Nature of dividing nuclei in skeletal muscle of growing rats
Open accessAbstract
Much is known about the early stages of muscle development-the proliferation of myoblasts, their fusion into myotubes, and the transformation of myotubes into young muscle fibers. However, the mode of growth of muscle in the young animal remains obscure. It is known that muscle growth is extensive (e.g. in the chicken the pectoralis muscle enlarges from 0.7 g at hatching to 300 g in the adult) and is mainly the result of hypertrophy of the fibers (1), with little, if any, increase in their number (2). Moreover, it is generally assumed that, unlike what happens in most other tissues, there is no division of the nuclei and, consequently, no increase in their number (3). This view is supported by experiments showing that,
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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 [147]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
THE USE OF LEAD CITRATE AT HIGH pH AS AN ELECTRON-OPAQUE STAIN IN ELECTRON MICROSCOPY
Reynolds, E. S. (1963) · The Journal of Cell Biology · doi:10.1083/jcb.17.1.208 · Cited by 24,938 · see citing works
A formaldehyde-glutaraldehyde fixative of high osmolality for use in electron-microscopy
Karnovsky, M. J., & Karnovsky, M. J. (1965) · The Journal of Cell Biology · Cited by 5,078 · see citing works
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 · see citing works
Messier, B., & Leblond, C. P. (1960) · American Journal of Anatomy · doi:10.1002/aja.1001060305 · Cited by 810 · see citing works
Self-citationStockdale, F. E., & Holtzer, H. (1961) · Experimental Cell Research · doi:10.1016/0014-4827(61)90450-5 · Cited by 554 · see citing works
AUTORADIOGRAPHY WITH THE ELECTRON MICROSCOPE
Salpeter, M. M., & Bachmann, L. (1964) · The Journal of Cell Biology · doi:10.1083/jcb.22.2.469 · Cited by 373 · see citing works
Increase in the number of nuclei and weight in skeletal muscle of rats of various ages
Enesco, M., & Puddy, D. A. (1964) · American Journal of Anatomy · doi:10.1002/aja.1001140204 · Cited by 198 · see citing works
Moss, F. P. (1968) · American Journal of Anatomy · doi:10.1002/aja.1001220308 · Cited by 183 · see citing works
Self-citationRadioautographic study of skeletal muscle regeneration
Bintliff, S., & Walker, B. E. (1960) · American Journal of Anatomy · doi:10.1002/aja.1001060304 · Cited by 96 · see citing works
Mitosis during postnatal growth in skeletal and cardiac muscle of the rat.
Shafiq, S. A., Gorycki, M. A., & Mauro, A. (1968) · PubMed · Cited by 90 · see citing works
COMPARISON OF EMULSIONS AND TECHNIQUES IN ELECTRON MICROSCOPE RADIOAUTOGRAPHY
Granboulan, P. (1965) · Elsevier eBooks · doi:10.1016/b978-0-12-395731-3.50008-7 · Cited by 80 · see citing works
The mode of increase in the number of skeletal muscle nuclei in the postnatal rat
MacConnachie, H. F., Enesco, M., & Leblond, C. P. (1964) · American Journal of Anatomy · doi:10.1002/aja.1001140205 · Cited by 75 · see citing works
Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
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 · see citing works
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
Self-citationSkeletal 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
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
Dynamics of muscle fibre growth during postnatal mouse development
White, R. B., Biérinx, A.-S., Gnocchi, V. F., & Zammit, P. S. (2010) · BMC Developmental Biology · doi:10.1186/1471-213x-10-21 · Cited by 512 · see citing works
Satellite cell content is specifically reduced in type II skeletal muscle fibers in the elderly
Verdijk, L. B., Koopman, R., Schaart, G., Meijer, K., Savelberg, H. H. C. M., & van Loon, L. J. C. (2007) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00278.2006 · Cited by 489 · see citing works
The Muscle Satellite Cell: A Review
Campion, D. R. (1984) · International review of cytology · doi:10.1016/s0074-7696(08)62444-4 · Cited by 476 · see citing works
Wagers, A. J., & Conboy, I. M. (2005) · Cell · doi:10.1016/j.cell.2005.08.021 · Cited by 416 · see citing works
Tissue-specific stem cells: Lessons from the skeletal muscle satellite cell
Brack, A. S., & Rando, T. (2012) · Cell Stem Cell · doi:10.1016/j.stem.2012.04.001 · Cited by 409 · see citing works
Verdijk, L. B., Gleeson, B. G., Jonkers, R. A. M., Meijer, K., Savelberg, H. H. C. M., Dendale, P., & van Loon, L. J. C. (2009) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/gln050 · Cited by 372 · see citing works
The regeneration of skeletal muscle — a review
Carlson, B. M. (1973) · American Journal of Anatomy · doi:10.1002/aja.1001370202 · Cited by 363 · see citing works
Satellite cells in human skeletal muscle plasticity
Snijders, T., Nederveen, J. P., McKay, B. R., Joanisse, S., Verdijk, L. B., van Loon, L. J. C., & Parise, G. (2015) · Frontiers in Physiology · doi:10.3389/fphys.2015.00283 · Cited by 359 · see citing works
The effect of immobilization on the longitudinal growth of striated muscle fibres.
WILLIAMS, P. E., & Goldspink, G. (1973) · PubMed · Cited by 331 · 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
Plasmid DNA Is Superior to Viral Vectors for Direct Gene Transfer into Adult Mouse Skeletal Muscle
Davis, H. L., DEMENEIX, B. A., Quantin, B., Coulombe, J., & Whalen, R. G. (1993) · Human Gene Therapy · doi:10.1089/hum.1993.4.6-733 · Cited by 307 · see citing works
Regeneration of single skeletal muscle fibers in vitro
Bischoff, R. (1975) · The Anatomical Record · doi:10.1002/ar.1091820207 · Cited by 278 · see citing works
Cellular Aspect of Muscle Growth: Myogenic Cell Proliferation
Allen, R. E., Merkel, R. A., & Young, R. B. (1979) · Journal of Animal Science · doi:10.2527/jas1979.491115x · Cited by 260 · see citing works
Excitation‐transcription coupling in skeletal muscle: the molecular pathways of exercise
Gundersen, K. (2010) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/j.1469-185x.2010.00161.x · Cited by 254 · see citing works
Dirks, M. L., Wall, B. T., Snijders, T., Ottenbros, C. L. P., Verdijk, L. B., & van Loon, L. J. C. (2013) · Acta Physiologica · doi:10.1111/apha.12200 · Cited by 252 · see citing works
The impact of sarcopenia and exercise training on skeletal muscle satellite cells
Snijders, T., Verdijk, L. B., & van Loon, L. J. C. (2009) · Ageing Research Reviews · doi:10.1016/j.arr.2009.05.003 · Cited by 245 · see citing works
Acetylcholine receptors and myasthenia
Lindstrom, J. M. (2000) · Muscle & Nerve · doi:10.1002/(sici)1097-4598(200004)23:4 · Cited by 277 · see citing works
Regulation of muscle growth in neonates
Davis, T. A., & Fiorotto, M. L. (2008) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0b013e32831cef9f · Cited by 237 · see citing works
All muscle satellite cells are equal, but are some more equal than others?
Zammit, P. S. (2008) · Journal of Cell Science · doi:10.1242/jcs.019661 · Cited by 201 · see citing works
The dynamic nature of the so-called “fiber types” of mammalian skeletal muscle
Guth, L., & Yellin, H. (1971) · Experimental Neurology · doi:10.1016/0014-4886(71)90196-8 · Cited by 204 · 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
A reliable, standardized method for ultrastructural electron microscopic radioautography
Kopriwa, B. M. (1973) · Histochemistry and Cell Biology · doi:10.1007/bf00306855 · Cited by 198 · 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] 。”
Population of Muscle Satellite Cells in Relation to Age and Mitotic Activity
Allbrook, D. B., Han, M., & Hellmuth, A. E. (1971) · Pathology · doi:10.1080/00313027109073739 · Cited by 192 · see citing works
The genetic basis of pectoralis major myopathies in modern broiler chicken lines
Bailey, R. A., Watson, K., Bilgili, S. F., & Avendaño, S. (2015) · Poultry Science · doi:10.3382/ps/pev304 · Cited by 194 · see citing works
Regulation and phylogeny of skeletal muscle regeneration.
Baghdadi, M. B., & Tajbakhsh, S. (2018) · Developmental Biology · doi:10.1016/j.ydbio.2017.07.026 · Cited by 166 · see citing works
The mdx mouse model as a surrogate for D uchenne muscular dystrophy
Partridge, T. A. (2013) · FEBS Journal · doi:10.1111/febs.12267 · Cited by 187 · see citing works
Stem cell activation in skeletal muscle regeneration
Fu, X., Wang, H.-T., & Hu, P. (2015) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-014-1819-5 · Cited by 161 · see citing works
Machingal, M. A., Corona, B. T., Walters, T. J., Kesireddy, V., Koval, C. N., Dannahower, A., Zhao, W., Yoo, J. J., & Christ, G. J. (2011) · Tissue Engineering Part A · doi:10.1089/ten.tea.2010.0682 · Cited by 182 · see citing works
Myogenic cells in development and growth of fish
Koumans, J. T. M., & Akster, H. A. (1995) · Comparative Biochemistry and Physiology Part A Physiology · doi:10.1016/0300-9629(94)00150-r · Cited by 184 · see citing works
Suetta, C., Frandsen, U., Mackey, A. L., Jensen, L., Hvid, L. G., Bayer, M. L., Petersson, S. J., Schrøder, H. D., Andersen, J. L., Aagaard, P., et al. (2013) · The Journal of Physiology · doi:10.1113/jphysiol.2013.257121 · Cited by 182 · see citing works
Sola, O. M., Christensen, D. L., & Martin, A. W. (1973) · Experimental Neurology · doi:10.1016/0014-4886(73)90182-9 · Cited by 182 · see citing works
Pervasive satellite cell contribution to uninjured adult muscle fibers
Pawlikowski, B. T., Pulliam, C., Betta, N. D., Kardon, G., & Olwin, B. B. (2015) · Skeletal Muscle · doi:10.1186/s13395-015-0067-1 · Cited by 182 · see citing works
The muscle satellite cell at 50: the formative years
Scharner, J., & Zammit, P. S. (2011) · Skeletal Muscle · doi:10.1186/2044-5040-1-28 · Cited by 180 · see citing works
Caspase-3 Regulation of Diaphragm Myonuclear Domain during Mechanical Ventilation–induced Atrophy
McClung, J. M., Kavazis, A. N., DeRuisseau, K. C., Falk, D. J., Deering, M. A., Lee, Y., Sugiura, T., & Powers, S. K. (2006) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200601-142oc · Cited by 180 · see citing works
SATELLITE CELL REGULATION FOLLOWING MYOTRAUMA CAUSED BY RESISTANCE EXERCISE
Vierck, J. L., O'Reilly, B. A., HOSSNER, K. L., António, J., Byrne, K. M., Bucci, L. R., & Dodson, M. V. (2000) · Cell Biology International · doi:10.1006/cbir.2000.0499 · Cited by 179 · see citing works
Cardasis, C. A., & Cooper, G. (1975) · Journal of Experimental Zoology · doi:10.1002/jez.1401910305 · Cited by 171 · 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
Heterogeneity in the muscle satellite cell population
Biressi, S., & Rando, T. A. (2010) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2010.09.003 · Cited by 168 · see citing works
DEVELOPMENT OF STRIATED MUSCLE
Fischman, D. A. (1972) · Elsevier eBooks · doi:10.1016/b978-0-12-119101-6.50010-x · Cited by 168 · see citing works
Laurent, G. J., Sparrow, M. P., & Millward, D. J. (1978) · Biochemical Journal · doi:10.1042/bj1760407 · Cited by 166 · see citing works
The regenerative response of single mature muscle fibers isolated in vitro
Konigsberg, U. R., Lipton, B. H., & Konigsberg, I. R. (1975) · Developmental Biology · doi:10.1016/0012-1606(75)90065-2 · Cited by 164 · see citing works
Murach, K. A., White, S. H., Wen, Y., Ho, A., Dupont-Versteegden, E. E., McCarthy, J. J., & Peterson, C. A. (2017) · Skeletal Muscle · doi:10.1186/s13395-017-0132-z · Cited by 156 · see citing works
Requirement of myomaker-mediated stem cell fusion for skeletal muscle hypertrophy
Goh, Q., & Millay, D. P. (2017) · eLife · doi:10.7554/elife.20007 · Cited by 157 · see citing works
Ontell, M. (1974) · The Anatomical Record · doi:10.1002/ar.1091780206 · Cited by 152 · see citing works
X‐Irradiation improves mdx mouse muscle as a model of myofiber loss in DMD
Wakeford, S., Watt, D. J., & Partridge, T. A. (1991) · Muscle & Nerve · doi:10.1002/mus.880140108 · Cited by 144 · see citing works
Neonatal muscle growth: A quantitative study
Ontell, M., & Dunn, R. F. (1978) · American Journal of Anatomy · doi:10.1002/aja.1001520408 · Cited by 142 · 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
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
The fate of newly formed satellite cells during compensatory muscle hypertrophy
Schiaffino, S., Pierobon Bormioli, S., & Aloisi, M. (1976) · Virchows Archiv B Cell Pathology · doi:10.1007/bf02899148 · Cited by 132 · see citing works
IGF-1 induces human myotube hypertrophy by increasing cell recruitment
Jacquemin, V., Furling, D., Bigot, A., Butler-Browne, G. S., & Mouly, V. (2004) · Experimental Cell Research · doi:10.1016/j.yexcr.2004.05.023 · Cited by 130 · see citing works
Lekic, P., Rubbino, I., Krasnoshtein, F., Cheifetz, S., McCulloch, C. A., & Tenenbaum, H. C. (1997) · The Anatomical Record · doi:10.1002/(sici)1097-0185(199703)247:3 · Cited by 42 · see citing works
Johnston, I. A. (1993) · Marine Biology · doi:10.1007/bf00350053 · Cited by 125 · see citing works
POSTEMBRYONIC GROWTH AND DIFFERENTIATION OF STRIATED MUSCLE
Goldspink, G. (1972) · Elsevier eBooks · doi:10.1016/b978-0-12-119101-6.50012-3 · Cited by 122 · 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
Nap1-mediated actin remodeling is essential for mammalian myoblast fusion
Nowak, S. J., Nahirney, P. C., Hadjantonakis, A., & Baylies, M. K. (2009) · Journal of Cell Science · doi:10.1242/jcs.047597 · Cited by 112 · see citing works
Dodson, M. V., Allen, R. E., & HOSSNER, K. L. (1985) · Endocrinology · doi:10.1210/endo-117-6-2357 · Cited by 111 · see citing works
Johnson, B. J., Halstead, N., White, M. E., Hathaway, M. R., DiCostanzo, A., & Dayton, W. R. (1998) · Journal of Animal Science · doi:10.2527/1998.76112779x · Cited by 110 · 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
Gabella, G. (1979) · Cell and Tissue Research · doi:10.1007/bf00238048 · Cited by 108 · 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
Reduced Satellite Cell Numbers with Spinal Cord Injury and Aging in Humans
Verdijk, L. B., Dirks, M. L., Snijders, T., Prompers, J. J., Beelen, M., Jonkers, R. A. M., Thijssen, D. H. J., Hopman, M. T. E., & van Loon, L. J. C. (2012) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0b013e3182667c2e · Cited by 107 · 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
Anderson, J. E. (2006) · Journal of Experimental Biology · doi:10.1242/jeb.02088 · Cited by 103 · see citing works
Neonatal muscle: An electron microscopic study
Ontell, M. (1977) · The Anatomical Record · doi:10.1002/ar.1091890410 · Cited by 102 · see citing works
Neal, A., Boldrin, L., & Morgan, J. E. (2012) · PLoS ONE · doi:10.1371/journal.pone.0037950 · Cited by 99 · see citing works
Somitogenesis: From somite to skeletal muscle
Musumeci, G., Castrogiovanni, P., Coleman, R., Szychlinska, M. A., Salvatorelli, L., Parenti, R., Magro, G. G., & Imbesi, R. (2015) · Acta Histochemica · doi:10.1016/j.acthis.2015.02.011 · Cited by 97 · see citing works
The concept of skeletal muscle memory: Evidence from animal and human studies
Snijders, T., Aussieker, T., Holwerda, A. M., Parise, G., van Loon, L. J. C., & Verdijk, L. B. (2020) · Acta Physiologica · doi:10.1111/apha.13465 · Cited by 96 · see citing works
STAT3 in Skeletal Muscle Function and Disorders
Guadagnin, E., Mázala, D. A. G., & Chen, Y. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19082265 · Cited by 91 · see citing works
The origin, molecular regulation and therapeutic potential of myogenic stem cell populations
Otto, A., Collins‐Hooper, H., & Patel, K. (2009) · Journal of Anatomy · doi:10.1111/j.1469-7580.2009.01138.x · Cited by 94 · see citing works
Kandalla, P. K., Goldspink, G., Butler-Browne, G. S., & Mouly, V. (2011) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2011.02.007 · Cited by 89 · see citing works
Optimization of bovine satellite cell-derived myotube formation in vitro
Dodson, M. V., Martin, E., Brannon, M. A., Mathison, B. A., & McFarland, D. C. (1987) · Tissue and Cell · doi:10.1016/0040-8166(87)90001-2 · Cited by 84 · see citing works
Park, C. Y., Pierce, S. A., von Drehle, M., Ivey, K. N., Morgan, J. A., Blau, H. M., & Srivastava, D. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1013493107 · Cited by 82 · see citing works
Maier, A., McEwan, J. C., Dodds, K. G., Fischman, D. A., Fitzsimons, R. B., & Harris, A. (1992) · Journal of Muscle Research and Cell Motility · doi:10.1007/bf01737997 · Cited by 81 · see citing works
Myonuclear content regulates cell size with similar scaling properties in mice and humans
Hansson, K., Eftestøl, E., Bruusgaard, J. C., Juvkam, I. S., Cramer, A., Malthe‐Sørenssen, A., Millay, D. P., & Gundersen, K. (2020) · Nature Communications · doi:10.1038/s41467-020-20057-8 · Cited by 79 · see citing works
Koumans, J. T. M., Akster, H. A., Booms, G. H. R., & Osse, J. W. M. (1993) · Journal of Fish Biology · doi:10.1111/j.1095-8649.1993.tb00411.x · Cited by 78 · see citing works
Is the myonuclear domain size fixed?
van der Meer, S. F. T., Jaspers, R. T., & Degens, H. (2011) · PubMed · Cited by 78 · see citing works
Moresi, V., Pristerà, A., Scicchitano, B. M., Molinaro, M., Teodori, L., Sassoon, D. A., Adamo, S., & Coletti, D. (2008) · Stem Cells · doi:10.1634/stemcells.2007-0493 · Cited by 76 · see citing works
Powell, R. L., Dodson, M. V., & Cloud, J. G. (1989) · Journal of Experimental Zoology · doi:10.1002/jez.1402500314 · Cited by 76 · see citing works
Myosatellite cells, growth, and regeneration in murine dystrophic muscle: A quantitative study
Ontell, M., Feng, K. C., Klueber, K. M., Dunn, R. F., & Taylor, F. H. (1984) · The Anatomical Record · doi:10.1002/ar.1092080203 · Cited by 74 · see citing works
Purification of human muscle satellite cells by flow cytometry
Baroffio, A., Aubry, J., Kaelin, A., Krause, R. M., Hamann, M., & Bader, C. R. (1993) · Muscle & Nerve · doi:10.1002/mus.880160511 · Cited by 68 · see citing works
Impaired regeneration: A role for the muscle microenvironment in cancer cachexia
Talbert, E. E., & D, D. C. G. (2015) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2015.09.009 · Cited by 67 · see citing works
Piestun, Y., Yahav, S., & Halevy, O. (2015) · Poultry Science · doi:10.3382/ps/pev245 · Cited by 65 · see citing works
Stem cells and heterotopic ossification: Lessons from animal models
Lees‐Shepard, J. B., & Goldhamer, D. J. (2018) · Bone · doi:10.1016/j.bone.2018.01.029 · Cited by 63 · see citing works
The Effects of Ergogenic Compounds on Myogenic Satellite Cells
Vierck, J. L., ICENOGGLE, D. L., Bucci, L. R., & Dodson, M. V. (2003) · Medicine & Science in Sports & Exercise · doi:10.1249/01.mss.0000065005.96298.01 · Cited by 63 · see citing works
Numbers of myosatellite cells in white axial muscle of growing fish: Cyprinus carpio L. (teleostei)
Koumans, J. T. M., Akster, H. A., Booms, G. H. R., Lemmens, C. J. J., & Osse, J. W. M. (1991) · American Journal of Anatomy · doi:10.1002/aja.1001920409 · Cited by 63 · see citing works
Rouger, K., Brault, M., Daval, N., Leroux, I., Guigand, L., Lesoeur, J., Fernandez, B., & Chérel, Y. (2004) · Cell and Tissue Research · doi:10.1007/s00441-004-0911-9 · Cited by 61 · see citing works
Tertiary myotubes in postnatal growing pig muscle detected by their myosin isoform composition1
Mascarello, F., Stecchini, M. L., Rowlerson, A. M., & Ballocchi, E. (1992) · Journal of Animal Science · doi:10.2527/1992.7061806x · Cited by 61 · see citing works
Transdetermination: Drosophila imaginal disc cells exhibit stem cell-like potency
McClure, K. D., & Schubiger, G. (2007) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2007.01.007 · Cited by 60 · see citing works
Molnar, G., Ho, M.-L., & Schroedl, N. A. (1996) · Tissue and Cell · doi:10.1016/s0040-8166(96)80057-7 · Cited by 60 · see citing works
Gabella, G. (1994) · Handbook of experimental pharmacology · doi:10.1007/978-3-642-78920-5_1 · Cited by 58 · see citing works
DNA synthesis and differentiation in developing white adipose tissue
Pilgrim, C. (1971) · Developmental Biology · doi:10.1016/0012-1606(71)90108-4 · Cited by 58 · see citing works
Methods for animal satellite cell culture under a variety of conditions
Burton, N. M., Vierck, J. F., Krabbenhoft, L., Bryne, K. M., & Dodson, M. V. (2000) · Methods in Cell Science · doi:10.1023/a:1009830114804 · Cited by 57 · see citing works
Barjot, C., Cotten, M.-L., Goblet, C., Whalen, R. G., & Bacou, F. (1995) · Journal of Muscle Research and Cell Motility · doi:10.1007/bf00130243 · Cited by 55 · 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
The myonuclear domain in adult skeletal muscle fibres: past, present and future
Bagley, J. R., Denes, L. T., McCarthy, J. J., Wang, E. T., & Murach, K. A. (2023) · The Journal of Physiology · doi:10.1113/jp283658 · Cited by 56 · see citing works
- Authors
- Moss, F. P., & Leblond, C. P.
- Affiliations
- McGill University (CA)
- Venue
- The Journal of Cell Biology
- Publisher
- Rockefeller University Press
- Published
- 1970-02-01
- Volume
- 44
- Issue
- 2
- Pages
- 459-461
- ISSN
- 0021-9525 (ISSN-L)
- 1540-8140
- PMC
- PMC2107938
- OpenAlex
- W1981218555
- Cited by
- 289
- References
- 12
- Citations by year
- 2026: 3 · 2025: 3 · 2024: 5 · 2023: 4 · 2022: 7 · 2021: 8 · 2020: 7 · 2019: 6 · 2018: 6 · 2017: 11 · 2016: 4 · 2015: 16 · 2014: 4 · 2013: 12 · 2012: 8
- FWCI
- 5.67
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- cc-by-nc-sa
- Locations
- The Journal of Cell Biology (publishedVersion)
- PubMed Central (publishedVersion, cc-by-nc-sa)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- skeletal muscle growth, muscle fiber hypertrophy, myoblast proliferation, myotube fusion, myoblasts, myogenesis, cell division, young rats, muscle fiber number
- MeSH terms
- Animals, Autoradiography, Basement Membrane, Cell Nucleus, Cytoplasm, Male, Microscopy, Electron, Muscle Proteins, Muscles, Tritium, Muscle Development, 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