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Oxytocin is involved in steroid hormone–stimulated bovine satellite cell proliferation and differentiation in vitro

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Understanding the influence of trenbolone acetate and polyamines on proliferation of bovine satellite cells

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Comparative analysis of cattle breeds as satellite cell donors for cultured beefPreprint

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Inhalation of low‐dose basil ( Ocimum basilicum ) essential oil improved cardiovascular health and plasma lipid markers in high fat diet‐induced obese rats

Hong, S. J., Kim, D., Lee, J.-K., Boo, C. G., Youn, M. Y., Le, B., Kim, J. K., & Shin, E. (2022) · Journal of Food Science · doi:10.1111/1750-3841.16196 · Cited by 12 · see citing works

Effects of ovariectomy on body measurements, carcass composition, and meat quality of Huainan chickens

Guo, X., Ma, C., Fang, Q., Zhou, B., Wan, Y., & Jiang, R. (2016) · Animal Production Science · doi:10.1071/an15815 · Cited by 12 · see citing works

Ostarine-Induced Myogenic Differentiation in C2C12, L6, and Rat Muscles

Leciejewska, N., Kolodziejski, P. A., Sassek, M., Nogowski, L., Małek, E., & Pruszyńska‐Oszmałek, E. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23084404 · Cited by 11 · see citing works

Sexual dimorphism through androgen signaling; from external genitalia to muscles

Ipulan, L. A. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.940229 · Cited by 11 · 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

Quality and Risk Control in Cultivated Meat Production

de Macedo, R. E. F., Ferreira, G. A., Poniewas, L., Barchiki, F., Rebelatto, C. L. K., Daga, D. R., Costa, L. B., & Rosa, E. A. R. (2024) · Springer eBooks · doi:10.1007/978-3-031-55968-6_11 · Cited by 10 · see citing works

RAD140 (Testolone) negatively impacts skeletal muscle adaptation, frailty status and mortality risk in female mice

Brown, A. M., Ganjayi, M. S., & Baumann, C. W. (2023) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/1440-1681.13824 · Cited by 10 · see citing works

Androgen receptors in the bonnethead, Sphyrna tiburo: cDNA cloning and tissue-specific expression in the male reproductive tract

Tyminski, J. P., Gelsleichter, J. J., & Motta, P. J. (2015) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2015.08.018 · Cited by 9 · see citing works

A potent liver-mediated mechanism for loss of muscle mass during androgen deprivation therapy

Lam, T., McLean, M. P., Hayden, A. J., Poljak, A., Cheema, B. S., Gurney, H., Stone, G., Bahl, N., Reddy, N., Shahidipour, H., et al. (2019) · Endocrine Connections · doi:10.1530/ec-19-0179 · Cited by 8 · see citing works

Polyamine pathway is associated with muscle anabolic effects by androgen receptor ligand

Kanou, M., Nakamura, K., Horie, K., Sakai, H., Yanagihara, Y., Sakakibara, I., Yamana, K., & Imai, Y. (2020) · JCSM Rapid Communications · doi:10.1002/rco2.28 · Cited by 8 · see citing works

Downregulation of Androgen Receptors upon Anabolic-Androgenic Steroids: A Cause or a Flawed Hypothesis of the Muscle-Building Plateau?

Santos, H. O., & Haluch, C. E. F. (2022) · Muscles · doi:10.3390/muscles1020010 · Cited by 8 · see citing works

The quasi-parallel lives of satellite cells and atrophying muscle

Biressi, S. (2015) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2015.00140 · Cited by 8 · see citing works

Human Pluripotent Stem Cell‐Derived Skeletal Muscle Organoid Model of Aging‐Induced Sarcopenia

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The role of ubiquitination in spinal and bulbar muscular atrophy

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ESTERÓIDES ANABÓLICOS E EXERCÍCIO: AÇÃO E EFEITOS COLATERAIS

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Nandrolone Stimulates Myod Expression During Muscle Regeneration in the Condition of Myonecrosis Induced by Bothrops jararacussu Venom Poisoning

de Souza, R. W. A., Gonçalves, W. A., Cavalcante, W. L. G., Dal‐Pai‐Silva, M., & Gallacci, M. (2010) · Journal of Toxicology and Environmental Health · doi:10.1080/15287391003751729 · Cited by 7 · see citing works

Age-Dependent Changes in Skeletal MuscleRegeneration

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Bioengineered human pre-vascularized microtissues reconstruct vascular niche and regenerative microenvironment to enhance functional skeletal muscle regeneration

Cheng, L., Gao, Y. P., Li, J., Liang, Q., Li, M., Yang, J., Su, X., Zhang, J., Tian, W., & Liao, L. (2025) · Biomaterials · doi:10.1016/j.biomaterials.2025.123645 · Cited by 6 · see citing works

Impaired muscle performance

Marcus, R., Westlen-Boyer, K., & LaStayo, P. (2012) · Elsevier eBooks · doi:10.1016/b978-0-323-02948-3.00023-7 · Cited by 8 · see citing works

Perfil hormonal del envejecimiento muscular

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Normal muscle growth

Carlson, B. M. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-820278-4.00003-7 · Cited by 6 · see citing works

21 REVIEW Androgen regulation of satellite cell function

Chen, Y., Zajac, J. D., & Maclean, H. E. (2013)

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

Androgens and skeletal muscle: cellular and molecular action mechanisms underlying the anabolic actions

Dubois, V., Laurent, M., Boonen, S., Vanderschueren, D., & Claessens, F. (2012) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-011-0883-3 · Cited by 197 · 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

Unravelling androgen action in skeletal muscle: a satellite-cell specific knockout of the androgen receptor

Dubois, V., Laurent, M. R., Sinnesael, M., Cielen, N., Helsen, C., Clinckemalie, L., Spans, L., Gayan‐Ramirez, G., Deldicque, L., Hespel, P., et al. (2014)