Neural control of aging skeletal muscle

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

Human aging, muscle mass, and fiber type composition.

Evans, W. J., & Lexell, J. (1995) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/50a.special_issue.11 · Cited by 1,308

Localized Igf-1 transgene expression sustains hypertrophy and regeneration in senescent skeletal muscle

Musarò, A., McCullagh, K., Paul, A., Houghton, L., Dobrowolny, G., Molinaro, M., Barton, E. R., L Sweeney, H., & Rosenthal, N. (2001) · Nature Genetics · doi:10.1038/84839 · Cited by 1,137 · cited 1×

Interactions between motoneurones and muscles in respect of the characteristic speeds of their responses

Buller, A., Eccles, J. C., & Eccles, R. M. (1960) · The Journal of Physiology · doi:10.1113/jphysiol.1960.sp006395 · Cited by 1,123

Voltage Dependent Charge Movement in Skeletal Muscle: a Possible Step in Excitation–Contraction Coupling

Schneider, M. F., & Chandler, W. K. (1973) · Nature · doi:10.1038/242244a0 · Cited by 998

Influence of aging on peripheral nerve function and regeneration

Verdú, E., Ceballos, D., Vilches, J., & Navarro, X. (2000) · Journal of the Peripheral Nervous System · doi:10.1046/j.1529-8027.2000.00026.x · Cited by 857

Potentiation of developing neuromuscular synapses by the neurotrophins NT-3 and BDNF

Lohof, A. M., Ip, N. Y., & Poo, M.-M. (1993) · Nature · doi:10.1038/363350a0 · Cited by 755

The neurotrophin hypothesis for synaptic plasticity

Schinder, A. F. (2000) · Trends in Neurosciences · doi:10.1016/s0166-2236(00)01672-6 · Cited by 740

Viral mediated expression of insulin-like growth factor I blocks the aging-related loss of skeletal muscle function

Barton-Davis, E. R., Shoturma, D. I., Musarò, A., Rosenthal, N. A., & Sweeney, H. L. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.26.15603 · Cited by 700

Early and Selective Loss of Neuromuscular Synapse Subtypes with Low Sprouting Competence in Motoneuron Diseases

Frey, D., Schneider, C., Xu, L., Borg, J., Spooren, W. P. J. M., & Caroni, P. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-07-02534.2000 · Cited by 683

Mechanisms of Muscle Denervation in Aging: Insights from a Mouse Model of Amyotrophic Lateral Sclerosis

Park, K. H. J. (2015) · Aging and Disease · doi:10.14336/ad.2015.0506 · Cited by 27

Motor responses to experimental Achilles tendon pain

Henriksen, M., Aaboe, J., Graven‐Nielsen, T., Bliddal, H., & Langberg, H. (2010) · British Journal of Sports Medicine · doi:10.1136/bjsm.2010.072561 · Cited by 27

Sarcopenia: An emphasis on occlusion training and dietary protein.

Loenneke, J. P., & Pujol, T. J. (2011) · Europe PMC (PubMed Central) · Cited by 26

Motor neuron targeting of IGF-1 attenuates age-related external Ca2+-dependent skeletal muscle contraction in senescent mice

Payne, A. M., Messi, M. L., Zheng, Z., & Delbono, O. (2006) · Experimental Gerontology · doi:10.1016/j.exger.2006.11.003 · Cited by 28

Thigh Muscle Strength in Senior Athletes and Healthy Controls

McCrory, J. L., Salacinski, A. J., Hunt, S. E., & Greenspan, S. L. (2009) · The Journal of Strength and Conditioning Research · doi:10.1519/jsc.0b013e3181bab46d · Cited by 26

Age-Related Changes in Skeletal Muscle of Cattle

Costagliola, A., Wojcik, S. P., Pagano, T. B., Biase, D. D., Russo, V., Iovane, V., Grieco, E., Papparella, S., & Paciello, O. (2016) · Veterinary Pathology · doi:10.1177/0300985815624495 · Cited by 27

Neurofilament-light chains (NF-L), a biomarker of neuronal damage, is increased in patients with severe sarcopenia: results of the SarcoPhAge study

Ladang, A., Kovacs, S., Lengelé, L., Locquet, M., Beaudart, C., Reginster, J., Bruyère, O., & Cavalier, E. (2023) · Aging Clinical and Experimental Research · doi:10.1007/s40520-023-02521-9 · Cited by 25

Interactions Between Reactive Oxygen Species Generated by Contractile Activity and Aging in Skeletal Muscle?

Jackson, M. J. (2013) · Antioxidants and Redox Signaling · doi:10.1089/ars.2013.5383 · Cited by 27

Age-related changes affect rat rotator cuff muscle function

Plate, J. F., Pace, L. A., Seyler, T. M., Jiménez-Moreno, R., Smith, T. L., Tuohy, C. J., & Mannava, S. (2013) · Journal of Shoulder and Elbow Surgery · doi:10.1016/j.jse.2013.04.017 · Cited by 25

Aging of the striatum: mechanisms and interventions

Umegaki, H., Roth, G. S., & Ingram, D. K. (2008) · AGE · doi:10.1007/s11357-008-9066-z · Cited by 23

Repeatability of locomotor performance and of morphology – locomotor performance relationships

Conradsen, C., Walker, J. A., Perna, C., & McGuigan, K. (2016) · Journal of Experimental Biology · doi:10.1242/jeb.141259 · Cited by 23

Skill acquisition as a function of age, hand and task difficulty: Interactions between cognition and action

Raw, R. K., Wilkie, R. M., Allen, R. J., Warburton, M., Leonetti, M., Williams, J. H. G., & Mon-Williams, M. A. (2019) · PLoS ONE · doi:10.1371/journal.pone.0211706 · Cited by 26

On the mechanisms underlying attenuated redox responses to exercise in older individuals: A hypothesis

Jackson, M. J. (2020) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2020.10.026 · Cited by 24

Influence of IGF-I serum concentration on muscular regeneration capacity in patients with sarcopenia

Jarmusch, S., Baber, L., Bidlingmaier, M., Ferrari, U., Hofmeister, F., Hintze, S., Mehaffey, S., Meinke, P., Neuerburg, C., Schoser, B. G. H., et al. (2021) · BMC Musculoskeletal Disorders · doi:10.1186/s12891-021-04699-3 · Cited by 23

Lipogenic regulators are elevated with age and chronic overload in rat skeletal muscle

Rivas, D. A., Morris, E. P., & Fielding, R. A. (2011) · Acta Physiologica · doi:10.1111/j.1748-1716.2011.02289.x · Cited by 24

Motor Sequence Learning in Healthy Older Adults Is Not Necessarily Facilitated by Transcranial Direct Current Stimulation (tDCS)

Raw, R. K., Allen, R. J., Mon-Williams, M. A., & Wilkie, R. M. (2016) · Geriatrics · doi:10.3390/geriatrics1040032 · Cited by 21

TrkB expression at the neuromuscular junction is reduced during aging

Personius, K. E., & Parker, S. D. (2012) · Muscle & Nerve · doi:10.1002/mus.23616 · Cited by 24

Progression of motor neuron disease is accelerated and the ability to recover is compromised with advanced age in rNLS8 mice

Spiller, K. J., Restrepo, C. R., Khan, T., Stieber, A., Kwong, L. K., Trojanowski, J. Q., & Lee, V. M. ‐. (2016) · Acta Neuropathologica Communications · doi:10.1186/s40478-016-0377-5 · Cited by 23

Follistatin-induced muscle hypertrophy in aged mice improves neuromuscular junction innervation and function

Iyer, C. C., Chugh, D., Bobbili, P. J., Blatnik, A. J., Crum, A. E., Yi, A. F., Kaspar, B. K., Meyer, K., Burghes, A. H. M., & Arnold, W. D. (2021) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2021.03.005 · Cited by 22

Ultrasound of peripheral nerves in acromegaly: changes at 1‐year follow‐up

Resmini, E., Tagliafico, A. S., Nizzo, R., Bianchi, F., Minuto, F. M., Derchi, L. E., Martinoli, C., & Ferone, D. (2008) · Clinical Endocrinology · doi:10.1111/j.1365-2265.2008.03468.x · Cited by 22

Skeletal Muscle Fiber Size and Gene Expression in the Oldest-Old With Differing Degrees of Mobility

Naro, F., Venturelli, M., Monaco, L., Toniolo, L., Muti, E., Milanese, C., Zhao, J., Richardson, R. S., Schena, F. F., & Reggiani, C. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.00313 · Cited by 22

Age-related functional changes and susceptibility to eccentric contraction-induced damage in skeletal muscle cell

Choi, S.-J. (2016) · Integrative Medicine Research · doi:10.1016/j.imr.2016.05.004 · Cited by 21

Reduced adenosine diphosphate sensitivity in skeletal muscle mitochondria increases reactive oxygen species production in mouse models of aging and oxidative stress but not denervation

Pharaoh, G. A., Brown, J. L., Ranjit, R., Ungvari, Z. I., & Remmen, H. V. (2020) · JCSM Rapid Communications · doi:10.1002/rco2.29 · Cited by 21

The role of attenuated redox and heat shock protein responses in the age-related decline in skeletal muscle mass and function

McArdle, A., & Jackson, M. J. (2017) · Essays in Biochemistry · doi:10.1042/ebc20160088 · Cited by 19

Exercise-induced gene expression changes in skeletal muscle of old mice

Endo, Y., Zhang, Y., Olumi, S., Karvar, M., Argawal, S., Neppl, R. L., & Sinha, I. (2021) · Genomics · doi:10.1016/j.ygeno.2021.06.035 · Cited by 20

Long‐term, induced expression of Hand2 in peripheral sympathetic neurons ameliorates sarcopenia in geriatric mice

Rodrigues, A. C. Z., Messi, M. L., Wang, Z., Bonilla, H. J., Freeman, W. M., & Delbono, O. (2021) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12790 · Cited by 20

Mesenchymal Stem Cell Transplantation for the Treatment of Age-Related Musculoskeletal Frailty

Mahindran, E., Law, J. X., Ng, M. H., & Nordin, F. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms221910542 · Cited by 21

Common Genetic Variation in the IGF1 Associates with Maximal Force Output

Huuskonen, A. S., Lappalainen, J., Oksala, N., Santtila, M., Häkkinen, K., Kyröläinen, H., & Atalay, M. (2011) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0b013e3182220179 · Cited by 21

Effects of disease-afflicted and aging neurons on the musculoskeletal system

Valdez, G. (2019) · Bone · doi:10.1016/j.bone.2019.01.023 · Cited by 22

Effects of aging and maternal protein restriction on the muscle fibers morphology and neuromuscular junctions of rats after nutritional recovery

Confortim, H. D., Jerônimo, L. C., Centenaro, L. A., Pinheiro, P. F. F., Brancalhão, R. M. C., Matheus, S. M. M., & Torrejais, M. M. (2015) · Micron · doi:10.1016/j.micron.2014.12.006 · Cited by 20

Estimation of the number and size of motor units in intrinsic laryngeal muscles using morphometric methods

Neto, H. S., & Marques, M. J. (2008) · Clinical Anatomy · doi:10.1002/ca.20624 · Cited by 19

Heart and neural crest derivative 2‐induced preservation of sympathetic neurons attenuates sarcopenia with aging

Rodrigues, A. C. Z., Wang, Z., Messi, M. L., Bonilla, H. J., Liu, L., Freeman, W. M., & Delbono, O. (2020) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12644 · Cited by 22

Maternal protein restriction during pregnancy and lactation affects the development of muscle fibers and neuromuscular junctions in rats

Confortim, H. D., Jerônimo, L. C., Centenaro, L. A., Pinheiro, P. F. F., Matheus, S. M. M., & Torrejais, M. M. (2016) · Muscle & Nerve · doi:10.1002/mus.25187 · Cited by 19

Dynamics of postural control during bilateral stance – Effect of support area, visual input and age

Raffalt, P. C., Spedden, M. E., & Geertsen, S. S. (2019) · Human Movement Science · doi:10.1016/j.humov.2019.05.007 · Cited by 18

Voluntary wheel running with and without follistatin overexpression improves NMJ transmission but not motor unit loss in late life of C57BL/6J mice

Chugh, D., Iyer, C. C., Bobbili, P., Blatnik, A. J., Kaspar, B. K., Meyer, K., Burghes, A. H., Clark, B. C., & Arnold, W. D. (2021) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2021.01.012 · Cited by 17

Age-Dependent Changes Cooperatively Impact Skeletal Muscle Regeneration after Compartment Syndrome Injury

Zhou, Y., Lovell, D., Bethea, M. M., Wang, Z., Christ, G. J., Söker, S., & Criswell, T. L. (2014) · American Journal Of Pathology · doi:10.1016/j.ajpath.2014.03.018 · Cited by 18

Brainstem noradrenergic neurons: Identifying a hub at the intersection of cognition, motility, and skeletal muscle regulation

Delbono, O., Wang, Z., & Messi, M. L. (2022) · Acta Physiologica · doi:10.1111/apha.13887 · Cited by 17

Motor unit activity when young and old adults perform steady contractions while supporting an inertial load

Pascoe, M. A., Gould, J. R., & Enoka, R. M. (2012) · Journal of Neurophysiology · doi:10.1152/jn.00437.2012 · Cited by 17

Age independent and position-dependent alterations in motor unit activity of the biceps brachii

Harwood, B. J., Edwards, D. L., & Jakobi, J. M. (2010) · European Journal of Applied Physiology · doi:10.1007/s00421-010-1438-2 · Cited by 17

Self-Reported Physical Activity and Relations to Growth and Neurotrophic Factors in Diabetes Mellitus: The Framingham Offspring Study

Spartano, N. L., Davis‐Plourde, K. L., Himali, J. J., Murabito, J. M., Vasan, R. S., Beiser, A., & Seshadri, S. S. (2019) · Journal of Diabetes Research · doi:10.1155/2019/2718465 · Cited by 17

Age-dependent action of reactive oxygen species on transmitter release in mammalian neuromuscular junctions

Shakirzyanova, A., Valeeva, G. R., Giniatullin, А. R., Naumenko, N. V., Fulle, S., Akulov, A. N., Atalay, M., Nikolsky, E. E., & Giniatullin, R. A. (2015) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2015.10.023 · Cited by 16

Myosin heavy chain isoform expression in the Vastus Lateralis muscle of aging African green vervet monkeys

Feng, X., Zhang, T., Xu, Z., Choi, S.-J., Qian, J. X., Furdui, C. M., Register, T. C., & Delbono, O. (2012) · Experimental Gerontology · doi:10.1016/j.exger.2012.05.007 · Cited by 18

Mesenchymal Stem Cell-Derived Extracellular Vesicles: Hype or Hope for Skeletal Muscle Anti-Frailty

Mahindran, E., Zaman, W. S. W. K., Noordin, K. B. A. A., Tan, Y.-F., & Nordin, F. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24097833 · Cited by 16

Nutritional Considerations in Preventing Muscle Atrophy

Creţoiu, S. M., & Zugravu, C. (2018) · Advances in experimental medicine and biology · doi:10.1007/978-981-13-1435-3_23 · Cited by 17

Maintaining Muscle Function Across the Lifespan

Arnold, W. D., & Colón, C. J. P. (2020) · American Journal of Physical Medicine & Rehabilitation · doi:10.1097/phm.0000000000001429 · Cited by 15

Preservation of Motor Neuron Ca2+ Channel Sensitivity to Insulin‐Like Growth Factor‐1 in Brain Motor Cortex from Senescent Rat

Shan, H. Q., Messi, M. L., Zheng, Z., Wang, Z., & Delbono, O. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2003.047746 · Cited by 15

Insulin-Like Growth Factors in the Peripheral Nervous System

Sakowski, S. A., & Feldman, E. L. (2012) · Endocrinology and Metabolism Clinics of North America · doi:10.1016/j.ecl.2012.04.020 · Cited by 15

Role of Sustained Overexpression of Central Nervous System IGF-I in the Age-Dependent Decline of Mouse Excitation-Contraction Coupling

Jiménez-Moreno, R., Messi, M. L., Zheng, Z., Wang, Z., Ye, P., D’Ercole, J. A., & Delbono, O. (2006) · The Journal of Membrane Biology · doi:10.1007/s00232-006-0044-z · Cited by 14

Sarcopenia Diagnosis and Management in Hematological Malignancies and Differences with Cachexia and Frailty

Colloca, G. F., Bellieni, A., Capua, B. D., Iervolino, M., Bracci, S., Fusco, D., Tagliaferri, L., Landi, F., & Valentini, V. (2023) · Cancers · doi:10.3390/cancers15184600 · Cited by 14

Neuromuscular transmission modulation by adenosine upon aging

Pousinha, P. A., Correia, A. M., Sebastião, A. M., & Ribeiro, J. A. (2012) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2012.01.008 · Cited by 13

Epigenetics of Skeletal Muscle Aging

Sharples, A. P., Seaborne, R. A. E., & Stewart, C. E. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-811060-7.00019-x · Cited by 14

The giant miniature endplate potentials frequency is increased in aged rats

Pousinha, P. A., Correia, A. M., Sebastião, A. M., & Ribeiro, J. A. (2014) · Neuroscience Letters · doi:10.1016/j.neulet.2014.10.035 · Cited by 12

Exercise training exacerbates tourniquet ischemia-induced decreases in GLUT4 expression and muscle atrophy in rats

Tsai, Y., Hou, C., Liao, Y., Chen, C., Lin, F.-C., Lee, W.-C., Chou, S., & Kuo, C. (2006) · Life Sciences · doi:10.1016/j.lfs.2005.11.021 · Cited by 12

Tongue Structure and Function

Sokoloff, A. J., & Burkholder, T. J. (2012) · Springer eBooks · doi:10.1007/978-1-4614-4466-4_12 · Cited by 12

Inhibition of the endocannabinoid system reverses obese phenotype in aged mice and partly restores skeletal muscle function

Fajardo, L., Sanchez, P., Salles, J., Rigaudière, J., Patrac, V., Caspar‐Bauguil, S., Bergoglgio, C., Moro, C., Walrand, S., & Bacquer, O. L. (2023) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00258.2022 · Cited by 11

Assessment of neuromuscular and haemodynamic effects of cisatracurium and vecuronium under sevoflurane-remifentanil anaesthesia in elderly patients

Keleş, G. T., Yentür, A., Çavuş, Z., & Sakarya, M. (2004) · European Journal of Anaesthesiology · doi:10.1017/s0265021504000225 · Cited by 11

Excitation-Contraction Coupling Regulation in Aging Skeletal Muscle

Delbono, O. (2010) · Springer eBooks · doi:10.1007/978-90-481-9713-2_6 · Cited by 12

Skeletal muscle transcriptomics identifies common pathways in nerve crush injury and ageing

Staunton, C. A., Owen, E., Hemmings, K., Vasilaki, A., McArdle, A., Barrett‐Jolley, R., & Jackson, M. J. (2022) · Skeletal Muscle · doi:10.1186/s13395-021-00283-4 · Cited by 11

Molecular composition of skeletal muscle in infants and adults: a comparative proteomic and transcriptomic study

Schaiter, A., Hentschel, A., Kleefeld, F., Schuld, J., Umathum, V. G., Procida‐Kowalski, T., Nelke, C., Roth, A., Hahn, A., Krämer, H. H., et al. (2024) · Scientific Reports · doi:10.1038/s41598-024-74913-4 · Cited by 12

The Interaction of Aging and 10 Years of Racing on Ultraendurance Running Performance

Rae, D. E., Bosch, A. N., Collins, M., & Lambert, M. (2005) · Journal of Aging and Physical Activity · doi:10.1123/japa.13.2.210 · Cited by 10

The role of L- and T-type Ca2+ currents during the in vitro aging of murine myogenic (i28) cells in culture

Luin, E., & Ruzzier, F. (2006) · Cell Calcium · doi:10.1016/j.ceca.2006.09.006 · Cited by 10

Ageing of human myofibres in the Vastus Lateralis muscle: A narrative review

Granic, A., Simoes, D. C. M., Bowen, T. S., Almaghtuf, N., Richardson, G. D., & Sayer, A. A. (2026) · Ageing Research Reviews · doi:10.1016/j.arr.2026.103022 · Cited by 9

Lower Limb Strength Profile in Elderly with Different Pathologies: Comparisons with Healthy Subjects

Bullo, V., Roma, E., Gobbo, S., Duregon, F., Bergamo, M., Bianchini, G., Doria, E., Cugusi, L., Blasio, A. D., Bocalini, D. S., et al. (2020) · Geriatrics · doi:10.3390/geriatrics5040083 · Cited by 9

Pericytes in Skeletal Muscle

Gautam, J., & Yao, Y. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-11093-2_4 · Cited by 10

Skeletal muscle sympathetic denervation disrupts the neuromuscular junction postterminal organization: A single-cell quantitative approach

Wang, Z.-M., Messi, M. L., Rodrigues, A. C. Z., & Delbono, O. (2022) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2022.103730 · Cited by 9

The Impact of Age on Skeletal Muscle Progenitor Cell Survival and Fate After Injury

Zhou, Y., Lovell, D., Bethea, M. M., Yoseph, B. P., Poteracki, J. M., Söker, S., & Criswell, T. L. (2017) · Tissue Engineering Part C Methods · doi:10.1089/ten.tec.2017.0216 · Cited by 9

Is whole-body vibration beneficial for seniors?

Lachance, C. C., Weir, P. L., Kenno, K. A., & Horton, S. (2012) · European Review of Aging and Physical Activity · doi:10.1007/s11556-011-0094-9 · Cited by 9

Isometric force complexity may not fully originate from the nervous system

Raffalt, P. C., Yentes, J. M., & Spedden, M. E. (2023) · Human Movement Science · doi:10.1016/j.humov.2023.103111 · Cited by 8

IGF-1 Antibody Prolongs the Effective Duration Time of Botulinum Toxin in Decreasing Muscle Strength

Jin, L., Pan, L., Liu, W., Guo, Y., Zheng, Y., Guan, Q., & Nie, Z. (2013) · International Journal of Molecular Sciences · doi:10.3390/ijms14059051 · Cited by 8

The cost of being stable: Trade-offs between effort and stability across a landscape of redundant motor solutionsPreprint

Sohn, M. H., & Ting, L. H. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/477083 · Cited by 8

A Biomechanical Simulation of Forearm Flexion Using the Finite Element Approach

Liang, C., Jiang, F., Kawaguchi, D., & Chen, X. (2023) · Bioengineering · doi:10.3390/bioengineering11010023 · Cited by 7

Effects of Aging on Orbicularis Oculi Muscle Strength and Ultrastructure in Dermatochalasis: A Pilot Study

Krajewska-Węglewicz, L., Felczak, P., & Dorobek, M. (2024) · Journal of Clinical Medicine · doi:10.3390/jcm14010162 · Cited by 7

Investigating the Stroke- and Aging-Related Changes in Global and Instantaneous Intermuscular Coupling Using Cross-Fuzzy Entropy

Tian, N., Chen, Y., Sun, W., Liu, H., Wang, X., Yan, T., & Song, R. (2021) · IEEE Transactions on Neural Systems and Rehabilitation Engineering · doi:10.1109/tnsre.2021.3101615 · Cited by 7

Modern Concepts of Cholinergic Neurotransmission at the Motor Synapse

Malomouzh, A. I., & Nikolsky, E. E. (2018) · Biochemistry (Moscow) Supplement Series A Membrane and Cell Biology · doi:10.1134/s1990747818030078 · Cited by 8

Effects of cardiac output on the onset of rocuronium-induced neuromuscular block in elderly patients

Shiraishi, N., Aono, M., Kameyama, Y., Yamamoto, M., Kitajima, O., & Suzuki, T. (2018) · Journal of Anesthesia · doi:10.1007/s00540-018-2510-z · Cited by 7

Skeletal muscle-specific calpastatin overexpression mitigates muscle weakness in aging and extends life span

Schroder, E. A., Wang, L., Wen, Y., Callahan, L. A., & Supinski, G. S. (2021) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00883.2020 · Cited by 7

Age-Related Remodeling of Neuromuscular Junctions

Mantilla, C. B., & Sieck, G. C. (2010) · Springer eBooks · doi:10.1007/978-90-481-9713-2_3 · Cited by 6

Oxidative stress in skeletal muscle: Unraveling the potential beneficial and deleterious roles of reactive oxygen species

Jackson, M. J., Pollock, N., Staunton, C. A., Stretton, C., Vasilaki, A., & McArdle, A. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-818606-0.00034-1 · Cited by 6

Semiautomatic morphometric analysis of skeletal muscle obtained by needle biopsy in older adults

Bonilla, H. J., Messi, M. L., Sadieva, K. A., Hamilton, C. A., Buchman, A. S., & Delbono, O. (2020) · GeroScience · doi:10.1007/s11357-020-00266-1 · Cited by 6

Calcium current kinetics in young and aged human cultured myotubes

Luin, E., Lorenzon, P., Wernig, A., & Ruzzier, F. (2008) · Cell Calcium · doi:10.1016/j.ceca.2008.04.002 · Cited by 6

Update on therapies for sarcopenia: novel approaches for age-related muscle wasting and weakness

Lynch, G. S. (2004) · Expert Opinion on Therapeutic Patents · doi:10.1517/13543776.14.9.1329 · Cited by 6

Muscle fibers from senescent mice retain excitation–contraction coupling properties in culture

Wang, Z.-M., Zheng, Z., Messi, M. L., & Delbono, O. (2007) · In Vitro Cellular & Developmental Biology - Animal · doi:10.1007/s11626-007-9047-z · Cited by 5

cPLA2 in musculoskeletal and autoimmune diseases: Molecular mechanisms and therapeutic insights.

He, C., Huang, G.-W., Bi, J., Fu, W.-Y., & Liu, C.-J. (2026) · Cytokine & growth factor reviews · doi:10.1016/j.cytogfr.2026.01.002 · Cited by 4

Potentiation by sevoflurane of rocuronium-induced neuromuscular block is greater in older than younger adult patients: a randomised controlled trial

Takagi, S., Kitajima, O., Yamamoto, M., Matsui, M., & Suzuki, T. (2020) · British Journal of Anaesthesia · doi:10.1016/j.bja.2020.05.047 · Cited by 4

Age-related changes in contractile properties and morphology on chemically skinned single fibers from young and old human skeletal muscles.

최승준, & 임재영 (2012) · Exercise Science · doi:10.15857/ksep.2012.21.3.309 · Cited by 4

Non-Cholinergic Signaling Pathways at Vertebrate Neuromuscular Junctions

Artem, I. B. (2012) · InTech eBooks · doi:10.5772/48337 · Cited by 5

Abstracts of the Myology Seminar: Are deferrable the mobility impairments in older aging? | Accademia Galileiana di Scienze Lettere ed Arti, Padua, Italy, February 16, 2016

Editors, T. (2016) · European Journal of Translational Myology · doi:10.4081/ejtm.2016.5831 · Cited by 4

The evidence for old age motor neuron death: A scoping review

Cheung, S. W., & Fogarty, M. J. (2026) · Physiological Reports · doi:10.14814/phy2.70967 · Cited by 3

Myokines as molecular mediators of the muscle–brain axis: Mechanisms linking sarcopenia to cognitive decline and implications for preventive strategies in ageing — A narrative review

Dharmansyah, D., Rahayuwati, L., Defi, I. R., Pramukti, I., & Mutyara, K. (2026) · Experimental Gerontology · doi:10.1016/j.exger.2026.113247 · Cited by 4

In the land of not-unhappiness: On the state-of-the-art of targeting aging and age-related diseases by biomedical research

Klinaki, E., & Ogrodnik, M. B. (2024) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2024.111929 · Cited by 3

Healthy aging and exercise

Gökdemir, Ö., & Özçakar, N. (2022) · The Journal of Turkish Family Physician · doi:10.15511/tjtfp.22.00304 · Cited by 3

Bioinformatic Analysis of the Sciatic Nerve Transcriptomes of Mice after 30-Day Spaceflight on Board the Bion-M1 Biosatellite

Kuznetsov, M., Rezvyakov, P. N., Lisyukov, A. N., Gusev, O., Nikolskiy, E. E., & Islamov, R. R. (2019) · Russian Journal of Genetics · doi:10.1134/s1022795419030104 · Cited by 3

Increased skeletal muscle akt content in a murine model of motor neuron disease

Cunningham, L. R. (2005) · Summit (Simon Fraser University) · Cited by 3

The rise and deceleration of neuronal excitability in aging and Alzheimer’s disease: Mechanisms, implications, and therapeutic targets

Delbono, O., Wang, Z., & Messi, M. L. (2025) · Ageing Research Reviews · doi:10.1016/j.arr.2025.102999 · Cited by 3

Altered H19/miR‐675 expression in skeletal muscle is associated with low muscle mass in community‐dwelling older adults

Antoun, E., Migliavacca, E., Garratt, E. S., Barton, S. J., Titcombe, P., Westbury, L. D., Baczynska, A., Dodds, R., Roberts, H. C., Sayer, A. A., et al. (2021) · JCSM Rapid Communications · doi:10.1002/rco2.44 · Cited by 3

The Roles of myomiRs in the Pathogenesis of Sarcopenia: From Literature to In Silico Analysis

Jia, H., Nurgulsim, K., Khan, R., & Ayari‐Akkari, A. (2025) · Molecular Biotechnology · doi:10.1007/s12033-025-01373-0 · Cited by 2

Mechanisms of decline in muscle quality in sarcopenia

Yamada, T. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-822146-4.00007-7 · Cited by 2

Enriched Environmental Conditions Ameliorate Age-Dependent Alterations in the Somatosensory System, but Do Not Affect the Motor System of the Rat Spinal Cord

Hilbig, H., Beier, V., Köster, K., Stoll, C., Richter, D., & Dinse, H. R. (2006) · Neuroembryology and Aging · doi:10.1159/000109345 · Cited by 2

Knee Muscle Activation Characteristics During Closed Kinetic Chain Directional Loading in Healthy Young Males and Females

Flaxman, T. E. (2011) · Library and Archives Canada (Government of Canada) · doi:10.20381/ruor-4498 · Cited by 2

The effects of whole-body vibration exercise on muscular strength in seniors

Lachance, C. C. (2012) · Cited by 2

Summary

Delbono, O. (2015)

Excitation-Contraction Coupling Regulation in Aging Skeletal Muscle

Delbono, O. (2010) · Springer eBooks · doi:10.1007/978-90-481-9713-2_6 · Cited by 12

Innervation and neuromuscular control in ageing skeletal muscle

Hepple, R. T., & Rice, C. L. (2015) · The Journal of Physiology · doi:10.1113/jp270561 · Cited by 417

Rejuvenation of the aged neuromuscular junction by exercise

Kreko‐Pierce, T., & Eaton, B. A. (2018) · Cell Stress · doi:10.15698/cst2018.02.123 · Cited by 8

Motor neurone targeting of IGF‐1 prevents specific force decline in ageing mouse muscle

Payne, A. M., Zheng, Z., Messi, M. L., Milligan, C., Rodríguez, E. G., & Delbono, O. (2005) · The Journal of Physiology · doi:10.1113/jphysiol.2005.100032 · Cited by 72