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

Identification of the haematopoietic stem cell niche and control of the niche size

Zhang, J., Niu, C. S., Ye, L., Huang, H., He, X. C., Tong, W.-G., Ross, J., Haug, J., Johnson, T. J., Feng, J. Q., et al. (2003) · Nature · doi:10.1038/nature02041 · Cited by 2,948 · see citing works

Muscle Regeneration by Bone Marrow-Derived Myogenic Progenitors

Ferrari, G., Cusella, G., Angelis, D., Coletta, M., Paolucci, E., Stornaiuolo, A., Cossu, G., & Mavilio, F. (1998) · Science · doi:10.1126/science.279.5356.1528 · Cited by 2,721 · 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

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

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

Involvement of Follicular Stem Cells in Forming Not Only the Follicle but Also the Epidermis

Taylor, G., Lehrer, M. S., Jensen, P. J., Sun, T.-T., & Lavker, R. M. (2000) · Cell · doi:10.1016/s0092-8674(00)00050-7 · Cited by 1,070 · 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

Biological Progression from Adult Bone Marrow to Mononucleate Muscle Stem Cell to Multinucleate Muscle Fiber in Response to Injury

LaBarge, M. A., & Blau, H. M. (2002) · Cell · doi:10.1016/s0092-8674(02)01078-4 · Cited by 798 · see citing works

Asymmetric distribution of numb protein during division of the sensory organ precursor cell confers distinct fates to daughter cells

Rhyu, M. S., Jan, L. Y., & Jan, Y. N. (1994) · Cell · doi:10.1016/0092-8674(94)90112-0 · Cited by 770 · see citing works

Myogenic specification of side population cells in skeletal muscle

Asakura, A., Seale, P., Girgis-Gabardo, A., & Rudnicki, M. A. (2002) · The Journal of Cell Biology · doi:10.1083/jcb.200202092 · Cited by 681 · see citing works

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 · see citing works

Intestinal stem cells protect their genome by selective segregation of template DNA strands

Potten, C. S., Owen, G., & Booth, D. (2002) · Journal of Cell Science · doi:10.1242/jcs.115.11.2381 · Cited by 633 · see citing works

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 · see citing works

numb, a gene required in determination of cell fate during sensory organ formation in Drosophila embryos

Uemura, T., Younger-Shepherd, S., Ackerman, L. D., Jan, L. Y., & Jan, Y. N. (1989) · Cell · doi:10.1016/0092-8674(89)90849-0 · Cited by 505 · 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

Asymmetric Localization of a Mammalian Numb Homolog during Mouse Cortical Neurogenesis

Zhong, W., Feder, J. N., Jiang, M., Jan, L. Y., & Jan, Y. N. (1996) · Neuron · doi:10.1016/s0896-6273(00)80279-2 · Cited by 478 · see citing works

Dare to Be Different: Asymmetric Cell Division in Drosophila, C. elegans and Vertebrates

Betschinger, J., & Knoblich, J. A. (2004) · Current Biology · doi:10.1016/j.cub.2004.08.017 · Cited by 449 · see citing works

Numb Antagonizes Notch Signaling to Specify Sibling Neuron Cell Fates

Spana, E. P., & Doe, C. Q. (1996) · Neuron · doi:10.1016/s0896-6273(00)80277-9 · Cited by 433 · see citing works

Single hematopoietic stem cells generate skeletal muscle through myeloid intermediates

Camargo, F. D., Green, R., Capetenaki, Y., Jackson, K. A., & Goodell, M. A. (2003) · Nature Medicine · doi:10.1038/nm963 · Cited by 410 · see citing works

Numb Is an Endocytic Protein

Santolini, E., Puri, C., Salcini, A. E., Gagliani, M. C., Pelicci, P. G., Tacchetti, C., & Fiore, P. P. D. (2000) · The Journal of Cell Biology · doi:10.1083/jcb.151.6.1345 · Cited by 363 · see citing works

Progenitor cell maintenance requires numb and numblike during mouse neurogenesis

Petersen, P. H., Zou, K., Hwang, J. K., Jan, Y. N., & Zhong, W. (2002) · Nature · doi:10.1038/nature01124 · Cited by 330 · see citing works

INHIBITION OF MYOBLAST FUSION AFTER ONE ROUND OF DNA SYNTHESIS IN 5-BROMODEOXYURIDINE

Bischoff, R., & Holtzer, H. (1970) · The Journal of Cell Biology · doi:10.1083/jcb.44.1.134 · Cited by 322 · see citing works

The segregation of DNA in epithelial stem cells

Potten, C. S., Hume, W. J., Reid, P. J., & Cairns, J. (1978) · Cell · doi:10.1016/0092-8674(78)90274-x · Cited by 313 · see citing works

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 · 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

The skeletal muscle satellite cell: stem cell or son of stem cell?

Zammit, P. S., & Beauchamp, J. R. (2001) · Differentiation · doi:10.1046/j.1432-0436.2001.680407.x · Cited by 259 · see citing works

NUMB Localizes in the Basal Cortex of Mitotic Avian Neuroepithelial Cells and Modulates Neuronal Differentiation by Binding to NOTCH-1

Wakamatsu, Y., Maynard, T. M., Jones, S. U., & Weston, J. A. (1999) · Neuron · doi:10.1016/s0896-6273(00)80754-0 · Cited by 256 · see citing works

Highly Persistent Label-Retaining Cells in the Hair Follicles of Mice and Their Fate Following Induction of Anagen

Morris, R. J., & Potten, C. S. (1999) · Journal of Investigative Dermatology · doi:10.1046/j.1523-1747.1999.00537.x · Cited by 249 · see citing works

Somatic stem cells and the kinetics of mutagenesis and carcinogenesis

Cairns, J. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.162369899 · Cited by 239 · see citing works

DNA damage tumor suppressor genes and genomic instability

Motoyama, N., & Naka, K. (2003) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2003.12.003 · Cited by 237 · see citing works

Asymmetric cell division

Roegiers, F., & Jan, Y. N. (2004) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2004.02.010 · Cited by 223 · see citing works

Asymmetric segregation of Numb: a mechanism for neural specification from Drosophila to mammals

Cayouette, M., & RAFF, M. C. (2002) · Nature Neuroscience · doi:10.1038/nn1202-1265 · Cited by 195 · 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

Distinct human NUMB isoforms regulate differentiation vs. proliferation in the neuronal lineage

Verdi, J. M., Bashirullah, A., Goldhawk, D. E., Kubu, C. J., Jamali, M., Meakin, S. O., & Lipshitz, H. D. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.18.10472 · Cited by 188 · 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

δ-Tubulin and ɛ-tubulin: two new human centrosomal tubulins reveal new aspects of centrosome structure and function

Chang, P., & Stearns, T. (1999) · Nature Cell Biology · doi:10.1038/71350 · 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

Cosegregation of chromosomes containing immortal DNA strands in cells that cycle with asymmetric stem cell kinetics.

Merok, J. R., Lansita, J. A., Tunstead, J. R., & Sherley, J. L. (2002) · PubMed · Cited by 137 · see citing works

Numb and α‐Adaptin regulate Sanpodo endocytosis to specify cell fate in Drosophila external sensory organs

Hutterer, A., & Knoblich, J. A. (2005) · EMBO Reports · doi:10.1038/sj.embor.7400500 · Cited by 129 · see citing works

Deconstructing stemness

Mikkers, H. M. M., & Frisén, J. (2005) · The EMBO Journal · doi:10.1038/sj.emboj.7600749 · Cited by 97 · see citing works

Cellular Senescence: Ex Vivo p53‐Dependent Asymmetric Cell Kinetics

Rambhatla, L., Bohn, S. A., Stadler, P. B., Boyd, J. T., Coss, R. A., & Sherley, J. L. (2001) · BioMed Research International · doi:10.1155/s1110724301000079 · Cited by 74 · see citing works

Skeletal muscle stem and progenitor cells: Reconciling genetics and lineage

Tajbakhsh, S. (2005) · Experimental Cell Research · doi:10.1016/j.yexcr.2005.03.033 · Cited by 70 · see citing works

Diversifying Neural Cells through Order of Birth and Asymmetry of Division

Zhong, W. (2003) · Neuron · doi:10.1016/s0896-6273(02)01178-9 · Cited by 65 · see citing works

Asymmetric localization of Numb:EGFP in dividing neuroepithelial cells during neurulation in Danio rerio

Reugels, A. M., Boggetti, B., Scheer, N., & Campos‐Ortega, J. A. (2006) · Developmental Dynamics · doi:10.1002/dvdy.20699 · Cited by 41 · see citing works

The Enigma of the Numb-Notch Relationship during Mammalian Embryogenesis

Petersen, P. H., Tang, H., Zou, K., & Zhong, W. (2006) · Developmental Neuroscience · doi:10.1159/000090761 · Cited by 41 · see citing works

Localization-Dependent and -Independent Roles of Numb Contribute to Cell-Fate Specification in Drosophila

Bhalerao, S., Berdnik, D., Tőrők, T., & Knoblich, J. A. (2005) · Current Biology · doi:10.1016/j.cub.2005.07.061 · Cited by 32 · see citing works

Random Segregation of DNA Strands in Epidermal Basal Cells

Kuroki, T., & Murakami, Y. (1989) · Japanese Journal of Cancer Research · doi:10.1111/j.1349-7006.1989.tb01690.x · Cited by 27 · see citing works

The Human MYOD1 Transgene Is Suppressed by 5-Bromodeoxyuridine in Mouse Myoblasts

Ogino, H., Satou, W., Fujii, M., Suzuki, T., He, Y., Michishita, E., & Ayusawa, D. (2002) · The Journal of Biochemistry · doi:10.1093/oxfordjournals.jbchem.a003309 · Cited by 9 · see citing works

Satellite Cells and the Muscle Stem Cell Niche

Yin, H., Price, F., & Rudnicki, M. A. (2013) · Physiological Reviews · doi:10.1152/physrev.00043.2011 · Cited by 2,166 · see citing works

Hematopoietic Stem Cells Reversibly Switch from Dormancy to Self-Renewal during Homeostasis and Repair

Wilson, A., Laurenti, E., Oser, G., van der Wath, R. C., Blanco-Bose, W., Jaworski, M., Offner, S., Dunant, C. F., Eshkind, L., Bockamp, E., et al. (2008) · Cell · doi:10.1016/j.cell.2008.10.048 · Cited by 1,908 · see citing works

Substrate Elasticity Regulates Skeletal Muscle Stem Cell Self-Renewal in Culture

Gilbert, P. M., Havenstrite, K. L., Magnusson, K. E. G., Sacco, A., Leonardi, N. A., Kraft, P., Nguyen, N. K., Thrun, S., Lutolf, M. P., & Blau, H. M. (2010) · Science · doi:10.1126/science.1191035 · Cited by 1,587 · 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

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

Molecular regulation of stem cell quiescence

Cheung, T. H., & Rando, T. A. (2013) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3591 · Cited by 1,148 · see citing works

Pax7-expressing satellite cells are indispensable for adult skeletal muscle regeneration

Sambasivan, R., Yao, R., Kissenpfennig, A., Van Wittenberghe, L., Paldi, A., Gayraud-Morel, B., Guenou, H., Malissen, B., Tajbakhsh, S., & Galy, A. (2011) · Development · doi:10.1242/dev.067587 · Cited by 939 · see citing works

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 · 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

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 · 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 591 · see citing works

Asymmetric cell division: recent developments and their implications for tumour biology

Knoblich, J. A. (2010) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3010 · Cited by 568 · see citing works

Growth and Regeneration of Adult β Cells Does Not Involve Specialized Progenitors

Teta, M., Rankin, M. M., Long, S. Y., Stein, G. M., & Kushner, J. A. (2007) · Developmental Cell · doi:10.1016/j.devcel.2007.04.011 · Cited by 551 · see citing works

Skeletal muscle satellite cells and adult myogenesis

Le Grand, F., & Rudnicki, M. A. (2007) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2007.09.012 · Cited by 544 · see citing works

Role of Inflammation in Muscle Homeostasis and Myogenesis

Costamagna, D., Costelli, P., Sampaolesi, M., & Penna, F. (2015) · Mediators of Inflammation · doi:10.1155/2015/805172 · Cited by 390 · see citing works

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 · see citing works

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 512 · see citing works

A Subpopulation of Adult Skeletal Muscle Stem Cells Retains All Template DNA Strands after Cell Division

Rocheteau, P., Gayraud-Morel, B., Siegl-Cachedenier, I., Blasco, M. A., & Tajbakhsh, S. (2012) · Cell · doi:10.1016/j.cell.2011.11.049 · Cited by 510 · see citing works

Niche Regulation of Muscle Satellite Cell Self-Renewal and Differentiation

Kuang, S., Gillespie, M. A., & Rudnicki, M. A. (2008) · Cell Stem Cell · doi:10.1016/j.stem.2007.12.012 · Cited by 507 · see citing works

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 · see citing works

Mechanisms of asymmetric cell division: flies and worms pave the way

Gönczy, P. (2008) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2388 · Cited by 487 · see citing works

The Role ofPaxGenes in the Development of Tissues and Organs:Pax3andPax7Regulate Muscle Progenitor Cell Functions

BUCKINGHAM, M. E., & Relaix, F. (2007) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.23.090506.123438 · Cited by 484 · see citing works

Maintenance of muscle stem-cell quiescence by microRNA-489

Cheung, T. H., Quach, N. L., Charville, G. W., Liu, L., Park, L., Edalati, A., Yoo, B., Hoang, P., & Rando, T. A. (2012) · Nature · doi:10.1038/nature10834 · Cited by 461 · see citing works

Myogenic progenitor cells and skeletal myogenesis in vertebrates

BUCKINGHAM, M. E. (2006) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2006.08.008 · Cited by 452 · 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

Mitotic Spindle Orientation in Asymmetric and Symmetric Cell Divisions during Animal Development

Morin, X., & Bellaïche, Y. (2011) · Developmental Cell · doi:10.1016/j.devcel.2011.06.012 · Cited by 423 · 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

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

Dividing cellular asymmetry: asymmetric cell division and its implications for stem cells and cancerPreprint

Neumüller, R. A., & Knoblich, J. A. (2009) · Genes & Development · doi:10.1101/gad.1850809 · Cited by 402 · see citing works

Skeletal muscle hypertrophy and regeneration: interplay between the myogenic regulatory factors (MRFs) and insulin-like growth factors (IGFs) pathways

Zanou, N., & Gailly, P. L. (2013) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-013-1330-4 · Cited by 361 · see citing works

Tissue-Resident Adult Stem Cell Populations of Rapidly Self-Renewing Organs

Barker, N., Bartfeld, S., & Clevers, H. C. (2010) · Cell stem cell · doi:10.1016/j.stem.2010.11.016 · Cited by 352 · 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

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

Muscle regeneration: cellular and molecular events.

Karalaki, M., Fili, S., Philippou, Α., & Koutsilieris, M. (2009) · PubMed · Cited by 330 · see citing works

When stem cells grow old: phenotypes and mechanisms of stem cell aging

Schultz, M. B., & Sinclair, D. A. (2016) · Development · doi:10.1242/dev.130633 · Cited by 331 · see citing works

A Population of Myogenic Stem Cells That Survives Skeletal Muscle Aging

Collins, C. A., Zammit, P. S., Ruiz, A. P., Morgan, J. E., & Partridge, T. A. (2007) · Stem Cells · doi:10.1634/stemcells.2006-0372 · Cited by 320 · see citing works

Molecular circuitry of stem cell fate in skeletal muscle regeneration, ageing and disease

Almada, A. E., & Wagers, A. J. (2016) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm.2016.7 · Cited by 314 · 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

Reciprocal inhibition between Pax7 and muscle regulatory factors modulates myogenic cell fate determination

Olguín, H. C., Yang, Z., Tapscott, S. J., & Olwin, B. B. (2007) · The Journal of Cell Biology · doi:10.1083/jcb.200608122 · Cited by 311 · see citing works

Adult stem cells at work: regenerating skeletal muscle

Schmidt, M., Schüler, S. C., Hüttner, S. S., von Eyß, B., & von Maltzahn, J. (2019) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-019-03093-6 · Cited by 313 · see citing works

Multi-isotope imaging mass spectrometry quantifies stem cell division and metabolism

Steinhauser, M. L., Bailey, A. P., Senyo, S. E., Guillermier, C., Perlstein, T. S., Gould, A. P., Lee, R. T., & Lechène, C. (2012) · Nature · doi:10.1038/nature10734 · Cited by 307 · see citing works

Reciprocal signalling by Notch–Collagen V–CALCR retains muscle stem cells in their niche

Baghdadi, M. B., Castel, D., Machado, L., Fukada, S., Birk, D. E., Relaix, F., Tajbakhsh, S., & Mourikis, P. (2018) · Nature · doi:10.1038/s41586-018-0144-9 · Cited by 299 · see citing works

MicroRNA-146a directs the symmetric division of Snail-dominant colorectal cancer stem cells

Hwang, W., Jiang, J., Yang, S.-H., Huang, T. S., Lan, H., Teng, H., Yang, C.-Y., Tsai, Y., Lin, C.-H., Wang, H., et al. (2014) · Nature Cell Biology · doi:10.1038/ncb2910 · Cited by 303 · see citing works

Manifestations and mechanisms of stem cell aging

Liu, L. A., & Rando, T. A. (2011) · The Journal of Cell Biology · doi:10.1083/jcb.201010131 · Cited by 306 · see citing works

THE HUBBLE SPACE TELESCOPE WIDE FIELD CAMERA 3 EARLY RELEASE SCIENCE DATA: PANCHROMATIC FAINT OBJECT COUNTS FOR 0.2-2 μm WAVELENGTH

Windhorst, R. A., Cohen, S. H., Hathi, N. P., McCarthy, P. J., Ryan, R. E., Yan, H., Baldry, I. K., Driver, S. P., Frogel, J. A., Hill, D. T., et al. (2011) · The Astrophysical Journal Supplement Series · doi:10.1088/0067-0049/193/2/27 · Cited by 298 · see citing works

The genetics of vertebrate myogenesis

Bryson‐Richardson, R. J., & Currie, P. D. (2008) · Nature Reviews Genetics · doi:10.1038/nrg2369 · Cited by 285 · 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

Constitutive Notch Activation Upregulates Pax7 and Promotes the Self-Renewal of Skeletal Muscle Satellite Cells

Wen, Y., Bi, P., Liu, W., Asakura, A., Keller, C., & Kuang, S. (2012) · Molecular and Cellular Biology · doi:10.1128/mcb.06753-11 · Cited by 271 · see citing works

Coordination of Satellite Cell Activation and Self-Renewal by Par-Complex-Dependent Asymmetric Activation of p38α/β MAPK

Troy, A., Cadwallader, A. B., Fedorov, Y., Tyner, K., Tanaka, K. K., & Olwin, B. B. (2012) · Cell Stem Cell · doi:10.1016/j.stem.2012.05.025 · Cited by 268 · 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

Pregnancy and the risk of breast cancer

Britt, K. L., Ashworth, A., & Smalley, M. J. (2007) · Endocrine Related Cancer · doi:10.1677/erc-07-0137 · Cited by 397 · see citing works

Telomeres and telomerase in normal and cancer stem cells

Shay, J. W., & Wright, W. E. (2010) · FEBS Letters · doi:10.1016/j.febslet.2010.05.026 · Cited by 253 · see citing works

Syndecan-4-Expressing Muscle Progenitor Cells in the SP Engraft as Satellite Cells during Muscle Regeneration

Kelly, K. K., Hall, J. K., Troy, A. A., Cornelison, D., Majka, S. M., & Olwin, B. B. (2009) · Cell stem cell · doi:10.1016/j.stem.2009.01.016 · Cited by 249 · see citing works

Lipid modulation of skeletal muscle mass and function

Lipina, C., & Hundal, H. S. (2017) · Journal of Cachexia, Sarcopenia and Muscle · doi:10.1002/jcsm.12144 · Cited by 247 · see citing works

Heterochronic parabiosis for the study of the effects of aging on stem cells and their niches

Conboy, I. M., & Rando, T. A. (2012) · Cell Cycle · doi:10.4161/cc.20437 · Cited by 239 · 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

Ageing affects DNA methylation drift and transcriptional cell-to-cell variability in mouse muscle stem cells

Hernando-Herraez, I., Evano, B., Stubbs, T., Commere, P.-H., Jan Bonder, M., Clark, S., Andrews, S., Tajbakhsh, S., & Reik, W. (2019) · Nature Communications · doi:10.1038/s41467-019-12293-4 · Cited by 236 · see citing works

Autocrine and Paracrine Angiopoietin 1/Tie-2 Signaling Promotes Muscle Satellite Cell Self-Renewal

Abou-Khalil, R., Grand, F. L., Pallafacchina, G., Valable, S., Authier, F., Rudnicki, M. A., Gherardi, R. K., Germain, S., Chrétien, F. C., Sotiropoulos, A., et al. (2009) · Cell stem cell · doi:10.1016/j.stem.2009.06.001 · Cited by 236 · see citing works

Stem cell niches in mammals

Mitsiadis, T. A., Barrandon, O., Rochat, A., Barrandon, Y., & Bari, C. D. (2007) · Experimental Cell Research · doi:10.1016/j.yexcr.2007.07.027 · Cited by 227 · 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

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

Immortality of cell lines: challenges and advantages of establishment

Irfan Maqsood, M., Matin, M. M., Bahrami, A. R., & Ghasroldasht, M. M. (2013) · Cell Biology International · doi:10.1002/cbin.10137 · Cited by 217 · see citing works

Imaging stem-cell-driven regeneration in mammals

Schroeder, T. (2008) · Nature · doi:10.1038/nature07043 · Cited by 205 · see citing works

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 201 · see citing works

Lying low but ready for action: the quiescent muscle satellite cell

Montarras, D., L’honoré, A., & BUCKINGHAM, M. E. (2013) · FEBS Journal · doi:10.1111/febs.12372 · Cited by 199 · see citing works

Hypoxia promotes satellite cell self-renewal and enhances the efficiency of myoblast transplantation

Liu, W., Wen, Y., Bi, P., Lai, X., Liu, X., Liu, X., & Kuang, S. (2012) · Development · doi:10.1242/dev.079665 · Cited by 198 · see citing works

Organelle positioning and cell polarity

Bornens, M. (2008) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2524 · Cited by 191 · see citing works

Spindle orientation, asymmetric division and tumour suppression in Drosophila stem cells

González, C. (2007) · Nature Reviews Genetics · doi:10.1038/nrg2103 · Cited by 189 · see citing works

The multiple functions of Numb

Gulino, A., Marcotullio, L. D., & Screpanti, I. (2009) · Experimental Cell Research · doi:10.1016/j.yexcr.2009.11.017 · Cited by 192 · see citing works

Recent Progress on Tissue-Resident Adult Stem Cell Biology and Their Therapeutic Implications

Mimeault, M., & Batra, S. K. (2008) · Stem Cell Reviews and Reports · doi:10.1007/s12015-008-9008-2 · Cited by 190 · see citing works

Immortal Strands? Give Me a Break

Lansdorp, P. M. (2007) · Cell · doi:10.1016/j.cell.2007.06.017 · Cited by 188 · see citing works

The stem cells of small intestinal crypts: where are they?

Potten, C. S., Gândara, R., Mahida, Y., Loeffler, M., & Wright, N. A. (2009) · Cell Proliferation · doi:10.1111/j.1365-2184.2009.00642.x · Cited by 184 · see citing works

3D Timelapse Analysis of Muscle Satellite Cell Motility

Siegel, A. L., Atchison, K., Fisher, K. E., Davis, G. E., & Cornelison, D. (2009) · Stem Cells · doi:10.1002/stem.178 · Cited by 184 · see citing works

Tracking adult stem cells

Snippert, H. J. G., & Clevers, H. C. (2011) · EMBO Reports · doi:10.1038/embor.2010.216 · Cited by 180 · see citing works

Satellite Cells

Chang, N. C., & Rudnicki, M. A. (2014) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/b978-0-12-416022-4.00006-8 · Cited by 180 · see citing works

Attributes of adult stem cells

Alison, M., & Islam, S. (2008) · The Journal of Pathology · doi:10.1002/path.2498 · Cited by 172 · see citing works

Heterogeneity in the muscle satellite cell population

Biressi, S., & Rando, T. A. (2010) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2010.09.003 · Cited by 168 · see citing works

Tumor Dormancy and Cancer Stem Cells: Implications for the Biology and Treatment of Breast Cancer Metastasis

Allan, A. L., Vantyghem, S. A., Tuck, A. B., & Chambers, A. F. (2007) · Breast Disease · doi:10.3233/bd-2007-26108 · Cited by 168 · see citing works

Stretching the limits: from homeostasis to stem cell plasticity in wound healing and cancer

Ge, Y., & Fuchs, E. (2018) · Nature reviews genetics · doi:10.1038/nrg.2018.9 · Cited by 160 · see citing works

Bone marrow long label-retaining cells reside in the sinusoidal hypoxic niche

Kubota, Y., Takubo, K., & Suda, T. (2007) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2007.11.086 · Cited by 160 · see citing works

Melanoma Stem Cells: The Dark Seed of Melanoma

Zabierowski, S. E., & Herlyn, M. (2008) · Journal of Clinical Oncology · doi:10.1200/jco.2007.15.5465 · Cited by 157 · see citing works

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 · see citing works

Early forming label-retaining muscle stem cells require p27kip1 for maintenance of the primitive state

Chakkalakal, J. V., Christensen, J., Xiang, W., Tierney, M. T., Boscolo, F. S., Sacco, A., & Brack, A. S. (2014) · Development · doi:10.1242/dev.100842 · Cited by 148 · see citing works

NUMB-ing down cancer by more than just a NOTCH

Pece, S., Confalonieri, S., Romano, P. R., & Fiore, P. P. D. (2010) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2010.10.001 · Cited by 147 · see citing works

Asymmetric division of clonal muscle stem cells coordinates muscle regeneration in vivo

Gurevich, D., Nguyen, P. D., Siegel, A. L., Ehrlich, O., Sonntag, C., Phan, J. M. N., Berger, S., Ratnayake, D., Hersey, L., Berger, J., et al. (2016) · Science · doi:10.1126/science.aad9969 · Cited by 146 · see citing works

Skeletal muscle stem cell birth and properties

Sambasivan, R., & Tajbakhsh, S. (2007) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2007.09.013 · Cited by 143 · see citing works

Satellite Cells and Skeletal Muscle Regeneration

Dumont, N. A., Bentzinger, C. F., Sincennes, M., & Rudnicki, M. A. (2015) · Comprehensive physiology · doi:10.1002/j.2040-4603.2015.tb00646.x · Cited by 143 · see citing works

Defining the transcriptional signature of skeletal muscle stem cells1,2

Yablonka‐Reuveni, Z., Day, K. R., Vine, A. L., & Shefer, G. (2007) · Journal of Animal Science · doi:10.2527/jas.2007-0473 · Cited by 141 · 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

Skeletal muscle stem cells in comfort and stress

Evano, B., & Tajbakhsh, S. (2018) · npj Regenerative Medicine · doi:10.1038/s41536-018-0062-3 · Cited by 132 · see citing works

Mitochondria as a Potential Regulator of Myogenesis

Wagatsuma, A., & Sakuma, K. (2013) · The Scientific World JOURNAL · doi:10.1155/2013/593267 · Cited by 134 · 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

Control of the adaptive response of the heart to stress via the Notch1 receptor pathway

Croquelois, A., Domenighetti, A. A., Nemir, M., Lepore, M. G., Rosenblatt‐Velin, N., Radtke, F., & Pedrazzini, T. (2008) · The Journal of Experimental Medicine · doi:10.1084/jem.20081427 · Cited by 133 · see citing works

Metabolism and the Control of Cell Fate Decisions and Stem Cell Renewal

Ito, K., & Ito, K. (2016) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-111315-125134 · Cited by 137 · see citing works

Microenvironmental modulation of asymmetric cell division in human lung cancer cells

Pine, S. R., Ryan, B. M., Varticovski, L., Robles, A. I., & Harris, C. C. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0909390107 · Cited by 133 · 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

Notch-Induced miR-708 Antagonizes Satellite Cell Migration and Maintains Quiescence

Baghdadi, M. B., de Firmino, J. B., Soni, K., Evano, B., Girolamo, D. D., Mourikis, P., Castel, D., & Tajbakhsh, S. (2018) · Cell stem cell · doi:10.1016/j.stem.2018.09.017 · Cited by 132 · see citing works

Quantitative proliferation dynamics and random chromosome segregation of hair follicle stem cells

Waghmare, S. K., Bansal, R., Lee, J., Zhang, Y. V., McDermitt, D. J., & Tumbar, T. (2008) · The EMBO Journal · doi:10.1038/emboj.2008.72 · Cited by 130 · see citing works

Proteolytic Processing of Delta-like 1 by ADAM Proteases

Dyczynska, E., Sun, D., Yi, H., Sehara‐Fujisawa, A., Blobel, C., & Żółkiewska, A. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m605451200 · Cited by 129 · see citing works

Template DNA-Strand Co-Segregation and Asymmetric Cell Division in Skeletal Muscle Stem Cells

Shinin, V., Gayraud-Morel, B., & Tajbakhsh, S. (2008) · Methods in molecular biology · doi:10.1007/978-1-59745-060-7_19 · Cited by 43 · see citing works

Satellite cells shed light on asymmetrical DNA strand segregation

Skipper, M. (2006) · Nature Reviews Genetics · doi:10.1038/nrg1930

A Subpopulation of Adult Skeletal Muscle Stem Cells Retains All Template DNA Strands after Cell Division

Rocheteau, P., Gayraud-Morel, B., Siegl-Cachedenier, I., Blasco, M. A., & Tajbakhsh, S. (2012) · Cell · doi:10.1016/j.cell.2011.11.049 · Cited by 510 · see citing works

High incidence of non-random template strand segregation and asymmetric fate determination in dividing stem cells and their progeny. PLoS Biol

Conboy, M. J., Karasov, A. O., & R, T. A. (2007)

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