The fate of newly formed satellite cells during compensatory muscle hypertrophy
Abstract
Compensatory hypertrophy was induced in the rat extensor digitorum longus muscle by extirpation of the synergistic tibialis anterior. Injections of 3H-thymidine (2 muCi/g body weight) was given at 24, 48, and 72 h after the operation. In animals killed immediately after the last injection both satellite cell nuclei and true muscle nuclei were labeled, whereas in animals killed 4 weeks later only true muscle nuclei were labeled. The results are interpreted as indicating incorporation of newly formed satellite cells into the fibers during compensatory hypertrophy.
Integrity signals
Registry
Cites
Statistics
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?
Studies concluding that satellite cells are necessary for muscle fiber hypertrophy utilize young or developing mice (<4 months of age).
“With respect to muscle fiber hypertrophy, studies concluding that satellite cells are necessary for muscle fiber hypertrophy utilize young or developing mice [146,147] (<4 months of age).”
From Potential Roles of n-3 PUFAs during Skeletal Muscle Growth and Regeneration (2018) · cites this paper as [146]
Cites
Satellite cells as the source of nuclei in muscles of growing rats
Moss, F. P., & Leblond, C. P. (1971) · The Anatomical Record · doi:10.1002/ar.1091700405 · Cited by 1,025 · see citing works
Nature of dividing nuclei in skeletal muscle of growing rats
Moss, F. P., & Leblond, C. P. (1970) · The Journal of Cell Biology · doi:10.1083/jcb.44.2.459 · Cited by 289 · see citing works
Work-induced growth of skeletal muscle in normal and hypophysectomized rats
Goldberg, A. (1967) · American Journal of Physiology-Legacy Content · doi:10.1152/ajplegacy.1967.213.5.1193 · Cited by 218 · see citing works
Cell proliferation in rat skeletal muscle during early stages of compensatory hypertrophy
Schiaffino, S., Bormioli, S. P., & Aloisi, M. (1972) · Virchows Archiv B Cell Pathology Including Molecular Pathology · doi:10.1007/bf02889406 · Cited by 108 · see citing works
Self-citationHanzl�kov�, V. R., Mackov�, E., & Hn�k, P. (1975) · Cell and Tissue Research · doi:10.1007/bf00222049 · Cited by 64 · see citing works
Adaptive changes in developing rat skeletal muscle in response to functional overload
Schiaffino, S., & Bormioli, S. P. (1973) · Experimental Neurology · doi:10.1016/0014-4886(73)90129-5 · Cited by 44 · see citing works
Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
Skeletal Muscle Adaptability: Significance for Metabolism and Performance
Saltin, B., & Gollnick, P. D. (1983) · Comprehensive physiology · doi:10.1002/cphy.cp100119 · Cited by 917 · see citing works
Signaling in Muscle Atrophy and Hypertrophy
Sandri, M. (2008) · Physiology · doi:10.1152/physiol.00041.2007 · Cited by 830 · see citing works
Regulation of skeletal muscle growth by the IGF1-Akt/PKB pathway: insights from genetic models
Schiaffino, S., & Mammucari, C. (2011) · Skeletal Muscle · doi:10.1186/2044-5040-1-4 · Cited by 816 · see citing works
“Satellite-cell proliferation and fusion leading to increase in myonuclei occurs during postnatal muscle growth [110] and during compensatory hypertrophy induced by ablation of synergistic muscles [ 111 ], as demonstrated by electron microscope autoradiographs after 3 H-thymidine labeling.”
BackgroundSelf-citationThe Skeletal Muscle Satellite Cell: The Stem Cell That Came in From the Cold
Zammit, P. S., Partridge, T. A., & Yablonka‐Reuveni, Z. (2006) · Journal of Histochemistry & Cytochemistry · doi:10.1369/jhc.6r6995.2006 · Cited by 684 · see citing works
Effective fiber hypertrophy in satellite cell-depleted skeletal muscle
McCarthy, J. J., Mula, J., Miyazaki, M., Erfani, R., Garrison, K., Farooqui, A. B., Srikuea, R., Lawson, B. A., Grimes, B., Keller, C., et al. (2011) · Development · doi:10.1242/dev.068858 · Cited by 616 · see citing works
Skeletal muscle satellite cells
Schultz, E., & McCormick, K. M. (1994) · Reviews of physiology, biochemistry and pharmacology · doi:10.1007/bfb0030904 · Cited by 526 · see citing works
New fundamental resistance exercise determinants of molecular and cellular muscle adaptations
Toigo, M., & Boutellier, U. (2006) · European Journal of Applied Physiology · doi:10.1007/s00421-006-0238-1 · Cited by 437 · see citing works
Regeneration of Mammalian Skeletal Muscle: Basic Mechanisms and Clinical Implications
Ciciliot, S., & Schiaffino, S. (2010) · Current Pharmaceutical Design · doi:10.2174/138161210790883453 · Cited by 384 · see citing works
Self-citationLocalized infusion of IGF-I results in skeletal muscle hypertrophy in rats
Adams, G. R., & McCue, S. A. (1998) · Journal of Applied Physiology · doi:10.1152/jappl.1998.84.5.1716 · Cited by 377 · see citing works
Satellite cell activity is required for hypertrophy of overloaded adult rat muscle
Rosenblatt, J. D., Yong, D., & Parry, D. J. (1994) · Muscle & Nerve · doi:10.1002/mus.880170607 · Cited by 356 · see citing works
Skeletal muscle satellite cells: Changes in proliferation potential as a function of age
Schultz, E., & Lipton, B. H. (1982) · Mechanisms of Ageing and Development · doi:10.1016/0047-6374(82)90105-1 · Cited by 335 · see citing works
Myonuclei acquired by overload exercise precede hypertrophy and are not lost on detraining
Bruusgaard, J. C., Johansen, I. B., Egner, I. M., Rana, Z. A., & Gundersen, K. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0913935107 · Cited by 327 · see citing works
Adams, G. R., & Haddad, F. (1996) · Journal of Applied Physiology · doi:10.1152/jappl.1996.81.6.2509 · Cited by 287 · see citing works
Regulation of the muscle fiber micro environment by activated satellite cells during hypertrophy
Fry, C. S., Lee, J. D., Jackson, J. R., Kirby, T. J., Stasko, S. A., Liu, H., Dupont‐Versteegden, E. E., McCarthy, J. J., & Peterson, C. A. (2014) · The FASEB Journal · doi:10.1096/fj.13-239426 · Cited by 273 · see citing works
Invited Review: Autocrine/paracrine IGF-I and skeletal muscle adaptation.
Adams, G. (2002) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01264.2001 · Cited by 22 · see citing works
Mechanisms Modulating Skeletal Muscle Phenotype
Blaauw, B., Schiaffino, S., & Reggiani, C. (2013) · Comprehensive physiology · doi:10.1002/cphy.c130009 · Cited by 278 · see citing works
Self-citationBlaauw, B., Canato, M., Agatea, L., Toniolo, L., Mammucari, C., Masiero, E., Abraham, R., Sandri, M., Schiaffino, S., & Reggiani, C. (2009) · The FASEB Journal · doi:10.1096/fj.09-131870 · Cited by 244 · see citing works
Self-citationPlasticity of myonuclear number in hypertrophied and atrophied mammalian skeletal muscle fibers
Allen, D. L., Monke, S. R., Talmadge, R. J., Roy, R. R., & Edgerton, V. R. (1995) · Journal of Applied Physiology · doi:10.1152/jappl.1995.78.5.1969 · Cited by 240 · see citing works
Kadi, F., & Thornell, L. (2000) · Histochemistry and Cell Biology · doi:10.1007/s004180050012 · Cited by 232 · see citing works
Roberts, M. D., McCarthy, J. J., Hornberger, T. A., Phillips, S. M., Mackey, A. L., Nader, G. A., Boppart, M. D., Kavazis, A. N., Reidy, P. T., Ogasawara, R., et al. (2023) · Physiological Reviews · doi:10.1152/physrev.00039.2022 · Cited by 214 · see citing works
Time course of changes in markers of myogenesis in overloaded rat skeletal muscles
Adams, G. R., Haddad, F., & Baldwin, K. M. (1999) · Journal of Applied Physiology · doi:10.1152/jappl.1999.87.5.1705 · Cited by 218 · see citing works
Satellite cell depletion prevents fiber hypertrophy in skeletal muscle
Egner, I. M., Bruusgaard, J. C., & Gundersen, K. (2016) · Development · doi:10.1242/dev.134411 · Cited by 203 · see citing works
The effects of aging on satellite cells in skeletal muscles of mice and rats
Snow, M. H. (1977) · Cell and Tissue Research · doi:10.1007/bf00220299 · Cited by 201 · see citing works
Time course of molecular responses of human skeletal muscle to acute bouts of resistance exercise
Bickel, C. S., Slade, J. M., Mahoney, E., Haddad, F., Dudley, G. A., & Adams, G. R. (2005) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00895.2004 · Cited by 200 · see citing works
Cellular and molecular responses to increased skeletal muscle loading after irradiation.
Adams, G., Caiozzo, V., Haddad, F., & Baldwin, K. (2002) · American Journal of Physiology - Cell Physiology · doi:10.1152/ajpcell.00173.2002 · Cited by 227 · see citing works
Bone and skeletal muscle: neighbors with close ties
DiGirolamo, D. J., Kiel, D. P., & Esser, K. A. (2013) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.1969 · Cited by 193 · see citing works
“和骨内膜再吸收进行。出生后的肌肉生长则完全是 肌纤维增大 ( 肥大 ) 的结果,尽管对驱动这一过程的 机制有过广泛争议,肌肉肥大长期以来一直被认为 需要卫星细胞的增殖活动及其与原有肌肉纤维的融 合 [33-35] ,但最近的证据显示了肌纤维在缺乏卫星细 胞时的肥大增生 [36] 。”
Interaction between satellite cells and skeletal muscle fibers
Bischoff, R. (1990) · Development · doi:10.1242/dev.109.4.943 · Cited by 192 · see citing works
Bischoff, R. (1990) · Development · doi:10.1242/dev.110.3.653-s · Cited by 182 · see citing works
Multiple signaling pathways mediate LIF-induced skeletal muscle satellite cell proliferation
Spangenburg, E. E., & Booth, F. W. (2002) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00574.2001 · Cited by 181 · see citing works
Role of satellite cells in muscle growth and maintenance of muscle mass
Pallafacchina, G., Blaauw, B., & Schiaffino, S. (2012) · Nutrition Metabolism and Cardiovascular Diseases · doi:10.1016/j.numecd.2012.02.002 · Cited by 173 · see citing works
Self-citationSelected contribution: acute cellular and molecular responses to resistance exercise.
Haddad, F., & Adams, G. (2002) · Journal of applied physiology · doi:10.1152/japplphysiol.01153.2001 · Cited by 192 · see citing works
Muscle memory and a new cellular model for muscle atrophy and hypertrophy
Gundersen, K. (2016) · Journal of Experimental Biology · doi:10.1242/jeb.124495 · Cited by 169 · see citing works
Molecular Mechanisms of Skeletal Muscle Hypertrophy
Schiaffino, S., Reggiani, C., Akimoto, T., & Blaauw, B. (2020) · Journal of Neuromuscular Diseases · doi:10.3233/jnd-200568 · Cited by 169 · see citing works
Self-citationGene shifting: a novel therapy for mitochondrial myopathy
Taivassalo, T. (1999) · Human Molecular Genetics · doi:10.1093/hmg/8.6.1047 · Cited by 160 · see citing works
Yamamoto, M., Kudoh, A., Arishima, K., & EGUCHI, Y. (1997) · The Anatomical Record · doi:10.1002/(sici)1097-0185(199702)247:2 · Cited by 12 · see citing works
Egner, I. M., Bruusgaard, J. C., Eftestøl, E., & Gundersen, K. (2013) · The Journal of Physiology · doi:10.1113/jphysiol.2013.264457 · Cited by 159 · see citing works
Modulation of myonuclear number in functionally overloaded and exercised rat plantaris fibers
Roy, R. R., Monke, S. R., Allen, D. L., & Edgerton, V. R. (1999) · Journal of Applied Physiology · doi:10.1152/jappl.1999.87.2.634 · Cited by 154 · see citing works
Molecular and Cellular Determinants of Skeletal Muscle Atrophy and Hypertrophy
Sartorelli, V., & Fulco, M. (2004) · Science s STKE · doi:10.1126/stke.2442004re11 · Cited by 145 · see citing works
Starring or supporting role? Satellite cells and skeletal muscle fiber size regulation
Murach, K. A., Fry, C. S., Kirby, T. J., Jackson, J. R., Lee, J. D., White, S. H., Dupont-Versteegden, E. E., McCarthy, J. J., & Peterson, C. A. (2018) · Physiology · doi:10.1152/physiol.00019.2017 · Cited by 137 · see citing works
Snow, M. H. (1990) · The Anatomical Record · doi:10.1002/ar.1092270407 · Cited by 137 · see citing works
Chapter 9 Cell Heterogeneity in The Myogenic Lineage
Cossu, G., & Molinaro, M. (1987) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(08)60625-0 · Cited by 135 · see citing works
Dupont‐Versteegden, E. E., Murphy, R. J. L., Houlé, J. D., Gurley, C. M., & Peterson, C. A. (1999) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1999.277.3.c589 · Cited by 125 · see citing works
Fusion and beyond: Satellite cell contributions to loading-induced skeletal muscle adaptation
Murach, K. A., Fry, C. S., Dupont‐Versteegden, E. E., McCarthy, J. J., & Peterson, C. A. (2021) · The FASEB Journal · doi:10.1096/fj.202101096r · Cited by 120 · see citing works
Satellite cells and myofiber growth in the rat soleus and extensor digitorum longus muscles
Kelly, A. M. (1978) · Developmental Biology · doi:10.1016/0012-1606(78)90174-4 · Cited by 118 · see citing works
Tamaki, T., Akatsuka, A., Tokunaga, M., Ishige, K., Uchiyama, S., & Shiraishi, T. (1997) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1997.273.1.c246 · Cited by 117 · see citing works
Cell cycle commitment of rat muscle satellite cells.
Bischoff, R. (1990) · The Journal of Cell Biology · doi:10.1083/jcb.111.1.201 · Cited by 113 · see citing works
McCall, G. E., Allen, D. L., Linderman, J. K., Grindeland, R. E., Roy, R. R., Mukku, V. R., & Edgerton, V. R. (1998) · Journal of Applied Physiology · doi:10.1152/jappl.1998.84.4.1407 · Cited by 110 · see citing works
No change in myonuclear number during muscle unloading and reloading
Bruusgaard, J. C., Egner, I. M., Larsen, T. K., Dupre-Aucouturier, S., Desplanches, D., & Gundersen, K. (2012) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00436.2012 · Cited by 107 · see citing works
Mechanical overload‐induced muscle‐derived extracellular vesicles promote adipose tissue lipolysis
Vechetti, I. J., Peck, B. D., Wen, Y., Walton, R. G., Valentino, T. R., Alimov, A. P., Dungan, C. M., Pelt, D. W. V., von Walden, F., Alkner, B. A., et al. (2021) · The FASEB Journal · doi:10.1096/fj.202100242r · Cited by 105 · see citing works
Regulation of skeletal muscle fiber size, shape and function
Edgerton, V. R., & Roy, R. R. (1991) · Journal of Biomechanics · doi:10.1016/0021-9290(91)90383-x · Cited by 104 · see citing works
Potential Roles of n-3 PUFAs during Skeletal Muscle Growth and Regeneration
Tachtsis, B., Camera, D., & Lacham-Kaplan, O. (2018) · Nutrients · doi:10.3390/nu10030309 · Cited by 104 · see citing works
Satellite cell proliferation and skeletal muscle hypertrophy
Adams, G. R. (2006) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/h06-053 · Cited by 103 · see citing works
Myoblast transplantation: the current status of a potential therapeutic tool for myopathies.
Skuk, D., & Tremblay, J. P. (2003) · PubMed · Cited by 98 · see citing works
Murach, K. A., Englund, D. A., Dupont‐Versteegden, E. E., McCarthy, J. J., & Peterson, C. A. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.00635 · Cited by 96 · see citing works
Resistance exercise training promotes fiber type-specific myonuclear adaptations in older adults
Moro, T., Brightwell, C. R., Volpi, E., Rasmussen, B. B., & Fry, C. S. (2020) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00723.2019 · Cited by 85 · see citing works
The role of satellite cells in muscle hypertrophy
Blaauw, B., & Reggiani, C. (2014) · Journal of Muscle Research and Cell Motility · doi:10.1007/s10974-014-9376-y · Cited by 78 · see citing works
Fukuda, S., Kaneshige, A., Kaji, T., Noguchi, Y.-T., Takemoto, Y., Zhang, L., Tsujikawa, K., Kokubo, H., Uezumi, A., Maehara, K., et al. (2019) · eLife · doi:10.7554/elife.48284 · Cited by 75 · see citing works
Regrowth of skeletal muscle atrophied from inactivity.
Machida, S., & Booth, F. (2004) · Medicine & Science in Sports & Exercise · doi:10.1249/01.mss.0000106175.24978.84 · Cited by 77 · see citing works
Mackey, A. L., Karlsen, A., Couppé, C., Mikkelsen, U. R., Nielsen, R. H., Magnusson, S. P., & Kjær, M. (2013) · Acta Physiologica · doi:10.1111/apha.12195 · Cited by 63 · see citing works
Essential role of satellite cells in the growth of rat soleus muscle fibers
Kawano, F., Takeno, Y., Nakai, N., Higo, Y., Terada, M., Ohira, T., Nonaka, I., & Ohira, Y. (2008) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00497.2007 · Cited by 59 · see citing works
Dirks, M. L., Tieland, M., Verdijk, L. B., Losen, M., Nilwik, R., Mensink, M., de Groot, L. C. P. G. M., & van Loon, L. J. C. (2017) · Journal of the American Medical Directors Association · doi:10.1016/j.jamda.2017.02.006 · Cited by 56 · see citing works
A quantitative study of satellite cells and myonuclei in stretched avian slow tonic muscle
Winchester, P., & Gonyea, W. J. (1992) · The Anatomical Record · doi:10.1002/ar.1092320306 · Cited by 56 · see citing works
PAX3/7 expression coincides with myod during chronic skeletal muscle overload
Hyatt, J. K., McCall, G. E., Kander, E. M., Zhong, H., Roy, R. R., & Huey, K. A. (2008) · Muscle & Nerve · doi:10.1002/mus.21006 · Cited by 54 · see citing works
Control of muscle fibre size: a crucial factor in ageing
Hughes, S. M., & Schiaffino, S. (1999) · Acta Physiologica Scandinavica · doi:10.1046/j.1365-201x.1999.00619.x · Cited by 50 · see citing works
Self-citationSatellite cell numbers in senile rat levator ani muscle
Nnodim, J. O. (2000) · Mechanisms of Ageing and Development · doi:10.1016/s0047-6374(99)00076-7 · Cited by 42 · see citing works
Mechanisms Modulating Skeletal Muscle Phenotype
Blaauw, B., Schiaffino, S., & Reggiani, C. (2013) · Comprehensive physiology · doi:10.1002/j.2040-4603.2013.tb00534.x · Cited by 38 · see citing works
Self-citationSolsona, R., Pavlin, L., Bernardi, H., & Sanchez, A. M. J. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22052741 · Cited by 39 · see citing works
Eftestøl, E., Egner, I. M., Lunde, I. G., Ellefsen, S., Andersen, T., Sjåland, C., Gundersen, K., & Bruusgaard, J. C. (2016) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00016.2016 · Cited by 36 · see citing works
Functional Overloading Facilitates the Regeneration of Injured Soleus Muscles in Mice
Morioka, S., Goto, K., Kojima, A., Naito, T., Matsuba, Y., Akema, T., Fujiya, H., Sugiura, T., Ohira, Y., Beppu, M., et al. (2008) · The Journal of Physiological Sciences · doi:10.2170/physiolsci.rp004008 · Cited by 29 · see citing works
Sakuma, K., Nishikawa, J., Nakao, R., Nakano, H., Sano, M., & Yasuhara, M. (2003) · Histochemistry and Cell Biology · doi:10.1007/s00418-003-0499-2 · Cited by 28 · see citing works
Hinterberger, T. J., & Barald, K. F. (1990) · Development · doi:10.1242/dev.109.1.139 · Cited by 28 · see citing works
Does an NSAID a day keep satellite cells at bay?
Mackey, A. L. (2013) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00044.2013 · Cited by 25 · see citing works
Frequency of bifurcated muscle fibers in hyperthrophic rat soleus muscle
Snow, M. H., & Chortkoff, B. S. (1987) · Muscle & Nerve · doi:10.1002/mus.880100406 · Cited by 25 · see citing works
Muscle satellite cells in malnourished and nutritionally rehabilitated children
Hansen‐Smith, F. M., Picou, D. I. M., & Golden, M. H. (1979) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(79)90040-6 · Cited by 23 · see citing works
Exercise Promotes Tissue Regeneration: Mechanisms Involved and Therapeutic Scope
Liu, C., Wu, X., Vulugundam, G., Gokulnath, P., Li, G., & Xiao, J. (2023) · Sports Medicine - Open · doi:10.1186/s40798-023-00573-9 · Cited by 20 · see citing works
Interstitial space and collagen alterations of the developing rat diaphragm
Gosselin, L. E., Martinez, D. A., VAILAS, A. C., & Sieck, G. C. (1993) · Journal of Applied Physiology · doi:10.1152/jappl.1993.74.5.2450 · Cited by 19 · see citing works
Barsky, S. T., & Monks, D. A. (2025) · Biology of Sex Differences · doi:10.1186/s13293-025-00707-6 · Cited by 19 · see citing works
Eftestøl, E., Ochi, E., Juvkam, I. S., Hansson, K., & Gundersen, K. (2022) · Acta Physiologica · doi:10.1111/apha.13879 · Cited by 17 · see citing works
Turner, D., Gorski, P., Seaborne, R. A., Viggars, M., Murphy, M., Jarvis, J., Martin, N., Stewart, C., & Sharples, A. (2021) · Journal of Cellular Physiology · doi:10.1002/jcp.30328 · Cited by 14 · see citing works
Mølsted, S., Andersen, J. L., Harrison, A. P., Eidemak, I., & Mackey, A. L. (2015) · Muscle & Nerve · doi:10.1002/mus.24633 · Cited by 17 · see citing works
Satellite cell dynamics during skeletal muscle hypertrophy
Saliu, T. P., Goh, J. Z., Kang, G., Burke, B. I., Ismaeel, A., & McCarthy, J. J. (2024) · Biochemical Society Transactions · doi:10.1042/bst20240201 · Cited by 15 · see citing works
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 17 · see citing works
Burke, B. I., Ismaeel, A., & McCarthy, J. J. (2024) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00362.2024 · Cited by 15 · see citing works
Tamaki, T., Uchiyama, Y., Okada, Y., Tono, K., Nitta, M., Hoshi, A., & Akatsuka, A. (2009) · Histochemistry and Cell Biology · doi:10.1007/s00418-009-0585-1 · Cited by 13 · see citing works
Molecular predictors of resistance training outcomes in young untrained female adults
Smith, M. A., Sexton, C. L., Smith, K. A., Osburn, S. C., Godwin, J. S., Beausejour, J. P., Ruple, B. A., Goodlett, M. D., Edison, J. L., Frugé, A. D., et al. (2023) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00605.2022 · Cited by 11 · see citing works
Joplin, R., Franchi, L. L., & Salmons, S. (1987) · PubMed · Cited by 12 · see citing works
Zhang, R., Liu, H., Liu, J., Hu, J., Yan, X., Wang, D.-M.-C., Li, L., & Wang, J. (2015) · PLoS ONE · doi:10.1371/journal.pone.0143378 · Cited by 11 · see citing works
Everett, A. W., & Sparrow, M. P. (1987) · Journal of Muscle Research and Cell Motility · doi:10.1007/bf01574590 · Cited by 11 · see citing works
Insights into human muscle biology from human primary skeletal muscle cell culture
Francis, T., Soendenbroe, C., Lazarus, N. R., Mackey, A. L., & Harridge, S. D. R. (2025) · Journal of Muscle Research and Cell Motility · doi:10.1007/s10974-025-09696-w · Cited by 10 · see citing works
Klotho regulates the myogenic response of muscle to mechanical loading and exercise
Ochi, E., Barrington, A., Wehling‐Henricks, M., Avila, M. H., Kuro‐o, M., & Tidball, J. G. (2023) · Experimental Physiology · doi:10.1113/ep091263 · Cited by 9 · see citing works
Zhang, R., Liu, H., Li, Q., Wang, Y., Liu, J., Hu, J., Yan, X., Gou, H., Li, L., & Wang, J. (2014) · Poultry Science · doi:10.3382/ps.2014-04145 · Cited by 9 · see citing works
Molecular Mechanisms Controlling Skeletal Muscle Mass
Sakuma, K., & Yamaguchi, A. (2015) · InTech eBooks · doi:10.5772/60876 · Cited by 9 · see citing works
Savikj, M., Ruby, M. A., Kostovski, E., Iversen, P. O., Zierath, J. R., Krook, A., & Widegren, U. (2018) · Physiological Reports · doi:10.14814/phy2.13739 · Cited by 6 · see citing works
Bidirectional myofiber transition through altering the photobiomodulation condition
Lin, C.-Y., Niwa, A., Hou, C.-Y., Tsai, C., & Chang, H. C. (2020) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/j.jphotobiol.2020.112041 · Cited by 6 · see citing works
Is the myonuclear domain ceiling hypothesis dead?
Aman, F. I., Khatib, E., AlNeaimi, A., Mohamed, A. A. M., Almulla, A. S., Zaidan, A. I., Alshafei, J., Habbal, O., Eldesouki, S., & Qaisar, R. (2021) · Singapore Medical Journal · doi:10.11622/smedj.2021103 · Cited by 6 · see citing works
The Muscle Satellite Cell and Its Role in Muscle Transplantation (A Short Review)
Mayr, R. (1981) · Springer eBooks · doi:10.1007/978-3-7091-8618-3_2 · Cited by 6 · see citing works
Iwamori, K., Kubota, M., Zhang, L., Kodama, K., Kubo, A., Kokubo, H., Akimoto, T., & Fukada, S. (2024) · Skeletal Muscle · doi:10.1186/s13395-024-00357-z · Cited by 5 · see citing works
Role of Mammalian Target of Rapamycin (mTOR) in Muscle Growth
Panzhinskiy, E., Culver, B. W., Ren, J. T., Bagchi, D., & Nair, S. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-396454-0.00022-9 · Cited by 5 · see citing works
Skeletal muscle stem cells: function and potential role in therapy
Watt, D. J., & Jones, G. E. (1997) · Elsevier eBooks · doi:10.1016/b978-012563455-7/50005-2 · Cited by 5 · see citing works
- Authors
- Schiaffino, S., Pierobon Bormioli, S., & Aloisi, M.
- Affiliations
- University of Padua (IT)
- Corresponding author
- Schiaffino, S.
- Venue
- Virchows Archiv B Cell Pathology
- Published
- 1976-12
- Volume
- 21
- Issue
- 1
- Pages
- 113-118
- ISSN
- 0340-6075 (ISSN-L)
- OpenAlex
- W172002323
- Cited by
- 132
- References
- 6
- Citations by year
- 2026: 1 · 2025: 3 · 2024: 3 · 2023: 5 · 2022: 3 · 2021: 5 · 2020: 4 · 2019: 4 · 2018: 5 · 2017: 2 · 2016: 4 · 2015: 6 · 2014: 3 · 2013: 8 · 2012: 5
- FWCI
- 0.56
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Virchows Archiv B Cell Pathology Including Molecular Pathology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Muscle metabolism and nutrition
- Life Sciences › Agricultural and Biological Sciences › Animal Science and Zoology › Meat and Animal Product Quality
- Keywords
- satellite cells, muscle fiber development, extensor digitorum longus, muscle regeneration, 3H-thymidine labeling
- MeSH terms
- Animals, Autoradiography, Hypertrophy, Male, Microscopy, Electron, Muscle Contraction, Muscles, Thymidine, Time Factors, Tritium, Rats
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
