Denervation-activated STAT3–IL-6 signalling in fibro-adipogenic progenitors promotes myofibres atrophy and fibrosis

Targeting the IL-6/JAK/STAT3 signalling axis in cancer

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Muscle injury activates resident fibro/adipogenic progenitors that facilitate myogenesis

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Stem Cell Function, Self-Renewal, and Behavioral Heterogeneity of Cells from the Adult Muscle Satellite Cell Niche

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Mesenchymal progenitors distinct from satellite cells contribute to ectopic fat cell formation in skeletal muscle

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Interleukin-6 Is an Essential Regulator of Satellite Cell-Mediated Skeletal Muscle Hypertrophy

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Type 2 Innate Signals Stimulate Fibro/Adipogenic Progenitors to Facilitate Muscle Regeneration

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Interleukin‐6 myokine signaling in skeletal muscle: a double‐edged sword?

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Nilotinib reduces muscle fibrosis in chronic muscle injury by promoting TNF-mediated apoptosis of fibro/adipogenic progenitors

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Regulation of Muscle Growth and Regeneration by the Immune System

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The role of pyocyanin in Pseudomonas aeruginosa infection

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Facioscapulohumeral Disease as a myodevelopmental disease: Applying Ockham’s razor to its various features

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IL-33-ST2 signaling in fibro-adipogenic progenitors alleviates immobilization-induced muscle atrophy in mice

Takahashi, Y., Yoda, M., Tsuji, O., Horiuchi, K., Watanabe, K., & Nakamura, M. (2024) · Skeletal Muscle · doi:10.1186/s13395-024-00338-2 · Cited by 6

Transcriptome Analysis of Differentially Expressed Genes and Molecular Pathways Involved in C2C12 Cells Myogenic Differentiation

Tao, L., Huang, W., Li, Z., Wang, W., Lei, X., Chen, J., Song, X., Lu, F., Fan, S., & Zhang, L. (2024) · Molecular Biotechnology · doi:10.1007/s12033-024-01259-7 · Cited by 6

Aging impairs skeletal muscle regeneration by promoting fibro/fatty degeneration and inhibiting inflammation resolution via fibro-adipogenic progenitorsPreprint

García‐Carrizo, F., Gohlke, S., Lenihan-Geels, G. N., Jank, A., Leer, M., Soultoukis, G. A., Oveisi, M., Herpich, C., Garrido, C. A., Kotsaris, G., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.11.27.568776 · Cited by 5

Notoginsenoside R2 attenuates hepatic fibrosis via STAT3-dependent hepatic stellate cells senescence induction and inflammatory microenvironment suppression

Deng, K., Li, M., Li, Y., Xiang, L., Wang, Y., Shi, H., Cheng, J., Huang, S., & Lv, Z. (2025) · Journal of Ginseng Research · doi:10.1016/j.jgr.2025.05.007 · Cited by 5

Pdgfrα+ stromal cells, a key regulator for tissue homeostasis and dysfunction in distinct organs

Kang, X., Zhao, K., Huang, Z., Fukada, S., Qi, X., & Miao, H. (2024) · Genes & Diseases · doi:10.1016/j.gendis.2024.101264 · Cited by 5

Sympathetic innervation maintains the murine quiescent skeletal muscle stem cell pool via perivascular-derived Angpt1

Rotini, A., Berthier, J., Martínez‐Sarrà, E., Berge, G., Ozturk, T., Koumaiha, Z., Didier, N., Salucci, S., Stettler, O., Gervais, M., et al. (2025) · Developmental Cell · doi:10.1016/j.devcel.2025.07.006 · Cited by 6

Exercised cytokines promote endurance

Correia, J. C., & Ruas, J. L. (2020) · Science · doi:10.1126/science.abb4116 · Cited by 5

Tendon Aging: A Silent Enemy Revealed Strategies for Effective Treatment

Gu, W., Wang, G., Zhang, H., & Yu, Y. (2025) · Aging Medicine · doi:10.1002/agm2.70027 · Cited by 4

Tenascin-C from the tissue microenvironment promotes muscle stem cell maintenance and function through Annexin A2

Cecchini, A., Loreti, M., Kaufman, C. D., Stamenkovic, C., Guarnaccia, G., Renero, A., Nicoletti, C., Kervadec, A., Mayer, D., Delaware, S., et al. (2025) · Communications Biology · doi:10.1038/s42003-025-09189-z · Cited by 7

Exercise mitigates IL-27-induced muscle atrophy following myocardial infarction through anti-inflammatory mechanisms

Li, Y., Yin, G., Li, S., Zheng, Q., Jiang, Y., Li, C., Yang, L., Li, H., Chen, X., Yang, P., et al. (2026) · Journal of Translational Medicine · doi:10.1186/s12967-025-07527-7 · Cited by 4

Biotoxins in muscle regeneration research

Mahdy, M. A. A. (2019) · Journal of Muscle Research and Cell Motility · doi:10.1007/s10974-019-09548-4 · Cited by 4

It’s not all about muscle: fibroadipogenic progenitors contribute to facioscapulohumeral muscular dystrophy

Serra, C., & Wagner, K. R. (2020) · Journal of Clinical Investigation · doi:10.1172/jci136133 · Cited by 4

Fibro-adipogenesis in Injured Rotator Cuff Muscle

Subhash, A. K., Davies, M., Gatto, A. P., Bogdanov, J. M., Lan, R., Jensen, A. R., Feeley, B. T., & Petrigliano, F. A. (2022) · Current Tissue Microenvironment Reports · doi:10.1007/s43152-021-00033-0 · Cited by 4

Muscle stem cell niche dynamics during muscle homeostasis and regeneration

Yin, Y., He, G. J., Hu, S., Tse, E. H. Y., & Cheung, T. H. (2024) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2024.02.008 · Cited by 4

Sunitinib-mediated inhibition of STAT3 in skeletal muscle and spinal cord does not affect the disease in a mouse model of ALS

Tortarolo, M., Cecconi, A. D. R., Camporeale, L., Margotta, C., Nardo, G., Pasetto, L., Bonetto, V., Galbiati, M., Crippa, V., Poletti, A., et al. (2024) · Neurobiology of Disease · doi:10.1016/j.nbd.2024.106576 · Cited by 4

Reawakening GDNF's regenerative past in mice and humans

Samos, A., McGaughey, V., Rieger, S., & Lisse, T. S. (2022) · Regenerative Therapy · doi:10.1016/j.reth.2022.03.008 · Cited by 3

Regenerating motor neurons prime muscle stem cells for myogenesis by enhancing protein synthesis and mitochondrial bioenergeticsPreprint

Choi, J. J., Shin, E. J., Han, W. M., Anderson, S. E., Mohiuddin, M., Lee, N. H., Trần, T. H., Nakhai, S. A., Jeong, H., Shcherbina, A., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.05.24.113456 · Cited by 4

Single‐nucleus transcriptomics reveals subsets of degenerative myonuclei after rotator cuff tear‐induced muscle atrophy

Sun, Z., Cheng, X., Wang, Z., Qiao, C., Qian, H., Yuan, T., Lv, Z., Sun, W., Zhang, H., Liu, Y., et al. (2024) · Cell Proliferation · doi:10.1111/cpr.13763 · Cited by 5

Interleukin Networks in GVHD: Mechanistic Crosstalk, Therapeutic Targeting, and Emerging Paradigms

Niu, Y., Liu, C., Li, P., Zhao, J., Jin, J., & Yang, J. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26178620 · Cited by 3

Molecular basis of muscle wasting and emerging therapeutic strategies targeting degenerative muscle disorders

Jude, M., Rajasingh, S., Alway, S. E., & Rajasingh, J. (2026) · Experimental Cell Research · doi:10.1016/j.yexcr.2026.114969 · Cited by 4

Biochemical dissection of STAT3 signaling in amyotrophic lateral sclerosis

Apolloni, S., & D’Ambrosi, N. (2024) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-24-00862 · Cited by 3

Deciphering the role of IGFBP5 in delaying fibrosis and sarcopenia in aging skeletal muscle: therapeutic implications and molecular mechanisms

Shi, L., Ding, Z., & Chen, J. (2025) · Frontiers in Pharmacology · doi:10.3389/fphar.2025.1557703 · Cited by 3

Modulation of the JAK2-STAT3 pathway promotes expansion and maturation of human iPSC-derived myogenic progenitor cells

Caputo, L., Stamenkovic, C., Tierney, M. T., Cecchini, A., Nicolau, M., Guarnaccia, G., Barajas, J. R., Falzarano, M. S., Bassel‐Duby, R., Ferlini, A., et al. (2025) · Stem Cell Reports · doi:10.1016/j.stemcr.2025.102692 · Cited by 3

The Impact of Cervical Multifidus Sarcopenia on Outcomes After Laminoplasty for Cervical Ossification of the Posterior Longitudinal Ligament

Zhao, Y., Tian, Y., Sun, D., Zhang, J., & Cai, S. (2025) · Journal of Bone and Joint Surgery · doi:10.2106/jbjs.25.00685 · Cited by 3

Distinct human skeletal muscle-derived CD90 progenitor subsets for myo-fibro-adipogenic disease modeling and treatment in multiplexed conditions

Li, A., Anbuchelvan, M., Fathi, A. T., Abu-Zahra, M., Evseenko, D. A., Petrigliano, F. A., & Dar, A. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1173794 · Cited by 3

Dystrophin S3059 phosphorylation partially attenuates denervation atrophy in mouse tibialis anterior muscles

Swiderski, K., Naim, T., Trieu, J., Chee, A., Herold, M. J., Kueh, A. J., Goodman, C. A., Gregorevic, P., & Lynch, G. S. (2024) · Physiological Reports · doi:10.14814/phy2.16145 · Cited by 3

Changes in strength performance of highly trained athletes after COVID-19

Cao, J., Sheng-tao, Y., Wang, J., & Zhang, P. (2024) · PLoS ONE · doi:10.1371/journal.pone.0308955 · Cited by 3

Coronavirus disease and the musculoskeletal system

Daher, M., & Sebaaly, A. (2022) · The Egyptian Orthopaedic Journal · doi:10.4103/eoj.eoj_34_22 · Cited by 3

Tissue-resident skeletal muscle macrophages promote recovery from viral pneumonia-induced sarcopenia in normal agingPreprint

Runyan, C. E., Luo, L., Welch, L. C., Lu, Z., Chen, F., Schleck, M. J., Nafikova, R. A., Grant, R. A., Aillon, R. P., Senkow, K. J., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.01.09.631996 · Cited by 4

HO-1 Suppression by Co-Culture-Derived IL-6 Alleviates Ferritinophagy-Dependent Oxidative Stress to Potentiate Myogenic Differentiation

Zhang, M., Liu, S., Wang, Y., Shan, S., & Cang, M. (2025) · Cells · doi:10.3390/cells14161234 · Cited by 2

Discovery of BE2012, a First-in-Class REV-ERBα/β Antagonist with Favorable Selectivity and Pharmacokinetics, and In Vivo Efficacy in Inducing Key Myogenic Factors for Muscle Repair upon Acute Muscle Injury

Maram, L., Valfort, A.-C., Rahman, M. H., Okda, H. E., Elagawany, M., Politte, H., Appourchaux, K., Bedia‐Diaz, G., Côté, I., Hegazy, L., et al. (2025) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.5c02749 · Cited by 2

Muscle Fibrosis in Amyotrophic Lateral Sclerosis: Molecular Mechanisms, Diagnostic Advances, and Therapeutic Strategies

Sun, Y., Huang, C., Pan, Y., Zhang, H., & He, X. (2026) · Molecular Neurobiology · doi:10.1007/s12035-025-05658-y · Cited by 2

Fibro-adipogenic progenitor cells from murine SMA muscles are intrinsically adipogenic

Luo, Y. E., Abe-Teh, Z., Alsaghir, T. Y., Heiden, K. D., Basso, K. B. G., & Barton, E. R. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2525423123 · Cited by 2

Relationship between muscle FNDC5, FGF21 mRNA, miR-150 and bone loss after sciatic denervation

Priego, T., Nebot, E., Moreno‐Rupérez, Á., Granado, M., Jaque, D., Pietschmann, P., Martı́n, A. I., & López‐Calderón, A. (2026) · Journal of Physiology and Biochemistry · doi:10.1007/s13105-026-01203-0 · Cited by 2

Skeletal Muscle Denervation: Sciatic and Tibial Nerve Transection Technique

Goto, K., & Ohashi, K. (2023) · Methods in molecular biology · doi:10.1007/978-1-0716-3036-5_16 · Cited by 2

Endothelial‐mesenchymal transition in skeletal muscle: Opportunities and challenges from 3D microphysiological systems

Francescato, R., Moretti, M., & Bersini, S. (2024) · Bioengineering & Translational Medicine · doi:10.1002/btm2.10644 · Cited by 2

Cellular activation patterns of CD10+ fibro-adipogenic progenitors across acquired disease states in human skeletal muscle biopsies

Schütz, P. W., Cheung, S., Yi, L., & Rossi, F. M. V. (2023) · Free Neuropathology · doi:10.17879/freeneuropathology-2024-5162 · Cited by 2

Pathological changes in the osteoarticular system during COVID-19 drug therapy (review of literature)

Tsed, A. N., Mushtin, N. E., Дулаев, А. К., & Шмелев, А. В. (2022) · Grekov s Bulletin of Surgery · doi:10.24884/0042-4625-2022-181-2-85-91 · Cited by 2

A Step in the ALS Direction: Lessons from the Purinome

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Multifocal lipoatrophy secondary to insulin injection in a patient with type 2 diabetes, hepatitis B virus infection, and liver cirrhosis

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Partial resistance to HDAC inhibitors in FAPs of dystrophic muscles at late stages of disease is associated to epigenetic and transcriptional features of cellular senescencePreprint

Consalvi, S., Tucciarone, L., Macrì, E., Bardi, M. D., Picozza, M., Salvatori, I., Renzini, A., Valente, S., Mai, A., Moresi, V., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.04.26.441412 · Cited by 2

Tenascin-C from the tissue microenvironment promotes muscle stem cell self-renewal through Annexin A2Preprint

Loreti, M., Cecchini, A., Kaufman, C. D., Stamenkovic, C., Renero, A., Nicoletti, C., Kervadec, A., Guarnaccia, G., Mayer, D., Colas, A. R., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.10.29.620732 · Cited by 2

Versatile role of fibro-adipogenic progenitors in neuromuscular junction homeostasis and pathology

Li, R., Li, J., Zou, S., & Yin, X. (2026) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2026.153286 · Cited by 1

Methods of muscle atrophy analysis at the single-nucleus level

Grima-Terrén, M., Rommelfanger, M. K., Campanario, S., Cisneros, A., Calls, A., Ramírez‐Pardo, I., Isern, J., Serrano, A. L., Perdiguero, E., & Muñoz‐Cánoves, P. (2026) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2026.112178 · Cited by 1

Macrophage and fibro-adipogenic progenitor communication in skeletal muscle regeneration: tissue homeostasis and pathogenic remodeling

Shrestha, S., Politeski, A., & Dick, S. A. (2026) · Journal of Leukocyte Biology · doi:10.1093/jleuko/qiag054 · Cited by 1

Single-cell resolution of skeletal muscle aging: Current paradigms and perspectives

Wang, Y., Yang, Y., Guan, W., Yu, W., Li, N., & Wang, D. (2026) · Ageing Research Reviews · doi:10.1016/j.arr.2026.103272 · Cited by 1

Comprehensive transcriptomic profiling reveals impaired polyamine metabolism as a contributor to age-related muscle decline

Ruggieri, V., Bracaglia, A., Esposito, L., Tumino, N., Fiore, P. F., Botta, S., Macone, A., Ohana, J., Bouché, M., Latella, L., et al. (2026) · iScience · doi:10.1016/j.isci.2026.117000 · Cited by 2

Convolutional Neural Network Optimization Algorithm-Based Magnetic Resonance Imaging in Analysis of Chronic Pain Caused by the Myofascial Trigger Point

Jin, X., Fan, L., & Yao, Y. (2021) · Scientific Programming · doi:10.1155/2021/4505147 · Cited by 1

MiRNA-206 Affects the Recovery of Sciatic Function by Stimulating BDNF Activity through the Down-regulation of Notch3 Expression.

Wang, M., Wu, S., Wang, J., Fan, D., Li, Z., Tian, S., Yao, S., Zhang, H., & Gao, H. (2023) · PubMed Central · Cited by 1

Circulating TGF-β1 Levels: Linking Muscle and Trauma

La, L., & Tuan, R. S. (2023) · Biomarkers in disease · doi:10.1007/978-3-031-07395-3_37 · Cited by 1

Comparison of Three Antagonists of Hedgehog Pathway to Promote Skeletal Muscle Regeneration after High Dose Irradiation

Graziosi, E. R., François, S., Nasser, F., Gauthier, M., Oger, M., Favier, A., Drouet, M., Jullien, N. D., & Riccobono, D. (2024) · Radiation Research · doi:10.1667/rade-23-00140.1 · Cited by 1

Pharmacologic Inhibition of Glutamate Dehydrogenase 1 Improves Functional Recovery of Neuromuscular Junctions and Muscle Function in Duchenne Muscular Dystrophy

Pereira‐Nunes, A., Ammarah, U., Shang, M., Charatsidou, I., Sharma, H., Sorroche, B. P., Nobis, M., Burg, T., Verschoren, S., Relaix, F., et al. (2025) · American Journal Of Pathology · doi:10.1016/j.ajpath.2025.05.003 · Cited by 1

Matrix Stiffness and Architecture Drive Fibro-adipogenic Progenitors’ Activation into MyofibroblastsPreprint

Loomis, T., Hu, L.-Y., Wohlgemuth, R. P., Chellakudam, R. R., & Smith, L. (2022) · Research Square · doi:10.21203/rs.3.rs-1467095/v2 · Cited by 1

MiR-27b-3p reduces muscle fibrosis during chronic skeletal muscle injury by targeting tgf-βr1/smad3 pathwayPreprint

yao, H., qian, J., Bian, X., Tang, Y., Xiao, Y., he, G., Tang, H., Liu, X., zhang, A., xie, Q., et al. (2024) · Research Square · doi:10.21203/rs.3.rs-3975799/v1 · Cited by 1

Pathophysiological remodeling of the skeletal muscle microenvironment in patients with lung cancerPreprint

Battey, E., Irazoki, A., Wang, J., Sørensen, J., Modvig, J. L., Themsen, S. S. B., Voldstedlund, C. T., Knos, C., Andersen, N. R., Frank, E., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.11.19.689342 · Cited by 4

Niclosamide Targets Inflammatory and Profibrotic Pathways in Amyotrophic Lateral SclerosisPreprint

Milani, M., Mammarella, E., Rossi, S., Lattante, S., Sabatelli, M., Cozzolino, M., D’Ambrosi, N., & Apolloni, S. (2021) · doi:10.21203/rs.3.rs-138253/v1

[Role of interleukin-6 in human umbilical vein endothelial cell to mesenchymal cell transformation].

Guo, L., He, J., Cui, L., Mi, J., Zhang, S., Sun, J., Du, J., Wen, D. L., Zhang, H. C., Jiang, J., et al. (2021) · PubMed · doi:10.3760/cma.j.cn.501120-20201215-00530

IL-6 Protein Expression is Increased in Fast Glycolytic Muscle Fibers Over Time in the SOD1G93A Mouse model.Preprint

Moreno‐Martínez, L., Calvo, A. C., Moreno‐García, L., García-Salamero, G., Lunetta, C., Penco, S., Tarlarini, C., Zaragoza, P., García‐Redondo, A., & Osta, R. (2021) · Research Square · doi:10.21203/rs.3.rs-785505/v1

City of Las Vegas Detention and Enforcement commission on accreditation of law enforcement accreditation program evaluation report

Kelly, K., McNeely, C., & Seda, S. (2020) · PubMed Central · doi:10.34917/2143862

Matrix Stiffness and Architecture Drive Fibro-adipogenic Progenitors’ Activation into MyofibroblastsPreprint

Loomis, T., Hu, L.-Y., Wohlgemuth, R. P., Chellakudam, R. R., & Smith, L. (2022) · Research Square · doi:10.21203/rs.3.rs-1467095/v1

Rhabdomyolysis in a hospitalized patient with COVID-19 – case report

Trifonescu, M. I., Molagic, V., Tilişcan, C., Ganea, O. A., Turan, G., Stratan, L. M., Vişan, A., Iftode, N., Aramă, Ș. S., & Aramă, V. (2021) · Romanian Journal of Infectious Diseases · doi:10.37897/rjid.2021.4.7

Circulating TGF-β1 Levels: Linking Muscle and Trauma

La, L., & Tuan, R. S. (2022) · Biomarkers in disease · doi:10.1007/978-3-030-87302-8_37-1

Estabelecimento de modelo de reimplante radicular após avulsão de raízes motoras espinais em camundongos C57BL/6J

Lombardi, J. (2021) · doi:10.47749/t/unicamp.2021.1265876

Muscle-resident mesenchymal progenitors sense and repair peripheral nerve injury via the GDNF-BDNF axisPreprint

Yoo, K., Jo, Y., Yoo, T., Hann, S., Park, I., Kim, Y.-E., Kim, Y. L., Rhee, J., Song, I.-W., Kim, J.-H., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.03.25.586563

Muscle-resident mesenchymal progenitors sense and repair peripheral nerve injury via the GDNF-BDNF axisPreprint

Yoo, K., Jo, Y., Yoo, T., Hann, S., Park, I., Kim, Y.-E., Kim, Y. L., Rhee, J., Song, I.-W., Kim, J.-H., et al. (2024) · eLife · doi:10.7554/elife.97662.1

Muscle-resident mesenchymal progenitors sense and repair peripheral nerve injury via the GDNF-BDNF axisPreprint

Yoo, K., Jo, Y., Yoo, T., Hann, S., Park, I., Kim, Y.-E., Kim, Y. L., Rhee, J., Song, I.-W., Kim, J.-H., et al. (2024) · eLife · doi:10.7554/elife.97662.2

Percepção de indivíduos hospitalizados por Covid-19 sobre benefícios, barreiras e facilitadores para a participação em um Programa de Reabilitação Pulmonar: um estudo qualitativo

Polato, R. R. (2023) · doi:10.34019/ufjf/di/2023/00094

Fibro-adipogenic progenitors prevent skeletal muscle degeneration at acute phase upon tendon rupture in a murine tibialis anterior tenotomy model

Ding, Z.-C., He, J., Shi, L., Qian, J., Mei, S.-H., Kang, X., & Chen, J. (2025) · World Journal of Stem Cells · doi:10.4252/wjsc.v17.i6.105491

Alterations of the Intestinal Barrier and Inflammatory Response, Caused by Chronic Ozone Exposure in a Rat Model

Miranda-Martínez, A., Rodrı́guez-Martı́nez, E., Valdés‐Fuentes, M., & Rivas-Arancibia, S. (2025) · Antioxidants · doi:10.3390/antiox14081000

Chemogenetic Mitochondrial H 2 O 2 Generation Triggers Dose-Dependent Skeletal Muscle Wasting SignaturesPreprint

Meneses‐Valdés, R., Gallero, S., Hentze, J., Nielsen, S. F., Nielsen, J., Jaimovich, E., Henríquez‐Olguín, C., & Jensen, T. E. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.08.19.671046

Epigenetic Drugs Splitomicin, Suberohydroxamic Acid, CPTH6, BVT-948, and PBIT Moderate Fibro-Fatty Development in Arrhythmogenic Cardiomyopathy

Lippi, M., Moimas, S., Braga, L., Santin, Y., Galotta, A., Giacca, M., Pompilio, G., & Sommariva, E. (2025) · Biomolecules · doi:10.3390/biom15111565

Influence of Neonatal Exposure to Hyperoxia on Skeletal Muscle in a Rat Model

Awata, K., Santosa, I., Arai, Y., Nakagawa, M., Suganuma, H., & Shoji, H. (2025) · Pediatric Reports · doi:10.3390/pediatric17060125

Additional file 1 of Targeting S100A4 with niclosamide attenuates inflammatory and profibrotic pathways in models of amyotrophic lateral sclerosis

Milani, M., Mammarella, E., Rossi, S., Miele, C., Lattante, S., Sabatelli, M., Cozzolino, M., D’Ambrosi, N., & Apolloni, S. (2021) · Figshare · doi:10.6084/m9.figshare.14775706

Additional file 1 of Studying intramuscular fat deposition and muscle regeneration: insights from a comparative analysis of mouse strains, injury models, and sex differences

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Additional file 1 of miR-27b-3p reduces muscle fibrosis during chronic skeletal muscle injury by targeting TGF-βR1/Smad pathway

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