TNF-α is a mitogen in skeletal muscle

A rapid micrqpreparation technique for extraction of DNA-binding proteins from limiting numbers of mammalian cells

Andrews, N. C., & Faller, D. V. (1991) · Nucleic Acids Research · doi:10.1093/nar/19.9.2499 · Cited by 2,292

TRADD–TRAF2 and TRADD–FADD Interactions Define Two Distinct TNF Receptor 1 Signal Transduction Pathways

Hsu, H., Shu, H., Pan, M., & Goeddel, D. V. (1996) · Cell · doi:10.1016/s0092-8674(00)80984-8 · Cited by 1,998

Myogenic satellite cells: physiology to molecular biology

Hawke, T. J., & Garry, D. J. (2001) · Journal of Applied Physiology · doi:10.1152/jappl.2001.91.2.534 · Cited by 1,646

NF-κB Controls Cell Growth and Differentiation through Transcriptional Regulation of Cyclin D1

D, D. C. G., Albanese, C., Reuther, J. Y., Pestell, R. G., & Baldwin, A. S. (1999) · Molecular and Cellular Biology · doi:10.1128/mcb.19.8.5785 · Cited by 1,304

The cytokine handbook

Thomson, A. W. (1994) · Cited by 1,114

Pro‐ and anti‐inflammatory cytokine balance in strenuous exercise in humans

Ostrowski, K., Rohde, T., Asp, S., Schjerling, P., & Pedersen, B. K. (1999) · The Journal of Physiology · doi:10.1111/j.1469-7793.1999.287ad.x · Cited by 1,014

Single-Cell Analysis of Regulatory Gene Expression in Quiescent and Activated Mouse Skeletal Muscle Satellite Cells

Cornelison, D., & Wold, B. J. (1997) · Developmental Biology · doi:10.1006/dbio.1997.8721 · Cited by 934

Isolation and properties of cDNA clones encoding SRF, a transcription factor that binds to the c-fos serum response element

Norman, C. M., Runswick, M. J., Pollock, R. M., & Treisman, R. (1988) · Cell · doi:10.1016/0092-8674(88)90244-9 · Cited by 933

Identification of a protein-binding site that mediates transcriptional response of the c-fos gene to serum factors

Treisman, R. (1986) · Cell · doi:10.1016/0092-8674(86)90882-2 · Cited by 886

Plasticity of the Differentiated State

Blau, H. M., Pavlath, G. K., Hardeman, E. C., Chiu, C., Silberstein, L., Webster, S. G., Miller, S. C., & Webster, C. (1985) · Science · doi:10.1126/science.2414846 · Cited by 840

Inflammatory monocytes recruited after skeletal muscle injury switch into antiinflammatory macrophages to support myogenesis

Arnold, L., Henry, A., Poron, F., Baba-Amer, Y., van Rooijen, N., Plonquet, A., Gherardi, R. K., & Chazaud, B. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20070075 · Cited by 2,002

IKKβ/NF-κB Activation Causes Severe Muscle Wasting in Mice

Cai, D., Frantz, J. D., Tawa, N. E., Melendez, P. A., Oh, B.-C., Lidov, H. G. W., Hasselgren, P.-O., Frontera, W. R., Lee, J., Glass, D. J., et al. (2004) · Cell · doi:10.1016/j.cell.2004.09.027 · Cited by 1,367

Regulatory interactions between muscle and the immune system during muscle regeneration

Tidball, J. G., & Villalta, S. A. (2010) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00735.2009 · Cited by 1,105

Macrophage polarization: an opportunity for improved outcomes in biomaterials and regenerative medicine

Brown, B. N., Ratner, B. D., Goodman, S. B., Amar, S., & Badylak, S. F. (2012) · Biomaterials · doi:10.1016/j.biomaterials.2012.02.034 · Cited by 926

Satellite Cells and Skeletal Muscle Regeneration

Dumont, N. A., Bentzinger, C. F., Sincennes, M., & Rudnicki, M. A. (2015) · Comprehensive Physiology · doi:10.1002/cphy.c140068 · Cited by 719

Skeletal muscle: A review of molecular structure and function, in health and disease

Mukund, K., & Subramaniam, S. (2019) · WIREs Systems Biology and Medicine · doi:10.1002/wsbm.1462 · Cited by 805

Notch Signaling Is Necessary to Maintain Quiescence in Adult Muscle Stem Cells

Bjornson, C. R. R., Cheung, T. H., Liu, L., Tripathi, P. V., Steeper, K. M., & Rando, T. A. (2012) · Stem Cells · doi:10.1002/stem.773 · Cited by 598

Muscle stem cells in development, regeneration, and diseasePreprint

Shi, X., & Garry, D. J. (2006) · Genes & Development · doi:10.1101/gad.1419406 · Cited by 502

Small heat shock proteins: Role in cellular functions and pathology

Raman, B., Ramakrishna, T., & Rao, C. M. (2014) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2014.12.019 · Cited by 481

Mechanisms of Muscle Injury, Repair, and Regeneration

Tidball, J. G. (2011) · Comprehensive physiology · doi:10.1002/cphy.c100092 · Cited by 471

Human skeletal muscle possesses an epigenetic memory of hypertrophy

Seaborne, R. A., Strauss, J., Cocks, M., Shepherd, S., O’Brien, T. D., van Someren, K. A., Bell, P. G., Murgatroyd, C., Morton, J. P., Stewart, C. E., et al. (2018) · Scientific Reports · doi:10.1038/s41598-018-20287-3 · Cited by 334

Muscle regeneration: cellular and molecular events.

Karalaki, M., Fili, S., Philippou, Α., & Koutsilieris, M. (2009) · PubMed · Cited by 328

Tumor necrosis factor-alpha inhibits myogenic differentiation through myod protein destabilization

Langen, R. C. J., van der Velden, J. L. J., Schols, A. M. W. J., Kelders, M. C. J. M., Wouters, E. F. M., & Janssen‐Heininger, Y. M. W. (2004) · The FASEB Journal · doi:10.1096/fj.03-0251com · Cited by 319

Molecular circuitry of stem cell fate in skeletal muscle regeneration, ageing and disease

Almada, A. E., & Wagers, A. J. (2016) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm.2016.7 · Cited by 322

Targeted ablation of IKK2 improves skeletal muscle strength, maintains mass, and promotes regeneration

Mourkioti, F., Kratsios, P., Luedde, T., Song, Y.-H., Delafontaine, P., Adami, R., Parente, V., Bottinelli, R., Pasparakis, M., & Rosenthal, N. A. (2006) · Journal of Clinical Investigation · doi:10.1172/jci28721 · Cited by 326

TNF-α regulates myogenesis and muscle regeneration by activating p38 MAPK

Chen, S., Jin, B., & Li, Y.-P. (2006) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00486.2006 · Cited by 309

Inflammation induced loss of skeletal muscle

Londhe, P., & Guttridge, D. C. (2015) · Bone · doi:10.1016/j.bone.2015.03.015 · Cited by 276

The p38α/β MAPK functions as a molecular switch to activate the quiescent satellite cell

Jones, N. C., Tyner, K. J., Nibarger, L., Stanley, H. M., Cornelison, D., Fedorov, Y. V., & Olwin, B. B. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200408066 · Cited by 272

The promotion of a constructive macrophage phenotype by solubilized extracellular matrix

Sicari, B. M., Dziki, J. L., Siu, B. F., Medberry, C. J., Dearth, C. L., & Badylak, S. F. (2014) · Biomaterials · doi:10.1016/j.biomaterials.2014.06.060 · Cited by 255

Dual and Beneficial Roles of Macrophages During Skeletal Muscle Regeneration

Chazaud, B., Brigitte, M., Yacoub‐Youssef, H., Arnold, L., Gherardi, R. K., Sonnet, C., Lafuste, P., & Chrétien, F. (2008) · Exercise and Sport Sciences Reviews · doi:10.1097/jes.0b013e318190ebdb · Cited by 270

Monocyte/macrophage interactions with myogenic precursor cells during skeletal muscle regeneration

Saclier, M., Cuvellier, S., Magnan, M., Mounier, R., & Chazaud, B. (2013) · FEBS Journal · doi:10.1111/febs.12166 · Cited by 270

The effects of obesity on skeletal muscle regeneration

Akhmedov, D., & Berdeaux, R. (2013) · Frontiers in Physiology · doi:10.3389/fphys.2013.00371 · Cited by 241

Anti‐TNFα (Remicade®) therapy protects dystrophic skeletal muscle from necrosis

Grounds, M. D., & Torrisi, J. (2004) · The FASEB Journal · doi:10.1096/fj.03-1024com · Cited by 239

Coupling between Myogenesis and Angiogenesis during Skeletal Muscle Regeneration Is Stimulated by Restorative Macrophages

Latroche, C., Weiss‐Gayet, M., Muller, L., Gitiaux, C., Leblanc, P., Liot, S., Larbi, S. B., Abou-Khalil, R., Verger, N., Bardot, P., et al. (2017) · Stem Cell Reports · doi:10.1016/j.stemcr.2017.10.027 · Cited by 234

Age-related changes in skeletal muscle: changes to life-style as a therapy

McCormick, R., & Vasilaki, A. (2018) · Biogerontology · doi:10.1007/s10522-018-9775-3 · Cited by 227

Rethinking Regenerative Medicine: A Macrophage-Centered Approach

Brown, B. N., Sicari, B. M., & Badylak, S. F. (2014) · Frontiers in Immunology · doi:10.3389/fimmu.2014.00510 · Cited by 196

Regulating activation of transplanted cells controls tissue regeneration

Hill, E. E., Boontheekul, T., & Mooney, D. J. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0506004103 · Cited by 188

The role of systemic inflammation in age‐related muscle weakness and wasting

Degens, H. (2009) · Scandinavian Journal of Medicine and Science in Sports · doi:10.1111/j.1600-0838.2009.01018.x · Cited by 188

Local NSAID infusion inhibits satellite cell proliferation in human skeletal muscle after eccentric exercise

Mikkelsen, U. R., Langberg, H., Helmark, I. C., Skovgaard, D., Andersen, L. L., Kjær, M., & Mackey, A. L. (2009) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00707.2009 · Cited by 185

Cytokine Profile in Quadriceps Muscles of Patients with Severe COPD

Barreiro, E., Schols, A. M. W. J., Polkey, M. I., Galdiz, J. B., Gosker, H. R., Swallow, E. B., Coronell, C., Gea, J., & on behalf of the ENIGMA in COPD project (2007) · Thorax · doi:10.1136/thx.2007.078030 · Cited by 175

Divergent Roles of Inflammation in Skeletal Muscle Recovery From Injury

Howard, E. E., Pasiakos, S. M., Blesso, C. N., Fussell, M. A., & Rodriguez, N. R. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.00087 · Cited by 187

Chronic inflammation in skeletal muscle impairs satellite cells function during regeneration: can physical exercise restore the satellite cell niche?

Perandini, L. A., Chimin, P., Lutkemeyer, D. D. S., & Câmara, N. O. S. (2018) · FEBS Journal · doi:10.1111/febs.14417 · Cited by 167

Variable Tidal Volumes Improve Lung Protective Ventilation Strategies in Experimental Lung Injury

Spieth, P. M., Carvalho, A. R., Pelosi, P. P., Hoehn, C., Meissner, C., Kasper, M. E., Hübler, M., von Neindorff, M., Dassow, C., Barrenschee, M., et al. (2009) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200806-975oc · Cited by 152

Skeletal muscle regeneration and impact of aging and nutrition

Domingues-Faria, C., Vasson, M.-P., Goncalves-Mendes, N., Boirie, Y., & Walrand, S. (2016) · Ageing Research Reviews · doi:10.1016/j.arr.2015.12.004 · Cited by 157

Entry of muscle satellite cells into the cell cycle requires sphingolipid signaling

Nagata, Y., Partridge, T. A., Matsuda, R., & Zammit, P. S. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.200605028 · Cited by 153

Bubble Continuous Positive Airway Pressure Enhances Lung Volume and Gas Exchange in Preterm Lambs

Pillow, J. J., Hillman, N. H., Moss, T. J. M., Polglase, G. R., Bold, G. T., Beaumont, C., Ikegami, M., & Jobe, A. H. (2007) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200609-1368oc · Cited by 153

Marking the tempo for myogenesis: Pax7 and the regulation of muscle stem cell fate decisions

Olguín, H. C., & Pisconti, A. (2011) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2011.01348.x · Cited by 155

Regulation of IRS1/Akt insulin signaling by microRNA-128a during myogenesis

Motohashi, N., Alexander, M. S., Shimizu‐Motohashi, Y., Myers, J. A., Kawahara, G., & Kunkel, L. M. (2013) · Journal of Cell Science · doi:10.1242/jcs.119966 · Cited by 140

Shared signaling systems in myeloid cell-mediated muscle regeneration

Tidball, J. G., Dorshkind, K. A., & Wehling‐Henricks, M. (2014) · Development · doi:10.1242/dev.098285 · Cited by 151

NF-κB signaling in skeletal muscle: prospects for intervention in muscle diseases

Mourkioti, F., & Rosenthal, N. A. (2008) · Journal of Molecular Medicine · doi:10.1007/s00109-008-0308-4 · Cited by 134

Cellular Players in Skeletal Muscle Regeneration

Ceafalan, L., Popescu, B., & Hinescu, M. (2014) · BioMed Research International · doi:10.1155/2014/957014 · Cited by 134

Prevention of Muscle Aging by Myofiber-Associated Satellite Cell Transplantation

Hall, J. K., Banks, G. B., Chamberlain, J. S., & Olwin, B. B. (2010) · Science Translational Medicine · doi:10.1126/scitranslmed.3001081 · Cited by 121

Transplantation of devitalized muscle scaffolds is insufficient for appreciable de novo muscle fiber regeneration after volumetric muscle loss injury

Garg, K., Ward, C., Rathbone, C., & Corona, B. T. (2014) · Cell and Tissue Research · doi:10.1007/s00441-014-2006-6 · Cited by 109

A Perspective on Immunomodulation and Tissue Repair

Mokarram, N., & Bellamkonda, R. V. (2013) · Annals of Biomedical Engineering · doi:10.1007/s10439-013-0941-0 · Cited by 115

In vitro response of macrophage polarization to a keratin biomaterial

Fearing, B. V., & Dyke, M. E. V. (2014) · Acta Biomaterialia · doi:10.1016/j.actbio.2014.04.003 · Cited by 111

Tumor necrosis factor alpha (TNF-α) inactivates the PI3-kinase/PKB pathway and induces atrophy and apoptosis in L6 myotubes

Sishi, B., & Engelbrecht, A. (2011) · Cytokine · doi:10.1016/j.cyto.2011.01.009 · Cited by 101

Human skeletal muscle macrophages increase following cycle training and are associated with adaptations that may facilitate growth

Walton, R. G., Kosmac, K., Mula, J., Fry, C. S., Peck, B. D., Groshong, J. S., Finlin, B. S., Zhu, B., Kern, P. A., & Peterson, C. A. (2019) · Scientific Reports · doi:10.1038/s41598-018-37187-1 · Cited by 97

Reduced muscle necrosis and long-term benefits in dystrophic mdx mice after cV1q (blockade of TNF) treatment

Radley‐Crabb, H. G., Davies, M. J., & Grounds, M. D. (2008) · Neuromuscular Disorders · doi:10.1016/j.nmd.2007.11.002 · Cited by 91

Fibroblast Growth Factor Inducible 14 (Fn14) Is Required for the Expression of Myogenic Regulatory Factors and Differentiation of Myoblasts into Myotubes

Dogra, C., Hall, S. L., Wedhas, N., Linkhart, T. A., & Kumar, A. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m608668200 · Cited by 91

Cytokines in Muscle Damage

Philippou, Α., Maridaki, M. D., Theos, A., & Koutsilieris, M. (2012) · Advances in clinical chemistry · doi:10.1016/b978-0-12-394383-5.00010-2 · Cited by 92

TACE release of TNF-α mediates mechanotransduction-induced activation of p38 MAPK and myogenesis

Zhan, M., Jin, B., Chen, S., Reecy, J. M., & Li, Y.-P. (2007) · Journal of Cell Science · doi:10.1242/jcs.03372 · Cited by 90

Tissue Engineering and Regenerative Medicine Approaches to Enhance the Functional Response to Skeletal Muscle Injury

Sicari, B. M., Dearth, C. L., & Badylak, S. F. (2013) · The Anatomical Record · doi:10.1002/ar.22794 · Cited by 88

Genome Engineering of Stem Cells for Autonomously Regulated, Closed-Loop Delivery of Biologic Drugs

Brunger, J. M., Zutshi, A., Willard, V. P., Gersbach, C. A., & Guilak, F. (2017) · Stem Cell Reports · doi:10.1016/j.stemcr.2017.03.022 · Cited by 88

The Many Roles of Macrophages in Skeletal Muscle Injury and Repair

Wang, X., & Zhou, L. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.952249 · Cited by 101

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

Myeloid Cell-Derived Tumor Necrosis Factor-Alpha Promotes Sarcopenia and Regulates Muscle Cell Fusion with Aging Muscle Fibers

Wang, Y., Welc, S. S., Wehling‐Henricks, M., & Tidball, J. G. (2018) · Aging Cell · doi:10.1111/acel.12828 · Cited by 80

Differential Cytokine Gene Expression in the Diaphragm in Response to Strenuous Resistive Breathing

Vassilakopoulos, T., Divangahi, M., Rallis, G., Kishta, O. A., Petrof, B. J., Comtois, A. S., & Hussain, S. N. A. (2004) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200308-1071oc · Cited by 77

Can muscle regeneration fail in chronic inflammation: a weakness in inflammatory myopathies?

Loell, I., & Lundberg, I. E. (2010) · Journal of Internal Medicine · doi:10.1111/j.1365-2796.2010.02334.x · Cited by 81

Modulation of the renin–angiotensin system in white adipose tissue and skeletal muscle: focus on exercise training

Frantz, E. D. C., Prodel, E., Bráz, I. D., Giori, I. G., Bargut, T. C. L., Magliano, D. C., & da Nóbrega, A. C. L. (2018) · Clinical Science · doi:10.1042/cs20180276 · Cited by 75

Stem Cell and Macrophage Roles in Skeletal Muscle Regenerative Medicine

Scala, P., Rehak, L., Giudice, V., Ciaglia, E., Puca, A. A., Selleri, C., Porta, G. D., & Maffulli, N. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms221910867 · Cited by 77

Tumor Necrosis Factor-α Inhibition of Skeletal Muscle Regeneration Is Mediated by a Caspase-Dependent Stem Cell Response

Moresi, V., Pristerà, A., Scicchitano, B. M., Molinaro, M., Teodori, L., Sassoon, D. A., Adamo, S., & Coletti, D. (2008) · Stem Cells · doi:10.1634/stemcells.2007-0493 · Cited by 79

Aryl hydrocarbon receptor-dependent apoptotic cell death induced by the flavonoid chrysin in human colorectal cancer cells

Ronnekleiv‐Kelly, S. M., Nukaya, M., Díaz-Díaz, C. J., Megna, B. W., Carney, P. R., Geiger, P. G., & Kennedy, G. D. (2015) · Cancer Letters · doi:10.1016/j.canlet.2015.10.014 · Cited by 72

Immunomodulation and Mobilization of Progenitor Cells by Extracellular Matrix Bioscaffolds for Volumetric Muscle Loss Treatment

Dziki, J. L., Sicari, B. M., Wolf, M. T., Cramer, M. C., & Badylak, S. F. (2016) · Tissue Engineering Part A · doi:10.1089/ten.tea.2016.0340 · Cited by 72

αB-crystallin, a small heat shock protein, modulates NF-κB activity in a phosphorylation-dependent manner and protects muscle myoblasts from TNF-α induced cytotoxicity

Adhikari, A. S., Singh, B. N., Rao, K. S., & Rao, C. M. (2011) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2011.04.009 · Cited by 69

CX3CL1—a macrophage chemoattractant induced by a single bout of exercise in human skeletal muscle

Strömberg, A., Olsson, K., Dijksterhuis, J. P., Rullman, E., Schulte, G., & Gustafsson, T. (2016) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00236.2015 · Cited by 67

Aging of the immune system and impaired muscle regeneration: a failure of immunomodulation of adult myogenesis

Tidball, J. G., Flores, I., Welc, S. S., Wehling-Henricks, M., & Ochi, E. (2021) · Experimental Gerontology · doi:10.1016/j.exger.2020.111200 · Cited by 66

Pulsed ultrasound associated with gold nanoparticle gel reduces oxidative stress parameters and expression of pro-inflammatory molecules in an animal model of muscle injury

Victor, E. G., Lock, P. C. S., Possato, J. C., da Rosa, G. L., Munari, U. B., de Souza, C. T., Pinho, R. A., da Silva, L. A., STRECK, E. L., & Paula, M. M. D. S. (2012) · Journal of Nanobiotechnology · doi:10.1186/1477-3155-10-11 · Cited by 66

Bubble CPAP: Is the Noise Important? An In Vitro Study

Pillow, J. J., & Travadi, J. (2005) · Pediatric Research · doi:10.1203/01.pdr.0000157721.66812.07 · Cited by 65

Phosphorylation of αB-crystallin: Role in stress, aging and patho-physiological conditions

Raman, B., Akula, K. K., Ramakrishna, T., & Rao, C. M. (2015) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2015.09.017 · Cited by 64

Muscle Satellite Cells: Exploring the Basic Biology to Rule Them

de Almeida, C., Fernandes, S., Ribeiro, A. F., Okamoto, O. K., & Vainzof, M. (2016) · Stem Cells International · doi:10.1155/2016/1078686 · Cited by 68

The effects PCSO-524®, a patented marine oil lipid and omega-3 PUFA blend derived from the New Zealand green lipped mussel (Perna canaliculus), on indirect markers of muscle damage and inflammation after muscle damaging exercise in untrained men: a randomized, placebo controlled trial

Mickleborough, T. D., Sinex, J. A., Platt, D., Chapman, R. F., & Hirt, M. B. (2015) · Journal of the International Society of Sports Nutrition · doi:10.1186/s12970-015-0073-z · Cited by 61

Macrophages escape Klotho gene silencing in the mdx mouse model of Duchenne muscular dystrophy and promote muscle growth and increase satellite cell numbers through a Klotho-mediated pathway

Wehling‐Henricks, M., Welc, S. S., Samengo, G., Rinaldi, C., Lindsey, C., Wang, Y., Lee, J., Kuro‐o, M., & Tidball, J. G. (2017) · Human Molecular Genetics · doi:10.1093/hmg/ddx380 · Cited by 59

Muscle Stem Cell Fate Is Controlled by the Cell-Polarity Protein Scrib

Ono, Y., Urata, Y., Goto, S., Nakagawa, S., Humbert, P. O., Li, T., & Zammit, P. S. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.01.045 · Cited by 59

An anti-RANKL treatment reduces muscle inflammation and dysfunction and strengthens bone in dystrophic mice

Hamoudi, D., Marcadet, L., Boulanger‐Piette, A., Yagita∥, H., Bouredji, Z., Argaw, A., & Frenette, J. (2019) · Human Molecular Genetics · doi:10.1093/hmg/ddz124 · Cited by 59

The immune response to resistive breathing

Vassilakopoulos, T., Roussos, C., & Zakynthinos, S. (2004) · European Respiratory Journal · doi:10.1183/09031936.04.00067904 · Cited by 56

Substrate and strain alter the muscle-derived mesenchymal stem cell secretome to promote myogenesis

Lisio, M. D., Jensen, T., Sukiennik, R. A., Huntsman, H. D., & Boppart, M. D. (2014) · Stem Cell Research & Therapy · doi:10.1186/scrt463 · Cited by 60

Markers of degeneration and regeneration in Duchenne muscular dystrophy.

Abdelsalam, E. M. N., Abdel-Meguid, I. E., & Korraa, S. S. (2009) · PubMed Central · Cited by 55

Local NSAID infusion does not affect protein synthesis and gene expression in human muscle after eccentric exercise

Mikkelsen, U. R., Schjerling, P., Helmark, I. C., Reitelseder, S., Holm, L., Skovgaard, D. C., Langberg, H., Kjær, M., & Heinemeier, K. M. (2010) · Scandinavian Journal of Medicine and Science in Sports · doi:10.1111/j.1600-0838.2010.01170.x · Cited by 53

Biomaterials‐Based Technologies in Skeletal Muscle Tissue Engineering

Luo, W., Zhang, H., Wan, R., Cai, Y., Liu, Y., Wu, Y., Yang, Y., Chen, J., Zhang, D., Luo, Z., et al. (2024) · Advanced Healthcare Materials · doi:10.1002/adhm.202304196 · Cited by 53

Stem Cell Transplantation for Muscular Dystrophy: The Challenge of Immune Response

Maffioletti, S. M., Noviello, M., English, K., & Tedesco, F. S. (2014) · BioMed Research International · doi:10.1155/2014/964010 · Cited by 53

A role for RNA post-transcriptional regulation in satellite cell activation

Farina, N. H., Hausburg, M. A., Betta, N. D., Pulliam, C., Srivastava, D., Cornelison, D., & Olwin, B. B. (2012) · Skeletal Muscle · doi:10.1186/2044-5040-2-21 · Cited by 51

Damaged Myofiber-Derived Metabolic Enzymes Act as Activators of Muscle Satellite Cells

Tsuchiya, Y., Kitajima, Y., Masumoto, H., & Ono, Y. (2020) · Stem Cell Reports · doi:10.1016/j.stemcr.2020.08.002 · Cited by 52

Cytokine Response of Cultured Skeletal Muscle Cells Stimulated with Proinflammatory Factors Depends on Differentiation Stage

Podbregar, M., Lainščak, M., Prelovsek, O., & Mars, T. (2013) · TheScientificWorldJournal · doi:10.1155/2013/617170 · Cited by 49

l ‐glutamine Improves Skeletal Muscle Cell Differentiation and Prevents Myotube Atrophy After Cytokine (TNF‐α) Stress Via Reduced p38 MAPK Signal Transduction

Girven, M., Dugdale, H. F., Owens, D. J., Hughes, D. C., Stewart, C. E., & Sharples, A. P. (2016) · Journal of Cellular Physiology · doi:10.1002/jcp.25380 · Cited by 48

An anti-inflammatory role for leukemia inhibitory factor receptor signaling in regenerating skeletal muscle

Hunt, L., Upadhyay, A., Jazayeri, J., Tudor, E., & White, J. (2012) · Histochemistry and Cell Biology · doi:10.1007/s00418-012-1018-0 · Cited by 47

IL-4 administration exerts preventive effects via suppression of underlying inflammation and TNF-α-induced apoptosis in steroid-induced osteonecrosis

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Epithelial and endothelial damage induced by mechanical ventilation modes

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Cell Cycle Regulation During Proliferation and Differentiation of Mammalian Muscle Precursor Cells

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Nicolas, N., Marazzi, G., Kelley, K., & Sassoon, D. A. (2005) · Developmental Biology · doi:10.1016/j.ydbio.2005.02.022 · Cited by 43

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van de Vyver, M., & Myburgh, K. H. (2012) · Journal of Muscle Research and Cell Motility · doi:10.1007/s10974-012-9303-z · Cited by 43

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Expression of myogenic regulatory factors and myo-endothelial remodeling in sporadic inclusion body myositis

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Andrés-Mateos, E., Mejías, R., Soleimani, A., Lin, B., Burks, T. N., Marx, R., Lin, B., Zellars, R., Zhang, Y.-G., Huso, D., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0048884 · Cited by 40

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Silveira, P., Scheffer, D. D. L., Glaser, V., Remor, A., Pinho, R. A., Júnior, A. S. A., & Latini, A. (2016) · Free radical research · doi:10.3109/10715762.2016.1147649 · Cited by 41

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