The DOI matches its Crossref record; 151 of the 151 references it cites were found in a registry or an index.
Function of the myogenic regulatory factors Myf5, MyoD, Myogenin and MRF4 in skeletal muscle, satellite cells and regenerative myogenesis
Abstract
Discovery of the myogenic regulatory factor family of transcription factors MYF5, MYOD, Myogenin and MRF4 was a seminal step in understanding specification of the skeletal muscle lineage and control of myogenic differentiation during development. These factors are also involved in specification of the muscle satellite cell lineage, which becomes the resident stem cell compartment inadult skeletal muscle. While MYF5, MYOD, Myogenin and MRF4 have subtle roles in mature muscle, they again play a crucial role in directing satellite cell function to regenerate skeletal muscle: linking the genetic control of developmental and regenerative myogenesis. Here, I review the role of the myogenic regulatory factors in developing and mature skeletal muscle, satellite cell specification and muscle regeneration.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“First, up-regulation of Myf5 by ApN in skeletal muscle [56] allows the activation of satellite cells and their commitment to regenerate the skeletal muscle [67].”
From Adiponectin and Its Mimics on Skeletal Muscle: Insulin Sensitizers, Fat Burners, Exercise Mimickers, Muscling Pills … or Everything Together? (2020) · cites this paper as [67]
In the citing paper
“Third, ApN can coordinate the last step of skeletal muscle regeneration. Indeed, it activates the expression of two key factors of muscle differentiation, Myogenin and Mrf4 [56], which are essential for provoking cell fusion into multinucleated myotubes [67] (Figure 3).”
From Adiponectin and Its Mimics on Skeletal Muscle: Insulin Sensitizers, Fat Burners, Exercise Mimickers, Muscling Pills … or Everything Together? (2020) · cites this paper as [67]
In the citing paper
“Skeletal muscles of mdx-ApN mice displayed higher expression of two major factors of muscle proliferation (Myf5 and MyoD), and two major factors of muscle differentiation (Myogenin and Mrf4) [56,67].”
From Adiponectin and Its Mimics on Skeletal Muscle: Insulin Sensitizers, Fat Burners, Exercise Mimickers, Muscling Pills … or Everything Together? (2020) · cites this paper as [67]
Citations
Cites
SATELLITE CELL OF SKELETAL MUSCLE FIBERS
Mauro, A. (1961) · The Journal of Cell Biology · doi:10.1083/jcb.9.2.493 · Cited by 3,683
Expression of a single transfected cDNA converts fibroblasts to myoblasts
Davis, R. L., Weintraub, H. M., & Lassar, A. B. (1987) · Cell · doi:10.1016/0092-8674(87)90585-x · Cited by 3,388
Skeletal muscle mass and distribution in 468 men and women aged 18–88 yr
Janssen, I., Heymsfield, S. B., Wang, Z., & Ross, R. (2000) · Journal of Applied Physiology · doi:10.1152/jappl.2000.89.1.81 · Cited by 3,087
X chromosome-linked muscular dystrophy (mdx) in the mouse
Bulfield, G., Siller, W. G., Wight, P. A., & Moore, K. J. (1984) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.81.4.1189 · Cited by 1,765
MyoD or Myf-5 is required for the formation of skeletal muscle
Rudnicki, M. A., Schnegelsberg, P. N. J., Stead, R. H., Braun, T. W., Arnold, H.-H., & Jaenisch, R. (1993) · Cell · doi:10.1016/0092-8674(93)90621-v · Cited by 1,731
The myoD Gene Family: Nodal Point During Specification of the Muscle Cell Lineage
Weintraub, H. M., Davis, R. L., Tapscott, S. J., Thayer, M., Krause, M., Benezra, R., Blackwell, T. K., Turner, D. L., Rupp, R. A. W., Hollenberg, S. M., et al. (1991) · Science · doi:10.1126/science.1846704 · Cited by 1,581
Asymmetric self-renewal and commitment of satellite stem cells in muscle
Kuang, S., Kuroda, K., Le Grand, F., & Rudnicki, M. A. (2007) · Cell · doi:10.1016/j.cell.2007.03.044 · Cited by 1,449
Collins, C. A., Olsen, I., Zammit, P. S., Heslop, L., Petrie, A., Partridge, T. A., & Morgan, J. E. (2005) · Cell · doi:10.1016/j.cell.2005.05.010 · Cited by 1,445
Muscle deficiency and neonatal death in mice with a targeted mutation in the myogenin gene
Hasty, P., Bradley, A., Morris, J. H., Edmondson, D. G., Venuti, J. M., Olson, E. N., & Klein, W. H. (1993) · Nature · doi:10.1038/364501a0 · Cited by 1,364
Myogenin, a factor regulating myogenesis, has a domain homologous to MyoD
Wright, W. E., Sassoon, D. A., & Lin, V. K. (1989) · Cell · doi:10.1016/0092-8674(89)90583-7 · Cited by 1,261
Flagged first, then by citations
Cited by
Sorted by citations
MicroRNA therapy stimulates uncontrolled cardiac repair after myocardial infarction in pigs
Gabisonia, K., Prosdocimo, G., Aquaro, G. D., Carlucci, L., Zentilin, L., Secco, I., Ali, H., Braga, L., Gorgodze, N., Bernini, F., et al. (2019) · Nature · doi:10.1038/s41586-019-1191-6 · Cited by 478
Csapo, R., Gumpenberger, M., & Wessner, B. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.00253 · Cited by 458
Macrophage-derived glutamine boosts satellite cells and muscle regeneration
Shang, M., Cappellesso, F., Amorim, R., Serneels, J., Virga, F., Eelen, G., Carobbio, S., Rincón, M. Y., Maechler, P., Bock, K. D., et al. (2020) · Nature · doi:10.1038/s41586-020-2857-9 · Cited by 270
Myogenin promotes myocyte fusion to balance fibre number and size
Ganassi, M., Badodi, S., Quiroga, H. P. O., Zammit, P. S., Hinits, Y., & Hughes, S. M. (2018) · Nature Communications · doi:10.1038/s41467-018-06583-6 · Cited by 190
Myogenin is an essential regulator of adult myofibre growth and muscle stem cell homeostasis
Ganassi, M., Badodi, S., Wanders, K., Zammit, P. S., & Hughes, S. M. (2020) · eLife · doi:10.7554/elife.60445 · Cited by 159
Feng, L., Li, B., Xi, Y., Cai, M., & Tian, Z. (2021) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00344.2021 · Cited by 162
Fat infiltration in skeletal muscle: Influential triggers and regulatory mechanism
Wang, L., Valencak, T. G., & Shan, T. (2024) · iScience · doi:10.1016/j.isci.2024.109221 · Cited by 149
Mitochondrial fatty acid synthesis coordinates oxidative metabolism in mammalian mitochondria
Nowinski, S. M., Solmonson, A., Rusin, S. F., Maschek, J. A., Bensard, C., Fogarty, S., Jeong, M.-Y., Lettlová, S., Berg, J. A., Morgan, J. T., et al. (2020) · eLife · doi:10.7554/elife.58041 · Cited by 141
In Vitro Tissue‐Engineered Skeletal Muscle Models for Studying Muscle Physiology and Disease
Khodabukus, A., Prabhu, N. K., Wang, J., & Bursac, N. (2018) · Advanced Healthcare Materials · doi:10.1002/adhm.201701498 · Cited by 136
RAGE in the pathophysiology of skeletal muscle
Riuzzi, F., Sorci, G., Sagheddu, R., Chiappalupi, S., Salvadori, L., & Donato, R. (2018) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12350 · Cited by 117
Wong, C. Y. J., Al‐Salami, H., & Dass, C. R. (2020) · Journal of Pharmacy and Pharmacology · doi:10.1111/jphp.13359 · Cited by 112
Human myotube formation is determined by MyoD–Myomixer/Myomaker axis
Zhang, H., Wen, J., Bigot, A., Chen, J., Shang, R., Mouly, V., & Bi, P. (2020) · Science Advances · doi:10.1126/sciadv.abc4062 · Cited by 102
Ganassi, M., & Zammit, P. S. (2022) · European Journal of Translational Myology · doi:10.4081/ejtm.2022.10064 · Cited by 111
A Zfp609 circular RNA regulates myoblast differentiation by sponging miR-194-5p
Wang, Y., Li, M., Wang, Y., Liu, J., Zhang, M., Fang, X., Chen, H., & Zhang, C. (2018) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2018.09.039 · Cited by 92
Steyn, P. J., Dzobo, K., Smith, R., & Myburgh, K. H. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20215273 · Cited by 95
Methods for Accurate Assessment of Myofiber Maturity During Skeletal Muscle Regeneration
Yoshimoto, Y., Ikemoto‐Uezumi, M., Hitachi, K., Fukada, S., & Uezumi, A. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00267 · Cited by 92
Controlling cellular organization in bioprinting through designed 3D microcompartmentalization
Samandari, M., Alipanah, F., Majidzadeh‐A, K., Álvarez, M. M., Santiago, G. T., & Tamayol, A. (2021) · Applied Physics Reviews · doi:10.1063/5.0040732 · Cited by 87
Britson, K. A., Ling, J. P., Braunstein, K. E., Montagne, J. M., Kastenschmidt, J. M., Wilson, A., Ikenaga, C., Tsao, W., Pinal‐Fernandez, I., Russell, K. A., et al. (2022) · Science Translational Medicine · doi:10.1126/scitranslmed.abi9196 · Cited by 86
Ma, B., He, X., Lu, Z., Zhang, L., Li, J., Jiang, Y., Zhou, G., & Gao, F. (2018) · Poultry Science · doi:10.3382/ps/pey291 · Cited by 87
Long acting GLP-1 analog liraglutide ameliorates skeletal muscle atrophy in rodents
Gurjar, A. A., Kushwaha, S., Chattopadhyay, S., Das, N., Pal, S., China, S. P., Kumar, H., Trivedi, A. K., Guha, R., Chattopadhyay, N., et al. (2020) · Metabolism · doi:10.1016/j.metabol.2019.154044 · Cited by 79
Defining and identifying satellite cell-opathies within muscular dystrophies and myopathies
Ganassi, M., Muntoni, F., & Zammit, P. S. (2021) · Experimental Cell Research · doi:10.1016/j.yexcr.2021.112906 · Cited by 83
Myogenic Differentiation of Stem Cells for Skeletal Muscle Regeneration
Yu, D., Cai, Z., Li, D., Zhang, Y., He, M., Yang, Y., Liu, D., Xie, W., Li, Y., & Xiao, W. (2021) · Stem Cells International · doi:10.1155/2021/8884283 · Cited by 86
Dong, M., Zhang, L., Wu, P., Feng, L., Jiang, W., Liu, Y., Kuang, S., Li, S., Mi, H., Tang, L., et al. (2022) · Journal of Animal Science and Biotechnology/Journal of animal science and biotechnology · doi:10.1186/s40104-022-00747-7 · Cited by 77
Yan, Y., Li, M., Lin, J., Ji, Y., Wang, K., Yan, D., Shen, Y., Wang, W., Huang, Z., Jiang, H., et al. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.947387 · Cited by 84
Pathomechanisms and biomarkers in facioscapulohumeral muscular dystrophy: roles of DUX4 and PAX7
Banerji, C. R. S., & Zammit, P. S. (2021) · EMBO Molecular Medicine · doi:10.15252/emmm.202013695 · Cited by 76
Wang, S., Zhao, X., Liu, Q., Wang, Y., Li, S., & Xu, S. (2022) · Redox Biology · doi:10.1016/j.redox.2022.102255 · Cited by 78
Feraco, A., Gorini, S., Armani, A., Camajani, E., Rizzo, M., & Caprio, M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22179327 · Cited by 78
Abou-Samra, M., Selvais, C. M., Dubuisson, N., & Brichard, S. M. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21072620 · Cited by 72
Reductive stress impairs myogenic differentiation
Rajasekaran, N. S., Shelar, S. B., Jones, D. P., & Hoidal, J. R. (2020) · Redox Biology · doi:10.1016/j.redox.2020.101492 · Cited by 70
Ribeiro, A. F., Souza, L. S., de Almeida, C., Ishiba, R., Fernandes, S., Ayub-Guerrieri, D., dos Santos, A. L. F., Onofre-Oliveira, P. C. G., & Vainzof, M. (2019) · Scientific Reports · doi:10.1038/s41598-019-48156-7 · Cited by 69
Molecular Mechanisms Regulating Muscle Plasticity in Fish
Koganti, P. P., Yao, J., & Cleveland, B. M. (2020) · Animals · doi:10.3390/ani11010061 · Cited by 69
Human and mouse skeletal muscle stem and progenitor cells in health and disease
Mierzejewski, B., Archacka, K., Grabowska, I., Florkowska, A., Ciemerych, M. A., & Brzóska, E. (2020) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2020.01.004 · Cited by 70
Archacka, K., Grabowska, I., Mierzejewski, B., Graffstein, J., Górzyńska, A., Krawczyk, M., Różycka, A. M., Kalaszczyńska, I., Muras, G., Stremińska, W., et al. (2021) · Stem Cell Research & Therapy · doi:10.1186/s13287-021-02530-3 · Cited by 68
Master control: transcriptional regulation of mammalian Myod
Wardle, F. C. (2019) · Journal of Muscle Research and Cell Motility · doi:10.1007/s10974-019-09538-6 · Cited by 64
Banerji, C. R. S., Henderson, D., Tawil, R., & Zammit, P. S. (2020) · Human Molecular Genetics · doi:10.1093/hmg/ddaa164 · Cited by 62
Pancheri, E., Guglielmi, V., Wilczynski, G. M., Malatesta, M., Tonin, P., Tomelleri, G., Nowis, D., & Vattemi, G. N. A. (2020) · Cancers · doi:10.3390/cancers12092540 · Cited by 62
Chen, W., Lin, I., Lee, C., & Chen, Y. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22042123 · Cited by 61
New Human Chromosomal Sites with “Safe Harbor” Potential for Targeted Transgene Insertion
Pellenz, S., Phelps, M., Tang, W., Hovde, B. T., Sinit, R. B., Fu, W., Li, H., Chen, E. Y., & Monnat, R. J. (2019) · Human Gene Therapy · doi:10.1089/hum.2018.169 · Cited by 71
lncMGPF is a novel positive regulator of muscle growth and regeneration
Lv, W., Jin, J., Xu, Z., Luo, H., Guo, Y., Wang, X., Wang, S., Zhang, J., Zuo, H., Bai, W., et al. (2020) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12623 · Cited by 60
McDonald, C. M., Ramírez‐Sánchez, I., Oskarsson, B., Joyce, N. C., Aguilar, C., Nicorici, A., Dayan, J. G., Goude, E., Abresch, R. T., Villarreal, F. J., et al. (2020) · Muscle & Nerve · doi:10.1002/mus.27108 · Cited by 56
Shi, D., & Grifone, R. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.738978 · Cited by 58
Llano‐Diez, M., Fury, W., Okamoto, H., Bai, Y., Gromada, J., & Larsson, L. (2019) · Skeletal Muscle · doi:10.1186/s13395-019-0194-1 · Cited by 58
Guo, L., Cui, H., Zhao, G., Liu, R., Li, Q., Zheng, M., Guo, Y., & Wen, J. (2018) · BMC Genomics · doi:10.1186/s12864-018-5209-5 · Cited by 54
Epigenetic modifications in muscle regeneration and progression of Duchenne muscular dystrophy
Rugowska, A., Starosta, A., & Konieczny, P. (2021) · Clinical Epigenetics · doi:10.1186/s13148-021-01001-z · Cited by 65
Xu, D., Wan, B., Qiu, K., Wang, Y., Zhang, X., Jiao, N., Yan, E., Wu, J. W., Yu, R., Gao, S., et al. (2023) · Advanced Science · doi:10.1002/advs.202305080 · Cited by 55
Integrative single-cell RNA-seq and ATAC-seq analysis of myogenic differentiation in pig
Cai, S., Hu, B., Wang, X., Liu, T., Lin, Z., Tong, X., Xu, R., Chen, M., Duo, T., Zhu, Q., et al. (2023) · BMC Biology · doi:10.1186/s12915-023-01519-z · Cited by 60
Emerging role and function of Hippo-YAP/TAZ signaling pathway in musculoskeletal disorders
Han, J., Zhang, J., Zhang, X., Luo, W., Liu, L., Zhu, Y., Liu, Q., & Zhang, X. (2024) · Stem Cell Research & Therapy · doi:10.1186/s13287-024-04011-9 · Cited by 59
Myostatin gene promoter: structure, conservation and importance as a target for muscle modulation
Grade, C. V. C., Mantovani, C. S., & Alvares, L. E. (2019) · Journal of Animal Science and Biotechnology/Journal of animal science and biotechnology · doi:10.1186/s40104-019-0338-5 · Cited by 54
Anderson, J. E. (2021) · European Journal of Applied Physiology · doi:10.1007/s00421-021-04865-4 · Cited by 53
Skeletal muscle atrophy, regeneration, and dysfunction in heart failure: Impact of exercise training
Gallagher, H., Hendrickse, P. W., Pereira, M. G., & Bowen, T. S. (2023) · Journal of sport and health science/Journal of Sport and Health Science · doi:10.1016/j.jshs.2023.04.001 · Cited by 56
Azm, F. R. A., Kong, F., Tan, Q., Zhu, Y., Yu, H., Yao, J., & Luo, Z. (2020) · Aquaculture · doi:10.1016/j.aquaculture.2020.736169 · Cited by 50
Bioengineered in vitro skeletal muscles as new tools for muscular dystrophies preclinical studies
Fernández‐Costa, J. M., Fernández‐Garibay, X., Velasco‐Mallorquí, F., & Ramón‐Azcón, J. (2021) · Journal of Tissue Engineering · doi:10.1177/2041731420981339 · Cited by 48
Single-cell sequencing deconvolutes cellular responses to exercise in human skeletal muscle
Lovrić, A., Rassolie, A., Alam, S., Mandić, M., Saini, A. S., Altun, M., Fernandez‐Gonzalo, R., Gustafsson, T. P., & Rullman, E. (2022) · Communications Biology · doi:10.1038/s42003-022-04088-z · Cited by 51
Liang, W., Han, M., Guan, L., Dang, W., Wu, H., Meng, X., Zhen, Y., Lin, W., Ao, R., Hu, X., et al. (2024) · Biomaterials · doi:10.1016/j.biomaterials.2024.122529 · Cited by 47
Functional Non-coding RNA During Embryonic Myogenesis and Postnatal Muscle Development and Disease
Luo, H., Lv, W., Tong, Q., Jin, J., Xu, Z., & Zuo, B. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.628339 · Cited by 49
Sun, H., Sun, J., Li, M., Qian, L., Zhang, L., Huang, Z., Shen, Y., Law, B. Y. K., Liu, L., & Gu, X. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.730070 · Cited by 47
Skrivergaard, S., Rasmussen, M. K., Therkildsen, M., & Young, J. F. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22168376 · Cited by 49
MuSCs and IPCs: roles in skeletal muscle homeostasis, aging and injury
Jiang, H., Liu, B., Lin, J., Xue, T., Han, Y., Lu, C., Zhou, S., Gu, Y., Xu, F., Shen, Y., et al. (2024) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-023-05096-w · Cited by 53
Regulation of myogenic cell proliferation and differentiation during mammalian skeletal myogenesis
Wu, J., & Yue, B. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.116563 · Cited by 51
Grifone, R., Shao, M., Saquet, A., & Shi, D. (2020) · Cells · doi:10.3390/cells9081891 · Cited by 46
Zhang, N., Mendieta-Esteban, J., Magli, A., Lilja, K. C., Perlingeiro, R. C. R., Martı́-Renom, M. A., Tsirigos, A., & Dynlacht, B. D. (2020) · Nature Communications · doi:10.1038/s41467-020-19999-w · Cited by 49
Pyruvate dehydrogenase B regulates myogenic differentiation via the FoxP1–Arih2 axis
Jiang, X. J., Ji, S., Yuan, F., Li, T., Cui, S., Wang, W., Ye, X., Wang, R., Chen, Y. Q., & Zhu, S. (2022) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.13166 · Cited by 44
AdipoRon, a new therapeutic prospect for Duchenne muscular dystrophy
Abou‐Samra, M., Selvais, C. M., Boursereau, R., Lecompte, S., Noel, L., & Brichard, S. M. (2020) · Journal of Cachexia, Sarcopenia and Muscle · doi:10.1002/jcsm.12531 · Cited by 44
Skeletal muscle mass is controlled by the MRF4–MEF2 axis
Schiaffino, S., Dyar, K. A., & Calabria, E. (2018) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0000000000000456 · Cited by 44
Bioengineered human skeletal muscle capable of functional regeneration
Fleming, J. W., Capel, A. J., Rimington, R. P., Wheeler, P. C., Leonard, A. N., BISHOP, N. C., Davies, O. G., & Lewis, M. P. (2020) · BMC Biology · doi:10.1186/s12915-020-00884-3 · Cited by 45
Immunometabolism of macrophages regulates skeletal muscle regeneration
Chen, Y.-F., Lee, C., Wu, H.-H., Lin, W., & Lee, O. K. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.948819 · Cited by 46
Transcriptome analysis of embryonic muscle development in Chengkou Mountain Chicken
Ren, L., Liu, A., Wang, Q., Wang, H., Dong, D., & Liu, L. (2021) · BMC Genomics · doi:10.1186/s12864-021-07740-w · Cited by 43
Available In Vitro Models for Human Satellite Cells from Skeletal Muscle
Romagnoli, C., Iantomasi, T., & Brandi, M. L. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222413221 · Cited by 44
Duran, B. O. D. S., Zanella, B. T. T., Perez, E. S., Mareco, E. A., Blasco, J., Dal‐Pai‐Silva, M., & de la serrana, D. G. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23031180 · Cited by 42
Seo, E., Truong, C.-S., & Jun, H. (2022) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2022.115490 · Cited by 42
Bolívar‐Monsalve, E. J., Ceballos‐González, C. F., Chávez-Madero, C., de la Cruz‐Rivas, B. G., Velásquez‐Marín, S., Mora‐Godínez, S., Reyes‐Cortés, L. M., Khademhosseini, A., Weiss, P. S., Samandari, M., et al. (2022) · Advanced Healthcare Materials · doi:10.1002/adhm.202200448 · Cited by 41
Zhang, Z., Zhao, X., Wang, C., Huang, Y., Han, Y., & Guo, B. (2022) · Acta Biomaterialia · doi:10.1016/j.actbio.2022.08.036 · Cited by 41
Ghanim, H., Dhindsa, S., Batra, M., Green, K., Abuaysheh, S., Kuhadiya, N. D., Makdissi, A., Chaudhuri, A., & Dandona, P. (2019) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2018-01832 · Cited by 41
Cell interactome in sarcopenia during aging
González‐Blanco, L., Bermúdez, M., Bermejo-Millo, J. C., Gutiérrez‐Rodríguez, J., Solano, J. J., Antuña, E., Menéndez‐Valle, I., Caballero, B., Vega‐Naredo, I., Potes, Y., et al. (2022) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12937 · Cited by 41
Wang, M., Yang, J., Wu, Y., Li, H., Zhong, Y.-B., Luo, Y., & Xie, R. (2024) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.13535 · Cited by 40
Hsu, J. Y., Danis, E. P., Nance, S., O’Brien, J., Gustafson, A. L., Wessells, V. M., Goodspeed, A. E., Talbot, J. C., Amacher, S. L., Jedlicka, P., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110323 · Cited by 40
Felicioni, F., Pereira, A. D., Caldeira-Brant, A. L., Santos, T. G., Paula, T., Magnabosco, D., Bortolozzo, F. P., Tsoi, S. C. ‐., Dyck, M. K., Dixon, W. T., et al. (2020) · Journal of Anatomy · doi:10.1111/joa.13152 · Cited by 38
Exploring the lncRNAs Related to Skeletal Muscle Fiber Types and Meat Quality Traits in Pigs
Li, R., Li, B., Jiang, A., Cao, Y., Hou, L., Zhang, Z., Zhang, X., Liu, H., Kim, K., & Wu, W. (2020) · Genes · doi:10.3390/genes11080883 · Cited by 39
Kim, B., Ko, D., Choi, S. H., & Park, S. (2023) · Current Research in Food Science · doi:10.1016/j.crfs.2023.100545 · Cited by 38
Yan, Z., Yan, Z., Liu, S., Yin, Y., Yang, T. L., & Chen, Q. (2021) · Frontiers in Nutrition · doi:10.3389/fnut.2021.714567 · Cited by 37
Immunoregulation in cancer-associated cachexia
Wu, Q., Liu, Z., Li, B., Liu, Y., & Wang, P. (2023) · Journal of Advanced Research · doi:10.1016/j.jare.2023.04.018 · Cited by 42
Kim, C. H., Lee, H. J., Jung, D. Y., Kim, M., Jung, H. Y., Hong, H., Choi, Y., Yong, H. I., & Jo, C. (2023) · Food Bioscience · doi:10.1016/j.fbio.2023.102923 · Cited by 37
Zhou, Y., Liu, X., Huang, C., & Lin, D. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232213996 · Cited by 36
Mitochondrial mechanisms in the pathogenesis of chronic inflammatory musculoskeletal disorders
Wu, K., Shieh, J.-S., Qin, L., & Guo, J. J. (2024) · Cell & Bioscience · doi:10.1186/s13578-024-01259-9 · Cited by 39
Fatty infiltration in the musculoskeletal system: pathological mechanisms and clinical implications
Zhu, Y., Hu, Y., Pan, Y., Li, M., Niu, Y., Zhang, T., Sun, H., Zhou, S., Liu, M., Zhang, Y., et al. (2024) · Frontiers in Endocrinology · doi:10.3389/fendo.2024.1406046 · Cited by 44
Zhou, L., Lu, R., Huang, C., & Lin, D. (2021) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2021.685362 · Cited by 38
Cao, S., Xiao, Y., Huang, R., Zhao, D., Xu, W., Li, S., Tang, J., Qu, F., Jin, J., Xie, S., et al. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.913800 · Cited by 37
High Altitude Mediated Skeletal Muscle Atrophy: Protective Role of Curcumin
Chaudhary, P., Sharma, Y. K., Sharma, S., Singh, S. N., & Suryakumar, G. (2019) · Biochimie · doi:10.1016/j.biochi.2018.10.012 · Cited by 35
Cell-based meat: The molecular aspect
Azhar, A., Zeyaullah, M., Bhunia, S., Kacham, S., Patil, G., Muzammil, K., Khan, M. S., & Sharma, S. (2023) · Frontiers in Food Science and Technology · doi:10.3389/frfst.2023.1126455 · Cited by 35
Long-Term Cryopreservation and Revival of Tissue-Engineered Skeletal Muscle
Grant, L., Raman, R., Cvetkovic, C., Ferrall‐Fairbanks, M. C., Pagan‐Diaz, G. J., Hadley, P., Ko, E. C., Platt, M. O., & Bashir, R. (2018) · Tissue Engineering Part A · doi:10.1089/ten.tea.2018.0202 · Cited by 35
Hansen, P. J., & Tríbulo, P. (2019) · Biology of Reproduction · doi:10.1093/biolre/ioz030 · Cited by 39
Millward, D. J. (2021) · Nutrients · doi:10.3390/nu13030729 · Cited by 44
Isesele, P., & Mazurak, V. C. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.682091 · Cited by 38
DNA methylation of exercise-responsive genes differs between trained and untrained men
Geiger, C., Needhamsen, M., Emanuelsson, E. B., Norrbom, J., Steindorf, K., Sundberg, C. J., Reitzner, S. M., & Lindholm, M. E. (2024) · BMC Biology · doi:10.1186/s12915-024-01938-6 · Cited by 40
Xue, T., Zheng, H., Zhao, Y., Zhao, Z., Wang, J., Zhang, Y., Li, Y., Wang, S., Liu, Y., Xue, C., et al. (2024) · Communications Biology · doi:10.1038/s42003-024-07400-1 · Cited by 34
Telles, G. D., Libardi, C. A., Conceição, M. S., VECHIN, F. C., Lixandrão, M. E., de Andrade, A. L. L., Guedes, D. N., Ugrinowitsch, C., & CAMERA, D. M. (2021) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0000000000002632 · Cited by 33
Role of Adipokines in Sarcopenia
Lu, W., Feng, W., Lai, J., Yuan, D., Xiao, W., & Li, Y. (2023) · Chinese Medical Journal · doi:10.1097/cm9.0000000000002255 · Cited by 34
H3K27me3 Depletion during Differentiation Promotes Myogenic Transcription in Porcine Satellite Cells
Wang, S., Sun, Y., Ren, R., Xie, J., Tian, X., Zhao, S., Li, X., & Cao, J. (2019) · Genes · doi:10.3390/genes10030231 · Cited by 33
Xiao, F., Wang, J., Liu, H., Zhuang, M., Wen, X., Zhao, H., & Wu, K. (2023) · Animals · doi:10.3390/ani13243886 · Cited by 35
Brief Electrical Stimulation Promotes Recovery after Surgical Repair of Injured Peripheral Nerves
Gordon, T. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25010665 · Cited by 32
Metadata
- Authors
- Zammit, P. S.
- Affiliations
- King's College London (GB)
- Corresponding author
- Zammit, Peter S.
- ORCID
- Zammit, Peter S.
- Venue
- Seminars in Cell & Developmental Biology
- Publisher
- Elsevier BV
- Published
- 2017-12
- Volume
- 72
- Pages
- 19-32
- ISSN
- 1084-9521 (ISSN-L)
- OpenAlex
- W2769580895
- Cited by
- 887
- References
- 151
- Citations by year
- 2026: 114 · 2025: 108 · 2024: 156 · 2023: 112 · 2022: 117 · 2021: 108 · 2020: 95 · 2019: 48 · 2018: 28 · 2017: 1
- FWCI
- 4.37
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Seminars in Cell and Developmental Biology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Medical Research Council (MR/P023215/1)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Congenital heart defects research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Keywords
- myogenic regulatory factors, Myf5, MyoD, myogenin, MRF4, skeletal muscle development, satellite cells, muscle regeneration, myogenesis, muscle stem cells, transcription factors
- MeSH terms
- Animals, Regeneration, MyoD Protein, Myogenic Regulatory Factors, Myogenin, Muscle, Skeletal, Gene Expression Regulation, Developmental, Muscle Development, Satellite Cells, Skeletal Muscle, Myogenic Regulatory Factor 5
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review