The DOI matches its Crossref record; 29 of the 29 references it cites were found in a registry or an index.
A single type of progenitor cell maintains normal epidermis
Open accessAbstract
According to the current model of adult epidermal homeostasis, skin tissue is maintained by two discrete populations of progenitor cells: self-renewing stem cells; and their progeny, known as transit amplifying cells, which differentiate after several rounds of cell division. By making use of inducible genetic labelling, we have tracked the fate of a representative sample of progenitor cells in mouse tail epidermis at single-cell resolution in vivo at time intervals up to one year. Here we show that clone-size distributions are consistent with a new model of homeostasis involving only one type of progenitor cell. These cells are found to undergo both symmetric and asymmetric division at rates that ensure epidermal homeostasis. The results raise important questions about the potential role of stem cells on tissue maintenance in vivo.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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?
In the citing paper
“adult epidermal homeostasis seems to rely solely on active stem cells34”
From Molecular regulation of stem cell quiescence (2013) · cites this paper as [34]
Citations
Cites
Cre reporter strains produced by targeted insertion of EYFP and ECFP into the ROSA26 locus
Srinivas, S., Watanabe, T., Lin, C.-S., William, C. M., Tanabe, Y., Jessell, T. M., & Costantini, F. (2001) · BMC Developmental Biology · doi:10.1186/1471-213x-1-4 · Cited by 3,121
Defining the Epithelial Stem Cell Niche in Skin
Tumbar, T., Guasch, G., Greco, V., Blanpain, C., Lowry, W. E., Rendl, M., & Fuchs, E. (2004) · Science · doi:10.1126/science.1092436 · Cited by 2,031
Ito, M., Liu, Y., Yang, Z., Nguyen, J., Liang, F., Morris, R. J., & Cotsarelis, G. (2005) · Nature Medicine · doi:10.1038/nm1328 · Cited by 1,317
Capturing and profiling adult hair follicle stem cells
Morris, R. J., Liu, Y., Marles, L., Yang, Z., Trempus, C., Li, S., Lin, J. S., Sawicki, J. A., & Cotsarelis, G. (2004) · Nature Biotechnology · doi:10.1038/nbt950 · Cited by 1,283
Asymmetric cell divisions promote stratification and differentiation of mammalian skin
Lechler, T., & Fuchs, E. (2005) · Nature · doi:10.1038/nature03922 · Cited by 998
Conboy, I. M., & Rando, T. A. (2002) · Developmental Cell · doi:10.1016/s1534-5807(02)00254-x · Cited by 905
Lajtha, L. G. (1979) · Differentiation · doi:10.1111/j.1432-0436.1979.tb01007.x · Cited by 562
Stem cells of the skin epithelium
Alonso, L. C., & Fuchs, E. V. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1734203100 · Cited by 531
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
Temple, S., & RAFF, M. C. (1986) · Cell · doi:10.1016/0092-8674(86)90843-3 · Cited by 455
Flagged first, then by citations
Cited by
Sorted by citations
Items 101–200 of 847
Snippert, H. J. G., & Clevers, H. C. (2011) · EMBO Reports · doi:10.1038/embor.2010.216 · Cited by 184
de Navascués, J., Perdigoto, C. N., Bian, Y., Schneider, M., Bardin, A. J., Martínez-Arias, A., & Simons, B. D. (2012) · The EMBO Journal · doi:10.1038/emboj.2012.106 · Cited by 185
Self-citationDiscrete limbal epithelial stem cell populations mediate corneal homeostasis and wound healing
Altshuler, A., Amitai-Lange, A., Tarazi, N., Dey, S., Strinkovsky, L., Hadad-Porat, S., Bhattacharya, S., Nasser, W., Imeri, J., Ben-David, G., et al. (2021) · Cell stem cell · doi:10.1016/j.stem.2021.04.003 · Cited by 181
Human skin stem cells and the ageing process
Zouboulis, C. C., Adjaye, J., Akamatsu, H., Moe-Behrens, G., & Niemann, C. (2008) · Experimental Gerontology · doi:10.1016/j.exger.2008.09.001 · Cited by 176
Defining Adult Stem Cell Function at Its Simplest: The Ability to Replace Lost Cells through Mitosis
Post, Y., & Clevers, H. C. (2019) · Cell stem cell · doi:10.1016/j.stem.2019.07.002 · Cited by 181
Demehri, S., Liu, Z., Lee, J., Lin, M., Crosby, S. D., Roberts, C. J., Grigsby, P. W., Miner, J. H., Farr, A. G., & Kopan, R. (2008) · PLoS Biology · doi:10.1371/journal.pbio.0060123 · Cited by 174
Jensen, U. B., Yan, X., Triel, C., Woo, S., Christensen, R., & Owens, D. M. (2008) · Journal of Cell Science · doi:10.1242/jcs.025502 · Cited by 180
Attributes of adult stem cells
Alison, M., & Islam, S. (2008) · The Journal of Pathology · doi:10.1002/path.2498 · Cited by 182
Finding One's Niche in the Skin
Fuchs, E. V. (2009) · Cell stem cell · doi:10.1016/j.stem.2009.05.001 · Cited by 171
Stem Cell Heterogeneity and Plasticity in Epithelia
Donati, G., & Watt, F. M. (2015) · Cell stem cell · doi:10.1016/j.stem.2015.04.014 · Cited by 175
Somatic stem cell heterogeneity: diversity in the blood, skin and intestinal stem cell compartments
Goodell, M. A., Nguyen, H., & Shroyer, N. F. (2015) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3980 · Cited by 182
Sic Transit Gloria: Farewell to the Epidermal Transit Amplifying Cell?
Jones, P. H., Simons, B. D., & Watt, F. M. (2007) · Cell stem cell · doi:10.1016/j.stem.2007.09.014 · Cited by 172
Self-citationWNT-SHH Antagonism Specifies and Expands Stem Cells prior to Niche Formation
Ouspenskaia, T., Matos, I., Mertz, A. F., Fiore, V. F., & Fuchs, E. V. (2016) · Cell · doi:10.1016/j.cell.2015.11.058 · Cited by 169
Normal stem cells and cancer stem cells: similar and different
Shackleton, M. J. (2010) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2010.04.002 · Cited by 168
Gomes, F. L. A. F., Zhang, G., Carbonell, F., Correa, J. A., Harris, W. A., Simons, B. D., & Cayouette, M. (2010) · Development · doi:10.1242/dev.059683 · Cited by 170
Self-citationAlcolea, M. P., Greulich, P., Wabik, A., Frede, J., Simons, B. D., & Jones, P. H. (2014) · Nature Cell Biology · doi:10.1038/ncb2963 · Cited by 164
Self-citationRai, T. S., Cole, J. J., Nelson, D. M., Dikovskaya, D., Faller, W. J., Vizioli, M. G., Hewitt, R. N., Anannya, O., McBryan, T., Manoharan, I., et al. (2014) · Genes & Development · doi:10.1101/gad.247528.114 · Cited by 162
Quantitative lineage tracing strategies to resolve multipotency in tissue-specific stem cellsPreprint
Wuidart, A., Ousset, M., Rulands, S., Simons, B. D., Keymeulen, A. V., & Blanpain, C. (2016) · Genes & Development · doi:10.1101/gad.280057.116 · Cited by 173
Self-citationStem cell dynamics in the hair follicle niche
Rompolas, P., & Greco, V. (2013) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2013.12.005 · Cited by 167
Spatial competition shapes the dynamic mutational landscape of normal esophageal epithelium
Colom, B., Alcolea, M. P., Piedrafita, G., Hall, M., Wabik, A., Dentro, S. C., Fowler, J. C., Herms, A., King, C., Ong, S. H., et al. (2020) · Nature Genetics · doi:10.1038/s41588-020-0624-3 · Cited by 161
Self-citationSox9 Controls Self-Renewal of Oncogene Targeted Cells and Links Tumor Initiation and Invasion
Larsimont, J., Youssef, K. K., Sánchez‐Danés, A., Sukumaran, V., Defrance, M., Delatte, B., Liagre, M., Baatsen, P., Marine, J., Lippens, S., et al. (2015) · Cell stem cell · doi:10.1016/j.stem.2015.05.008 · Cited by 155
Cell competition in development, homeostasis and cancer
van Neerven, S. M., & Vermeulen, L. (2022) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-022-00538-y · Cited by 163
Fuchs (2016) · doi:10.1016/bs.ctdb.2015.11.033 · Cited by 152
Regenerating the skin: a task for the heterogeneous stem cell pool and surrounding niche
Solanas, G., & Benitah, S. A. (2013) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3675 · Cited by 152
Concise Review: Wnt Signaling Pathways in Skin Development and Epidermal Stem Cells
Veltri, A., Lang, C. M. R., & Lien, W. (2017) · Stem Cells · doi:10.1002/stem.2723 · Cited by 152
Optimality in the Development of Intestinal Crypts
Itzkovitz, S., Blat, I. C., Jacks, T., Clevers, H. C., & van Oudenaarden, A. (2012) · Cell · doi:10.1016/j.cell.2011.12.025 · Cited by 151
Clevers, H. C. (2015) · Science · doi:10.1126/science.aad7016 · Cited by 152
Transforming Growth Factor-? and Endoglin Signaling Orchestrate Wound Healing
Valluru, M. K., Staton, C. A., Reed, M., & Brown, N. J. (2011) · Frontiers in Physiology · doi:10.3389/fphys.2011.00089 · Cited by 148
Stem cell self-renewal in intestinal crypt
Simons, B. D., & Clevers, H. C. (2011) · Experimental Cell Research · doi:10.1016/j.yexcr.2011.07.010 · Cited by 154
Self-citationLuis, N. M., Morey, L., Mejetta, S., Pascual, G., Janich, P., Kuebler, B., Roma, G., Nascimento, E., Frye, M., Di Croce, L., et al. (2011) · Cell stem cell · doi:10.1016/j.stem.2011.07.013 · Cited by 142
Acquisition of epithelial plasticity in human chronic liver disease
Gribben, C., Galanakis, V., Calderwood, A., Williams, E. C., Chazarra-Gil, R., Larraz, M., Frau, C., Puengel, T., Guillot, A., Rouhani, F. J., et al. (2024) · Nature · doi:10.1038/s41586-024-07465-2 · Cited by 142
Symmetric vs. Asymmetric Stem Cell Divisions: An Adaptation against Cancer?
Shahriyari, L., & Komarova, N. L. (2013) · PLoS ONE · doi:10.1371/journal.pone.0076195 · Cited by 149
Par3–mInsc and Gαi3 cooperate to promote oriented epidermal cell divisions through LGN
Williams, S. E., Ratliff, L. A., Postiglione, M. P., Knoblich, J. A., & Fuchs, E. V. (2014) · Nature Cell Biology · doi:10.1038/ncb3001 · Cited by 135
Kalabis, J., Oyama, K., Okawa, T., Nakagawa, H., Michaylira, C. Z., Stairs, D. B., de Figueiredo, J. L., Mahmood, U., Diehl, J. A., Herlyn, M., et al. (2008) · Journal of Clinical Investigation · doi:10.1172/jci35012 · Cited by 137
Next generation organoids for biomedical research and applications
Lou, Y., & Leung, A. W. (2017) · Biotechnology Advances · doi:10.1016/j.biotechadv.2017.10.005 · Cited by 138
In Vivo Single-Cell Detection of Metabolic Oscillations in Stem Cells
Stringari, C., Wang, H., Geyfman, M., Crosignani, V., Kumar, V., Takahashi, J. S., D, B. A. M., & Gratton, E. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.12.007 · Cited by 131
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 134
Defining the clonal dynamics leading to mouse skin tumour initiation
Sánchez‐Danés, A., Hannezo, É., Larsimont, J., Liagre, M., Youssef, K. K., Simons, B. D., & Blanpain, C. (2016) · Nature · doi:10.1038/nature19069 · Cited by 131
Self-citationKroeze, K. L., Boink, M. A., Sampat-Sardjoepersad, S. C., Waaijman, T., Scheper, R. J., & Gibbs, S. (2011) · Journal of Investigative Dermatology · doi:10.1038/jid.2011.245 · Cited by 130
TEIXEIRA, V. H., Nadarajan, P., Graham, T. A., Pipinikas, C., Brown, J., Falzon, M., Nye, E. L., Poulsom, R., Lawrence, D. R., Wright, N. A., et al. (2013) · eLife · doi:10.7554/elife.00966 · Cited by 126
Self-citationKeratin K15 as a Biomarker of Epidermal Stem Cells
Bose, A., Teh, M., Mackenzie, I. C., & Waseem, A. (2013) · International Journal of Molecular Sciences · doi:10.3390/ijms141019385 · Cited by 124
Oral epithelial stem cells in tissue maintenance and disease: the first steps in a long journey
Jones, K. B., & Klein, O. D. (2013) · International Journal of Oral Science · doi:10.1038/ijos.2013.46 · Cited by 124
Barker, N., van Es, J. H., Jaks, V., Kasper, M., Snippert, H. J. G., Toftgård, R., & Clevers, H. C. (2008) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2008.72.003 · Cited by 128
Notch1 mutations drive clonal expansion in normal esophageal epithelium but impair tumor growth
Abby, E., Dentro, S. C., Hall, M. W. J., Fowler, J. C., Ong, S. H., Sood, R., Herms, A., Piedrafita, G., Abnizova, I., Siebel, C. W., et al. (2023) · Nature Genetics · doi:10.1038/s41588-022-01280-z · Cited by 121
Self-citationHeterogeneity and plasticity of epidermal stem cells
Schepeler, T., Page, M. E., & Jensen, K. B. (2014) · Development · doi:10.1242/dev.104588 · Cited by 125
Dynamic stem cell heterogeneity
Krieger, T. G., & Simons, B. D. (2015) · Development · doi:10.1242/dev.101063 · Cited by 125
Self-citationIntestinal Stem Cells and Their Defining Niche
Tan, D. W., & Barker, N. (2014) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/b978-0-12-416022-4.00003-2 · Cited by 119
Li, L., Newton, P. T., Bouderlique, T., Šejnohová, M., Zikmund, T., Kozhemyakina, E. A., Xie, M., Křivánek, J., Kaiser, J., Qian, H., et al. (2016) · The FASEB Journal · doi:10.1096/fj.201600918r · Cited by 116
A self-organization framework for symmetry breaking in the mammalian embryo
Wennekamp, S., Mesecke, S., Nédélec, F., & Hiiragi, T. (2013) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3602 · Cited by 122
Markers of Epidermal Stem Cell Subpopulations in Adult Mammalian SkinPreprint
Kretzschmar, K., & Watt, F. M. (2014) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a013631 · Cited by 118
Epithelial stem cells in corneal regeneration and epidermal gene therapy
Pellegrini, G., Rama, P., Mavilio, F., & Luca, M. D. (2008) · The Journal of Pathology · doi:10.1002/path.2441 · Cited by 116
Single-Cell Analysis Uncovers Clonal Acinar Cell Heterogeneity in the Adult Pancreas
Wollny, D., Zhao, S., Everlien, I., Lun, X., Brunken, J., Brüne, D., Ziebell, F., Tabansky, I., Weichert, W., Marciniak-Czochra, A. K., et al. (2016) · Developmental Cell · doi:10.1016/j.devcel.2016.10.002 · Cited by 116
The emergence of the stem cell niche
Hicks, M. R., & Pyle, A. D. (2022) · Trends in Cell Biology · doi:10.1016/j.tcb.2022.07.003 · Cited by 114
Epidermal Development in Mammals: Key Regulators, Signals from Beneath, and Stem Cells
Liu, S., Zhang, H., & Duan, E. (2013) · International Journal of Molecular Sciences · doi:10.3390/ijms140610869 · Cited by 110
Master equations and the theory of stochastic path integrals
Weber, M. F., & Frey, E. (2017) · Reports on Progress in Physics · doi:10.1088/1361-6633/aa5ae2 · Cited by 123
Mitotic spindle (DIS)orientation and DISease: Cause or consequence?
Noatynska, A., Gotta, M., & Meraldi, P. (2012) · The Journal of Cell Biology · doi:10.1083/jcb.201209015 · Cited by 108
Outcompeting p53-Mutant Cells in the Normal Esophagus by Redox Manipulation
Fernández‐Antorán, D., Piedrafita, G., Murai, K., Ong, S. H., Herms, A., Frezza, C., & Jones, P. H. (2019) · Cell stem cell · doi:10.1016/j.stem.2019.06.011 · Cited by 111
Self-citationGenetics of Gonadal Stem Cell Renewal
Greenspan, L. J., de Cuevas, M., & Matunis, E. L. (2015) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-100913-013344 · Cited by 107
Gomez, C., Chua, W., Miremadi, A., Quist, S., Headon, D. J., & Watt, F. M. (2013) · Stem Cell Reports · doi:10.1016/j.stemcr.2013.04.001 · Cited by 107
Klein, A. M., Brash, D. E., Jones, P. H., & Simons, B. D. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0909738107 · Cited by 109
Self-citationReactive oxygen species produced by altered tumor metabolism impacts cancer stem cell maintenance
Tuy, K., Rickenbacker, L., & Hjelmeland, A. B. (2021) · Redox Biology · doi:10.1016/j.redox.2021.101953 · Cited by 107
Blanpain, C. (2010) · Nature · doi:10.1038/464686a · Cited by 105
Endogenous lung stem cells and contribution to disease
Snyder, J. C., Teisanu, R., & Stripp, B. R. (2008) · The Journal of Pathology · doi:10.1002/path.2473 · Cited by 108
Gokoffski, K. K., Wu, H., Beites, C. L., Kim, J., Kim, E. J., Matzuk, M. M., Johnson, J. E. B., Lander, A. D., & Calof, A. L. (2011) · Development · doi:10.1242/dev.065870 · Cited by 104
BMP-driven NRF2 activation in esophageal basal cell differentiation and eosinophilic esophagitis
Jiang, M. Z., Ku, W.-Y., Zhou, Z., Dellon, E. S., Falk, G. W., Nakagawa, H., Wang, M., Liu, K., Wang, J., Katzka, D. A., et al. (2015) · Journal of Clinical Investigation · doi:10.1172/jci78850 · Cited by 108
Dynamic regulation of tissue fluidity controls skin repair during wound healing
Sarate, R. M., Hochstetter, J., Valet, M., Hallou, A., Song, Y., Bansaccal, N., Ligare, M., Aragona, M., Engelman, D., Bauduin, A., et al. (2024) · Cell · doi:10.1016/j.cell.2024.07.031 · Cited by 104
Self-citationDevelopment and Homeostasis of the Skin EpidermisPreprint
Sotiropoulou, P., & Blanpain, C. (2012) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a008383 · Cited by 112
Stem cells and origins of cancer in the upper gastrointestinal tract
Hayakawa, Y., Nakagawa, H., Rustgi, A. K., Que, J., & Wang, T. C. (2021) · Cell stem cell · doi:10.1016/j.stem.2021.05.012 · Cited by 103
Lgr6 marks epidermal stem cells with a nerve-dependent role in wound re-epithelialization
Huang, S., Kuri, P., Aubert, Y., Brewster, M., Li, N., Farrelly, O. M., Rice, G., Bae, H., Prouty, S. M., Dentchev, T., et al. (2021) · Cell stem cell · doi:10.1016/j.stem.2021.05.007 · Cited by 102
Cell dynamics and gene expression control in tissue homeostasis and development
Rué, P., & Arias, A. M. (2015) · Molecular Systems Biology · doi:10.15252/msb.20145549 · Cited by 99
MicroRNA-203 functions as a tumor suppressor in basal cell carcinoma
Sonkoly, E., Lovén, J., Xu, N., Meisgen, F., Wei, T., Brodin, P., Jaks, V., Kasper, M., Shimokawa, T., Harada, M., et al. (2012) · Oncogenesis · doi:10.1038/oncsis.2012.3 · Cited by 99
Oriented divisions, fate decisions
Williams, S. E., & Fuchs, E. V. (2013) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2013.08.003 · Cited by 102
EMILIN1–α4/α9 integrin interaction inhibits dermal fibroblast and keratinocyte proliferation
Danussi, C., Petrucco, A., Wassermann, B., Pivetta, E., Modica, T. M. E., Belluz, L. D. B., Colombatti, A., & Spessotto, P. (2011) · The Journal of Cell Biology · doi:10.1083/jcb.201008013 · Cited by 100
Palmitoylation Regulates Epidermal Homeostasis and Hair Follicle Differentiation
Mill, P., Lee, A., Fukata, Y., Tsutsumi, R., Fukata, M., Keighren, M., Porter, R. M., McKie, L., Smyth, I., & Jackson, I. J. (2009) · PLoS Genetics · doi:10.1371/journal.pgen.1000748 · Cited by 99
Füllgrabe, A., Joost, S., Are, A., Jacob, T., Sivan, U., Haegebarth, A., Linnarsson, S., Simons, B. D., Clevers, H. C., Toftgård, R., et al. (2015) · Stem Cell Reports · doi:10.1016/j.stemcr.2015.09.013 · Cited by 98
Self-citationThe RNA-binding protein YBX1 regulates epidermal progenitors at a posttranscriptional level
Kwon, E., Todorova, K. A., Wang, J., Horos, R., Lee, K. K., Neel, V., Negri, G. L., Sorensen, P. H. B., Lee, S. W., Hentze, M. W., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-04092-0 · Cited by 98
Extracellular Matrix as a Regulator of Epidermal Stem Cell Fate
Chermnykh, E., Kalabusheva, E., & Vorotelyak, E. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19041003 · Cited by 95
Defining stem cell types: understanding the therapeutic potential of ESCs, ASCs, and iPS cells
Álvarez, C. V., García-Lavandeira, M., Garcia-Rendueles, M. E. R., Díaz‐Rodriguez, E., Garcia-Rendueles, Á. R., Pérez-Romero, S., Vila, T. V., Rodrigues, J. S., Lear, P., & Bravo, S. B. (2012) · Journal of Molecular Endocrinology · doi:10.1530/jme-12-0072 · Cited by 97
Coupling organelle inheritance with mitosis to balance growth and differentiation
Asare, A., Levorse, J. M., & Fuchs, E. V. (2017) · Science · doi:10.1126/science.aah4701 · Cited by 94
Petersson, M., Brylka, H., Kraus, A., John, S., Rappl, G., Schettina, P., & Niemann, C. (2011) · The EMBO Journal · doi:10.1038/emboj.2011.199 · Cited by 93
The extracellular matrix dictates regional competence for tumour initiation
Bansaccal, N., Vieugué, P., Sarate, R. M., Song, Y., Minguijón, E., Miroshnikova, Y. A., Zeuschner, D., Collin, A. M., Allard, J., Engelman, D., et al. (2023) · Nature · doi:10.1038/s41586-023-06740-y · Cited by 96
Stem cell competition: finding balance in the niche
Stine, R. R., & Matunis, E. L. (2013) · Trends in Cell Biology · doi:10.1016/j.tcb.2013.03.001 · Cited by 96
Neutral competition of stem cells is skewed by proliferative changes downstream of Hh and Hpo
Amoyel, M., Simons, B. D., & Bach, E. A. (2014) · The EMBO Journal · doi:10.15252/embj.201387500 · Cited by 93
Self-citationA Beginner’s Introduction to Skin Stem Cells and Wound Healing
Garcia, D. D., Filipová, A., Veloz, I. G., & Martínez‐Fierro, M. L. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222011030 · Cited by 96
Inferring Cell-State Transition Dynamics from Lineage Trees and Endpoint Single-Cell Measurements
Hormoz, S., Singer, Z. S., Linton, J. M., Antebi, Y. E., Shraiman, B. I., & Elowitz, M. B. (2016) · Cell Systems · doi:10.1016/j.cels.2016.10.015 · Cited by 94
Hallmarks of stemness in mammalian tissues
Beumer, J., & Clevers, H. C. (2024) · Cell stem cell · doi:10.1016/j.stem.2023.12.006 · Cited by 92
Elucidating the identity and behavior of spermatogenic stem cells in the mouse testis
Yoshida, S. (2012) · Reproduction · doi:10.1530/rep-11-0320 · Cited by 90
Human keratinocytes have two interconvertible modes of proliferation
Roshan, A., Murai, K., Fowler, J. C., Simons, B. D., Nikolaidou-Neokosmidou, V., & Jones, P. H. (2015) · Nature Cell Biology · doi:10.1038/ncb3282 · Cited by 95
Self-citationQuiescence Entry, Maintenance, and Exit in Adult Stem Cells
Mohammad, K., Dakik, P., Medkour, Y., Mitrofanova, D., & Titorenko, V. I. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20092158 · Cited by 94
Niwa, O., Barcellos‐Hoff, M. H., Globus, R. K., Harrison, J. D., Hendry, J. H., Jacob, P., Martin, M. T., Seed, T. M., Shay, J. W., Story, M. D., et al. (2015) · Annals of the ICRP · doi:10.1177/0146645315595585 · Cited by 91
Keratinocyte stem cells: Friends and foes
Pincelli, C., & Marconi, A. (2010) · Journal of Cellular Physiology · doi:10.1002/jcp.22275 · Cited by 89
Epidermal Tissue Adapts to Restrain Progenitors Carrying Clonal p53 Mutations
Murai, K., Skrupskelyte, G., Piedrafita, G., Hall, M., Kostiou, V., Ong, S. H., Nagy, T., Cagan, A., Goulding, D., Klein, A. M., et al. (2018) · Cell stem cell · doi:10.1016/j.stem.2018.08.017 · Cited by 89
Self-citationA comparison of epithelial-to-mesenchymal transition and re-epithelialization
Leopold, P. L., Vincent, J., & Wang, H. (2012) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2012.07.003 · Cited by 93
Ovary and fimbrial stem cells: biology, niche and cancer origins
Ng, A., & Barker, N. (2015) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm4056 · Cited by 94
Moving epithelia: Tracking the fate of mammalian limbal epithelial stem cells
Girolamo, N. D. (2015) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2015.04.002 · Cited by 87
Piedrafita, G., Kostiou, V., Wabik, A., Colom, B., Fernández‐Antorán, D., Herms, A., Murai, K., Hall, B. A., & Jones, P. H. (2020) · Nature Communications · doi:10.1038/s41467-020-15258-0 · Cited by 89
Self-citationDefining the Design Principles of Skin Epidermis Postnatal Growth
Dekoninck, S., Hannezo, É., Sifrim, A., Miroshnikova, Y. A., Aragona, M., Malfait, M., Gargouri, S., de Neunheuser, C., Dubois, C., Voet, T., et al. (2020) · Cell · doi:10.1016/j.cell.2020.03.015 · Cited by 85
Self-citationKent, D. G., Li, J., Tanna, H., Fink, J., Kirschner, K., Pask, D. C., Silber, Y., Hamilton, T. L., Sneade, R., Simons, B. D., et al. (2013) · PLoS Biology · doi:10.1371/journal.pbio.1001576 · Cited by 87
Self-citationLearning from regeneration research organisms: The circuitous road to scar free wound healing
Erickson, J. R., & Echeverri, K. (2017) · Developmental Biology · doi:10.1016/j.ydbio.2017.09.025 · Cited by 92
Cockburn, K., Annusver, K., Gonzalez, D. G., Ganesan, S., May, D. P., Mesa, K. R., Kawaguchi, K., Kasper, M., & Greco, V. (2022) · Nature Cell Biology · doi:10.1038/s41556-022-01021-8 · Cited by 84
Metadata
- Authors
- Clayton, E., Doupé, D. P., Klein, A. M., Winton, D. J., Simons, B. D., & Jones, P. H.
- Affiliations
- MRC Cancer Unit (GB)
- University of Cambridge (GB)
- Cancer Research UK (GB)
- Corresponding author
- Jones, Philip H.
- Venue
- Nature
- Published
- 2007-02-28
- Volume
- 446
- Issue
- 7132
- Pages
- 185-189
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W1979812265
- Cited by
- 853
- References
- 29
- Citations by year
- 2026: 22 · 2025: 22 · 2024: 38 · 2023: 22 · 2022: 32 · 2021: 36 · 2020: 41 · 2019: 44 · 2018: 47 · 2017: 51 · 2016: 49 · 2015: 46 · 2014: 59 · 2013: 61 · 2012: 79
- FWCI
- 61.13
- Type
- journal article
- Language
- en
- Open access
- Licence
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Durham Research Online (Durham University) (submittedVersion, cc-by)
- Topics
- Health Sciences › Medicine › Dermatology › Hair Growth and Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Skin and Cellular Biology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Keywords
- epidermal homeostasis, skin stem cells, progenitor cells, asymmetric cell division, symmetric cell division, transit amplifying cells, clone size distribution, tissue maintenance
- MeSH terms
- Epidermal Cells, Animals, Cell Differentiation, Cell Division, Clone Cells, Homeostasis, Models, Biological, Stem Cells, Cell Lineage, Mice
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