The DOI matches its Crossref record; 50 of the 53 references it cites were found in a registry or an index.
Satellite cells in human skeletal muscle; from birth to old age
Open accessAbstract
Changes in satellite cell content play a key role in regulating skeletal muscle growth and atrophy. Yet, there is little information on changes in satellite cell content from birth to old age in humans. The present study defines muscle fiber type-specific satellite cell content in human skeletal muscle tissue over the entire lifespan. Muscle biopsies were collected in 165 subjects, from different muscles of children undergoing surgery (<18 years; n = 13) and from the vastus lateralis muscle of young adult (18–49 years; n = 50), older (50–69 years; n = 53), and senescent subjects (70–86 years; n = 49). In a subgroup of 51 aged subjects (71 ± 6 years), additional biopsies were collected after 12 weeks of supervised resistance-type exercise training. Immunohistochemistry was applied to assess skeletal muscle fiber type-specific composition, size, and satellite cell content. From birth to adulthood, muscle fiber size increased tremendously with no major changes in muscle fiber satellite cell content, and no differences between type I and II muscle fibers. In contrast to type I muscle fibers, type II muscle fiber size was substantially smaller with increasing age in adults (r = −0.56; P < 0.001). This was accompanied by an age-related reduction in type II muscle fiber satellite cell content (r = −0.57; P < 0.001). Twelve weeks of resistance-type exercise training significantly increased type II muscle fiber size and satellite cell content. We conclude that type II muscle fiber atrophy with aging is accompanied by a specific decline in type II muscle fiber satellite cell content. Resistance-type exercise training represents an effective strategy to increase satellite cell content and reverse type II muscle fiber atrophy.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The text we found for this paper looks like another document, so the self-check wasn’t run.
Citations
Cites
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
Skeletal muscle mass and distribution in 468 men and women aged 18–88 yr
Janssen, I., Heymsfield, S. B., Wang, Z., & Ross, R. (2000) · Journal of Applied Physiology · doi:10.1152/jappl.2000.89.1.81 · Cited by 3,087
What is the cause of the ageing atrophy?
Lexell, J. E., Taylor, C. C., & Sjöstróm, M. (1988) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(88)90132-3 · Cited by 2,080
Myogenic satellite cells: physiology to molecular biology
Hawke, T. J., & Garry, D. J. (2001) · Journal of Applied Physiology · doi:10.1152/jappl.2001.91.2.534 · Cited by 1,646
High-Intensity Strength Training in Nonagenarians: Effects on Skeletal Muscle
Fiatarone, M. A. (1990) · JAMA · doi:10.1001/jama.1990.03440220053029 · Cited by 1,593 · cited 2×
“Resistance-type exercise training represents an effective interventional strategy to increase muscle mass and function in the elderly (Fiatarone et al. 1990; Frontera et al. 1988).”
BackgroundStrength conditioning in older men: skeletal muscle hypertrophy and improved function
Frontera, W. R., Meredith, C. N., O'Reilly, K. P., Knuttgen, H. G., & Evans, W. J. (1988) · Journal of Applied Physiology · doi:10.1152/jappl.1988.64.3.1038 · Cited by 1,386
Percutaneous Needle Biopsy of Skeletal Muscle in Physiological and Clinical Research
Bergström, J. P. (1975) · Scandinavian Journal of Clinical and Laboratory Investigation · doi:10.3109/00365517509095787 · Cited by 1,173
Age and gender comparisons of muscle strength in 654 women and men aged 20–93 yr
Lindle, R. S., Metter, E. J., Lynch, N. A., Fleg, J. L., Fozard, J. L., Tobin, J. D., Roy, T. A., & Hurley, B. F. (1997) · Journal of Applied Physiology · doi:10.1152/jappl.1997.83.5.1581 · Cited by 971
Muscle satellite cells adopt divergent fates
Zammit, P. S., Golding, J. P., Nagata, Y., Hudon, V., Partridge, T. A., & Beauchamp, J. R. (2004) · The Journal of Cell Biology · doi:10.1083/jcb.200312007 · Cited by 924
Visser, M., Kritchevsky, S. B., Goodpaster, B. H., Newman, A. B., Nevitt, M., Stamm, E., & Harris, T. B. (2002) · Journal of the American Geriatrics Society · doi:10.1046/j.1532-5415.2002.50217.x · Cited by 845
Cited by
Sorted by citations
Items 201–300 of 398
Muscle fibroblasts and stem cells stimulate motor neurons in an age and exercise‐dependent manner
Soendenbroe, C., Schjerling, P., Bechshøft, C. J. L., Svensson, R. B., Schaeffer, L., Kjær, M., Chazaud, B., Jacquier, A., & Mackey, A. L. (2024) · Aging Cell · doi:10.1111/acel.14413 · Cited by 13
A simple model of immune and muscle cell crosstalk during muscle regeneration
Kojouharov, H. V., Chen‐Charpentier, B. M., Solís, F. J., Biguetti, C. C., & Brotto, M. A. P. (2021) · Mathematical Biosciences · doi:10.1016/j.mbs.2021.108543 · Cited by 16
Ong, C., Lee, J. H., Leow, M. K., & Puthucheary, Z. (2021) · Translational Pediatrics · doi:10.21037/tp-20-298 · Cited by 14
Binet, E. R., McKenna, C. F., Salvador, A. F., Martinez, I. G., Alamilla, R. A., Collao, N., Bodnariuc, G., Khan, N. A., Paluska, S. A., Burd, N. A., et al. (2022) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00274.2022 · Cited by 15
Pax7-Positive Cells/Satellite Cells in Human Extraocular Muscles
Lindström, M., Tjust, A. E., & Domellöf, F. P. (2015) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.15-16544 · Cited by 14
A Comparison of Ovine Facial and Limb Muscle as a Primary Cell Source for Engineered Skeletal Muscle
Rodriguez, B. L., Nguyen, M. H., Armstrong, R. E., Vega-Soto, E. E., Polkowski, P. M., & Larkin, L. M. (2019) · Tissue Engineering Part A · doi:10.1089/ten.tea.2019.0087 · Cited by 15
Capillary facilitation of skeletal muscle function in health and disease
Parise, G., Murrant, C. L., Cocks, M. S., Snijders, T., Baum, O., & Plyley, M. J. (2019) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/apnm-2019-0416 · Cited by 14
Self-citationKim, C.-J., Kim, S.-H., Lee, E.-Y., Hwang, Y.-H., Lee, S. Y., & Joo, S.-T. (2024) · Food Science of Animal Resources · doi:10.5851/kosfa.2024.e72 · Cited by 13
Muscle regeneration and muscle stem cells in metabolic disease
Chung, J. D., Porrello, E. R., & Lynch, G. S. (2024) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2024.11.041 · Cited by 16
Age related changes of the motor excitabilities and central and peripheral muscle strength
Chuang, Y.-F., Chen, C., Hsu, M., Huang, N.-J., Huang, Y., Chan, H., & Chang, Y. (2018) · Journal of Electromyography and Kinesiology · doi:10.1016/j.jelekin.2018.12.007 · Cited by 12
Modeling muscle regeneration in RNA toxicity mice
Yadava, R. S., Mandal, M., Giese, J. M., Rigo, F., Bennett, C. F., & Mahadevan, M. S. (2021) · Human Molecular Genetics · doi:10.1093/hmg/ddab108 · Cited by 13
A Coupled Mechanobiological Model of Muscle Regeneration In Cerebral Palsy
Khuu, S., Fernandez, J. W., & Handsfield, G. (2021) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2021.689714 · Cited by 8
Guzman, S. D., Judge, J., Shigdar, S. M., Paul, T. A., Davis, C. S., Macpherson, P. C. D., Markworth, J. F., Remmen, H. V., Richardson, A. G., McArdle, A., et al. (2022) · Frontiers in Aging · doi:10.3389/fragi.2021.821904 · Cited by 14
Prokopidis, K., Giannos, P., Witard, O. C., Peckham, D. G., & Ispoglou, T. (2022) · PLoS ONE · doi:10.1371/journal.pone.0273766 · Cited by 13
Train your T cells: How skeletal muscles and T cells keep each other fit during aging
Slaets, H., Fonteyn, L., Eijnde, B. O., & Hellings, N. (2023) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2023.03.006 · Cited by 12
Pericytes in Muscular Dystrophies
Moyle, L. A., Tedesco, F. S., & Benedetti, S. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-16908-4_15 · Cited by 15
Notch, Numb and Numb‐like responses to exercise‐induced muscle damage in human skeletal muscle
Bubak, M. P., Stout, K. W., Tomtschik, J., Peterson, E., Cardozo, C. P., Graham, Z., & Gallagher, P. M. (2022) · Experimental Physiology · doi:10.1113/ep090364 · Cited by 12
Inflammation-associated miR-155 activates differentiation of muscular satellite cells
Onodera, Y., Teramura, T., Takehara, T., Itokazu, M., Mori, T., & Fukuda, K. (2018) · PLoS ONE · doi:10.1371/journal.pone.0204860 · Cited by 11
Skoglund, E., GrönholdtKlein, M., Rullman, E., Thornell, L. E., Strömberg, A., Hedman, A., Cederholm, T., Ulfhake, B., & Gustafsson, T. P. (2019) · The Journals of Gerontology Series A · doi:10.1093/gerona/glz068 · Cited by 12
Schaaf, G., Canibano‐Fraile, R., van Gestel, T. J. M., van der Ploeg, A. T., & Pijnappel, W. W. M. P. (2019) · Annals of Translational Medicine · doi:10.21037/atm.2019.04.48 · Cited by 14
Chemoradiation impairs myofiber hypertrophic growth in a pediatric tumor model
Paris, N. D., Kallenbach, J. G., Bachman, J. F., Blanc, R. S., Johnston, C. J., Hernady, E., Williams, J. P., & Chakkalakal, J. V. (2020) · Scientific Reports · doi:10.1038/s41598-020-75913-w · Cited by 12
Exercise, Exerkines, and Sarcopenia
Chung, H. S., & Choi, K. M. (2026) · Diabetes & Metabolism Journal · doi:10.4093/dmj.2025.0972 · Cited by 12
Laminin-111 Improves the Anabolic Response to Mechanical Load in Aged Skeletal Muscle
Garg, K., Mahmassani, Z. S., Dvoretskiy, S., Valero, M. C., Huntsman, H. D., Lapp, S., Wu, Y., Hauschka, S. D., Burkin, D. J., & Boppart, M. D. (2020) · The Journals of Gerontology Series A · doi:10.1093/gerona/glaa308 · Cited by 12
Melatonin ameliorates age-related sarcopenia by inhibiting fibrogenic conversion of satellite cell
Zhu, G.-Z., Zhao, K., Li, H.-Z., Wu, D.-Z., Chen, Y.-B., Han, D., Gao, J.-W., Chen, X., Yu, Y.-P., Huang, Z., et al. (2024) · Molecular Medicine · doi:10.1186/s10020-024-00998-2 · Cited by 15
LBP1C-2 from Lycium barbarum maintains skeletal muscle satellite cell pool by interaction with FGFR1
Meng, J., Lv, Z., Chen, X., Sun, C., Jin, C., Ding, K., & Chen, C. (2023) · iScience · doi:10.1016/j.isci.2023.106573 · Cited by 13
Preventative and therapeutic potential of tocotrienols on musculoskeletal diseases in ageing
Gany, S. L. S., Chin, K., Tan, J. K., Aminuddin, A., & Makpol, S. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1290721 · Cited by 12
Zhou, Y., Chen, J., Li, Z., Tan, S., Yan, C., Luo, S., Zhou, L., Song, J., Huan, X., Wang, Y., et al. (2022) · Frontiers in Neurology · doi:10.3389/fneur.2022.879261 · Cited by 11
Pérez, K., McGirr, J., Limbad, C., Doi, R., Nederveen, J. P., Nilsson, M. I., Tarnopolsky, M. A., Campisi, J., & Melov, S. (2021) · medRxiv · doi:10.1101/2021.01.22.21250336 · Cited by 12
Oleate Ameliorates Palmitate-Induced Impairment of Differentiative Capacity in C2C12 Myoblast Cells
Xue, M., Zhang, F., Ji, X., Yu, H., Jiang, X., Qiu, Y., Yu, J., Chen, J., Yang, F., & Bao, Z. (2021) · Stem Cells and Development · doi:10.1089/scd.2020.0168 · Cited by 10
Filippo, E. S. D., Bondi, D., Pietrangelo, T., Fanò, G., & Fulle, S. (2020) · Journal of Science in Sport and Exercise · doi:10.1007/s42978-020-00065-2 · Cited by 10
Brown, A. D., Stewart, C. E., & Burniston, J. G. (2022) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.13034 · Cited by 9
Noguchi, K. S., Mcleod, J. C., Phillips, S. M., Richardson, J. A., & Tang, A. (2023) · Physical Therapy · doi:10.1093/ptj/pzad095 · Cited by 9
Motohashi, N., Minegishi, K., & Aoki, Y. (2023) · Cell Death and Disease · doi:10.1038/s41419-023-06192-2 · Cited by 10
Ruple, B. A., Mattingly, M. L., Godwin, J. S., McIntosh, M. C., Kontos, N. J., Agyin-Birikorang, A., Michel, J. M., Plotkin, D. L., Chen, S., Ziegenfuss, T. N., et al. (2024) · The FASEB Journal · doi:10.1096/fj.202302103rrr · Cited by 9
Sullivan, B. P., Larson, A. A., Shams, A. S., McMillin, S. L., Ebeling, M. C., Peng, S., Kyba, M., & Lowe, D. A. (2024) · Aging Cell · doi:10.1111/acel.14441 · Cited by 9
Gorski, T., Casartelli, N. C., Fitzgerald, G., Horstman, A. M. H., Masschelein, E., Essers, K. J., Maffiuletti, N. A., Sutter, R., Leunig, M., & Bock, K. D. (2024) · Skeletal Muscle · doi:10.1186/s13395-024-00364-0 · Cited by 9
Microscopic and molecular aspects of skeletal muscle alterations in cerebral palsy
Edman, S., Horwath, O., Pontén, E., Dayanidhi, S., & von Walden, F. (2025) · Developmental Medicine & Child Neurology · doi:10.1111/dmcn.70044 · Cited by 11
Exercise attenuates the hallmarks of aging: Novel perspectives
Qiu, Y., Fernández‐Garcia, B., Lehmann, H. I., Li, G., Kroemer, G., López-Otín, C., & Xiao, J. (2025) · Journal of sport and health science/Journal of Sport and Health Science · doi:10.1016/j.jshs.2025.101108 · Cited by 16
Lilja, M. R., Moberg, M., Apró, W., Martínez-Aranda, L. M., Rundqvist, H., Langlet, B. S., Gustafsson, T. P., & Lundberg, T. R. (2023) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00698.2022 · Cited by 11
Satellite cells in the growth and maintenance of muscle
Bachman, J. F., & Chakkalakal, J. V. (2024) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2024.01.020 · Cited by 9
Premature aging in chronic kidney disease and chronic obstructive pulmonary disease
Kooman, J. P., Shiels, P. G., & Stenvinkel, P. (2015) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0000000000000218 · Cited by 9
The Influence and Delivery of Cytokines and their Mediating Effect on Muscle Satellite Cells
Nederveen, J. P., Joanisse, S., Snijders, T., & Parise, G. (2017) · Current Stem Cell Reports · doi:10.1007/s40778-017-0089-1 · Cited by 10
Self-citationGautam, J., & Yao, Y. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-11093-2_4 · Cited by 10
Lim, C., Dunford, E. C., Valentino, S. E., Oikawa, S. Y., McGlory, C., Baker, S., MacDonald, M. J., & Phillips, S. M. (2020) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0000000000002573 · Cited by 9
Short-term metformin ingestion by healthy older adults improves myoblast function
Mahmassani, Z. S., McKenzie, A. I., Petrocelli, J. J., de Hart, N. M. M. P., Reidy, P. T., Fix, D. K., Ferrara, P. J., Funai, K., & Drummond, M. J. (2021) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00469.2020 · Cited by 10
Effect of resistance training on satellite cells in old mice – a transcriptome study
Hsu, W.-B., Lin, S.-J., Hung, J.-S., Chen, M.-H., Lin, C.-Y., Hsu, W.-H., & Hsu, W.-W. R. (2022) · Bone and Joint Research · doi:10.1302/2046-3758.112.bjr-2021-0079.r2 · Cited by 9
Shamim, B., Camera, D. M., & Whitfield, J. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.625044 · Cited by 8
Sarcopenia and sarcopenic obesity in cardiovascular disease: a comprehensive review
Tan, L. F., Sia, C., & Merchant, R. A. (2025) · Singapore Medical Journal · doi:10.4103/singaporemedj.smj-2024-233 · Cited by 10
Age-dependent mechanical and microstructural properties of the rabbit soleus muscle
Leichsenring, K., Viswanathan, A., Kutschke, S., Siebert, T., & Böl, M. (2021) · Acta Biomaterialia · doi:10.1016/j.actbio.2021.07.066 · Cited by 8
Mei, C. T. Y., Ying, S. S. S., Yanshan, D. L., Koh, S. V., Karthikeyan, G., Xia, O. J., Low, X. L., Quek, H. Y., Shuyi, A. O., Low, L. L., et al. (2024) · PLoS ONE · doi:10.1371/journal.pone.0291702 · Cited by 8
The Role of the MYL4 Gene in Porcine Muscle Development and Its Molecular Regulatory Mechanisms
Ye, Y., Wu, G., Wang, H., Duan, M., Shang, P., & Chamba, Y. (2024) · Animals · doi:10.3390/ani14091370 · Cited by 8
Sarcopenia: an Aging Perspective and Management Options
Teixeira, A. M., Nosrani, S. E., Parvani, M., Viola, J., & Mohammadi, S. (2025) · International Journal of Sports Medicine · doi:10.1055/a-2577-2577 · Cited by 10
Nutritional strategies targeting age-related skeletal muscle fibrosis: underlying mechanisms
Cuijpers, I., Katsburg, J., van Loon, L. J. C., Troost, F. J., & Sthijns, M. M. J. P. E. (2025) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2025.2498676 · Cited by 8
Ashton, K. J., Kiessling, C. J., Thompson, J. M., Aziz, A. Y., Thomas, W. G., Headrick, J. P., & Reichelt, M. E. (2022) · Experimental Gerontology · doi:10.1016/j.exger.2022.112011 · Cited by 7
Heidari, D., Shirvani, H., Bazgir, B., & Shamsoddini, A. (2023) · PubMed Central · doi:10.22074/cellj.2023.1986679.1206 · Cited by 7
Zheng, M., Shao, Y. M., Gong, C., Wu, Y., Liu, W., & Chen, M. (2024) · European Geriatric Medicine · doi:10.1007/s41999-024-01101-y · Cited by 7
Muscle Homeostasis Is Disrupted in Burned Adults
Clark, A. T., Song, J., Xiao, Y., Carlson, D., Huebinger, R. M., Liu, M. M., Madni, T. D., Imran, J. B., Taveras, L. R., Weis, H. B., et al. (2019) · Journal of Burn Care & Research · doi:10.1093/jbcr/irz190 · Cited by 7
Nerve Lesions in Volkmann Ischemic Contracture
Özer, K. (2020) · The Journal Of Hand Surgery · doi:10.1016/j.jhsa.2020.03.027 · Cited by 7
Schweitzer, A. M., Koehle, M. S., Fliss, M. D., & Mitchell, C. J. (2025) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00992.2024 · Cited by 7
Shaikh, S., Ahmad, K., Lim, J. H., Ahmad, S. S., Lee, E. J., & Choi, I. (2025) · Pharmaceuticals · doi:10.3390/ph18091407 · Cited by 7
Wang, X., Zong, X., Ye, M., Jin, C., Xu, T., Yang, J., Gao, C., Wang, X., & Yan, H. (2024) · Cells · doi:10.3390/cells13070650 · Cited by 6
Zhong, J., Yuan, H., Yang, J., Du, Y. Y., Li, Z., Liu, X., Yang, H., Wang, Z., Wang, Z., Jiang, L., et al. (2024) · Frontiers in Medicine · doi:10.3389/fmed.2024.1378846 · Cited by 8
Normann, A. J., Mo, C. C., Wilson, R. L., Perez, M., Cutler, C. S., Uno, H., Thompson, L. V., Skinner, T. L., Richardson, P. G. G., Marinac, C. R., et al. (2024) · JMIR Research Protocols · doi:10.2196/64905 · Cited by 6
Mori, T., Onodera, Y., Itokazu, M., Takehara, T., Shigi, K., Iwawaki, N., Akagi, M., & Teramura, T. (2022) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2022.111619 · Cited by 6
Walz, I., Waibel, S. M., Kuhner, A., Gollhofer, A., & Maurer, C. (2023) · BMC Geriatrics · doi:10.1186/s12877-023-04150-3 · Cited by 6
Deschrevel, J., Maes, K., Andries, A., Beukelaer, N. D., Corvelyn, M., Costamagna, D., Campenhout, A. V., Wachter, E. D., Desloovere, K., Agten, A., et al. (2023) · PLoS ONE · doi:10.1371/journal.pone.0294395 · Cited by 6
Histological analysis of the medial gastrocnemius muscle in young healthy children
Andries, A., Deschrevel, J., Maes, K., Beukelaer, N. D., Corvelyn, M., Staut, L., Houwer, H. D., Costamagna, D., Nijs, S., Metsemakers, W., et al. (2024) · Frontiers in Physiology · doi:10.3389/fphys.2024.1336283 · Cited by 6
Satellite cell activation as a critical step in skeletal muscle plasticity
Verdijk, L. B. (2014) · Experimental Physiology · doi:10.1113/expphysiol.2014.081273 · Cited by 6
Self-citationMuscle Stem Cells: A Model System for Adult Stem Cell Biology
Cornelison, D., & Perdiguero, E. (2017) · Methods in molecular biology · doi:10.1007/978-1-4939-6771-1_1 · Cited by 6
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
Gaulton, N., Wakelin, G., Young, L. V., Wotherspoon, S., Kamal, M. J., Parise, G., Nederveen, J. P., Holwerda, A. M., Verdijk, L. B., van Loon, L. J. C., et al. (2022) · The FASEB Journal · doi:10.1096/fj.202201349rr · Cited by 7
Self-citationSatellite cells: promoting adaptation over a lifetime
Parise, G. (2013) · Acta Physiologica · doi:10.1111/apha.12219 · Cited by 6
Wang, J., Groennebaek, T., Nielsen, R. R., Pryds, K., de Paoli, F. V., Bøtker, H. E., & Vissing, K. (2025) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00275.2025 · Cited by 5
Skeletal muscle memory: implications for sports, aging and nutrition
Pérez-Castillo, Í. M., Ruiz-Caride, S. R., Rueda, R., Chicharro, J. L., Segura-Ortiz, F., & Bouzamondo, H. (2025) · Frontiers in Nutrition · doi:10.3389/fnut.2025.1701520 · Cited by 7
The impact of cellular senescence on aging skeletal muscle
Kamal, M. J., Bevington, R. T., Johnson, A., & Parise, G. (2025) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2025.1719279 · Cited by 7
Zhao, X., Wu, X., He, L., Xiao, J., Xiang, R., Sha, L., Tang, M., Yu, H., Qu, Y., Xiao, C., et al. (2025) · Scandinavian Journal of Medicine and Science in Sports · doi:10.1111/sms.70014 · Cited by 7
46th Walter J. Zeiter Lecture, Exercise Is Rehabilitation Medicine: Our History and Future
Becker, B. E. (2015) · PM&R · doi:10.1016/j.pmrj.2015.02.013 · Cited by 6
The congenital clubfoot – immunohistological analysis of the extracellular matrix
Kerling, A., Stoltenburg, G., Grams, L., Tegtbur, U., Horstmann, H., Kück, M., & Mellerowicz, H. (2018) · Orthopedic Research and Reviews · doi:10.2147/orr.s156449 · Cited by 5
The Performance of Powerlifting Athletes During Their Lifetime
Ugalde, J. A. H. (2021) · MHSALUD Revista en Ciencias del Movimiento Humano y Salud · doi:10.15359/mhs.19-1.4 · Cited by 5
The influence of biological sex in human skeletal muscle transcriptome during ageing
Huang, X., Chen, M., Xiao, Y., Zhu, F., Chen, L., Tian, X., & Hong, L. (2023) · Biogerontology · doi:10.1007/s10522-023-10070-x · Cited by 5
Linhares, D. G., Alves, A. D. S., Barreto, Y. A., Narciso, O. B., Filho, A. V. D. S., Cardozo, G. G., da Costa, M. G., de Castro, J. B. P., & Vale, R. G. D. S. (2023) · Muscles Ligaments and Tendons Journal · doi:10.32098/mltj.04.2023.05 · Cited by 5
Leveraging Biomaterial Platforms to Study Aging-Related Neural and Muscular Degeneration
Hidalgo‐Alvarez, V., & Madl, C. M. (2024) · Biomolecules · doi:10.3390/biom14010069 · Cited by 5
Sex-Based Differences in Muscle Stem Cell Regulation Following Exercise
Beaudry, K. M., & Lisio, M. D. (2024) · Exercise and Sport Sciences Reviews · doi:10.1249/jes.0000000000000337 · Cited by 5
Physical Activity and Redox Balance in the Elderly: Signal Transduction Mechanisms
Galli, D., Carubbi, C., Masselli, E., Vaccarezza, M., Presta, V., Pozzi, G., Ambrosini, L., Gobbi, G., Vitale, M., & Mirandola, P. (2021) · Applied Sciences · doi:10.3390/app11052228 · Cited by 6
Yamamoto, S., Honma, K., Fujii, M., Kakimoto, M., Kirihara, S., Nakayama, H., Kitamori, K., Sato, I., Hirohata, S., & Watanabe, S. (2023) · Annals of Anatomy - Anatomischer Anzeiger · doi:10.1016/j.aanat.2023.152104 · Cited by 5
Jensen, K. Y., Nielsen, J. L., Schrøder, H. D., Jacobsen, M., Boyle, E., Jørgensen, A. N., Bech, R. D., Frandsen, U., Aagaard, P., & Diederichsen, L. P. (2022) · Neuromuscular Disorders · doi:10.1016/j.nmd.2022.04.006 · Cited by 5
Bonnet, N., Capeding, M. R., Siegwald, L., Garcia‐Garcerà, M., Desgeorges, T., Tytgat, H. L. P., Krattinger, L.-F., Lebumfacil, J. D., Phee, L., Moll, J. M., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-66930-2 · Cited by 5
Betz, M. W., Brandt, J. D., Aussieker, T., Monsegue, A. P., Houtvast, D. C. J., Gehlert, S., Verdijk, L. B., van Loon, L. J. C., Gosker, H. R., LANGEN, R. C. J., et al. (2024) · ERJ Open Research · doi:10.1183/23120541.00203-2024 · Cited by 4
Self-citationBonanni, R., Falvino, A., Matticari, A., Rinaldi, A. M., D’Arcangelo, G., Cifelli, P., Iundusi, R., Gasbarra, E., Tancredi, V., Cariati, I., et al. (2025) · Frontiers in Physiology · doi:10.3389/fphys.2025.1616693 · Cited by 4
Smith, E. F., Thomas, M., Kutukcu, E. C., Torres‐Sánchez, I., Santiago, M. G., Quijano-Campos, J. C., Sylvester, K. P., Burtin, C., Šajnić, A., Brandt, J. D., et al. (2020) · ERJ Open Research · doi:10.1183/23120541.00808-2020 · Cited by 4
Li, B., Wang, H., Li, A., An, C., Zhu, L., Liu, S., & Zhuang, Z. (2022) · Frontiers in Marine Science · doi:10.3389/fmars.2022.916373 · Cited by 4
Differential effects of vitamin D on upper and lower body fat-free mass: potential mechanisms
Kirwan, R. (2022) · Molecular Biology Reports · doi:10.1007/s11033-022-07998-7 · Cited by 4
Skeletal muscle fibre morphology in childhood—insights into myopenia in pediatric liver disease
Hager, A., Mazurak, V. C., Noga, M., Gilmour, S. M., & Mager, D. R. (2023) · Applied Physiology Nutrition and Metabolism · doi:10.1139/apnm-2023-0033 · Cited by 4
Osteosarcopenia as a satellite of aging
Isaeva, B. I., & Магомедовна, А.-Х. К. (2023) · Meditsinskiy sovet = Medical Council · doi:10.21518/ms2023-147 · Cited by 4
Wang, Z., Cao, J., Mou, J., Sun, D., Yan, D., & Liu, P. (2023) · Orthopaedic Surgery · doi:10.1111/os.13964 · Cited by 4
Lim, C., & changkeun, K. (2020) · Exercise Science · doi:10.15857/ksep.2020.29.1.77 · Cited by 4
A review of the status of sarcopenia in elderly hospitalized patients
Xian, X., Zhang, J., & Yang, H. (2025) · Medicine · doi:10.1097/md.0000000000043365 · Cited by 3
FGFR1 and FGFR4 are essential regulators of muscle stem cell quiescence
Yeh, C.-J., Nakka, K. K., Yablonka‐Reuveni, Z., & Lepper, C. (2025) · Cell Communication and Signaling · doi:10.1186/s12964-025-02533-0 · Cited by 4
Cell Death in Skeletal Muscle Diseases: Diverse Roles and Pathological Processes
Yang, Y.-L., & Guo, L. (2026) · Cells · doi:10.3390/cells15090744 · Cited by 3
Liu, Q., Zhu, M., Salekin, F., McCoy, B. M., Kennedy, V., Tian, J., Mazucanti, C. H., Chia, C. W., & Egan, J. M. (2024) · Cells · doi:10.3390/cells13221903 · Cited by 3
Metadata
- Authors
- Verdijk, L. B., Snijders, T., Drost, M., Delhaas, T., Kadi, F., & van Loon, L. J. C.
- Affiliations
- Maastricht University Medical Centre (NL)
- Örebro University (SE)
- Corresponding author
- Verdijk, Lex B.
- Venue
- AGE
- Published
- 2013-10-12
- Volume
- 36
- Issue
- 2
- Pages
- 545-557
- ISSN
- 0161-9152 (ISSN-L)
- 1574-4647
- PMC
- PMC4039250
- OpenAlex
- W2087317993
- Cited by
- 399
- References
- 53
- Citations by year
- 2026: 19 · 2025: 30 · 2024: 43 · 2023: 44 · 2022: 47 · 2021: 42 · 2020: 41 · 2019: 32 · 2018: 25 · 2017: 22 · 2016: 13 · 2015: 27 · 2014: 12 · 2013: 2
- FWCI
- 8.06
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- AGE (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Research Publications (Maastricht University) (publishedVersion, other-oa)
- Research Bank (Australian Catholic University) (submittedVersion)
- VUBIR (Vrije Universiteit Brussel) (submittedVersion)
- Research Publications (Maastricht University) (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Health Sciences › Nursing › Nutrition and Dietetics › Muscle metabolism and nutrition
- Health Sciences › Medicine › Physiology (medical) › Nutrition and Health in Aging
- Keywords
- satellite cells, skeletal muscle, muscle fiber type, fast-twitch muscle, muscle fiber size, muscle atrophy, aging, resistance training, lifespan, vastus lateralis, muscle growth
- MeSH terms
- Adolescent, Adult, Aged, Aged, 80 and over, Aging, Biopsy, Child, Child, Preschool, Female, Humans, Immunohistochemistry, Infant, Infant, Newborn, Laminin, Male, Middle Aged, Reference Values, Exercise Tolerance, Muscle Fibers, Fast-Twitch, Muscle Fibers, Slow-Twitch, Myosin Heavy Chains, CD56 Antigen, Satellite Cells, Skeletal Muscle, Young Adult
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