The ubiquitin–proteasome system in regulation of the skeletal muscle homeostasis and atrophy: from basic science to disorders

Repertoires of Autophagy in the Pathogenesis of Ocular Diseases

Li, Y., Jiang, Q. L., Cao, G.-F., Yao, J., & Yan, B. (2015) · Cellular Physiology and Biochemistry · doi:10.1159/000373980 · Cited by 16,351

Induction of the Vitamin D Receptor Attenuates Autophagy Dysfunction-Mediated Cell Death Following Traumatic Brain Injury

Cui, C., Cui, J., Jin, F., Cui, Y., Li, R., Jiang, X., Tian, Y., Wang, R. C., Jiang, P., & Gao, J. (2017) · Cellular Physiology and Biochemistry · doi:10.1159/000479571 · Cited by 5,214

p62/SQSTM1 Binds Directly to Atg8/LC3 to Facilitate Degradation of Ubiquitinated Protein Aggregates by Autophagy

Pankiv, S., Clausen, T. H., Lamark, T., Brech, A., Bruun, J.-A., Outzen, H., Øvervatn, A., Bjørkøy, G., & Johansen, T. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m702824200 · Cited by 4,578

The Ubiquitin-Proteasome Proteolytic Pathway: Destruction for the Sake of Construction

Glickman, M. H., & Ciechanover, A. J. (2002) · Physiological Reviews · doi:10.1152/physrev.00027.2001 · Cited by 4,304

Autophagy regulates lipid metabolism

Singh, R., Kaushik, S., Wang, Y., Xiang, Y., Novak, I., Komatsu, M., Tanaka, K., Cuervo, A. M., & Czaja, M. J. (2009) · Nature · doi:10.1038/nature07976 · Cited by 3,975

Identification of ubiquitin ligases required for skeletal muscle atrophy.

Bodine, S. C., Latres, E., Baumhueter, S., Lai, V. K.-M., Nunez, L., Clarke, B. A., Poueymirou, W. T., Panaro, F. J., Na, E., Dharmarajan, K., et al. (2001) · Science · doi:10.1126/science.1065874 · Cited by 3,521

Foxo transcription factors induce the atrophy-related ubiquitin ligase atrogin-1 and cause skeletal muscle atrophy.

Sandri, M., Sandri, C., Gilbert, A., Skurk, C., Calabria, E., Picard, A., Walsh, K., Schiaffino, S., Lecker, S. H., & Goldberg, A. L. (2004) · Cell · doi:10.1016/s0092-8674(04)00400-3 · Cited by 3,012

The role of autophagy during the early neonatal starvation period

Kuma, A., Hatano, M., Matsui, M., Yamamoto, A., Nakaya, H., Yoshimori, T., Ohsumi, Y., Tokuhisa, T., & Mizushima, N. (2004) · Nature · doi:10.1038/nature03029 · Cited by 2,865

Mitochondrial dysfunction: roles in skeletal muscle atrophy

Chen, X., Ji, Y., Liu, R., Zhu, X., Wang, K., Yang, X., Liu, B., Gao, Z., Huang, Y. H., Shen, Y., et al. (2023) · Journal of Translational Medicine · doi:10.1186/s12967-023-04369-z · Cited by 362

Cancer cachexia: molecular mechanisms and treatment strategies

Setiawan, T., Sari, I. N., Wijaya, Y. T., Julianto, N. M., Muhammad, J. A., Lee, H., Chae, J. H., & Kwon, H. Y. (2023) · Journal of Hematology & Oncology · doi:10.1186/s13045-023-01454-0 · Cited by 342

Inflammation: Roles in Skeletal Muscle Atrophy

Ji, Y., Li, M., Chang, M., Liu, R., Qiu, J., Wang, K., Deng, C., Shen, Y., Zhu, J., Wang, W., et al. (2022) · Antioxidants · doi:10.3390/antiox11091686 · Cited by 329

Chronic critical illness and post-intensive care syndrome: from pathophysiology to clinical challenges

Voiriot, G., Oualha, M., Pierre, A., Salmon-Gandonnière, C., Gaudet, A., Jouan, Y., Kallel, H., Radermacher, P., Vodovar, D., Sarton, B., et al. (2022) · Annals of Intensive Care · doi:10.1186/s13613-022-01038-0 · Cited by 229

Mitochondrial dysfunction and skeletal muscle atrophy: Causes, mechanisms, and treatment strategies

Kubat, G. B., Bouhamida, E., Ülger, Ö., Türkel, İ., Pedriali, G., Ramaccini, D., Ekinci, Ö., Özerkliğ, B., Atalay, Ö., Patergnani, S., et al. (2023) · Mitochondrion · doi:10.1016/j.mito.2023.07.003 · Cited by 134

Diabetic Muscular Atrophy: Molecular Mechanisms and Promising Therapies

Shen, Y., Li, M., Wang, K., Qi, G., Liu, H., Wang, W., Ji, Y., Chang, M., Deng, C., Xu, F., et al. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.917113 · Cited by 104

Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting

Henrot, P., Dupin, I., Schilfarth, P., Esteves, P., Blervaque, L., Zysman, M., Gouzi, F., Hayot, M., Pomiès, P., & Berger, P. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24076454 · Cited by 85

The Effect of Omega-3 Fatty Acids on Sarcopenia: Mechanism of Action and Potential Efficacy

Therdyothin, A., Phiphopthatsanee, N., & Isanejad, M. (2023) · Marine Drugs · doi:10.3390/md21070399 · Cited by 85

Design and synthesis of new 4-(2-nitrophenoxy)benzamide derivatives as potential antiviral agents: molecular modeling and in vitro antiviral screening

Abdallah, A. E., Alesawy, M. S., Eissa, S. I., El‐Fakharany, E. M., Kalaba, M. H., Sharaf, M. H., Shama, N. M. A., Mahmoud, S. H., Mostafa, A., Al-Karmalawy, A. A., et al. (2021) · New Journal of Chemistry · doi:10.1039/d1nj02710g · Cited by 60

The metabolite butyrate produced by gut microbiota inhibits cachexia-associated skeletal muscle atrophy by regulating intestinal barrier function and macrophage polarization

Liu, H., Xi, Q., Tan, S., Qu, Y., Meng, Q., Zhang, Y., Cheng, Y.-X., & Wu, G. (2023) · International Immunopharmacology · doi:10.1016/j.intimp.2023.111001 · Cited by 54

Monotropein Improves Dexamethasone-Induced Muscle Atrophy via the AKT/mTOR/FOXO3a Signaling Pathways

Wang, P., Kang, S. Y., Kim, S. J., Park, Y., & Jung, H. W. (2022) · Nutrients · doi:10.3390/nu14091859 · Cited by 49

Sarcopenia and cachexia: molecular mechanisms and therapeutic interventions

Wang, T., Zhou, D., & Hong, Z. (2025) · MedComm · doi:10.1002/mco2.70030 · Cited by 46

The effects of omega-3 polyunsaturated fatty acids on muscle and whole-body protein synthesis: a systematic review and meta-analysis

Therdyothin, A., Prokopidis, K., Galli, F., Witard, O. C., & Isanejad, M. (2024) · Nutrition Reviews · doi:10.1093/nutrit/nuae055 · Cited by 45

Partial replacement of soybean meal by yellow mealworm (Tenebrio molitor) meal influences the flesh quality of Nile tilapia (Oreochromis niloticus)

Zhang, L., Wu, H., Li, W., Qiao, F., Zhang, W., Du, Z., & Zhang, M. (2022) · Animal nutrition · doi:10.1016/j.aninu.2022.09.007 · Cited by 42

Lactobacillus rhamnosus JY02 Ameliorates Sarcopenia by Anti-Atrophic Effects in a Dexamethasone-Induced Cellular and Murine Model

Lee, J., Kang, M., Yoo, J., Lee, S., Kang, M., Yun, B., Kim, J. N., Moon, H., Chung, Y., & Oh, S. (2023) · Journal of Microbiology and Biotechnology · doi:10.4014/jmb.2303.03001 · Cited by 37

The Current Landscape of Pharmacotherapies for Sarcopenia

Bahat, G., & Özkök, S. (2024) · Drugs & Aging · doi:10.1007/s40266-023-01093-7 · Cited by 41

Skeletal muscle atrophy after sciatic nerve damage: Mechanistic insights

Yadav, A., & Dabur, R. (2024) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2024.176506 · Cited by 38

Molecular Regulation of Skeletal Muscle Growth and Organelle Biosynthesis: Practical Recommendations for Exercise Training

Solsona, R., Pavlin, L., Bernardi, H., & Sanchez, A. M. J. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22052741 · Cited by 42

Chemotherapy-Induced Molecular Changes in Skeletal Muscle

Pedrosa, M. B., Barbosa, S., Vitorino, R. M. P., Ferreira, R. M., Moreira‐Gonçalves, D., & Santos, L. L. (2023) · Biomedicines · doi:10.3390/biomedicines11030905 · Cited by 44

Invited review: Muscle protein breakdown and its assessment in periparturient dairy cows

Sadri, H., Ghaffari, M. H., & Sauerwein, H. (2022) · Journal of Dairy Science · doi:10.3168/jds.2022-22068 · Cited by 43

Ventilator‐induced diaphragm dysfunction: phenomenology and mechanism(s) of pathogenesis

Powers, S. K. (2024) · The Journal of Physiology · doi:10.1113/jp283860 · Cited by 35

Muscle weakness after critical illness: unravelling biological mechanisms and clinical hurdles

Pierre, A., Favory, R., Bourel, C., Howsam, M., Romien, R., Lancel, S., & Préau, S. (2025) · Critical Care · doi:10.1186/s13054-025-05462-z · Cited by 39

Firearms-related skeletal muscle trauma: pathophysiology and novel approaches for regeneration

Moriscot, A. S., Miyabara, E. H., Langeani, B., Belli, A., Egginton, S., & Bowen, T. S. (2021) · npj Regenerative Medicine · doi:10.1038/s41536-021-00127-1 · Cited by 36

Molecular mechanisms of post‐burn muscle wasting and the therapeutic potential of physical exercise

Dombrecht, D., Daele, U. V., Asbroeck, B. V., Schieffelers, D. R., Guns, P., Gebruers, N., Meirte, J., & van Breda, E. (2023) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.13188 · Cited by 28

Inflammation o'clock: interactions of circadian rhythms with inflammation‐induced skeletal muscle atrophy

da Silva, F. M., Esser, K. A., Murach, K. A., & Greene, N. P. (2023) · The Journal of Physiology · doi:10.1113/jp284808 · Cited by 31

Vitamin D Impacts on Skeletal Muscle Dysfunction in Patients with COPD Promoting Mitochondrial Health

Russo, C., Valle, M. S., Casabona, A., Spicuzza, L., Sambataro, G., & Malaguarnera, L. (2022) · Biomedicines · doi:10.3390/biomedicines10040898 · Cited by 32

Deciphering Immune Landscape Remodeling Unravels the Underlying Mechanism for Synchronized Muscle and Bone Aging

Yin, P., Chen, M., Rao, M., Lin, Y., Zhang, M., Xu, R., Hu, X., Chen, R., Chai, W., Huang, X., et al. (2023) · Advanced Science · doi:10.1002/advs.202304084 · Cited by 29

Nutrient weight against sarcopenia: regulation of the IGF-1/PI3K/Akt/FOXO pathway in quinoa metabolites

Liu, P., Hu, Y., Wang, M.-J., & Kang, L. (2021) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2021.10.001 · Cited by 25

The Inhibition of Autophagy and Pyroptosis by an Ethanol Extract of Nelumbo nucifera Leaf Contributes to the Amelioration of Dexamethasone-Induced Muscle Atrophy

Park, E., Choi, H., Truong, C.-S., & Jun, H. (2023) · Nutrients · doi:10.3390/nu15040804 · Cited by 23

Mechanotransduction and Skeletal Muscle Atrophy: The Interplay Between Focal Adhesions and Oxidative Stress

Kamal, K. Y., & Trombetta-Lima, M. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26062802 · Cited by 25

USP18 is an essential regulator of muscle cell differentiation and maturation

Olie, C. S., Pinto-Fernández, A., Damianou, A., Vendrell, I., Mei, H., den Hamer, B., van der Wal, E., de Greef, J. C., Aronica, E., Raz, V., et al. (2023) · Cell Death and Disease · doi:10.1038/s41419-023-05725-z · Cited by 21

Sporadic Inclusion Body Myositis at the Crossroads between Muscle Degeneration, Inflammation, and Aging

Guglielmi, V., Cheli, M., Tonin, P., & Vattemi, G. N. A. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25052742 · Cited by 21

The role of exercise-induced short-chain fatty acids in the gut–muscle axis: implications for sarcopenia prevention and therapy

Fang, J., Yan, W., Sun, X., & Chen, J. (2025) · Frontiers in Microbiology · doi:10.3389/fmicb.2025.1665551 · Cited by 23

Biomarkers of Skeletal Muscle Atrophy Based on Atrogenes Evaluation: A Systematic Review and Meta-Analysis Study

Gouvêa, A. L., Alves, A. L. R., Martinez, C. G., Sousa, J., & Kurtenbach, E. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26083516 · Cited by 22

Inflammation and Oxidative Stress as Common Mechanisms of Pulmonary, Autonomic and Musculoskeletal Dysfunction after Spinal Cord Injury

Rosales-Antequera, C., Viscor, G., & Araneda, O. F. (2022) · Biology · doi:10.3390/biology11040550 · Cited by 20

Impact of cancer cachexia on respiratory muscle function and the therapeutic potential of exercise

Murphy, B. T., Mackrill, J. J., & O’Halloran, K. D. (2022) · The Journal of Physiology · doi:10.1113/jp283569 · Cited by 20

A Ketogenic Diet in Combination with Gemcitabine Mitigates Pancreatic Cancer-Associated Cachexia in Male and Female KPC Mice

Cortez, N. E., Pathak, S. J., Lanzi, C. R., Hong, B. V., Sule, R. O., Crone, R., Wang, F., Chen, S., Gomes, A. V., Baar, K., et al. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241310753 · Cited by 19

Physiological Overview of the Potential Link between the UPS and Ca2+ Signaling

Lee, D., & Hong, J. H. (2022) · Antioxidants · doi:10.3390/antiox11050997 · Cited by 19

PSMA2 knockdown impacts expression of proteins involved in immune and cellular stress responses in human lung cells

Rashid, M., Lorzadeh, S., Gao, A., Ghavami, S., & Coombs, K. M. (2022) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2022.166617 · Cited by 19

Gintonin-enriched fraction protects against sarcopenic obesity by promoting energy expenditure and attenuating skeletal muscle atrophy in high-fat diet-fed mice

Jin, H., Oh, H., Nah, S.-Y., & Lee, B.-Y. (2021) · Journal of Ginseng Research · doi:10.1016/j.jgr.2021.10.003 · Cited by 17

Early postmortem muscle proteome and metabolome of beef longissimus thoracis muscle classified by pH at 6 hours postmortem

Schulte, M. D., Hochmuth, K. G., Steadham, E. M., Lonergan, S. M., Hansen, S. L., & Huff-Lonergan, E. J. (2022) · Journal of Proteomics · doi:10.1016/j.jprot.2022.104756 · Cited by 17

The role of non-coding RNAs in muscle aging: regulatory mechanisms and therapeutic potential

Shin, Y. J., Kwon, K., Suh, Y., & Lee, K. (2024) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2023.1308274 · Cited by 16

Selenium Status Affects Hypertrophic Growth of Skeletal Muscle in Growing Zebrafish by Mediating Protein Turnover

Wang, L., Yin, J., Zhang, F., Yu, H., Chen, F.-F., Zhang, Z.-Y., & Zhang, X. (2021) · Journal of Nutrition · doi:10.1093/jn/nxab082 · Cited by 16

Laurel Attenuates Dexamethasone-Induced Skeletal Muscle Atrophy In Vitro and in a Rat Model

Jia, H., Yamashita, T., Li, X., & Kato, H. (2022) · Nutrients · doi:10.3390/nu14102029 · Cited by 17

Umbelliferone attenuates diabetic sarcopenia by modulating mitochondrial quality and the ubiquitin-proteasome system

Kim, D., Kang, Y.-H., & Kang, M. (2025) · Phytomedicine · doi:10.1016/j.phymed.2025.156930 · Cited by 15

Transcriptome sequencing and analysis reveals the molecular mechanism of skeletal muscle atrophy induced by denervation

Chen, X., Li, M., Chen, B., Wang, W., Zhang, L., Ji, Y., Chen, Z., Ni, X., Shen, Y., & Sun, H. (2021) · Annals of Translational Medicine · doi:10.21037/atm-21-1230 · Cited by 14

Inclusion Body Myositis and Neoplasia: A Narrative Review

Damian, L. O., Login, C., Solomon, C. M., Belizna, C. C., Encică, S., Urian, L. G., Jurcuț, C., Stancu, B., & Vulturar, R. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23137358 · Cited by 15

Resistance training-induced changes in muscle proteolysis and extracellular matrix remodeling biomarkers in the untrained and trained states

Scarpelli, M. C., Bergamasco, J. G. A., Godwin, J. S., Mesquita, P. H. C., Chaves, T. S., da Silva, D. G., Bittencourt, D., Dias, N. F., Medalha, R. A., Filho, P. C. C., et al. (2024) · European Journal of Applied Physiology · doi:10.1007/s00421-024-05484-5 · Cited by 14

Lifelong dietary protein restriction induces denervation and skeletal muscle atrophy in mice

Ersoy, U., Altinpinar, A. E., Kanakis, I., Alameddine, M., Gioran, A., Chondrogianni, N., Ozanne, S. E., Peffers, M. J., Jackson, M. J., Goljanek‐Whysall, K., et al. (2024) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2024.09.005 · Cited by 14

Advancing insights into microgravity induced muscle changes using Caenorhabditis elegans as a model organism

Beckett, L., Williams, P. M., Toh, L. S., Hessel, V., Gerstweiler, L., Fisk, I. D., Toronjo‐Urquiza, L., & Chauhan, V. M. (2024) · npj Microgravity · doi:10.1038/s41526-024-00418-z · Cited by 14

Cardiac proteostasis in obesity and cardiovascular disease

Guerra, J., Matta, L., & Bartelt, A. (2024) · Herz · doi:10.1007/s00059-024-05233-6 · Cited by 12

The “Sunshine Vitamin” and Its Antioxidant Benefits for Enhancing Muscle Function

Russo, C., Santangelo, R., Malaguarnera, L., & Valle, M. S. (2024) · Nutrients · doi:10.3390/nu16142195 · Cited by 12

Mechanisms and therapeutic strategies for NLRP3 degradation via post-translational modifications in ubiquitin-proteasome and autophagy lysosomal pathway

Su, K., Tang, M., Wu, J., Ye, N., Jiang, X., Zhao, M., Zhang, R., Cai, X., Zhang, X., Lin, L., et al. (2025) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2025.117476 · Cited by 12

Conditioned Generative Modeling of Molecular Glues: A Realistic AI Approach for Synthesizable Drug-like Molecules

Islam, N. N., & Caulfield, T. R. (2025) · Biomolecules · doi:10.3390/biom15060849 · Cited by 12

Moderating AKT signaling with baicalein protects against weight loss by preventing muscle atrophy in a cachexia model caused by CT26 colon cancer

Song, G., Park, W. Y., Jiao, W., Park, J. Y., Jung, S. J., Ma, S., Lee, J., Lee, K. Y., Choe, S., Park, J., et al. (2024) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2024.119670 · Cited by 12

Understanding the biology of volumetric muscle loss for an individualized exercise rehabilitation approach in breast cancer patients

Invernizzi, M., Venetis, K., Sajjadi, E., Piciotti, R., Alessandro de, S. I. R. E., & Fusco, N. (2021) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2021.03.007 · Cited by 13

The protective effect of cannabinoids against colorectal cancer cachexia through modulation of inflammation and immune responses

Ng, S.-K., Chung, D.-J., Chang, L., Luo, C.-K., Jwo, S.-H., Lee, Y.-H., Lin, J., Wang, C., & Wei, T.-T. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.114467 · Cited by 12

2-D08 treatment regulates C2C12 myoblast proliferation and differentiation via the Erk1/2 and proteasome signaling pathways

Liu, H., Lee, S.-M., & Joung, H. (2021) · Journal of Muscle Research and Cell Motility · doi:10.1007/s10974-021-09605-x · Cited by 11

A Bioassay-Guided Fractionation of Rosemary Leaf Extract Identifies Carnosol as a Major Hypertrophy Inducer in Human Skeletal Muscle Cells

Morel, S., Hugon, G., Vitou, M., Védère, M., Fons, F., Rapior, S., Saint, N., & Carnac, G. (2021) · Nutrients · doi:10.3390/nu13124190 · Cited by 12

N-Acetylcysteine Attenuates Sepsis-Induced Muscle Atrophy by Downregulating Endoplasmic Reticulum Stress

Chen, R., Zheng, Y., Zhou, C., Dai, H., Wang, Y.-R., Chu, Y., & Luo, J. (2024) · Biomedicines · doi:10.3390/biomedicines12040902 · Cited by 10

A Novel Muscle Atrophy Mechanism: Myocyte Degeneration Due to Intracellular Iron Deprivation

Suh, D. K., Lee, W.-Y., Yeo, W. J., Kyung, B. S., Jung, K. W., Seo, H. K., Lee, Y.-S., & Suh, D. W. (2022) · Cells · doi:10.3390/cells11182853 · Cited by 12

The Gentle Side of the UPS: Ubiquitin-Proteasome System and the Regulation of the Myogenic Program

Olguín, H. C. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.821839 · Cited by 11

Little involvement of recycled-amino acids from proteasomal proteolysis in de novo protein synthesis

Osana, S., Kitajima, Y., Naoki, S., Takada, H., Murayama, K., Kano, Y., & Nagatomi, R. (2022) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2022.09.113 · Cited by 11

Pathomechanistic Networks of Motor System Injury in Amyotrophic Lateral Sclerosis

Dey, B., Kumar, A., & Patel, A. B. (2023) · Current Neuropharmacology · doi:10.2174/1570159x21666230824091601 · Cited by 9

Artificial neural network inference analysis identified novel genes and gene interactions associated with skeletal muscle aging

Tarum, J., Ball, G., Gustafsson, T. P., Altun, M., & Santos, L. (2024) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.13562 · Cited by 11

Transcriptome analysis of muscle atrophy in Leizhou black goats: identification of key genes and insights into limb-girdle muscular dystrophy

Wang, K., Xu, M., Han, X., Liu, H., Han, J., Sun, W., & Zhou, H. (2025) · BMC Genomics · doi:10.1186/s12864-025-11282-w · Cited by 9

Impaired proteostasis in obese skeletal muscle relates to altered immunoproteasome activity

Fletcher, E., Wiggs, M. P., Greathouse, K. L., Morgan, G. B., & Gordon, P. M. (2022) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/apnm-2021-0764 · Cited by 9

Carcass composition, meat quality, leg muscle status, and its mRNA expression profile in broilers affected by valgus-varus deformity

Cai, C., Zhang, L., Liu, X., Li, J., Ma, Y., Jiang, R., Li, Z., Li, G., Tian, Y., Kang, X., et al. (2023) · Poultry Science · doi:10.1016/j.psj.2023.102682 · Cited by 9

LPS-Induced Modifications in Macrophage Transcript and Secretion Profiles Are Linked to Muscle Wasting and Glucose Intolerance

Ryu, H., Jeong, H. H., Lee, S., Lee, M., Kim, M., & Lee, B. (2023) · Journal of Microbiology and Biotechnology · doi:10.4014/jmb.2309.09037 · Cited by 8

Antioxidative effects of vitamin D in muscle dysfunction

Russo, C., Valle, M. S., & Malaguarnera, L. (2023) · Redox Experimental Medicine · doi:10.1530/rem-23-0013 · Cited by 9

Deubiquitinases in muscle physiology and disorders

Olie, C. S., O'Brien, D. P., Jones, H. B. L., Liang, Z., Damianou, A., Sur‐Erdem, İ., Pinto-Fernández, A., Raz, V., & Kessler, B. M. (2024) · Biochemical Society Transactions · doi:10.1042/bst20230562 · Cited by 8

Dominantly inherited muscle disorders: understanding their complexity and exploring therapeutic approaches

Findlay, A. R. (2024) · Disease Models & Mechanisms · doi:10.1242/dmm.050720 · Cited by 9

IL-6 Promotes Muscle Atrophy by Increasing Ubiquitin–Proteasome Degradation of Muscle Regeneration Factors After Cerebral Infarction in Rats

Chen, F., Fu, J., & Feng, H. (2025) · NeuroMolecular Medicine · doi:10.1007/s12017-024-08825-x · Cited by 8

The aminopeptidase LAP3 suppression accelerates myogenic differentiation via the AKT‐TFE3 pathway in C2C12 myoblasts

Osana, S., Kitajima, Y., Naoki, S., Murayama, K., Takada, H., Tabuchi, A., Kano, Y., & Nagatomi, R. (2023) · Journal of Cellular Physiology · doi:10.1002/jcp.31070 · Cited by 8

The E3 ubiquitin ligase Nedd4L preserves skeletal muscle stem cell quiescence by inhibiting their activation

Blackburn, D. M., Sahinyan, K., Hernández-Corchado, A., Lazure, F., Richard, V. R., Raco, L., Perron, G., Zahedi, R. P., Borchers, C. H., Lepper, C., et al. (2024) · iScience · doi:10.1016/j.isci.2024.110241 · Cited by 7

Coumestrol attenuates dexamethasone-induced muscle atrophy via AMPK-FOXO1/3 signaling

Hah, Y., Lee, W. K., Lee, S.-Y., Seo, J.-H., Kim, E. J., Choe, Y.-I., Kim, S. G., & Yoo, J. (2022) · Journal of Functional Foods · doi:10.1016/j.jff.2022.105387 · Cited by 8

circAGO3 facilitates NF-κB pathway-mediated inflammatory atrophy in chicken skeletal muscle via the miR-34b-5p/TRAF3 axis

Zhao, X., Tang, S., Lei, Z., Shen, X., Zhang, Y., Han, S., Yin, H., & Cui, C. (2024) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2024.137614 · Cited by 8

Identification of differentially expressed genes and SNPs linked to harvest body weight of genetically improved rohu carp, Labeo rohita

Nandanpawar, P. C., Sahoo, L., Sahoo, B., Murmu, K., Chaudhari, A., Kumar, A., & Das, P. (2023) · Frontiers in Genetics · doi:10.3389/fgene.2023.1153911 · Cited by 7

Effects of C-Peptide on Dexamethasone-Induced In Vitro and In Vivo Models as a Potential Therapeutic Agent for Muscle Atrophy

Kim, J., Yang, Y.-M., Choi, E., Lee, S., & Choi, J. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms242015433 · Cited by 6

Current understanding on the role of proteolysis on meat quality

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