The DOI matches its Crossref record; 297 of the 299 references it cites were found in a registry or an index.
Control of satellite cell function in muscle regeneration and its disruption in ageing
Abstract
Skeletal muscle contains a designated population of adult stem cells, called satellite cells, which are generally quiescent. In homeostasis, satellite cells proliferate only sporadically and usually by asymmetric cell division to replace myofibres damaged by daily activity and maintain the stem cell pool. However, satellite cells can also be robustly activated upon tissue injury, after which they undergo symmetric divisions to generate new stem cells and numerous proliferating myoblasts that later differentiate to muscle cells (myocytes) to rebuild the muscle fibre, thereby supporting skeletal muscle regeneration. Recent discoveries show that satellite cells have a great degree of population heterogeneity, and that their cell fate choices during the regeneration process are dictated by both intrinsic and extrinsic mechanisms. Extrinsic cues come largely from communication with the numerous distinct stromal cell types in their niche, creating a dynamically interactive microenvironment. This Review discusses the role and regulation of satellite cells in skeletal muscle homeostasis and regeneration. In particular, we highlight the cell-intrinsic control of quiescence versus activation, the importance of satellite cell-niche communication, and deregulation of these mechanisms associated with ageing. The increasing understanding of how satellite cells are regulated will help to advance muscle regeneration and rejuvenation therapies.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Tissue regeneration requires coordination between resident stem cells and local niche cells1,2.”
From Senescence atlas reveals an aged-like inflamed niche that blunts muscle regeneration (2023) · cites this paper as [2]
Citations
Cites
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
Embryonic Stem Cell Lines Derived from Human Blastocysts
Thomson, J. A., Itskovitz‐Eldor, J., Shapiro, S. S., Waknitz, M. A., Swiergiel, J. J., Marshall, V. S., & Jones, J. M. (1998) · Science · doi:10.1126/science.282.5391.1145 · Cited by 15,947
Matrix elasticity directs stem cell lineage specification
Engler, A. J., Sen, S., Sweeney, H. L., & Discher, D. E. (2006) · Cell · doi:10.1016/j.cell.2006.06.044 · Cited by 13,915
Chronic Inflammation (Inflammaging) and Its Potential Contribution to Age-Associated Diseases
Franceschi, C., & Campisi, J. (2014) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/glu057 · Cited by 3,891
Rapamycin fed late in life extends lifespan in genetically heterogeneous mice
Harrison, D. E., Strong, R., Sharp, Z. D., Nelson, J. F., Astle, C. M., Flurkey, K., Nadon, N. L., Wilkinson, J. E., Frenkel, K., Carter, C. S., et al. (2009) · Nature · doi:10.1038/nature08221 · Cited by 3,766
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
The role of microRNA-1 and microRNA-133 in skeletal muscle proliferation and differentiation
Chen, J., Mandel, E. M., Thomson, J. M., Wu, Q., Callis, T. E., Hammond, S. M., Conlon, F. L., & Wang, D.-Z. (2005) · Nature Genetics · doi:10.1038/ng1725 · Cited by 2,807
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
Satellite Cells and the Muscle Stem Cell Niche
Yin, H., Price, F., & Rudnicki, M. A. (2013) · Physiological Reviews · doi:10.1152/physrev.00043.2011 · Cited by 2,166
Arnold, L., Henry, A., Poron, F., Baba-Amer, Y., van Rooijen, N., Plonquet, A., Gherardi, R. K., & Chazaud, B. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20070075 · Cited by 2,002
Cited by
Sorted by citations
Items 401–480 of 480
Southerland, K. W., Xu, Y., Peters, D. T., Lin, X., Wei, X., Xiang, Y., Fei, K., Olivere, L. A., Morowitz, J. M., Otto, J. C., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26638311
Southerland, K. W., Xu, Y., Peters, D., Lin, X., Wei, X., Xiang, Y., Fei, K., Olivere, L. A., Morowitz, J. M., Otto, J. C., et al. (2024) · Figshare · doi:10.6084/m9.figshare.24547047
Florczyk, U., Polak, K., Jelínková, Š., Bronisz-Budzyńska, I., Sabo, R., Bolisetty, S., Agarwal, A., Werner, E., Józkowicz, A., Stępniewski, J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26732860
Florczyk, U., Polak, K., Jelínková, Š., Bronisz-Budzyńska, I., Sabo, R., Bolisetty, S., Agarwal, A., Werner, E., Józkowicz, A., Stępniewski, J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26027675
Southerland, K. W., Xu, Y., Peters, D. T., Lin, X., Wei, X., Xiang, Y., Fei, K., Olivere, L. A., Morowitz, J. M., Otto, J. C., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26638314
Chen, Q., He, S., Xue, X., Zhang, W., Li, H., He, X., Pu, Y., Yue-hui, M., Jiang, L., Zhao, Y., et al. (2025) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.5c09967
Wu, X., Chen, M., Fan, R., Wang, H., Ma, R., Tang, X., Wang, H., Wei, W., Wong, J., Xu, G., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2025.12.26.696560
Yokoyama, S., Kido, T., Yoneda, M., Springer, D., Awasthi, P. P., Chari, R., Patterson, A. D., & Kimura, S. (2025) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-025-06045-5 · Cited by 1
IGF-1 regulates PEAR1 through Egr1 to promote skeletal muscle post-injury regeneration
Wang, J., Li, Y., Zhang, Y., Zhao, Y., Tong, H., & Li, S. (2026) · Developmental Biology · doi:10.1016/j.ydbio.2026.01.003
No evidence of the presence of dystrophin protein in rodent muscle stem cellsPreprint
Matouk, M., Morin, A., Royer, L., Macaux, G., Gaci, A., Jobart‐Malfait, A., Evano, B., Sarde, L., Stantzou, A., Petkova, M. V., et al. (2026) · Research Square · doi:10.21203/rs.3.rs-7997649/v1
Simultaneous improvement of breast muscle yield and meat quality in Langshan chickens
Chen, J., Zhang, X., Zhang, L., Xing, T., Gao, F., & Zhao, L. (2026) · Poultry Science · doi:10.1016/j.psj.2026.106552
NRMLncR, a myocyte-enriched long non-coding RNA, enhances myogenesis in mousePreprint
Li, Y., Zhou, Y., Li, Q. Y., Arrington, J. V., Abdelhai, M. F., Wang, Y., Ren, J., Cheng, Y.-Y., Xie, M., Tao, W. A., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.02.11.704964
Gilad, N., Darlyuk‐Saadon, I., Mohanam, M. P., & Engelberg, D. (2026) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2026.111338
Wang, Y., Li, H., Li, Y., Kong, W., & Li, Y. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27062677
Cho, S., Lee, Y., Hwang, Y. H., Goo, J., Han, J., Woo, J., Nam, G., Jeong, C., Kim, I., & Kim, I.-S. (2026) · Journal of Controlled Release · doi:10.1016/j.jconrel.2026.114862
Tumors mimic the niche to inhibit neighboring stem cell differentiationPreprint
Zhang, Y., Wang, Y., Song, J., Yan, L., Wang, Z., Song, D., Wang, H., Yang, S., Niu, L., Sun, C., et al. (2026) · eLife · doi:10.7554/elife.108910.2
A decline in skeletal muscle NOX4 abrogates adaptive homeostasis and exacerbates ageingPreprint
Xirouchaki, C. E., Coughlan, E., García-Domínguez, E., Giri, S., McGrath, M. J., Wiede, F., Sadoshima, J., Roman, W., Gomez-Cabrera, M. C., Philp, A., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.03.27.714615
Murakami, R., Tabuchi, A., Kobayashi, T., Yagishita, K., Hoshino, D., Poole, D. C., & Kano, Y. (2026) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00115.2026 · Cited by 2
Mallard, J. (2022) · theses.fr (ABES) · doi:10.70675/f8b2c96bzc4cdz4249z8e59z5f87c7ca2462
Rôle de Srf dans le contrôle de la fusion des myoblastes
Kobon, K. (2022) · theses.fr (ABES) · doi:10.70675/8b6bc030zd923z447eza0b8z6cdc49037dcd
Dotou, M. (2023) · theses.fr (ABES) · doi:10.70675/ea22a042z96ccz45fdz9667z82a8825cb567
Renalase knockdown inhibits proliferation of mouse satellite cells
Kato, Y., Tokinoya, K., Aoki, K., & Takekoshi, K. (2026) · Molecular Biology Reports · doi:10.1007/s11033-026-11803-0
Pan, R.-R., Tang, R.-X., Qian, Z.-F., & Gong, J.-Y. (2026) · Current Medical Science · doi:10.1007/s11596-026-00193-w
Stewart, M., Hu, L.-Y., Loomis, T., Brashear, S. E., Torre, L. D. L., Sulthan, A. M., Villalba, M., Davids, J. R., Wang, Y. J., Kulkarni, V., et al. (2026) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00808.2025
Chatterjee, N., Pandita, U., & Misra, S. K. (2026) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.5c02171
Tang, W., Lin, B., Jin, M., Liu, T., Zhou, J., Jin, Y., Chen, Y., Zhu, Y., Liu, G., Hu, P., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-72824-8
Rewiring the repair niche for therapeutic skeletal muscle regeneration
Huang, K., Liu, W., Peng, C., Wan, R., Luo, W., Qin, Z., Chen, C. Y., & Luo, Z. (2026) · Genes & Diseases · doi:10.1016/j.gendis.2026.102238
TDP-43 sustains satellite cells to maintain and regenerate skeletal muscle
Ewachiw, T. E., Vallery, T. K., Dhar, S., Clarkson, H., Elston, T. L., Gay, H., & Olwin, B. B. (2026) · Stem Cell Reports · doi:10.1016/j.stemcr.2026.103050
Mazzola, G., Alalwan, T. A., Rondanelli, M., & Perna, S. (2026) · Experimental Gerontology · doi:10.1016/j.exger.2026.113178
Yu, Y., He, Y., Wang, Y., Wu, C., Zhou, R., Chen, F., & Ma, W. (2026) · The FASEB Journal · doi:10.1096/fj.202601360r
Hansson, K. (2026) · The Journal of Physiology · doi:10.1113/jp291492
Song, G., Cong, W., Lu, H., Wang, J., Wang, Y., Zhao, Y., Wang, S., Zhu, S., Midgley, A. C., Li, W., et al. (2026) · Bioactive Materials · doi:10.1016/j.bioactmat.2026.05.002
Chen, C. J., Mulat, Y., Jiang, D., & Lin, H. (2026) · iScience · doi:10.1016/j.isci.2026.116296
Caloric restriction rejuvenates aged adult stem cells: From mechanisms to interventions
Chai, Y., Liu, X., Bi, J., Zeng, J., Yao, M., Shi, F., & Xu, S. (2026) · Ageing Research Reviews · doi:10.1016/j.arr.2026.103204
Cornish, S. M., & Peralta-Huertas, J. (2026) · Biomolecules · doi:10.3390/biom16060850 · Cited by 1
Kawaminami, M., Kimoto, S., Yamamoto, H., & Hasegawa, Y. (2026) · Biogerontology · doi:10.1007/s10522-026-10459-4
Cell-type resolved transcriptional network analysis of in vivo cellular senescence following injury
Sabalic, A., Moiseeva, V., Cisneros, A., Deryagin, O., Perdiguero, E., Muñoz‐Cánoves, P., & García‐Ojalvo, J. (2026) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1014429 · Cited by 1
Self-citationChREBP Is Dispensable for Myofiber Type Switch but Promotes Skeletal Muscle Regeneration
Lu, J., Chen, J., Zhang, G., Ma, H., Sun, P., Wang, C., Yu, X., Feng, K., Wang, C., Hu, C., et al. (2026) · Nutrients · doi:10.3390/nu18122012
A Myocyte‐Enriched Long Non‐Coding RNA NRMLncR Enhances Myogenesis in Mouse
Li, Y., Zhou, Y., L.I., Q., Arrington, J., Hu, Z., Abdelhai, M. F., Wang, Y., Ren, J., Cheng, Y.-Y., Xie, M., et al. (2026) · The FASEB Journal · doi:10.1096/fj.202601027r
Nanotechnological Strategies to Promote Skeletal Muscle Regeneration in Aging
Carton, F., & Malatesta, M. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27146167
Exercise-induced mitochondrial remodeling in energy-demanding organs during aging
Zhou, Z., Gao, J., Wang, M., & Zhang, H. (2026) · iScience · doi:10.1016/j.isci.2026.116791 · Cited by 1
Muscle satellite cells and aging
Johnson, A., Bevington, R. T., Rumelski, S., Kassamali, N., & Parise, G. (2026) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00232.2026
He, L., Qiang, S. U. N., Qiao, Y., Wang, Z., Zhou, Q., Han, L., Wu, Z., Sun, H., & Wang, H. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.07.13.738242
Impaired Myogenic Differentiation Is a Shared Feature Across Genetic Myopathies
Soule, T., Slavin, M. B., Pontifex, C. S., Dabaja, M. Z., Melnyk, A., Dufour, A., Dumont, N. A., Shutt, T. E., & Pfeffer, G. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27146338
Zushi, K., Seki, M., Mizuochi, R., Shitamitsu, K., Elgaabari, A., Tanaka, S., Miyamoto, J., Mizoguchi, K., Fujimaru, R., Han, J., et al. (2026) · Scientific Reports · doi:10.1038/s41598-026-60835-w
Wang, X., Wang, Y., Yuan, R., Smith, G. R., Ruf-Zamojski, F. M., Homma, S. T., Sealfon, S. C., & Zhou, L. (2026) · iScience · doi:10.1016/j.isci.2026.116933
Toward an Integrated Strategy for Volumetric Muscle Loss Regeneration
Dcosta, C., Zhang, K. L., Duazo, M., Grubišić, V., Hamzah, R. N., & Alghazali, K. M. (2026) · Journal of Clinical Medicine · doi:10.3390/jcm15155901
Jaklin, F. J., Keller, L., Spittler, A., Reissig, L., & Aszmann, O. C. (2026) · Annals of Anatomy - Anatomischer Anzeiger · doi:10.1016/j.aanat.2026.153348
NSUN2 suppresses ferroptosis via the KLF4/GPX4 axis to preserve stem cells and tissues
Zhan, Y., Deng, B., Zeng, X., Guo, Y., Xie, M., Tang, C., Li, Y., Tian, Y., Huang, L., Yang, Z., et al. (2026) · Redox Biology · doi:10.1016/j.redox.2026.104323
TRF2 couples muscle stem cell identity to regenerative repair
Lee, J., Nakka, K. K., Calhoun, R. P., Hachmer, S., Gupta, A., Arezza, E., Megeney, L. A., Seale, P., Greenberg, R. A., Dilworth, F. J., et al. (2026) · Science Advances · doi:10.1126/sciadv.aei7316
Loss of TDP-43 drives premature aging and impairs skeletal muscle stem cell pool restorationPreprint
Pikatza‐Menoio, O., Sutcu, H. H., Rodríguez-Hidalgo, M., Elicegui, A., Vidal-Gil, A., Levchuk, M., Hernandez-Montalvo, N., Moreno‐Martínez, L., Armas, J. M. B., Osta, R., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.08.02.742226
Xu, H., Zhang, X., Zhang, Y., Zhao, M., Li, X., & Choi, S. H. (2026) · Animals · doi:10.3390/ani16162564
Niche-dependent immunometabolic regulation of tissue repair and regeneration
Xie, X., Zeng, L., Chi, Z., & Wang, D. (2026) · Immunity & Inflammation · doi:10.1007/s44466-026-00052-2
Godlewski, A., Wróblewski, M., Kuk, J., Moritz, M., Dobrak, F., Kołodziejska, R., & Woźniak, A. (2026) · Genes · doi:10.3390/genes17080964
Aging-, obesity-, and diabetes-related sarcopenia: Pathogenesis and interventions
Han, S., Xiong, Q., 吴庆前, Han, C., Zhang, Y., Zou, J., Guo, R., Gao, Y., & Meng, Z.-X. (2026) · Chinese Medical Journal · doi:10.1097/cm9.0000000000004152
Li, Z., Li, J., Zhu, X., Qin, G., Zheng, Y., Chen, L., Duan, R., & Shi, H. (2026) · Ageing Research Reviews · doi:10.1016/j.arr.2026.103316
Kim, I., Song, Y., Choo, S., & Lee, S. S. (2026) · Ageing Research Reviews · doi:10.1016/j.arr.2026.103320
Fu, S., Meng, Y., Liang, K., & Feng, M. (2026) · Biomolecules · doi:10.3390/biom16091238
Barrera, V., Trevino, J. H., Denton, T. T., Rasmussen, B. B., Rathbone, C. R., Ortiz, Y. S., Porras, M. A. G., & Giambini, H. (2026) · Journal of Orthopaedic Research® · doi:10.1002/jor.70269
DPF3a couples H3K36me2-dependent chromatin remodeling to genome architecture during myogenesisPreprint
Yu, M., Xue, J., Zhang, Q., Pan, Y., Hao, M., Hu, M., Liu, M., Feng, Y., Yao, Y., Peng, M., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.08.25.746968
Tang, T., Zhou, J., Jia, X., Shao, J., Wang, M., Xia, S., Chen, S., Sun, W., Wang, J., & Lai, S. (2026) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2026.1926968
Woven dECM yarn scaffolds enable volumetric muscle loss regeneration via immunomodulation
Song, G., Cong, W., Lu, H., Wang, Y., Zhao, Y., Wang, S., Zhu, S., Fan, M., Kong, D., Wang, K., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-77032-y
Closing the gap in aging science: unlocking the potential of nanoparticles in senescence therapy
Kanbur, E., & Aydin, Ö. F. (2026) · Biogerontology · doi:10.1007/s10522-026-10489-y
The ageing microenvironment in sarcopenia: early alterations and targeted therapeutic strategies
Zhang, L., Li, G., Long, L., Pan, L., Bai, Y., Ni, L., Han, L., & Cao, R. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1929891
Sen, A., Baris, O. R., Schaumkessel, Y., Kallabis, S., Gabillard-Lefort, C., Desquiret‐Dumas, V., Wiesner, R. J., & Pla‐Martín, D. (2026) · Cell Reports · doi:10.1016/j.celrep.2026.117979
Li, T., Guo, T., Wang, P., Zhi, Z., Cao, Y., Cui, M., & Zhang, J. (2026) · Poultry Science · doi:10.1016/j.psj.2026.107762
Myogenic Fusogen‐Engineered Lipid Nanoparticles Enhance mRNA Delivery in Skeletal Muscle
Zhang, F., Xu, Z., Duan, Y., Sun, Y., Wu, S., Long, T., Durbacz, M. Z., Zhang, L., Xiao, Y., Pien, Y.-C., et al. (2026) · Advanced Functional Materials · doi:10.1002/adfm.78165
Saisomboon, S., Vaeteewoottacharn, K., Settha, N., Pattanachot, J., Thanan, R., Leelavatcharamas, V., Petsong, K., Patramanon, R., Chaoruangrit, A., & Boonmars, T. (2026) · Veterinary World · doi:10.14202/vetworld.2026.4025-4041
Xie, W., Tian, Y., Jia, X., Du, W., Gao, C., Lei, Y., Yang, L., Wang, K., Sun, G., Kang, X., et al. (2026) · Poultry Science · doi:10.1016/j.psj.2026.107856
Lee, E. J., Ahmad, K., Shaikh, S., Lim, J. H., Ahmad, S. S., Seo, M., & Choi, I. (2026) · Food Science of Animal Resources · doi:10.1007/s44463-026-00108-2
Carbon dots in tissue repair: from cell behavior to microenvironment remodeling
Li, X., Luo, J., & Li, S. (2026) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2026.1912437
Παπανικολάου, Κ., Jamurtas, A. Z., Draganidis, D., Baloyiannis, I., Poulios, A., Rosvoglou, A., Papadopoulos, C., Papadimas, G., Chrysanthou‐Piterou, M., Havaki, S., et al. (2026) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2026.10.010
Lu, Z., Sheng, R., Backman, L. J., Liu, C., Zheng, D., Zhang, W., & Chen, J. (2026) · BMEMat · doi:10.1002/bmm2.70139
Liu, J., Liu, Y., Sun, X., Zhang, X., Xing, T., Zhang, L., Gao, F., & Zhao, L. (2026) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2026.154869
Skeletal Muscle Aging Is a Significant Contributor to Systemic Aging
Li, M.-M., Liu, X., Li, Y., Li, H., Wang, Y., Qiu, K., & Kong, W. (2026) · Biomolecules · doi:10.3390/biom16101527
Cell Transplantation for Skeletal Muscle Regeneration: Current Strategies and Clinical Translation
Cinemre, D. A., Cinemre, G. C., Rozmukhamedova, S., Arunchander, T., Gharaibeh, B., & Deasy, B. M. (2026) · IntechOpen eBooks · doi:10.5772/intechopen.1016937
Hideaki, S. A. T. O., Tatsukawa, T., Nakajima, K., Watanabe, Y., Sakuma, H., Kobayashi, Y., Sakurai, Y., Tokuno, S., Minami, Y., Inoue, Y., et al. (2026) · Research Square · doi:10.21203/rs.3.rs-10338126/v1
Liao, Z., Liao, Z., & Xiao, M. (2026) · Research Square · doi:10.21203/rs.3.rs-11180171/v1
Human muscle-on-a-chip platforms for disease modeling and drug screening
Tensfeldt, A., Harriot, A. D., Ward, C. W., & Kim, D.-H. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-16110-0.00012-1
Mechanical memory in aging: From adaptive sensing to pathological entrenchment
Huang, M., Ma, X., Gao, R., Miao, Q., Wang, G., Liu, Z., Wang, K., & Luo, M. B. (2026) · Interdisciplinary medicine · doi:10.1002/inmd.70180
Metadata
- Authors
- Sousa-Victor, P., García-Prat, L., & Muñoz-Cánoves, P.
- ORCID
- Muñoz-Cánoves, Pura
- Venue
- Nature Reviews Molecular Cell Biology
- Published
- 2021-10-18
- Volume
- 23
- Issue
- 3
- Pages
- 204-226
- ISSN
- 1471-0072 (ISSN-L)
- 1471-0080
- OpenAlex
- W3205354997
- Cited by
- 476
- References
- 299
- Citations by year
- 2026: 107 · 2025: 126 · 2024: 118 · 2023: 78 · 2022: 45 · 2021: 2
- FWCI
- 6.48
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Nature Reviews Molecular Cell Biology (publishedVersion)
- PubMed (publishedVersion)
- Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT) (submittedVersion)
- Funders
- Canadian Institutes of Health Research (201910MFE-430959-284655)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Congenital heart defects research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Mesenchymal stem cell research
- Keywords
- satellite cells, skeletal muscle regeneration, muscle aging, muscle stem cells, quiescence, cell activation, asymmetric cell division, symmetric cell division, myogenesis, stem cell niche, niche microenvironment, stromal cells, muscle homeostasis, cell-intrinsic regulation
- MeSH terms
- Cell Differentiation, Stem Cells, Muscle, Skeletal, Satellite Cells, Skeletal Muscle
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review