Muscle wasting and aging: Experimental models, fatty infiltrations, and prevention

Sarcopenia: European consensus on definition and diagnosis

Cruz-Jentoft, A. J., Baeyens, J. P., Bauer, J. M., Boirie, Y., Cederholm, T., Landi, F., Martin, F. C., Michel, J.-P., Rolland, Y., Schneider, S. M., et al. (2010) · Age and Ageing · doi:10.1093/ageing/afq034 · Cited by 11,601 · see citing works

A short physical performance battery assessing lower extremity function: association with self-reported disability and prediction of mortality and nursing home admission

Guralnik, J. M., Simonsick, E. M., Ferrucci, L., Glynn, R. J., Berkman, L. F., Blazer, D. G., Scherr, P. A., & Wallace, R. B. (1994) · Journal of Gerontology · doi:10.1093/geronj/49.2.m85 · Cited by 9,792 · see citing works

Epidemiology of Sarcopenia among the Elderly in New Mexico

Baumgartner, R. N., Koehler, K. M., Gallagher, D., Romero, L., Heymsfield, S. B., Ross, R. R., Garry, P. J., & Lindeman, R. D. (1998) · American Journal of Epidemiology · doi:10.1093/oxfordjournals.aje.a009520 · Cited by 4,004 · see citing works

Identification of ubiquitin ligases required for skeletal muscle atrophy.

Bodine, S. C., Latres, E., Baumhueter, S., Lai, V. K.-M., Nunez, L., Clarke, B. A., Poueymirou, W. T., Panaro, F. J., Na, E., Dharmarajan, K., et al. (2001) · Science · doi:10.1126/science.1065874 · Cited by 3,521 · see citing works

Sarcopenia: An Undiagnosed Condition in Older Adults. Current Consensus Definition: Prevalence, Etiology, and Consequences. International Working Group on Sarcopenia

Fielding, R. A., Vellas, B., Evans, W. J., Bhasin, S., Morley, J. E., Newman, A. B., Abellan van Kan, G., Andrieu, S., Bauer, J., Breuille, D., et al. (2011) · Journal of the American Medical Directors Association · doi:10.1016/j.jamda.2011.01.003 · Cited by 3,256 · cited 4× · see citing works

The Loss of Skeletal Muscle Strength, Mass, and Quality in Older Adults: The Health, Aging and Body Composition Study

Goodpaster, B. H., Park, S. W., Harris, T. B., Kritchevsky, S. B., Nevitt, M., Schwartz, A. V., Simonsick, E. M., Tylavsky, F. A., Visser, M., Newman, A. B., et al. (2006) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/61.10.1059 · Cited by 3,083 · cited 1× · see citing works

The Transforming Growth Factor-Beta Family

Massagué, J. (1990) · Annual Review of Cell Biology · doi:10.1146/annurev.cb.06.110190.003121 · Cited by 3,041 · see citing works

Foxo transcription factors induce the atrophy-related ubiquitin ligase atrogin-1 and cause skeletal muscle atrophy.

Sandri, M., Sandri, C., Gilbert, A., Skurk, C., Calabria, E., Picard, A., Walsh, K., Schiaffino, S., Lecker, S. H., & Goldberg, A. L. (2004) · Cell · doi:10.1016/s0092-8674(04)00400-3 · Cited by 3,012 · see citing works

Targeted disruption of the mouse transforming growth factor-β1 gene results in multifocal inflammatory disease

Shull, M. M., Ormsby, I., Kier, A. B., Pawlowski, S., Diebold, R. J., Yin, M., Allen, R., Sidman, C., Proetzel, G., Calvin, D., et al. (1992) · Nature · doi:10.1038/359693a0 · Cited by 2,985 · see citing works

Lower extremity function and subsequent disability: consistency across studies, predictive models, and value of gait speed alone compared with the short physical performance battery

Guralnik, J. M., Ferrucci, L., Pieper, C. F., Leveille, S. G., Markides, K. S., Ostir, G. V., Studenski, S., Berkman, L. F., & Wallace, R. B. (2000) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/55.4.m221 · Cited by 2,898 · see citing works

Rejuvenation of aged progenitor cells by exposure to a young systemic environment

Conboy, I. M., Conboy, M. J., Wagers, A. J., Girma, E. R., Weissman, I. L., & Rando, T. A. (2005) · Nature · doi:10.1038/nature03260 · Cited by 2,287 · see citing works

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 · see citing works

The IGF-1/PI3K/Akt pathway prevents expression of muscle atrophy-induced ubiquitin ligases by inhibiting FOXO transcription factors.

Stitt, T. N., Drujan, D., Clarke, B. A., Panaro, F., Timofeyva, Y., Kline, W. O., Gonzalez, M., Yancopoulos, G. D., & Glass, D. J. (2004) · Molecular Cell · doi:10.1016/s1097-2765(04)00211-4 · Cited by 1,964 · see citing works

Inhibition of Adipogenesis by Wnt Signaling

Ross, S. E., Hemati, N., Longo, K. A., Bennett, C. N., Lucas, P. C., Erickson, R. L., & MacDougald, O. A. (2000) · Science · doi:10.1126/science.289.5481.950 · Cited by 1,876 · see citing works

Invited Review: Aging and sarcopenia

Doherty, T. J. (2003) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00347.2003 · Cited by 1,764 · see citing works

The ageing systemic milieu negatively regulates neurogenesis and cognitive function

Villeda, S. A., Luo, J., Mosher, K. I., Zou, B., Britschgi, M., Bieri, G., Stan, T. M., Fainberg, N., Ding, Z., Eggel, A., et al. (2011) · Nature · doi:10.1038/nature10357 · Cited by 1,763 · see citing works

Consensus definition of sarcopenia, cachexia and pre-cachexia: joint document elaborated by Special Interest Groups (SIG) “cachexia-anorexia in chronic wasting diseases” and “nutrition in geriatrics”

Muscaritoli, M., Anker, S. D., Argilés, J., Aversa, Z., Bauer, J. M., Biolo, G., Boirie, Y., Bosaeus, I., Cederholm, T., Costelli, P., et al. (2010) · Clinical Nutrition · doi:10.1016/j.clnu.2009.12.004 · Cited by 1,732 · see citing works

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 · see citing works

Increased Wnt signaling during aging alters muscle stem cell fate and increases fibrosis

Brack, A. S., Conboy, M. J., Roy, S., Lee, M., Kuo, C. J., Keller, C., & Rando, T. A. (2007) · Science · doi:10.1126/science.1144090 · Cited by 1,564 · see citing works

Multiple types of skeletal muscle atrophy involve a common program of changes in gene expression

Lecker, S. H., Jagoe, R. T., Gilbert, A., Gomes, M., Baracos, V., Bailey, J., Price, S. R., Mitch, W. E., & Goldberg, A. L. (2004) · The FASEB Journal · doi:10.1096/fj.03-0610com · Cited by 1,539 · see citing works

Balance in elderly patients: the "get-up and go" test.

Mathias, S., Nayak, U. S., & Isaacs, B. (1986) · PubMed · Cited by 1,539 · see citing works

Mechanisms regulating skeletal muscle growth and atrophy

Schiaffino, S., Dyar, K. A., Ciciliot, S., Blaauw, B., & Sandri, M. (2013) · The FEBS Journal · doi:10.1111/febs.12253 · Cited by 1,492 · see citing works

Longitudinal study of muscle strength, quality, and adipose tissue infiltration

Delmonico, M. J., Harris, T. B., Visser, M., Park, S. W., Conroy, M. B., Velasquez-Mieyer, P., Boudreau, R., Manini, T. M., Nevitt, M., Newman, A. B., et al. (2009) · The American Journal of Clinical Nutrition · doi:10.3945/ajcn.2009.28047 · Cited by 1,446 · see citing works

Aging of skeletal muscle: a 12-yr longitudinal study

Frontera, W. R., Hughes, V. A., Fielding, R. A., Fiatarone, M. A., Evans, W. J., & Roubenoff, R. (2000) · Journal of Applied Physiology · doi:10.1152/jappl.2000.88.4.1321 · Cited by 1,443 · see citing works

Muscle Mass, Muscle Strength, and Muscle Fat Infiltration as Predictors of Incident Mobility Limitations in Well-Functioning Older Persons

Visser, M., Goodpaster, B. H., Kritchevsky, S. B., Newman, A. B., Nevitt, M., Rubin, S. M., Simonsick, E. M., Harris, T. B., & Study, F. T. H. A. (2005) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/60.3.324 · Cited by 1,403 · see citing works

Sarcopenia, dynapenia, and the impact of advancing age on human skeletal muscle size and strength; a quantitative review

Mitchell, W. K., Williams, J., Atherton, P., Larvin, M., Lund, J., & Narici, M. (2012) · Frontiers in Physiology · doi:10.3389/fphys.2012.00260 · Cited by 1,377 · see citing works

IKKβ/NF-κB Activation Causes Severe Muscle Wasting in Mice

Cai, D., Frantz, J. D., Tawa, N. E., Melendez, P. A., Oh, B.-C., Lidov, H. G. W., Hasselgren, P.-O., Frontera, W. R., Lee, J., Glass, D. J., et al. (2004) · Cell · doi:10.1016/j.cell.2004.09.027 · Cited by 1,367 · see citing works

Decline in skeletal muscle mitochondrial function with aging in humans

Short, K. R., Bigelow, M. L., Kahl, J., Singh, R., Coenen-Schimke, J., Raghavakaimal, S., & Nair, K. S. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0501559102 · Cited by 1,333 · see citing works

Mesenchymal progenitors distinct from satellite cells contribute to ectopic fat cell formation in skeletal muscle

Uezumi, A., Fukada, S., Yamamoto, N., Takeda, S., & Tsuchida, K. (2010) · Nature Cell Biology · doi:10.1038/ncb2014 · Cited by 1,315 · see citing works

Cellular and molecular mechanisms of muscle atrophy

Bonaldo, P., & Sandri, M. (2013) · Disease Models & Mechanisms · doi:10.1242/dmm.010389 · Cited by 1,284 · see citing works

Attenuation of skeletal muscle and strength in the elderly: the Health ABC Study

Goodpaster, B. H., Carlson, C. L., Visser, M., Kelley, D. E., Scherzinger, A., Harris, T. B., Stamm, E., & Newman, A. B. (2001) · Journal of Applied Physiology · doi:10.1152/jappl.2001.90.6.2157 · Cited by 1,226 · see citing works

Resistance Exercise in Individuals With and Without Cardiovascular Disease: 2007 Update: A Scientific Statement From the American Heart Association Council on Clinical Cardiology and Council on Nutrition, Physical Activity, and Metabolism

Williams, M. A., Haskell, W. L., Ades, P. A., Amsterdam, E. A., Bittner, V., Franklin, B. A., Gulanick, M., Laing, S. T., & Stewart, K. J. (2007) · Circulation · doi:10.1161/circulationaha.107.185214 · Cited by 1,211 · see citing works

Anabolic signaling deficits underlie amino acid resistance of wasting, aging muscle

Cuthbertson, D., Smith, K., Babraj, J., Leese, G., Waddell, T., Atherton, P., Wackerhage, H., Taylor, P. M., & Rennie, M. J. (2005) · The FASEB Journal · doi:10.1096/fj.04-2640fje · Cited by 1,211 · see citing works

Skeletal Muscle Cutpoints Associated with Elevated Physical Disability Risk in Older Men and Women

Janssen, I. (2004) · American Journal of Epidemiology · doi:10.1093/aje/kwh058 · Cited by 1,190 · see citing works

Muscle strength and speed of movement in relation to age and muscle morphology

Larsson, L., Grimby, G., & Karlsson, J. (1979) · Journal of Applied Physiology · doi:10.1152/jappl.1979.46.3.451 · Cited by 1,135 · see citing works

Sarcopenia with limited mobility: an international consensus

Morley, J. E., Abbatecola, A. M., Argiles, J. M., Baracos, V., Bauer, J., Bhasin, S., Cederholm, T., Stewart Coats, A. J., Cummings, S. R., Evans, W. J., et al. (2011) · Journal of the American Medical Directors Association · doi:10.1016/j.jamda.2011.04.014 · Cited by 1,125 · see citing works

Notch-Mediated Restoration of Regenerative Potential to Aged Muscle

Conboy, I. M., Conboy, M. J., Smythe, G. M., & Rando, T. A. (2003) · Science · doi:10.1126/science.1087573 · Cited by 1,121 · see citing works

Skeletal muscle hypertrophy and atrophy signaling pathways

Glass, D. J. (2005) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2005.04.018 · Cited by 1,106 · see citing works

Growth Hormone and the Insulin-Like Growth Factor System in Myogenesis*

Florini, J. R., Ewton, D. Z., & Coolican, S. A. (1996) · Endocrine Reviews · doi:10.1210/edrv-17-5-481 · Cited by 1,092 · see citing works

Subcutaneous abdominal fat and thigh muscle composition predict insulin sensitivity independently of visceral fat

Goodpaster, B. H., Leland Thaete, F., Simoneau, J.-A., & Kelley, D. E. (1997) · Diabetes · doi:10.2337/diacare.46.10.1579 · Cited by 1,012 · see citing works

Geriatric muscle stem cells switch reversible quiescence into senescence

Sousa-Victor, P., Gutarra, S., García-Prat, L., Rodriguez-Ubreva, J., Ortet, L., Ruiz-Bonilla, V., Jardí, M., Ballestar, E., González, S., Serrano, A. L., et al. (2014) · Nature · doi:10.1038/nature13013 · Cited by 1,010 · see citing works

The Molecular Basis of Skeletal Muscle Atrophy

Jackman, R. W., & Kandarian, S. C. (2004) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00579.2003 · Cited by 1,008 · see citing works

Hindlimb unloading rodent model: technical aspects

Morey, E. R., & Globus, R. K. (2002) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00969.2001 · Cited by 998 · see citing works

Longitudinal Muscle Strength Changes in Older Adults: Influence of Muscle Mass, Physical Activity, and Health

HUGHES, V. A., Frontera, W. R., Wood, M., Evans, W. J., Dallal, G. E., Roubenoff, R., & Singh, M. A. F. (2001) · The Journals of Gerontology Series A · doi:10.1093/gerona/56.5.b209 · Cited by 924 · see citing works

Skeletal Muscle Power

Reid, K. F., & Fielding, R. A. (2012) · Exercise and Sport Sciences Reviews · doi:10.1097/jes.0b013e31823b5f13 · Cited by 858 · cited 2× · see citing works

The aged niche disrupts muscle stem cell quiescence

Chakkalakal, J. V., Jones, K. M., Basson, M. A., & Brack, A. S. (2012) · Nature · doi:10.1038/nature11438 · Cited by 851 · see citing works

Leg muscle mass and composition in relation to lower extremity performance in men and women aged 70 to 79: the health, aging and body composition study

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 · see citing works

Alternative definitions of sarcopenia, lower extremity performance, and functional impairment with aging in older men and women

Delmonico, M. J., Harris, T. B., Lee, J., Visser, M., Nevitt, M., Kritchevsky, S. B., Tylavsky, F. A., Newman, A. B., & for the Health, A. A. B. C. S. (2007) · Journal of the American Geriatrics Society · doi:10.1111/j.1532-5415.2007.01140.x · Cited by 819 · see citing works

Type 2 Innate Signals Stimulate Fibro/Adipogenic Progenitors to Facilitate Muscle Regeneration

Heredia, J. E., Mukundan, L., Chen, F. M., Mueller, A. A., Deo, R. C., Locksley, R. M., Rando, T. A., & Chawla, A. (2013) · Cell · doi:10.1016/j.cell.2013.02.053 · Cited by 818 · see citing works

Contractile properties of skeletal muscles from young, adult and aged mice.

Brooks, S. V., & Faulkner, J. A. (1988) · The Journal of Physiology · doi:10.1113/jphysiol.1988.sp017279 · Cited by 777 · cited 8× · see citing works

Regulation of Wnt Signaling during Adipogenesis

Bennett, C. N., Ross, S. E., Longo, K. A., Bajnok, L., Hemati, N., Johnson, K. W., Harrison, S. D., & MacDougald, O. A. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m204527200 · Cited by 743 · see citing works

Nilotinib reduces muscle fibrosis in chronic muscle injury by promoting TNF-mediated apoptosis of fibro/adipogenic progenitors

Lemos, D. R., Babaeijandaghi, F., Low, M., Chang, C.-K., Lee, S. T., Fiore, D., Zhang, R.-H., Natarajan, A., Nedospasov, S. A., & Rossi, F. M. V. (2015) · Nature Medicine · doi:10.1038/nm.3869 · Cited by 740 · see citing works

The Effect of Testosterone Replacement on Endogenous Inflammatory Cytokines and Lipid Profiles in Hypogonadal Men

Malkin, C. J., Pugh, P. J., Jones, R. D., Kapoor, D., Channer, K. S., & Jones, T. H. (2004) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2003-031069 · Cited by 731 · see citing works

Adverse Effects of Testosterone Therapy in Adult Men: A Systematic Review and Meta-Analysis

Fernández-Balsells, M. M., Murad, M. H., Lane, M., Lampropulos, J. F., Albuquerque, F., Mullan, R. J., Agrwal, N., Elamin, M. B., Gallegos-Orozco, J. F., Wang, A. T., et al. (2010) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2009-2575 · Cited by 713 · see citing works

The global prevalence of glucose-6-phosphate dehydrogenase deficiency: A systematic review and meta-analysis

Nkhoma, E. T., Poole, C., Vannappagari, V. X., Hall, S. A., & Beutler, E. (2009) · Blood Cells Molecules and Diseases · doi:10.1016/j.bcmd.2008.12.005 · Cited by 709 · see citing works

Glucose‐6‐phosphate dehydrogenase, NADPH, and cell survival

Stanton, R. C. (2012) · IUBMB Life · doi:10.1002/iub.1017 · Cited by 706 · see citing works

Glucocorticoid-Induced Skeletal Muscle Atrophy

Schakman, O., Kalista, S., Barbé, C., Loumaye, A., & Thissen, J. P. (2013) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2013.05.036 · Cited by 705 · see citing works

Added value of physical performance measures in predicting adverse health-related events: results from the health, aging and body composition study

Cesari, M., Kritchevsky, S. B., Newman, A. B., Simonsick, E. M., Harris, T. B., Penninx, B. W., Brach, J. S., Tylavsky, F. A., Satterfield, S., Bauer, D. C., et al. (2009) · Journal of the American Geriatrics Society · doi:10.1111/j.1532-5415.2008.02126.x · Cited by 702 · see citing works

Fibrosis and adipogenesis originate from a common mesenchymal progenitor in skeletal muscle

Uezumi, A., Ito, T., Morikawa, D., Shimizu, N., Yoneda, T., Segawa, M., Yamaguchi, M., Ogawa, R., Matev, M. M., Miyagoe-Suzuki, Y., et al. (2011) · Journal of Cell Science · doi:10.1242/jcs.086629 · Cited by 680 · see citing works

Rejuvenation of the muscle stem cell population restores strength to injured aged muscles

Cosgrove, B. D., Gilbert, P. M., Porpiglia, E., Mourkioti, F., Lee, S. P., Corbel, S. Y., Llewellyn, M. E., Delp, S. L., & Blau, H. M. (2014) · Nature Medicine · doi:10.1038/nm.3464 · Cited by 677 · see citing works

Increased cytokine production in mononuclear cells of healthy elderly people

Fagiolo, U., Cossarizza, A., Scala, E., Fanales‐Belasio, E., Ortolani, C., Cozzi, E., Monti, D., Franceschi, C., & Paganelli, R. (1993) · European Journal of Immunology · doi:10.1002/eji.1830230950 · Cited by 665 · see citing works

From space to Earth: Advances in human physiology from 20 years of bed rest studies (1986–2006)

Pavy-Le Traon, A., Heer, M., Narici, M. V., Rittweger, J., & Vernikos, J. (2007) · European Journal of Applied Physiology · doi:10.1007/s00421-007-0474-z · Cited by 658 · see citing works

Intermuscular fat: a review of the consequences and causes

Addison, O., Marcus, R. L., LaStayo, P. C., & Ryan, A. S. (2014) · International Journal of Endocrinology · doi:10.1155/2014/309570 · Cited by 656 · see citing works

Role of muscle loss in the age-associated reduction in VO2 max

Fleg, J. L., & Lakatta, E. G. (1988) · Journal of Applied Physiology · doi:10.1152/jappl.1988.65.3.1147 · Cited by 631 · see citing works

Impact of Aerobic Exercise Training on Age-Related Changes in Insulin Sensitivity and Muscle Oxidative Capacity

Short, K. R., Vittone, J. L., Bigelow, M. L., Proctor, D. N., Rizza, R. A., Coenen-Schimke, J. M., & Nair, K. S. (2003) · Diabetes · doi:10.2337/diabetes.52.8.1888 · Cited by 631 · see citing works

Mitochondrial dysfunction and sarcopenia of aging: from signaling pathways to clinical trials

Marzetti, E., Calvani, R., Cesari, M., Buford, T. W., Lorenzi, M., Behnke, B. J., & Leeuwenburgh, C. (2013) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2013.06.024 · Cited by 627 · see citing works

Effects of weight loss on regional fat distribution and insulin sensitivity in obesity.

Goodpaster, B. H., Kelley, D. E., Wing, R. R., Meier, A., & Thaete, F. L. (1999) · Diabetes · doi:10.2337/diabetes.48.4.839 · Cited by 608 · see citing works

[42] Glucose-6-phosphate dehydrogenase 6-phosphogluconic dehydrogenase

Kornberg, A., Horecker, B. L., Horecker, B. L., & Smyrniotis, P. Z. (1955) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(55)01046-x · Cited by 601 · see citing works

Notch Signaling Is Necessary to Maintain Quiescence in Adult Muscle Stem Cells

Bjornson, C. R. R., Cheung, T. H., Liu, L., Tripathi, P. V., Steeper, K. M., & Rando, T. A. (2012) · Stem Cells · doi:10.1002/stem.773 · Cited by 598 · see citing works

Endurance Exercise as a Countermeasure for Aging

Lanza, I. R., Short, D. K., Short, K. R., Raghavakaimal, S., Basu, R., Joyner, M. J., McConnell, J. P., & Nair, K. S. (2008) · Diabetes · doi:10.2337/db08-0349 · Cited by 582 · see citing works

p38 MAPK signaling underlies a cell-autonomous loss of stem cell self-renewal in skeletal muscle of aged mice

Bernet, J. D., Doles, J. D., Hall, J. K., Kelly Tanaka, K., Carter, T. A., & Olwin, B. B. (2014) · Nature Medicine · doi:10.1038/nm.3465 · Cited by 573 · see citing works

Glucose‐6‐phosphate dehydrogenase: a “housekeeping” enzyme subject to tissue‐specific regulation by hormones, nutrients, and oxidant stress

Kletzien, R. F., Harris, P. K. W., & Foellmi, L. A. (1994) · The FASEB Journal · doi:10.1096/fasebj.8.2.8119488 · Cited by 551 · see citing works

<i>Physiology of a Microgravity Environment</i> Invited Review: Microgravity and skeletal muscle

Fitts, R. H., Riley, D. R., & Widrick, J. J. (2000) · Journal of Applied Physiology · doi:10.1152/jappl.2000.89.2.823 · Cited by 548 · see citing works

Effects of aging on in vivo synthesis of skeletal muscle myosin heavy-chain and sarcoplasmic protein in humans

Balagopal, P., Rooyackers, O., Adey, D., Ades, P. A., & Nair, K. S. (1997) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1997.273.4.e790 · Cited by 541 · see citing works

Growth hormone and the insulin-like growth factor system in myogenesis

Florini, J. R. (1996) · Endocrine Reviews · doi:10.1210/er.17.5.481 · Cited by 536 · see citing works

Mitochondrial hexokinases, novel mediators of the antiapoptotic effects of growth factors and Akt

Robey, R. B., & Hay, N. (2006) · Oncogene · doi:10.1038/sj.onc.1209595 · Cited by 534 · see citing works

Importance of Glucose-6-phosphate Dehydrogenase Activity for Cell Growth

Tian, W.-N., Braunstein, L. D., Pang, J., Stuhlmeier, K. M., Xi, Q. J., Tian, X., & Stanton, R. C. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.17.10609 · Cited by 534 · see citing works

A Critical Requirement for Notch Signaling in Maintenance of the Quiescent Skeletal Muscle Stem Cell State

Mourikis, P., Sambasivan, R., Castel, D., Rocheteau, P., Bizzarro, V., & Tajbakhsh, S. (2012) · Stem Cells · doi:10.1002/stem.775 · Cited by 526 · see citing works

Loss of skeletal muscle mass in aging: Examining the relationship of starvation, sarcopenia and cachexia

Thomas, D. R. (2007) · Clinical Nutrition · doi:10.1016/j.clnu.2007.03.008 · Cited by 521 · see citing works

Insulin-like Growth Factor-1 (IGF-1) Inversely Regulates Atrophy-induced Genes via the Phosphatidylinositol 3-Kinase/Akt/Mammalian Target of Rapamycin (PI3K/Akt/mTOR) Pathway*

Latres, E., Amini, A. R., Amini, A. A., Griffiths, J. S., Martin, F. J., Wei, Y., Lin, H. C., Yancopouloš, G., & Glass, D. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m407517200 · Cited by 514 · see citing works

Fasting enhances growth hormone secretion and amplifies the complex rhythms of growth hormone secretion in man.

Ho, K. Y., Veldhuis, J. D., Johnson, M. L., Furlanetto, R., Evans, W. S., Alberti, K. G., & Thorner, M. O. (1988) · Journal of Clinical Investigation · doi:10.1172/jci113450 · Cited by 503 · see citing works

Skeletal muscle myocytes undergo protein loss and reactive oxygen-mediated NF-κB activation in response to tumor necrosis factor α

Li, Y., Schwartz, R. J., Waddell, I. D., Holloway, B. R., & Reid, M. B. (1998) · The FASEB Journal · doi:10.1096/fasebj.12.10.871 · Cited by 502 · see citing works

Histochemical and biochemical changes in human skeletal muscle with age in sedentary males, age 22–65 years

Larsson, L., Sjödin, B., & Karlsson, J. (1978) · Acta Physiologica Scandinavica · doi:10.1111/j.1748-1716.1978.tb06187.x · Cited by 498 · see citing works

A review of the clinical evidence for exercise in osteoarthritis of the hip and knee

Bennell, K. L., & Hinman, R. S. (2011) · Journal of Science and Medicine in Sport · doi:10.1016/j.jsams.2010.08.002 · Cited by 492 · 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

Imbalance between pSmad3 and Notch induces CDK inhibitors in old muscle stem cells

Carlson, M. E., Hsu, M., & Conboy, I. M. (2008) · Nature · doi:10.1038/nature07034 · Cited by 483 · see citing works

Age and aerobic exercise training effects on whole body and muscle protein metabolism

Short, K. R., Vittone, J. L., Bigelow, M. L., Proctor, D. N., & Nair, K. S. (2004) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00366.2003 · Cited by 470 · cited 5× · see citing works

Weight stability masks sarcopenia in elderly men and women

Gallagher, D., Ruts, E., Visser, M., Heshka, S., Baumgartner, R. N., Wang, J., Pierson, R. N., Pi-Sunyer, F. X., & Heymsfield, S. B. (2000) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.2000.279.2.e366 · Cited by 466 · see citing works

Age Changes in Body Composition Revealed by Computed Tomography

Borkan, G. A., Hults, D. E., Gerzof, S. G., Robbins, A. H., & Silbert, C. K. (1983) · Journal of Gerontology · doi:10.1093/geronj/38.6.673 · Cited by 460 · see citing works

Histochemical and enzymatic comparison of the gastrocnemius muscle of young and elderly men and women

Coggan, A. R., Spina, R. J., King, D. S., Rogers, M. A., Rogers, M. A., Brown, M., Nemeth, P. M., & Holloszy, J. O. (1992) · Journal of Gerontology · doi:10.1093/geronj/47.3.b71 · Cited by 456 · see citing works

Silencing of Epidermal Growth Factor Receptor Suppresses Hypoxia-Inducible Factor-2–Driven VHL −/− Renal Cancer

Smith, K., Gunaratnam, L., Morley, M., Franovic, A., Mekhail, K., & Lee, S. (2005) · Cancer Research · doi:10.1158/0008-5472.can-05-0169 · Cited by 456 · see citing works

Growth Hormone and Sex Steroid Administration in Healthy Aged Women and Men: A Randomized Controlled Trial

Blackman, M. R. (2002) · JAMA · doi:10.1001/jama.288.18.2282 · Cited by 455 · see citing works

The developmental origins of sarcopenia

Sayer, A. A., Syddall, H., Martin, H., Patel, H., Baylis, D., & Cooper, C. (2008) · The Journal of nutrition, health and aging · doi:10.1007/bf02982703 · Cited by 450 · see citing works

Skeletal muscle fat infiltration: impact of age, inactivity, and exercise

Marcus, R. L., Addison, O., Kidde, J. P., Dibble, L. E., & Lastayo, P. C. (2010) · The Journal of nutrition, health and aging · doi:10.1007/s12603-010-0081-2 · Cited by 449 · see citing works

Animal Models of Steatosis

Koteish, A. A., & Diehl, A. M. (2001) · Seminars in Liver Disease · doi:10.1055/s-2001-12932 · Cited by 447 · see citing works

Effects of physical activity on strength and skeletal muscle fat infiltration in older adults: a randomized controlled trial

Goodpaster, B. H., Chomentowski, P., Ward, B. K., Rossi, A., Glynn, N. W., Delmonico, M. J., Kritchevsky, S. B., Pahor, M., & Newman, A. B. (2008) · Journal of Applied Physiology · doi:10.1152/japplphysiol.90425.2008 · Cited by 446 · see citing works

Mitochondrial function and apoptotic susceptibility in aging skeletal muscle

Chabi, B., Ljubicic, V., Menzies, K. J., Huang, J. H., Saleem, A., & Hood, D. A. (2008) · Aging Cell · doi:10.1111/j.1474-9726.2007.00347.x · Cited by 437 · see citing works

The central role of muscle stem cells in regenerative failure with aging

Blau, H. M., Cosgrove, B. D., & Ho, A. T. V. (2015) · Nature Medicine · doi:10.1038/nm.3918 · Cited by 437 · see citing works

Senescence in innate immune responses: reduced neutrophil phagocytic capacity and CD16 expression in elderly humans

Butcher, S. K., Chahal, H., Nayak, L., Sinclair, A., Henriquez, N. V., Sapey, E., O'Mahony, D., & Lord, J. M. (2001) · Journal of Leukocyte Biology · doi:10.1189/jlb.70.6.881 · Cited by 436 · see citing works

The size and strength of the quadriceps muscles of old

Men, Y., Young, A., Stokes, M. J., & Crowe, M. J. (1985) · Clinical Physiology · doi:10.1111/j.1475-097x.1985.tb00590.x · Cited by 433 · see citing works

Inhibition of JAK-STAT signaling stimulates adult satellite cell function

Price, F. D., von Maltzahn, J., Bentzinger, C. F., Dumont, N. A., Yin, H., Chang, N. C., Wilson, D. H., Frenette, J., & Rudnicki, M. A. (2014) · Nature Medicine · doi:10.1038/nm.3655 · Cited by 433 · see citing works

Dll1- and Dll4-Mediated Notch Signaling Are Required for Homeostasis of Intestinal Stem Cells

Pellegrinet, L., Rodilla, V., Liu, Z., Chen, S., Koch, U., Espinosa, L., Kaestner, K. H., Kopan, R., Lewis, J. H., & Radtke, F. (2011) · Gastroenterology · doi:10.1053/j.gastro.2011.01.005 · Cited by 426 · see citing works

Skeletal muscle fiber quality in older men and women

Frontera, W. R., Suh, D., Krivickas, L. S., HUGHES, V. A., Goldstein, R., & Roubenoff, R. (2000) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.2000.279.3.c611 · Cited by 424 · see citing works

Cellular and molecular mechanisms underlying age-related skeletal muscle wasting and weakness

Ryall, J. G., Schertzer, J. D., & Lynch, G. S. (2008) · Biogerontology · doi:10.1007/s10522-008-9131-0 · Cited by 423 · see citing works

Autophagy Impairment in Muscle Induces Neuromuscular Junction Degeneration and Precocious Aging

Carnio, S., LoVerso, F., Baraibar, M. A., Longa, E., Khan, M. M., Maffei, M., Reischl, M., Canepari, M., Loefler, S., Kern, H., et al. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.07.061 · Cited by 423 · see citing works

Muscle transplantation between young and old rats: age of host determines recovery

Carlson, B. M., & Faulkner, J. A. (1989) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1989.256.6.c1262 · Cited by 417 · see citing works

Skeletal muscle atrophy and increased intramuscular fat after incomplete spinal cord injury

Gorgey, A. S., & Dudley, G. A. (2007) · Spinal Cord · doi:10.1038/sj.sc.3101968 · Cited by 415 · see citing works

Opposing roles for p16Ink4a and p19Arf in senescence and ageing caused by BubR1 insufficiency

Baker, D. J., Perez-Terzic, C., Jin, F., Pitel, K. S., Niederländer, N. J., Jeganathan, K., Yamada, S., Reyes, S., Rowe, L., Hiddinga, H. J., et al. (2008) · Nature Cell Biology · doi:10.1038/ncb1744 · Cited by 408 · cited 1× · see citing works

Acute effects of resistance exercise on muscle protein synthesis rate in young and elderly men and women

Yarasheski, K. E., Zachwieja, J. J., & Bier, D. M. (1993) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1993.265.2.e210 · Cited by 406 · see citing works

Myostatin inhibition in muscle, but not adipose tissue, decreases fat mass and improves insulin sensitivity

Guo, T., Jou, W., Chanturiya, T., Portas, J., Gavrilova, O., & McPherron, A. C. (2009) · PLoS ONE · doi:10.1371/journal.pone.0004937 · Cited by 402 · see citing works

World Population Ageing 2015

Nations, U. (2017) · Statistical Papers - United Nations (Ser. A), Population and Vital Statistics Report · doi:10.18356/88fa44e7-en · Cited by 400 · see citing works

Satellite cells in human skeletal muscle; from birth to old age

Verdijk, L. B., Snijders, T., Drost, M., Delhaas, T., Kadi, F., & van Loon, L. J. C. (2014) · AGE · doi:10.1007/s11357-013-9583-2 · Cited by 399 · see citing works

Skeletal muscle autophagy and apoptosis during aging: Effects of calorie restriction and life-long exercise

Wohlgemuth, S. E., Seo, A. Y., Marzetti, E., Lees, H. A., & Leeuwenburgh, C. (2010) · Experimental Gerontology · doi:10.1016/j.exger.2009.11.002 · Cited by 397 · see citing works

Effect of leucine metabolite β-hydroxy-β-methylbutyrate on muscle metabolism during resistance-exercise training

Nissen, S., Sharp, R., Ray, M., Rathmacher, J. A., Rice, D., Fuller, J. C., Connelly, A. S., & Abumrad, N. (1996) · Journal of Applied Physiology · doi:10.1152/jappl.1996.81.5.2095 · Cited by 393 · see citing works

Differential impact of age, sex steroid hormones, and obesity on basal versus pulsatile growth hormone secretion in men as assessed in an ultrasensitive chemiluminescence assay

Veldhuis, J. D., Liem, A. Y., South, S. A., WELTMAN, A. L., Weltman, J. Y., Clemmons, D., Abbott, R. D., Mulligan, T., Johnson, M. L., & Pincus, S. M. (1995) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.80.11.7593428 · Cited by 385 · see citing works

Skeletal muscle hypertrophy following resistance training is accompanied by a fiber type-specific increase in satellite cell content in elderly men

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

Effects of exercise on depressive symptoms in older adults with poorly responsive depressive disorder

Mather, A. S., Rodriguez, C., Guthrie, M., McHarg, A. M., Reid, I., & McMurdo, M. E. T. (2002) · The British Journal of Psychiatry · doi:10.1192/bjp.180.5.411 · Cited by 370 · see citing works

Prolonged space flight-induced alterations in the structure and function of human skeletal muscle fibres

Fitts, R. H., Trappe, S. W., COSTILL, D. L., Gallagher, P. M., Creer, A. C., Colloton, P. A., Peters, J., Romatowski, J. G., Bain, J. L. W., & Riley, D. A. (2010) · The Journal of Physiology · doi:10.1113/jphysiol.2010.188508 · Cited by 369 · see citing works

Atrogin-1, MuRF-1, and sarcopenia

Gumucio, J. P., & Mendias, C. L. (2012) · Endocrine · doi:10.1007/s12020-012-9751-7 · Cited by 368 · see citing works

Skeletal muscle glycolytic and oxidative enzyme capacities are determinants of insulin sensitivity and muscle composition in obese women.

Simoneau, J., Colberg, S. R., Thaete, F. L., & Kelley, D. E. (1995) · The FASEB Journal · doi:10.1096/fasebj.9.2.7781930 · Cited by 362 · cited 1× · see citing works

Regional changes in muscle mass following 17 weeks of bed rest

LeBlanc, A. D., Schneider, V. S., Evans, H. J., Pientok, C., Rowe, R., & Spector, E. (1992) · Journal of Applied Physiology · doi:10.1152/jappl.1992.73.5.2172 · Cited by 359 · cited 1× · see citing works

Efficacy of myonuclear addition may explain differential myofiber growth among resistance-trained young and older men and women

Petrella, J. K., Kim, J.-S., Cross, J. M., Kosek, D. J., & Bamman, M. M. (2006) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00190.2006 · Cited by 356 · see citing works

Lower limb skeletal muscle function after 6 wk of bed rest

Berg, H. E., Larsson, L., & Tesch, P. A. (1997) · Journal of Applied Physiology · doi:10.1152/jappl.1997.82.1.182 · Cited by 352 · see citing works

Muscle atrophy and bone loss after 90 days' bed rest and the effects of flywheel resistive exercise and pamidronate: Results from the LTBR study

Rittweger, J., Frost, H. M., Schießl, H., Ohshima, H., Alkner, B. A., Tesch, P. A., & Felsenberg, D. (2005) · Bone · doi:10.1016/j.bone.2004.11.014 · Cited by 351 · see citing works

Low Testosterone in Men with Type 2 Diabetes: Significance and Treatment

Grossmann, M. (2011) · The Journal of Clinical Endocrinology &amp; Metabolism · doi:10.1210/jc.2011-0118 · Cited by 350 · see citing works

Functional and morphological recovery of dystrophic muscles in mice treated with deacetylase inhibitors

Minetti, G., Colussi, C., Adami, R., Serra, C., Mozzetta, C., Parente, V., Fortuni, S., Straino, S., Sampaolesi, M., Padova, M. D., et al. (2006) · Nature Medicine · doi:10.1038/nm1479 · Cited by 341 · see citing works

Adipogenesis and aging: does aging make fat go MAD

Kirkland, J. L., Tchkonia, T., Pirtskhalava, T., Han, J., & Karagiannides, I. (2002) · Experimental Gerontology · doi:10.1016/s0531-5565(02)00014-1 · Cited by 339 · 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

Defective myoblasts identified in Duchenne muscular dystrophy

Blau, H. M., Webster, C., & Pavlath, G. K. (1983) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.80.15.4856 · Cited by 335 · see citing works

Enhanced Glutathione Levels and Oxidoresistance Mediated by Increased Glucose-6-phosphate Dehydrogenase Expression

Salvemini, F., Franzè, A., Iervolino, A., Filosa, S., Salzano, S., & Ursini, M. V. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.5.2750 · Cited by 333 · see citing works

Reduced physical activity increases intermuscular adipose tissue in healthy young adults

Manini, T. M., Clark, B. C., Nalls, M. A., Goodpaster, B. H., Ploutz-Snyder, L. L., & Harris, T. B. (2007) · The American Journal of Clinical Nutrition · doi:10.1093/ajcn/85.2.377 · Cited by 332 · see citing works

Muscle hypertrophy and fast fiber type conversions in heavy resistance-trained women.

Staron, R. S., Malicky, E. S., Leonardi, M. J., Falkel, J. E., Hagerman, F. C., & Dudley, G. A. (1990) · European Journal of Applied Physiology and Occupational Physiology · doi:10.1007/bf00572189 · Cited by 328 · see citing works

Mitochondrial pathways in sarcopenia of aging and disuse muscle atrophy

Calvani, R., Joseph, A.-M., Adhihetty, P. J., Miccheli, A., Bossola, M., Leeuwenburgh, C., Bernabei, R., & Marzetti, E. (2013) · bchm · doi:10.1515/hsz-2012-0247 · Cited by 328 · see citing works

Sarcopenia and increased adipose tissue infiltration of muscle in elderly African American women

Song, M.-Y., Ruts, E., Kim, J., Janumala, I., Heymsfield, S., & Gallagher, D. (2004) · The American Journal of Clinical Nutrition · doi:10.1093/ajcn/79.5.874 · Cited by 324 · see citing works

Skeletal muscle mitochondrial energetics are associated with maximal aerobic capacity and walking speed in older adults

Coen, P. M., Jubrias, S. A., Distefano, G., Amati, F., Mackey, D. C., Glynn, N. W., Manini, T. M., Wohlgemuth, S. E., Leeuwenburgh, C., Cummings, S. R., et al. (2013) · The Journals of Gerontology: Series A · doi:10.1093/gerona/gls196 · Cited by 323 · see citing works

Targeted expression of catalase to mitochondria prevents age-associated reductions in mitochondrial function and insulin resistance

Lee, H.-Y., Choi, C. S., Birkenfeld, A. L., Alves, T. C., Jornayvaz, F. R., Jurczak, M. J., Zhang, D., Woo, D. K., Shadel, G. S., Ladiges, W., et al. (2010) · Cell Metabolism · doi:10.1016/j.cmet.2010.11.004 · Cited by 319 · see citing works

Normal values for handgrip strength in 920 men and women aged over 65 years, and longitudinal changes over 4 years in 620 survivors

Bassey, E. J., & Harries, U. (1993) · Clinical Science · doi:10.1042/cs0840331 · Cited by 318 · see citing works

Regenerative potential of human skeletal muscle during aging

Renault, V. M., Thorne, L., Eriksson, P., Butler-Browne, G. S., & Mouly, V. (2002) · Aging Cell · doi:10.1046/j.1474-9728.2002.00017.x · Cited by 318 · see citing works

Reversal of cancer-related wasting using oral supplementation with a combination of β-hydroxy-β-methylbutyrate, arginine, and glutamine

May, P. E., Barber, A. E., D'Olimpio, J. T., Hourihane, A., & Abumrad, N. N. (2002) · The American Journal of Surgery · doi:10.1016/s0002-9610(02)00823-1 · Cited by 318 · see citing works

The GH/IGF1 axis and signaling pathways in the muscle and bone: mechanisms underlying age-related skeletal muscle wasting and osteoporosis

Perrini, S., Laviola, L., Carreira, M. C., Cignarelli, A., Natalicchio, A., & Giorgino, F. (2010) · Journal of Endocrinology · doi:10.1677/joe-09-0431 · Cited by 317 · see citing works

Spaceflight and Bone Turnover: Correlation with a New Rat Model of Weightlessness

Morey, E. R. (1979) · BioScience · doi:10.2307/1307797 · Cited by 315 · see citing works

Muscle morphology, enzymatic activity, and muscle strength in elderly men: A follow‐up study

ANIANSSON, A., Hedberg, M., Henning, G., & Grimby, G. (1986) · Muscle & Nerve · doi:10.1002/mus.880090702 · Cited by 314 · see citing works

Senescence-accelerated mouse (SAM): a biogerontological resource in aging research

Takeda, T. (1999) · Neurobiology of Aging · doi:10.1016/s0197-4580(99)00008-1 · Cited by 311 · see citing works

Peroxisome-proliferator-activated receptor γ suppresses Wnt/β-catenin signalling during adipogenesis

Moldes, M., Zuo, Y., Morrison, R. F., Silva, D., Park, B.-H., Liu, J., & Farmer, S. R. (2003) · Biochemical Journal · doi:10.1042/bj20030426 · Cited by 308 · see citing works

Effects of beta-hydroxy-beta-methylbutyrate (HMB) on exercise performance and body composition across varying levels of age, sex, and training experience: A review

Wilson, G. J., Wilson, J. M., & Manninen, A. H. (2008) · Nutrition &amp; Metabolism · doi:10.1186/1743-7075-5-1 · Cited by 306 · see citing works

Knee extensor and plantar flexor muscle size and function following 90 days of bed rest with or without resistance exercise

Alkner, B. A., & Tesch, P. A. (2004) · European Journal of Applied Physiology · doi:10.1007/s00421-004-1172-8 · Cited by 306 · see citing works

Role of exercise on sarcopenia in the elderly.

Montero-Fernández, N., & Rexach, J. A. S. (2013) · PubMed · Cited by 306 · see citing works

Identification and characterization of PDGFRα+ mesenchymal progenitors in human skeletal muscle

Uezumi, A., Fukada, S., Yamamoto, N., Ikemoto‐Uezumi, M., Nakatani, M., Morita, M., Yamaguchi, A., Yamada, H., Nishino, I., Hamada, Y., et al. (2014) · Cell Death and Disease · doi:10.1038/cddis.2014.161 · Cited by 304 · see citing works

Role of different proteolytic systems in the degradation of muscle proteins during denervation atrophy.

Furuno, K., Goodman, M. N., & Goldberg, A. L. (1990) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)38923-9 · Cited by 300 · see citing works

Evidence for a myogenic stem cell that is exhausted in dystrophic muscle

Heslop, L., Morgan, J. E., & Partridge, T. A. (2000) · Journal of Cell Science · doi:10.1242/jcs.113.12.2299 · Cited by 297 · see citing works

Intramuscular adipose tissue, sarcopenia, and mobility function in older individuals

Marcus, R. L., Addison, O., Dibble, L. E., Foreman, K. B., Morrell, G., & LaStayo, P. (2012) · Journal of Aging Research · doi:10.1155/2012/629637 · Cited by 296 · see citing works

Resistance exercise acutely increases MHC and mixed muscle protein synthesis rates in 78–84 and 23–32 yr olds

Hasten, D. L., Pak-Loduca, J., Obert, K. A., & Yarasheski, K. E. (2000) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.2000.278.4.e620 · Cited by 294 · see citing works

Immune Modulation of Stem Cells and Regeneration

Aurora, A., & Olson, E. (2014) · Cell Stem Cell · doi:10.1016/j.stem.2014.06.009 · Cited by 293 · see citing works

Effect of β-hydroxy-β-methylbutyrate (HMB) on lean body mass during 10 days of bed rest in older adults

Deutz, N. E. P., Pereira, S. L., Hays, N. P., Oliver, J. S., Edens, N. K., Evans, C. M., & Wolfe, R. R. (2013) · Clinical Nutrition · doi:10.1016/j.clnu.2013.02.011 · Cited by 287 · cited 6× · see citing works

Satellite cells and myonuclei in young and elderly women and men

Kadi, F., Charifi, N., Denis, C., & Lexell, J. E. (2003) · Muscle & Nerve · doi:10.1002/mus.10510 · Cited by 283 · see citing works

Lifelong physical exercise delays age-associated skeletal muscle decline

Zampieri, S., Pietrangelo, L., Loefler, S., Fruhmann, H., Vogelauer, M., Burggraf, S., Pond, A., Grim-Stieger, M., Cvecka, J., Sedliak, M., et al. (2015) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/glu006 · Cited by 282 · see citing works

Is stair climb power a clinically relevant measure of leg power impairments in at-risk older adults?

Bean, J. F., Kiely, D. K., LaRose, S., Alian, J., & Frontera, W. R. (2007) · Archives of Physical Medicine and Rehabilitation · doi:10.1016/j.apmr.2007.02.004 · Cited by 278 · see citing works

Global analysis of gene expression patterns during disuse atrophy in rat skeletal muscle

Stevenson, E. J., Giresi, P. G., Koncarevic, A., & Kandarian, S. C. (2003) · The Journal of Physiology · doi:10.1111/j.1469-7793.2003.00033.x · Cited by 271 · see citing works

Constitutive Notch Activation Upregulates Pax7 and Promotes the Self-Renewal of Skeletal Muscle Satellite Cells

Wen, Y., Bi, P., Liu, W., Asakura, A., Keller, C., & Kuang, S. (2012) · Molecular and Cellular Biology · doi:10.1128/mcb.06753-11 · Cited by 271 · see citing works

Nutritional role of the leucine metabolite β-hydroxy β-methylbutyrate (HMB)

Nissen, S., & Abumrad, N. N. (1997) · The Journal of Nutritional Biochemistry · doi:10.1016/s0955-2863(97)00048-x · Cited by 269 · see citing works

Alterations in muscle attenuation following detraining and retraining in resistance-trained older adults

Taaffe, D. R., Henwood, T. R., Nalls, M. A., Walker, D. G., Lang, T. F., & Harris, T. B. (2009) · Gerontology · doi:10.1159/000182084 · Cited by 269 · see citing works

Exercise training decreases DNA damage and increases DNA repair and resistance against oxidative stress of proteins in aged rat skeletal muscle

Radák, Z., Naito, H., Kaneko, T., Tahara, S., Nakamoto, H., Takahashi, R., Cardozo-Pelaez, F., & Goto, S. (2002) · Pfl�gers Archiv European Journal of Physiology · doi:10.1007/s00424-002-0918-6 · Cited by 269 · see citing works

Genomic and proteomic profiling reveals reduced mitochondrial function and disruption of the neuromuscular junction driving rat sarcopenia

Ibebunjo, C., Chick, J. M., Kendall, T., Eash, J. K., Li, C., Zhang, Y., Vickers, C., Wu, Z., Clarke, B. A., Shi, J., et al. (2013) · Molecular and Cellular Biology · doi:10.1128/mcb.01036-12 · Cited by 267 · see citing works

Muscle hypertrophy in men and women

Cureton, K. J., Collins, M. A., Hill, D. W., & McELHANNON, F. M. (1988) · Medicine & Science in Sports & Exercise · doi:10.1249/00005768-198808000-00003 · Cited by 266 · see citing works

Strength of Isometric and Isokinetic Contractions

Murray, M., Gardner, G. M., MOLLINGER, L. A., & SEPIC, S. B. (1980) · Physical Therapy · doi:10.1093/ptj/60.4.412 · Cited by 265 · see citing works

G6PD protects from oxidative damage and improves healthspan in mice

Pereira, S. N., Fernández-Marcos, P. J., Brioche, T., Gómez‐Cabrera, M. C., Salvador‐Pascual, A., Flores, J. M., Viña, J., & Serrano, M. (2016) · Nature Communications · doi:10.1038/ncomms10894 · Cited by 265 · see citing works

Sepsis is associated with increased mRNAs of the ubiquitin-proteasome proteolytic pathway in human skeletal muscle.

Tiao, G. M., Hobler, S. C., Wang, J. J., Meyer, T. A., Luchette, F. A., Fischer, J. E., & Hasselgren, P.-O. (1997) · Journal of Clinical Investigation · doi:10.1172/jci119143 · Cited by 264 · see citing works

Identification of a molecular signature of sarcopenia

Giresi, P. G., Stevenson, E. J., Theilhaber, J., Koncarevic, A., Parkington, J. D., Fielding, R. A., & Kandarian, S. C. (2005) · Physiological Genomics · doi:10.1152/physiolgenomics.00249.2004 · Cited by 263 · see citing works

The origin of intermuscular adipose tissue and its pathophysiological implications

Vettor, R., Milan, G., Franzin, C., Sanna, M., Coppi, P. D., Rizzuto, R., & Federspil, G. (2009) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00229.2009 · Cited by 263 · see citing works

Effect of β-hydroxy-β-methylbutyrate, arginine, and lysine supplementation on strength, functionality, body composition, and protein metabolism in elderly women

Flakoll, P. J., Sharp, R. L., Baier, S. M., Levenhagen, D. K., Carr, C., & Nissen, S. (2004) · Nutrition · doi:10.1016/j.nut.2004.01.009 · Cited by 262 · see citing works

Fibroadipogenic progenitors mediate the ability of HDAC inhibitors to promote regeneration in dystrophic muscles of young, but not old Mdx mice

Mozzetta, C., Consalvi, S., Saccone, V., Tierney, M. T., Diamantini, A., Mitchell, K. J., Marazzi, G., Borsellino, G., Battistini, L., Sassoon, D. A., et al. (2013) · EMBO Molecular Medicine · doi:10.1002/emmm.201202096 · Cited by 261 · see citing works

Associations between body composition and gait-speed decline: results from the health, aging, and body composition study

Beavers, K. M., Beavers, D. P., Houston, D. K., Harris, T. B., Hue, T. F., Koster, A., Newman, A. B., Simonsick, E. M., Studenski, S. A., Nicklas, B. J., et al. (2013) · The American Journal of Clinical Nutrition · doi:10.3945/ajcn.112.047860 · Cited by 259 · see citing works

Importance of glucose-6-phosphate dehydrogenase activity in cell death

Tian, W.-N., Braunstein, L. D., Apse, K. A., Pang, J., Rose, M., Tian, X., & Stanton, R. C. (1999) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1999.276.5.c1121 · Cited by 258 · see citing works

Composition of Skeletal Muscle Evaluated with Computed Tomography

Goodpaster, B. H., Thaete, F. L., & Kelley, D. E. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb06416.x · Cited by 257 · see citing works

Satellite cell numbers in young and older men 24 hours after eccentric exercise

Dreyer, H. C., Blanco, C. E., Sattler, F. R., Schroeder, E. T., & Wiswell, R. A. (2006) · Muscle &amp; Nerve · doi:10.1002/mus.20461 · Cited by 256 · see citing works

Mitochondrial biogenesis in exercise and in ageing☆

Viña, J., Gómez‐Cabrera, M. C., Borrás, C., Froio, T., Sanchis‐Gomar, F., Martinez-Bello, V. E., & Pallardó, F. V. (2009) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2009.06.006 · Cited by 251 · see citing works

Activity-Dependent Signaling Pathways Controlling Muscle Diversity and Plasticity

Schiaffino, S., Sandri, M., & Murgia, M. (2007) · Physiology · doi:10.1152/physiol.00009.2007 · Cited by 251 · see citing works

Metabolic Regulation of Oocyte Cell Death through the CaMKII-Mediated Phosphorylation of Caspase-2

Nutt, L. K., Margolis, S. S., Jensen, M. V., Herman, C. E., Dunphy, W. G., Rathmell, J. C., & Kornbluth, S. A. (2005) · Cell · doi:10.1016/j.cell.2005.07.032 · Cited by 249 · see citing works

Age effect on transcript levels and synthesis rate of muscle MHC and response to resistance exercise

Balagopal, P., Coenen-Schimke, J. M., Ades, P. A., Adey, D., & Nair, K. S. (2001) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.2001.280.2.e203 · Cited by 248 · 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

Molecular aging and rejuvenation of human muscle stem cells

Carlson, M. E., Suetta, C., Conboy, M. J., Aagaard, P., Mackey, A., Kjaer, M., & Conboy, I. (2009) · EMBO Molecular Medicine · doi:10.1002/emmm.200900045 · Cited by 245 · see citing works

Metabolic functions of glucocorticoid receptor in skeletal muscle

Kuo, T., Harris, C. A., & Wang, J.-C. (2013) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2013.03.003 · Cited by 240 · see citing works

Physiopathological Mechanism of Sarcopenia

Walrand, S., Guillet, C., Salles, J., Cano, N., & Boirie, Y. (2011) · Clinics in Geriatric Medicine · doi:10.1016/j.cger.2011.03.005 · Cited by 235 · cited 1× · see citing works

Nutritional Treatment for Acquired Immunodeficiency Virus‐Associated Wasting Using β‐Hydroxy β‐Methylbutyrate, Glutamine, and Arginine: A Randomized, Double‐Blind, Placebo‐Controlled Study

Clark, R. E., Feleke, G., Din, M., Yasmin, T., Singh, G., Khan, F. A., & Rathmacher, J. A. (2000) · Journal of Parenteral and Enteral Nutrition · doi:10.1177/0148607100024003133 · Cited by 230 · see citing works

Resistance exercise training increases mixed muscle protein synthesis rate in frail women and men ≥76 yr old

Yarasheski, K. E., Pak-Loduca, J., Hasten, D. L., Obert, K. A., Brown, M. B., & Sinacore, D. R. (1999) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1999.277.1.e118 · Cited by 226 · see citing works

Elderly men and women benefit equally from prolonged resistance-type exercise training

Leenders, M., Verdijk, L. B., van der Hoeven, L., van Kranenburg, J., Nilwik, R., & van Loon, L. J. C. (2013) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/gls241 · Cited by 226 · see citing works

Age-related muscle dysfunction

Thompson, L. V. (2009) · Experimental Gerontology · doi:10.1016/j.exger.2008.05.003 · Cited by 226 · see citing works

Body Composition in 70-Year-Old Adults Responds to Dietary β-Hydroxy-β-Methylbutyrate Similarly to That of Young Adults

Vukovich, M. D., Stubbs, N. B., & Bohlken, R. M. (2001) · The Journal of Nutrition · doi:10.1093/jn/131.7.2049 · Cited by 222 · see citing works

Decline in isokinetic force with age: muscle cross-sectional area and specific force

Jubrias, S. A., Odderson, I. R., Esselman, P. C., & Conley, K. E. (1997) · Pfl�gers Archiv European Journal of Physiology · doi:10.1007/s004240050392 · Cited by 222 · see citing works

Glucose-6-Phosphate Dehydrogenase Overexpression Decreases Endothelial Cell Oxidant Stress and Increases Bioavailable Nitric Oxide

Leopold, J. A., Zhang, Y., Scribner, A. W., Stanton, R. C., & Loscalzo, J. (2003) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/01.atv.0000056744.26901.ba · Cited by 219 · see citing works

Age-Related Differences in Knee Muscle Strength in Normal Women

MURRAY, M. P., Duthie, E. H., Gambert, S. R., Sepic, S. B., & MOLLINGER, L. A. (1985) · Journal of Gerontology · doi:10.1093/geronj/40.3.275 · Cited by 218 · see citing works

Aberrant mitochondrial homeostasis in the skeletal muscle of sedentary older adults

Safdar, A., Hamadeh, M. J., Kaczor, J. J., Raha, S., deBeer, J., & Tarnopolsky, M. A. (2010) · PLoS ONE · doi:10.1371/journal.pone.0010778 · Cited by 217 · see citing works

Translational signaling responses preceding resistance training-mediated myofiber hypertrophy in young and old humans

Mayhew, D. L., Kim, J.-S., Cross, J. M., Ferrando, A. A., & Bamman, M. M. (2009) · Journal of Applied Physiology · doi:10.1152/japplphysiol.91234.2008 · Cited by 215 · see citing works

Global analysis of gene expression patterns during disuse atrophy in rat skeletal muscle

Stevenson, E. J., Giresi, P. G., Koncarevic, A., et al. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2003.044701 · Cited by 212 · see citing works

Reduced Satellite Cell Numbers and Myogenic Capacity in Aging Can Be Alleviated by Endurance Exercise

Shefer, G., Rauner, G., Yablonka‐Reuveni, Z., & Benayahu, D. (2010) · PLoS ONE · doi:10.1371/journal.pone.0013307 · Cited by 211 · see citing works

Overexpression of Glucose-6-Phosphate Dehydrogenase Is Associated with Lipid Dysregulation and Insulin Resistance in Obesity

Park, J., Rho, H. K., Kim, K. H., Choe, S. S., Lee, Y. S., & Kim, J. B. (2005) · Molecular and Cellular Biology · doi:10.1128/mcb.25.12.5146-5157.2005 · Cited by 209 · see citing works

Skeletal muscle density: effects of obesity and non-insulin-dependent diabetes mellitus

Kelley, D., Slasky, B., & Janosky, J. (1991) · The American Journal of Clinical Nutrition · doi:10.1093/ajcn/54.3.509 · Cited by 206 · see citing works

Effects of aerobic exercise training on antioxidant enzyme activities and mRNA levels in soleus muscle from young and aged rats

Lambertucci, R. H., Levada‐Pires, A. C., Rossoni, L. V., Curi, R., & Pithon‐Curi, T. C. (2006) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2006.12.006 · Cited by 205 · see citing works

Arm and leg composition determined by computed tomography in young and elderly men

Rice, C. L., Cunningham, D. A., Paterson, D. H., & Lefcoe, M. S. (1989) · Clinical Physiology · doi:10.1111/j.1475-097x.1989.tb00973.x · Cited by 205 · see citing works

Pathogenesis of sarcopenia and the relationship with fat mass: descriptive review

Li, C., Yu, K., Shyh‐Chang, N., Jiang, Z., Liu, T., Ma, S., Luo, L., Guang, L., Liang, K., Ma, W., et al. (2022) · Journal of Cachexia, Sarcopenia and Muscle · doi:10.1002/jcsm.12901 · Cited by 626 · see citing works

Imaging of sarcopenia: old evidence and new insights

Albano, D., Messina, C., Vitale, J. A., & Sconfienza, L. M. (2019) · European Radiology · doi:10.1007/s00330-019-06573-2 · Cited by 400 · see citing works

Epidemiology of sarcopenia and insight into possible therapeutic targets

Dennison, E. M., Sayer, A. A., & Cooper, C. C. (2017) · Nature Reviews Rheumatology · doi:10.1038/nrrheum.2017.60 · Cited by 296 · see citing works

Mouse models of sarcopenia: classification and evaluation

Xie, W., He, M., Yu, D., Wu, Y., Wang, X., Lv, S., Xiao, W., & Li, Y. (2021) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12709 · Cited by 233 · see citing works

Sarcopenia: imaging assessment and clinical application

Chianca, V., Albano, D., Messina, C., Gitto, S., Ruffo, G., Guarino, S., Grande, F. D., & Sconfienza, L. M. (2021) · Abdominal Radiology · doi:10.1007/s00261-021-03294-3 · Cited by 207 · see citing works

Muscle Lipid Metabolism: Role of Lipid Droplets and Perilipins

Morales, P. E., Bucarey, J. L., & Espinosa, A. (2017) · Journal of Diabetes Research · doi:10.1155/2017/1789395 · Cited by 171 · see citing works

Experimental Models of Sarcopenia: Bridging Molecular Mechanism and Therapeutic Strategy

Mankhong, S., Kim, S., Moon, S., Kwak, H., Park, D., & Kang, J. (2020) · Cells · doi:10.3390/cells9061385 · Cited by 143 · see citing works

Signaling pathways regulating the fate of fibro/adipogenic progenitors (FAPs) in skeletal muscle regeneration and disease

Giuliani, G., Rosina, M., & Reggio, A. (2021) · FEBS Journal · doi:10.1111/febs.16080 · Cited by 138 · see citing works

Single‐cell RNA sequencing and lipidomics reveal cell and lipid dynamics of fat infiltration in skeletal muscle

Xu, Z., You, W., Chen, W., Zhou, Y., Nong, Q., Valencak, T. G., Wang, Y., & Shan, T. (2020) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12643 · Cited by 131 · see citing works

Early structural and functional signature of 3‐day human skeletal muscle disuse using the dry immersion model

Demangel, R., Treffel, L., Py, G., Brioche, T., Pagano, A. F., Bareille, M., Beck, A., Pessemesse, L., Candau, R., Gharib, C., et al. (2017) · Journal of Physiology · doi:10.1113/jp273895 · Cited by 98 · see citing works

Short‐term disuse promotes fatty acid infiltration into skeletal muscle

Pagano, A. F., Brioche, T., Arc-Chagnaud, C., Demangel, R., Chopard, A., & Py, G. (2017) · Journal of Cachexia, Sarcopenia and Muscle · doi:10.1002/jcsm.12259 · Cited by 99 · see citing works

Hospital‐associated deconditioning: Not only physical, but also cognitive

Chen, Y. S., Almirall‐Sánchez, A., Mockler, D., Adrion, E., Domínguez‐Vivero, C., & Romero‐Ortuño, R. (2022) · International Journal of Geriatric Psychiatry · doi:10.1002/gps.5687 · Cited by 113 · see citing works

IL-1β- and IL-4-polarized macrophages have opposite effects on adipogenesis of intramuscular fibro-adipogenic progenitors in humans

Moratal, C., Raffort, J., Arrighi, N., Rekima, S., Schaub, S., Dechesne, C. A., Chinetti, G., & Dani, C. (2018) · Scientific Reports · doi:10.1038/s41598-018-35429-w · Cited by 101 · see citing works

Sarcopenia: Beyond Muscle Atrophy and into the New Frontiers of Opportunistic Imaging, Precision Medicine, and Machine Learning

Lenchik, L., & Boutin, R. D. (2018) · Seminars in Musculoskeletal Radiology · doi:10.1055/s-0038-1641573 · Cited by 98 · see citing works

Hyperbaric oxygen therapy for healthy aging: From mechanisms to therapeutics

Fu, Q., Duan, R., Sun, Y., & Li, Q. (2022) · Redox Biology · doi:10.1016/j.redox.2022.102352 · Cited by 73 · see citing works

Screening Accuracy of SARC-F for Sarcopenia in the Elderly: A Diagnostic Meta-Analysis

Lü, J., Ding, L.-Y., Xu, Q., Zhu, S., Xu, X., Hua, H., Chen, L., & Xu, H. (2020) · The journal of nutrition health & aging · doi:10.1007/s12603-020-1471-8 · Cited by 70 · see citing works

Opportunistic Measurement of Skeletal Muscle Size and Muscle Attenuation on Computed Tomography Predicts 1-Year Mortality in Medicare Patients

Lenchik, L., Lenoir, K. M., Tan, J., Boutin, R. D., Callahan, K. E., Kritchevsky, S. B., & Wells, B. J. (2018) · The Journals of Gerontology Series A · doi:10.1093/gerona/gly183 · Cited by 70 · see citing works

PPARγ Controls Ectopic Adipogenesis and Cross-Talks with Myogenesis During Skeletal Muscle Regeneration

Dammone, G., Karaz, S., Lukjanenko, L., Winkler, C., Sizzano, F., Jacot, G. E., Migliavacca, E., Palini, A. G., Desvergne, B., Gilardi, F., et al. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19072044 · Cited by 69 · see citing works

Evaluation of an Antioxidant and Anti-inflammatory Cocktail Against Human Hypoactivity-Induced Skeletal Muscle Deconditioning

Arc-Chagnaud, C., Py, G., Fovet, T., Roumanille, R., Demangel, R., Pagano, A. F., Delobel, P., Blanc, S., Jasmin, B. J., Blottner, D., et al. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.00071 · Cited by 59 · see citing works

Mitochondrial Bioenergetics and Turnover during Chronic Muscle Disuse

Memme, J. M., Slavin, M. B., Moradi, N., & Hood, D. A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22105179 · Cited by 59 · see citing works

Skeletal Muscle Deconditioning in Breast Cancer Patients Undergoing Chemotherapy: Current Knowledge and Insights From Other Cancers

Mallard, J., Hucteau, E., Hureau, T. J., & Pagano, A. F. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.719643 · Cited by 57 · see citing works

Association of high body mass index, waist circumference, and body fat percentage with sarcopenia in older women

Yoo, M. C., Won, C. W., & Soh, Y. (2022) · BMC Geriatrics · doi:10.1186/s12877-022-03643-x · Cited by 59 · see citing works

Chemotherapy impairs skeletal muscle mitochondrial homeostasis in early breast cancer patients

Mallard, J., Hucteau, E., Charles, A., Bender, L., Baeza, C., Pélissié, M., Trensz, P., Pflumio, C., Kalish‐Weindling, M., Gény, B., et al. (2022) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12991 · Cited by 50 · see citing works

The effect of calorie restriction on mouse skeletal muscle is sex, strain and time-dependent

Boldrin, L., Ross, J. A., Whitmore, C. L., Doreste, B., Beaver, C., Eddaoudi, A., Pearce, D. J., & Morgan, J. E. (2017) · Scientific Reports · doi:10.1038/s41598-017-04896-y · Cited by 51 · see citing works

Adiponectin receptor agonist AdipoRon improves skeletal muscle function in aged mice

Balasubramanian, P., Schaar, A. E., Gustafson, G. E., Smith, A. B., Howell, P. R., Greenman, A., Baum, S., Colman, R. J., Lamming, D. W., Diffee, G., et al. (2022) · eLife · doi:10.7554/elife.71282 · Cited by 49 · see citing works

Molecular and Functional Networks Linked to Sarcopenia Prevention by Caloric Restriction in Rhesus Monkeys

Rhoads, T. W., Clark, J. P., Gustafson, G. E., Miller, K. N., Conklin, M. W., DeMuth, T. M., Berres, M. E., Eliceiri, K. W., Vaughan, L. K., Lary, C. W., et al. (2020) · Cell Systems · doi:10.1016/j.cels.2019.12.002 · Cited by 50 · see citing works

The altered human serum metabolome induced by a marathon

Stander, Z., Luies, L., Mienie, L. J., Keane, K. M., Howatson, G., Clifford, T., Stevenson, E., & Loots, D. T. (2018) · Metabolomics · doi:10.1007/s11306-018-1447-4 · Cited by 50 · see citing works

Control of Muscle Fibro-Adipogenic Progenitors by Myogenic Lineage is Altered in Aging and Duchenne Muscular Dystrophy

Moratal, C., Arrighi, N., Dechesne, C. A., & Dani, C. (2019) · Cellular Physiology and Biochemistry · doi:10.33594/000000196 · Cited by 45 · see citing works

Mitochondrial dysfunction in age-related sarcopenia: mechanistic insights, diagnostic advances, and therapeutic prospects

Huang, Y., Wang, C., Cui, H., Sun, G., Qi, X., & Yao, X. (2025) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2025.1590524 · Cited by 45 · see citing works

Morphological and Functional Aspects of Human Skeletal Muscle

Trovato, F., Imbesi, R., Conway, N., & Castrogiovanni, P. (2016) · Journal of Functional Morphology and Kinesiology · doi:10.3390/jfmk1030289 · Cited by 41 · see citing works

Resistance training regulates gene expression of molecules associated with intramyocellular lipids, glucose signaling and fiber size in old rats

Ribeiro, M. B. T., Guzzoni, V., Hord, J. M., Lopes, G. N., Marqueti, R. D. C., de Andrade, R. V., Selistre-de-Araújo, H. S., & Durigan, J. L. Q. (2017) · Scientific Reports · doi:10.1038/s41598-017-09343-6 · Cited by 40 · see citing works

Prognostic Value of Sarcopenia in Patients With Diffuse Large B-Cell Lymphoma Treated With R-CHOP: A Systematic Review and Meta-Analysis

Xu, X., Dong-liang, H., Tian, M., Wu, H., & Jin, X. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.816883 · Cited by 39 · see citing works

Glycerol-induced injury as a new model of muscle regeneration

Mahdy, M. A. A. (2018) · Cell and Tissue Research · doi:10.1007/s00441-018-2846-6 · Cited by 37 · see citing works

Preventive Effects of Schisandrin A, A Bioactive Component of Schisandra chinensis, on Dexamethasone-Induced Muscle Atrophy

Yeon, M., Choi, H., & Jun, H. (2020) · Nutrients · doi:10.3390/nu12051255 · Cited by 34 · see citing works

Early-stage inflammation changes in supraspinatus muscle after rotator cuff tear

Stengaard, K., Hejbøl, E. K., Jensen, P. T., Degn, M., Ta, T. M. L., Stensballe, A., Andersen, D. C., Schrøder, H. D., Lambertsen, K. L., & Frich, L. H. (2022) · Journal of Shoulder and Elbow Surgery · doi:10.1016/j.jse.2021.12.046 · Cited by 33 · see citing works

Glucose 6-P Dehydrogenase—An Antioxidant Enzyme with Regulatory Functions in Skeletal Muscle during Exercise

García-Domínguez, E., Carretero, A., Viña-Almunia, A., Doménech, J., González, G. O., Viña, J., & Gómez‐Cabrera, M. C. (2022) · Cells · doi:10.3390/cells11193041 · Cited by 32 · see citing works

An externally validated deep learning model for the accurate segmentation of the lumbar paravertebral muscles

Niemeyer, F., Zanker, A., Jonas, R., Tao, Y., Galbusera, F., & Wilke, H. (2022) · European Spine Journal · doi:10.1007/s00586-022-07320-w · Cited by 28 · see citing works

Appendicular skeletal muscle mass: A more sensitive biomarker of disease severity than BMI in adults with mitochondrial diseases

Hou, Y., Xie, Z., Zhao, X., Yuan, Y., Dou, P., & Wang, Z. (2019) · PLoS ONE · doi:10.1371/journal.pone.0219628 · Cited by 27 · see citing works

Integrated study on comparative transcriptome and skeletal muscle function in aged rats

Zhou, J., Liao, Z., Chen, J., Zhao, K., & Xiao, Q. (2018) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2018.01.001 · Cited by 25 · see citing works

Preserved Capacity for Adaptations in Strength and Muscle Regulatory Factors in Elderly in Response to Resistance Exercise Training and Deconditioning

Fritzen, A. M., Thøgersen, F. B., Qadri, K. A. N., Krag, T. O. B., Sveen, M., Vissing, J., & Jeppesen, T. D. (2020) · Journal of Clinical Medicine · doi:10.3390/jcm9072188 · Cited by 25 · see citing works

Differential analysis of chromatin accessibility and gene expression profiles identifies cis-regulatory elements in rat adipose and muscle

Nair, V. D., Vasoya, M., Nair, V., Smith, G. R., Pinças, H., Ge, Y., Douglas, C. M., Esser, K. A., & Sealfon, S. C. (2021) · Genomics · doi:10.1016/j.ygeno.2021.09.013 · Cited by 25 · see citing works

Paraspinal Muscle Degeneration: A Potential Risk Factor for New Vertebral Compression Fractures After Percutaneous Kyphoplasty

Si, F., Yuan, S., Zang, L., Fan, N., Wu, Q., Wang, T., & Wang, A. (2022) · Clinical Interventions in Aging · doi:10.2147/cia.s374857 · Cited by 25 · see citing works

Cerium Oxide Nanoparticle Administration to Skeletal Muscle Cells under Different Gravity and Radiation Conditions

Genchi, G. G., Degl’Innocenti, A., Martinelli, C., Battaglini, M., Pasquale, D. D., Prato, M., Marras, S., Pugliese, G., Drago, F., Mariani, A., et al. (2021) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.1c14176 · Cited by 22 · see citing works

Trimetazidine and exercise provide comparable improvements to high fat diet-induced muscle dysfunction through enhancement of mitochondrial quality control

Zhang, W., You, B., Qi, D., Qiu, L., Ripley-Gonzalez, J. W., Zheng, F., Fu, S., Li, C., Dun, Y., & Liu, S. (2021) · Scientific Reports · doi:10.1038/s41598-021-98771-6 · Cited by 22 · see citing works

Increased Fibro-Adipogenic Progenitors and Intramyocellular Lipid Accumulation in Obesity-Related Skeletal Muscle Dysfunction

Jia, G., & Sowers, J. R. (2018) · Diabetes · doi:10.2337/dbi18-0047 · Cited by 20 · see citing works

Mechanical stress promotes biological functions of C2C12 myoblasts by activating PI3K/AKT/mTOR signaling pathway

Da, Y., Mou, Y., Wang, M., Yuan, X. H., Yan, F., Lan, W., & Zhang, F. (2019) · Molecular Medicine Reports · doi:10.3892/mmr.2019.10808 · Cited by 20 · see citing works

In Vitro, In Vivo, and In Silico Methods for Assessment of Muscle Size and Muscle Growth Regulation

Rupert, J. E., Jengelley, D. H. A., & Zimmers, T. A. (2020) · Shock · doi:10.1097/shk.0000000000001498 · Cited by 19 · see citing works

Age, diabetes mellitus, and dialysis modality are associated with risk of poor muscle strength and physical function in hemodialysis and peritoneal dialysis patients

Silva, M. Z. C., Antônio, K. J., Reis, J. M. S., Alves, L. S., Caramori, J. C. T., & Vogt, B. P. (2021) · Kidney Research and Clinical Practice · doi:10.23876/j.krcp.20.159 · Cited by 19 · see citing works

Development of skeletal muscle atrophy and intermuscular adipose tissue in patients with early breast cancer treated with chemotherapy

Mallard, J., Hucteau, E., Bender, L., Charlot, A., Debrut, L., Pflumio, C., Trensz, P., Schött, R., Favret, F., Pivot, X. B., et al. (2022) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00373.2022 · Cited by 19 · see citing works

Understanding the development of sarcopenic obesity

Gross, D. C., Cheever, C. R., & Batsis, J. A. (2023) · Expert Review of Endocrinology & Metabolism · doi:10.1080/17446651.2023.2267672 · Cited by 19 · see citing works

Muscle Resting and TGF-β Inhibitor Treatment Prevent Fatty Infiltration Following Skeletal Muscle Injury

Pagano, A. F., Arc‐Chagnaud, C., Brioche, T., Chopard, A., & Py, G. (2019) · Cellular Physiology and Biochemistry · doi:10.33594/000000121 · Cited by 19 · see citing works

SIRT1-dependent mechanisms and effects of resveratrol for amelioration of muscle wasting in NASH mice

Liu, C.-W., Huang, C., Hsu, C.-F., Li, T., Tsai, Y.-L., Lin, M., Tsai, H., Huang, S., Yang, Y., Hsieh, Y., et al. (2020) · BMJ Open Gastroenterology · doi:10.1136/bmjgast-2020-000381 · Cited by 18 · see citing works

Extracellular vesicle-derived miRNAs improve stem cell-based therapeutic approaches in muscle wasting conditions

Yedigaryan, L., Martínez‐Sarrà, E., Giacomazzi, G., Giarratana, N., van der Veer, B. K., Rotini, A., Querceto, S., Grosemans, H., Cortés-Calabuig, Á., Salucci, S., et al. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.977617 · Cited by 18 · see citing works

Mechanisms, assessment, and exercise interventions for skeletal muscle dysfunction post-chemotherapy in breast cancer: from inflammation factors to clinical practice

Zhong, P., Li, X., & Li, J. (2025) · Frontiers in Oncology · doi:10.3389/fonc.2025.1551561 · Cited by 18 · see citing works

The Whole-transcriptome Landscape of Diabetes-related Sarcopenia Reveals the Specific Function of Novel lncRNA Gm20743

Yu, J., Loh, K., Yang, H.-Q., Du, M.-R., Wu, Y.-X., Liao, Z., Guo, A., Yang, Y., Chen, B., Zhao, Y., et al. (2022) · Communications Biology · doi:10.1038/s42003-022-03728-8 · Cited by 17 · see citing works

Earthworm, Perionyx excavatus as an alternate protein source for Nile tilapia: Effects on growth performance, blood biochemistry, erythrocyte morphology and intestinal health

Das, B., Islam, S. M., Nag, S. K., Al-Azim, Vatsos, I. N., & Siddik, M. A. B. (2024) · Aquaculture International · doi:10.1007/s10499-024-01533-0 · Cited by 16 · see citing works

A Comprehensive Review of Essential Aspects of Molecular Pathophysiological Mechanisms with Emerging Interventions for Sarcopenia in Older People

Prajapati, P., Kumar, A., Chaudary, R., Mangrulkar, S. V., Arya, M., & Kushwaha, S. (2023) · Current Molecular Pharmacology · doi:10.2174/1874467216666230308142137 · Cited by 17 · see citing works

Effects of transforming growth factor‐β1 treatment on muscle regeneration and adipogenesis in glycerol‐injured muscle

Mahdy, M. A. A., Warita, K., & Hosaka, Y. Z. (2017) · Animal Science Journal · doi:10.1111/asj.12845 · Cited by 15 · see citing works

Combined protein and calcium β-hydroxy-β-methylbutyrate induced gains in leg fat free mass: a double-blinded, placebo-controlled study

Stahn, A. C., Maggioni, M. A., Gunga, H., & Terblanche, E. (2020) · Journal of the International Society of Sports Nutrition · doi:10.1186/s12970-020-0336-1 · Cited by 15 · see citing works

Clinical and prognostic role of 2-[18F]FDG PET/CT and sarcopenia in treatment-naïve patients with T-cell lymphoblastic lymphoma

Tan, X., Yuan, H., Li, D., Sun, X., Ding, C., & Jiang, L. (2022) · Annals of Hematology · doi:10.1007/s00277-022-04988-4 · Cited by 14 · see citing works

Application of imaging methods and the latest progress in sarcopenia

Li, C., Huang, Y., Wang, H., Lu, J., & He, B. (2024) · Chinese Journal of Academic Radiology · doi:10.1007/s42058-024-00142-3 · Cited by 13 · see citing works

Radiographic analysis of fatty infiltration of the extraocular muscles in thyroid eye disease

Cohen, L. M., Liou, V. D., Cunnane, M. E., & Yoon, M. K. (2020) · Orbit · doi:10.1080/01676830.2020.1817100 · Cited by 13 · see citing works

Characterizing skeletal muscle dysfunction in women with polycystic ovary syndrome

McDonnell, T., Cussen, L., McIlroy, M., & O’Reilly, M. (2022) · Therapeutic Advances in Endocrinology and Metabolism · doi:10.1177/20420188221113140 · Cited by 13 · see citing works

Pim1 knockout alleviates sarcopenia in aging mice via reducing adipogenic differentiation of PDGFRα+ mesenchymal progenitors

Shang, G., Han, L., Wang, Z., Song, M., Wang, D., Tan, Y., Li, Y., Li, Y., Zhang, W., & Zhong, M. (2021) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12770 · Cited by 12 · see citing works

Muscular Swedish mutant APP-to-Brain axis in the development of Alzheimer’s disease

Pan, J., Lee, D., Sun, D., Zhao, K., Xiong, L., Guo, H.-H., Ren, X., Chen, P., de Boer, R. L., Lu, Y., et al. (2022) · Cell Death and Disease · doi:10.1038/s41419-022-05378-4 · Cited by 12 · see citing works

Sarcopenia in distal radius fractures: systematic review of the literature and current findings

Artiaco, S., Fusini, F., Pennacchio, G., Colzani, G., Battiston, B., & Bianchi, P. (2020) · European Journal of Orthopaedic Surgery & Traumatology · doi:10.1007/s00590-020-02697-0 · Cited by 12 · see citing works

The Relationship between Exercise Capacity and Muscle Strength, Physical Activity, Fatigue and Quality of Life in Patients with Cancer Cachexia

Polat, K., Karadibak, D., Güç, Z. G., Yavuzşen, T., & Öztop, İ. (2023) · Nutrition and Cancer · doi:10.1080/01635581.2023.2276486 · Cited by 11 · see citing works

Histological and biochemical evaluation of supplementing broiler diet with β-hydroxy-methyl butyrate calcium (β-HMB-Ca).

Ahmed, S. K., Al-Shamire, J. S., & Dhyaa, A. A. (2018) · Europe PMC (PubMed Central) · Cited by 11 · see citing works

The role of sarcopenic obesity for the prediction of prognosis of patients with gastrointestinal cancer

Chen, W., Yuan, Q., Li, X., Yao, J., Yuan, L., Chen, X., & Gao, B. (2024) · Cancer Medicine · doi:10.1002/cam4.7452 · Cited by 9 · see citing works

Experimental models as a tool for research on sarcopenia: A narrative review

Alonso-Puyo, J., Izagirre-Fernandez, O., Crende, O., Valdivia, A., García-Gallastegui, P., & Sanz, B. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102534 · Cited by 11 · see citing works

Rodent model intervention for prevention and optimal management of sarcopenia: A systematic review on the beneficial effects of nutrients & non-nutrients and exercise to improve skeletal muscle health

Vijayakumar, M., Kannappan, P., Janani, B., & Kim, C. Y. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102543 · Cited by 10 · see citing works

Evolution of Physical Status From Diagnosis to the End of First-Line Treatment in Breast, Lung, and Colorectal Cancer Patients: The PROTECT-01 Cohort Study Protocol

Mallard, J., Hucteau, E., Schött, R., Petit, T., Demarchi, M., Belletier, C., Abdelghani, M. B., Carinato, H., Chiappa, P., Fischbach, C., et al. (2020) · Frontiers in Oncology · doi:10.3389/fonc.2020.01304 · Cited by 10 · see citing works

ß-Hydroxy-ß-methylbutyrate: A feed supplement influencing performance, bone metabolism, intestinal morphology, and muscle quality of laying hens: a preliminary one-point study

Tomaszewska, E., Świątkiewicz, S., Arczewska-Włosek, A., Wojtysiak, D., Dobrowolski, P., Domaradzki, P., Puzio, I., Rudyk, H., Brezvyn, O. M., & Muszyński, S. (2024) · Poultry Science · doi:10.1016/j.psj.2024.103597 · Cited by 9 · see citing works

Sarcopenia is attenuated by mairin in SAMP8 mice via the inhibition of FAPs fibrosis through the AMPK-TGF-β-SMAD axis

Zhong, W., Jia, H., Zhu, H., Tian, Y., Huang, W., & Yang, Q. (2024) · Gene · doi:10.1016/j.gene.2024.148873 · Cited by 9 · see citing works

Muskelverletzungen des Sportlers

Loizides, A., Gruber, H., Peer, S., & Plaikner, M. (2017) · Der Radiologe · doi:10.1007/s00117-017-0292-1 · Cited by 9 · see citing works

The Impact of Ulmus macrocarpa Extracts on a Model of Sarcopenia-Induced C57BL/6 Mice

Lee, C. H., Kwon, Y., Park, S., Kim, T.-H., Kim, M. S., Kim, E. J., Jung, J. I., Min, S., Park, K., Jeong, J. H., et al. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25116197 · Cited by 10 · see citing works

Yoga education program for older women diagnosed with sarcopenia: A multicity 10-year follow-up experiment

Pandya, S. P. (2018) · Journal of Women & Aging · doi:10.1080/08952841.2018.1510245 · Cited by 8 · see citing works

The Preventive Effect of Specific Collagen Peptides against Dexamethasone-Induced Muscle Atrophy in Mice

Oh, J., Park, S. H., Kim, D. S., Choi, W., Jang, J., Rahmawati, L., Jang, W. Y., Lim, H. K., Hwang, J. Y., Gu, G. R., et al. (2023) · Molecules · doi:10.3390/molecules28041950 · Cited by 7 · see citing works

Limited Benefit of Marine Protein Hydrolysate on Physical Function and Strength in Older Adults: A Randomized Controlled Trial

Nygård, L. K., Mundal, I. P., Dahl, L., Benth, J. Š., & Rokstad, A. M. M. (2021) · Marine Drugs · doi:10.3390/md19020062 · Cited by 7 · see citing works

Utility of multidetector computed tomography quantitative measurements in identifying sarcopenia: a propensity score matched study

Zuo, Y.-Q., Gao, Z., Wang, Z., Liu, Q., Yang, X., Yin, Y.-L., & Feng, P. (2021) · Skeletal Radiology · doi:10.1007/s00256-021-03953-y · Cited by 6 · see citing works

Effects of mammalian target of rapamycin on proliferation, apoptosis and differentiation of myoblasts undergoing mechanical stress.

Wang, M., Mou, Y., Da, Y., Yuan, X. H., Yan, F., Lan, W., & Zhang, F. (2018) · Europe PMC (PubMed Central) · Cited by 6 · see citing works

Changes of Wnt/β-catenin signalling, BMP2, and BMP4 in the jejunum during ageing in rats

Dun, Y., Chen, J., Liu, J., Guo, Y., Zhang, C., & Yuan, D. (2020) · Arab Journal of Gastroenterology · doi:10.1016/j.ajg.2019.12.004 · Cited by 6 · see citing works

The important role of fatty infiltration of skeletal muscle in aging: skeletal muscle function, pathological mechanisms, and intervention

Yang, M., Zhou, F., Wang, C., sun, T., zhao, W., Liu, L., Meng, Y., & tian, L. (2026) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00473.2025 · Cited by 5 · see citing works

Custom-made 3D-printed boot as a model of disuse-induced atrophy in murine skeletal muscle

Masiero, G., Ferrarese, G., Perazzolo, E., Baraldo, M., Nogara, L., & Tezze, C. (2024) · PLoS ONE · doi:10.1371/journal.pone.0304380 · Cited by 5 · see citing works

Vitamin D, Sarcopenia and Aging

Skaaby, T., Thuesen, B. H., & Linneberg, A. R. (2018) · Frontiers of hormone research · doi:10.1159/000486084 · Cited by 5 · see citing works

Age-related variations in trunk composition and patterns of regional bone and soft tissue changes in adult Caucasian women by DXA

Theodorou, S. J., Theodorou, D. J., Kigka, V. I., Gkiatas, I. S., & FOTOPOULOS, A. D. (2023) · Rheumatology International · doi:10.1007/s00296-023-05514-z · Cited by 5 · see citing works

Pdgfrα+ stromal cells, a key regulator for tissue homeostasis and dysfunction in distinct organs

Kang, X., Zhao, K., Huang, Z., Fukada, S., Qi, X., & Miao, H. (2024) · Genes & Diseases · doi:10.1016/j.gendis.2024.101264 · Cited by 5 · see citing works

Using an electronic frailty index and patient reported outcomes to predict sarcopenia risk

Altherr, C. A., Luo, X., Ding, H., Liu, Z., Warden, S. J., Moorthi, R. N., & Imel, E. A. (2025) · Scientific Reports · doi:10.1038/s41598-025-19311-0 · Cited by 4 · see citing works

Skeletal Muscle System

Acuña, M. J., Brandan, E., & Motta‐Santos, D. (2019) · Springer eBooks · doi:10.1007/978-3-030-22696-1_11 · Cited by 4 · see citing works

Aging Muscles, Myositis, Pain, and Peripheral Neuropathies: PET Manifestations in the Elderly

Katal, S., Taubman, K., Han, J., & Gholamrezanezhad, A. (2022) · PET Clinics · doi:10.1016/j.cpet.2022.09.009 · Cited by 3 · see citing works

The effect of pre-slaughter electrical stunning on bleeding efficiency, meat quality, histology, and microbial count of several goat muscles

Al-Amri, I. S., Kadim, I. T., AlKindi, A. Y., Haq, Q. M. I., Al-Ajmi, D. S., Haemd, A., Quibol, R., Al-Magbali, R. S., Khalaf, S. K., & Hosni, K. S. A. (2023) · South African Journal of Animal Science · doi:10.4314/sajas.v52i5.07 · Cited by 3 · see citing works

Opportunistic retrospective assessment of HUAC, bone density, SFT and breast density on CT images and relationship with severity of COVID-19

Subaşı, M., Düger, M., Erol, C., & Durur-Subasi, İ. (2023) · Journal of Mind and Medical Sciences · doi:10.22543/2392-7674.1371 · Cited by 3 · see citing works

The Impact of FBN1-α5β1 Axis in Fibro/Adipogenic Progenitor Cells (FAPCD9-) on Intramuscular Fat Content in Pigs.

Tong, X., Zhu, Q., Duo, T.-Q., Liang, Z.-Y., Zhang, C., Cai, S., Wang, X.-Y., Liu, Y.-H., Li, Y., Liu, X.-H., et al. (2024) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.4c00059 · Cited by 7 · see citing works

Intermuscular adipose tissue drives bone loss in postmenopausal osteoporosis via fibro-adipogenic progenitors-mediated osteoclastogenesis

Luo, L., Tang, Y., Huang, Z.-W., Dai, M.-X., Lai, S.-Q., Gao, J.-W., Le, S.-Y., Wang, L., & Tu, C. (2026) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2026.112830 · Cited by 2 · see citing works

Sarcopenia definitions: Critical issues

Iolascon, G., & Moretti, A. (2018) · Edorium Journal of Disability and Rehabilitation · doi:10.5348/d05-2018-36-ed-2 · Cited by 2 · see citing works

Isolated fatty infiltration of the gastrocnemius medial head, a cadaveric case study

Rabey, K. N., Satkunam, L. E., Webber, C. A., & Hocking, J. C. (2021) · Human Pathology Case Reports · doi:10.1016/j.ehpc.2021.200480 · Cited by 2 · see citing works

Correlation of Vitamin D Serum Levels with Muscle Mass, Muscle Strength, and Physical Performance in the Elderly Community in Mohammad Hoesin General Hospital Palembang

Bachry, N. C., Riviati, N., Kusnadi, Y., & Bahar, E. (2021) · Bioscientia Medicina Journal of Biomedicine and Translational Research · doi:10.32539/bsm.v5i2.225 · Cited by 2 · see citing works

Quantification of 11 metabolites in rat urine after exposure to organophosphates

Leninsky, M. A., Sobolev, V. E., Sokolova, M. O., Войтенко, Н. Г., & Skvortsov, N. V. (2024) · Laboratory Animal Research · doi:10.1186/s42826-024-00209-3 · Cited by 1 · see citing works

A generalized equation for predicting peak oxygen consumption during treadmill exercise testing: mitigating the bias from total body mass scaling

Santana, E. J., Cauwenberghs, N., Celestin, B. E., Kuznetsova, T., Gardner, C. D., Arena, R. A., Kaminsky, L. A., Harber, M. P., Ashley, E. A., Christle, J. W., et al. (2024) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2024.1393363 · Cited by 1 · see citing works

Aging biology and geriatric disease in dogs and cats

Armstrong, P., & Oh, W. (2025) · Journal of Veterinary Science · doi:10.4142/jvs.25220 · Cited by 1 · see citing works

Skeletal Muscle Fat Infiltration with Aging An Important Factor of Sarcopenia

Pagano, A. F., Arc‐Chagnaud, C., Brioche, T., Chopard, A., & Py, G. (2019) · CRC Press eBooks · doi:10.1201/9780429155260-13

Role of fibro-adipogenic progenitors in skeletal muscle aging

Wan, R., Zhang, H., Liu, S., Jiao, C., Chen, H., Luo, Z., & Shang, X. (2023) · Aging Pathobiology and Therapeutics · doi:10.31491/apt.2023.06.116 · Cited by 8 · see citing works

Targeting fibro-adipogenic progenitor cells in aging muscle: Exercise regulation and strategies to enhance regeneration and repair

Alway, S. E., & Rajasingh, J. (2026) · Sports Medicine and Health Science · doi:10.1016/j.smhs.2026.07.005

Rethinking Muscle Aging Through the Lens of Fibro-Adipogenic Progenitors

Zhang, F., Zhang, X.-Z., Yu, Z., Zhuang, C.-L., & Han, L. (2025) · Aging and Disease · doi:10.14336/ad.2025.1162 · Cited by 2 · see citing works

Treating age‐related loss of muscle mass and function: Where should we be focusing?

Ham, D. J., Fry, C. S., Ruparelia, A. A., Ngo, S. T., & Lamon, S. (2026) · The Journal of Physiology · doi:10.1113/jp289838 · Cited by 5 · see citing works