Niche Regulation of Muscle Satellite Cell Self-Renewal and Differentiation

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 · see citing works

Cellular and Molecular Regulation of Muscle Regeneration

CHARGÉ, S. B. P., & Rudnicki, M. A. (2004) · Physiological Reviews · doi:10.1152/physrev.00019.2003 · Cited by 2,691 · see citing works

Pax7 Is Required for the Specification of Myogenic Satellite Cells

Seale, P., Sabourin, L. A., Girgis-Gabardo, A., Mansouri, A., Gruß, P., & Rudnicki, M. A. (2000) · Cell · doi:10.1016/s0092-8674(00)00066-0 · Cited by 2,345 · see citing works

Rejuvenation of aged progenitor cells by exposure to a young systemic environment

Conboy, I. M., Conboy, M. J., Wagers, A. J., Girma, E. R., Weissman, I. L., & Rando, T. A. (2005) · Nature · doi:10.1038/nature03260 · Cited by 2,287 · see citing works

The stem-cell niche as an entity of action

Scadden, D. T. (2006) · Nature · doi:10.1038/nature04957 · Cited by 1,859 · see citing works

Socializing with the Neighbors

Fuchs, E. V., Tumbar, T., & Guasch, G. (2004) · Cell · doi:10.1016/s0092-8674(04)00255-7 · Cited by 1,711 · see citing works

Mutation selection and the natural history of cancer

Cairns, J. (1975) · Nature · doi:10.1038/255197a0 · Cited by 1,592 · see citing works

Increased Wnt signaling during aging alters muscle stem cell fate and increases fibrosis

Brack, A. S., Conboy, M. J., Roy, S., Lee, M., Kuo, C. J., Keller, C., & Rando, T. A. (2007) · Science · doi:10.1126/science.1144090 · Cited by 1,564 · see citing works

Stem Cells and Their Niches

Moore, K. A., & Lemischka, I. R. (2006) · Science · doi:10.1126/science.1110542 · Cited by 1,541 · see citing works

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 · see citing works

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 · see citing works

Wnt Signaling: Multiple Pathways, Multiple Receptors, and Multiple Transcription Factors

Gordon, M. D., & Nusse, R. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.r600015200 · Cited by 1,333 · see citing works

Notch-Mediated Restoration of Regenerative Potential to Aged Muscle

Conboy, I. M., Conboy, M. J., Smythe, G. M., & Rando, T. A. (2003) · Science · doi:10.1126/science.1087573 · Cited by 1,121 · see citing works

Direct Isolation of Satellite Cells for Skeletal Muscle Regeneration

Montarras, D., Morgan, J., Collins, C., Relaix, F., Zaffran, S., Cumano, A., Partridge, T., & Buckingham, M. (2005) · Science · doi:10.1126/science.1114758 · Cited by 1,100 · see citing works

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 · see citing works

Pericytes of human skeletal muscle are myogenic precursors distinct from satellite cells

Dellavalle, A., Sampaolesi, M., Tonlorenzi, R., Tagliafico, E., Sacchetti, B., Perani, L., Innocenzi, A., Gálvez, B. G., Messina, G., Roberta Morosetti, A., et al. (2007) · Nature Cell Biology · doi:10.1038/ncb1542 · Cited by 1,001 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

The Regulation of Notch Signaling Controls Satellite Cell Activation and Cell Fate Determination in Postnatal Myogenesis

Conboy, I. M., & Rando, T. A. (2002) · Developmental Cell · doi:10.1016/s1534-5807(02)00254-x · Cited by 905 · see citing works

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 · see citing works

Skeletal muscle stem cells express anti-apoptotic ErbB receptors during activation from quiescence.

Golding, J. P., Calderbank, E. F., Partridge, T. A., & Beauchamp, J. (2007) · Experimental Cell Research · doi:10.1016/j.yexcr.2006.10.019 · Cited by 801 · see citing works

Myostatin negatively regulates satellite cell activation and self-renewal

McCroskery, S., Thomas, M., Maxwell, L., Sharma, M., & Kambadur, R. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200207056 · Cited by 784 · see citing works

Mesoangioblast stem cells ameliorate muscle function in dystrophic dogs

Sampaolesi, M., Blot, S., D’Antona, G., Granger, N. P., Tonlorenzi, R., Innocenzi, A., Mognol, P., Thibaud, J. L., Gálvez, B. G., Barthélémy, I., et al. (2006) · Nature · doi:10.1038/nature05282 · Cited by 768 · see citing works

Muscle Satellite Cells and Endothelial Cells: Close Neighbors and Privileged Partners

Christov, C., Chrétien, F. C., Abou-Khalil, R., Bassez, G., Vallet, G., Authier, F., Bassaglia, Y., Shinin, V., Tajbakhsh, S., Chazaud, B., et al. (2007) · Molecular Biology of the Cell · doi:10.1091/mbc.e06-08-0693 · Cited by 702 · see citing works

HGF/SF Is Present in Normal Adult Skeletal Muscle and Is Capable of Activating Satellite Cells

Tatsumi, R., Anderson, J. E., Nevoret, C. J., Halevy, O., & Allen, R. E. (1998) · Developmental Biology · doi:10.1006/dbio.1997.8803 · Cited by 685 · see citing works

A Temporal Switch from Notch to Wnt Signaling in Muscle Stem Cells Is Necessary for Normal Adult Myogenesis

Brack, A. S., Conboy, I. M., Conboy, M. J., Shen, J., & Rando, T. A. (2008) · Cell Stem Cell · doi:10.1016/j.stem.2007.10.006 · Cited by 682 · see citing works

Cell Therapy of α-Sarcoglycan Null Dystrophic Mice Through Intra-Arterial Delivery of Mesoangioblasts

Sampaolesi, M., Torrente, Y., Innocenzi, A., Tonlorenzi, R., D’Antona, G., Pellegrino, M. A., Barresi, R., Bresolin, N., Angelis, M. G. C. D., Campbell, K. P., et al. (2003) · Science · doi:10.1126/science.1082254 · Cited by 639 · see citing works

Retrospective Birth Dating of Cells in Humans

Spalding, K. L., Bhardwaj, R. D., Buchholz, B. A., Druid, H., & Frisén, J. (2005) · Cell · doi:10.1016/j.cell.2005.04.028 · Cited by 626 · see citing works

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 · see citing works

Wnt Signaling Induces the Myogenic Specification of Resident CD45+ Adult Stem Cells during Muscle Regeneration

Polesskaya, A., Seale, P., & Rudnicki, M. A. (2003) · Cell · doi:10.1016/s0092-8674(03)00437-9 · Cited by 515 · see citing works

The meso-angioblast: A multipotent, self-renewing cell that originates from the dorsal aorta and differentiates into most mesodermal tissues

Minasi, M. G., Riminucci, M., De Angelis, L., Borello, U., Berarducci, B., Innocenzi, A., Caprioli, A., Sirabella, D., Baiocchi, M., De Maria, R., et al. (2002) · Development · doi:10.1242/dev.129.11.2773 · Cited by 514 · see citing works

Satellite-cell pool size does matter: Defining the myogenic potency of aging skeletal muscle

Shefer, G., de Mark, D. P. V., Richardson, J. B., & Yablonka‐Reuveni, Z. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2006.02.022 · Cited by 506 · see citing works

Molecular Signature of Quiescent Satellite Cells in Adult Skeletal Muscle

Fukada, S.-I., Uezumi, A., Ikemoto, M., Masuda, S., Segawa, M., Tanimura, N., Yamamoto, H., Miyagoe-Suzuki, Y., & Takeda, S. (2007) · Stem Cells · doi:10.1634/stemcells.2007-0019 · Cited by 506 · see citing works

Asymmetric division and cosegregation of template DNA strands in adult muscle satellite cells

Shinin, V., Gayraud-Morel, B., Gomès, D., & Tajbakhsh, S. (2006) · Nature Cell Biology · doi:10.1038/ncb1425 · Cited by 504 · see citing works

Isolation of Adult Mouse Myogenic Progenitors

Sherwood, R. I., Christensen, J. L., Conboy, I. M., Conboy, M. J., Rando, T. A., Weissman, I. L., & Wagers, A. J. (2004) · Cell · doi:10.1016/j.cell.2004.10.021 · Cited by 491 · see citing works

Distinct roles for Pax7 and Pax3 in adult regenerative myogenesis

Kuang, S., CHARGÉ, S. B. P., Seale, P., Huh, M. S., & Rudnicki, M. A. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.200508001 · Cited by 490 · see citing works

The intracellular domain of mouse Notch: a constitutively activated repressor of myogenesis directed at the basic helix-loop-helix region of MyoD

Kopan, R., Nye, J. S., & Weintraub, H. (1994) · Development · doi:10.1242/dev.120.9.2385 · Cited by 488 · see citing works

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 · see citing works

Phospho-caveolin-1 mediates integrin-regulated membrane domain internalization

del Pozo, M. Á., Balasubramanian, N., Alderson, N. B., Kiosses, W. B., Grande-García, A., Anderson, R. G. W., & Schwartz, M. A. (2005) · Nature Cell Biology · doi:10.1038/ncb1293 · Cited by 424 · see citing works

Skeletal Myogenic Progenitors Originating from Embryonic Dorsal Aorta Coexpress Endothelial and Myogenic Markers and Contribute to Postnatal Muscle Growth and Regeneration

Angelis, L. D., Berghella, L., Coletta, M., Lattanzi, L., Zanchi, M., Gabriella, M., Ponzetto, C., & Cossu, G. (1999) · The Journal of Cell Biology · doi:10.1083/jcb.147.4.869 · Cited by 421 · see citing works

Haematopoietic stem cells do not asymmetrically segregate chromosomes or retain BrdU

Kiel, M. J., He, S., Ashkenazi, R., Gentry, S. N., Teta, M., Kushner, J. A., Jackson, T. L., & Morrison, S. J. (2007) · Nature · doi:10.1038/nature06115 · Cited by 417 · see citing works

Muscle transplantation between young and old rats: age of host determines recovery

Carlson, B. M., & Faulkner, J. A. (1989) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1989.256.6.c1262 · Cited by 417 · see citing works

Roles for the integrin VLA-4 and its counter receptor VCAM-1 in myogenesis

Rosen, G., Sanes, J. R., Lachance, R. M., Cunningham, J. M., Roman, J., & Dean, D. C. (1992) · Cell · doi:10.1016/0092-8674(92)90633-n · Cited by 404 · see citing works

Syndecan-3 and Syndecan-4 Specifically Mark Skeletal Muscle Satellite Cells and Are Implicated in Satellite Cell Maintenance and Muscle Regeneration

Cornelison, D., Filla, M. S., Stanley, H. M., Rapraeger, A. C., & Olwin, B. B. (2001) · Developmental Biology · doi:10.1006/dbio.2001.0416 · Cited by 399 · see citing works

Human circulating AC133+ stem cells restore dystrophin expression and ameliorate function in dystrophic skeletal muscle

Torrente, Y., Belicchi, M., Sampaolesi, M., Pisati, F., Meregalli, M., D’Antona, G., Tonlorenzi, R., Porretti, L., Gavina, M., Mamchaoui, K., et al. (2004) · Journal of Clinical Investigation · doi:10.1172/jci20325 · Cited by 396 · see citing works

Satellite Cell Proliferative Compartments in Growing Skeletal Muscles

Schultz, E. (1996) · Developmental Biology · doi:10.1006/dbio.1996.0097 · Cited by 394 · see citing works

Expression pattern of M‐cadherin in normal, denervated, and regenerating mouse muscles

Irintchev, A., Zeschnigk, M., Starzinski‐Powitz, A., & Wernig, A. (1994) · Developmental Dynamics · doi:10.1002/aja.1001990407 · Cited by 368 · see citing works

The emerging biology of satellite cells and their therapeutic potential

Kuang, S., & Rudnicki, M. A. (2008) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2007.12.004 · Cited by 339 · see citing works

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 · see citing works

Essential and separable roles for Syndecan-3 and Syndecan-4 in skeletal muscle development and regeneration

Cornelison, D. D. W., Wilcox-Adelman, S. A., Goetinck, P. F., Rauvala, H., Rapraeger, A. C., & Olwin, B. B. (2004) · Genes & Development · doi:10.1101/gad.1214204 · Cited by 317 · see citing works

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 · see citing works

Label-retaining epithelial cells in mouse mammary gland divide asymmetrically and retain their template DNA strands

Smith, G. H. (2005) · Development · doi:10.1242/dev.01609 · Cited by 288 · see citing works

High Incidence of Non-Random Template Strand Segregation and Asymmetric Fate Determination In Dividing Stem Cells and their Progeny

Conboy, M. J., Karasov, A. O., & Rando, T. A. (2007) · PLoS Biology · doi:10.1371/journal.pbio.0050102 · Cited by 287 · see citing works

The α7β1 integrin in muscle development and disease

Burkin, D. J., & Kaufman, S. J. (1999) · Cell and Tissue Research · doi:10.1007/s004410051279 · Cited by 286 · see citing works

Expression of Functional CXCR4 by Muscle Satellite Cells and Secretion of SDF-1 by Muscle-Derived Fibroblasts is Associated with the Presence of Both Muscle Progenitors in Bone Marrow and Hematopoietic Stem/Progenitor Cells in Muscles

Ratajczak, M. Z., Majka, M., Kucia, M., Drukała, J., Pietrzkowski, Z. J., Peiper, S. C., & Janowska‐Wieczorek, A. (2003) · Stem Cells · doi:10.1634/stemcells.21-3-363 · Cited by 280 · see citing works

Regeneration of single skeletal muscle fibers in vitro

Bischoff, R. (1975) · The Anatomical Record · doi:10.1002/ar.1091820207 · Cited by 278 · see citing works

The p38α/β MAPK functions as a molecular switch to activate the quiescent satellite cell

Jones, N. C., Tyner, K. J., Nibarger, L., Stanley, H. M., Cornelison, D., Fedorov, Y. V., & Olwin, B. B. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200408066 · Cited by 272 · see citing works

Premature myogenic differentiation and depletion of progenitor cells cause severe muscle hypotrophy in Delta1 mutants

Schuster-Gossler, K., Cordes, R., & Gossler, A. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0608281104 · Cited by 262 · see citing works

Fibroblast Growth Factor in the Extracellular Matrix of Dystrophic (mdx) Mouse Muscle

DiMario, J. X., Buffinger, N., Yamada, S., & Strohman, R. C. (1989) · Science · doi:10.1126/science.2717945 · Cited by 262 · see citing works

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 · see citing works

Mesoangioblasts — vascular progenitors for extravascular mesodermal tissues

Cossu, G., & Bianco, P. (2003) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2003.08.001 · Cited by 246 · see citing works

Repression of myogenic differentiation by aFGF, bFGF, and K-FGF is dependent on cellular heparan sulfate

Olwin, B., & Rapraeger, A. (1992) · Journal of Cell Biology · doi:10.1083/jcb.118.3.631 · Cited by 246 · see citing works

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 · see citing works

RBP-J ( Rbpsuh ) is essential to maintain muscle progenitor cells and to generate satellite cells

Vasyutina, E. L., Lenhard, D. C., Wende, H., Erdmann, B., Epstein, J. A., & Birchmeier, C. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0610647104 · Cited by 238 · see citing works

Restoration of Human Dystrophin Following Transplantation of Exon-Skipping-Engineered DMD Patient Stem Cells into Dystrophic Mice

Benchaouir, R., Meregalli, M., Farini, A., D’Antona, G., Belicchi, M., Goyenvalle, A., Battistelli, M., Bresolin, N., Bottinelli, R., Garcı́a, L., et al. (2007) · Cell stem cell · doi:10.1016/j.stem.2007.09.016 · Cited by 236 · see citing works

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 · see citing works

TWEAK, via its receptor Fn14, is a novel regulator of mesenchymal progenitor cells and skeletal muscle regeneration

Girgenrath, M., Weng, S., Kostek, C. A., Browning, B., Wang, M., Brown, S. A. N., Winkles, J. A., Michaelson, J. S., Allaire, N., Schneider, P., et al. (2006) · The EMBO Journal · doi:10.1038/sj.emboj.7601441 · Cited by 213 · see citing works

BDNF is expressed in skeletal muscle satellite cells and inhibits myogenic differentiation

Mousavi, K., & Jasmin, B. J. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.5398-05.2006 · Cited by 210 · see citing works

Satellite cell activation in stretched skeletal muscle and the role of nitric oxide and hepatocyte growth factor

Tatsumi, R., Liu, X., Pulido, A., Morales, M. N., SAKATA, T., Dial, S. M., Hattori, A., Ikeuchi, Y., & Allen, R. E. (2006) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00513.2005 · Cited by 210 · see citing works

Developmental Fate of Skeletal Muscle Satellite Cells

Lipton, B. H., & Schultz, E. (1979) · Science · doi:10.1126/science.472747 · Cited by 201 · see citing works

Support for the immortal strand hypothesis: neural stem cells partition DNA asymmetrically in vitro

Karpowicz, P. A., Morshead, C. M., Kam, A., Jervis, E., Ramunas, J., Cheng, V. Y. S., & van der Kooy, D. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200502073 · Cited by 191 · see citing works

Segregation of myogenic lineages in Drosophila requires Numb

Ruiz‐Gómez, M., & Bate, M. (1997) · Development · doi:10.1242/dev.124.23.4857 · Cited by 182 · see citing works

Delta 1-activated Notch inhibits muscle differentiation without affecting Myf5 and Pax3 expression in chick limb myogenesis

Delfini, M.-C., Hirsinger, E., Pourquié, O., & Duprez, D. (2000) · Development · doi:10.1242/dev.127.23.5213 · Cited by 175 · see citing works

An autoradiographic study of satellite cell differentiation into regenerating myotubes following transplantation of muscles in young rats

Snow, M. H. (1978) · Cell and Tissue Research · doi:10.1007/bf00224941 · Cited by 169 · see citing works

The regenerative response of single mature muscle fibers isolated in vitro

Konigsberg, U. R., Lipton, B. H., & Konigsberg, I. R. (1975) · Developmental Biology · doi:10.1016/0012-1606(75)90065-2 · Cited by 164 · see citing works

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 · see citing works

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 · see citing works

inscuteable and numb mediate asymmetric muscle progenitor cell divisions during Drosophila myogenesisPreprint

Carmena, A., Murugasu-Oei, B., Menon, D., Jiménez, F., & Chia, W. (1998) · Genes & Development · doi:10.1101/gad.12.3.304 · Cited by 148 · see citing works

Nitric oxide‐dependence of satellite stem cell activation and quiescence on normal skeletal muscle fibers

Wozniak, A. C., & Anderson, J. E. (2006) · Developmental Dynamics · doi:10.1002/dvdy.21012 · Cited by 145 · see citing works

Long-term persistence and migration of myogenic cells injected into pre-irradiated muscles of mdx mice

Morgan, J. E., Pagel, C. N., Sherrratt, T., & Partridge, T. A. (1993) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(93)90224-m · Cited by 142 · see citing works

Insulin-like growth factor 1 and muscle growth: implication for satellite cell proliferation

Machida, S., & Booth, F. W. (2004) · Proceedings of The Nutrition Society · doi:10.1079/pns2004354 · Cited by 132 · see citing works

The epigenetic network regulating muscle development and regeneration

Palacios, D., & Puri, P. (2005) · Journal of Cellular Physiology · doi:10.1002/jcp.20489 · Cited by 124 · see citing works

Satellite cells from dystrophic (Mdx) mice display accelerated differentiation in primary cultures and in isolated myofibers

Yablonka‐Reuveni, Z., & Anderson, J. E. (2005) · Developmental Dynamics · doi:10.1002/dvdy.20602 · Cited by 123 · see citing works

Gene Expression during Vascular Pericyte Differentiation

Doherty, M. J., & Canfield, A. E. (1999) · Critical Reviews in Eukaryotic Gene Expression · doi:10.1615/critreveukaryotgeneexpr.v9.i1.10 · Cited by 121 · see citing works

The modulation of caveolin‐1 expression controls satellite cell activation during muscle repair

Volonté, D., Liu, Y., & Galbiati, F. (2004) · The FASEB Journal · doi:10.1096/fj.04-2215fje · Cited by 121 · see citing works

The Mammalian Golgi Regulates Numb Signaling in Asymmetric Cell Division by Releasing ACBD3 during Mitosis

Zhou, Y., Atkins, J. B., Rompani, S. B., Bancescu, D. L., Petersen, P. H., Tang, H., Zou, K., Stewart, S. B., & Zhong, W. (2007) · Cell · doi:10.1016/j.cell.2007.02.037 · Cited by 115 · see citing works

Megf10 regulates the progression of the satellite cell myogenic program

Holterman, C. E., Grand, F. L., Kuang, S., Seale, P., & Rudnicki, M. A. (2007) · The Journal of Cell Biology · doi:10.1083/jcb.200709083 · Cited by 102 · see citing works

Pericyte differentiation.

Schor, A. M., Canfield, A. E., Sutton, A. B., Arciniegas, E., & Allen, T. D. (1995) · PubMed · Cited by 81 · see citing works

Sulfs are regulators of growth factor signaling for satellite cell differentiation and muscle regeneration

Langsdorf, A. E., Do, A.-T., Kusche‐Gullberg, M., Emerson, C. P., & Ai, X. (2007) · Developmental Biology · doi:10.1016/j.ydbio.2007.08.053 · Cited by 80 · see citing works

Caveolin-1(−/−)- and Caveolin-2(−/−)-Deficient Mice Both Display Numerous Skeletal Muscle Abnormalities, with Tubular Aggregate Formation

Schubert, W., Sotgia, F., Cohen, A. W., Capozza, F., Bonuccelli, G., Bruno, C., Minetti, C., Bonilla, E., DiMauro, S., & Lisanti, M. P. (2007) · American Journal Of Pathology · doi:10.2353/ajpath.2007.060687 · Cited by 72 · see citing works

Age‐related impeded regeneration of mouse minced anterior tibial muscle

Zacks, S. I., & Sheff, M. F. (1982) · Muscle & Nerve · doi:10.1002/mus.880050213 · Cited by 56 · see citing works

p38 MAP kinase regulates the expression of XMyf5 and affects distinct myogenic programs during Xenopus development

Keren, A., Bengal, E., & Frank, D. (2005) · Developmental Biology · doi:10.1016/j.ydbio.2005.09.020 · Cited by 51 · see citing works

Heparan sulfates in skeletal muscle development and physiology

Jenniskens, G. J., Veerkamp, J. H., & Kuppevelt, T. H. V. (2005) · Journal of Cellular Physiology · doi:10.1002/jcp.20450 · Cited by 45 · see citing works

Asymmetric localization of numb in the chick somite and the influence of myogenic signals

Holowacz, T., Zeng, L., & Lassar, A. B. (2006) · Developmental Dynamics · doi:10.1002/dvdy.20672 · Cited by 41 · see citing works

Reenthronement of the Muscle Satellite Cell

Partridge, T. A. (2004) · Cell · doi:10.1016/j.cell.2004.10.022 · Cited by 33 · see citing works

Asymmetric cell divisions are concentrated in the dermomyotome dorsomedial lip during epaxial primary myotome morphogenesis

Venters, S. J., & Ordahl, C. P. (2005) · Anatomy and Embryology · doi:10.1007/s00429-005-0461-2 · Cited by 29 · see citing works

Myogenic reprogramming of retina-derived cells following their spontaneous fusion with myotubes

Kirillova, I., Gussoni, E., Goldhamer, D. J., & Yablonka‐Reuveni, Z. (2007) · Developmental Biology · doi:10.1016/j.ydbio.2007.08.056 · Cited by 29 · see citing works

IP3 receptors and Ca2+ signals in adult skeletal muscle satellite cells in situ

Molgó, J., Colasante, C., Adams, D. S., & Jaimovich, E. (2004) · Biological Research · doi:10.4067/s0716-97602004000400019 · Cited by 15 · see citing works

Extracellular matrix: A dynamic microenvironment for stem cell niche

Gattazzo, F., Urciuolo, A., & Bonaldo, P. (2014) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2014.01.010 · Cited by 1,304 · see citing works

Satellite cells, connective tissue fibroblasts and their interactions are crucial for muscle regeneration

Murphy, M. M., Lawson, J. A., Mathew, S. J., Hutcheson, D. A., & Kardon, G. (2011) · Development · doi:10.1242/dev.064162 · Cited by 1,249 · see citing works

Building Muscle: Molecular Regulation of MyogenesisPreprint

Bentzinger, C. F., Wang, Y. X., & Rudnicki, M. A. (2012) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a008342 · Cited by 1,198 · see citing works

Type 2 Innate Signals Stimulate Fibro/Adipogenic Progenitors to Facilitate Muscle Regeneration

Heredia, J. E., Mukundan, L., Chen, F. M., Mueller, A. A., Deo, R. C., Locksley, R. M., Rando, T. A., & Chawla, A. (2013) · Cell · doi:10.1016/j.cell.2013.02.053 · Cited by 818 · see citing works

Repairing skeletal muscle: regenerative potential of skeletal muscle stem cells.

Tedesco, F. S., Dellavalle, A., Díaz-Manera, J., Messina, G., & Cossu, G. (2010) · Journal of Clinical Investigation · doi:10.1172/jci40373 · Cited by 667 · see citing works

microRNA-1 and microRNA-206 regulate skeletal muscle satellite cell proliferation and differentiation by repressing Pax7

Chen, J., Tao, Y., Li, J., Deng, Z., Yan, Z., Xiao, X., & Wang, D.-Z. (2010) · The Journal of Cell Biology · doi:10.1083/jcb.200911036 · Cited by 587 · see citing works

The NAD+-Dependent SIRT1 Deacetylase Translates a Metabolic Switch into Regulatory Epigenetics in Skeletal Muscle Stem Cells

Ryall, J. G., Dell’Orso, S., Derfoul, A., Juan, A., Zare, H., Feng, X., Clermont, D., Koulnis, M., Gutierrez-Cruz, G., Fulco, M., et al. (2015) · Cell Stem Cell · doi:10.1016/j.stem.2014.12.004 · Cited by 575 · see citing works

Periosteum contains skeletal stem cells with high bone regenerative potential controlled by Periostin

de Lageneste, O. D., Julien, A., Abou-Khalil, R., Frangi, G., Carvalho, C., Cagnard, N., Cordier, C., Conway, S. J., & Colnot, C. (2018) · Nature Communications · doi:10.1038/s41467-018-03124-z · Cited by 559 · see citing works

Fetal programming of skeletal muscle development in ruminant animals1

Du, ‬., Tong, J., Zhao, J., Underwood, K. R., Zhu, M., Ford, S. P., & Nathanielsz, P. W. (2009) · Journal of Animal Science · doi:10.2527/jas.2009-2311 · Cited by 564 · see citing works

Wnt7a Activates the Planar Cell Polarity Pathway to Drive the Symmetric Expansion of Satellite Stem Cells

Grand, F. L., Jones, A., Seale, V., Scimè, A., & Rudnicki, M. A. (2009) · Cell stem cell · doi:10.1016/j.stem.2009.03.013 · Cited by 531 · see citing works

Collagen VI regulates satellite cell self-renewal and muscle regeneration

Urciuolo, A., Quarta, M., Morbidoni, V., Gattazzo, F., Molon, S., Grumati, P., Montemurro, F., Tedesco, F. S., Blaauw, B., Cossu, G., et al. (2013) · Nature Communications · doi:10.1038/ncomms2964 · Cited by 511 · see citing works

Neurogenesis in the embryonic and adult brain: same regulators, different roles

Urbán, N., & Guillemot, F. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00396 · Cited by 493 · see citing works

Insulin-like growth factors (IGFs), IGF receptors, and IGF-binding proteins: Roles in skeletal muscle growth and differentiation

Duan, C., Ren, H., & Gao, S. (2010) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2010.04.009 · Cited by 492 · see citing works

The central role of muscle stem cells in regenerative failure with aging

Blau, H. M., Cosgrove, B. D., & Ho, A. T. V. (2015) · Nature Medicine · doi:10.1038/nm.3918 · Cited by 437 · see citing works

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

Qazi, T. H., Mooney, D. J., Pumberger, M., Geißler, S., & Duda, G. N. (2015) · Biomaterials · doi:10.1016/j.biomaterials.2015.02.110 · Cited by 433 · see citing works

Tissue-specific stem cells: Lessons from the skeletal muscle satellite cell

Brack, A. S., & Rando, T. (2012) · Cell Stem Cell · doi:10.1016/j.stem.2012.04.001 · Cited by 409 · see citing works

TNF/p38α/Polycomb Signaling to Pax7 Locus in Satellite Cells Links Inflammation to the Epigenetic Control of Muscle Regeneration

Palacios, D., Mozzetta, C., Consalvi, S., Caretti, G., Saccone, V., Proserpio, V., Marquez, V. E., Valente, S., Mai, A., Forcales, S. V., et al. (2010) · Cell Stem Cell · doi:10.1016/j.stem.2010.08.013 · Cited by 392 · see citing works

Fibronectin Regulates Wnt7a Signaling and Satellite Cell Expansion

Bentzinger, C. F., Wang, Y. X., von Maltzahn, J., Soleimani, V. D., Yin, H., & Rudnicki, M. A. (2013) · Cell Stem Cell · doi:10.1016/j.stem.2012.09.015 · Cited by 386 · see citing works

Myogenic progenitor cells control extracellular matrix production by fibroblasts during skeletal muscle hypertrophy

Fry, C. S., Kirby, T. J., Kosmac, K., McCarthy, J. J., & Peterson, C. A. (2017) · Cell stem cell · doi:10.1016/j.stem.2016.09.010 · Cited by 372 · see citing works

microRNA-206 promotes skeletal muscle regeneration and delays progression of Duchenne muscular dystrophy in mice

Liu, N., Williams, A. H., Maxeiner, J. M., Bezprozvannaya, S., Shelton, J. M., Richardson, J. A., Bassel‐Duby, R., & Olson, E. N. (2012) · Journal of Clinical Investigation · doi:10.1172/jci62656 · Cited by 349 · see citing works

Skeletal muscle stem cells in developmental versus regenerative myogenesis

Tajbakhsh, S. (2009) · Journal of Internal Medicine · doi:10.1111/j.1365-2796.2009.02158.x · Cited by 333 · see citing works

Regulatory factors and cell populations involved in skeletal muscle regeneration

Broek, R. W. T., Grefte, S., & den Hoff, J. W. V. (2010) · Journal of Cellular Physiology · doi:10.1002/jcp.22127 · Cited by 315 · see citing works

Myostatin/activin pathway antagonism: molecular basis and therapeutic potential

Han, H. Q., Zhou, X., Mitch, W. E., & Goldberg, A. L. (2013) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2013.05.019 · Cited by 314 · see citing works

The Molecular Regulation of Muscle Stem Cell FunctionPreprint

Rudnicki, M. A., Grand, F. L., McKinnell, I. W., & Kuang, S. (2008) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2008.73.064 · Cited by 261 · see citing works

Adhesion in the stem cell niche: biological roles and regulation

Chen, S., Lewallen, M. E., & Xie, T. (2012) · Development · doi:10.1242/dev.083139 · Cited by 246 · see citing works

Prostaglandin E2 is essential for efficacious skeletal muscle stem-cell function, augmenting regeneration and strength

Ho, A. T. V., Palla, A. R., Blake, M. R., Yucel, N. D., Wang, Y. X., Magnusson, K. E. G., Holbrook, C. A., Kraft, P. E., Delp, S. L., & Blau, H. M. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1705420114 · Cited by 244 · see citing works

Structural, biochemical, cellular, and functional changes in skeletal muscle extracellular matrix with aging

Kragstrup, T. W., Kjær, M., & Mackey, A. L. (2011) · Scandinavian Journal of Medicine and Science in Sports · doi:10.1111/j.1600-0838.2011.01377.x · Cited by 241 · see citing works

Regulation of muscle growth in neonates

Davis, T. A., & Fiorotto, M. L. (2008) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0b013e32831cef9f · Cited by 237 · see citing works

Basal lamina remodeling at the skeletal muscle stem cell niche mediates stem cell self-renewal

Rayagiri, S. S., Ranaldi, D., Raven, A., Mohamad Azhar, N. I. F., Lefebvre, O., Zammit, P. S., & Borycki, A.-G. (2018) · Nature Communications · doi:10.1038/s41467-018-03425-3 · Cited by 218 · see citing works

Polycomb EZH2 controls self-renewal and safeguards the transcriptional identity of skeletal muscle stem cellsPreprint

Juan, A. H., Derfoul, A., Feng, X., Ryall, J. G., Dell’Orso, S., Pasut, A., Zare, H., Simone, J. M., Rudnicki, M. A., & Sartorelli, V. (2011) · Genes & Development · doi:10.1101/gad.2027911 · Cited by 218 · see citing works

A Transcriptional Mechanism Integrating Inputs from Extracellular Signals to Activate Hippocampal Stem Cells

Andersen, J., Urbán, N., Achimastou, A., Ito, A., Simic, M., Ullom, K., Martynoga, B., Lebel, M., Göritz, C., Frisén, J., et al. (2014) · Neuron · doi:10.1016/j.neuron.2014.08.004 · Cited by 212 · see citing works

Colonization of the Satellite Cell Niche by Skeletal Muscle Progenitor Cells Depends on Notch Signals

Bröhl, D., Vasyutina, E. L., Czajkowski, M. T., Griger, J., Raßek, C., Rahn, H.-P., Purfürst, B., Wende, H., & Birchmeier, C. (2012) · Developmental Cell · doi:10.1016/j.devcel.2012.07.014 · Cited by 214 · see citing works

Extracellular matrix regulation in the muscle satellite cell niche

Thomas, K. A., Engler, A. J., & Meyer, G. A. (2014) · Connective Tissue Research · doi:10.3109/03008207.2014.947369 · Cited by 194 · see citing works

Identification of telocytes in skeletal muscle interstitium: implication for muscle regeneration

Popescu, L. M., Manole, E., Serboiu, C. S., Manole, C. G., Ceafalan, L. C., Gherghiceanu, M., & Popescu, B. O. (2011) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2011.01330.x · Cited by 195 · see citing works

Minireview: Mechano-Growth Factor: A Putative Product of IGF-I Gene Expression Involved in Tissue Repair and Regeneration

Matheny, R. W., Nindl, B. C., & Adamo, M. L. (2010) · Endocrinology · doi:10.1210/en.2009-1217 · Cited by 186 · see citing works

Maternal obesity downregulates myogenesis and β-catenin signaling in fetal skeletal muscle

Tong, J. F., Yan, X., Zhu, M. J., Ford, S. P., Nathanielsz, P. W., & Du, ‬. (2009) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.90924.2008 · Cited by 182 · see citing works

A Review of the Pathophysiology and Potential Biomarkers for Peripheral Artery Disease

Krishna, S. M., Moxon, J. V., & Golledge, J. (2015) · International Journal of Molecular Sciences · doi:10.3390/ijms160511294 · Cited by 179 · see citing works

Sequenced response of extracellular matrix deadhesion and fibrotic regulators after muscle damage is involved in protection against future injury in human skeletal muscle

Mackey, A. L., Brandstetter, S., Schjerling, P., Bojsen‐Møller, J., Qvortrup, K., Pedersen, M. M., Doessing, S., Kjær, M., Magnusson, S. P., & Langberg, H. (2011) · The FASEB Journal · doi:10.1096/fj.10-176487 · Cited by 171 · see citing works

Wnt7a stimulates myogenic stem cell motility and engraftment resulting in improved muscle strength

Bentzinger, C. F., von Maltzahn, J., Dumont, N. A., Stark, D. A., Wang, Y. X., Nhan, K., Frenette, J., Cornelison, D., & Rudnicki, M. A. (2014) · The Journal of Cell Biology · doi:10.1083/jcb.201310035 · Cited by 163 · see citing works

Skeletal muscle stem cells adopt a dormant cell state post mortem and retain regenerative capacity

Latil, M., Rocheteau, P., Châtre, L., Sanulli, S., Mémet, S., Ricchetti, M., Tajbakhsh, S., & Chrétien, F. (2012) · Nature Communications · doi:10.1038/ncomms1890 · Cited by 165 · see citing works

The Skeletal Muscle Satellite Cell

Yablonka‐Reuveni, Z. (2011) · Journal of Histochemistry & Cytochemistry · doi:10.1369/0022155411426780 · Cited by 164 · see citing works

Increased Stiffness in Aged Skeletal Muscle Impairs Muscle Progenitor Cell Proliferative Activity

Lacraz, G., Rouleau, A.-J., Couture, V., Söllrald, T., Drouin, G., Veillette, N., Grandbois, M., & Grenier, G. (2015) · PLoS ONE · doi:10.1371/journal.pone.0136217 · Cited by 156 · see citing works

Telocytes in regenerative medicine

Bei, Y., Wang, F., Yang, C., & Xiao, J. (2015) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.12594 · Cited by 154 · see citing works

Biomaterials in Tendon and Skeletal Muscle Tissue Engineering: Current Trends and Challenges

Beldjilali‐Labro, M., Garcia, A. G., Farhat, F., Bédoui, F., Grosset, J.-F., Dufresne, M., & Legallais, C. (2018) · Materials · doi:10.3390/ma11071116 · Cited by 153 · see citing works

Mechanisms of skeletal muscle aging: insights from <i>Drosophila</i> and mammalian models

Demontis, F., Piccirillo, R., Goldberg, A. L., & Perrimon, N. (2013) · Disease Models &amp; Mechanisms · doi:10.1242/dmm.012559 · Cited by 238 · see citing works

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 · see citing works

Biomaterial-based delivery for skeletal muscle repair

Cezar, C. A., & Mooney, D. J. (2014) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2014.09.008 · Cited by 142 · see citing works

A home away from home: Challenges and opportunities in engineering in vitro muscle satellite cell niches

Cosgrove, B. D., Sacco, A., Gilbert, P. M., & Blau, H. M. (2009) · Differentiation · doi:10.1016/j.diff.2009.08.004 · Cited by 135 · see citing works

Srf-Dependent Paracrine Signals Produced by Myofibers Control Satellite Cell-Mediated Skeletal Muscle Hypertrophy

Guerci, A., Lahoute, C., Hébrard, S., Collard, L., Graindorge, D., Favier, M., Cagnard, N., Batonnet‐Pichon, S., Précigout, G., Garcı́a, L., et al. (2012) · Cell Metabolism · doi:10.1016/j.cmet.2011.12.001 · Cited by 138 · see citing works

Myostatin and its Regulation: A Comprehensive Review of Myostatin Inhibiting Strategies

Baig, M. H., Ahmad, K., Moon, J. S., Park, S.-Y., Ho Lim, J., Chun, H. J., Qadri, A. F., Hwang, Y. C., Jan, A. T., Ahmad, S. S., et al. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.876078 · Cited by 135 · see citing works

Muscular dystrophy in the mdx mouse is a severe myopathy compounded by hypotrophy, hypertrophy and hyperplasia

Duddy, W. J., Duguez, S., Johnston, H., Cohen, T. V., Phadke, A., Gordish‐Dressman, H., Nagaraju, K., Gnocchi, V. F., Low, S., & Partridge, T. A. (2015) · Skeletal Muscle · doi:10.1186/s13395-015-0041-y · Cited by 130 · see citing works

The Muscle Stem Cell Niche in Health and Disease

Mashinchian, O., Pisconti, A., Moal, E. L., & Bentzinger, C. F. (2017) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2017.08.003 · Cited by 127 · see citing works

Syndecan-3 and Notch cooperate in regulating adult myogenesis

Pisconti, A., Cornelison, D., Olguín, H. C., Antwine, T. L., & Olwin, B. B. (2010) · The Journal of Cell Biology · doi:10.1083/jcb.201003081 · Cited by 126 · see citing works

Extrinsic regulation of satellite cell specification

Bentzinger, C. F., von Maltzahn, J., & Rudnicki, M. A. (2010) · Stem Cell Research & Therapy · doi:10.1186/scrt27 · Cited by 126 · see citing works

The Adventitia: A Progenitor Cell Niche for the Vessel Wall

Majesky, M. W., Dong, X. R., Hoglund, V. J., Daum, G., & Mahoney, W. M. (2011) · Cells Tissues Organs · doi:10.1159/000331413 · Cited by 125 · see citing works

Macrophage-released ADAMTS1 promotes muscle stem cell activation

Du, H., Shih, C., Wosczyna, M. N., Mueller, A. A., Cho, J., Aggarwal, A., Rando, T. A., & Feldman, B. J. (2017) · Nature Communications · doi:10.1038/s41467-017-00522-7 · Cited by 128 · see citing works

Muscle stem cells at a glance

Wang, Y. X., Dumont, N. A., & Rudnicki, M. A. (2014) · Journal of Cell Science · doi:10.1242/jcs.151209 · Cited by 125 · see citing works

Spatial influence on breast muscle morphological structure, myofiber size, and gene expression associated with the wooden breast myopathy in broilers

Clark, D. L., & Velleman, S. G. (2016) · Poultry Science · doi:10.3382/ps/pew243 · Cited by 124 · see citing works

In vivo partial reprogramming of myofibers promotes muscle regeneration by remodeling the stem cell niche

Wang, C., Rabadan Ros, R., Martinez-Redondo, P., Ma, Z., Shi, L., Xue, Y., Guillen-Guillen, I., Huang, L., Hishida, T., Liao, H.-K., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-23353-z · Cited by 119 · see citing works

Engineered skeletal muscles for disease modeling and drug discovery

Wang, J., Khodabukus, A., Rao, L., VanDusen, K. W., Abutaleb, N. O., & Bursac, N. (2019) · Biomaterials · doi:10.1016/j.biomaterials.2019.119416 · Cited by 117 · see citing works

Notch1 and Notch2 Coordinately Regulate Stem Cell Function in the Quiescent and Activated States of Muscle Satellite Cells

Fujimaki, S., Seko, D., Kitajima, Y., Yoshioka, K., Tsuchiya, Y., Masuda, S., & Ono, Y. (2017) · Stem Cells · doi:10.1002/stem.2743 · Cited by 112 · see citing works

Bidirectional roles of skeletal muscle fibro-adipogenic progenitors in homeostasis and disease

Chen, W., You, W., Valencak, T. G., & Shan, T. (2022) · Ageing Research Reviews · doi:10.1016/j.arr.2022.101682 · Cited by 118 · see citing works

The Muscle Stem Cell Niche: Regulation of Satellite Cells During Regeneration

Boonen, K. J. M., & Post, M. J. (2008) · Tissue Engineering Part B Reviews · doi:10.1089/ten.teb.2008.0045 · Cited by 114 · see citing works

Emerin in health and disease

Koch, A. J., & Holaska, J. M. (2014) · Seminars in Cell &amp; Developmental Biology · doi:10.1016/j.semcdb.2013.12.008 · Cited by 114 · see citing works

Protein imbalance in the development of skeletal muscle wasting in tumour‐bearing mice

Brown, J. L., Lee, D. E., Rosa-Caldwell, M., Brown, L., Perry, R. A., Haynie, W. S., Huseman, K., Sataranatarajan, K., Remmen, H. V., Washington, T. A., et al. (2018) · Journal of Cachexia, Sarcopenia and Muscle · doi:10.1002/jcsm.12354 · Cited by 98 · see citing works

Nitric Oxide Sustains Long-Term Skeletal Muscle Regeneration by Regulating Fate of Satellite Cells Via Signaling Pathways Requiring Vangl2 and Cyclic GMP

Buono, R., Vantaggiato, C., Pisa, V., Azzoni, E., Bassi, M. T., Brunelli, S., Sciorati, C., & Clementi, E. (2011) · Stem Cells · doi:10.1002/stem.783 · Cited by 113 · see citing works

Hyaluronic acid matrices show matrix stiffness in 2D and 3D dictates cytoskeletal order and myosin-II phosphorylation within stem cells

Rehfeldt, F., Brown, A. E., Raab, M., Cai, S., Zajac, A. L., Zemel, A., & Discher, D. E. (2012) · Integrative Biology · doi:10.1039/c2ib00150k · Cited by 112 · see citing works

Epigenetic regulation of myogenesis

Perdiguero, E., Sousa‐Victor, P., Ballestar, E., & Muñoz‐Cánoves, P. (2009) · Epigenetics · doi:10.4161/epi.4.8.10258 · Cited by 103 · see citing works

Adhesion within the stem cell niches

Raymond, K., Deugnier, M., Faraldo, M. M., & Glukhova, M. A. (2009) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2009.05.004 · Cited by 101 · see citing works

Muscle Tissue Engineering Using Gingival Mesenchymal Stem Cells Encapsulated in Alginate Hydrogels Containing Multiple Growth Factors

Ansari, S., Chen, C., Xu, X., Annabi, N., Zadeh, H. H., Wu, B. M., Khademhosseini, A., Shi, S., & Moshaverinia, A. (2016) · Annals of Biomedical Engineering · doi:10.1007/s10439-016-1594-6 · Cited by 101 · see citing works

Early Life Nutrition Modulates Muscle Stem Cell Number: Implications for Muscle Mass and Repair

Woo, M., ISGANAITIS, E. M., Cerletti, M., Fitzpatrick, C., Wagers, A. J., Jimenez-Chillaron, J., & Patti, M. (2011) · Stem Cells and Development · doi:10.1089/scd.2010.0349 · Cited by 97 · see citing works

Engineering Craniofacial Structures: Facing the Challenge

Zaky, S. H., & Cancedda, R. (2009) · Journal of Dental Research · doi:10.1177/0022034509349926 · Cited by 95 · see citing works

Adult Stem Cell Niches

Rezza, A., Sennett, R., & Rendl, M. (2014) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/b978-0-12-416022-4.00012-3 · Cited by 95 · see citing works

Skeletal muscle satellite cells: Mediators of muscle growth during development and implications for developmental disorders

Dayanidhi, S., & Lieber, R. L. (2014) · Muscle & Nerve · doi:10.1002/mus.24441 · Cited by 93 · see citing works

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 · see citing works

Skeletal Muscle as a Paradigm for Regenerative Biology and Medicine

Gayraud-Morel, B., Chrétien, F. C., & Tajbakhsh, S. (2009) · Regenerative Medicine · doi:10.2217/17460751.4.2.293 · Cited by 93 · see citing works

HMGB1/RAGE regulates muscle satellite cell homeostasis via p38 MAPK/myogenin-dependent repression of Pax7 transcription

Riuzzi, F., Sorci, G., Sagheddu, R., & Donato, R. (2012) · Journal of Cell Science · doi:10.1242/jcs.092163 · Cited by 91 · see citing works

Muscle stem cells in developmental and regenerative myogenesis

Kang, J.-S., & Krauss, R. S. (2010) · Current Opinion in Clinical Nutrition and Metabolic Care · doi:10.1097/mco.0b013e328336ea98 · Cited by 90 · see citing works

Fat deposition and accumulation in the damaged and inflamed skeletal muscle: cellular and molecular players

Sciorati, C., Clementi, E., Manfredi, A. A., & Rovere, P. Q. (2015) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-015-1857-7 · Cited by 92 · see citing works

Blood Vessels and the Satellite Cell Niche

Mounier, R., Chrétien, F., & Chazaud, B. (2011) · Current Topics in Developmental Biology · doi:10.1016/b978-0-12-385940-2.00005-x · Cited by 89 · see citing works

Emerin and histone deacetylase 3 (HDAC3) cooperatively regulate expression and nuclear positions of MyoD, Myf5, and Pax7 genes during myogenesis

Demmerle, J., Koch, A. J., & Holaska, J. M. (2013) · Chromosome Research · doi:10.1007/s10577-013-9381-9 · Cited by 89 · see citing works

Optimized method for extraction of exosomes from human primary muscle cells

Gall, L. L., Ouandaogo, Z. G., Anakor, E., Connolly, O., Butler-Browne, G. S., Lainé, J., Duddy, W. J., & Duguez, S. (2020) · Skeletal Muscle · doi:10.1186/s13395-020-00238-1 · Cited by 90 · see citing works

Chromatin: the interface between extrinsic cues and the epigenetic regulation of muscle regeneration

Guasconi, V., & Puri, P. (2009) · Trends in Cell Biology · doi:10.1016/j.tcb.2009.03.002 · Cited by 88 · see citing works

Nrf2 deficiency promotes apoptosis and impairs PAX7/MyoD expression in aging skeletal muscle cells

Narasimhan, M., Hong, J., Atieno, N., Muthusamy, V. R., Davidson, C. J., Abu-Rmaileh, N., Richardson, R. S., Gomes, A. V., Hoidal, J. R., & Rajasekaran, N. S. (2014) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2014.02.023 · Cited by 87 · see citing works

Extracellular matrix: the critical contributor to skeletal muscle regeneration—a comprehensive review

Ahmad, K., Shaikh, S., Chun, H. J., Ali, S. M., Lim, J. H., Ahmad, S. S., Lee, E. J., & Choi, I. (2023) · Inflammation and Regeneration · doi:10.1186/s41232-023-00308-z · Cited by 85 · see citing works

Macrophages in Injured Skeletal Muscle: A Perpetuum Mobile Causing and Limiting Fibrosis, Prompting or Restricting Resolution and Regeneration

Bosurgi, L., Manfredi, A., & Rovere-Querini, P. (2011) · Front. Immun. · doi:10.3389/fimmu.2011.00062 · Cited by 80 · see citing works

Unacylated Ghrelin Induces Oxidative Stress Resistance in a Glucose Intolerance and Peripheral Artery Disease Mouse Model by Restoring Endothelial Cell miR-126 Expression

Togliatto, G., Trombetta, A., Dentelli, P., Gallo, S., Rosso, A., Cotogni, P., Granata, R., Falcioni, R., Delale, T., Ghigo, E., et al. (2014) · Diabetes · doi:10.2337/db14-0991 · Cited by 84 · see citing works

Unacylated Ghrelin Promotes Skeletal Muscle Regeneration Following Hindlimb Ischemia via SOD‐2–Mediated miR‐221/222 Expression

Togliatto, G., Trombetta, A., Dentelli, P., Cotogni, P., Rosso, A., Tschöp, M. H., Granata, R., Ghigo, E., & Brizzi, M. F. (2013) · Journal of the American Heart Association · doi:10.1161/jaha.113.000376 · Cited by 84 · see citing works

The hypoxia-inducible factors HIF1α and HIF2α are dispensable for embryonic muscle development but essential for postnatal muscle regeneration

Yang, X., Yang, S., Wang, C., & Kuang, S. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.756312 · Cited by 85 · see citing works

Angiotensin II Inhibits Satellite Cell Proliferation and Prevents Skeletal Muscle Regeneration

Yoshida, T., Galvez, S., Tiwari, S., Rezk, B. M., Semprun‐Prieto, L., Higashi, Y., Sukhanov, S., Yablonka‐Reuveni, Z., & Delafontaine, P. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.449074 · Cited by 83 · see citing works

Satellite cell number and cell cycle kinetics in response to acute myotrauma in humans: immunohistochemistryversusflow cytometry

McKay, B. R., Toth, K., Tarnopolsky, M. A., & Parise, G. (2010) · The Journal of Physiology · doi:10.1113/jphysiol.2010.190876 · Cited by 82 · see citing works

Muscle satellite cell proliferation and association: new insights from myofiber time-lapse imaging

Siegel, A. L., Kuhlmann, P., & Cornelison, D. (2011) · Skeletal Muscle · doi:10.1186/2044-5040-1-7 · Cited by 82 · see citing works

Growth Factors for Skeletal Muscle Tissue Engineering

Syverud, B. C., VanDusen, K. W., & Larkin, L. M. (2016) · Cells Tissues Organs · doi:10.1159/000444671 · Cited by 82 · see citing works

Activation of Toll-like receptor 3 amplifies mesenchymal stem cell trophic factors and enhances therapeutic potency

Mastri, M., Shah, Z., McLaughlin, T. J., Greene, C., Baum, L., Suzuki, G., & Lee, T. (2012) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00191.2012 · Cited by 81 · see citing works

MASTR directs MyoD-dependent satellite cell differentiation during skeletal muscle regenerationPreprint

Mokalled, M. H., Johnson, A. N., Creemers, E. E., & Olson, E. N. (2012) · Genes & Development · doi:10.1101/gad.179663.111 · Cited by 81 · see citing works

Regulation of promyogenic signal transduction by cell–cell contact and adhesion

Krauss, R. S. (2010) · Experimental Cell Research · doi:10.1016/j.yexcr.2010.05.008 · Cited by 79 · see citing works

Lipid droplet dynamics regulate adult muscle stem cell fate

Yue, F., Oprescu, S. N., Qiu, J., Gu, L., Zhang, L., Chen, J., Narayanan, N., Deng, M., & Kuang, S. (2022) · Cell Reports · doi:10.1016/j.celrep.2021.110267 · Cited by 78 · see citing works

O 2 Regulates Skeletal Muscle Progenitor Differentiation through Phosphatidylinositol 3-Kinase/AKT Signaling

Majmundar, A. J., Skuli, N., Mesquita, R. C., Kim, M. N., Yodh, A. G., Nguyen-McCarty, M., & Simon, M. C. (2011) · Molecular and Cellular Biology · doi:10.1128/mcb.05857-11 · Cited by 75 · see citing works

Harnessing Fiber Diameter-Dependent Effects of Myoblasts Toward Biomimetic Scaffold-Based Skeletal Muscle Regeneration

Narayanan, N., Jiang, C., Wang, C., Uzunallı, G., Whittern, N., Chen, D., Jones, O. G., Kuang, S., & Deng, M. (2020) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2020.00203 · Cited by 77 · see citing works

Human Skeletal Muscle–derived CD133+ Cells Form Functional Satellite Cells After Intramuscular Transplantation in Immunodeficient Host Mice

Meng, J., Chun, S., Asfahani, R., Lochmüller, H., Francesco Muntoni, A., & Morgan, J. E. (2014) · Molecular Therapy · doi:10.1038/mt.2014.26 · Cited by 74 · see citing works

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 251 · see citing works

The Satellite Cell Niche in Skeletal Muscle

Brun, C. E., Chevalier, F. P., Dumont, N. A., & Rudnicki, M. A. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-802734-9.00010-x · Cited by 10 · see citing works

The Role of Satellite Cells and Stem Cells in Muscle Regeneration

Kawabe, Y.-I., & Rudnicki, M. A. (2011) · Springer eBooks · doi:10.1007/978-1-4419-1795-9_77 · Cited by 1 · see citing works

Oriented Cell Divisions and Muscle Satellite Cell Heterogeneity

Cossu, G., & Tajbakhsh, S. (2007) · Cell · doi:10.1016/j.cell.2007.05.029 · Cited by 49 · see citing works

Orienting Muscle Stem Cells for Regeneration in Homeostasis, Aging, and Disease

Feige, P., Brun, C. E., Ritso, M., & Rudnicki, M. A. (2018) · Cell stem cell · doi:10.1016/j.stem.2018.10.006 · Cited by 227 · see citing works