Role of TNF-α signaling in regeneration of cardiotoxin-injured muscle

Dynamic properties of mammalian skeletal muscles.

Close, R. I. (1972) · Physiological Reviews · doi:10.1152/physrev.1972.52.1.129 · Cited by 1,890

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

Cyclin D1 Expression Is Regulated Positively by the p42/p44 and Negatively by the p38/HOG Pathway

Lavoie, J. N., L’Allemain, G., Brunet, A., Müller, R., & Pouysségur, J. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.34.20608 · Cited by 1,210

The cytokine handbook

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

Inactivation of MyoD in mice leads to up-regulation of the myogenic HLH gene Myf-5 and results in apparently normal muscle development

Rudnicki, M. A., Braun, T. W., Hinuma, S., & Jaenisch, R. (1992) · Cell · doi:10.1016/0092-8674(92)90508-a · Cited by 984

MEF2: a calcium-dependent regulator of cell division, differentiation and death

McKinsey, T. A., Zhang, C. L., & Olson, E. N. (2002) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(01)02031-x · Cited by 701

The Mitogenic and Myogenic Actions of Insulin-like Growth Factors Utilize Distinct Signaling Pathways

Coolican, S. A., Samuel, D. S., Ewton, D. Z., McWade, F. J., & Florini, J. R. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.10.6653 · Cited by 646

The Cell Cycle: A Review

Schafer, K. A. (1998) · Veterinary Pathology · doi:10.1177/030098589803500601 · Cited by 641

TNF‐α acts via p38 MAPK to stimulate expression of the ubiquitin ligase atrogin1/MAFbx in skeletal muscle

Li, Y.-P., Chen, Y., John, J., Moylan, J. S., Jin, B., Mann, D. L., & Reid, M. B. (2005) · The FASEB Journal · doi:10.1096/fj.04-2364com · Cited by 634

p38 and Extracellular Signal-Regulated Kinases Regulate the Myogenic Program at Multiple Steps

Wu, Z.-G., Woodring, P. J., Bhakta, K. S., Tamura, K., Wen, F., Feramisco, J., Karin, M., Wang, J. Y. J., & Puri, P. (2000) · Molecular and Cellular Biology · doi:10.1128/mcb.20.11.3951-3964.2000 · Cited by 524

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

Regulation of Muscle Growth and Regeneration by the Immune System

Tidball, J. G. (2017) · Nature Reviews Immunology · doi:10.1038/nri.2016.150 · Cited by 740

Biomaterials based strategies for skeletal muscle tissue engineering: existing technologies and future trends.

Qazi, T., Mooney, D., Pumberger, M., Geissler, S., & Duda, G. (2015) · Biomaterials · doi:10.1016/j.biomaterials.2015.02.110 · Cited by 386

Mechanisms of Muscle Injury, Repair, and Regeneration

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

Apoptotic cell death in disease—Current understanding of the NCCD 2023

Vitale, I., Pietrocola, F., Guilbaud, E., Aaronson, S. A., Abrams, J., Adam, D., Agostini, M., Agostinis, P., Alnemri, E. S., Altucci, L., et al. (2023) · Cell Death and Differentiation · doi:10.1038/s41418-023-01153-w · Cited by 352

Phenotypic Transitions of Macrophages Orchestrate Tissue Repair

Novak, M. L., & Koh, T. J. (2013) · American Journal Of Pathology · doi:10.1016/j.ajpath.2013.06.034 · Cited by 370

Skeletal muscle regeneration is modulated by inflammation

Yang, W., & Hu, P. (2018) · Journal of Orthopaedic Translation · doi:10.1016/j.jot.2018.01.002 · Cited by 366

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

Advances in signaling in vertebrate regeneration as a prelude to regenerative medicinePreprint

Stoick-Cooper, C. L., Moon, R. T., & Weidinger, G. (2007) · Genes & Development · doi:10.1101/gad.1540507 · Cited by 309

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

Regeneration of skeletal muscle

Turner, N. J., & Badylak, S. F. (2011) · Cell and Tissue Research · doi:10.1007/s00441-011-1185-7 · Cited by 309

NF-κB Signaling: A Tale of Two Pathways in Skeletal Myogenesis

Bakkar, N., & Guttridge, D. C. (2010) · Physiological Reviews · doi:10.1152/physrev.00040.2009 · Cited by 203

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 195

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

Cytokine Signaling in Skeletal Muscle Wasting

Zhou, J., Liu, B., Liang, C., Li, Y., & Song, Y.-H. (2016) · Trends in Endocrinology & Metabolism · doi:10.1016/j.tem.2016.03.002 · Cited by 172

Stem Cell Aging in Skeletal Muscle Regeneration and Disease

Yamakawa, H., Kusumoto, D., Hashimoto, H., & Yuasa, S. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21051830 · Cited by 187

Incorporation of macrophages into engineered skeletal muscle enables enhanced muscle regeneration

Juhas, M. E., Abutaleb, N. O., Wang, J. T., Ye, J., Shaikh, Z., Sriworarat, C., Qian, Y., & Bursac, N. (2018) · Nature Biomedical Engineering · doi:10.1038/s41551-018-0290-2 · Cited by 149

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

Regenerative function of immune system: Modulation of muscle stem cells

Saini, J., McPhee, J. S., Al-Dabbagh, S., Stewart, C. E., & Al‐Shanti, N. (2016) · Ageing Research Reviews · doi:10.1016/j.arr.2016.03.006 · Cited by 130

Beyond atrophy: redox mechanisms of muscle dysfunction in chronic inflammatory disease

Reid, M. B., & Moylan, J. S. (2011) · The Journal of Physiology · doi:10.1113/jphysiol.2010.203356 · Cited by 126

Cellular Players in Skeletal Muscle Regeneration

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

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

Emerging use of stem cells in regenerative medicine

Teo, A. K. K., & Vallier, L. (2010) · Biochemical Journal · doi:10.1042/bj20100102 · Cited by 111

Vitamin D status and biomarkers of inflammation in runners

Larson‐Meyer, D. E., WILLIS, W., Smith, & Broughton (2012) · Open Access Journal of Sports Medicine · doi:10.2147/oajsm.s31022 · Cited by 106

Is caspase‐dependent apoptosis only cell differentiation taken to the extreme?

Fernando, P., & Megeney, L. A. (2006) · The FASEB Journal · doi:10.1096/fj.06-5912hyp · Cited by 104

Potential Roles of n-3 PUFAs during Skeletal Muscle Growth and Regeneration

Tachtsis, B., Camera, D., & Lacham-Kaplan, O. (2018) · Nutrients · doi:10.3390/nu10030309 · Cited by 104

Promoting musculoskeletal system soft tissue regeneration by biomaterial-mediated modulation of macrophage polarization

Ye, J., Xie, C., Wang, C., Huang, J., Yin, Z., Heng, B. C., Chen, X., & Shen, W. (2021) · Bioactive Materials · doi:10.1016/j.bioactmat.2021.04.017 · Cited by 97

Engineering skeletal muscle repair

Juhas, M. E., & Bursac, N. (2013) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2013.04.013 · Cited by 91

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

TWEAK and cIAP1 Regulate Myoblast Fusion Through the Noncanonical NF-κB Signaling Pathway

Enwere, E. K., Holbrook, J., Mrad, R. L., Vineham, J., Timusk, K., Sivaraj, B., Isaac, M. B., Uehling, D., Al‐awar, R., LaCasse, E. C., et al. (2012) · Science Signaling · doi:10.1126/scisignal.2003086 · Cited by 85

Advances in biomaterials for skeletal muscle engineering and obstacles still to overcome

Smoak, M. M., & Mikos, A. G. (2020) · Materials Today Bio · doi:10.1016/j.mtbio.2020.100069 · Cited by 81

Skeletal Muscle Regeneration in Cardiotoxin-Induced Muscle Injury Models

Wang, Y., Lu, J., & Liu, Y. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232113380 · 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

β3‐Integrin mediates satellite cell differentiation in regenerating mouse muscle

Liu, H., Niu, A., Chen, S., & Li, Y. (2011) · The FASEB Journal · doi:10.1096/fj.10-170449 · Cited by 75

Muscle cell‐derived cytokines in skeletal muscle regeneration

Waldemer, R. J., Kim, D., & Chen, J. (2022) · FEBS Journal · doi:10.1111/febs.16372 · Cited by 79

uPA deficiency exacerbates muscular dystrophy in MDX mice

Suelves, M., Vidal, B., Serrano, A. L., Tjwa, M., Roma, J. M., López‐Alemany, R., Luttun, A., de Lagrán, M. M., Díaz, M. À., Jardı́, M., et al. (2007) · The Journal of Cell Biology · doi:10.1083/jcb.200705127 · Cited by 70

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

Impaired regeneration: A role for the muscle microenvironment in cancer cachexia

Talbert, E. E., & Guttridge, D. C. (2015) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2015.09.009 · Cited by 71

Diet‐induced obesity alters anabolic signalling in mice at the onset of skeletal muscle regeneration

Brown, L. A., Lee, D. E., Patton, J. F., Perry, R. A., Brown, J. L., Baum, J., Smith‐Blair, N., Greene, N. P., & Washington, T. A. (2015) · Acta Physiologica · doi:10.1111/apha.12537 · Cited by 71

Neutrophil Depletion Attenuates Muscle Injury after Exhaustive Exercise

Kawanishi, N., Mizokami, T., NIIHARA, H., Yada, K., & Suzuki, K. (2016) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0000000000000980 · Cited by 65

Blueberry Anthocyanins-Enriched Extracts Attenuate Cyclophosphamide-Induced Cardiac Injury

Liu, Y., Tan, D., Shi, L., Liu, X., Zhang, Y., Tong, C., Song, D., & Hou, M. (2015) · PLoS ONE · doi:10.1371/journal.pone.0127813 · Cited by 64

Cellular Prion Protein Promotes Regeneration of Adult Muscle Tissue

Stella, R., Massimino, M. L., Sandri, M., Sorgato, M. C., & Bertoli, A. (2010) · Molecular and Cellular Biology · doi:10.1128/mcb.01040-09 · Cited by 64

Biologic scaffolds for musculotendinous tissue repair

Turner, N. J., & Badylak, S. F. (2013) · European Cells and Materials · doi:10.22203/ecm.v025a09 · Cited by 65

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

TIMP3: a physiological regulator of adult myogenesis

Liu, H., Chen, S., Jin, B., Carson, J. A., Niu, A., Durham, W., Lai, J.-Y., & Li, Y.-P. (2010) · Journal of Cell Science · doi:10.1242/jcs.057620 · Cited by 60

Injectable and degradable methacrylic acid hydrogel alters macrophage response in skeletal muscle

Carleton, M. M., & Sefton, M. V. (2019) · Biomaterials · doi:10.1016/j.biomaterials.2019.119477 · Cited by 58

Long-term administration of the TNF blocking drug Remicade (cV1q) to mdx mice reduces skeletal and cardiac muscle fibrosis, but negatively impacts cardiac function

Ermolova, N. V., Martinez, L., Vetrone, S. A., Jordan, M. C., Roos, K. P., Sweeney, H. L., & Spencer, M. J. (2014) · Neuromuscular Disorders · doi:10.1016/j.nmd.2014.04.006 · Cited by 56

Progressive nuclear factor‐κB activation resistant to inhibition by contraction and curcumin in mdx mice

Durham, W. J., Arbogast, S., Gerken, E., Li, Y., & Reid, M. B. (2006) · Muscle & Nerve · doi:10.1002/mus.20579 · Cited by 55

Acute resistance exercise increases the expression of chemotactic factors within skeletal muscle

Gatta, P. A. D., Cameron‐Smith, D., & Peake, J. M. (2014) · European Journal of Applied Physiology · doi:10.1007/s00421-014-2936-4 · Cited by 54

Advanced Techniques for Skeletal Muscle Tissue Engineering and Regeneration

Kang, M. S., Lee, S. H., Park, W. J., Lee, J. E., Kim, B., & Han, D. (2020) · Bioengineering · doi:10.3390/bioengineering7030099 · Cited by 54

Overload‐induced skeletal muscle extracellular matrix remodelling and myofibre growth in mice lacking IL‐6

White, J. P., Reecy, J. M., Washington, T. A., Sato, S., Le, M. E., Davis, J. M., Wilson, L. B., & Carson, J. A. (2009) · Acta Physiologica · doi:10.1111/j.1748-1716.2009.02029.x · Cited by 53

Death receptors and mitochondria: Two prime triggers of neural apoptosis and differentiation

Solá, S., Morgado, A. L., & Rodrigues, C. M. P. (2012) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2012.09.021 · Cited by 52

Metabolic Changes During Cancer Cachexia Pathogenesis

Shyh‐Chang, N. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-981-10-6020-5_11 · Cited by 52

Cellular Prion Protein Regulates Its Own α-Cleavage through ADAM8 in Skeletal Muscle

Liang, J., Wang, W., Sorensen, D., Medina, S. J., Ilchenko, S. A., Kiselar, J., Surewicz, W. K., Booth, S. A., & Kong, Q. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.360891 · Cited by 49

Understanding the muscular dystrophy caused by deletion of choline kinase beta in mice

Wu, G., Sher, R. B., Cox, G. A., & Vance, D. E. (2009) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2009.02.006 · 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

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

Ciemerych, M. A., Archacka, K., Grabowska, I., & Gawor, M. (2011) · Results and problems in cell differentiation · doi:10.1007/978-3-642-19065-0_20 · Cited by 47

Apoptosis signal-regulating kinase 1 is an intracellular inducer of p38 MAPK-mediated myogenic signalling in cardiac myoblasts

Choi, T. G., Lee, J., Ha, J., & Kim, S. S. (2011) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2011.04.001 · Cited by 46

Arpp/Ankrd2, a member of the muscle ankyrin repeat proteins (MARPs), translocates from the I-band to the nucleus after muscle injury

Tsukamoto, Y., Hijiya, N., Yano, S., Yokoyama, S., Nakada, C., Uchida, T., Matsuura, K., & Moriyama, M. (2007) · Histochemistry and Cell Biology · doi:10.1007/s00418-007-0348-9 · Cited by 42

Regenerative pharmacology in the treatment of genetic diseases: The paradigm of muscular dystrophy

Mozzetta, C., Minetti, G., & Puri, P. (2008) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2008.08.033 · Cited by 39

Near-Infrared Imaging of Injured Tissue in Living Subjects Using IR-820

Prajapati, S. I., Martinez, C. O., Bahadur, A. N., Wu, I. Q., Zheng, W., Lechleiter, J. D., McManus, L. M., Chisholm, G. B., Michalek, J. E., Shireman, P. K., et al. (2009) · Molecular Imaging · doi:10.2310/7290.2009.00005 · Cited by 39

Amelioration of Duchenne muscular dystrophy in mdx mice by elimination of matrix-associated fibrin-driven inflammation coupled to the αMβ2 leukocyte integrin receptor

Vidal, B., Ardite, E., Suelves, M., Ruiz‐Bonilla, V., Janué, A., Flick, M. J., Degen, J. L., Serrano, A. L., & Muñoz‐Cánoves, P. (2012) · Human Molecular Genetics · doi:10.1093/hmg/dds012 · Cited by 39

Ceramide accumulation and up-regulation of proinflammatory interleukin-1β exemplify lipotoxicity to mediate declines of reproductive efficacy of broiler hens

Pan, Y.-E., Liu, Z.-C., Chang, C., Xie, Y.-L., Chen, C.-Y., Chen, C., Walzem, R. L., & Chen, S. (2011) · Domestic Animal Endocrinology · doi:10.1016/j.domaniend.2011.12.001 · Cited by 38

Regulation of muscle stem cells activation: the role of growth factors and extracellular matrix.

Brzóska, E., Ciemerych, M., Przewoźniak, M., & Zimowska, M. (2011) · Vitamins and hormones · doi:10.1016/b978-0-12-386015-6.00031-7 · Cited by 36

Modulation of overload-induced inflammation by aging and anabolic steroid administration.

Thompson, R. W., McClung, J., Baltgalvis, K. A., Davis, J. M., & Carson, J. A. (2006) · Experimental Gerontology · doi:10.1016/j.exger.2006.08.013 · Cited by 41

Dietary apple polyphenols have preventive effects against lengthening contraction‐induced muscle injuries

Nakazato, K., Ochi, E., & Waga, T. (2009) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.200900145 · Cited by 35

Neuroprotective effect of TNFα against the β-amyloid neurotoxicity mediated by CDK5 kinase

Orellana, D. I., Quintanilla, R. A., & Maccioni, R. B. (2006) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2006.10.010 · Cited by 36

Anti-interleukin-6 receptor antibody (MR16-1) promotes muscle regeneration via modulation of gene expressions in infiltrated macrophages

Fujita, R., Kawano, F., Ohira, T., Nakai, N., Shibaguchi, T., Nishimoto, N., & Ohira, Y. (2014) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2014.01.014 · Cited by 34

Rejuvenating stem cells to restore muscle regeneration in aging

Bengal, E., Perdiguero, E., Serrano, A. L., & Muñoz‐Cánoves, P. (2017) · F1000Research · doi:10.12688/f1000research.9846.1 · Cited by 30

TNFα and IFNγ cooperate for efficient pro- to anti-inflammatory transition of macrophages during muscle regeneration

Babaeijandaghi, F., Paiero, A., Long, R., Tung, L. W., Smith, S. P., Cheng, R., Smandych, J., Kajabadi, N., Chang, C.-K., Ghassemi, A., et al. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2209976119 · Cited by 35

Tumor necrosis factor alpha regulates myogenesis to inhibit differentiation and promote proliferation in satellite cells

Shirakawa, T., Rojasawasthien, T., Inoue, A., Matsubara, T., Kawamoto, T., & Kokabu, S. (2021) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2021.09.067 · Cited by 32

Immunomodulatory capacity of the local mesenchymal stem cells transplantation after severe skeletal muscle injury in female rats

Helal, M. A. M., Shaheen, N., & Zahra, F. A. A. (2016) · Immunopharmacology and Immunotoxicology · doi:10.1080/08923973.2016.1222617 · Cited by 32

Effect of Phytobiotic Composition on Production Parameters, Oxidative Stress Markers and Myokine Levels in Blood and Pectoral Muscle of Broiler Chickens

Chodkowska, K. A., Abramowicz-Pindor, P. A., Tuśnio, A., Gawin, K., Taciak, M., & Barszcz, M. (2022) · Animals · doi:10.3390/ani12192625 · Cited by 31

Src mediates the mechanical activation of myogenesis by activating TNFα-converting enzyme

Niu, A., Wen, Y., Liu, H., Zhan, M., Jin, B., & Li, Y.-P. (2013) · Journal of Cell Science · doi:10.1242/jcs.125328 · Cited by 31

Effects of Dandelion Extract on the Proliferation of Rat Skeletal Muscle Cells and the Inhibition of a Lipopolysaccharide-Induced Inflammatory Reaction

Liu, Q., Zhao, H., Gao, Y., Meng, Y., Zhao, X., & Pan, S. (2018) · Chinese Medical Journal · doi:10.4103/0366-6999.235878 · Cited by 30

Skeletal muscle response to inflammation—Lessons for chronic obstructive pulmonary disease

Reid, W. D., Rurak, J., & Harris, R. (2009) · Critical Care Medicine · doi:10.1097/ccm.0b013e3181b6ea1d · Cited by 30

Characterization of Dystrophic Calcification Induced in Mice by Cardiotoxin

Zhao, Y., Urganus, A. L., Spevak, L., Shrestha, S., Doty, S. B., Boskey, A. L., & Pachman, L. M. (2009) · Calcified Tissue International · doi:10.1007/s00223-009-9271-5 · Cited by 28

Accelerated regeneration of the skeletal muscle in RNF13-knockout mice is mediated by macrophage-secreted IL-4/IL-6

Meng, J., Zou, X., Wu, R., Zhong, R., Zhu, D., & Zhang, Y. (2014) · Protein & Cell · doi:10.1007/s13238-014-0025-4 · Cited by 28

Inflammation in Skeletal Muscle Regeneration

Tidball, J. G. (2008) · Springer eBooks · doi:10.1007/978-1-4020-6768-6_12 · Cited by 27

Protection by Mikania laevigata (guaco) extract against the toxicity of Philodryas olfersii snake venom

Collaço, R. D. C., Cogo, J. C., Α, L. R.-S., Rocha, T., Oshima‐Franco, Y., & Randazzo‐Moura, P. (2012) · Toxicon · doi:10.1016/j.toxicon.2012.05.014 · Cited by 26

Differential expression of choline kinase isoforms in skeletal muscle explains the phenotypic variability in the rostrocaudal muscular dystrophy mouse

Wu, G., Sher, R. B., Cox, G. A., & Vance, D. E. (2009) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2009.12.003 · Cited by 26

Redox Mechanisms of Muscle Dysfunction in Inflammatory Disease

Reid, M. B., Andrade, F. H., Balke, C. W., & Esser, K. A. (2005) · Physical Medicine and Rehabilitation Clinics of North America · doi:10.1016/j.pmr.2005.08.016 · Cited by 25

Role of nutrition in patients with coexisting chronic obstructive pulmonary disease and sarcopenia

Nan, Y., Zhou, Y., Dai, Z., Yan, T., Zhong, P., Zhang, F., Chen, Q., & Peng, L. (2023) · Frontiers in Nutrition · doi:10.3389/fnut.2023.1214684 · Cited by 25

Eccentric exercise results in a prolonged increase in interleukin-6 and tumor necrosis factor-α levels in rat skeletal muscle

Zuo, Q., Qu, F., Li, N., Wang, S., Liu, J.-Y., Xu, C., & Yu, X.-K. (2019) · Journal of Muscle Research and Cell Motility · doi:10.1007/s10974-019-09554-6 · Cited by 17

Role of Protein Arginine Methyltransferases and Inflammation in Muscle Pathophysiology

So, H.-K., Kim, S., Kang, J., & Lee, S.-J. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.712389 · Cited by 23

The monoacylglycerol lipase inhibitor JZL184 decreases inflammatory response in skeletal muscle contusion in rats.

Jiang, S.-K., Zhang, M., Tian, Z.-L., Wang, M., Zhao, R., Wang, L.-L., Li, S.-S., Liu, M., Li, J.-Y., Zhang, M.-Z., et al. (2015) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2015.04.018 · Cited by 21

Dilated cardiomyopathy-mediated heart failure induces a unique skeletal muscle myopathy with inflammation

Song, T., Manoharan, P., Millay, D. P., Koch, S. E., Rubinstein, J., Heiny, J. A., & Sadayappan, S. (2019) · Skeletal Muscle · doi:10.1186/s13395-019-0189-y · Cited by 22

Redox-dependent regulation of satellite cells following aseptic muscle trauma: Implications for sports performance and nutrition

Παπανικολάου, Κ., Veskoukis, A. S., Draganidis, D., Baloyiannis, I., Deli, C. K., Poulios, A., Jamurtas, A. Z., & Fatouros, I. G. (2020) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2020.10.001 · Cited by 22

Myoblasts Inhibit Prostate Cancer Growth by Paracrine Secretion of Tumor Necrosis Factor-α

Stölting, M., Ferrari, S. M., Handschin, C., Becskei, A., Provenzano, M., Sulser, T., & Eberli, D. (2012) · The Journal of Urology · doi:10.1016/j.juro.2012.10.071 · Cited by 21

Transcriptional analysis of scar-free wound healing during early stages of tail regeneration in the green anole lizard, Anolis carolinensis

Xu, C., Hutchins, E. D., Tokuyama, M. A., Wilson‐Rawls, J., & Kusumi, K. (2019) · Journal of Immunology and Regenerative Medicine · doi:10.1016/j.regen.2019.100025 · Cited by 22

Selection of multipotent cells and enhanced muscle reconstruction by myogenic macrophage-secreted factors

Malerba, A., Vitiello, L., Segat, D., Dazzo, E., Frigo, M., Scambi, I., Coppi, P. D., Boldrin, L., Martelli, L., Pasut, A., et al. (2009) · Experimental Cell Research · doi:10.1016/j.yexcr.2009.01.005 · Cited by 22

Single cell analysis reveals satellite cell heterogeneity for proinflammatory chemokine expression

Andre, A. B., Rees, K. P., O’Connor, S. A., Severson, G. W., Newbern, J. M., Wilson‐Rawls, J., Plaisier, C. L., & Rawls, A. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1084068 · Cited by 22

Injury and Subsequent Regeneration of Muscles for Activation of Local Innate Immunity to Facilitate the Development and Relapse of Autoimmune Myositis in C57BL/6 Mice

Kimura, N., Hirata, S., Miyasaka, N., Kawahata, K., & Kohsaka, H. (2015) · Arthritis & Rheumatology · doi:10.1002/art.39017 · Cited by 20

Comparative evaluation of in vivo biocompatibility and biodegradability of regenerated silk scaffolds reinforced with/without natural silk fibers

Mobini, S., Taghizadeh-Jahed, M., Khanmohammadi, M., Moshiri, A., Naderi, M.-M., Heidari‐Vala, H., Helan, J. A., Khanjani, S., Springer, A., Akhondi, M. M., et al. (2015) · Journal of Biomaterials Applications · doi:10.1177/0885328215601925 · Cited by 20

Muscle-specific deletion of SOCS3 increases the early inflammatory response but does not affect regeneration after myotoxic injury

Swiderski, K., Thakur, S. S., Naim, T., Trieu, J., Chee, A., Stapleton, D., Koopman, R., & Lynch, G. S. (2016) · Skeletal Muscle · doi:10.1186/s13395-016-0108-4 · Cited by 21

KLF2 in Myeloid Lineage Cells Regulates the Innate Immune Response during Skeletal Muscle Injury and Regeneration

Manoharan, P., Song, T., Radzyukevich, T. L., Sadayappan, S., Lingrel, J. B., & Heiny, J. A. (2019) · iScience · doi:10.1016/j.isci.2019.07.009 · Cited by 17

Enhancing health span: muscle stem cells and hormesis

Calabrese, E. J., & Calabrese, V. (2022) · Biogerontology · doi:10.1007/s10522-022-09949-y · Cited by 17

Direct bone formation during distraction osteogenesis does not require TNFα receptors and elevated serum TNFα fails to inhibit bone formation in TNFR1 deficient mice

Wahl, E. C., Aronson, J., Liu, L., Skinner, R. A., Miller, M. J., Cockrell, G. E., Fowlkes, J. L., Thrailkill, K. M., Bunn, R. C., Ronis, M. J. J., et al. (2009) · Bone · doi:10.1016/j.bone.2009.09.011 · Cited by 16

Acid Sphingomyelinase Controls Early Phases of Skeletal Muscle Regeneration by Shaping the Macrophage Phenotype

Roux-Biejat, P., Coazzoli, M., Marrazzo, P., Zecchini, S., Renzo, I. D., Prata, C., Napoli, A., Moscheni, C., Giovarelli, M., Barbalace, M. C., et al. (2021) · Cells · doi:10.3390/cells10113028 · Cited by 16

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

TNF- regulates myogenesis and muscle regeneration by activating p38 MAPK

Chen, S.-E., Jin, B., & Li, Y.-P. (2006)

The Role of Tumor Necrosis Factor-alpha (TNF-α) in Skeletal Muscle Regeneration

Collins, R. A., & Grounds, M. D. (2001) · Journal of Histochemistry & Cytochemistry · doi:10.1177/002215540104900807 · Cited by 161

Physiological role of tumor necrosis factor α in traumatic muscle injury

Warren, G. L., Hulderman, T., Jensen, N., McKinstry, M., Mishra, M., Luster, M. I., & Simeonova, P. P. (2002) · The FASEB Journal · doi:10.1096/fj.02-0187fje · Cited by 248

TNF-α与ERK1/2在心脏毒素诱导的肌损伤再生修复中的作用研究

陈睿, 佘燕玲, 周珊瑶, 史华彩, & 黎程 (2016) · 新医学