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

SATELLITE CELL OF SKELETAL MUSCLE FIBERS

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Muscle Regeneration by Bone Marrow-Derived Myogenic Progenitors

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Cellular and Molecular Regulation of Muscle Regeneration

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Pax7 Is Required for the Specification of Myogenic Satellite Cells

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

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Stem Cells

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Myogenic satellite cells: physiology to molecular biology

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Little Evidence for Developmental Plasticity of Adult Hematopoietic Stem Cells

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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

The E2F transcription factor is a cellular target for the RB protein

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Trophic Actions of Bone Marrow-Derived Mesenchymal Stromal Cells for Muscle Repair/Regeneration

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Muscular dystrophies share pathogenetic mechanisms with muscle sarcomas

Fanzani, A., Monti, E., Donato, R., & Sorci, G. (2013) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2013.07.001 · Cited by 29

Regulation of Skeletal Muscle Development and Disease by microRNAs

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ATOH8: a novel marker in human muscle fiber regeneration

Güttsches, A., Balakrishnan-Renuka, A., Kley, R. A., Tegenthoff, M., Brand‐Saberi, B., & Vorgerd, M. (2014) · Histochemistry and Cell Biology · doi:10.1007/s00418-014-1299-6 · Cited by 26

Myofiber Baf60c controls muscle regeneration by modulating Dkk3-mediated paracrine signaling

Xu, J., Li, X., Chen, W., Zhang, Z., Zhou, Y., Gou, Y., Lv, C.-A., Lu, J., Qiu, X., Ma, S., et al. (2023) · The Journal of Experimental Medicine · doi:10.1084/jem.20221123 · Cited by 26

Regulation of gene expression mediating indeterminate muscle growth in teleosts

Ahammad, A. K. S., Md., A., Asakawa, S., Watabe, S., & Kinoshita, S. (2015) · Mechanisms of Development · doi:10.1016/j.mod.2015.02.006 · Cited by 25

Administration of granulocyte colony-stimulating factor facilitates the regenerative process of injured mice skeletal muscle via the activation of Akt/GSK3αβ signals

Naito, T., Goto, K., Morioka, S., Matsuba, Y., Akema, T., Sugiura, T., Ohira, Y., Beppu, M., & Yoshioka, T. (2008) · European Journal of Applied Physiology · doi:10.1007/s00421-008-0946-9 · Cited by 26

Cardiomyopathy induced by T-2 toxin in rats

Jacevic, V. M., Wu, Q., Nepovimová, E., & Kuča, K. (2020) · Food and Chemical Toxicology · doi:10.1016/j.fct.2020.111138 · Cited by 26

Endothelial and Myogenic Differentiation of Hematopoietic Progenitor Cells in Inflammatory Myopathies

Hollemann, D., Budka, H., Löscher, W. N., Yanagida, G., Fischer, M. B., & Wanschitz, J. (2008) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0b013e31817d8064 · Cited by 26

A Novel In Vitro Model for Studying Quiescence and Activation of Primary Isolated Human Myoblasts

Sellathurai, J., Cheedipudi, S. M., Dhawan, J., & Schrøder, H. D. (2013) · PLoS ONE · doi:10.1371/journal.pone.0064067 · Cited by 27

Effect of differentiation on microRNA expression in bovine skeletal muscle satellite cells by deep sequencing

Zhang, W. W., Sun, X. F., Tong, H. L., Wang, Y., Li, S. F., Yan, Y., & Li, G. P. (2016) · Cellular & Molecular Biology Letters · doi:10.1186/s11658-016-0009-x · Cited by 25

Melatonin mediates monochromatic green light-induced satellite cell proliferation and muscle growth in chick embryo

Bai, X., Cao, J., Dong, Y., Wang, Z., & Chen, Y. (2019) · PLoS ONE · doi:10.1371/journal.pone.0216392 · Cited by 27

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

Regulatory role of RNA N6-methyladenosine modifications during skeletal muscle development

Yu, B., Liu, J., Zhang, J., Mu, T., Feng, X., Ma, R., & Gu, Y. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.929183 · Cited by 26

Functional modulation of satellite cells in long‐term denervated human laryngeal muscle

Donghui, C., Shicai, C., Wei, W., Fei, L., Jianjun, J., Gang, C., & Hong-liang, Z. (2009) · The Laryngoscope · doi:10.1002/lary.20796 · 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

Genome-wide identification of enhancers and transcription factors regulating the myogenic differentiation of bovine satellite cells

Lyu, P., Settlage, R. E., & Jiang, H. (2021) · BMC Genomics · doi:10.1186/s12864-021-08224-7 · Cited by 25

Impact of thermal stress during incubation on gene expression in embryonic muscle of Peking ducks (Anasplatyrhynchos domestica)

Liu, H., Liu, J., Yan, X., Li, Q., Zhao, Y., Wang, Y., Zhang, R., Wang, G., Wang, H., Li, X., et al. (2015) · Journal of Thermal Biology · doi:10.1016/j.jtherbio.2015.08.013 · Cited by 24

Stem cell decision making and critical-like exploratory networks

Halley, J. D., Burden, F. R., & Winkler, D. A. (2009) · Stem Cell Research · doi:10.1016/j.scr.2009.03.001 · Cited by 23

A high-content, high-throughput siRNA screen identifies cyclin D2 as a potent regulator of muscle progenitor cell fusion and a target to enhance muscle regeneration

Khanjyan, M. V., Yang, J., Kayalı, R., Caldwell, T. A., & Bertoni, C. (2013) · Human Molecular Genetics · doi:10.1093/hmg/ddt184 · Cited by 26

Muscle Fibre Regeneration in Human Skeletal Muscle Diseases

Karpati, G., & Molnár, M. J. (2008) · Springer eBooks · doi:10.1007/978-1-4020-6768-6_10 · Cited by 24

Muscle as an Endocrine Organ

Legaard, G. E., & Pedersen, B. K. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-814593-7.00013-x · Cited by 24

Beneficial Role of Exercise in the Modulation of mdx Muscle Plastic Remodeling and Oxidative Stress

Frinchi, M., Morici, G., Mudò, G., Bonsignore, M. R., & Liberto, V. D. (2021) · Antioxidants · doi:10.3390/antiox10040558 · Cited by 23

Dystrophin Orchestrates the Epigenetic Profile of Muscle Cells Via miRNAs

Marrone, A. K., & Shcherbata, H. R. (2011) · Frontiers in Genetics · doi:10.3389/fgene.2011.00064 · Cited by 23

A Disintegrin and Metalloprotease 10 (ADAM10) Is Indispensable for Maintenance of the Muscle Satellite Cell Pool

Mizuno, S., Yoda, M., Shimoda, M., Tohmonda, T., Okada, Y., Toyama, Y., Takeda, S., Nakamura, M., Matsumoto, M., & Horiuchi, K. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.653477 · Cited by 24

Expression of the paired box domain Pax7 protein in myogenic cells isolated from the porcine semitendinosus muscle after birth

Patruno, M., Caliaro, F., Martinello, T., & Mascarello, F. (2007) · Tissue and Cell · doi:10.1016/j.tice.2007.08.006 · Cited by 23

Proteome analysis of differentiating human myoblasts by dialysis‐assisted two‐dimensional gel electrophoresis (DAGE)

Gonnet, F., Bouazza, B., Millot, G. A., Ziaei, S., Garcı́a, L., Butler-Browne, G. S., Mouly, V., Tortajada, J., Danos, O., & Svinartchouk, F. (2008) · PROTEOMICS · doi:10.1002/pmic.200700261 · Cited by 23

Biomolecular bases of the senescence process and cancer. A new approach to oncological treatment linked to ageing

Badiola, I., Santaolalla, F., García-Gallastegui, P., del Rey, A. S., Unda, F. J., & Ibarretxe, G. (2015) · Ageing Research Reviews · doi:10.1016/j.arr.2015.03.004 · 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

Required Role of Apoptotic Myogenic Precursors and Toll‐like Receptor Stimulation for the Establishment of Autoimmune Myositis in Experimental Murine Models

Sciorati, C., Monno, A., Ascherman, D. P., Seletti, E., Manfredi, A. A., & Rovere, P. Q. (2014) · Arthritis & Rheumatology · doi:10.1002/art.38985 · Cited by 21

Single-cell RNA Sequencing Reveals Heterogeneity of Cultured Bovine Satellite Cells

Lyu, P., Qi, Y., Tu, Z. J., & Jiang, H. (2021) · Frontiers in Genetics · doi:10.3389/fgene.2021.742077 · Cited by 24

Cilia‐Mediated Insulin/Akt and ST2/JNK Signaling Pathways Regulate the Recovery of Muscle Injury

Yamakawa, D., Tsuboi, J., Kasahara, K., Matsuda, C., Nishimura, Y., Kodama, T., Katayama, N., Watanabe, M., & Inagaki, M. (2022) · Advanced Science · doi:10.1002/advs.202202632 · Cited by 21

The Function and Regulation Mechanism of Non-Coding RNAs in Muscle Development

Yang, Y., Wu, J., Liu, W., Zhao, Y., & Chen, H. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241914534 · Cited by 22

Myoblasts Inhibit Prostate Cancer Growth by Paracrine Secretion of Tumor Necrosis Factor-α

Stölting, M., Ferrari, S. M., Handschin, C., Becskei, A., Provenzano, M., Sulser, T., & Eberli, D. (2012) · The Journal of Urology · doi:10.1016/j.juro.2012.10.071 · Cited by 21

Toxic Injury to Muscle Tissue of Rats Following Acute Oximes Exposure

Jacevic, V. M., Nepovimová, E., & Kuča, K. (2019) · Scientific Reports · doi:10.1038/s41598-018-37837-4 · Cited by 21

Transcriptomic Profile of Primary Culture of Skeletal Muscle Cells Isolated from Semitendinosus Muscle of Beef and Dairy Bulls

Ciecierska, A., Motyl, T., & Sadkowski, T. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21134794 · Cited by 21

Regulating Quiescence: New Insights into Hematopoietic Stem Cell Biology

Passegue, E. A., & Wagers, A. J. (2006) · Developmental Cell · doi:10.1016/j.devcel.2006.03.002 · Cited by 21

Satellite cell count, VO 2max, and p 38 MAPK in inactive to moderately active young men

Macaluso, F., Brooks, N. E., van de Vyver, M., van Tubbergh, K., Niesler, C. U., & Myburgh, K. H. (2011) · Scandinavian Journal of Medicine and Science in Sports · doi:10.1111/j.1600-0838.2011.01389.x · Cited by 21

From skeletal muscle damage and regeneration to the hypertrophy induced by exercise: what is the role of different macrophage subsets?

Minari, A. L. A., & dos Santos, R. V. T. (2021) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00038.2021 · Cited by 21

Aberrant cell cycle reentry in human and experimental inclusion body myositis and polymyositis

Kwon, B., Kumar, P., Lee, H., Zeng, L., Walsh, K. X., Fu, Q., Barakat, A., & Querfurth, H. W. (2014) · Human Molecular Genetics · doi:10.1093/hmg/ddu077 · Cited by 20

A Three-Dimensional Culture Model of Reversibly Quiescent Myogenic Cells

Aguanno, S., Petrelli, C., Siena, S. D., Angelis, L. D., Pellegrini, M., & Naro, F. (2019) · Stem Cells International · doi:10.1155/2019/7548160 · Cited by 19

The Association of Mitochondrial Copy Number With Sarcopenia in Adult Survivors of Childhood Cancer

McCastlain, K., Howell, C. R., Welsh, C. E., Wang, Z., Wilson, C. L., Mulder, H. L., Easton, J. B., Mertens, A. C., Zhang, J., Yasui, Y., et al. (2021) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/djab084 · Cited by 22

TGF-β isoforms inhibit IGF-1-induced migration and regulate terminal differentiation in a cell-specific manner

Schabort, E. J., van der Merwe, M., & Niesler, C. U. (2011) · Journal of Muscle Research and Cell Motility · doi:10.1007/s10974-011-9241-1 · Cited by 20

Avian Satellite Cell Plasticity

Jankowski, M., Mozdziak, P. E., Petitte, J. N., Kulus, M., & Kempisty, B. (2020) · Animals · doi:10.3390/ani10081322 · Cited by 19

Stem cells: a model for screening, discovery and development of drugs

Kitambi, S. S., & Chandrasekar, G. (2011) · Stem Cells and Cloning Advances and Applications · doi:10.2147/sccaa.s16417 · Cited by 19

Satellite cell activation and number following acute and chronic exercise: A mini review

Martin, N. R., & Lewis, M. P. (2012) · Cellular and Molecular Exercise Physiology · doi:10.7457/cmep.v1i1.e3 · Cited by 20

E2F5 and LEK1 Translocation to the nucleus is an early event demarcating myoblast quiescence

Reed, S. A., Ouellette, S. E., Liu, X., Allen, R. E., & Johnson, S. (2007) · Journal of Cellular Biochemistry · doi:10.1002/jcb.21256 · Cited by 20

Cultured meat: advances in stem cell biology, tissue engineering, and bioprocess optimisation for scalable and sustainable production—a review

Kim, S. M., Jeong, Y., Jo, H., Park, Y., & Moon, S. (2025) · International Journal of Food Science & Technology · doi:10.1093/ijfood/vvaf220 · Cited by 17

IGF1 promotes human myotube differentiation toward a mature metabolic and contractile phenotype

Dreher, S. I., Grubba, P., von Toerne, C., Moruzzi, A., Maurer, J. A., Goj, T., Birkenfeld, A. L., Peter, A., Loskill, P., Hauck, S. M., et al. (2024) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00654.2023 · Cited by 20

A latent Axin2+/Scx+ progenitor pool is the central organizer of tendon healing

Grinstein, M., Tsai, S. L., Montoro, D. T., Freedman, B. R., Dingwall, H. L., Villaseñor, S., Zou, K., Sade-Feldman, M., Tanaka, M. J., Mooney, D. J., et al. (2024) · npj Regenerative Medicine · doi:10.1038/s41536-024-00370-2 · Cited by 21

Muscle stem cell activation in a mouse model of rotator cuff injury

Davies, M., Garcia, S. M., Tamaki, S. J., Liu, X., Lee, S., Jose, A., Pomerantz, J. H., & Feeley, B. T. (2017) · Journal of Orthopaedic Research® · doi:10.1002/jor.23679 · Cited by 18

A gene-trap strategy identifies quiescence-induced genes in synchronized myoblasts

Sambasivan, R., Pavlath, G. K., & Dhawan, J. (2008) · Journal of Biosciences · doi:10.1007/s12038-008-0019-6 · Cited by 18

Potential of dietary nitrate in angiogenesis

Rammos, C. (2015) · World Journal of Cardiology · doi:10.4330/wjc.v7.i10.652 · Cited by 17

Ability of stem and progenitor cells in the dental pulp to form hard tissue

Hosoya, A., & Nakamura, H. (2015) · Japanese Dental Science Review · doi:10.1016/j.jdsr.2015.03.002 · Cited by 17

Developmentally regulated alternative splicing is perturbed in type 1 diabetic skeletal muscle

Nutter, C. A., Jaworski, E. A., Verma, S. K., Perez‐Carrasco, Y., & Kuyumcu‐Martinez, M. N. (2017) · Muscle & Nerve · doi:10.1002/mus.25599 · Cited by 17

Nitrite circumvents canonical cGMP signaling to enhance proliferation of myocyte precursor cells

Totzeck, M., Schicho, A., Stock, P., Kelm, M., Rassaf, T., & Hendgen-Cotta, U. B. (2014) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-014-2305-y · Cited by 17

One bout of vibration exercise with vascular occlusion activates satellite cells

Aguayo, D., Mueller, S. M., Boutellier, U., Auer, M., Jung, H. H., Flück, M., & Toigo, M. (2015) · Experimental Physiology · doi:10.1113/ep085330 · Cited by 16

The role of the aging microenvironment on the fate of PDGFRβ lineage cells in skeletal muscle repair

Lu, A., Tseng, C., Guo, P., Gao, Z., Whitney, K. E., Kolonin, M. G., & Huard, J. (2022) · Stem Cell Research & Therapy · doi:10.1186/s13287-022-03072-y · Cited by 16

TIMP2 promotes intramuscular fat deposition by regulating the extracellular matrix in chicken

Cui, H., Luo, N., Guo, L., Lu, L. I. U., Xing, S., Zhao, G., & Wen, J. (2022) · Journal of Integrative Agriculture · doi:10.1016/j.jia.2022.08.071 · Cited by 16

Characterization of in vitro cultured myoblasts isolated from duck (Anas platyrhynchos) embryo

Liu, H., Li, L., Chen, X., Cao, W., Zhang, R., Yu, H., Xu, F., He, H., & Wang, J. (2011) · Cytotechnology · doi:10.1007/s10616-011-9356-7 · Cited by 16

Engineering skeletal muscle - from two to three dimensions

Ngan, C., Quigley, A. F., Kapsa, R. M. I., & Choong, P. (2017) · Journal of Tissue Engineering and Regenerative Medicine · doi:10.1002/term.2265 · Cited by 16

Identification of satellite cells from anole lizard skeletal muscle and demonstration of expanded musculoskeletal potential

Palade, J., Djordjevic, D., Hutchins, E. D., George, R. M., Cornelius, J. A., Rawls, A., Ho, J. W. K., Kusumi, K., & Wilson‐Rawls, J. (2017) · Developmental Biology · doi:10.1016/j.ydbio.2017.08.037 · Cited by 16

Skeletal muscle stem cell characteristics and myonuclei content in patients with rheumatoid arthritis: a cross-sectional study

Boutrup, R. J., Farup, J., Vissing, K., Kjær, M., & Mikkelsen, U. R. (2018) · Rheumatology International · doi:10.1007/s00296-018-4028-y · Cited by 16

Efficacy of methylprednisolone on T-2 toxin-induced cardiotoxicity in vivo: A pathohistological study

Jacevic, V. M., Wu, Q., Nepovimová, E., & Kuča, K. (2019) · Environmental Toxicology and Pharmacology · doi:10.1016/j.etap.2019.103221 · Cited by 17

The metabolic sensor PASK is a histone 3 kinase that also regulates H3K4 methylation by associating with H3K4 MLL2 methyltransferase complex

Karakkat, J. V., Kaimala, S., Sreedharan, S. P., Jayaprakash, P., Adeghate, E. A., Ansari, S. A., Guccione, E., Mensah‐Brown, E. P. K., & Emerald, B. S. (2019) · Nucleic Acids Research · doi:10.1093/nar/gkz786 · Cited by 16

Traction and attraction: haptotaxis substrates collagen and fibronectin interact with chemotaxis by HGF to regulate myoblast migration in a microfluidic device

Roveimiab, Z., Lin, F., & Anderson, J. E. (2020) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00417.2019 · Cited by 16

Satellite cell pool expansion is affected by skeletal muscle characteristics

Macaluso, F., Brooks, N. E., Niesler, C. U., & Myburgh, K. H. (2012) · Muscle & Nerve · doi:10.1002/mus.23721 · Cited by 16

Transthyretin: A Transporter Protein Essential for Proliferation of Myoblast in the Myogenic Program

Lee, E., Pokharel, S., Jan, A. T., Huh, S., Galope, R., Lim, J. H., Lee, D.-M., Choi, S., Nahm, S., Kim, Y., et al. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18010115 · Cited by 16

Bioelectric Properties of Myogenic Progenitor Cells

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

Understanding the relationship between cancer associated cachexia and hypoxia-inducible factor-1

Muthamil, S., Kim, H. Y., Jang, H., Lyu, J., Shin, U. C., Go, Y., Park, S., Lee, H. G., & Park, J. H. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.114802 · Cited by 16

Differential roles of HIC-5 isoforms in the regulation of cell death and myotube formation during myogenesis

Gao, Z., Deblis, R., Glenn, H. L., & Schwartz, L. M. (2007) · Experimental Cell Research · doi:10.1016/j.yexcr.2007.05.023 · Cited by 15

Electric fish: new insights into conserved processes of adult tissue regeneration

Unguez, G. A. (2013) · Journal of Experimental Biology · doi:10.1242/jeb.082396 · Cited by 15

Deiodinases and stem cells: an intimate relationship

Salvatore, D. (2017) · Journal of Endocrinological Investigation · doi:10.1007/s40618-017-0737-4 · Cited by 15

Mathematical Model of Muscle Wasting in Cancer Cachexia

Farhang‐Sardroodi, S., & Wilkie, K. P. (2020) · Journal of Clinical Medicine · doi:10.3390/jcm9072029 · Cited by 16

A molecular imaging analysis of Cx43 association with Cdo during skeletal myoblast differentiation

Nosi, D., Mercatelli, R., Chellini, F., Soria, S., Pini, A., Formigli, L., & Quercioli, F. (2012) · Journal of Biophotonics · doi:10.1002/jbio.201200063 · Cited by 15

Is Postexercise Muscle Soreness a Valid Indicator of Muscular Adaptations?

Schoenfeld, B. J., & Contreras, B. M. (2013) · Strength and conditioning journal · doi:10.1519/ssc.0b013e3182a61820 · Cited by 15

Diminished satellite cell fusion and S6K1 expression in myotubes derived from skeletal muscle of low birth weight neonatal pigs

Chen, Y., Zhu, H., McCauley, S. R., Zhao, L., Johnson, S., Rhoads, R. P., & El‐Kadi, S. W. (2017) · Physiological Reports · doi:10.14814/phy2.13075 · Cited by 18

A single bout of high‐intensity exercise modulates the expression of vitamin D receptor and vitamin D‐metabolising enzymes in horse skeletal muscle

Puangthong, C., Sukhong, P., Saengnual, P., Srikuea, R., & Chanda, M. (2020) · Equine Veterinary Journal · doi:10.1111/evj.13346 · Cited by 15

Myosin heavy chain isoform transitions in canine skeletal muscles during postnatal growth

Štrbenc, M., Smerdu, V., Pogačnik, A., & Fazarinc, G. (2006) · Journal of Anatomy · doi:10.1111/j.1469-7580.2006.00599.x · Cited by 15

Deciphering the miRNA transcriptome of Rongchang pig longissimus dorsi at weaning and slaughter time points

Chen, X., Zhao, C., Dou, M., Sun, Y., Yu, T., Pang, W., & Yang, G. (2020) · Journal of Animal Physiology and Animal Nutrition · doi:10.1111/jpn.13314 · Cited by 14

Mononuclear Cells from Dedifferentiation of Mouse Myotubes Display Remarkable Regenerative Capability

Yang, Z., Liu, Q., Mannix, R. J., Xu, X., Li, H., Ma, Z., Ingber, D. E., Allen, P. D., & Wang, Y. (2014) · Stem Cells · doi:10.1002/stem.1742 · Cited by 14

Bioreactor Systems for Tissue Engineering II

Kasper, C., van Griensven, M., & Pörtner, R. (2010) · Springer eBooks · doi:10.1007/978-3-642-16051-6 · Cited by 15

Satellite Cells: Regenerative Mechanisms and Applicability in Muscular Dystrophy

de Souza, G. T., Zanette, R. D. S. S., do Amaral, D. L. A. S., da Guia, F. C., Maranduba, C. P., de Souza, C. M., Guimarães, E. D. S. G., Rettore, J. V. P., Rabelo, N. C., do Carmo, A. M. R., et al. (2015) · Stem Cells International · doi:10.1155/2015/487467 · Cited by 14

Bioinformatics analysis of differentially expressed genes in rotator cuff tear patients using microarray data

Ren, Y., Duan, Y., Sun, Y., Yang, T., & Tian, M.-Q. (2018) · Journal of Orthopaedic Surgery and Research · doi:10.1186/s13018-018-0989-5 · Cited by 13

The Muscle Satellite Cell: The Story of a Cell on the Edge!

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Roles of the proteasome and inhibitor of DNA binding 1 protein in myoblast differentiation

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