Cited by 929Muscle Physiology and DisordersCongenital heart defects researchDevelopmental Biology and Gene Regulation

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

Zammit, Peter S.·2017·Seminars in Cell & Developmental Biology

DOI 10.1016/j.semcdb.2017.11.011

Open this paper in CoChat — free account

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.

Integrity signals

Registry

Crossref · 10.1016/j.semcdb.2017.11.011

Cites

151 of 151 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

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?

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
A Pax3/Pax7-dependent population of skeletal muscle progenitor cells
Relaix, F., Rocancourt, D., Mansouri, A., & BUCKINGHAM, M. E. (2005) · Nature · doi:10.1038/nature03594 · Cited by 1,167
Satellite cells as the source of nuclei in muscles of growing rats
Moss, F. P., & Leblond, C. P. (1971) · The Anatomical Record · doi:10.1002/ar.1091700405 · Cited by 1,025
Myogenin gene disruption results in perinatal lethality because of severe muscle defect
Nabeshima, Y., Hanaoka, K., Hayasaka, M., Esuml, E., Li, S., Nonaka, I., & Nabeshima, Y.-I. (1993) · Nature · doi:10.1038/364532a0 · Cited by 954
Single-Cell Analysis of Regulatory Gene Expression in Quiescent and Activated Mouse Skeletal Muscle Satellite Cells
Cornelison, D., & Wold, B. J. (1997) · Developmental Biology · doi:10.1006/dbio.1997.8721 · Cited by 934
Muscle satellite cells adopt divergent fates
Zammit, P. S., Golding, J. P., Nagata, Y., Hudon, V., Partridge, T. A., & Beauchamp, J. R. (2004) · The Journal of Cell Biology · doi:10.1083/jcb.200312007 · Cited by 924
Expression of Cd34 and Myf5 Defines the Majority of Quiescent Adult Skeletal Muscle Satellite Cells
Beauchamp, J. R., Heslop, L., Yu, D. S., Tajbakhsh, S., Kelly, R. G., Wernig, A., BUCKINGHAM, M. E., Partridge, T. A., & Zammit, P. S. (2000) · The Journal of Cell Biology · doi:10.1083/jcb.151.6.1221 · Cited by 917
A novel human muscle factor related to but distinct from MyoD1 induces myogenic conversion in 10T1/2 fibroblasts.
Braun, T. W., Buschhausen-Denker, G., Bober, E., Tannich, E., & Arnold, H.-H. (1989) · The EMBO Journal · doi:10.1002/j.1460-2075.1989.tb03429.x · Cited by 906
Redefining the Genetic Hierarchies Controlling Skeletal Myogenesis: Pax-3 and Myf-5 Act Upstream of MyoD
Tajbakhsh, S., Rocancourt, D., Cossu, G., & BUCKINGHAM, M. E. (1997) · Cell · doi:10.1016/s0092-8674(00)80189-0 · Cited by 842
Early stages of chick somite development
Christ, B., & Ordahl, C. P. (1995) · Anatomy and Embryology · doi:10.1007/bf00304424 · Cited by 795
Identification of MRF4: a new member of the muscle regulatory factor gene family.Preprint
Rhodes, S. J., & Konieczny, S. F. (1989) · Genes & Development · doi:10.1101/gad.3.12b.2050 · Cited by 788
Pax3 and Pax7 have distinct and overlapping functions in adult muscle progenitor cells
Relaix, F., Montarras, D., Zaffran, S., Gayraud-Morel, B., Rocancourt, D., Tajbakhsh, S., Mansouri, A., Cumano, A., & BUCKINGHAM, M. E. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200508044 · Cited by 736
MyoD is required for myogenic stem cell function in adult skeletal muscle
Megeney, L. A., Kablar, B., Garrett, K., Anderson, J. E., & Rudnicki, M. A. (1996) · Genes & Development · doi:10.1101/gad.10.10.1173 · Cited by 724
Satellite Cells and Skeletal Muscle Regeneration
Dumont, N. A., Bentzinger, C. F., Sincennes, M., & Rudnicki, M. A. (2015) · Comprehensive Physiology · doi:10.1002/cphy.c140068 · Cited by 719
Targeted inactivation of the muscle regulatory gene Myf-5 results in abnormal rib development and perinatal death
Braun, T. W., Rudnicki, M. A., Arnold, H.-H., & Jaenisch, R. (1992) · Cell · doi:10.1016/0092-8674(92)90507-9 · Cited by 702
The Skeletal Muscle Satellite Cell: The Stem Cell That Came in From the Cold
Zammit, P. S., Partridge, T. A., & Yablonka‐Reuveni, Z. (2006) · Journal of Histochemistry & Cytochemistry · doi:10.1369/jhc.6r6995.2006 · Cited by 684
Mrf4 determines skeletal muscle identity in Myf5:Myod double-mutant mice
Kassar-Duchossoy, L., Gayraud-Morel, B., Gomès, D., Rocancourt, D., BUCKINGHAM, M. E., Shinin, V., & Tajbakhsh, S. (2004) · Nature · doi:10.1038/nature02876 · Cited by 677
Myogenin expression, cell cycle withdrawal, and phenotypic differentiation are temporally separable events that precede cell fusion upon myogenesis.
Andrés, V., & Walsh, K. (1996) · The Journal of Cell Biology · doi:10.1083/jcb.132.4.657 · Cited by 621
Pax7 and myogenic progression in skeletal muscle satellite cells
Zammit, P. S., Relaix, F., Nagata, Y., Ruiz, A. P., Collins, C. A., Partridge, T. A., & Beauchamp, J. R. (2006) · Journal of Cell Science · doi:10.1242/jcs.02908 · Cited by 614
A common somitic origin for embryonic muscle progenitors and satellite cells
Gros, J., Manceau, M., Thomé, V., & Marcelle, C. (2005) · Nature · doi:10.1038/nature03572 · Cited by 596
Adult satellite cells and embryonic muscle progenitors have distinct genetic requirements
Lepper, C., Conway, S. J., & Fan, C. (2009) · Nature · doi:10.1038/nature08209 · Cited by 580
Know Your Neighbors: Three Phenotypes in Null Mutants of the Myogenic bHLH Gene MRF4
Olson, E. N., Arnold, H.-H., Rigby, P. W. J., & Wold, B. J. (1996) · Cell · doi:10.1016/s0092-8674(00)81073-9 · Cited by 577
Pax-7 up-regulation inhibits myogenesis and cell cycle progression in satellite cells: a potential mechanism for self-renewal
Olguín, H. C., & Olwin, B. B. (2004) · Developmental Biology · doi:10.1016/j.ydbio.2004.08.015 · Cited by 573
Pax3/Pax7 mark a novel population of primitive myogenic cells during developmentPreprint
Kassar-Duchossoy, L., Giacone, E., Gayraud-Morel, B., Jory, A., Gomès, D., & Tajbakhsh, S. (2005) · Genes & Development · doi:10.1101/gad.345505 · Cited by 556
Comparative Study of Injury Models for Studying Muscle Regeneration in Mice
Hardy, D., Besnard, A., Latil, M., Jouvion, G., Briand, D., Thépenier, C., Pascal, Q., Guguin, A., Gayraud-Morel, B., Cavaillon, J., et al. (2016) · PLoS ONE · doi:10.1371/journal.pone.0147198 · Cited by 546
A Somitic Compartment of Tendon Progenitors
Brent, A. E., Schweitzer, R., & Tabin, C. J. (2003) · Cell · doi:10.1016/s0092-8674(03)00268-x · Cited by 530
Dynamics of muscle fibre growth during postnatal mouse development
White, R. B., Biérinx, A.-S., Gnocchi, V. F., & Zammit, P. S. (2010) · BMC Developmental Biology · doi:10.1186/1471-213x-10-21 · Cited by 512
Intrinsic and extrinsic mechanisms regulating satellite cell function
Dumont, N. A., Wang, Y. X., & Rudnicki, M. A. (2015) · Development · doi:10.1242/dev.114223 · Cited by 491
Genome-wide MyoD Binding in Skeletal Muscle Cells: A Potential for Broad Cellular Reprogramming
Cao, Y., Yao, Z., Sarkar, D., Lawrence, M., Sanchez, G. J., Parker, M. H., MacQuarrie, K. L., Davison, J., Morgan, M. T., Ruzzo, W. L., et al. (2010) · Developmental Cell · doi:10.1016/j.devcel.2010.02.014 · Cited by 480
Myf‐6, a new member of the human gene family of myogenic determination factors: evidence for a gene cluster on chromosome 12.
Braun, T. W., Bober, E., Winter, B., Rosenthal, N. A., & Arnold, H.-H. (1990) · The EMBO Journal · doi:10.1002/j.1460-2075.1990.tb08179.x · Cited by 478
Herculin, a fourth member of the MyoD family of myogenic regulatory genes.
Miner, J. H., & Wold, B. J. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.3.1089 · Cited by 459
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
Temporal expression of regulatory and structural muscle proteins during myogenesis of satellite cells on isolated adult rat fibers
Yablonka‐Reuveni, Z., & Rivera, A. J. (1994) · Developmental Biology · doi:10.1006/dbio.1994.1226 · Cited by 454
Cell heterogeneity upon myogenic differentiation: down-regulation of MyoD and Myf-5 generates ‘reserve cells
Yoshida, N., Yoshida, S., Koishi, K., Masuda, K., & Nabeshima, Y.-I. (1998) · Journal of Cell Science · doi:10.1242/jcs.111.6.769 · Cited by 425
Selective accumulation of MyoD and Myogenin mRNAs in fast and slow adult skeletal muscle is controlled by innervation and hormones
Hughes, S. M., Taylor, J. M., Tapscott, S. J., Gurley, C. M., Carter, W. J., & Peterson, C. A. (1993) · Development · doi:10.1242/dev.118.4.1137 · Cited by 422
Inducible lineage tracing of Pax7‐descendant cells reveals embryonic origin of adult satellite cells
Lepper, C., & Fan, C. (2010) · genesis · doi:10.1002/dvg.20630 · Cited by 377
Reduced Differentiation Potential of Primary MyoD−/− Myogenic Cells Derived from Adult Skeletal Muscle
Sabourin, L. A., Girgis-Gabardo, A., Seale, P., Asakura, A., & Rudnicki, M. A. (1999) · The Journal of Cell Biology · doi:10.1083/jcb.144.4.631 · Cited by 371
THE HISTOGENESIS OF RAT INTERCOSTAL MUSCLE
Kelly, A. M., & Zacks, S. I. (1969) · The Journal of Cell Biology · doi:10.1083/jcb.42.1.135 · Cited by 366
Muscle Satellite Cells Are Primed for Myogenesis but Maintain Quiescence with Sequestration of Myf5 mRNA Targeted by microRNA-31 in mRNP Granules
Crist, C. G., Montarras, D., & Buckingham, M. (2012) · Cell Stem Cell · doi:10.1016/j.stem.2012.03.011 · Cited by 346
Pattern of Pax7 expression during myogenesis in the posthatch chicken establishes a model for satellite cell differentiation and renewal
Halevy, O., Piestun, Y., Allouh, M. Z., Rosser, B. W. C., Rinkevich, Y., Reshef, R., ROZENBOIM, I., Wleklinski‐Lee, M., & Yablonka‐Reuveni, Z. (2004) · Developmental Dynamics · doi:10.1002/dvdy.20151 · Cited by 334
Inactivation of the myogenic bHLH gene MRF4 results in up-regulation of myogenin and rib anomalies.Preprint
Zhang, W., Behringer, R. R., & Olson, E. N. (1995) · Genes & Development · doi:10.1101/gad.9.11.1388 · Cited by 325
The Muscle Regulatory Factors MyoD and Myf-5 Undergo Distinct Cell Cycle–specific Expression in Muscle Cells
Kitzmann, M., Carnac, G., Vandromme, M., Primig, M., Lamb, N. J. C., & Fernandez, A. (1998) · The Journal of Cell Biology · doi:10.1083/jcb.142.6.1447 · Cited by 323
Myogenin is required for late but not early aspects of myogenesis during mouse development.
Venuti, J. M., Morris, J., Vivian, J. L., Olson, E. N., & Klein, W. H. (1995) · The Journal of Cell Biology · doi:10.1083/jcb.128.4.563 · Cited by 316
MyoD−/− Satellite Cells in Single-Fiber Culture Are Differentiation Defective and MRF4 Deficient
Cornelison, D., Olwin, B. B., Rudnicki, M. A., & Wold, B. J. (2000) · Developmental Biology · doi:10.1006/dbio.2000.9682 · Cited by 314
Identification of skeletal muscle precursor cells in vivo by use of MyoD1 and myogenin probes
Grounds, M. D., Garrett, K. L., Lai, M. C., Wright, W. E., & Beilharz, M. W. (1992) · Cell & Tissue Research · doi:10.1007/bf00318695 · Cited by 313
Muscle progenitor cells failing to respond to positional cues adopt non-myogenic fates in myf-5 null mice
Tajbakhsh, S., Rocancourt, D., & BUCKINGHAM, M. E. (1996) · Nature · doi:10.1038/384266a0 · Cited by 309
Kinetics of Myoblast Proliferation Show That Resident Satellite Cells Are Competent to Fully Regenerate Skeletal Muscle Fibers
Zammit, P. S., Heslop, L., Hudon, V., Rosenblatt, J. D., Tajbakhsh, S., BUCKINGHAM, M. E., Beauchamp, J. R., & Partridge, T. A. (2002) · Experimental Cell Research · doi:10.1006/excr.2002.5653 · Cited by 306
Alveolar rhabdomyosarcomas in conditional Pax3:Fkhr mice: cooperativity of Ink4a/ARF and Trp53 loss of functionPreprint
Keller, C., Arenkiel, B. R., Coffin, C. M., Bardeesy, N. M., DePinho, R. A., & Capecchi, M. R. (2004) · Genes & Development · doi:10.1101/gad.1244004 · Cited by 304
Expression of the muscle regulatory factor MRF4 during somite and skeletal myofiber development
Hinterberger, T. J., Sassoon, D. A., Rhodes, S. J., & Konieczny, S. F. (1991) · Developmental Biology · doi:10.1016/s0012-1606(05)80014-4 · Cited by 302
Embryonic and fetal limb myogenic cells are derived from developmentally distinct progenitors and have different requirements for β-cateninPreprint
Hutcheson, D. A., Zhao, J., Merrell, A. J., Haldar, M., & Kardon, G. (2009) · Genes & Development · doi:10.1101/gad.1769009 · Cited by 301
Temporal expression of myogenic regulatory genes during activation, proliferation, and differentiation of rat skeletal muscle satellite cells
Smith, C. K., Janney, M. J., & Allen, R. E. (1994) · Journal of Cellular Physiology · doi:10.1002/jcp.1041590222 · Cited by 290
Myf5-Positive Satellite Cells Contribute to Pax7-Dependent Long-Term Maintenance of Adult Muscle Stem Cells
Günther, S., Kim, J., Kostin, S., Lepper, C., Fan, C.-M., & Braun, T. (2013) · Cell Stem Cell · doi:10.1016/j.stem.2013.07.016 · Cited by 280
The Transition from Proliferation to Differentiation Is Delayed in Satellite Cells from Mice Lacking MyoD
Yablonka‐Reuveni, Z., Rudnicki, M. A., Rivera, A. J., Primig, M., Anderson, J. E., & Natanson, P. (1999) · Developmental Biology · doi:10.1006/dbio.1999.9284 · Cited by 271
Muscle satellite cell heterogeneity and self-renewal
Motohashi, N., & Asakura, A. (2014) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2014.00001 · Cited by 262
The termination of the afferent nerve fibre in the muscle spindle of the frog
Katz, B. (1961) · Philosophical transactions of the Royal Society of London. Series B, Biological sciences · doi:10.1098/rstb.1961.0001 · Cited by 261
The depletion of skeletal muscle satellite cells with age is concomitant with reduced capacity of single progenitors to produce reserve progeny
Day, K., Shefer, G., Shearer, A., & Yablonka-Reuveni, Z. (2010) · Developmental Biology · doi:10.1016/j.ydbio.2010.01.006 · Cited by 254
Fibre types in skeletal muscle: a personal account
Schiaffino, S. (2010) · Acta Physiologica · doi:10.1111/j.1748-1716.2010.02130.x · Cited by 247
Distinct Origins and Genetic Programs of Head Muscle Satellite Cells
Harel, I., Nathan, E., Tirosh-Finkel, L., Zigdon, H., Guimarães‐Camboa, N., Evans, S. Μ., & Tzahor, E. (2009) · Developmental Cell · doi:10.1016/j.devcel.2009.05.007 · Cited by 244
Insertion of Cre into the Pax3 locus creates a new allele of Splotch and identifies unexpected Pax3 derivatives
Engleka, K. A., Gitler, A. D., Zhang, M., Zhou, D. D., High, F. A., & Epstein, J. A. (2005) · Developmental Biology · doi:10.1016/j.ydbio.2005.02.002 · Cited by 240
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
The organogenesis of murine striated muscle: A cytoarchitectural study
Ontell, M., & Kozeka, K. (1984) · American Journal of Anatomy · doi:10.1002/aja.1001710202 · Cited by 226
Satellite cell proliferation and the expression of myogenin and desmin in regenerating skeletal muscle: evidence for two different populations of satellite cells.
Rantanen, J., Hurme, T., Lukka, R., Heino, J., & Kalimo, H. (1995) · PubMed · Cited by 223
Nestin-GFP reporter expression defines the quiescent state of skeletal muscle satellite cells
Day, K. R., Shefer, G., Richardson, J. B., Enikolopov, G., & Yablonka‐Reuveni, Z. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2006.12.026 · Cited by 222
Disruption of the mouse MRF4 gene identifies multiple waves of myogenesis in the myotome
Patapoutian, A., Yoon, J. K., Miner, J. H., Wang, S., Stark, K. L., & Wold, B. J. (1995) · Development · doi:10.1242/dev.121.10.3347 · Cited by 220
Muscle satellite cells are a functionally heterogeneous population in both somite-derived and branchiomeric muscles
Ono, Y., Boldrin, L., Knopp, P., Morgan, J. E., & Zammit, P. S. (2009) · Developmental Biology · doi:10.1016/j.ydbio.2009.10.005 · Cited by 217
Somitic origin of limb muscle satellite and side population cells
Schienda, J., Engleka, K. A., Jun, S. J., Hansen, M. S. T., Epstein, J. A., Tabin, C. J., Kunkel, L. M., & Kardon, G. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0510164103 · Cited by 216
All muscle satellite cells are equal, but are some more equal than others?
Zammit, P. S. (2008) · Journal of Cell Science · doi:10.1242/jcs.019661 · Cited by 213
Molecular and Cellular Regulation of Skeletal Myogenesis
Comai, G., & Tajbakhsh, S. (2014) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/b978-0-12-405943-6.00001-4 · Cited by 213
Nfix Regulates Fetal-Specific Transcription in Developing Skeletal Muscle
Messina, G., Biressi, S., Monteverde, S., Magli, A., Cassano, M., Perani, L., Roncaglia, E., Tagliafico, E., Starnes, L., Campbell, C. E., et al. (2010) · Cell · doi:10.1016/j.cell.2010.01.027 · Cited by 210
Differential expression of muscle regulatory factor genes in normal and denervated adult rat hindlimb muscles
Voytik, S. L., Przyborski, M., Badylak, S. F., & Konieczny, S. F. (1993) · Developmental Dynamics · doi:10.1002/aja.1001980307 · Cited by 206
Myogenin Induces a Shift of Enzyme Activity from Glycolytic to Oxidative Metabolism in Muscles of Transgenic Mice
Hughes, S. M., Chi, M. M.-Y., Lowry, O. H., & Gundersen, K. (1999) · The Journal of Cell Biology · doi:10.1083/jcb.145.3.633 · Cited by 202
Progenitors of skeletal muscle satellite cells express the muscle determination gene, MyoD
Kanisicak, O., Mendez, J. J., Yamamoto, S., Yamamoto, M., & Goldhamer, D. J. (2009) · Developmental Biology · doi:10.1016/j.ydbio.2009.05.554 · Cited by 192
Differential modulation of cell cycle progression distinguishes members of the myogenic regulatory factor family of transcription factors
Singh, K., & Dilworth, F. J. (2013) · FEBS Journal · doi:10.1111/febs.12188 · Cited by 186
Inactivation of Myf‐6 and Myf‐5 genes in mice leads to alterations in skeletal muscle development.
Braun, T. W., & Arnold, H.-H. (1995) · The EMBO Journal · doi:10.1002/j.1460-2075.1995.tb07101.x · Cited by 181
Overlapping functions of the myogenic bHLH genes MRF4 and MyoD revealed in double mutant mice
Rawls, A., Valdez, M. R., Zhang, W., Richardson, J. A., Klein, W. H., & Olson, E. N. (1998) · Development · doi:10.1242/dev.125.13.2349 · Cited by 179
MyoD and myogenin are coexpressed in regenerating skeletal muscle of the mouse
Füchtbauer, E., & Westphal, H. (1992) · Developmental Dynamics · doi:10.1002/aja.1001930106 · Cited by 176
MyoD protein is differentially accumulated in fast and slow skeletal muscle fibres and required for normal fibre type balance in rodents
Hughes, S. M., Koishi, K., Rudnicki, M. A., & Maggs, A. M. (1997) · Mechanisms of Development · doi:10.1016/s0925-4773(96)00631-4 · Cited by 175
Identification of self-renewing myoblasts in the progeny of single human muscle satellite cells
Baroffio, A., Hamann, M., Bernheim, L., Bochaton‐Piallat, M., Gabbiani, G., & Bader, C. R. (1996) · Differentiation · doi:10.1046/j.1432-0436.1996.6010047.x · Cited by 170
Loss of myogenin in postnatal life leads to normal skeletal muscle but reduced body size
Knapp, J. R., Davie, J. K., Myer, A., Meadows, E., Olson, E. N., & Klein, W. H. (2006) · Development · doi:10.1242/dev.02249 · Cited by 167
The Myogenic Factor Myf5 Supports Efficient Skeletal Muscle Regeneration by Enabling Transient Myoblast Amplification
Ustanina, S., Carvajal, J. J., Rigby, P. W. J., & Braun, T. W. (2007) · Stem Cells · doi:10.1634/stemcells.2006-0736 · Cited by 160
Myogenin's Functions Do Not Overlap with Those of MyoD or Myf-5 during Mouse Embryogenesis
Rawls, A., Morris, J. H., Rudnicki, M. A., Braun, T. W., Arnold, H.-H., Klein, W. H., & Olson, E. N. (1995) · Developmental Biology · doi:10.1006/dbio.1995.0004 · Cited by 155
Entry of muscle satellite cells into the cell cycle requires sphingolipid signaling
Nagata, Y., Partridge, T. A., Matsuda, R., & Zammit, P. S. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.200605028 · Cited by 153
Satellite Cell Heterogeneity in Skeletal Muscle Homeostasis
Tierney, M. T., & Sacco, A. (2016) · Trends in Cell Biology · doi:10.1016/j.tcb.2016.02.004 · Cited by 151
MyoD protein accumulates in satellite cells and is neurally regulated in regenerating myotubes and skeletal muscle fibers
Koishi, K., Zhang, M., McLennan, I. S., & Harris, A. (1995) · Developmental Dynamics · doi:10.1002/aja.1002020304 · Cited by 149
Two Cell Lineages, myf5 and myf5-Independent, Participate in Mouse Skeletal Myogenesis
Haldar, M., Karan, G., Tvrdík, P., & Capecchi, M. R. (2008) · Developmental Cell · doi:10.1016/j.devcel.2008.01.002 · Cited by 142
Origin of satellite cells in avian skeletal muscles.
Armand, O., Boutineau, A. M., Mauger, A., Pautou, M.-P., & Kieny, M. (1983) · PubMed · Cited by 138
Failure of Myf5 to Support Myogenic Differentiation without Myogenin, MyoD, and MRF4
Valdez, M. R., Richardson, J. A., Klein, W. H., & Olson, E. N. (2000) · Developmental Biology · doi:10.1006/dbio.2000.9621 · Cited by 127
Increased survival of muscle stem cells lacking the MyoD gene after transplantation into regenerating skeletal muscle
Asakura, A., Hirai, H., Kablar, B., Morita, S., Ishibashi, J., Piras, B. A., Christ, A. J., Verma, M., Vineretsky, K. A., & Rudnicki, M. A. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0708145104 · Cited by 125
Cell Cycle–regulated Expression of the Muscle Determination Factor Myf5 in Proliferating Myoblasts
Lindon, C., Montarras, D., & Pinset, C. (1998) · The Journal of Cell Biology · doi:10.1083/jcb.140.1.111 · Cited by 122
Genetic and Epigenetic Determinants of Neurogenesis and Myogenesis
Fong, A. P., Yao, Z., Zhong, J. W., Cao, Y., Ruzzo, W. L., Gentleman, R. C., & Tapscott, S. J. (2012) · Developmental Cell · doi:10.1016/j.devcel.2012.01.015 · Cited by 119
Myogenin regulates a distinct genetic program in adult muscle stem cells
Meadows, E., Cho, J.-H., Flynn, J. M., & Klein, W. H. (2008) · Developmental Biology · doi:10.1016/j.ydbio.2008.07.024 · Cited by 118
Mechanisms of impaired differentiation in rhabdomyosarcoma
Keller, C., & D, D. C. G. (2013) · FEBS Journal · doi:10.1111/febs.12421 · Cited by 115
MRF4 negatively regulates adult skeletal muscle growth by repressing MEF2 activity
Moretti, I., Ciciliot, S., Dyar, K. A., Abraham, R., Murgia, M., Agatea, L., Akimoto, T., Bicciato, S., Forcato, M., Pierre, P., et al. (2016) · Nature Communications · doi:10.1038/ncomms12397 · Cited by 115
Different autonomous myogenic cell populations revealed by ablation of Myf5-expressing cells during mouse embryogenesis
Gensch, N., Borchardt, T., Schneider, A., Riethmacher, D., & Braun, T. W. (2008) · Development · doi:10.1242/dev.019331 · Cited by 113
Satellite cells from dystrophic muscle retain regenerative capacity
Boldrin, L., Zammit, P. S., & Morgan, J. E. (2014) · Stem Cell Research · doi:10.1016/j.scr.2014.10.007 · Cited by 112
Slow-dividing satellite cells retain long-term self-renewal ability in adult muscle
Ono, Y., Masuda, S., Nam, H.-S., Benezra, R., Miyagoe‐Suzuki, Y., & Takeda, S. (2012) · Journal of Cell Science · doi:10.1242/jcs.096198 · Cited by 109
Erythroid Krüppel-like factor exhibits an early and sequentially localized pattern of expression during mammalian erythroid ontogeny
Southwood, C. M., Downs, K. M., & Bieker, J. J. (1996) · Developmental Dynamics · doi:10.1002/(sici)1097-0177(199607)206:3 · Cited by 108
Organogenesis of the mouse extensor digitorum logus muscle: A quantitative study
Ontell, M., & Kozeka, K. (1984) · American Journal of Anatomy · doi:10.1002/aja.1001710203 · Cited by 107
BCL9 is an essential component of canonical Wnt signaling that mediates the differentiation of myogenic progenitors during muscle regeneration
Brack, A. S., Murphy-Seiler, F., Hanifi, J. M., Deka, J., Eyckerman, S., Keller, C., Aguet, M., & Rando, T. A. (2009) · Developmental Biology · doi:10.1016/j.ydbio.2009.08.014 · Cited by 107
Myotube Formation is Delayed but not Prevented in MyoD-deficient Skeletal Muscle: Studies in Regenerating Whole Muscle Grafts of Adult Mice
White, J. D., Scaffidi, A. K., Davies, M. J., McGeachie, J. K., Rudnicki, M. A., & Grounds, M. D. (2000) · Journal of Histochemistry & Cytochemistry · doi:10.1177/002215540004801110 · Cited by 100
Extracellular Matrix, Growth Factors, Genetics: Their Influence on Cell Proliferation and Myotube Formation in Primary Cultures of Adult Mouse Skeletal Muscle
Maley, M. A. L., Davies, M. J., & Grounds, M. D. (1995) · Experimental Cell Research · doi:10.1006/excr.1995.1217 · Cited by 97
Myf5 haploinsufficiency reveals distinct cell fate potentials for adult skeletal muscle stem cells
Gayraud-Morel, B., Chrétien, F. C., Jory, A., Sambasivan, R., Négroni, E., Flamant, P., Soubigou, G., Coppée, J., Santo, J. P. D., Cumano, A., et al. (2012) · Journal of Cell Science · doi:10.1242/jcs.097006 · Cited by 92
Myogenin can substitute for Myf5 in promoting myogenesis but less efficiently
Wang, Y., & Jaenisch, R. (1997) · Development · doi:10.1242/dev.124.13.2507 · Cited by 92
Activation of Cdc6 by MyoD is associated with the expansion of quiescent myogenic satellite cells
Zhang, K., Sha, J., & Harter, M. L. (2010) · The Journal of Cell Biology · doi:10.1083/jcb.200904144 · Cited by 89
Molecular evolution of the MyoD family of transcription factors.
Atchley, W. R., Fitch, W. M., & Bronner-Fraser, M. E. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.24.11522 · Cited by 88
Comparative expression profiling identifies differential roles for Myogenin and p38α MAPK signaling in myogenesis
Liu, Q., Zha, X., Faralli, H., Yin, H., Louis‐Jeune, C., Perdiguero, E., Pranckevičienė, E., Muñoz‐Cánoves, P., Rudnicki, M. A., Brand, M., et al. (2012) · Journal of Molecular Cell Biology · doi:10.1093/jmcb/mjs045 · Cited by 81
Alveolar rhabdomyosarcoma-associated proteins PAX3/FOXO1A and PAX7/FOXO1A suppress the transcriptional activity of MyoD-target genes in muscle stem cells
Calhabeu, F., Hayashi, S., Morgan, J. E., Relaix, F., & Zammit, P. S. (2012) · Oncogene · doi:10.1038/onc.2012.73 · Cited by 78
Role of MyoD in denervated, disused, and exercised muscle
Legerlotz, K., & Smith, H. K. (2008) · Muscle & Nerve · doi:10.1002/mus.21087 · Cited by 78
De‐phosphorylation of MyoD is linking nerve‐evoked activity to fast myosin heavy chain expression in rodent adult skeletal muscle
Ekmark, M., Rana, Z. A., Stewart, G., Hardie, D. G., & Gundersen, K. (2007) · The Journal of Physiology · doi:10.1113/jphysiol.2007.141457 · Cited by 77
Myf5 expression during fetal myogenesis defines the developmental progenitors of adult satellite cells
Biressi, S., Bjornson, C. R. R., Carlig, P. M. M., Nishijo, K., Keller, C., & Rando, T. A. (2013) · Developmental Biology · doi:10.1016/j.ydbio.2013.04.021 · Cited by 76
DifferentMRF4Knockout Alleles Differentially Disrupt Myf-5 Expression:cis-Regulatory Interactions at theMRF4/Myf-5Locus
Yoon, J. K., Olson, E. N., Arnold, H.-H., & Wold, B. J. (1997) · Developmental Biology · doi:10.1006/dbio.1997.8670 · Cited by 75
Cultured myf5 null and myoD null muscle precursor cells display distinct growth defects
Montarras, D., Lindon, C., Pinset, C., & Domeyne, P. (2000) · Biology of the Cell · doi:10.1016/s0248-4900(00)01110-2 · Cited by 72
Myf5 expression in satellite cells and spindles in adult muscle is controlled by separate genetic elements
Zammit, P. S., Carvajal, J. J., Golding, J. P., Morgan, J. E., Summerbell, D., Zolnerciks, J. K., Partridge, T. A., Rigby, P. W. J., & Beauchamp, J. R. (2004) · Developmental Biology · doi:10.1016/j.ydbio.2004.05.038 · Cited by 71
MyoD-expressing progenitors are essential for skeletal myogenesis and satellite cell development
Wood, W. M., Etemad, S. A., Yamamoto, M., & Goldhamer, D. J. (2013) · Developmental Biology · doi:10.1016/j.ydbio.2013.09.012 · Cited by 71
bHLH transcription factor MyoD affects myosin heavy chain expression pattern in a muscle-specific fashion
Seward, D. J., Haney, J. C., Rudnicki, M. A., & Swoap, S. J. (2001) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.2001.280.2.c408 · Cited by 67
Expression of the myogenic regulatory factor Mrf4 precedes or is contemporaneous with that of Myf5 in the somitic bud
Summerbell, D., Halai, C., & Rigby, P. W. J. (2002) · Mechanisms of Development · doi:10.1016/s0925-4773(02)00208-3 · Cited by 67
Myogenin Regulates Exercise Capacity and Skeletal Muscle Metabolism in the Adult Mouse
Flynn, J. M., Meadows, E., Fiorotto, M. L., & Klein, W. H. (2010) · PLoS ONE · doi:10.1371/journal.pone.0013535 · Cited by 64
Global transcriptional regulation of the locus encoding the skeletal muscle determination genes Mrf4 and Myf5Preprint
Carvajal, J. J., Keith, A. C., & Rigby, P. W. J. (2008) · Genes & Development · doi:10.1101/gad.442408 · Cited by 60
Conversion of MyoD to a Neurogenic Factor: Binding Site Specificity Determines Lineage
Fong, A. P., Yao, Z., Zhong, J. W., Johnson, N. M., Farr, G. H., Maves, L., & Tapscott, S. J. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.02.055 · Cited by 60
Embryonic founders of adult muscle stem cells are primed by the determination gene Mrf4
Sambasivan, R., Comai, G., Roux, I. L., Gomès, D., Konge, J. C., Dumas, G., Cimper, C., & Tajbakhsh, S. (2013) · Developmental Biology · doi:10.1016/j.ydbio.2013.04.018 · Cited by 58
Jun, Fos, MyoD1, and Myogenin proteins are increased in skeletal muscle fiber nuclei after denervation
Weis, J. (1994) · Acta Neuropathologica · doi:10.1007/bf00386255 · Cited by 55
Variations in the Efficiency of Lineage Marking and Ablation Confound Distinctions between Myogenic Cell Populations
Comai, G., Sambasivan, R., Gopalakrishnan, S., & Tajbakhsh, S. (2014) · Developmental Cell · doi:10.1016/j.devcel.2014.11.005 · Cited by 50
Loss-of-Function Mutations Reveal That the Drosophila nautilus Gene Is Not Essential for Embryonic Myogenesis or Viability
Balagopalan, L., Keller, C. A., & Abmayr, S. M. (2001) · Developmental Biology · doi:10.1006/dbio.2001.0162 · Cited by 48
Overexpression of Myogenin in Muscles of Transgenic Mice: Interaction with Id-1, Negative Crossregulation of Myogenic Factors, and Induction of Extrasynaptic Acetylcholine Receptor Expression
Gundersen, K., Rabben, I., Klocke, B. J., & Merlie, J. P. (1995) · Molecular and Cellular Biology · doi:10.1128/mcb.15.12.7127 · Cited by 47
The expression of the myogenic regulatory factors in denervated and normal muscles of different phenotypes
Walters, E. H., Stickland, N. C., & Loughna, P. T. (2000) · Journal of Muscle Research and Cell Motility · doi:10.1023/a:1005683825960 · Cited by 46
Myogenin induces higher oxidative capacity in pre-existing mouse muscle fibres after somatic DNA transfer
Ekmark, M., Grønevik, E., Schjerling, P., & Gundersen, K. (2003) · The Journal of Physiology · doi:10.1111/j.1469-7793.2003.00259.x · Cited by 45
Neuromuscular junction morphology, fiber‐type proportions, and satellite‐cell proliferation rates are altered in MyoD−/− mice
Macharia, R., Otto, A., Valášek, P., & Patel, K. (2010) · Muscle & Nerve · doi:10.1002/mus.21637 · Cited by 44
MRF4 protein expression in regenerating rat muscle
Zhou, Z., & Bornemann, A. (2001) · Journal of Muscle Research and Cell Motility · doi:10.1023/a:1013133616449 · Cited by 41
Myogenin induces higher oxidative capacity in pre-existing mouse muscle fibres after somatic DNA transfer
Ekmark, M., Grønevik, E., Schjerling, P., & Gundersen, K. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2002.036228 · Cited by 36
Myogenin Regulates Exercise Capacity but Is Dispensable for Skeletal Muscle Regeneration in Adult mdx Mice
Meadows, E., Flynn, J. M., & Klein, W. H. (2011) · PLoS ONE · doi:10.1371/journal.pone.0016184 · Cited by 35
Diaphragm contractile dysfunction in MyoD gene-inactivated mice
Staib, J. L., Swoap, S. J., & Powers, S. K. (2002) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00080.2002 · Cited by 33
Regeneration of Transgenic Skeletal Muscles with Altered Timing of Expression of the Basic Helix-Loop-Helix Muscle Regulatory Factor MRF4
Pavlath, G. K., Dominov, J. A., Kegley, K. M., & Miller, J. B. (2003) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)64303-9 · Cited by 30
Analyses of the differentiation potential of satellite cells from myoD -/-, mdx, and PMP22 C22 mice
Schuierer, M. M., Mann, C. J., Bildsoe, H., Huxley, C. M., & Hughes, S. M. (2005) · BMC Musculoskeletal Disorders · doi:10.1186/1471-2474-6-15 · Cited by 29
MRF-4 exhibits fiber type- and muscle-specific pattern of expression in postnatal rat muscle
Walters, E. H., Stickland, N. C., & Loughna, P. T. (2000) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.2000.278.5.r1381 · Cited by 29
MyoD- and nerve-dependent maintenance of MyoDexpression in mature muscle fibres acts through the DRR/PRR element
CHARGÉ, S. B. P., Brack, A. S., Bayol, S. A., & Hughes, S. M. (2008) · BMC Developmental Biology · doi:10.1186/1471-213x-8-5 · Cited by 28
The absence of MyoD in regenerating skeletal muscle affects the expression pattern of basement membrane, interstitial matrix and integrin molecules that is consistent with delayed myotube formation
Huijbregts, J. E., White, J. D., & Grounds, M. D. (2001) · Acta Histochemica · doi:10.1078/0065-1281-00607 · Cited by 27
Myf-5m1/Myf-6m1Compound Heterozygous Mouse Mutants Down-regulate Myf-5 Expression and Exert Rib Defects: Evidence for Long-RangecisEffects on Myf-5 Transcription
Floß, T., Arnold, H.-H., & Braun, T. W. (1996) · Developmental Biology · doi:10.1006/dbio.1996.0058 · Cited by 26
Control of Myf5 activation in adult skeletal myonuclei requires ERK signalling
Ruiz, A. P., Gnocchi, V. F., & Zammit, P. S. (2007) · Cellular Signalling · doi:10.1016/j.cellsig.2007.03.003 · Cited by 23
Absence of MyoD Increases Donor Myoblast Migration into Host Muscle
Smythe, G. M., & Grounds, M. D. (2001) · Experimental Cell Research · doi:10.1006/excr.2001.5257 · Cited by 20
A Selective Role for MRF4 in Innervated Adult Skeletal Muscle: Na V 1.4 Na + Channel Expression Is Reduced in MRF4-Null Mice
Thompson, A. L., Filatov, G., Chen, C., PORTER, I., Li, Y., Rich, M. M., & Kraner, S. D. (2005) · Gene Expression · doi:10.3727/000000005783992034 · Cited by 18
Loss of synaptic vesicles from neuromuscular junctions in aged MRF4-null mice
Wang, Q., Hebert, S. L., Rich, M. M., & Kraner, S. D. (2011) · Neuroreport · doi:10.1097/wnr.0b013e328344493c · Cited by 8
Response: Contributions of the Myf5-Independent Lineage to Myogenesis
Haldar, M., Karan, G., Watanabe, S., Günther, S., Braun, T. W., & Capecchi, M. R. (2014) · Developmental Cell · doi:10.1016/j.devcel.2014.11.010 · Cited by 7

Flagged first, then by citations

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
Skeletal Muscle Extracellular Matrix – What Do We Know About Its Composition, Regulation, and Physiological Roles? A Narrative Review
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

See all 929

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)
DOI: 10.1016/j.semcdb.2017.11.011
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
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
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

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

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks