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

Loss of Tob1 promotes muscle regeneration through muscle stem cell expansion

Kitajima, Y., Yoshioka, K., Mikumo, Y., Ohki, S., Maehara, K., Ohkawa, Y., & Ono, Y. (2024) · Journal of Cell Science · doi:10.1242/jcs.261886 · Cited by 1

Aerobic Exercise Protects against Cardiotoxin-Induced Skeletal Muscle Injury in a DDAH1-Dependent Manner

Feng, F., Luo, K., Yuan, X., Lan, T., Wang, S., Xu, X. Y., & Lu, Z. (2024) · Antioxidants · doi:10.3390/antiox13091069 · Cited by 1

Comparative Analysis of Skeletal Muscle Satellite Cells from Hanwoo Steers and Cows for Optimizing Cell-Based Meat Production

Kim, B., Kim, D., Choi, Y., Kim, J., Heo, S.-H., & Park, S. (2024) · Food Science of Animal Resources · doi:10.5851/kosfa.2024.e82 · Cited by 1

Ameliorating role of co-administration of granulocyte colony stimulating factor and sodium bicarbonate on the skeletal muscle of a rat model of chronic kidney disease (A histological and immunohistochemical study)

Ahmed, F. E., Hassen, E. Z., Mousa, F., & Abdelfadeel, K. (2024) · Ultrastructural Pathology · doi:10.1080/01913123.2024.2446242 · Cited by 1

Temporal Transcriptomic Analysis of Periodontal Disease Progression and Its Molecular Links to Systemic Diseases

Nantakeeratipat, T., Fujihara, C., & Takedachi, M. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26051998 · Cited by 1

Intramuscular Reactivity of the Modified Graphene Oxides and Their Bio-Reactivity in Aging Muscle

Jian, X., Wang, J., Hu, J., Li, Y., Wang, Q., Wang, H., Huang, J.-W., Ke, Y., & Liao, H. (2025) · Journal of Functional Biomaterials · doi:10.3390/jfb16040115 · Cited by 1

Comparative Transcriptomic Analysis Between High- and Low-Growth-Rate Meat-Type Rabbits Reveals Key Pathways Associated with Muscle Development

Yang, C., Zhu, L., Tang, L. P., Li, M., Zhang, X., 李丛艳, Zhang, C., Yuan, D., Zhang, M., & Xie, X. (2025) · Animals · doi:10.3390/ani15111585 · Cited by 1

Effects of Sleeve Gastrectomy and Treadmill Exercise on Skeletal Muscle and Ectopic Fat in High-Fat Diet-Induced Obese Rats

Noguchi, T., Yoshida, Y., Gotoh, K., Nagai, S., Sada, K., Matsuda, N., Suzuki, M., Kudo, A., Miyamoto, S., Ozeki, Y., et al. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26115294 · Cited by 1

Cultural optimization of pigeon muscle satellite cells and nutritional evaluation of the pigeon-derived cultivated meat

Dong, S., Chen, J., Li, S., Li, Y., Liang, X., Liu, Y., Zhang, M., Yang, F., Feng, R., & Liang, J. (2025) · Journal of Future Foods · doi:10.1016/j.jfutfo.2024.05.014 · Cited by 1

Evaluating the potential of graphene oxide to promote skeletal muscle complex regeneration

Chen, Y., Zhu, Z., Shen, Y., Liu, X., He, Y., Lyu, C., & Lu, J. (2025) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2025.1574145 · Cited by 1

Dietary biotin facilitates collagen deposition and myofiber growth and development, improving muscle chewiness and hardness in grass carp (Ctenopharyngodon idella)

Yang, Y., Jiang, W., Wu, P., Liu, Y., Ma, Y.-B., Kuang, S., Li, S., Tang, L., Zhong, C.-B., Feng, L., et al. (2025) · Food Bioscience · doi:10.1016/j.fbio.2025.107461 · Cited by 1

Novel insights into choline's role in promoting myofiber hypertrophy and mitochondrial function in muscle of sub-adult grass carp (Ctenopharyngodon idella)

Li, Q., Zhou, X., Feng, L., Jiang, W., Liu, Y., Ma, Y.-B., Kuang, S., Li, S., Tang, L., Zhong, C.-B., et al. (2025) · Animal nutrition · doi:10.1016/j.aninu.2025.03.023 · Cited by 1

Radiation-induced impairment of skeletal muscle regeneration

Čemažar, M., & Jurdana, M. (2025) · Radiology and Oncology · doi:10.2478/raon-2025-0048 · Cited by 1

Effect of the sdc4 gene knockdown on muscle development in zebrafish

Wang, A., Du, C., Liu, H., & Wang, H. (2025) · Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology · doi:10.1016/j.cbpb.2025.111171 · Cited by 1

Alleviating stocking density stress in juvenile rainbow trout (Oncorhynchus mykiss) through dietary nano-selenium: Effects on growth, antioxidant activity, and immune response

Ali, M., Akram, A., Jan, F. A., Ahmad, A., Hussain, A., Khan, F. U., & Arshad, M. (2025) · Journal of Trace Elements in Medicine and Biology · doi:10.1016/j.jtemb.2025.127798 · Cited by 1

Correlation of molecular and cellular signatures in primary skeletal muscle satellite cells derived from lean and diet-induced obese mice

Krabichler, F., Mayr, A. J., Seichter, K., Keshavarz, M., Knäbel, K., Stemmer, K., Koch, M., & Steingruber, L. (2025) · In Vitro Cellular & Developmental Biology - Animal · doi:10.1007/s11626-025-01130-2 · Cited by 1

Emerging roles of selenium nanoparticles in fish: Gene regulation, epigenetic modulation, and future directions for functional aquafeeds

Mahrous, E. S., Husseiny, W. A., & Elaswad, A. H. (2025) · Aquaculture · doi:10.1016/j.aquaculture.2025.743531 · Cited by 1

Transcriptomic Insights Reveal PRTFDC1 as a Novel Regulator of Myogenic Differentiation in Sujiang Pig Satellite Cells

Zhang, L., Ye, X., Sun, S., Zhang, L., Gu, Y., Cao, S., Zhou, M., Sun, W., Fu, C., Zhang, Q., et al. (2025) · Veterinary Sciences · doi:10.3390/vetsci12121197 · Cited by 1

Myogenic Potential in Labeo rohita Dorsal Muscle Cell Line and Development of CRISPR-Cas9 Construct for Myostatin Gene

Iqbal, G., Pinto, N., Sonwane, A., Rasal, K. D., Singh, L. S., Chikkathimmashetty, N. N., Pawaskar, D., & Goswami, M. (2025) · ACS Omega · doi:10.1021/acsomega.5c02861 · Cited by 1

Effects of Dietary Phenylalanine on Antioxidant Activity and Muscle Quality of Common Carp (Cyprinus carpio)

Sharifi, S. U., Naqeebullah, E., & Hemat, A. W. (2025) · Journal of Natural Science Review · doi:10.62810/jnsr.v3i4.331 · Cited by 1

Exercise and Dietary Factors in Skeletal Muscle Anabolism Across Aging: Inferences for the Insulin/IGF-1 Axis—A Narrative Review

Curiel-Cervantes, V. (2026) · Physiologia · doi:10.3390/physiologia6010005 · Cited by 1

Single-Cell Sequencing Reveals the Crosstalk Between MuSCs and FAPs in Ruminant Skeletal Muscle Development

Chen, Y., Gong, Y., Xu, X., Song, M., Sun, X., Luo, J., Guo, J., Li, L., & Zhang, H. (2026) · Cells · doi:10.3390/cells15020206 · Cited by 2

Functional role of THRAP3 in modulating thyroid hormone–mediated gene networks in C2C12 myotubes

Fukushima, T., Kuse, S., Hasegawa, Y., Fujioka, T., Nikawa, T., Masubuchi, S., & Sakakibara, I. (2026) · PLoS ONE · doi:10.1371/journal.pone.0341353 · Cited by 1

Dual-Mode Ventilation Promotes Diaphragm Function Recovery in Rats With Ventilator-Induced Diaphragmatic Dysfunction by Upregulating Insulin-Like Growth Factor-1

Zheng, X., Wu, L., Chen, Q., Lei, X., & Guo, S.-L. (2026) · Journal of Surgical Research · doi:10.1016/j.jss.2025.12.024 · Cited by 1

The ARHGAP10-202aa protein encoded by circARHGAP10 promotes skeletal muscle development and regeneration

Zhang, L., Ma, Y., Zhong, D., Gao, L., Huang, K., Li, X., Li, Z., Huang, J., Li, H., Chen, N., et al. (2026) · Journal of genetics and genomics/Journal of Genetics and Genomics · doi:10.1016/j.jgg.2026.01.008 · Cited by 1

Laser photobiomodulation enhances cell viability and regenerative gene expression in oxidative-stressed muscle cells

Silva-de-Oliveira, A. F. S., da Silva, J. L., dos Santos, N. T. B., Andraus, R. A. C., Poli‐Frederico, R. C., Oliveira, D. A. D. A. P., de Oliveira, R. F., & Luciana Prado, M. A. I. A. (2026) · Lasers in Medical Science · doi:10.1007/s10103-026-04811-w · Cited by 1

AmeloD regulates cell proliferation and differentiation process of ameloblasts through modulation of the sonic hedgehog (shh) signaling pathway

Oka, S., Chiba, Y., Sato, H., Chiba, M., Komine, I., Hirofuji, Y., Yamada, A., & Fukumoto, S. (2026) · Journal of Oral Biosciences · doi:10.1016/j.job.2026.100758 · Cited by 1

Hb-EGF directs systemic muscle repair

Dean, H. C., Saraswathy, V. M., Saini, A., Ou, T., McAdow, J. F., Tendolkar, A., Mokalled, M. H., & Johnson, A. N. (2026) · Development · doi:10.1242/dev.204993 · Cited by 1

Quercetin attenuates deoxynivalenol-induced muscle developmental disorders in broilers by modulating the PI3K/Akt/mTOR pathway and reducing apoptosis

Fang, Y., Fu, H., Jiang, X., Yang, H., Yin, Y., (112195), B. L., Chen, X., Shi, B., Cai, J., & Zhang, Z. (2026) · Poultry Science · doi:10.1016/j.psj.2026.106740 · Cited by 1

Effects of Chlorogenic Acid and 1,8-Cineole on Stress Resistance and Muscle Quality of Large Yellow Croaker (Larimichthys crocea)

Zhang, Y., Qu, P., Chen, P., Jiang, H., Zhang, C., Jiang, L., Mai, K., & Zhang, W. (2026) · Journal of Ocean University of China · doi:10.1007/s11802-026-6270-3 · Cited by 1

Epigenetics of Genes Displaying High and Preferential Expression in Myoblasts

Ehrlich, K. C., Lacey, M. R., Pradhan, S., & Ehrlich, M. (2026) · Epigenomes · doi:10.3390/epigenomes10010020 · Cited by 1

The Effect of Mechanical Loading on Mitophagy in Aged Myoblasts

Tolis, E., Chatzinikita, E., Moustogiannis, A., Giannopoulos, A., Maridaki, M. D., Koutsilieris, M., & Philippou, Α. (2026) · Cells · doi:10.3390/cells15060522 · Cited by 1

6‐Shogaol Attenuates Doxorubicin‐Induced Cardiac and Skeletal Muscle Atrophy by Inhibiting E3 Ubiquitin Ligases and Necroptosis

Sun, X., Wang, Y., Yang, Q., Xin, B., Huang, J., & Guo, C. (2026) · Phytotherapy Research · doi:10.1002/ptr.70276 · Cited by 1

Dynamic development of muscle during embryogenesis in Arbor Acres broilers and TaoYuan chickens revealed by RNA sequencing

Zhao, D., Shi, Y., Ouyang, Q., Zhang, H. S., Guo, Y., Song, Z., & He, X. (2026) · BMC Genomics · doi:10.1186/s12864-026-12795-8 · Cited by 1

Microbiota-associated metabolite pantothenic acid enhances skeletal muscle contusion repair via epigenetic regulation of macrophage M2 polarization

Wu, L., Zhang, Y., Zhang, G., Feng, X., Zhu, W., Yang, H., Ji, X., Yin, M., Li, S., Li, Y., et al. (2026) · Journal of Translational Medicine · doi:10.1186/s12967-026-08087-0 · Cited by 1

HuR-mediated regulation of mTOR mRNA stability promotes the commitment of satellite cells towards myogenesis

Tremblay, A. K., Sánchez, B. J., Colalillo, B., Mubaid, S., Sadek, J., Lian, X. J., Diaz-Gaxiola, A., Marco, S. D., & Gallouzi, I. (2026) · Cell Death and Disease · doi:10.1038/s41419-026-08759-1 · Cited by 1

Tauroursodeoxycholic acid (TUDCA) ameliorates age‐related skeletal muscle loss

Carvalho, M. U. W. B. D., Barssotti, L., dos Santos, L. M. B., Rosa, L. R. D. O., Gomes‐Marcondes, M. C. C., CARNEIRO, E. M., Barbosa, H. C. L., & Zangerolamo, L. (2026) · The Journal of Physiology · doi:10.1113/jp290683 · Cited by 2

Single-Cell RNA Sequencing Reveals Cellular Heterogeneity and Developmental Dynamics of Goose Satellite Cells During Embryogenesis

Wang, C., LIU, Y. F., Jiang, G., Li, C., Shi, K., Chen, S., Wang, H., & He, D. (2026) · Cells · doi:10.3390/cells15110983 · Cited by 1

Integrative analysis of RNA-seq and Ribo-seq reveals that lncRNA regulates chicken myogenesis through encoding peptide

Niu, Y., He, L., An, Z., Yuan, M., Ji, H., Wang, W., Wei, C., Han, R., Tian, W., Tian, Y., et al. (2026) · Journal of Animal Science and Biotechnology/Journal of animal science and biotechnology · doi:10.1186/s40104-026-01421-y · Cited by 2

Dietary inclusion of black soldier fly larvae as a partial protein source: effects on growth performance, carcass traits and meat quality of broilers

Jiang, Q., CHEN, S., Li, Y., Zhou, Z., Zhang, M., Sun, Y., Zhang, L., Li, Y., Zhang, X., Qu, Y., et al. (2026) · British Poultry Science · doi:10.1080/00071668.2026.2620609 · Cited by 1

Thermal manipulation during mid-embryogenesis alters myogenic gene expression and muscle morphometry in broilers

Lobato, H. C., de Souza, O. F., Vieira, M. C., Bernardes, L. F., de Araújo, V. F., Galvão, C. B., Ribeiro, A. F., Alfaro, C. D. A., Carrasco, K. X. N., Jorge, É. C., et al. (2026) · Journal of Thermal Biology · doi:10.1016/j.jtherbio.2026.104502 · Cited by 1

The cGAS–STING pathway contributes to cisplatin-induced skeletal muscle atrophy through altered proteostasis and myogenic signaling

Liu, X., Xu, M., Wang, H., Wang, H., Wang, H., Fang, W., Li, M., Huang, J., Chen, F. C., Wang, H., et al. (2026) · Cell Communication and Signaling · doi:10.1186/s12964-026-02989-8 · Cited by 1

A bioengineered platform reveals progressive impairment of skeletal muscles by metabolic dysfunction-associated steatotic liver disease-derived factors

Cortés-Reséndiz, A., Fernández‐Costa, J. M., Sabater-Arcis, M., Chiara, F. D., & Ramón‐Azcón, J. (2026) · Disease Models & Mechanisms · doi:10.1242/dmm.052820 · Cited by 1

Methods to Mimic In Vivo Muscle Cell Biology in Primary Human Myoblasts Using Quiescence as a Guidepost in Regenerative Medicine Research

Gudagudi, K. B., & Myburgh, K. H. (2021) · OMICS A Journal of Integrative Biology · doi:10.1089/omi.2020.0211 · Cited by 1

Muscle adaptation to sleeve gastrectomy: Potential role of nutritional supplementation and physical exercise

Saber, E. A., Aziz, N. M., Aleem, M. M. A. E., Kamel, M. Y., El‐Aleem, S. A. A., Ali, F. F., Ali, D. M. E., & Behery, A. F. (2021) · Acta Biochimica Polonica · doi:10.18388/abp.2020_5565 · Cited by 1

Time to surgery and myo-d expression in biceps muscle of adult brachial plexus injury: a preliminary study

Suroto, H., Wardana, G. R., Sugianto, J. A., Aprilya, D., & Samijo, S. K. (2023) · BMC Research Notes · doi:10.1186/s13104-023-06317-y · Cited by 1

The Presence of Two MyoD Genes in a Subset of Acanthopterygii Fish Is Associated with a Polyserine Insert in MyoD1

White, L. J., Russell, A. J., Pizzey, A. R., Dasmahapatra, K. K., & Pownall, M. E. (2023) · Journal of Developmental Biology · doi:10.3390/jdb11020019 · Cited by 1

Effect of fermented sarco oyster extract on age induced sarcopenia muscle repair by modulating regulatory T cells

Byun, K.-A., Oh, S., Batsukh, S., Rheu, K.-M., Lee, B.-J., Son, K. H., & Byun, K. (2023) · Fisheries and aquatic sciences · doi:10.47853/fas.2023.e34 · Cited by 1

Bioprocessing Considerations towards the Manufacturing of Therapeutic Skeletal and Smooth Muscle Cells

Franchi-Mendes, T., Silva, M., Cartaxo, A. L., Fernandes‐Platzgummer, A., Cabral, J. M. S., & da Silva, C. L. (2023) · Bioengineering · doi:10.3390/bioengineering10091067 · Cited by 1

Ectopic myogenesis and fibrosis accompany adipogenesis during thymic involution induced by repeated cocaine administration

Unuma, K., Wen, S., Aki, T., & Uemura, K. (2023) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2023.149201 · Cited by 1

Structural Analysis and Phylogenetic Relationship of a Lepidopteran Scopelodes kwangtungensis Based on its Complete Mitochondrial Genome Sequence

Chu, P., Xing, J., Li, F., Li, T., & Qiao, Z. (2024) · Pakistan Journal of Zoology · doi:10.17582/journal.pjz/20230730111147 · Cited by 1

Molecular cloning of TPM3 gene in qinchuan cattle and its effect on myoblast proliferation and differentiation

Guo, J., Wang, J., Zhang, K., Yang, Z., Li, B., Pan, Y., Yu, H., Yu, S., Raza, S. H. A., Abebe, B. K., et al. (2024) · Animal Biotechnology · doi:10.1080/10495398.2024.2345238 · Cited by 1

Comprehensive analysis of the expression patterns and function of the FTO–LINE1 axis in yak tissues and muscle satellite cells

Ma, Z., Chai, Z., Yang, H., Zhang, X., Zhao, H., Luo, X., Zhong, J., & Wu, Z. (2024) · Frontiers in Veterinary Science · doi:10.3389/fvets.2024.1448587 · Cited by 1

Deletion of RBM20 exon 9 impairs skeletal muscle growth and satellite cell function in pigs

Zhang, L., Fu, C., Zhou, M., Miao, W., Sun, W., Xu, J., Cao, S., & Zhu, S. (2024) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2024.151076 · Cited by 1

Relationships Among Growth, Carcass Characteristics, and Myf5 Myf6, MyoD, and MyoG Genes Expression Level in Saanen Male Kids with Varying Slaughter Weights

Şen, U., Gökçek, D., Yılmaz, Ö. F., Yüksel, H. M., Önder, H., Şirin, E., Bozkurt, S., Ocak, S., Yücel, C., Omarova, K., et al. (2024) · Animals · doi:10.3390/ani15010016 · Cited by 1

Identification of highly expressed genes and efficient core promoters specific to buffalo skeletal muscles

Huang, J., Guo, D., Zhu, R., Wang, H., Yang, C., Shi, D., & Shang, J. (2025) · Archives animal breeding/Archiv für Tierzucht · doi:10.5194/aab-68-67-2025 · Cited by 1

Cloning and Transcriptional Activity Analysis of the Bovine CDH11 Gene Promoter: Transcription Factors Sp1 and GR Regulate Bovine CDH11 Expression

Liu, Z., Bai, Y., Chen, Z., Niu, Y., Jia, X., Li, L., Zhang, X., Shi, B. S., Zhao, Z., Hu, J., et al. (2025) · Animals · doi:10.3390/ani15091217 · Cited by 1

Neuromuscular junction transcriptome analysis of spinal and bulbar muscular atrophy mice implicates sarcomere gene expression and calcium flux dysregulation in disease pathogenesis

Gromova, A., Cha, B., Nguyen, N., Garg, D., Coscolluela, C., Strickland, L. M., Luong, D., Longo, F., Sopher, B. L., ElMallah, M. K., et al. (2025) · Human Molecular Genetics · doi:10.1093/hmg/ddaf074 · Cited by 1

Functional Mutations in the VRTN Gene Influence Growth Traits and Meat Quality in Hainan Black Goats

Xu, M., Huang, J., Wang, K., Zhang, Y., Zhou, H., Wang, F., & Han, J. (2025) · Veterinary Sciences · doi:10.3390/vetsci12100936 · Cited by 3

Role of satellite cells in growth and regeneration of skeletal muscles

Ciecierska, A., Sadkowski, T., & Motyl, T. (2019) · Medycyna Weterynaryjna · doi:10.21521/mw.6349 · Cited by 1

Skeletal muscle protein catabolism, protein anabolism, and myogenesis after various types of insults

Ono, Y., Saito, M., Fujinami, Y., Inoue, S., & Kotani, J. (2020) · The Japanese Journal of SURGICAL METABOLISM and NUTRITION · doi:10.11638/jssmn.54.3_139 · Cited by 1

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Alshamaileh, H., Кулібаба, Р. О., Liashenko, Y. V., & Borzova, H. S. (2021) · The Scientific and Technical Bulletin of the Institute of Animal Science NAAS of Ukraine · doi:10.32900/10.32900/2312-8402-2021-125-69-78 · Cited by 1

Epigenetic modifications in induced pluripotent stem cells to boost myogenic commitment

Breuls, N., Giarratana, N., Yedigaryan, L., & Sampaolesi, M. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-99892-5.00019-0 · Cited by 1

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Prüller, J., & Zammit, P. S. (2020) · Springer eBooks · doi:10.1007/978-3-319-08831-0_2 · Cited by 1

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Papanikolaou, N. A., Nikolaidis, M., Amoutzias, G. D., Fouza, A., Papaioannou, M., Pandey, A., & Papavassiliou, A. G. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24032124 · Cited by 1

Noggin Combined With Dental Pulp Stem Cells Repair Muscle Injury Through Smad/Pax7 Signaling PathwayPreprint

Zhang, M., Yu, L.-M., Zhang, W., Deng, J., Sun, B., Chen, M., Huang, W., He, H., Han, X., & Liu, Y. (2021) · Research Square · doi:10.21203/rs.3.rs-861400/v1 · Cited by 1

Exon skipping in genes encoding lineage-defining myogenic transcription factors in rhabdomyosarcomaPreprint

Butler, E. B., Xu, L., Rakheja, D., Schwettmann, B., Toubbeh, S., Guo, L. M., Kim, J., Skapek, S. X., & Zheng, Y. (2022) · Molecular Case Studies · doi:10.1101/mcs.a006190 · Cited by 1

Comparative Transcriptome Profiling of Skeletal Muscle From Fujian White Rabbit (Oryctolagus cuniculus) at Different Growth Stages Using RNA-SeqPreprint

Chen, D., Lei, S., Sun, S., Chen, Y., Wang, J., Gao, C., & Xie, X. (2023) · Preprints.org · doi:10.20944/preprints202306.0379.v1 · Cited by 1

20(S)-ginsenoside Rg3 promotes myoblast differentiation and inhibits myotube atrophy by protecting mitochondrial function via AMPK/FoxO3 pathway in high glucose-induced modelPreprint

Wang, M., Chen, X., Yan, X., Zhao, Y., Cai, C., Li, Y., Liu, F., & Sun, L. (2023) · Research Square · doi:10.21203/rs.3.rs-3026554/v1 · Cited by 1

Metabolism regulates muscle stem cell self-renewal by connecting the microenvironment and histone acetylationPreprint

Ly, C., Chung, J. D., Nguyen, J. H. V., Tian, L., Schröder, J., Knaupp, A. S., Su, S., Trieu, J., Salmi, T. M., Amann‐Zalcenstein, D., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.07.04.547746 · Cited by 1

REST/NRSF preserves muscle stem cell identity and survival by repressing alternate cell fatesPreprint

Soleimani, V. D., Sahinyan, K., Blackburn, D. M., Simon, M.-M., Lazure, F., Kwan, T., Wilson, D. H., von Maltzahn, J., Yamada, Y., Jahani‐Asl, A., et al. (2024) · Research Square · doi:10.21203/rs.3.rs-4396883/v1 · Cited by 1

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De, B., Lei, B., Chen, Y., Lü, L., Liu, Y., Meng, F., Jia, T., Wang, S., Li, T., Liu, C., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.09.02.673668 · Cited by 1

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Júnior, A. F. R. (2018) · doi:10.11606/d.41.2018.tde-01062018-122959

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Sakamoto, K. (2018) · YAKUGAKU ZASSHI · doi:10.1248/yakushi.18-00091-3

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Pereira, A. D., Felicioni, F., Caldeira-Brant, A. L., Magnabosco, D., Bortolozzo, F. P., Tsoi, S. C. ‐., Dyck, M. K., Dixon, W. T., Martinelli, P. M., Jorge, É. C., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/524629

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Prüller, J., & Zammit, P. S. (2018) · Springer eBooks · doi:10.1007/978-3-319-37076-7_2-1

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Liu, L. (2019) · Queensland University of Technology · doi:10.5204/thesis.eprints.131581

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de Almeida, C. (2019) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.41.2019.tde-27082019-090701

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Phua, W. W. T. (2019) · doi:10.32657/10220/49672

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rasouli, H., Farzanegi, P., & Abbaszadeh, H. (2020) · Medical Laboratory Journal · doi:10.52547/mlj.14.6.41

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Sanvee, G. M., Bouitbir, J., & Kraehenbuehl, S. (2021) · Research Square · doi:10.21203/rs.3.rs-348598/v1

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Vepkhvadze, T. F., Vorotnikov, A. V., & Popov, D. V. (2021) · Biochemistry (Moscow) · doi:10.31857/s0320972521050080

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de Sena, I. G., & GOMES, T. D. S. (2021) · Multidisciplinary Reviews · doi:10.29327/multi.2021013

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Xie, S., Fang, C., Gao, Y., Yan, J., Luo, L., Sun, Y., & Liang, X. (2021) · Research Square · doi:10.21203/rs.3.rs-560801/v1

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Gremminger, V. L. (2021) · MOspace Institutional Repository (University of Missouri) · doi:10.32469/10355/85774

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Vlasman, S. (2021) · doi:10.15760/honors.1136

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Terruzzi, I. (2021) · Springer eBooks · doi:10.1007/978-3-030-80267-7_12

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Petry, B. (2021) · doi:10.11606/t.11.2021.tde-10092021-125732

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Telles, G. D. (2019) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.39.2019.tde-22102021-122843

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Carlson, B. M. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-820278-4.00011-6 · Cited by 1

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Contriciani, R. E. (2018) · doi:10.47749/t/unicamp.2018.1059186

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Zheng, X., Zhang, W., Wu, J., Hu, Y., Zhang, X., Hao, F., Han, J., Hao, W., Wang, R., Tian, M., et al. (2022) · Research Square · doi:10.21203/rs.3.rs-1473019/v1

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EBIHARA, R., Bhandari, S., Choe, S., Qahar, M., Mizunoya, W., Tatsumi, R., & NAKAMURA, M. (2022) · Journal of the Faculty of Agriculture Kyushu University · doi:10.5109/4772335

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(2022) · PeerJ · doi:10.7287/peerj.13150v0.1/reviews/2

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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

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

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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

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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