyes, M., & Kim, D. (2017) · ACS Nano · doi:10.1021/acsnano.7b00186 · Cited by 26

Muscle Stem Cells Give Rise to Rhabdomyosarcomas in a Severe Mouse Model of Duchenne Muscular Dystrophy

Sesillo, F. B., Fox, D. J., & Sacco, A. (2019) · Cell Reports · doi:10.1016/j.celrep.2018.12.089 · Cited by 26

Ex Vivo Gene Editing of the Dystrophin Gene in Muscle Stem Cells Mediated by Peptide Nucleic Acid Single Stranded Oligodeoxynucleotides Induces Stable Expression of Dystrophin in a Mouse Model for Duchenne Muscular Dystrophy

Nik‐Ahd, F., & Bertoni, C. (2014) · Stem Cells · doi:10.1002/stem.1668 · Cited by 26

Three-dimensional porous scaffold allows long-term wild-type cell delivery in dystrophic muscle

Carnio, S., Serena, E., Rossi, C. A., Coppi, P. D., Elvassore, N., & Vitiello, L. (2010) · Journal of Tissue Engineering and Regenerative Medicine · doi:10.1002/term.282 · Cited by 26

Secreted protein acidic and rich in cysteine internalization and its age‐related alterations in skeletal muscle progenitor cells

Nakamura, K., Yamanouchi, K., & Nishihara, M. (2013) · Aging Cell · doi:10.1111/acel.12168 · Cited by 26

Applicability of Adipose-Derived Stem Cells in Type 1 Diabetes Mellitus

Lin, H.-P., Chan, T.-M., Fu, R., Chuu, C., Chiu, S., Tseng, Y.-H., Liu, S., Lai, K., Shih, M., Lin, Z.-S., et al. (2015) · Cell Transplantation · doi:10.3727/096368915x686977 · Cited by 26

Slow-dividing satellite cells retain long-term self-renewal ability in adult muscle

Ono, Y., Masuda, S., Nam, H.-S., Benezra, R., Miyagoe‐Suzuki, Y., & Takeda, S. (2012) · Development · doi:10.1242/dev.080978 · Cited by 26

Skeletal muscle cell transplantation: models and methods

Mueller, A. L., & Bloch, R. J. (2019) · Journal of Muscle Research and Cell Motility · doi:10.1007/s10974-019-09550-w · Cited by 25

A novel lncRNA promotes myogenesis of bovine skeletal muscle satellite cells via PFN1‐RhoA/Rac1

Chen, M., Zhang, L., Guo, Y., Liu, X., Song, Y., Li, X., Ding, X., & Guo, H. (2021) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.16427 · Cited by 25

Tubastatin A maintains adult skeletal muscle stem cells in a quiescent state ex vivo and improves their engraftment ability in vivo

Arjona, M., Goshayeshi, A., Rodríguez-Mateo, C., Brett, J. O., Both, P., Ishak, H. D., & Rando, T. A. (2022) · Stem Cell Reports · doi:10.1016/j.stemcr.2021.11.012 · Cited by 25

Stem cell maintenance by manipulating signaling pathways: past, current and future

Chen, X. X., Ye, S., & Ying, Q. (2015) · BMB Reports · doi:10.5483/bmbrep.2015.48.12.215 · Cited by 25

Essential Role for p38α MAPK But Not p38γ MAPK in Igf2 Expression and Myoblast Differentiation

Lovett, F. A., Cosgrove, R. A., Gonzalez, I., & Pell, J. M. (2010) · Endocrinology · doi:10.1210/en.2010-0209 · Cited by 25

A myogenic precursor cell that could contribute to regeneration in zebrafish and its similarity to the satellite cell

Siegel, A. L., Gurevich, D., & Currie, P. D. (2013) · FEBS Journal · doi:10.1111/febs.12300 · Cited by 24

Emerging gene editing strategies for Duchenne muscular dystrophy targeting stem cells

Bertoni, C. (2014) · Frontiers in Physiology · doi:10.3389/fphys.2014.00148 · Cited by 24

Enhanced cartilage repair in ‘healer’ mice—New leads in the search for better clinical options for cartilage repair

Fitzgerald, J. (2016) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2016.04.018 · Cited by 24

Isolation of Muscle Stem Cells from Mouse Skeletal Muscle

Gayraud-Morel, B., Pala, F., Sakai, H., & Tajbakhsh, S. (2017) · Methods in molecular biology · doi:10.1007/978-1-4939-6771-1_2 · Cited by 24

Skeletal Muscle-Derived Human Mesenchymal Stem Cells: Influence of Different Culture Conditions on Proliferative and Myogenic Capabilities

Testa, S., Riera, C. S., Fornetti, E., Riccio, F., Fuoco, C., Bernardini, S., Baldi, J., Costantini, M., Foddai, M. L., Cannata, S. M., et al. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.553198 · Cited by 24

Preservation of satellite cell number and regenerative potential with age reveals locomotory muscle bias

Arpke, R. W., Shams, A. S., Collins, B. C., Larson, A. A., Lu, N., Lowe, D. A., & Kyba, M. (2021) · Skeletal Muscle · doi:10.1186/s13395-021-00277-2 · Cited by 25

Fibroblast growth factor 6 regulates sizing of the muscle stem cell pool

Zofkie, W., Southard, S. M., Braun, T. W., & Lepper, C. (2021) · Stem Cell Reports · doi:10.1016/j.stemcr.2021.10.006 · Cited by 27

Tabula Microcebus: A transcriptomic cell atlas of mouse lemur, an emerging primate model organismPreprint

Ezran, C., Liu, S., Chang, S., Ming, J., Botvinnik, O. B., Penland, L., Tarashansky, A. J., de Morrée, A., Travaglini, K. J., Zhao, J., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.12.12.469460 · Cited by 24

Spontaneous In Vivo Differentiation of Embryonic Stem Cell-Derived Pancreatic Endoderm-Like Cells Corrects Hyperglycemia in Diabetic Mice

Raikwar, S. P., & Zavazava, N. (2010) · Transplantation · doi:10.1097/tp.0b013e3181fdd98b · Cited by 23

MiR-27b promotes sheep skeletal muscle satellite cell proliferation by targeting myostatin gene

Zhang, W., Wang, S.-Y., Deng, S., Gao, L., Yang, L., Liu, X., & Guo-qing, S. (2018) · Journal of Genetics · doi:10.1007/s12041-018-0998-5 · Cited by 23

Molecular regulation of satellite cells via intercellular signaling

Yeh, C.-J., Sattler, K. M., & Lepper, C. (2023) · Gene · doi:10.1016/j.gene.2023.147172 · Cited by 26

Erythropoietin signaling promotes transplanted progenitor cell survival

Jia, Y., Warin, R., Yu, X., Epstein, R., & Noguchi, C. T. (2009) · The FASEB Journal · doi:10.1096/fj.09-130237 · Cited by 23

Extrinsic Regulation of Satellite Cell Function and Muscle Regeneration Capacity during Aging

Chakkalakal, J. V. (2012) · Journal of Stem Cell Research & Therapy · doi:10.4172/2157-7633.s11-001 · Cited by 26

Fundamentals of In Situ Tissue Regeneration

Lee, S. J., Yoo, J. J., & Atala, A. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-802225-2.00001-5 · Cited by 23

Mitochondrial fatty acid oxidation regulates adult muscle stem cell function through modulating metabolic flux and protein acetylation

Yue, F., Gu, L., Qiu, J., Oprescu, S. N., Beckett, L. M., Ellis, J. M., Donkin, S. S., & Kuang, S. (2025) · The EMBO Journal · doi:10.1038/s44318-025-00397-1 · Cited by 25

Systemic cell therapy for muscular dystrophies

Ausems, C. R. M., van Engelen, B. G. M., van Bokhoven, H., & Wansink, D. G. (2020) · Stem Cell Reviews and Reports · doi:10.1007/s12015-020-10100-y · Cited by 23

The activation of satellite cells by nanofibrous poly ɛ-caprolacton constructs

Hosseinzadeh, S., Soleimani, M., Rezayat, S. M., Ai, J., & Vasei, M. (2013) · Journal of Biomaterials Applications · doi:10.1177/0885328213481072 · Cited by 22

Restricted Myogenic Potential of Mesenchymal Stromal Cells Isolated from Umbilical Cord

Grabowska, I., Brzóska, E., Gawrysiak, A., Stremińska, W., Moraczewski, J., Polański, Z., Hoser, G., Kawiak, J., Machaj, E. K., Pojda, Z., et al. (2012) · Cell Transplantation · doi:10.3727/096368912x640493 · Cited by 22

A single cell bioengineering approach to elucidate mechanisms of adult stem cell self-renewal

Gilbert, P. M., Corbel, S. Y., Doyonnas, R., Havenstrite, K. L., Magnusson, K. E. G., & Blau, H. M. (2012) · Integrative Biology · doi:10.1039/c2ib00148a · Cited by 22

Biomaterial-Based Regenerative Strategies for Volumetric Muscle Loss: Challenges and Solutions

Cai, C. W., Grey, J. A., Hubmacher, D., & Han, W. M. (2024) · Advances in Wound Care · doi:10.1089/wound.2024.0079 · Cited by 23

Regenerative medicine provides alternative strategies for the treatment of anal incontinence

Gräs, S., Tolstrup, C. K., & Lose, G. (2016) · International Urogynecology Journal · doi:10.1007/s00192-016-3064-y · Cited by 21

Reduced prostaglandin I 2 signaling in Arid5b −/− primary skeletal muscle cells attenuates myogenesis

Murray, J., Whitson, R. H., & Itakura, K. (2017) · The FASEB Journal · doi:10.1096/fj.201700453rr · Cited by 21

Isolation of muscle stem cells from rat skeletal muscles

Sesillo, F. B., Wong, M., Cortez, A., & Alperin, M. (2019) · Stem Cell Research · doi:10.1016/j.scr.2019.101684 · Cited by 21

The chemokine receptor CXCR4 regulates satellite cell activation, early expansion, and self-renewal, in response to skeletal muscle injury

Shams, A. S., Arpke, R. W., Gearhart, M. D., Weiblen, J., Mai, B., Oyler, D., Bosnakovski, D., Mahmoud, O. M., Hassan, G. M., & Kyba, M. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.949532 · Cited by 21

TBP/TFIID-dependent activation of MyoD target genes in skeletal muscle cells

Malecová, B., Dall’Agnese, A., Madaro, L., Gatto, S., Toto, P. C., Albini, S., Ryan, T. L., Tora, L., & Puri, P. (2016) · eLife · doi:10.7554/elife.12534 · Cited by 22

Developmental stage determines efficiency of gene transfer to muscle satellite cells by in utero delivery of adeno-associated virus vector serotype 2/9

Stitelman, D. H., Brazelton, T. R., Bora, A., Traas, J., Merianos, D. J., Limberis, M. P., Davey, M. G., & Flake, A. W. (2014) · Molecular Therapy — Methods & Clinical Development · doi:10.1038/mtm.2014.40 · Cited by 21

Efficient engraftment of pluripotent stem cell-derived myogenic progenitors in a novel immunodeficient mouse model of limb girdle muscular dystrophy 2I

Azzag, K., Ortiz‐Cordero, C., Oliveira, N. A. D. J., Magli, A., Selvaraj, S., Tungtur, S. K., Upchurch, W. J., Iaizzo, P. A., Lu, Q. L., & Perlingeiro, R. C. R. (2020) · Skeletal Muscle · doi:10.1186/s13395-020-00228-3 · Cited by 21

Time- and dose-dependent effects of total-body ionizing radiation on muscle stem cells

Masuda, S., Hisamatsu, T., Seko, D., Urata, Y., Goto, S., Li, T., & Ono, Y. (2015) · Physiological Reports · doi:10.14814/phy2.12377 · Cited by 23

Dissecting cell diversity and connectivity in skeletal muscle for myogenesis

Liu, Y., Wu, B., Gong, L., An, C., Lin, J., Li, Q.-K., Jiang, D., Jin, K., Mechakra, A., Bunpetch, V., et al. (2019) · Cell Death and Disease · doi:10.1038/s41419-019-1647-5 · Cited by 21

Fresh muscle fiber fragments on a scaffold in rats–a new concept in urogynecology?

Boennelycke, M., Christensen, L. H., Nielsen, L. F., Gräs, S., & Lose, G. (2011) · American Journal of Obstetrics and Gynecology · doi:10.1016/j.ajog.2011.04.020 · Cited by 20

Genome Editing and Muscle Stem Cells as a Therapeutic Tool for Muscular Dystrophies

Pini, V., Morgan, J. E., Francesco Muntoni, A., & O’Neill, H. C. (2017) · Current Stem Cell Reports · doi:10.1007/s40778-017-0076-6 · Cited by 20

Establishment of stably expandable induced myogenic stem cells by four transcription factors

Lee, E. H., Kim, M., Kim, Y. D., Chung, M.-J., Elfadl, A. K., Ulah, H. M. A., Park, D., Lee, S., Park, H., Kim, T., et al. (2018) · Cell Death and Disease · doi:10.1038/s41419-018-1114-8 · Cited by 21

Pluripotent stem cell-induced skeletal muscle progenitor cells with givinostat promote myoangiogenesis and restore dystrophin in injured Duchenne dystrophic muscle

Xuan, W., Khan, M., & Ashraf, M. (2021) · Stem Cell Research & Therapy · doi:10.1186/s13287-021-02174-3 · Cited by 20

CRISPR/Cas9 editing of directly reprogrammed myogenic progenitors restores dystrophin expression in a mouse model of muscular dystrophy

Domenig, S. A., Bundschuh, N., Lenardič, A., Ghosh, A., Kim, I., Qabrati, X., D’Hulst, G., & Bar‐Nur, O. (2022) · Stem Cell Reports · doi:10.1016/j.stemcr.2021.12.003 · Cited by 21

Induced Pluripotent Stem Cells for Tissue-Engineered Skeletal Muscles

Zhao, S., Chen, J., Wu, L., Tao, X., Yaqub, N., & Chang, J. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241411520 · Cited by 23

Skeletal Myogenic Potential of Mouse Skin-Derived Precursors

Qiu, Z., Miao, C., Li, J., Lei, X., Liu, S., Guo, W., Cao, Y., & Duan, E. (2009) · Stem Cells and Development · doi:10.1089/scd.2009.0058 · Cited by 20

“Known Unknowns”: Current Questions in Muscle Satellite Cell Biology

Cornelison, D. (2017) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2017.08.006 · Cited by 20

Mechanotransduction, nuclear architecture and epigenetics in Emery Dreifuss Muscular Dystrophy: tous pour un, un pour tous

Bianchi, A., Manti, P. G., Lucini, F., & Lanzuolo, C. (2018) · Nucleus · doi:10.1080/19491034.2018.1460044 · Cited by 22

The Satellite Cell at 60: The Foundation Years

Engquist, E. N., & Zammit, P. S. (2021) · Journal of Neuromuscular Diseases · doi:10.3233/jnd-210705 · Cited by 21

An In Vitro Culture System That Supports Robust Expansion and Maintenance of In Vivo Engraftment Capabilities for Myogenic Progenitor Cells from Adult Mice

Wang, Z., Cheung, D. Y. C., Zhou, Y., Han, C., Fennelly, C., Criswell, T. L., & Söker, S. (2014) · BioResearch open access · doi:10.1089/biores.2014.0007 · Cited by 21

Autologous temporomandibular joint reconstruction independent of exogenous additives: a proof-of-concept study for guided self-generation

Wei, J., Herrler, T., Han, D., Liu, K., Huang, R., Guba, M. O., Dai, C., & Li, Q. (2016) · Scientific Reports · doi:10.1038/srep37904 · Cited by 19

Induction of Skeletal Muscle Progenitors and Stem Cells from human induced Pluripotent Stem Cells

Sato, T. (2020) · Journal of Neuromuscular Diseases · doi:10.3233/jnd-200497 · Cited by 19

Tetraspanin CD82 is necessary for muscle stem cell activation and supports dystrophic muscle function

Hall, A. J., Fontelonga, T. M., Wright, A., Gwilt, K. B., Widrick, J. J., Pasut, A., Villa, F., Miranti, C. K., Gibbs, D. E., Jiang, E., et al. (2020) · Skeletal Muscle · doi:10.1186/s13395-020-00252-3 · Cited by 19

Pax7+ Satellite Cells in Human Skeletal Muscle After Exercise: A Systematic Review and Meta-analysis

Dewi, L., Lin, Y., Nicholls, A., Condello, G., Huang, C., & Kuo, C. (2022) · Sports Medicine · doi:10.1007/s40279-022-01767-z · Cited by 21

Applications of skeletal muscle progenitor cells for neuromuscular diseases.

Hosoyama, T., Dyke, J. V., & Suzuki, M. (2012) · Europe PMC (PubMed Central) · Cited by 19

The clinical relevance of cell‐based therapy for the treatment of stress urinary incontinence

Gräs, S., & Lose, G. (2011) · Acta Obstetricia Et Gynecologica Scandinavica · doi:10.1111/j.1600-0412.2011.01184.x · Cited by 19

Meeting the meat: delineating the molecular machinery of muscle development

Jan, A. T., Lee, E. J., Ahmad, S., & Choi, I. (2016) · Journal of Animal Science and Technology · doi:10.1186/s40781-016-0100-x · Cited by 19

Epigenetic regulation of muscle development

Barreiro, E., & Tajbakhsh, S. (2017) · Journal of Muscle Research and Cell Motility · doi:10.1007/s10974-017-9469-5 · Cited by 19

Protective effect of Rhus coriaria fruit extracts against hydrogen peroxide-induced oxidative stress in muscle progenitors and zebrafish embryos

Najjar, F., Rizk, F., Carnac, G., Nassar, R., Jabak, S., Sobolev, A. P., Saada, Y. B., El-Sabban, M. E., & Hamadé, A. (2017) · PeerJ · doi:10.7717/peerj.4144 · Cited by 19

Potential Therapies Using Myogenic Stem Cells Combined with Bio-Engineering Approaches for Treatment of Muscular Dystrophies

Motohashi, N., Shimizu‐Motohashi, Y., Roberts, T. C., & Aoki, Y. (2019) · Cells · doi:10.3390/cells8091066 · Cited by 19

Smooth Muscle Differentiation of Penile Stem/Progenitor Cells Induced by Microenergy Acoustic Pulses In Vitro

Peng, D., Yuan, H., Liu, T., Wang, T., Reed‐Maldonado, A. B., Kang, N., Banie, L., Wang, G., Tang, Y., He, L., et al. (2019) · The Journal of Sexual Medicine · doi:10.1016/j.jsxm.2019.08.020 · Cited by 19

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

The Lateral Plate Mesoderm: A Novel Source of Skeletal Muscle

Qin, P., Patel, K., & Huang, R. (2014) · Results and problems in cell differentiation · doi:10.1007/978-3-662-44608-9_7 · Cited by 19

Human fetal skeletal muscle contains a myogenic side population that expresses the melanoma cell-adhesion molecule

Lapan, A. D., Rozkalne, A., & Gussoni, E. (2012) · Human Molecular Genetics · doi:10.1093/hmg/dds196 · Cited by 19

Beyond the bulk: overview and novel insights into the dynamics of muscle satellite cells during muscle regeneration

Byun, W. S., Lee, J., & Baek, J.-H. (2024) · Inflammation and Regeneration · doi:10.1186/s41232-024-00354-1 · Cited by 20

Mitochondrial Dynamics Drive Muscle Stem Cell Progression from Quiescence to Myogenic Differentiation

Sommers, O., Tomsine, R. A., & Khacho, M. (2024) · Cells · doi:10.3390/cells13211773 · Cited by 22

A Long Journey before Cycling: Regulation of Quiescence Exit in Adult Muscle Satellite Cells

Zhou, S., Han, L., & Wu, Z. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23031748 · Cited by 21

PPARγ and MyoD are differentially regulated by myostatin in adipose-derived stem cells and muscle satellite cells

Zhang, F., Deng, B., Wen, J., Chen, K., Liu, W., Ye, S., Huang, H., Jiang, S., & Xiong, Y. (2015) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2015.01.120 · Cited by 18

Muscle Diversity, Heterogeneity, and Gradients: Learning from Sarcoglycanopathies

Riera, C. S., Lozanoska‐Ochser, B., Testa, S., Fornetti, E., Bouché, M., & Madaro, L. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22052502 · Cited by 18

Impact of Stem Cells in Craniofacial Regenerative Medicine

Sanchez-Lara, P. A., Zhao, H., Bajpai, R., Abdelhamid, A. I., & Warburton, D. (2012) · Frontiers in Physiology · doi:10.3389/fphys.2012.00188 · Cited by 17

The Survival of Myoblasts After Intramuscular Transplantation Is Improved When Fewer Cells Are Injected

Pellegrini, K. L., & Beilharz, M. W. (2010) · Transplantation · doi:10.1097/tp.0b013e318208a8c0 · Cited by 17

Characterisation of equine satellite cell transcriptomic profile response to β -hydroxy- β -methylbutyrate (HMB)

Szcześniak, K. A., Ciecierska, A., Ostaszewski, P., & Sadkowski, T. (2016) · British Journal Of Nutrition · doi:10.1017/s000711451600324x · Cited by 17

CCAAT/enhancer binding protein β is required for satellite cell self-renewal

Lala-Tabbert, N., AlSudais, H., Marchildon, F., Fu, D., & Wiper‐Bergeron, N. (2016) · Skeletal Muscle · doi:10.1186/s13395-016-0112-8 · Cited by 17

Human Satellite Cell Isolation and Xenotransplantation

Garcia, S. M., Tamaki, S. J., Xu, X., & Pomerantz, J. H. (2017) · Methods in molecular biology · doi:10.1007/978-1-4939-7283-8_8 · Cited by 17

miR‑217‑5p regulates myogenesis in skeletal muscle stem cells by targeting FGFR2

Zhu, M., Chen, G., Yang, Y., Yang, J., Qin, B., & Gu, L. (2020) · Molecular Medicine Reports · doi:10.3892/mmr.2020.11133 · Cited by 18

Pax3-induced expansion enables the genetic correction of dystrophic satellite cells

Filareto, A., Rinaldi, F., Arpke, R. W., Darabi, R., Belanto, J. J., Toso, E. A., Miller, A. Z., Ervasti, J. M., McIvor, R. S., Kyba, M., et al. (2015) · Skeletal Muscle · doi:10.1186/s13395-015-0061-7 · Cited by 17

Increased Understanding of Stem Cell Behavior in Neurodegenerative and Neuromuscular Disorders by Use of Noninvasive Cell Imaging

Holvoet, B., Waele, L. D., Quattrocelli, M., Gheysens, O. S., Sampaolesi, M., Verfaillie, C. M., & Deroose, C. M. (2016) · Stem Cells International · doi:10.1155/2016/6235687 · Cited by 17

Isolation, Culture, and Immunostaining of Skeletal Muscle Myofibers from Wildtype and Nestin-GFP Mice as a Means to Analyze Satellite Cells

Stuelsatz, P., Keire, P. A., & Yablonka‐Reuveni, Z. (2017) · Methods in molecular biology · doi:10.1007/978-1-4939-6771-1_4 · Cited by 17

Nutritional Regulation of Muscle Stem Cells in Exercise and Disease: The Role of Protein and Amino Acid Dietary Supplementation

Beaudry, K. M., Binet, E. R., Collao, N., & Lisio, M. D. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.915390 · Cited by 16

Ultrasensitive and long-lasting bioluminescence immunoassay for point-of-care viral antigen detection

Kim, S., Cho, G., Lee, J. S., Doshi, K., Gharpure, S., Kim, J., Gwak, J., Hardie, J. M., Kanakasabapathy, M. K., Kandula, H., et al. (2025) · Nature Biomedical Engineering · doi:10.1038/s41551-025-01405-9 · Cited by 17

Stem cell dynamics in muscle regeneration: Insights from live imaging in different animal models

Ratnayake, D., & Currie, P. D. (2017) · BioEssays · doi:10.1002/bies.201700011 · Cited by 16

The effects of microenergy acoustic pulses on animal model of obesity‐associated stress urinary incontinence. Part 2: In situ activation of pelvic floor and urethral striated muscle progenitor cells

Kang, N., Peng, D., Wang, B., Ruan, Y., Zhou, J., Reed‐Maldonado, A. B., Banie, L., Wang, G., Xing, N., Tang, Y., et al. (2019) · Neurourology and Urodynamics · doi:10.1002/nau.24152 · Cited by 16

Human muscle production in vitro from pluripotent stem cells: Basic and clinical applications

Yan, L., Rodríguez‐delaRosa, A., & Pourquié, O. (2021) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2021.04.017 · Cited by 18

Healthy skeletal muscle aging: The role of satellite cells, somatic mutations and exercise

Franco, I., Fernandez‐Gonzalo, R., Vrtačnik, P., Lundberg, T. R., Eriksson, M., & Gustafsson, T. P. (2019) · International review of cytology · doi:10.1016/bs.ircmb.2019.03.003 · Cited by 18

Featured characteristics and pivotal roles of satellite cells in skeletal muscle regeneration

Song, T., & Sadayappan, S. (2019) · Journal of Muscle Research and Cell Motility · doi:10.1007/s10974-019-09553-7 · Cited by 20

Renin angiotensin system-induced muscle wasting: putative mechanisms and implications for clinicians

Afsar, B., Afsar, R. E., Caliskan, Y., Lentine, K. L., & Edwards, J. C. (2025) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-024-05043-8 · Cited by 15

Emerging new tools to study and treat muscle pathologies: genetics and molecular mechanisms underlying skeletal muscle development, regeneration, and disease

Crist, C. G. (2016) · The Journal of Pathology · doi:10.1002/path.4830 · Cited by 15

Bioelectric Properties of Myogenic Progenitor Cells

Fennelly, C., & Söker, S. (2018) · Bioelectricity · doi:10.1089/bioe.2018.0002 · Cited by 14

Sex Hormones and Satellite Cell Regulation in Women

Oxfeldt, M., Dalgaard, L. B., Farup, J., & Hansen, M. (2022) · Translational Sports Medicine · doi:10.1155/2022/9065923 · Cited by 17

Stem Cell Function, Self-Renewal, and Behavioral Heterogeneity of Cells from the Adult Muscle Satellite Cell Niche

Collins, C. A., Olsen, I., Zammit, P. S., Heslop, L., Petrie, A., Partridge, T. A., & Morgan, J. E. (2005) · Cell · doi:10.1016/j.cell.2005.05.010 · Cited by 1,445

An investigation of the stem cell potential of skeletal muscle satellite cells.

Collins, C. A. (2004) · OpenGrey (Institut de l'Information Scientifique et Technique)

Isolation, Culture, Functional Assays, and Immunofluorescence of Myofiber-Associated Satellite Cells

Vogler, T. O., Gadek, K. E., Cadwallader, A. B., Elston, T. L., & Olwin, B. B. (2016) · Methods in molecular biology · doi:10.1007/978-1-4939-3810-0_11 · Cited by 18

Transplantation of muscle stem cells

(2008) · Science-Business eXchange · doi:10.1038/scibx.2008.888

Isolation and clonal analysis of satellite cells from adult rats

Chen, Xiaoping, Liu, Hồng, Wang, Chang-Yong, Guo, Qing, Q., Fan, J., & Ming, M. (2001) · 中国生物医学工程学报：英文版