Function of the myogenic regulatory factors Myf5, MyoD, Myogenin and MRF4 in skeletal muscle, satellite cells and regenerative myogenesis

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

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

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

Effects of L‐Carnitine and Fenofibrate on Lipid Metabolism, Oxidative Status, and Flesh Quality of Yellow River Carp ( Cyprinus carpio )

Zhao, M., Zhi, S., Qin, C., Yang, L., & Nie, G. (2026) · Aquaculture Nutrition · doi:10.1155/anu/1500743

Biomolecular condensates as dynamic regulators of musculoskeletal homeostasis, disease, and therapeutic challenges

Miao, Q., Gao, R., Huang, M., Wang, G., Wang, W., & Luo, M. B. (2026) · Bone Research · doi:10.1038/s41413-026-00578-6

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Rodrigues, G. D. A., Silva, C. B., Lopes, B. Q., Monteiro, P. V., Valério, M. N., Lopes, M. M., Serão, N. V. L., Duarte, M., & Saraiva, A. (2026) · Meat and Muscle Biology · doi:10.22175/mmb.24700

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Wang, B. (2026) · Journal of Animal Science and Biotechnology/Journal of animal science and biotechnology · doi:10.1186/s40104-026-01475-y

Effects of a 4-wk high-fat diet on transcriptome and DNA methylation after muscle contractions in rat skeletal muscle

Nehashi, R., Kawata, K., Sotani, Y., Kusano, T., Kano, R., Takeda, R., Sudo, M., Kano, Y., & Hoshino, D. (2026) · Physiological Genomics · doi:10.1152/physiolgenomics.00168.2026

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Uçar, N., Özbek, M., Karaca, H., Simsek, M., Fırat, T., & Öner, H. (2026) · Bratislavské lekárske listy/Bratislava medical journal · doi:10.1007/s44411-026-00831-8

Phase-transition failure in aged skeletal muscle regeneration

Zhang, B., Shi, H., Guo, X., & Wang, Y. (2026) · Biogerontology · doi:10.1007/s10522-026-10500-6

The ageing microenvironment in sarcopenia: early alterations and targeted therapeutic strategies

Zhang, L., Li, G., Long, L., Pan, L., Bai, Y., Ni, L., Han, L., & Cao, R. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1929891

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Lee, W., 양성재, Yu, H., Kim, Y., Cho, S., Kim, H. Y., Kim, U., Kong, H., & Kim, S. B. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27177894

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Cui, W. (2026) · Revista Brasileira de Farmacognosia · doi:10.1007/s43450-026-00802-8

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Cao, X., Song, Y., Zhang, Z., Ji, H., Jiang, X., Li, N., Wang, L., Luo, X., Cui, H., & Sun, J. (2026) · All Life · doi:10.1080/26895293.2026.2724024

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Kim, D. B., Lee, H. J., Lee, H. W., Jang, H. G., Oh, S.-H., Kim, J. H., & Lee, S. Y. (2026) · Food Science of Animal Resources · doi:10.1007/s44463-026-00103-7

Integrated RNA-seq and ATAC-seq analyses reveal muscle development differences between european meat pigeon and shiqi pigeon during embryonic to post-hatching stages

Han, Y., Hong, P., Liu, Z., Chen, T., Chang, K., Chen, W., Zhong, Y., Qiu, Z., Zheng, Z., Li, X., et al. (2026) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2026.1908892

Decoding SUMOylation as a metabolic stress sensor in aging and age-related disorders: Mechanisms, tissue specificity and therapeutic potential

Liu, X., Chen, S., Liu, D., Zou, S., Deng, L., Gao, Y., Xu, W., Xie, Y., Peng, J., & Hao, L. (2026) · Ageing Research Reviews · doi:10.1016/j.arr.2026.103369

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Yadav, S., Sharma, T., Olea‐Flores, M., Padilla‐Benavides, T., & Imbalzano, A. N. (2026) · PLoS ONE · doi:10.1371/journal.pone.0358038

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Kumari, P., Raval, A. A., Rana, P. S. J. B., Kaushik, R., Sahi, A., Gundu, S., & Mahto, S. K. (2026) · Annals of Anatomy · doi:10.1016/j.aanat.2026.153381

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Yang, Z., Wu, C., Zou, J., & Yuan, Y. (2026) · Progress in Biophysics and Molecular Biology · doi:10.1016/j.pbiomolbio.2026.101955

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Adamcová, M., & Petráň, L. (2026) · Molecular Biomedicine · doi:10.1186/s43556-026-00597-z

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Lee, E. J., Ahmad, K., Shaikh, S., Lim, J. H., Ahmad, S. S., Seo, M., & Choi, I. (2026) · Food Science of Animal Resources · doi:10.1007/s44463-026-00108-2

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Ishikawa, A., Sato, H., Chiba, Y., Oka, S., Chiba, M., Yamada, A., & Fukumoto, S. (2026) · Pediatric Dental Journal · doi:10.1016/j.pdj.2026.100398

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Zhao, C., Gong, Y., Zheng, L. P., & Zhao, M. (2026) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.6c09331

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Liu, J., Liu, Y., Sun, X., Zhang, X., Xing, T., Zhang, L., Gao, F., & Zhao, L. (2026) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2026.154869

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Wang, Y., Liu, K., Luo, H., Zhang, W., Xu, X., Yang, Q., & Zhang, W. (2026) · Cell Biology International · doi:10.1002/cbin.70228

Potentially food-compatible cellulose acetate scaffolds functionalized with galactomannan and L-alanine: Effects on collagen production and early myogenic responses—A preliminary study

Ruengket, P., Maimansomsuk, S., Purananunak, C., Sinthuvanich, C., Phonphoem, W. P., Aramrak, A., Arikit, S., Yokthongwattana, C., Phuthong, W., Srikulnath, K., et al. (2026) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2026.154983

TRPV1 mediates tetrathiomolybdate-induced muscle hypertrophy via peroxynitrite-dependent redox signaling

Lu, S., 周, 一., Liu, L., 段志贵, Xiang, R., Wei, F., & Li, G. (2026) · Biochemical Pharmacology · doi:10.1016/j.bcp.2026.118566

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Kim, G. M., Baek, K., Lee, A. Y., Ko, T., Lee, M., Kim, J. H., & Kim, H. Y. (2026) · Applied Biological Chemistry · doi:10.1186/s13765-026-01150-w

Skeletal Muscle Gene Expression in Nellore Cattle Fed Guanidinoacetic Acid During the Growing and Finishing Phases

Soares, L. C. B., Huang, L., Ramírez-Zamudio, G. D., Ramos, M. E., Fidelis, S. D. S., Miranda, A. D. S., Merighe, G. K. F., Negrão, J. A., Dahlen, C. R., Cônsolo, N. R. B., et al. (2026) · Animals · doi:10.3390/ani16213353

Automated Quantitative Analysis of Myogenesis in Isolated Mouse and Rat Muscle Stem Cells

Garcia, P., Gurlekian, Z., Desaulniers, R., & Dumont, N. A. (2026) · Methods in molecular biology · doi:10.1007/978-1-0716-5643-3_11

Targeted Chromatin Profiling in Muscle Stem Cells Using a CUT&RUN-qPCR Strategy

Pintart, A., Cicciarello, D., & Scionti, I. (2026) · Methods in molecular biology · doi:10.1007/978-1-0716-5643-3_21

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Iwuchukwu, G. A., Gökçek, D., & Özdemir, Z. (2024) · Black Sea Journal of Agriculture · doi:10.47115/bsagriculture.1480033 · Cited by 3

A role for the myogenic determination gene Myf5 in adult regenerative myogenesis

Gayraud-Morel, B., Chrétien, F. C., Flamant, P., Gomès, D., Zammit, P. S., & Tajbakhsh, S. (2007) · Developmental Biology · doi:10.1016/j.ydbio.2007.08.059 · Cited by 240

Molecular mechanisms regulating myogenic determination and differentiation

Robert, L. S. P. (2000) · Frontiers in bioscience · doi:10.2741/perry · Cited by 369

The myogenic regulatory factors, determinants of muscle development, cell identity and regeneration

Hernández‐Hernández, J. M., García-González, E. G., Brun, C. E., & Rudnicki, M. A. (2017) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2017.11.010 · Cited by 669

In vivo satellite cell activation via Myf5 and MyoD in regenerating mouse skeletal muscle

Cooper, R. N., Tajbakhsh, S., Mouly, V., Cossu, G., BUCKINGHAM, M. E., & Butler-Browne, G. S. (1999) · Journal of Cell Science · doi:10.1242/jcs.112.17.2895 · Cited by 457