Myostatin Inhibition Enhances the Effects of Exercise on Performance and Metabolic Outcomes in Aged Mice

PGC-1α-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes

Mootha, V. K., Lindgren, C. M., Eriksson, K.-F., Subramanian, A., Sihag, S., Lehar, J., Puigserver, P., Carlsson, E., Ridderstråle, M., Laurila, E., et al. (2003) · Nature Genetics · doi:10.1038/ng1180 · Cited by 10,197

Risk Factors for Falls among Elderly Persons Living in the Community

Tinetti, M. E., Speechley, M. R., & Ginter, S. F. (1988) · New England Journal of Medicine · doi:10.1056/nejm198812293192604 · Cited by 6,507

Mechanisms controlling mitochondrial biogenesis and respiration through the thermogenic coactivator PGC-1

Wu, Z., Puigserver, P., Andersson, U., Zhang, C., Adelmant, G., Mootha, V., Troy, A., Cinti, S., Lowell, B., Scarpulla, R. C., et al. (1999) · Cell · doi:10.1016/s0092-8674(00)80611-x · Cited by 4,139

Lower-extremity function in persons over the age of 70 years as a predictor of subsequent disability

Guralnik, J. M., Ferrucci, L., Simonsick, E. M., Salive, M. E., & Wallace, R. B. (1995) · New England Journal of Medicine · doi:10.1056/nejm199503023320902 · Cited by 4,083

Regulation of skeletal muscle mass in mice by a new TGF-p superfamily member

McPherron, A. C., Lawler, A. M., & Lee, S.-J. (1997) · Nature · doi:10.1038/387083a0 · Cited by 4,013

Myostatin Mutation Associated with Gross Muscle Hypertrophy in a Child

Schuelke, M., Wagner, K. R., Stolz, L. E., Hübner, C., Riebel, T., Kömen, W., Braun, T., Tobin, J. F., & Lee, S.-J. (2004) · New England Journal of Medicine · doi:10.1056/nejmoa040933 · Cited by 1,399

Physical performance measures in the clinical setting

Studenski, S., Perera, S., Wallace, D., Chandler, J. M., Duncan, P. W., Rooney, E., Fox, M., & Guralnik, J. M. (2003) · Journal of the American Geriatrics Society · doi:10.1046/j.1532-5415.2003.51104.x · Cited by 1,218

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

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

Association of Long-Distance Corridor Walk Performance With Mortality, Cardiovascular Disease, Mobility Limitation, and Disability

Newman, A. B., Simonsick, E. M., Naydeck, B. L., Boudreau, R. M., Kritchevsky, S. B., Nevitt, M. C., Pahor, M., Satterfield, S., Brach, J. S., Studenski, S. A., et al. (2006) · JAMA · doi:10.1001/jama.295.17.2018 · Cited by 934

Effect of Myostatin Depletion on Weight Gain, Hyperglycemia, and Hepatic Steatosis during Five Months of High-Fat Feeding in Mice

Burgess, K., Xu, T., Brown, R. H., Han, B., & Welle, S. L. (2011) · PLoS ONE · doi:10.1371/journal.pone.0017090 · Cited by 28

Myostatin/activin blocking combined with exercise reconditions skeletal muscle expression profile of mdx mice

Kainulainen, H., Papaioannou, K., Silvennoinen, M., Autio, R., Saarela, J., Oliveira, B. M. S., Nyqvist, M., Pasternack, A. H., Hoen, P. A. C. ’., Kujala, U. M., et al. (2014) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2014.10.001 · Cited by 27

Animal models of cachexia and sarcopenia in chronic illness: Cardiac function, body composition changes and therapeutic results

Ishida, J., Saitoh, M., Doehner, W., von Haehling, S., Anker, M. S., Anker, S. D., & Springer, J. (2017) · International Journal of Cardiology · doi:10.1016/j.ijcard.2017.03.154 · Cited by 27

Therapeutic considerations of sarcopenia in heart failure patients

Saitoh, M., Ebner, N., von Haehling, S., Anker, S. D., & Springer, J. (2018) · Expert Review of Cardiovascular Therapy · doi:10.1080/14779072.2018.1424542 · Cited by 30

Dietary Creatine Supplementation in Gilthead Seabream (Sparus aurata) Increases Dorsal Muscle Area and the Expression of myod1 and capn1 Genes

Ramos-Pinto, L., Lopes, G., Sousa, V., Castro, L. F. C., Schrama, D., Rodrigues, P., & Valente, L. M. P. (2019) · Frontiers in Endocrinology · doi:10.3389/fendo.2019.00161 · Cited by 23

Local myostatin inhibition improves skeletal muscle glucose uptake in insulin-resistant high-fat diet-fed mice

Eilers, W., Chambers, D. J., Cleasby, M. E., & Foster, K. (2020) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00185.2019 · Cited by 29

Physiologic and metabolic safety of butyrylcholinesterase gene therapy in mice

Murthy, V., Gao, Y., Geng, L., LeBrasseur, N. K., White, T. A., Parks, R. J., & Brimijoin, S. (2014) · Vaccine · doi:10.1016/j.vaccine.2014.05.067 · Cited by 25

Whole Body Vibration Improves Brain and Musculoskeletal Health by Modulating the Expression of Tissue-Specific Markers: FNDC5 as a Key Regulator of Vibration Adaptations

Cariati, I., Bonanni, R., Pallone, G., Romagnoli, C., Rinaldi, A. M., Annino, G., D’Arcangelo, G., & Tancredi, V. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms231810388 · Cited by 25

Soluble activin receptor type IIB decoy receptor differentially impacts murine osteogenesis imperfecta muscle function

Jeong, Y., Daghlas, S. A., Kahveci, A. S., Salamango, D. J., Gentry, B. A., Brown, M., Rector, R. S., Pearsall, R. S., & Phillips, C. L. (2017) · Muscle & Nerve · doi:10.1002/mus.25706 · Cited by 24

Seasonal variation in pectoralis muscle and heart myostatin and tolloid-like proteinases in small birds: a regulatory role for seasonal phenotypic flexibility?

Swanson, D. L., King, M. O., & Harmon, E. B. (2014) · Journal of Comparative Physiology B · doi:10.1007/s00360-013-0798-4 · Cited by 24

AAV-Mediated Administration of Myostatin Pro-Peptide Mutant in Adult Ldlr Null Mice Reduces Diet-Induced Hepatosteatosis and Arteriosclerosis

Guo, W., Wong, S., & Bhasin, S. (2013) · PLoS ONE · doi:10.1371/journal.pone.0071017 · Cited by 24

Changes in lean mass and serum myostatin with habitual protein intake and high-velocity resistance training

Binns, A., Gray, M., Henson, A. C., & Fort, I. L. (2017) · The journal of nutrition health & aging · doi:10.1007/s12603-017-0883-6 · Cited by 26

CRISPR Genome Editing Technology: A Powerful Tool Applied to Developing Agribusiness

Maximiano, M. R., Távora, F. T. P. K., Prado, G. S., Dias, S. C., Mehta, Â., & Franco, O. L. (2021) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.1c01062 · Cited by 25

Benefits in cardiac function by CD38 suppression: Improvement in NAD+ levels, exercise capacity, heart rate variability and protection against catecholamine-induced ventricular arrhythmias

Agorrody, G., Peclat, T., Peluso, G., Gonano, L. A., Santos, L., van Schooten, W., Chini, C. C. S., Escande, C., Chini, E. N., & Contreras, P. (2022) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2022.01.008 · Cited by 24

Myostatin regulates energy homeostasis through autocrine- and paracrine-mediated microenvironment communication

Wang, H., Guo, S., Gao, H., Ding, J., Li, H., Kong, X., Zhang, S., He, M., Feng, Y., Wu, W., et al. (2024) · Journal of Clinical Investigation · doi:10.1172/jci178303 · Cited by 22

ActRIIB blockade increases force‐generating capacity and preserves energy supply in exercising mdx mouse muscle in vivo

Béchir, N., Pecchi, É., Vilmen, C., Fur, Y. L., Amthor, H., Bernard, M., Bendahan, D., & Giannesini, B. (2016) · The FASEB Journal · doi:10.1096/fj.201600271rr · Cited by 22

Late‐life time‐restricted feeding and exercise differentially alter healthspan in obesity

Schafer, M. J., Mazula, D. L., Brown, A. K., White, T. A., Atkinson, E. J., Pearsall, V. M., Aversa, Z., Verzosa, G., Smith, L. A., Matveyenko, A. V., et al. (2019) · Aging Cell · doi:10.1111/acel.12966 · Cited by 23

Sarcopenia and Endocrine Ageing: Are They Related?

Gupta, P., & Kumar, S. (2022) · Cureus · doi:10.7759/cureus.28787 · Cited by 28

Comparative gene expression and phenotype analyses of skeletal muscle from aged wild-type and PAPP-A-deficient mice

Conover, C. A., Bale, L. K., & Nair, K. S. (2016) · Experimental Gerontology · doi:10.1016/j.exger.2016.04.005 · Cited by 19

Impact of Genetic and Pharmacologic Inhibition of Myostatin in a Murine Model of Osteogenesis Imperfecta

Omosule, C. L., Gremminger, V. L., AGUILLARD, A., Jeong, Y., Harrelson, E. N., Miloscio, L., Mastaitis, J. W., Rafique, A., Kleiner, S., Pfeiffer, F. M., et al. (2020) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.4223 · Cited by 21

Bimagrumab: an investigational human monoclonal antibody against activin type II receptors for treating obesity

Kaur, M., & Misra, S. (2024) · Journal of Basic and Clinical Physiology and Pharmacology · doi:10.1515/jbcpp-2024-0065 · Cited by 17

Cancer Cachexia: Underlying Mechanisms and Potential Therapeutic Interventions

Directo, D. J., & Lee, S.-R. (2023) · Metabolites · doi:10.3390/metabo13091024 · Cited by 16

Myostatin: genetic variants, therapy and gene doping

Yamada, A. K., Verlengia, R., & Júnior, C. R. B. (2012) · Brazilian Journal of Pharmaceutical Sciences · doi:10.1590/s1984-82502012000300003 · Cited by 13

Highlighting the idea of exerkines in the management of cancer patients with cachexia: novel insights and a critical review

Hekmatikar, A. H. A., Nelson, A. R., & Petersen, A. C. (2023) · BMC Cancer · doi:10.1186/s12885-023-11391-3 · Cited by 13

Alterations in Adiposity and Glucose Homeostasis in Adult Gasp-1 Overexpressing Mice

Pèrié, L., Parenté, A., Baraige, F., Magnol, L., & Blanquet, V. (2017) · Cellular Physiology and Biochemistry · doi:10.1159/000485878 · Cited by 13

Inhibition of Myostatin Reduces Collagen Deposition in a Mouse Model of Oculopharyngeal Muscular Dystrophy (OPMD) With Established Disease

Harish, P., Forrest, L., Herath, S., Dickson, G., Malerba, A., & Popplewell, L. J. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.00184 · Cited by 11

Mitochondrial impairment induced by postnatal ActRIIB blockade does not alter function and energy status in exercising mouse glycolytic muscle in vivo

Béchir, N., Pecchi, É., Relizani, K., Vilmen, C., Fur, Y. L., Bernard, M., Amthor, H., Bendahan, D., & Giannesini, B. (2016) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00370.2015 · Cited by 11

Drugs of Muscle Wasting and Their Therapeutic Targets

Sakuma, K., & Yamaguchi, A. (2018) · Advances in experimental medicine and biology · doi:10.1007/978-981-13-1435-3_21 · Cited by 12

Telmisartan versus metformin in downregulating myostatin gene expression and enhancing insulin sensitivity in the skeletal muscles of type 2 diabetic rat model

Tammam, A. A.-E., Rizg, W. Y., Boushra, A. F., Alhelf, M., Alissa, M., Soliman, G. F., Ouais, G. N., Hosny, K. M., Alkhalidi, H. M., & Elebiary, A. M. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1228525 · Cited by 10

Idiopathic pulmonary fibrosis: aligning murine models to clinical trials in humans

Chang, A., Ry, P. M. V., & Raghu, G. (2023) · The Lancet Respiratory Medicine · doi:10.1016/s2213-2600(23)00325-9 · Cited by 10

Aging: A struggle for beneficial to overcome negative factors made by muscle and bone

Welc, S. S., Brotto, M., White, K. E., & Bonewald, L. F. (2025) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2025.112039 · Cited by 11

Ferulic Acid Promotes Growth of Both Fast Glycolytic and Slow Oxidative Skeletal Muscles in Corticosteroid-Induced Rat Myopathy

SAMIR, M. D. A. F. M. S. M. (2019) · The Medical Journal of Cairo University/The Medical Journal of Cairo University · doi:10.21608/mjcu.2019.53950 · Cited by 10

Two Types of Mouse Models for Sarcopenia Research: Senescence Acceleration and Genetic Modification Models

Baek, K., Jung, Y., Park, J. S., Kim, J., Hah, Y., Kim, S.-J., & Yoo, J. (2021) · Journal of Bone Metabolism · doi:10.11005/jbm.2021.28.3.179 · Cited by 10

Complex roles of myoglianin in regulating adult performance and lifespan

Augustin, H., Adcott, J., Elliott, C. J. H., & Partridge, L. (2017) · Fly · doi:10.1080/19336934.2017.1369638 · Cited by 11

Pharmacologic inhibition of myostatin with a myostatin antibody improves the skeletal muscle and bone phenotype of male insulin-deficient diabetic mice

Bunn, R. C., Adatorwovor, R., Smith, R. R., Ray, P. D., Fields, S. E., Keeble, A. R., Fry, C. S., Uppuganti, S., Nyman, J. S., Fowlkes, J. L., et al. (2023) · JBMR Plus · doi:10.1002/jbm4.10833 · Cited by 9

Inhibition of activin receptor 2 signalling ameliorates metabolic dysfunction–associated steatotic liver disease in western diet/L-NAME induced cardiometabolic disease

Swan, J., Szabó, Z., Peters, J., Kummu, O., Kemppi, A., Rahtu‐Korpela, L., Konzack, A., Hakkola, J., Pasternack, A. H., Ritvos, O., et al. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.116683 · Cited by 9

Sex differences in body composition but not neuromuscular function following long-term, doxycycline-induced reduction in circulating levels of myostatin in mice

Tavoian, D., Arnold, W. D., Mort, S. C., & Lacalle, S. D. (2019) · PLoS ONE · doi:10.1371/journal.pone.0225283 · Cited by 11

Ecto-CD38-NADase inhibition modulates cardiac metabolism and protects mice against doxorubicin-induced cardiotoxicity

Peclat, T., Agorrody, G., Colman, L., Kashyap, S., Zeidler, J. D., Chini, C. C. S., Warner, G. M., Thompson, K. L., Dalvi, P., Beckedorff, F., et al. (2024) · Cardiovascular Research · doi:10.1093/cvr/cvae025 · Cited by 9

Co-Administration of Myostatin-Targeting siRNA and ActRIIB-Fc Fusion Protein Increases Masseter Muscle Mass and Fiber Size

Bayarsaikhan, O., Kawai, N., Mori, H., Kinouchi, N., Nikawa, T., & Tanaka, E. I. (2017) · Journal of Nutritional Science and Vitaminology · doi:10.3177/jnsv.63.244 · Cited by 9

Myostatin

Lee, S.-J. (2012) · Muscle · doi:10.1016/b978-0-12-381510-1.00079-x · Cited by 8

The effect of eight weeks resistance and aerobic training on myostatin and follistatin expression in cardiac muscle of rats

Rashidlamir, A., Hosseini, S. R. A., Hejazi, K., & Motevalli, M. S. (2016) · Journal of Cardiovascular and Thoracic Research · doi:10.15171/jcvtr.2016.33 · Cited by 8

Experimental Increases in Foraging Costs Affect Pectoralis Muscle Mass and Myostatin Expression in Female, but Not Male, Zebra Finches (Taeniopygia guttata)

Zhang, Y., Yap, K. N., Williams, T. D., & Swanson, D. L. (2018) · Physiological and Biochemical Zoology · doi:10.1086/697153 · Cited by 8

Myostatin (GDF-8) as a therapeutic target for the prevention of osteoporotic fractures

Hamrick, M. W. (2010) · IBMS BoneKEy · doi:10.1138/20100423 · Cited by 7

Short‐term aerobic exercise prevents development of glucocorticoid myopathic features in aged skeletal muscle in a sex‐dependent manner

Laskin, G. R., Rentería, L. I., Muller‐Delp, J. M., Kim, J., Chase, P. B., Hwang, H. S., & Gordon, B. S. (2024) · The Journal of Physiology · doi:10.1113/jp286334 · Cited by 7

Identification of the minimum region of flatfish myostatin propeptide (Pep45-65) for myostatin inhibition and its potential to enhance muscle growth and performance in animals

Kim, J. H., Kim, J. H., Sutikno, L. A., Lee, S. B., Jin, D., Hong, Y., Kim, Y. S., & Jin, H. (2019) · PLoS ONE · doi:10.1371/journal.pone.0215298 · Cited by 7

Identification of Molecules from Coffee Silverskin That Suppresses Myostatin Activity and Improves Muscle Mass and Strength in Mice

Kim, J. H., Kim, J., Jang, J., Jang, J., Jin, D., Kim, Y., & Jin, H. (2021) · Molecules · doi:10.3390/molecules26092676 · Cited by 7

Muscle-brain crosstalk as a driver of brain health in aging

McNeish, B. L., Miljkovic, I., Liu-Ambrose, T. Y. L., Ambrosio, F., Esser, K. A., Fahnestock, M. L., & Rosano, C. (2025) · GeroScience · doi:10.1007/s11357-025-01833-0 · Cited by 10

2′-Fucosyllactose improved muscle health in middle-aged mice performing forced swimming exercise

Kim, J. K., Shin, C. S., Yoon, J.-W., Jeon, S.-M., Bang, J., Ku, S., & Jegal, K. H. (2024) · Journal of Functional Foods · doi:10.1016/j.jff.2024.106567 · Cited by 5

Protective Effect of Delta-Like 1 Homolog Against Muscular Atrophy in a Mouse Model

Lee, J. Y., Lee, M., Lee, D.-H., Lee, Y., Lee, B., Kang, E. S., & Soo, B. (2022) · Endocrinology and Metabolism · doi:10.3803/enm.2022.1446 · Cited by 6

Physical Resilience as a Predictor of Lifespan and Late-Life Health in Genetically Heterogeneous Mice

Brown, A. K., Mazula, D. L., Roberts, L., Roos, C. M., Zhang, B., Pearsall, V. M., Schafer, M. J., White, T. A., Huang, R., Kumar, N., et al. (2023) · The Journals of Gerontology Series A · doi:10.1093/gerona/glad207 · Cited by 5

Protective effect of myostatin gene deletion on aging-related muscle metabolic decline

Chabi, B., Pauly, M., Carillon, J., Carnac, G., Favier, F. B., Fouret, G., Bonafos, B., Vanterpool, F., Vernus, B., Coudray, C., et al. (2016) · Experimental Gerontology · doi:10.1016/j.exger.2016.01.016 · Cited by 5

Age-related changes in myostatin expression in rat skeletal muscles

Shibaguchi, T., Maeoka, T., Yoshihara, T., Naıto, H., Goto, K., Yoshioka, T., & Sugiura, T. (2018) · The Journal of Physical Fitness and Sports Medicine · doi:10.7600/jpfsm.7.221 · Cited by 5

Diabetes and Physical Activity

Banu, J. (2016) · Journal of Endocrinology and Diabetes · doi:10.15226/2374-6890/3/1/00140 · Cited by 4

Speed and endurance: you can have it all

Lee, S. (2010) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00618.2010 · Cited by 4

Exercise-induced exerkines in multiple sclerosis: Emphasizing the pivotal role of myokines

Alifarsangi, A., Khaksari, M., Rajizadeh, M. A., Zadeh, N. A., & Rafie, F. (2025) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2025.111565 · Cited by 3

Effects of Nicotinamide Mononucleotide Supplementation and Aerobic Exercise on Metabolic Health and Physical Performance in Aged Mice

Hsu, Y.-J., Lee, M., Fan, H.-Y., & Lo, Y.-C. (2025) · Nutrients · doi:10.3390/nu17193148 · Cited by 3

ETAS®, a Standardized Extract of Asparagus officinalis Stem, Alleviates Sarcopenia via Regulating Protein Turnover and Mitochondrial Quality

Chang, S., Chen, Y., Chang, Y.-C., Cheng, C.-C., & Chan, Y. (2025) · Pharmaceuticals · doi:10.3390/ph18091243 · Cited by 2

Low Aerobic Capacity Accelerates Lipid Accumulation and Metabolic Abnormalities Caused by High-Fat Diet-Induced Obesity in Postpartum Mice

Lee, M., Hsu, Y.-J., Sung, H., Wen, Y.-T., Wei, L., & Huang, C. (2022) · Nutrients · doi:10.3390/nu14183746 · Cited by 2

Sarcopenia and Its Intervention

Sakuma, K., & Yamaguchi, A. (2015) · Healthy ageing and longevity · doi:10.1007/978-3-319-14830-4_7 · Cited by 2

8 Weeks of Resistance Training Effect on Myostatin Gene Expression of Myocardium in Healthy Male Wistar Rats

Rashidlamir, A., Basami, M. R., Hosseini, S. R. A., Hejazi, K., & Anberani, S. M. M. (2016) · Quarterly of Horizon of Medical Sciences · doi:10.18869/acadpub.hms.22.2.111 · Cited by 2

Novel Intriguing Strategies Attenuating to Sarcopenia

Sakuma, K., & Yamaguchi, A. (2016) · Apple Academic Press eBooks · doi:10.1201/b19985-13 · Cited by 2

Activin type IIB receptor blockade does not limit adenosine triphosphate supply in mouse skeletal muscle in Vivo

Béchir, N., Pecchi, É., Vilmen, C., Bernard, M., Bendahan, D., & Giannesini, B. (2018) · Muscle & Nerve · doi:10.1002/mus.26306 · Cited by 1

The Effects of Poor Maternal Nutrition on Muscle Development in Lambs

Raja, J. (2013) · OpenCommons - UConn (University of Connecticut) · Cited by 1

Combinatorial and independent effects of exercise and myostatin/activin blocking on muscle gene expression profiling

Papaioannou, K.-G. G. (2013) · Jyväskylä University Digital Archive (University of Jyväskylä) · Cited by 1

Supplement with Cystoseira canariensis promotes an increase of resistance to the maximum load in the grastrocnemius muscle of female rats

Abdalla, D. R., Araújo, E. S. C., Carvalho, L. C., & Bertoncello, D. (2014) · Fisioterapia e Pesquisa · doi:10.1590/1809-2950/57421022014

Myostatin as a Potential Therapeutic Target for Obesity and Insulin Resistance

Jeong, K., & Choi, C. S. (2011) · The Korean Journal of Obesity · doi:10.7570/kjo.2011.20.3.91 · Cited by 1

The Effect of Myostatin on Glucose Metabolism and Insulin Sensitivity

Ghozlan, M. (2013) · Libraries and Cultural Resources (University of Calgary) · doi:10.11575/prism/28087

attenuates disuse muscle atrophy and weakness in Acute antibody-directed myostatin inhibition

Lynch, S. E., Murphy, K. T., Ryall, J. G., Ibebunjo, C., Judge, A. R., Beharry, A. W., Sandesara, P. B., Roberts, B. M., Ferreira, L. F., Sarah, M., et al. (2015)

Myostatin and Sarcopenia: Opportunities and Challenges - A Mini-Review

Kogod, A. (2014)

Pharmacological Intervention for Sarcopenia in Chronic Kidney Disease

Sakuma, K., & Yamaguchi, A. (2020) · Springer eBooks · doi:10.1007/978-981-15-2365-6_11

Novel Therapeutic Strategy for the Prevention of Bone Fractures

Hamrick, M. W. (2014) · Defense Technical Information Center (DTIC) · doi:10.21236/ada614236

Faculty Opinions recommendation of The Achilles' heel of senescent cells: from transcriptome to senolytic drugs.

Casper, R. F. (2018) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.725384204.793545606

Effects of differential and combinatorial inhibition of myostatin and activin A in the G610 murine model of osteogenesis imperfecta

Omosule, C. L. (2021) · MOspace Institutional Repository (University of Missouri) · doi:10.32469/10355/90078

Construction of myostatin gene knockout C2C12 cell line and expression of related microRNAPreprint

Weng, S., Zhang, W., Ma, Z., Shi, S., Zhao, M., Ji, X., & Wang, Y. (2023) · Research Square · doi:10.21203/rs.3.rs-3361771/v1

The function of Activin receptor type IIB signaling in adult skeletal muscle

Relizani, K. (2014) · theses.fr (ABES) · doi:10.70675/20978d43z02f0z4a1ezb428zf5dab86d9abf

Déconditionnement et régénération du muscle strié squelettique : rôle du niveau d’activité contractile sur le développement d’infiltrations graisseuses

Pagano, A. F. (2016) · theses.fr (ABES) · doi:10.70675/b2e8ea4ez5cd3z43a4zae84z3a8e6d8c661f

Dualités fonctionnelles de GASP-1 et GASP-2, deux protéines multi-domaines antagonistes de la myostatine

Parenté, A. (2019) · theses.fr (ABES) · doi:10.70675/3d9a23f5z3546z46f1z957cz5d167994539d

Reconditionnement musculaire dans un modèle murin de myopathie centronucléaire autosomique dominante par inactivation du gène myostatine

Arnould, D. (2018) · theses.fr (ABES) · doi:10.70675/ef3fd79fzd587z4f8ez8732z826b864b9165

Maintien de la masse musculaire et vieillissement : rôle de Cavβ1

Traoré, M. (2020) · theses.fr (ABES) · doi:10.70675/95ed9074z58a5z4b86z91e7z4894a80d2353

Targeting the Skeletal Muscle Microenvironment: A Novel Therapeutic Strategy for Skeletal Muscle Aging

Yu, Y., He, Y., Wang, Y., Wu, C., Zhou, R., Chen, F., & Ma, W. (2026) · The FASEB Journal · doi:10.1096/fj.202601360r

Aerobic exercise + weight loss decreases skeletal muscle myostatin expression and improves insulin sensitivity in older adults

Ryan, A. S., Li, G., Blumenthal, J. B., & Ortmeyer, H. K. (2013) · Obesity · doi:10.1002/oby.20216 · Cited by 74

Postnatal PPARδ Activation and Myostatin Inhibition Exert Distinct yet Complimentary Effects on the Metabolic Profile of Obese Insulin-Resistant Mice

Bernardo, B. L., Wachtmann, T. S., Cosgrove, P. G., Kühn, M., Opsahl, A., Judkins, K. M., Freeman, T. B., Hadcock, J. R., & LeBrasseur, N. K. (2010) · PLoS ONE · doi:10.1371/journal.pone.0011307 · Cited by 68

Metformin inhibits mitochondrial adaptations to aerobic exercise training in older adults

Konopka, A. R., Laurin, J. L., Schoenberg, H. M., Reid, J. J., Castor, W. M., Wolff, C. A., Musci, R. V., Safairad, O. D., Linden, M. A., Biela, L. M., et al. (2019) · Aging Cell · doi:10.1111/acel.12880 · Cited by 238

Combined Strategies for Maintaining Skeletal Muscle Mass and Function in Aging: Myostatin Inactivation and AICAR-Associated Oxidative Metabolism Induction

Pauly, M., Chabi, B., Favier, F. B., Vanterpool, F., Matecki, S., Fouret, G., Bonafos, B., Vernus, B., Feillet‐Coudray, C., Coudray, C., et al. (2014) · The Journals of Gerontology Series A · doi:10.1093/gerona/glu147 · Cited by 29

Effect Of Exercise Intervention On Expression And Translocation Of FAT/CD36 In Aging Mice

Sun, J., Su, Y., Qin, L., Zhou, Y., Dong, J., & Dong, J. (2019) · Medicine & Science in Sports & Exercise · doi:10.1249/01.mss.0000563430.14459.95