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mTORC1 controls the adaptive transition of quiescent stem cells from G0 to GAlert
Open accessAbstract
A unique property of many adult stem cells is their ability to exist in a non-cycling, quiescent state. Although quiescence serves an essential role in preserving stem cell function until the stem cell is needed in tissue homeostasis or repair, defects in quiescence can lead to an impairment in tissue function. The extent to which stem cells can regulate quiescence is unknown. Here we show that the stem cell quiescent state is composed of two distinct functional phases, G0 and an 'alert' phase we term G(Alert). Stem cells actively and reversibly transition between these phases in response to injury-induced systemic signals. Using genetic mouse models specific to muscle stem cells (or satellite cells), we show that mTORC1 activity is necessary and sufficient for the transition of satellite cells from G0 into G(Alert) and that signalling through the HGF receptor cMet is also necessary. We also identify G0-to-G(Alert) transitions in several populations of quiescent stem cells. Quiescent stem cells that transition into G(Alert) possess enhanced tissue regenerative function. We propose that the transition of quiescent stem cells into G(Alert) functions as an 'alerting' mechanism, an adaptive response that positions stem cells to respond rapidly under conditions of injury and stress, priming them for cell cycle entry.
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“inflammatory initiation of a cell cycle–primed Galert state in HSCs and other cells requires activation of mammalian target of rapamycin (Rodgers et al., 2014).”
From PU.1 enforces quiescence and limits hematopoietic stem cell expansion during inflammatory stress (2021) · cites this paper as Rodgers et al., 2014
Experimental — accuracy not yet measuredIn the citing paper
“Likewise, ‘priming’ of activation by systemic signaling factors has been reported to improve regeneration (Rodgers et al., 2014, 2017).”
From Aging induces aberrant state transition kinetics in murine muscle stem cells (2020) · cites this paper as Rodgers et al., 2014
In the citing paper
“Across all clusters, there were no distinct cell-cycle states observed, consistent with reports of the first division occurring ≥24 hours after our 18 h time point (Gilbert et al., 2010; Rodgers et al., 2014) (Fig. S2D).”
From Aging induces aberrant state transition kinetics in murine muscle stem cells (2020) · cites this paper as Rodgers et al., 2014
In the citing paper
“For instance, although we do not observe bistable transcriptional states between the most-quiescent and most-activated cells in our experiments, stable intermediary activation states might exist in vivo (Rodgers et al., 2014).”
From Aging induces aberrant state transition kinetics in murine muscle stem cells (2020) · cites this paper as Rodgers et al., 2014
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Citations
Cites
Adjusting batch effects in microarray expression data using empirical Bayes methods
Johnson, W. E., Li, C., & Rabinovic, A. (2007) · Biostatistics · doi:10.1093/biostatistics/kxj037 · Cited by 8,658
mTOR Signaling in Growth Control and Disease
Laplante, M., & Sabatini, D. M. (2012) · Cell · doi:10.1016/j.cell.2012.03.017 · Cited by 8,509
KEGG for integration and interpretation of large-scale molecular data sets
Kanehisa, M., Goto, S., Sato, Y., Furumichi, M., & Tanabe, M. (2012) · Nucleic Acids Research · doi:10.1093/nar/gkr988 · Cited by 4,848
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
G 1 Events and Regulation of Cell Proliferation
Pardee, A. B. (1989) · Science · doi:10.1126/science.2683075 · Cited by 2,182
Wilson, A., Laurenti, E., Oser, G., van der Wath, R. C., Blanco-Bose, W., Jaworski, M., Offner, S., Dunant, C. F., Eshkind, L., Bockamp, E., et al. (2008) · Cell · doi:10.1016/j.cell.2008.10.048 · Cited by 1,908
Muscle injury activates resident fibro/adipogenic progenitors that facilitate myogenesis
Joe, A. W. B., Yi, L., Natarajan, A., Le Grand, F., So, L., Wang, J., Rudnicki, M. A., & Rossi, F. M. V. (2010) · Nature Cell Biology · doi:10.1038/ncb2015 · Cited by 1,690
Rainer Breitling, A., Armengaud, P., Anna Amtmann, A., & Herzyk, P. (2004) · FEBS Letters · doi:10.1016/j.febslet.2004.07.055 · Cited by 1,478
Uezumi, A., Fukada, S., Yamamoto, N., Takeda, S., & Tsuchida, K. (2010) · Nature Cell Biology · doi:10.1038/ncb2014 · Cited by 1,315
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Items 501–600 of 774
Rodríguez-Outeiriño, L., Hernández‐Torres, F., de Acuña, F. R., Rastrojo, A., Creus, C., Carvajal, A., Salmerón, L. M., Montolio, M., Soblechero‐Martín, P., Arechavala‐Gomeza, V., et al. (2022) · Molecular Therapy — Nucleic Acids · doi:10.1016/j.omtn.2022.08.025 · Cited by 7
Sequencing Single Cells Reveals Sequential Stem Cell States
Linnarsson, S. (2015) · Cell stem cell · doi:10.1016/j.stem.2015.08.016 · Cited by 7
Identification of quiescent FOXC2+ spermatogonial stem cells in adult mammals
Wang, Z., Jin, C., Li, P., Li, Y., Tang, J., Yu, Z., Jiao, T., Ou, J., Wang, H., Zou, D., et al. (2023) · eLife · doi:10.7554/elife.85380 · Cited by 7
Rossi, A., Coum, A., Madelénat, M., Harris, L., Miedzik, A., Strohbuecker, S., Chai, A., Fiaz, H., Chaouni, R., Faull, P., et al. (2021) · bioRxiv · doi:10.1101/2021.01.06.425462 · Cited by 6
Qiu, L., Yu, P., Li, Q., Wen, C., Wang, H., Zhao, D., Zhang, T., Wang, C., Liu, L., Li, D., et al. (2025) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2025.117737 · Cited by 6
3D Mechanical Confinement Directs Muscle Stem Cell Fate and Function
Park, G., Grey, J. A., Mourkioti, F., & Han, W. M. (2025) · Advanced Biology · doi:10.1002/adbi.202400717 · Cited by 7
Emerging roles of ribosome translation in stem cells and stem cell therapy - a review
Gao, Y., Guo, L., Shi, G., Wang, R., Wang, X., & Lou, J. (2025) · Cell & Bioscience · doi:10.1186/s13578-025-01412-y · Cited by 6
Morizet, D., Foucher, I., Mignerey, I., Alunni, A., & Bally‐Cuif, L. (2025) · Science Advances · doi:10.1126/sciadv.adu3189 · Cited by 8
Xiao, C., & Xiong, J. (2023) · Cell Regeneration · doi:10.1186/s13619-023-00180-9 · Cited by 6
Guan, X., Pan, Z., Li, M., Shen, J.-R., Sun, Y., Yu, C., Fei, Z., Ma, Z., Zhou, J.-W., & Chen, J. (2025) · Future Foods · doi:10.1016/j.fufo.2025.100618 · Cited by 7
Cruz, M. R. D. S., Reinert, T., & Cristofanilli, M. (2017) · Clinical Pharmacology & Therapeutics · doi:10.1002/cpt.965 · Cited by 6
Luo, X., Jean‐Toussaint, R., Tian, Y., Balashov, S. V., Saçan, A., & Ajit, S. K. (2023) · Journal of Pain · doi:10.1016/j.jpain.2023.03.015 · Cited by 7
Werle, S. D., Ikonomi, N., Lausser, L. M., Kestler, A. M. T. U., Weidner, F. M., Schwab, J. D., Maier, J., Buchholz, M., Gress, T. M., Kestler, A. M. R., et al. (2023) · npj Systems Biology and Applications · doi:10.1038/s41540-023-00283-8 · Cited by 6
Dissecting dormancy and quiescence in hematopoietic stem cells
Ibneeva, L., & Grinenko, T. (2024) · Frontiers in Hematology · doi:10.3389/frhem.2024.1401713 · Cited by 7
Lost in Translation: Preserving Satellite Cell Function with Global Translational Control
Eliazer, S., & Brack, A. S. (2016) · Cell stem cell · doi:10.1016/j.stem.2015.12.006 · Cited by 6
Programming and reprogramming the brain: a meeting of minds in neural fate
Götz, M., & Jarriault, S. (2017) · Development · doi:10.1242/dev.150466 · Cited by 8
Methods and sensors for functional genomic studies of cell-cycle transitions in single cells
Zambon, A. C., Hsu, T., Kim, S. E., Klinck, M., Stowe, J. C., Henderson, L. M., Singer, D., Patam, L., Lim, C., McCulloch, A. D., et al. (2020) · Physiological Genomics · doi:10.1152/physiolgenomics.00065.2020 · Cited by 6
MTORC1 and the Rebirth of Stemness
Johnson, N. M., & Lengner, C. J. (2020) · Developmental Cell · doi:10.1016/j.devcel.2020.10.001 · Cited by 6
Meeting Report: Aging Research and Drug Discovery
Meron, E., Thaysen, M., Angeli, S., Antebi, A., Barzilai, N., Baur, J. A., Bekker‐Jensen, S., Birkisdóttir, M. B., Bischof, E. Y., Bruening, J., et al. (2022) · Aging · doi:10.18632/aging.203859 · Cited by 7
Petkov, S., Brenmoehl, J., Langhammer, M., Hoeflich, A., & Röntgen, M. (2022) · Cells · doi:10.3390/cells11061001 · Cited by 6
Extracellular Fluid Flow Induces Shallow Quiescence Through Physical and Biochemical Cues
Liu, B., Wang, X., Jiang, L., Xu, J., Zohar, Y., & Yao, G. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.792719 · Cited by 7
Murtaj, V., Butti, E., Martino, G., & Panina‐Bordignon, P. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1125785 · Cited by 8
Srivastava, S., Gala, H., Mishra, R. K., & Dhawan, J. (2017) · Methods in molecular biology · doi:10.1007/978-1-4939-7371-2_16 · Cited by 6
Yucel, N. D., & Blau, H. M. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-809880-6.00018-7 · Cited by 7
Proteogenomic landscape of gastric adenocarcinoma peritoneal metastases
Zhao, S., Wang, R., Song, S., Hao, D., Han, G., Song, X., Zhang, J., Pizzi, M. P., Shanbhag, N., Futreal, A., et al. (2023) · iScience · doi:10.1016/j.isci.2023.106913 · Cited by 5
Quiescence and aging of melanocyte stem cells and a novel association with programmed death-ligand 1
Palmer, J. W., Villavicencio, K. M., Idris, M. I., Baranyk, I. J., Polycarp, N., Dawson, A. D., Weddle, D., Pavan, W. J., Filipp, F. V., & Harris, M. L. (2024) · iScience · doi:10.1016/j.isci.2024.110908 · Cited by 6
Verkerke, M., Werkman, M. H., & Donega, V. (2025) · Stem Cell Reports · doi:10.1016/j.stemcr.2025.102533 · Cited by 5
Enhancer Rewiring Orchestrates Inflammation and Loss of Cell Identity During Muscle Stem Cell Aging
Shi, C., Yang, N., Pizano, E., Wang, L., Occean, J. R., Cui, C., Liu, L. A., Dunn, C., Boadu, F., Meng, Q., et al. (2025) · Aging Cell · doi:10.1111/acel.70289 · Cited by 6
Local problems need global solutions: The metabolic needs of regenerating organisms
Kübler, I. C., Kretzschmar, J., Brankatschk, M., & Sandoval‐Guzmán, T. (2022) · Wound Repair and Regeneration · doi:10.1111/wrr.13029 · Cited by 5
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Liang, X.-B., Dai, Z.-C., Zou, R., Tang, J., & Yao, C. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241713558 · Cited by 5
mTORC1 pathway activity biases cell fate choice
Wang, Y., Papayova, M., Warren, E., & Pears, C. J. (2024) · Scientific Reports · doi:10.1038/s41598-024-71298-2 · Cited by 6
Heterogeneity of quiescent and active neural stem cells in the postnatal brain
Dimitrakopoulos, D., Kakogiannis, D., & Kazanis, I. (2022) · The International Journal of Developmental Biology · doi:10.1387/ijdb.220010ik · Cited by 5
Ugale, A. S., Shunmugam, D., Pimpale, L. G., Rebhan, E.-M., & Baccarini, M. (2024) · The Journal of Cell Biology · doi:10.1083/jcb.202310137 · Cited by 5
Quiescence-Origin Senescence: A New Paradigm in Cellular Aging
Yao, G. (2024) · Biomedicines · doi:10.3390/biomedicines12081837 · Cited by 6
Rotini, A., Berthier, J., Martínez‐Sarrà, E., Berge, G., Ozturk, T., Koumaiha, Z., Didier, N., Salucci, S., Stettler, O., Gervais, M., et al. (2025) · Developmental Cell · doi:10.1016/j.devcel.2025.07.006 · Cited by 6
MET promotes the proliferation and differentiation of myoblasts
Li, Y., Zhou, H., Chen, Y., Zhong, D., Su, P., Yuan, H., Yang, X., Liao, Z., Qiu, X., Wang, X., et al. (2020) · Experimental Cell Research · doi:10.1016/j.yexcr.2020.111838 · Cited by 5
3022 – CELL SIZE IS A DETERMINANT OF STEM CELL POTENTIAL DURING AGING
Lengefeld, J., & Amon, A. (2021) · Experimental Hematology · doi:10.1016/j.exphem.2021.12.244 · Cited by 4
Feng, R., Wu, S., Li, R., Huang, K.-L., Zeng, T., Zhou, Z., Zhong, X., Songyang, Z., & Liu, F. (2023) · Stem Cells and Development · doi:10.1089/scd.2022.0243 · Cited by 6
Stem cells as a regenerative medicine approach in treatment of microvascular diabetic complications
Poojari, A. S., Wairkar, S., & Kulkarni, Y. A. (2023) · Tissue and Cell · doi:10.1016/j.tice.2023.102225 · Cited by 5
Mechanism of satellite cell regulation by myokines
Furuichi, Y., & FUJII, N. L. (2017) · The Journal of Physical Fitness and Sports Medicine · doi:10.7600/jpfsm.6.311 · Cited by 5
MuSK-BMP signaling in adult muscle stem cells maintains quiescence and regulates myofiber sizePreprint
Madigan, L. A., Jaime, D., Chen, I., & Fallon, J. R. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.05.17.541238 · Cited by 5
Otsuka, T., & Matsui, H. (2025) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2025.112087 · Cited by 6
Metabolic symphony coordinates the muscle regeneration niche
Lu, Y., Chi, Z., & Wang, D. (2025) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2025.07.006 · Cited by 6
PFKM governs metabolic shifts throughout skeletal muscle differentiation
Campos, M., Nguyen, S. T., Kong, X., Yang, Y., Watson, R. L., Gromova, A., Livelo, C. R., Franco, C. N., Cabral, J. E., Seabrook, L. J., et al. (2026) · Nature Metabolism · doi:10.1038/s42255-026-01457-4 · Cited by 4
Androgen action on myogenesis throughout the lifespan; comparison with neurogenesis
Barsky, S. T., & Monks, D. A. (2023) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2023.101101 · Cited by 6
Enhanced secretion of promyogenic exosomes by quiescent muscle cells
Prabhavathy, D., Ghosh, A., Pallavi Rao, T., Raychaudhuri, S., Adicherla, H., Devvanshi, H., Kshetrapal, P., & Dhawan, J. (2024) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2024.1381357 · Cited by 4
Kawashima, M., Nagata, I., Terada, E., Tamari, A., Kurauchi, M., Sakuraya, T., Sonomura, T., Oyanagi, E., Yano, H., Peake, J. M., et al. (2024) · Journal of Histochemistry & Cytochemistry · doi:10.1369/00221554241274882 · Cited by 4
ZIP13 marks muscle satellite cells and contributes to their quiescent and active phase balance
Yoshigai, E., Hara, T., Hashimoto, M., Tsuzuki, H., Abe, T., Inoue, K., Noguchi, A., Ohashi, T., & Fukada, T. (2025) · Scientific Reports · doi:10.1038/s41598-025-92501-y · Cited by 5
Stem Cell Aging and Rejuvenation in the Skeletal Muscle System
Libergoli, M., & Almada, A. E. (2025) · Rejuvenation Research · doi:10.1089/rej.2025.0028 · Cited by 4
Yang, L., Liao, J., Huang, H., Lee, T., & Qi, H. (2024) · Developmental Biology · doi:10.1016/j.ydbio.2024.02.002 · Cited by 4
Kim, R. T., & Whited, J. L. (2024) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.15210 · Cited by 3
mRNA translational control of regeneration
Amiri, M., Sonenberg, N., & Tahmasebi, S. (2025) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2025.102367 · Cited by 5
Laporte, D., & Sagot, I. (2025) · Biomolecules · doi:10.3390/biom15070960 · Cited by 4
Mom Knows Best: Imprinted Control of Hematopoietic Stem Cell Quiescence
Serrano‐López, J., & Cancelas, J. A. (2016) · Cell stem cell · doi:10.1016/j.stem.2016.01.004 · Cited by 4
Cell-intrinsic factors governing quiescence vis-à-vis activation of adult hematopoietic stem cells
Budgude, P., Vaidya, A., & Kale, V. P. (2022) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-022-04594-y · Cited by 5
High Throughput Screening of Mitochondrial Bioenergetics in Myoblasts and Differentiated Myotubes
Takeda, K., Takemasa, T., & Fujita, R. (2023) · Methods in molecular biology · doi:10.1007/978-1-0716-3036-5_7 · Cited by 4
Yang, Y., Huang, K., Jiang, H., Wang, S., Xu, X., Liu, Y., Liu, Q., Wei, M., & Li, Z. (2024) · The FASEB Journal · doi:10.1096/fj.202302599rr · Cited by 4
Gonzalez, M. L., Jacobs, R. D., Ely, K., & Johnson, S. (2019) · Journal of Animal Science · doi:10.1093/jas/skz330 · Cited by 4
Marko, R., Columbus, D. A., Julia, S.-W., Agus, S., Hanh, V. N., Ryan, F., Teresa, A. D., & Marta, L. F. (2019) · Journal of Nutrition · doi:10.1093/jn/nxz216 · Cited by 4
Spain, M. M., Braceros, K. C. A., & Tsukiyama, T. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/426288 · Cited by 4
Choi, J. J., Shin, E. J., Han, W. M., Anderson, S. E., Mohiuddin, M., Lee, N. H., Trần, T. H., Nakhai, S. A., Jeong, H., Shcherbina, A., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.05.24.113456 · Cited by 4
Metabolism of glucose and glutamine is critical for skeletal muscle stem cell activationPreprint
Ahsan, S., Raval, M. H., Ederer, M., Tiwari, R. L., Chareunsouk, A., & Rodgers, J. T. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.07.28.225847 · Cited by 4
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Tranter, J. D., Kumar, A., Nair, V. K., & Sah, R. (2023) · Comprehensive physiology · doi:10.1002/cphy.c230005 · Cited by 10
Han, L., Qiu, Y., He, L., Gao, C., Zhou, N., Fu, X., Xu, J., Lin, L., Wang, H., Biswal, S., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-65506-4 · Cited by 3
Cellular quiescence uncouples the proteome from the transcriptome in neural stem cells
Rossi, A., Coum, A., Madelenat, M., Harris, L., Strohbuecker, S., Chai, A., Fiaz, H., Chaouni, R., Faull, P. A., Heaven, N. C., et al. (2026) · The EMBO Journal · doi:10.1038/s44318-026-00693-4 · Cited by 3
Jude, M., Rajasingh, S., Alway, S. E., & Rajasingh, J. (2026) · Experimental Cell Research · doi:10.1016/j.yexcr.2026.114969 · Cited by 4
Hong, X., & Muñoz‐Cánoves, P. (2023) · Methods in molecular biology · doi:10.1007/978-1-0716-3036-5_6 · Cited by 3
Wei, X., Rigopoulos, A., Lienhard, M., Pöhle‐Kronawitter, S., Kotsaris, G., Franke, J., Berndt, N., Mejedo, J. O., Wu, H., Boerno, S. T., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-45618-z · Cited by 4
Zhou, S., Makashova, O. E., Chevillard, P., Josey, V., Li, B., & Prager‐Khoutorsky, M. (2024) · Journal of Neuroendocrinology · doi:10.1111/jne.13377 · Cited by 3
Navigating translational control of gene expression in satellite cells
Jiogo, H., & Crist, C. G. (2024) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2024.02.013 · Cited by 3
Luna‐Angulo, A. B., Landa‐Solís, C., Escobar‐Cedillo, R. E., Estrada-Mena, F. J., Sánchez‐Chapul, L., Gómez‐Díaz, B., Carrillo-Mora, P. U., Avilés‐Arnaut, H., Jiménez-Hernández, L., Jiménez-Hernández, D. A., et al. (2024) · Medicina · doi:10.3390/medicina60071060 · Cited by 3
Liu, Y., Ilinski, A., Gerstenfeld, L. C., & Bragdon, B. C. (2023) · Frontiers in Physiology · doi:10.3389/fphys.2023.1106474 · Cited by 3
Stange, K., Schumacher, T., Miersch, C., Whelan, R., Klünemann, M., & Röntgen, M. (2023) · Current Issues in Molecular Biology · doi:10.3390/cimb45040174 · Cited by 7
Absolute Quantification of mRNA Isoforms in Adult Stem Cells Using Microfluidic Digital PCR
Barman, S. D., Frimand, Z., & de Morrée, A. (2023) · BIO-PROTOCOL · doi:10.21769/bioprotoc.4811 · Cited by 3
Regeneration: Signaling superhighways
Sun, F., Simone, A. D., & Poss, K. D. (2023) · Current Biology · doi:10.1016/j.cub.2023.08.024 · Cited by 3
Myburgh, E., Geoghegan, V., Alves‐Ferreira, E. V. C., Nievas, Y. R., Grewal, J. S., Brown, E. H., McLuskey, K., & Mottram, J. C. (2024) · EMBO Reports · doi:10.1038/s44319-024-00084-y · Cited by 3
H’ng, C. H., Amarasinghe, S. L., Zhang, B., Chang, H., Qu, X., Powell, D., & Roselló‐Díez, A. (2024) · Nature Communications · doi:10.1038/s41467-024-47311-7 · Cited by 3
Sequential transcriptional programs underpin activation of hippocampal stem cells
Rigo, P., Ahmed-de-Prado, S., Johnston, R. L., Choudhury, C., Guillemot, F., & Harris, L. (2025) · Science Advances · doi:10.1126/sciadv.adu4523 · Cited by 7
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Relaix, F., Zoglio, V., Chebouti, S., de Lima, J. E., & Lafuste, P. (2025) · Journal of Muscle Research and Cell Motility · doi:10.1007/s10974-025-09701-2 · Cited by 3
Anti-Differentiation Effect of Oncogenic Met Receptor in Terminally-Differentiated Myotubes
Sala, V., Gallo, S., Gatti, S., Vigna, E., Ponzetto, A., & Crepaldi, T. (2015) · Biomedicines · doi:10.3390/biomedicines3010124 · Cited by 3
He, L., Ding, Y., Zhao, Y. F., So, K. K. H., Peng, X. L., Li, Y., Yuan, J., Sun, H., & Wang, H. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/797746 · Cited by 3
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Gheller, B. J. F., Blum, J., Bender, E. L., Gheller, M. E., Lim, E. W., Handzlik, M. K., Stover, P. J., Field, M. S., Cosgrove, B. D., Metallo, C. M., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/833798 · Cited by 3
Sequential transcriptional programs underpin activation of quiescent hippocampal stem cellsPreprint
Rigo, P., Ahmed-de-Prado, S., Johnston, R. L., Choudhury, C., Guillemot, F., & Harris, L. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.10.29.620545 · Cited by 3
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Metadata
- Authors
- Rodgers, J. T., King, K. Y., Brett, J. O., Cromie, M. J., Charville, G. W., Maguire, K. K., Brunson, C., Mastey, N., Liu, L., Tsai, C.-R., Goodell, M. A., & Rando, T. A.
- Affiliations
- Stanford Medicine (US)
- Baylor College of Medicine (US)
- VA Palo Alto Health Care System (US)
- Corresponding author
- Rando, Thomas A.
- ORCID
- Venue
- Nature
- Published
- 2014-05-25
- Volume
- 510
- Issue
- 7505
- Pages
- 393-396
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC4065227
- OpenAlex
- W1964204876
- Cited by
- 776
- References
- 35
- Citations by year
- 2026: 48 · 2025: 51 · 2024: 65 · 2023: 93 · 2022: 71 · 2021: 72 · 2020: 64 · 2019: 63 · 2018: 59 · 2017: 80 · 2016: 43 · 2015: 53 · 2014: 14
- FWCI
- 25.82
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- U.S. Department of Veterans Affairs (I01 BX002324)
- China Scholarship Council
- National Institute on Aging (R37AG023806, K99AG041764, R01AG023806, F30AG035521, R01AG047820, P01AG036695)
- National Heart, Lung, and Blood Institute (K08HL098898)
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK092883)
- National Institute of Arthritis and Musculoskeletal and Skin Diseases (R01AR062185)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › PI3K/AKT/mTOR signaling in cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Keywords
- stem cell quiescence, mTORC1, muscle stem cells, satellite cells, hepatocyte growth factor, tissue regeneration, injury response, cell cycle entry
- MeSH terms
- Mechanistic Target of Rapamycin Complex 1, Animals, Cell Cycle, Cells, Cultured, Gene Expression Regulation, Male, Mice, Inbred C57BL, Regeneration, Resting Phase, Cell Cycle, Muscle, Skeletal, Gene Expression Profiling, Satellite Cells, Skeletal Muscle, Multiprotein Complexes, Mice, TOR Serine-Threonine Kinases
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