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Sarcopenia and Cognitive Decline in Older Adults: Targeting the Muscle–Brain Axis

Arosio, B., Calvani, R., Ferri, E., Coelho-Junior, H. J., Carandina, A., Campanelli, F., Ghiglieri, V., Marzetti, E., & Picca, A. (2023) · Nutrients · doi:10.3390/nu15081853 · Cited by 165 · see citing works

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Sousa-Victor, P., García-Prat, L., Serrano, A. L., Perdiguero, E., & Muñoz-Cánoves, P. (2015) · Trends in Endocrinology & Metabolism · doi:10.1016/j.tem.2015.03.006 · Cited by 163 · see citing works

Partial Inhibition of mTORC1 in Aged Rats Counteracts the Decline in Muscle Mass and Reverses Molecular Signaling Associated with Sarcopenia

Joseph, G. A., Wang, S. X., Jacobs, C. E., Zhou, W., Kimble, G. C., Tse, H. W., Eash, J. K., Shavlakadze, T., & Glass, D. J. (2019) · Molecular and Cellular Biology · doi:10.1128/mcb.00141-19 · Cited by 161 · see citing works

Mitochondria initiate and regulate sarcopenia

Alway, S. E., Mohamed, J. S., & Myers, M. J. (2017) · Exercise and Sport Sciences Reviews · doi:10.1249/jes.0000000000000101 · Cited by 153 · see citing works

Regenerative decline of stem cells in sarcopenia

Sousa-Victor, P., & Muñoz-Cánoves, P. (2016) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2016.02.002 · Cited by 147 · see citing works

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

Brioche, T., Pagano, A. F., Py, G., & Chopard, A. (2016) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2016.04.006 · Cited by 129 · see citing works

Aging and sarcopenia associate with specific interactions between gut microbes, serum biomarkers and host physiology in rats

Siddharth, J., Chakrabarti, A., Pannérec, A., Karaz, S., Morin-Rivron, D., Masoodi, M., Feige, J. N., & Parkinson, S. J. (2017) · Aging · doi:10.18632/aging.101262 · Cited by 127 · see citing works

Mitochondrial Dysfunction Is a Common Denominator Linking Skeletal Muscle Wasting Due to Disease, Aging, and Prolonged Inactivity

Hyatt, H. W., & Powers, S. K. (2021) · Antioxidants · doi:10.3390/antiox10040588 · Cited by 127 · see citing works

Identification and Small Molecule Inhibition of an Activating Transcription Factor 4 (ATF4)-dependent Pathway to Age-related Skeletal Muscle Weakness and Atrophy

Ebert, S. M., Dyle, M. C., Bullard, S. A., Dierdorff, J. M., Murry, D. J., Fox, D. K., Bongers, K. S., Lira, V. A., Meyerholz, D. K., Talley, J. J., et al. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.681445 · Cited by 120 · see citing works

Neuromuscular Junction Dismantling in Amyotrophic Lateral Sclerosis

Cappello, V., & Francolini, M. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18102092 · Cited by 119 · see citing works

Voluntary resistance wheel exercise from mid-life prevents sarcopenia and increases markers of mitochondrial function and autophagy in muscles of old male and female C57BL/6J mice

White, Z. R., Terrill, J. R., White, R. B., McMahon, C., Sheard, P., Grounds, M. D., & Shavlakadze, T. (2016) · Skeletal Muscle · doi:10.1186/s13395-016-0117-3 · Cited by 119 · see citing works

p53 and ATF4 mediate distinct and additive pathways to skeletal muscle atrophy during limb immobilization

Fox, D. K., Ebert, S. M., Bongers, K. S., Dyle, M. C., Bullard, S. A., Dierdorff, J. M., Kunkel, S. D., & Adams, C. M. (2014) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00010.2014 · Cited by 119 · see citing works

Hallmarks of ageing in human skeletal muscle and implications for understanding the pathophysiology of sarcopenia in women and men

Granic, A., Suetterlin, K., Shavlakadze, T., Grounds, M. D., & Sayer, A. A. (2023) · Clinical Science · doi:10.1042/cs20230319 · Cited by 118 · see citing works

A robust neuromuscular system protects rat and human skeletal muscle from sarcopenia

Pannérec, A., Springer, M., Migliavacca, E., Ireland, A., Piasecki, M., Karaz, S., Jacot, G., Métairon, S., Danenberg, E., Raymond, F., et al. (2016) · Aging · doi:10.18632/aging.100926 · Cited by 110 · see citing works

Muscle function decline and mitochondria changes in middle age precede sarcopenia in mice

del Campo, A., Contreras‐Hernandez, I., Castro‐Sepúlveda, M., Campos, C. A., Figueroa, R., Tevy, M. F., Eisner, V., Casas, M., & Jaimovich, E. (2018) · Aging · doi:10.18632/aging.101358 · Cited by 110 · see citing works

Apoptosis in capillary endothelial cells in ageing skeletal muscle

Wang, H., Listrat, A., Meunier, B., Gueugneau, M., Coudy‐Gandilhon, C., Combaret, L., Taillandier, D., Polge, C., Attaix, D., Lethias, C., et al. (2014) · Aging Cell · doi:10.1111/acel.12169 · Cited by 109 · see citing works

Gut microbiota as a promising therapeutic target for age-related sarcopenia

Zhang, T., Cheng, J.-K., & Hu, Y. (2022) · Ageing Research Reviews · doi:10.1016/j.arr.2022.101739 · Cited by 102 · see citing works

Single nuclei profiling identifies cell specific markers of skeletal muscle aging, frailty, and senescence

Pérez, K., Ciotlos, S., McGirr, J., Limbad, C., Doi, R., Nederveen, J. P., Nilsson, M. I., Winer, D. A., Evans, W. J., Tarnopolsky, M. A., et al. (2022) · Aging · doi:10.18632/aging.204435 · Cited by 105 · see citing works

Failed reinnervation in aging skeletal muscle

Aare, S., Spendiff, S., Vuda, M., Elkrief, D., Pérez, A., Wu, Q., Mayaki, D., Hussain, S. N. A., Hettwer, S., & Hepple, R. T. (2016) · Skeletal Muscle · doi:10.1186/s13395-016-0101-y · Cited by 102 · see citing works

Distinct and additive effects of calorie restriction and rapamycin in aging skeletal muscle

Ham, D. J., Börsch, A., Chojnowska, K., Lin, S., Leuchtmann, A. B., Ham, A. S., Thürkauf, M., Delezie, J., Furrer, R., Bürri, D., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-29714-6 · Cited by 102 · see citing works

Thermal manipulation of the chicken embryo triggers differential gene expression in response to a later heat challenge

Loyau, T., Hennequet‐Antier, C., Coustham, V., Berri, C., Leduc, M., Crochet, S., Sannier, M., Duclos, M. J. M. J., Mignon-Grasteau, S., Tesseraud, S., et al. (2016) · BMC Genomics · doi:10.1186/s12864-016-2661-y · Cited by 102 · see citing works

Denervation drives mitochondrial dysfunction in skeletal muscle of octogenarians

Spendiff, S., Vuda, M., Gouspillou, G., Aare, S., Pérez, A., Morais, J. A., Jagoe, R. T., Filion, M., Glicksman, R., Kapchinsky, S., et al. (2016) · The Journal of Physiology · doi:10.1113/jp272487 · Cited by 100 · see citing works

The Interplay between Mitochondrial Morphology and Myomitokines in Aging Sarcopenia

Romanello, V. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms22010091 · Cited by 101 · see citing works

Microarray Analysis of Gene Expression Provides New Insights Into Denervation-Induced Skeletal Muscle Atrophy

Shen, Y., Zhang, R., Xu, L., Wan, Q., Zhu, J., Gu, J., Huang, Z., Ma, W., Shen, M., Ding, F., et al. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.01298 · Cited by 97 · see citing works

ATP Citrate Lyase Improves Mitochondrial Function in Skeletal Muscle

Das, S., Morvan, F., Jourde, B., Meier, V., Kahle, P., Brebbia, P., Toussaint, G., Glass, D. J., & Fornaro, M. (2015) · Cell Metabolism · doi:10.1016/j.cmet.2015.05.006 · Cited by 91 · see citing works

Skeletal muscle aging, cellular senescence, and senotherapeutics: current knowledge and future directions

Englund, D. A., Zhang, X., Aversa, Z., & LeBrasseur, N. K. (2021) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2021.111595 · Cited by 94 · see citing works

Inhibition of the Fission Machinery Mitigates OPA1 Impairment in Adult Skeletal Muscles

Romanello, V., Scalabrin, M., Albiero, M., Blaauw, B., Scorrano, L., & Sandri, M. (2019) · Cells · doi:10.3390/cells8060597 · Cited by 91 · see citing works

Fiber-Type Shifting in Sarcopenia of Old Age: Proteomic Profiling of the Contractile Apparatus of Skeletal Muscles

Dowling, P., Gargan, S., Swandulla, D., & Ohlendieck, K. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24032415 · Cited by 95 · see citing works

Mitochondrial calcium uptake declines during aging and is directly activated by oleuropein to boost energy metabolism and skeletal muscle performance

Gherardi, G., Weiser, A., Bermont, F., Migliavacca, E., Brinon, B., Jacot, G. E., Hermant, A., Sturlese, M., Nogara, L., Vascon, F., et al. (2024) · Cell Metabolism · doi:10.1016/j.cmet.2024.10.021 · Cited by 92 · see citing works

HDAC4 Controls Muscle Homeostasis through Deacetylation of Myosin Heavy Chain, PGC-1α, and Hsc70

Luo, L., Martin, S. C., Parkington, J. D., Cadena, S. M., Zhu, J., Ibebunjo, C., Summermatter, S., Londraville, N., Patora‐Komisarska, K., Widler, L., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.09.023 · Cited by 92 · see citing works

Drp1 knockdown induces severe muscle atrophy and remodelling, mitochondrial dysfunction, autophagy impairment and denervation

Dulac, M., Leduc‐Gaudet, J., Reynaud, O., Ayoub, M., Guérin, A., Finkelchtein, M., Hussain, S. N., & Gouspillou, G. (2020) · The Journal of Physiology · doi:10.1113/jp279802 · Cited by 90 · see citing works

Molecular and phenotypic analysis of rodent models reveals conserved and species-specific modulators of human sarcopenia

Börsch, A., Ham, D. J., Mittal, N., Tintignac, L. A., Migliavacca, E., Feige, J. N., Rüegg, M. A., & Zavolan, M. (2021) · Communications Biology · doi:10.1038/s42003-021-01723-z · Cited by 85 · see citing works

Molecular analyses provide insight into mechanisms underlying sarcopenia and myofibre denervation in old skeletal muscles of mice

Barns, M. E., Gondro, C., Tellam, R. L., Radley‐Crabb, H. G., Grounds, M. D., & Shavlakadze, T. (2014) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2014.04.025 · Cited by 84 · see citing works

Polyphenols and Their Potential Role in Preventing Skeletal Muscle Atrophy

Salucci, S., & Falcieri, E. (2020) · Nutrition Research · doi:10.1016/j.nutres.2019.11.004 · Cited by 83 · see citing works

Multi-omics research in sarcopenia: Current progress and future prospects

Liu, J., Dong, S., Shen, H., Yang, D.-Y., Chen, B., Ma, X., Peng, Y., Xiao, H., & Deng, H. (2022) · Ageing Research Reviews · doi:10.1016/j.arr.2022.101576 · Cited by 83 · see citing works

The need to more precisely define aspects of skeletal muscle regeneration

Grounds, M. D. (2014) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2014.09.010 · Cited by 79 · see citing works

Skeletal Muscle Atrophy: Discovery of Mechanisms and Potential Therapies

Ebert, S. M., Al-Zougbi, A., Bodine, S. C., & Adams, C. M. (2019) · Physiology · doi:10.1152/physiol.00003.2019 · Cited by 80 · see citing works

Central and Peripheral Neuromuscular Adaptations to Ageing

Borzuola, R., Giombini, A., Torre, G., Campi, S., Albo, E., Bravi, M., Borrione, P., FOSSATI, C., & Macaluso, A. (2020) · Journal of Clinical Medicine · doi:10.3390/jcm9030741 · Cited by 91 · see citing works

Vitamin E in Sarcopenia: Current Evidences on Its Role in Prevention and Treatment

Khor, S. C., Karim, N. A., Ngah, W. Z. W., Yusof, Y. A. M., & Makpol, S. (2014) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2014/914853 · Cited by 77 · see citing works

NMJ maintenance and repair in aging

Taetzsch, T., & Valdez, G. (2018) · Current Opinion in Physiology · doi:10.1016/j.cophys.2018.05.007 · Cited by 77 · see citing works

Effect of dietary n-3 PUFA supplementation on the muscle transcriptome in older adults

Yoshino, J., Smith, G. I., Kelly, S. C., Julliand, S., Reeds, D. N., & Mittendorfer, B. (2016) · Physiological Reports · doi:10.14814/phy2.12785 · Cited by 76 · see citing works

Impact of Mitophagy and Mitochondrial Unfolded Protein Response as New Adaptive Mechanisms Underlying Old Pathologies: Sarcopenia and Non-Alcoholic Fatty Liver Disease

Urbina-Varela, R., Castillo, N., Videla, L. A., & del Campo, A. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21207704 · Cited by 74 · see citing works

A neuromuscular perspective of sarcopenia pathogenesis: deciphering the signaling pathways involved

Moreira-Pais, A., Ferreira, R., Oliveira, P. A., & Duarte, J. A. (2022) · GeroScience · doi:10.1007/s11357-021-00510-2 · Cited by 74 · see citing works

Age‐related changes in the structure and function of mammalian neuromuscular junctions

Willadt, S., Nash, M., & Slater, C. R. (2017) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13521 · Cited by 68 · see citing works

Increased Adenine Nucleotide Degradation in Skeletal Muscle Atrophy

Miller, S. G., Hafen, P. S., & Brault, J. J. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms21010088 · Cited by 65 · see citing works

Blockade of Metallothioneins 1 and 2 Increases Skeletal Muscle Mass and Strength

Summermatter, S., Bouzan, A., Pierrel, E., Melly, S., Stauffer, D., Gutzwiller, S., Nolin, E., Dornelas, C., Fryer, C., Leighton-Davies, J., et al. (2017) · Molecular and Cellular Biology · doi:10.1128/mcb.00305-16 · Cited by 66 · see citing works

Alterations in the in vitro and in vivo regulation of muscle regeneration in healthy ageing and the influence of sarcopenia

Brzeszczyńska, J., Meyer, A. S., McGregor, R. A., Schilb, A., Degen, S., Tadini, V., Johns, N., LANGEN, R. C. J., Schols, A. M. W. J., Glass, D. J., et al. (2017) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12252 · Cited by 65 · see citing works

Integrated genomic and proteomic analyses identify stimulus-dependent molecular changes associated with distinct modes of skeletal muscle atrophy

Hunt, L. C., Graça, F. A., Pagala, V., Wang, Y., Li, Y., Yuan, Z., Fan, Y., Labelle, M., Peng, J., & Demontis, F. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109971 · Cited by 69 · see citing works

Neuromuscular impairment at different stages of human sarcopenia

Sarto, F., Franchi, M. V., McPhee, J. S., Stashuk, D. W., Paganini, M., Monti, E., Rossi, M., Sirago, G., Zampieri, S., Motanova, E. S., et al. (2024) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.13531 · Cited by 67 · see citing works

Slow or fast: Implications of myofibre type and associated differences for manifestation of neuromuscular disorders

Lloyd, E. M., Pinniger, G. J., Murphy, R. M., & Grounds, M. D. (2023) · Acta Physiologica · doi:10.1111/apha.14012 · Cited by 65 · see citing works

Skeletal muscle and childhood cancer: Where are we now and where we go from here

Goodenough, C. G., Partin, R. E., & Ness, K. K. (2021) · Aging and Cancer · doi:10.1002/aac2.12027 · Cited by 63 · see citing works

Sarcoglycan Alpha Mitigates Neuromuscular Junction Decline in Aged Mice by Stabilizing LRP4

Zhao, K., Shen, C., Li, L., Wu, H., Xing, G., Dong, Z., Jing, H., Chen, W., Zhang, H., Tan, Z., et al. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.0860-18.2018 · Cited by 59 · see citing works

Neuromuscular junctions are stable in patients with cancer cachexia

Boehm, I., Miller, J. D., Wishart, T. M., Wigmore, S. J., Skipworth, R. J. E., Jones, R. A., & Gillingwater, T. H. (2019) · Journal of Clinical Investigation · doi:10.1172/jci128411 · Cited by 63 · see citing works

Activating transcription factor 4 (ATF4) promotes skeletal muscle atrophy by forming a heterodimer with the transcriptional regulator C/EBPβ

Ebert, S. M., Bullard, S. A., Basisty, N., Marcotte, G. R., Skopec, Z. P., Dierdorff, J. M., Al‐Zougbi, A., Tomcheck, K. C., DeLau, A. D., Rathmacher, J. A., et al. (2020) · Journal of Biological Chemistry · doi:10.1074/jbc.ra119.012095 · Cited by 63 · see citing works

Short-term Low-Dose mTORC1 Inhibition in Aged Rats Counter-Regulates Age-Related Gene Changes and Blocks Age-Related Kidney Pathology

Shavlakadze, T., Zhu, J., Wang, S., Zhou, W., Morin, B., Egerman, M. A., Fan, L., Wang, Y., Iartchouk, O., Meyer, A., et al. (2018) · The Journals of Gerontology: Series A · doi:10.1093/gerona/glx249 · Cited by 59 · see citing works

Transcriptomic and epigenetic regulation of disuse atrophy and the return to activity in skeletal muscle

Fisher, A. G., Seaborne, R. A., Hughes, T. M., Gutteridge, A., Stewart, C., Coulson, J., Sharples, A., & Jarvis, J. (2017) · The FASEB Journal · doi:10.1096/fj.201700089rr · Cited by 54 · see citing works

Spermine oxidase maintains basal skeletal muscle gene expression and fiber size and is strongly repressed by conditions that cause skeletal muscle atrophy

Bongers, K. S., Fox, D. K., Kunkel, S. D., Stebounova, L. V., Murry, D. J., Pufall, M. A., Ebert, S. M., Dyle, M. C., Bullard, S. A., Dierdorff, J. M., et al. (2014) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00472.2014 · Cited by 61 · see citing works

High throughput screening of mitochondrial bioenergetics in human differentiated myotubes identifies novel enhancers of muscle performance in aged mice

Biesemann, N., Ried, J. S., Ding‐Pfennigdorff, D., Dietrich, A., Rudolph, C., Hahn, S., Hennerici, W., Asbrand, C., Leeuw, T., & Strübing, C. (2018) · Scientific Reports · doi:10.1038/s41598-018-27614-8 · Cited by 59 · see citing works

Resistance Training Enhances Skeletal Muscle Innervation Without Modifying the Number of Satellite Cells or their Myofiber Association in Obese Older Adults

Messi, M. L., Li, T., Wang, Z.-M., Marsh, A. P., Nicklas, B. J., & Delbono, O. (2015) · The Journals of Gerontology Series A · doi:10.1093/gerona/glv176 · Cited by 60 · see citing works

Mitochondrial Quality Control in Sarcopenia: Updated Overview of Mechanisms and Interventions

Liu, D., Fan, Y., Tao, X., Pan, W., Wu, Y., Wang, X., He, Y., Xiao, W., & Li, Y. (2021) · Aging and Disease · doi:10.14336/ad.2021.0427 · Cited by 60 · see citing works

Adaptive Remodeling of the Neuromuscular Junction with Aging

Deschenes, M. R., Flannery, R. E., Hawbaker, A., Patek, L. G., & Mifsud, M. (2022) · Cells · doi:10.3390/cells11071150 · Cited by 59 · see citing works

High mTORC1 signaling is maintained, while protein degradation pathways are perturbed in old murine skeletal muscles in the fasted state

White, Z. R., White, R. B., McMahon, C., Grounds, M. D., & Shavlakadze, T. (2016) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2016.06.012 · Cited by 59 · see citing works

Improvement of skeletal muscle performance in ageing by the metabolic modulator Trimetazidine

Ferraro, E., Pin, F., Gorini, S., Pontecorvo, L., Ferri, A., Mollace, V., Costelli, P., & Rosano, G. M. C. (2016) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12097 · Cited by 59 · see citing works

Biology of Activating Transcription Factor 4 (ATF4) and Its Role in Skeletal Muscle Atrophy

Ebert, S. M., Rasmussen, B. B., Judge, A. R., Judge, S. M., Larsson, L., Wek, R. C., Anthony, T. G., Marcotte, G. R., Miller, M. J., Yorek, M. A., et al. (2021) · Journal of Nutrition · doi:10.1093/jn/nxab440 · Cited by 61 · see citing works

The role of GDF11 in aging and skeletal muscle, cardiac and bone homeostasis

Egerman, M. A., & Glass, D. J. (2019) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.1080/10409238.2019.1610722 · Cited by 57 · see citing works

The translation of age-related body composition findings from rodents to humans

Pappas, L. E., & Nagy, T. R. (2018) · European Journal of Clinical Nutrition · doi:10.1038/s41430-018-0324-6 · Cited by 55 · see citing works

Mitofusin 2 Regulates Axonal Transport of Calpastatin to Prevent Neuromuscular Synaptic Elimination in Skeletal Muscles

Wang, L., Gao, J., Liu, J., Siedlak, S. L., Torres, S. L., Fujioka, H., Huntley, M. L., Jiang, Y., Ji, H., Yan, T., et al. (2018) · Cell Metabolism · doi:10.1016/j.cmet.2018.06.011 · Cited by 55 · see citing works

Transient systemic mtDNA damage leads to muscle wasting by reducing the satellite cell pool

Wang, X., Pickrell, A. M., Rossi, S. G., Pinto, M., Dillon, L. M., Hida, A., Rotundo, R. L., & Moraes, C. T. (2013) · Human Molecular Genetics · doi:10.1093/hmg/ddt251 · Cited by 54 · see citing works

Skeletal Muscle Degeneration and Regeneration in Mice and Flies

Rai, M., Nongthomba, U., & Grounds, M. D. (2014) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/b978-0-12-391498-9.00007-3 · Cited by 55 · see citing works

Effects of loaded voluntary wheel exercise on performance and muscle hypertrophy in young and old male C 57 B l/6 J mice

Soffe, Z., Radley‐Crabb, H. G., McMahon, C., Grounds, M. D., & Shavlakadze, T. (2015) · Scandinavian Journal of Medicine and Science in Sports · doi:10.1111/sms.12416 · Cited by 54 · see citing works

Gadd45a Protein Promotes Skeletal Muscle Atrophy by Forming a Complex with the Protein Kinase MEKK4

Bullard, S. A., Seo, S., Schilling, B., Dyle, M. C., Dierdorff, J. M., Ebert, S. M., DeLau, A. D., Gibson, B. W., & Adams, C. M. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.740308 · Cited by 56 · see citing works

Sarcopenia and Nutrition

Laviano, A., Gori, C. S., & Rianda, S. (2014) · Advances in food and nutrition research · doi:10.1016/b978-0-12-800270-4.00003-1 · Cited by 53 · see citing works

Integrated expression analysis of muscle hypertrophy identifies Asb2 as a negative regulator of muscle mass

Davey, J. R., Watt, K. I., Parker, B. L., Chaudhuri, R., Ryall, J. G., Cunningham, L., Qian, H., Sartorelli, V., Sandri, M., Chamberlain, J., et al. (2016) · JCI Insight · doi:10.1172/jci.insight.85477 · Cited by 51 · see citing works

Regrowth after skeletal muscle atrophy is impaired in aged rats, despite similar responses in signaling pathways

White, J., Confides, A. L., Moore-Reed, S. D., Hoch, J., & Dupont-Versteegden, E. (2015) · Experimental Gerontology · doi:10.1016/j.exger.2015.02.007 · Cited by 48 · see citing works

Genomic and Proteomic Profiling Reveals Reduced Mitochondrial Function and Disruption of the Neuromuscular Junction Driving Rat

(2016)

Article of Significant Interest Selected from This Issue by the Editors

(2012) · Molecular and Cellular Biology · doi:10.1128/mcb.01541-12

Mitochondrial pathways and sarcopenia in the geroscience era

Marzetti, E., Calvani, R., Coelho‐Júnior, H. J., & Picca, A. (2024) · The journal of nutrition health & aging · doi:10.1016/j.jnha.2024.100397 · Cited by 14 · see citing works

Molecular analyses provide insight into mechanisms underlying sarcopenia and myofibre denervation in old skeletal muscles of mice

Barns, M. E., Gondro, C., Tellam, R. L., Radley‐Crabb, H. G., Grounds, M. D., & Shavlakadze, T. (2014) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2014.04.025 · Cited by 84 · see citing works

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

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