Testosterone improves the regeneration of old and young mouse skeletal muscle

Longitudinal Effects of Aging on Serum Total and Free Testosterone Levels in Healthy Men

Harman, S. M., Metter, E. J., Tobin, J. D., Pearson, J., & Blackman, M. R. (2001) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.86.2.7219 · Cited by 2,760 · 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

Mediation of IGF-1-induced skeletal myotube hypertrophy by PI(3)K/Akt/mTOR and PI(3)K/Akt/GSK3 pathways

Rommel, C., Bodine, S. C., Clarke, B. A., Rossman, R., Nunez, L., Stitt, T. N., Yancopoulos, G. D., & Glass, D. J. (2001) · Nature Cell Biology · doi:10.1038/ncb1101-1009 · Cited by 1,583 · see citing works

Stem Cell Function, Self-Renewal, and Behavioral Heterogeneity of Cells from the Adult Muscle Satellite Cell Niche

Collins, C. A., Olsen, I., Zammit, P. S., Heslop, L., Petrie, A., Partridge, T. A., & Morgan, J. E. (2005) · Cell · doi:10.1016/j.cell.2005.05.010 · Cited by 1,445 · see citing works

Satellite cells, connective tissue fibroblasts and their interactions are crucial for muscle regeneration

Murphy, M. M., Lawson, J. A., Mathew, S. J., Hutcheson, D. A., & Kardon, G. (2011) · Development · doi:10.1242/dev.064162 · Cited by 1,249 · 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

Human growth hormone and human aging

CORPAS, E., HARMAN, S. M., & BLACKMAN, M. R. (1993) · Endocrine Reviews · doi:10.1210/edrv-14-1-20 · Cited by 911 · see citing works

Myostatin negatively regulates satellite cell activation and self-renewal

McCroskery, S., Thomas, M., Maxwell, L., Sharma, M., & Kambadur, R. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200207056 · Cited by 784 · see citing works

Differentiation Stage-Specific Inhibition of the Raf-MEK-ERK Pathway by Akt

Rommel, C., Clarke, B. A., Zimmermann, S., Nuñez, L., Rossman, R., Reid, K., Moelling, K., Yancopoulos, G. D., & Glass, D. J. (1999) · Science · doi:10.1126/science.286.5445.1738 · Cited by 759 · see citing works

The Mitogenic and Myogenic Actions of Insulin-like Growth Factors Utilize Distinct Signaling Pathways

Coolican, S. A., Samuel, D. S., Ewton, D. Z., McWade, F. J., & Florini, J. R. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.10.6653 · Cited by 646 · see citing works

Androgens Stimulate Myogenic Differentiation and Inhibit Adipogenesis in C3H 10T1/2 Pluripotent Cells through an Androgen Receptor-Mediated Pathway

Singh, R., Artaza, J. N., Taylor, W. E., Gonzalez-Cadavid, N. F., & Bhasin, S. (2003) · Endocrinology · doi:10.1210/en.2003-0741 · Cited by 555 · see citing works

Type beta transforming growth factor is an inhibitor of myogenic differentiation.

Massagué, J., Cheifetz, S., Endo, T., & Nadal‐Ginard, B. (1986) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.83.21.8206 · Cited by 550 · 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

Testosterone-induced increase in muscle size in healthy young men is associated with muscle fiber hypertrophy

Sinha-Hikim, I., Artaza, J., Woodhouse, L., Gonzalez-Cadavid, N., Singh, A. B., Lee, M. I., Storer, T. W., Casaburi, R., Shen, R., & Bhasin, S. (2002) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00502.2001 · Cited by 464 · see citing works

In vivo satellite cell activation via Myf5 and MyoD in regenerating mouse skeletal muscle

Cooper, R. N., Tajbakhsh, S., Mouly, V., Cossu, G., BUCKINGHAM, M. E., & Butler-Browne, G. S. (1999) · Journal of Cell Science · doi:10.1242/jcs.112.17.2895 · Cited by 457 · see citing works

Transforming Growth Factor-β1 Induces the Differentiation of Myogenic Cells into Fibrotic Cells in Injured Skeletal Muscle

Li, Y., Foster, W. H., Deasy, B. M., Chan, Y., Prisk, V. R., Tang, Y., Cummins, J. H., & Huard, J. (2004) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)63188-4 · Cited by 454 · see citing works

Hepatocyte growth factor activates quiescent skeletal muscle satellite cells in vitro

Allen, R. E., Sheehan, S. M., Taylor, R. G., Kendall, T. L., & Rice, G. M. (1995) · Journal of Cellular Physiology · doi:10.1002/jcp.1041650211 · Cited by 422 · see citing works

Testosterone-induced muscle hypertrophy is associated with an increase in satellite cell number in healthy, young men

Sinha-Hikim, I., Roth, S. M., Lee, M. I., & Bhasin, S. (2003) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00370.2002 · Cited by 344 · see citing works

A Population of Myogenic Stem Cells That Survives Skeletal Muscle Aging

Collins, C. A., Zammit, P. S., Ruiz, A. P., Morgan, J. E., & Partridge, T. A. (2007) · Stem Cells · doi:10.1634/stemcells.2006-0372 · Cited by 320 · 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

Effects of Testosterone Supplementation on Skeletal Muscle Fiber Hypertrophy and Satellite Cells in Community-Dwelling Older Men

Sinha-Hikim, I., Cornford, M., Gaytan, H., Lee, M. L., & Bhasin, S. (2006) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2006-0357 · Cited by 318 · see citing works

Regulatory factors and cell populations involved in skeletal muscle regeneration

Broek, R. W. T., Grefte, S., & den Hoff, J. W. V. (2010) · Journal of Cellular Physiology · doi:10.1002/jcp.22127 · Cited by 315 · see citing works

Androgen Receptor in Human Skeletal Muscle and Cultured Muscle Satellite Cells: Up-Regulation by Androgen Treatment

Sinha‐Hikim, I., Taylor, W. E., González-Cadavid, N. F., Zheng, W. D., & Bhasin, S. (2004) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2004-0084 · Cited by 312 · see citing works

Metabolic and Reproductive Features before and during Puberty in Daughters of Women with Polycystic Ovary Syndrome

Sir-Petermann, T., Codner, E., Pérez, V., Echiburú, B., Maliqueo, M., Ladrón de Guevara, A., Preisler, J., Crisosto, N., Sánchez, F., Cassorla, F., et al. (2009) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2008-2836 · Cited by 260 · 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

Relative roles of TGF‐β1 and Wnt in the systemic regulation and aging of satellite cell responses

Carlson, M. E., Conboy, M. J., Hsu, M., Barchas, L., Jeong, J., Agrawal, A., Mikels, A. J., Agrawal, S., Schaffer, D. V., & Conboy, I. M. (2009) · Aging Cell · doi:10.1111/j.1474-9726.2009.00517.x · Cited by 244 · see citing works

Loss of stem cell regenerative capacity within aged niches

Carlson, M. E., & Conboy, I. M. (2007) · Aging Cell · doi:10.1111/j.1474-9726.2007.00286.x · Cited by 233 · see citing works

Absolute strength and loss of strength as predictors of mobility decline in older adults: the InCHIANTI study

Hicks, G. E., Shardell, M., Alley, D. E., Miller, R. R., Bandinelli, S., Guralnik, J., Lauretani, F., Simonsick, E. M., & Ferrucci, L. (2012) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/glr055 · Cited by 229 · see citing works

Impaired skeletal muscle development and function in male, but not female, genomic <i>androgen receptor</i> knockout mice

MacLean, H. E., Chiu, W. S. M., Notini, A. J., Axell, A.-M., Davey, R. A., McManus, J. F., Ma, C., Plant, D. R., Lynch, G. S., & Zajac, J. D. (2008) · The FASEB Journal · doi:10.1096/fj.08-105726 · Cited by 209 · see citing works

Improvement of muscle healing through enhancement of muscle regeneration and prevention of fibrosis

Satô, K., Li, Y., Foster, W. H., Fukushima, K., Badlani, N., Adachi, N., Ūsas, A., Fu, F. H., & Huard, J. (2003) · Muscle & Nerve · doi:10.1002/mus.10436 · Cited by 208 · see citing works

Testosterone Supplementation Reverses Sarcopenia in Aging through Regulation of Myostatin, c-Jun NH2-Terminal Kinase, Notch, and Akt Signaling Pathways

Kovacheva, E. L., Hikim, A. P. S., Shen, R., Sinha, I., & Sinha‐Hikim, I. (2009) · Endocrinology · doi:10.1210/en.2009-1177 · Cited by 197 · see citing works

Effects of anabolic steroids on the muscle cells of strength-trained athletes

KADI, F., ERIKSSON, A., HOLMNER, S., & THORNELL, L.-E. (1999) · Medicine &amp; Science in Sports &amp; Exercise · doi:10.1097/00005768-199911000-00006 · Cited by 190 · see citing works

Regenerating and denervated human muscle fibers and satellite cells express neural cell adhesion molecule recognized by monoclonal antibodies to natural killer cells

Illa, I., Leon‐Monzon, M., & Dalakas, M. C. (1992) · Annals of Neurology · doi:10.1002/ana.410310109 · Cited by 178 · see citing works

The expression of androgen receptors in human neck and limb muscles: effects of training and self-administration of androgenic-anabolic steroids

Kadi, F., Bonnerud, P., Eriksson, A., & Thornell, L. (2000) · Histochemistry and Cell Biology · doi:10.1007/s004180050003 · Cited by 164 · see citing works

The Effect of Anabolic Steroids and Corticosteroids on Healing of Muscle Contusion Injury

Beiner, J. M., Jokl, P., Cholewicki, J., & Panjabi, M. M. (1999) · The American Journal of Sports Medicine · doi:10.1177/03635465990270011101 · Cited by 147 · see citing works

Differential regulation of bone and body composition in male mice with combined inactivation of androgen and estrogen receptor‐α

Callewaert, F., Venken, K., Ophoff, J., Gendt, K. D., Torcasio, A., van Lenthe, H., Oosterwyck, H. V., Boonen, S., Bouillon, R., Verhoeven, G., et al. (2008) · The FASEB Journal · doi:10.1096/fj.08-113456 · Cited by 142 · see citing works

TGF‐β‐activated Smad3 represses MEF2‐dependent transcription in myogenic differentiation

Liu, D., Kang, J. S., & Derynck, R. (2004) · The EMBO Journal · doi:10.1038/sj.emboj.7600179 · Cited by 140 · see citing works

A Direct Effect of Testosterone on Muscle Cells in Tissue Culture1

Powers, M. L., & Florini, J. R. (1975) · Endocrinology · doi:10.1210/endo-97-4-1043 · Cited by 136 · see citing works

Regulation of Myogenic Differentiation by Androgens: Cross Talk between Androgen Receptor/ β-Catenin and Follistatin/Transforming Growth Factor-β Signaling Pathways

Singh, R., Bhasin, S., Braga, M., Artaza, J. N., Pervin, S., Taylor, W. E., Krishnan, V., Sinha, S. K., Rajavashisth, T. B., & Jasuja, R. (2008) · Endocrinology · doi:10.1210/en.2008-0858 · Cited by 131 · see citing works

Continuous testosterone administration prevents skeletal muscle atrophy and enhances resistance to fatigue in orchidectomized male mice

Axell, A.-M., MacLean, H. E., Plant, D. R., Harcourt, L. J., Davis, J. A., Jimenez, M., Handelsman, D. J., Lynch, G. S., & Zajac, J. D. (2006) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00058.2006 · Cited by 125 · see citing works

Androgen Signaling in Myocytes Contributes to the Maintenance of Muscle Mass and Fiber Type Regulation But Not to Muscle Strength or Fatigue

Ophoff, J., Proeyen, K. V., Callewaert, F., Gendt, K. D., Bock, K. D., Bosch, A. V., Verhoeven, G., Hespel, P., & Vanderschueren, D. (2009) · Endocrinology · doi:10.1210/en.2008-1509 · Cited by 123 · see citing works

Neuromuscular contributions to age-related weakness

Clark, D. J., & Fielding, R. A. (2012) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/glr041 · Cited by 115 · see citing works

Testosterone up-regulates androgen receptors and decreases differentiation of porcine myogenic satellite cells in vitro.

Doumit, M. E., Cook, D. R., & Merkel, R. A. (1996) · Endocrinology · doi:10.1210/endo.137.4.8625915 · Cited by 114 · see citing works

Myocytic androgen receptor controls the strength but not the mass of limb muscles

Chambon, C., Duteil, D., Vignaud, A., Ferry, A., Messaddeq, N., Malivindi, R., Kato, S., Chambon, P., & METZGER, D. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1009536107 · Cited by 111 · see citing works

Growth factors and muscle ageing

Goldspink, G., & Harridge, S. D. R. (2004) · Experimental Gerontology · doi:10.1016/j.exger.2004.08.010 · Cited by 97 · see citing works

Low Circulating Levels of Insulin‐Like Growth Factors and Testosterone in Chronically Institutionalized Elderly Men

Abbasi, A. A., Drinka, P. J., Mattson, D. E., & Rudman, D. (1993) · Journal of the American Geriatrics Society · doi:10.1111/j.1532-5415.1993.tb06764.x · Cited by 93 · see citing works

The Role of GH and IGF-I in Mediating Anabolic Effects of Testosterone on Androgen-Responsive Muscle

Serra, C., Bhasin, S., Tangherlini, F., Barton, E. R., Ganno, M. L., Zhang, A., Shansky, J., Vandenburgh, H. H., Travison, T. G., Jasuja, R., et al. (2010) · Endocrinology · doi:10.1210/en.2010-0802 · Cited by 90 · see citing works

Voluntary running, skeletal muscle gene expression, and signaling inversely regulated by orchidectomy and testosterone replacement

Ibebunjo, C., Eash, J. K., Li, C., Ma, Q., & Glass, D. J. (2010) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00402.2010 · Cited by 81 · see citing works

Testosterone Treatment Results in Quiescent Satellite Cells Being Activated and Recruited into Cell Cycle in Rat Levator Ani Muscle

Joubert, Y., & Tobin, C. (1995) · Developmental Biology · doi:10.1006/dbio.1995.1144 · Cited by 79 · see citing works

IL-13 mediates the recruitment of reserve cells for fusion during IGF-1-induced hypertrophy of human myotubes

Jacquemin, V., Butler-Browne, G. S., Furling, D., & Mouly, V. (2007) · Journal of Cell Science · doi:10.1242/jcs.03371 · Cited by 77 · see citing works

Androgen receptor enhances myogenin expression and accelerates differentiation

Lee, D. K. (2002) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(02)00504-1 · Cited by 74 · see citing works

C2C12 myoblastoma cell differentiation and proliferation is stimulated by androgens and associated with a modulation of myostatin and Pax7 expression

Diel, P. R., Baadners, D., Schlüpmann, K., Velders, M., & Schwarz, J. P. (2008) · Journal of Molecular Endocrinology · doi:10.1677/jme-07-0175 · Cited by 74 · see citing works

Role of IGF-I and IGF-binding proteins within diaphragm muscle in modulating the effects of nandrolone

Lewis, M. I., Horvitz, G. D., Clemmons, D. R., & Fournier, M. (2002) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00191.2001 · Cited by 70 · see citing works

Effect of nandrolone decanoate administration on recovery from bupivacaine-induced muscle injury.

White, J., Baltgalvis, K. A., Sato, S., Wilson, L., & Carson, J. A. (2009) · Journal of applied physiology · doi:10.1152/japplphysiol.00668.2009 · Cited by 62 · see citing works

Aging Biology and Novel Targets for Drug Discovery

Couteur, D. G. L., McLachlan, A. J., Quinn, R. J., Simpson, S. J., & de Cabo, R. (2011) · The Journals of Gerontology Series A · doi:10.1093/gerona/glr095 · Cited by 60 · see citing works

Expression and neural control of follistatin versus myostatin genes during regeneration of mouse soleus

Armand, A., Gaspera, B. D., Launay, T., Charbonnier, F., Gallien, C. L., & Chanoine, C. (2003) · Developmental Dynamics · doi:10.1002/dvdy.10306 · Cited by 46 · see citing works

Testosterone up-regulates androgen receptors and decreases differentiation of porcine myogenic satellite cells in vitro

Doumit, M. E. (1996) · Endocrinology · doi:10.1210/en.137.4.1385 · Cited by 45 · see citing works

Usefulness of Preclinical Models for Assessing the Efficacy of Late-Life Interventions for Sarcopenia

Carter, C. S., Marzetti, E., Leeuwenburgh, C., Manini, T. M., Foster, T. C., Groban, L., Scarpace, P. J., & Morgan, D. (2011) · The Journals of Gerontology Series A · doi:10.1093/gerona/glr042 · Cited by 44 · see citing works

Effects of anabolic/androgenic steroids on regenerating skeletal muscles in the rat

Ferry, A., Noirez, Page, C. L., Salah, I. B., Daegelen, & Rieu (1999) · Acta Physiologica Scandinavica · doi:10.1046/j.1365-201x.1999.00549.x · Cited by 20 · see citing works

Frailty and sarcopenia as the basis for the phenotypic manifestation of chronic diseases in older adults

Angulo, J., Assar, M. E., & Rodríguez‐Mañas, L. (2016) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2016.06.001 · Cited by 185 · see citing works

Effects of sex steroids on bones and muscles: Similarities, parallels, and putative interactions in health and disease

Carson, J. A., & Manolagas, S. C. (2015) · Bone · doi:10.1016/j.bone.2015.04.015 · Cited by 171 · see citing works

How Sex Hormones Promote Skeletal Muscle Regeneration

Velders, M., & Diel, P. R. (2013) · Sports Medicine · doi:10.1007/s40279-013-0081-6 · Cited by 129 · see citing works

The Role of Testosterone in the Elderly: What Do We Know?

Barone, B., Napolitano, L., Abate, M., Cirillo, L., Reccia, P., Passaro, F., Turco, C., Morra, S., Mastrangelo, F., Scarpato, A., et al. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23073535 · Cited by 120 · see citing works

Mitochondrial and sex steroid hormone crosstalk during aging

Velarde, M. C. (2014) · Longevity &amp; Healthspan · doi:10.1186/2046-2395-3-2 · Cited by 96 · see citing works

Myonuclear Domain Flexibility Challenges Rigid Assumptions on Satellite Cell Contribution to Skeletal Muscle Fiber Hypertrophy

Murach, K. A., Englund, D. A., Dupont‐Versteegden, E. E., McCarthy, J. J., & Peterson, C. A. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.00635 · Cited by 96 · see citing works

Aging and Regeneration in Vertebrates

Sousounis, K., Baddour, J., & Tsonis, P. A. (2014) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/b978-0-12-391498-9.00008-5 · Cited by 94 · see citing works

Role of hormones in sarcopenia

Priego, T., Martı́n, A. I., González‐Hedström, D., Granado, M., & López‐Calderón, A. (2021) · Vitamins and hormones · doi:10.1016/bs.vh.2020.12.021 · Cited by 97 · see citing works

Genome-wide DNA methylation changes in skeletal muscle between young and middle-aged pigs

Jin, L., Jiang, Z., Xia, Y.-D., Lou, P., Chen, L., Wang, H.-M., Bai, L., Xie, Y.-C., Liu, Y.-H., Li, W., et al. (2014) · BMC Genomics · doi:10.1186/1471-2164-15-653 · Cited by 69 · see citing works

Skeletal Muscle Regeneration in Cardiotoxin-Induced Muscle Injury Models

Wang, Y., Lu, J., & Liu, Y. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232113380 · Cited by 77 · see citing works

Inhibition of Myostatin Signaling through Notch Activation following Acute Resistance Exercise

MacKenzie, M. G., Hamilton, D. L., Pepin, M. E., Patton, A., & Baar, K. (2013) · PLoS ONE · doi:10.1371/journal.pone.0068743 · Cited by 72 · see citing works

Prospective views for whey protein and/or resistance training against age-related sarcopenia

Liao, Y., Peng, Z., Chen, L., Zhang, Y., Cheng, Q., Nüssler, A. K., Bao, W., Liu, L., & Yang, W. (2019) · Aging and Disease · doi:10.14336/ad.2018.0325 · Cited by 68 · see citing works

Bone is Not Alone: the Effects of Skeletal Muscle Dysfunction in Chronic Kidney Disease

Avin, K. G., & Moorthi, R. N. (2015) · Current Osteoporosis Reports · doi:10.1007/s11914-015-0261-4 · Cited by 70 · see citing works

Increased Muscle Force Production and Bone Mineral Density in ActRIIB-Fc-Treated Mature Rodents

Chiu, C.-S., Peekhaus, N., Weber, H., Adamski, S., Murray, E. M., Zhang, H. Z., Zhao, J. Z., Ernst, R., Lineberger, J., Huang, L., et al. (2013) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/glt030 · Cited by 68 · see citing works

Effect of combinations of monochromatic lights on growth and productive performance of broilers

Cao, J., Wang, Z., Dong, Y., Zhang, Z., Li, J., Li, F., & Chen, Y. (2012) · Poultry Science · doi:10.3382/ps.2012-02413 · Cited by 67 · see citing works

The role of sex steroid hormones in the pathophysiology and treatment of sarcopenia

Kim, Y. J., Tamadon, A., Park, H. T., Kim, H., & Ku, S. (2016) · Osteoporosis and Sarcopenia · doi:10.1016/j.afos.2016.06.002 · Cited by 67 · see citing works

Impact of GLP-1 Receptor Agonist Therapy in Patients High Risk for Sarcopenia

Memel, Z., Gold, S. L., Pearlman, M., Muratore, A., & Martindale, R. (2025) · Current Nutrition Reports · doi:10.1007/s13668-025-00649-w · Cited by 63 · see citing works

Why is Skeletal Muscle Regeneration Impaired after Myonecrosis Induced by Viperid Snake Venoms?

Gutiérrez, J. M., Escalante, T., Hernández, R., Gastaldello, S., Saravia‐Otten, P., & Rucavado, A. (2018) · Toxins · doi:10.3390/toxins10050182 · Cited by 60 · see citing works

Changes in Perceived Recovery Status Scale Following High-Volume Muscle Damaging Resistance Exercise

Sikorski, E. M., Wilson, J. M., Lowery, R. P., Joy, J. M., Laurent, C. M., Wilson, S. M.-C., Hesson, D., Naimo, M. A., Averbuch, B., & Gilchrist, P. (2013) · The Journal of Strength and Conditioning Research · doi:10.1519/jsc.0b013e31827e8e78 · Cited by 59 · see citing works

The Therapeutic Intervention of Sex Steroid Hormones for Sarcopenia

Huang, L., & Wang, J. (2021) · Frontiers in Medicine · doi:10.3389/fmed.2021.739251 · Cited by 59 · see citing works

Mechanisms of muscle cells alterations and regeneration decline during aging

Chinvattanachot, G., Rivas, D., & Duque, G. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102589 · Cited by 58 · see citing works

Nutrition, pharmacological and training strategies adopted by six bodybuilders: case report and critical review

Gentil, P., de Lira, C. A. B., Paoli, A., dos Santos, J. A. B., da Silva, R. D. T., Pereira, J. R., da Silva, E. P., & Magosso, R. F. (2017) · European Journal of Translational Myology · doi:10.4081/ejtm.2017.6247 · Cited by 58 · see citing works

From mitochondria to sarcopenia: role of 17β-estradiol and testosterone

Tian, X., Lou, S., & Shi, R. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1156583 · Cited by 54 · see citing works

Genetic Evidence That Captured Retroviral Envelope syncytins Contribute to Myoblast Fusion and Muscle Sexual Dimorphism in Mice

Redelsperger, F., Raddi, N., Bacquin, A., Vernochet, C., Mariot, V., Gache, V., Blanchard‐Gutton, N., Charrin, S., Tiret, L., Dumonceaux, J., et al. (2016) · PLoS Genetics · doi:10.1371/journal.pgen.1006289 · Cited by 51 · 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

An overview on androgen-mediated actions in skeletal muscle and adipose tissue

Rizk, J. G., Sahu, R., & Duteil, D. (2023) · Steroids · doi:10.1016/j.steroids.2023.109306 · Cited by 52 · see citing works

Testosterone enables growth and hypertrophy in fusion impaired myoblasts that display myotube atrophy: deciphering the role of androgen and IGF-I receptors

Hughes, D. C., Stewart, C. E., Sculthorpe, N. F., Dugdale, H. F., Yousefian, F., Lewis, M. P., & Sharples, A. P. (2015) · Biogerontology · doi:10.1007/s10522-015-9621-9 · Cited by 47 · see citing works

Durable antibacterial cotton fabrics with chitosan based quaternary ammonium salt

Feng, X., Zheng, K., Wang, C., Chu, F., & Chen, Y. (2016) · Fibers and Polymers · doi:10.1007/s12221-016-5919-8 · Cited by 47 · see citing works

Multiple Hormonal Dysregulation as Determinant of Low Physical Performance and Mobility in Older Persons

Maggio, M. G., Lauretani, F., Vita, F., Basaria, S. S., Lippi, G., Buttò, V., Luci, M., Cattabiani, C., Ceresini, G., Verzicco, I., et al. (2014) · Current Pharmaceutical Design · doi:10.2174/13816128113196660062 · Cited by 44 · see citing works

Impaired hypertrophy in myoblasts is improved with testosterone administration

Deane, C. S., Hughes, D. C., Sculthorpe, N. F., Lewis, M. P., Stewart, C. E., & Sharples, A. P. (2013) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/j.jsbmb.2013.05.005 · Cited by 43 · see citing works

Laminin-111 Improves Skeletal Muscle Stem Cell Quantity and Function Following Eccentric Exercise

Zou, K., Lisio, M. D., Huntsman, H. D., Pincu, Y., Mahmassani, Z. S., Miller, M., Olatunbosun, D., Jensen, T., & Boppart, M. D. (2014) · Stem Cells Translational Medicine · doi:10.5966/sctm.2014-0044 · Cited by 38 · see citing works

Molecular Targets of Androgen Signaling that Characterize Skeletal Muscle Recovery and Regeneration

MacKrell, J. G., Yaden, B. C., Bullock, H. A., Chen, K., Shetler, P. K., Bryant, H. U., & Krishnan, V. (2015) · Nuclear Receptor Signaling · doi:10.1621/nrs.13005 · Cited by 38 · see citing works

A Comparison of Monochromatic and Mixed LED Light Color on Performance, Bone Mineral Density, Meat and Blood Properties, and Immunity of Broiler Chicks

Hassan, M. R., Sultana, S., Choe, H. S., & Ryu, K. S. (2013) · The Journal of Poultry Science · doi:10.2141/jpsa.0130049 · Cited by 34 · see citing works

Transcriptional regulation of myotrophic actions by testosterone and trenbolone on androgen-responsive muscle

Ye, F., McCoy, S. C., Ross, H. H., Bernardo, J. A., Beharry, A. W., Judge, S. M., Judge, A. R., Beck, D. T., Conover, C. F., Cannady, D. F., et al. (2014) · Steroids · doi:10.1016/j.steroids.2014.05.024 · Cited by 29 · see citing works

Sarcopenia in chronic kidney disease: from bench to bedside

Kim, D. W., & Song, S. H. (2023) · The Korean Journal of Internal Medicine · doi:10.3904/kjim.2022.338 · Cited by 30 · see citing works

Testosterone Promotes the Proliferation of Chicken Embryonic Myoblasts Via Androgen Receptor Mediated PI3K/Akt Signaling Pathway

Li, D., Wang, Q., Shi, K., Lu, Y., Yu, D., Shi, X., Du, W., & Yu, M. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21031152 · Cited by 26 · see citing works

Effects of oral contraceptive use on female sexual salivary hormones and indirect markers of muscle damage following eccentric cycling in women

Mackay, K., Gonzalez, C., Zbinden-Foncea, H., & Peñailillo, L. E. (2019) · European Journal of Applied Physiology · doi:10.1007/s00421-019-04254-y · Cited by 20 · see citing works

Febuxostat attenuates testosterone-induced benign prostatic hyperplasia in rats via inhibiting JAK/STAT axis

Abo‐Youssef, A. M., Afify, H., Azouz, A. A., Abdel-Rahman, H. M., Abdel‐Naim, A. B., & Allam, S. (2020) · Life Sciences · doi:10.1016/j.lfs.2020.118414 · Cited by 24 · see citing works

Sex differences in skeletal muscle size, function, and myosin heavy chain isoform expression during post‐injury regeneration in mice

You, J., Barai, P., & Chen, J. (2023) · Physiological Reports · doi:10.14814/phy2.15791 · Cited by 22 · see citing works

Mechanisms of Testosterone's Anabolic Effects on Muscle and Function: Controversies and New Insights

Bhasin, S., Wang, C., Chandra, M. R. G., Gagliano‐Jucá, T., & Jasuja, R. (2025) · Endocrine Reviews · doi:10.1210/endrev/bnaf041 · Cited by 24 · see citing works

Changes in Communication between Muscle Stem Cells and their Environment with Aging

Thorley, M., Malatras, A., Duddy, W. J., Gall, L. L., Mouly, V., Butler-Browne, G. S., & Duguez, S. (2015) · Journal of Neuromuscular Diseases · doi:10.3233/jnd-150097 · Cited by 21 · see citing works

Long-term high loading intensity of aerobic exercise improves skeletal muscle performance via the gut microbiota-testosterone axis

Zhang, L., Lang, H., Ran, L., Tian, G., Shen, H., Zhu, J., Zhang, Q., Yi, L., & Mi, M. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.1049469 · Cited by 19 · see citing works

Targeting muscle signaling pathways to minimize adverse effects of androgen deprivation

de Rooy, C., Grossmann, M., Zajac, J. D., & Cheung, A. S. (2015) · Endocrine Related Cancer · doi:10.1530/erc-15-0232 · Cited by 16 · see citing works

Increasing Circulating Testosterone: Impact of Herbal Dietary Supplements

Gunnels, T. A., & Bloomer, R. J. (2014) · Journal of Plant Biochemistry & Physiology · doi:10.4172/2329-9029.1000130 · Cited by 17 · see citing works

Castration induces satellite cell activation that contributes to skeletal muscle maintenance

Klose, A. M., Liu, W., Paris, N. D., Forman, S., Krolewski, J. J., Nastiuk, K. L., & Chakkalakal, J. V. (2018) · JCSM Rapid Communications · doi:10.1002/j.2617-1619.2018.tb00004.x · Cited by 15 · see citing works

Testosterone improves muscle function of the extensor digitorum longus in rats with sepsis

Wang, J., & Wu, T. (2020) · Bioscience Reports · doi:10.1042/bsr20193342 · Cited by 16 · see citing works

Receptor-Mediated Muscle Homeostasis as a Target for Sarcopenia Therapeutics

Yoon, J. H., & Kwon, K. (2021) · Endocrinology and Metabolism · doi:10.3803/enm.2021.1081 · Cited by 16 · see citing works

Healthy skeletal muscle aging: The role of satellite cells, somatic mutations and exercise

Franco, I., Fernandez‐Gonzalo, R., Vrtačnik, P., Lundberg, T. R., Eriksson, M., & Gustafsson, T. P. (2019) · International review of cytology · doi:10.1016/bs.ircmb.2019.03.003 · Cited by 17 · see citing works

Testosterone and Obesity in an Aging Society

Tsutsumi, T., & Tsuchiya, K. (2025) · Biomolecules · doi:10.3390/biom15111521 · Cited by 18 · see citing works

Effects of letrozole administration on growth and reproductive performance in Markhoz goat bucklings

Rezaei, A., Vaziry, A., Farshad, A., Farzinpour, A., & Rostamzadeh, J. (2019) · Theriogenology · doi:10.1016/j.theriogenology.2019.11.017 · Cited by 14 · see citing works

Increased Adipocyte Area in Injured Muscle With Aging and Impaired Remodeling in Female Mice

Fearing, C. M., Melton, D. W., Lei, X., Hancock, H. M., Wang, H., Sarwar, Z. U., Porter, L., McHale, M. J., McManus, L. M., & Shireman, P. K. (2015) · The Journals of Gerontology Series A · doi:10.1093/gerona/glv104 · Cited by 14 · see citing works

Anabolic Androgenic Steroids in Orthopaedic Surgery: Current Concepts and Clinical Applications

Weber, A. E., Gallo, M. C., Bolia, I. K., Cleary, E. J., Schroeder, T. E., & Hatch, G. F. R. (2022) · JAAOS Global Research and Reviews · doi:10.5435/jaaosglobal-d-21-00156 · Cited by 13 · see citing works

Influence of Androgen Receptor in Vascular Cells on Reperfusion following Hindlimb Ischaemia

Wu, J., Hadoke, P. W. F., Takov, K., Korczak, A., Denvir, M. A., & Smith, L. B. (2016) · PLoS ONE · doi:10.1371/journal.pone.0154987 · Cited by 13 · see citing works

Effect of Periodized Resistance Training on Skeletal Muscle During Androgen Deprivation Therapy for Prostate Cancer: A Pilot Randomized Trial

Dawson, J., Dorff, T. B., Tuzon, C. T., Rice, J. C., Schroeder, E. T., Lane, C. J., Gross, M. E., & Dieli-Conwright, C. M. (2021) · Integrative Cancer Therapies · doi:10.1177/15347354211035442 · Cited by 12 · see citing works

Unraveling the Paradoxical Action of Androgens on Muscle Stem Cells.

Seo, J., Kim, J.-H., & Kong, Y. (2019) · Europe PMC (PubMed Central) · doi:10.14348/molcells.2019.0004 · Cited by 12 · see citing works

Cell-specific functions of androgen receptor in skeletal muscles

Sakai, H., & Imai, Y. (2024) · Endocrine Journal · doi:10.1507/endocrj.ej23-0691 · Cited by 10 · see citing works

Association of Dental Caries with Muscle Mass, Muscle Strength, and Sarcopenia: A Community-Based Study

Yang, Y., Deng, S., Wang, C., Wang, Y., Shi, Y., Lin, J., Wang, N., Su, L., Yang, F., Wang, H., et al. (2022) · The journal of nutrition health & aging · doi:10.1007/s12603-022-1875-8 · Cited by 10 · see citing works

Gonadal Steroids in Regeneration and Repair of Neuromuscular Systems

Foecking, E. M., Fargo, K. N., Brown, T. J., Sengelaub, D. R., & Jones, K. J. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-801732-6.00008-2 · Cited by 9 · see citing works

Histological and biochemical changes in lymphatic vessels after skeletal muscle injury induced by lengthening contraction in male mice

Tamura, Y., Kawashima, T., Ji, R., Agata, N., Itoh, Y., & Kawakami, K. (2024) · Physiological Reports · doi:10.14814/phy2.15950 · Cited by 8 · see citing works

Mechanical stretch enhances sex steroidogenesis in C2C12 skeletal muscle cells

Feng, Y., Wu, J., Cheng, Z., Zhang, J., Lu, J., & Shi, R. (2019) · Steroids · doi:10.1016/j.steroids.2019.108434 · Cited by 8 · see citing works

Using image-based flow cytometry to monitor satellite cells proliferation and differentiation in vitro

Luk, H., McFarlin, B. K., & Vingren, J. L. (2016) · Methods · doi:10.1016/j.ymeth.2016.08.005 · Cited by 7 · see citing works

Nandrolone supplementation does not improve functional recovery in an aged animal model of volumetric muscle loss injury

Kim, J. T., Roberts, K. W. S., Dunlap, G., Perry, R. A., Washington, T. A., & Wolchok, J. C. (2022) · Journal of Tissue Engineering and Regenerative Medicine · doi:10.1002/term.3286 · Cited by 7 · see citing works

Gene expression of sex steroid metabolizing enzymes and receptors in the skeletal muscle of migrant and resident subspecies of white-crowned sparrow (Zonotrichia leucophrys)

Krause, J. S., Watkins, T. V., Reid, A. M. A., Cheah, J. C., Pérez, J. H., Bishop, V. R., Ramenofsky, M., Wingfield, J. C., & Meddle, S. (2022) · Oecologia · doi:10.1007/s00442-022-05204-w · Cited by 7 · see citing works

Growth, pectoralis muscle performance, and testis of pelung cockerels (Gallus gallus gallus [Linnaeus, 1758]) supplemented with blood clam shell powder (Anadara granosa [Linnaeus, 1758])

Yuneldi, R. F., Aırın, C. M., Saragih, H. T. S. S. G., Sarmin, S., Astutı, P., & Alimon, A. R. (2023) · Veterinary World · doi:10.14202/vetworld.2023.474-482 · Cited by 7 · see citing works

Blood flow restriction training: a new approach for preventing and treating sarcopenia in older adults

Li, W., Hu, M., Yin, Q., Liu, Y., Chen, L., Ru, Q., Xu, G., & Wu, Y. (2025) · Frontiers in Physiology · doi:10.3389/fphys.2025.1616874 · Cited by 6 · see citing works

Prostatic androgen receptor signaling shows an age-related and lobe-specific alteration in mice

Zhang, H., Liu, T. T., Ricke, E. A., & Ricke, W. A. (2024) · Scientific Reports · doi:10.1038/s41598-024-79879-x · Cited by 6 · see citing works

Molecular Pathogenesis of Sarcopenia: Regulatory Networks Involving MicroRNAs in Age-Related Skeletal Muscle Decline

Kalan, J. J., Varghese, L. N., & Katare, R. (2025) · Frontiers in Bioscience-Landmark · doi:10.31083/fbl38106 · Cited by 5 · see citing works

Telomere length as a marker of changes in body composition and fractures-an analysis of data from the NHANES 2001-2002

Guo, Y., Zhao, H., Wang, F., Xu, H.-W., Liu, X., Hu, T., & Wu, D. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1181544 · Cited by 5 · see citing works

Effect of sequential and intermittent white, green and blue monochromatic lights on productive traits, some immune and stress responses of broiler chickens

Zamanizad, M., Ghalamkari, G., Toghyani, M., Adeljoo, A. H., & Toghyani, M. (2019) · Livestock Science · doi:10.1016/j.livsci.2019.06.023 · Cited by 5 · see citing works

Androgen action on myogenesis throughout the lifespan; comparison with neurogenesis

Barsky, S. T., & Monks, D. A. (2023) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2023.101101 · Cited by 5 · see citing works

Adaptation to full weight‐bearing following disuse in rats: The impact of biological sex on musculoskeletal recovery

Issertine, M., Rosa‐Caldwell, M. E., Sung, D., Bouxsein, M., Rutkove, S. B., & Mortreux, M. (2024) · Physiological Reports · doi:10.14814/phy2.15938 · Cited by 4 · see citing works

Role of the planar cell polarity pathway in regulating ectopic hair cell-like cells induced by Math1 and testosterone treatment

Yang, X., Jin, K., Ma, R., Yang, J., Luo, W., Han, Z., Cong, N., Ren, D., & Chi, F. (2015) · Brain Research · doi:10.1016/j.brainres.2015.04.017 · Cited by 3 · see citing works

The Effects of the Wild African Potato (Hypoxis hemerocallidea) Supplementation on Streptozotocin-Induced Diabetic Wistar Rats Reproductive Function

Jordaan, A. E., du Plessis, S. S., & Aboua, Y. G. (2016) · Andrology-Open Access · doi:10.4172/2167-0250.1000165 · Cited by 3 · see citing works

rHGF interacts with rIGF-1 to activate the satellite cells in the striated urethral sphincter in rats: a promising treatment for urinary incontinence?

Gu, X., Fan, L., Ke, R., & Chen, Y. (2018) · Archives of Gynecology and Obstetrics · doi:10.1007/s00404-018-4930-2 · Cited by 2 · see citing works

Sex-Specific Association of Low Muscle Mass with Depression Status in Asymptomatic Adults: A Population-Based Study

Cho, S. J., Jung, S., Lee, M. Y., & Park, C. (2024) · Brain Sciences · doi:10.3390/brainsci14111093 · Cited by 2 · see citing works

The Future of Drugs in Sarcopenia

Zazzara, M. B., Penfold, R., & Onder, G. (2021) · Practical issues in geriatrics · doi:10.1007/978-3-030-80038-3_14 · Cited by 2 · see citing works

Effects of local nandrolone decanoate on TGF-1β and IGF-1 in the healing of the muscle wound

Al-Abdullah, T. M., & Al-Mashhadane, F. (2023) · Al-mağallaẗ al-ʻirāqiyyaẗ li-l-ʻulūm al-bayṭariyyaẗ/Iraqi journal of veterinary sciences · doi:10.33899/ijvs.2023.139125.2885 · Cited by 1 · see citing works

The use of bioassays to detect designer androgens in sports supplements

Cooper, E. R. (2016) · UTS ePRESS (University of Technology Sydney) · Cited by 1 · see citing works

The E ffec t of Nerve Growth Factor (NGF) Incorporation into Swine Intestinal Submucosa (SIS) Suture Material on the Healing Process in Gastrocnemius Muscle

Alexander, N. K. (2013) · Digital Commons - PCOM (Philadelphia College of Osteopathic Medicine)

THE EFFECT OF VARIATION IN ENDOCRINE MECHANISMS ON NATURAL DISPLAY BEHAVIOR IN CARIBBEAN ANOLIS LIZARDS

Castro, D. J. (2013) · Digital Commons - Trinity University (Trinity University)

Sex Hormone Influenced Differences in Skeletal Muscle Responses to Aging and Exercise

Brown, M., & Tiidus, P. M. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-802388-4.00010-0

Inactivation of Magel2 in a mouse model of Prader-Willi Syndrome alters autophagy in the hypothalamus and impairs muscle function

Kamaludin, A. A. (2016) · ERA: Education and Research Archive (University of Alberta) · doi:10.7939/r3cr5np7z

Steroid hormone receptors in aging and neurodegenerative diseases

Kumar, R., & McEwan, I. J. (2024) · Elsevier eBooks · doi:10.1016/b978-0-323-91141-2.00001-5

Androgen receptor imprints satellite cells stemness and preserves their reservoir for lifelong regeneration and optimal repairPreprint

Rizk, J. G., Ghaibour, K. C., Souali‐Crespo, S., Calvano, E., Bilger, A., Jacobs, H., Messaddeq, N., Cai, Q., Grandgirard, E., Sahu, R., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.10.30.685031

Secretion of neurotoxic vesicles by muscle cells of ALS patients

Gall, L. L. (2019) · theses.fr (ABES) · doi:10.70675/61e48a01z5133z45e6z8569z1b35b4b8fb4f

Androgen receptor imprints satellite cell stemness and preserves their reservoir for lifelong regeneration and optimal repair

Rizk, J. G., Ghaibour, K. C., Souali‐Crespo, S., Calvano, E., Bilger, A., Jacobs, H., Messaddeq, N., Cai, Q., Grandgirard, E., Sahu, R., et al. (2026) · Science Advances · doi:10.1126/sciadv.aec8073

397 TESTOSTERONE SUPPLEMENTATION INDUCES SKELETAL MUSCLE HYPERTROPHY, AND INCREASES SATELLITE CELL NUMBER AND REPLICATION IN HEALTHY OLDER MEN

Sinha‐Hikim, I., Cornford, M. E., Lee, M., & Bhasin, S. (2005) · Journal of Investigative Medicine · doi:10.2310/6650.2005.00005.396

Exercise conditioning in old mice improves skeletal muscle regeneration

Joanisse, S., Nederveen, J. P., Baker, J. M., Snijders, T., Iacono, C., & Parise, G. (2016) · The FASEB Journal · doi:10.1096/fj.201600143rr · Cited by 83 · see citing works

Effects of testosterone supplementation on skeletal muscle fiber hypertrophy and satellite cells in community-dwelling older men

- (n.d.) · UCLA - Biblioteca de Ciencias de la Salud

The effects of testosterone and ageing on skeletal muscle growth and androgen receptor expression

Williams, R. (2022) · Liverpool John Moores University · doi:10.24377/ljmu.t.00016152

Testosterone Supplementation Reverses Sarcopenia in Aging through Regulation of Myostatin, c-Jun NH2-Terminal Kinase, Notch, and Akt Signaling Pathways

Kovacheva, E. L., Hikim, A. P. S., Shen, R., Sinha, I., & Sinha‐Hikim, I. (2009) · Endocrinology · doi:10.1210/en.2009-1177 · Cited by 197 · see citing works