Tissue Stem Cells: New Tools and Functional Diversity

Induction of Pluripotent Stem Cells from Adult Human Fibroblasts by Defined Factors

Takahashi, K., Tanabe, K., Ohnuki, M., Narita, M., Ichisaka, T., Tomoda, K., & Yamanaka, S. (2007) · Cell · doi:10.1016/j.cell.2007.11.019 · Cited by 20,221 · see citing works

Single Lgr5 stem cells build crypt-villus structures in vitro without a mesenchymal niche

Sato, T., Vries, R. G., Snippert, H. J., van de Wetering, M., Barker, N., Stange, D. E., van Es, J. H., Abo, A., Kujala, P., Peters, P. J., et al. (2009) · Nature · doi:10.1038/nature07935 · Cited by 7,204 · see citing works

Identification of stem cells in small intestine and colon by marker gene Lgr5

Barker, N., van Es, J. H., Kuipers, J., Kujala, P., van den Born, M., Cozijnsen, M., Haegebarth, A., Korving, J., Begthel, H., Peters, P. J., et al. (2007) · Nature · doi:10.1038/nature06196 · Cited by 5,687 · see citing works

Label-retaining cells reside in the bulge area of pilosebaceous unit: Implications for follicular stem cells, hair cycle, and skin carcinogenesis

Cotsarelis, G., Sun, T.-T., & Lavker, R. M. (1990) · Cell · doi:10.1016/0092-8674(90)90696-c · Cited by 2,276 · see citing works

Adult pancreatic β-cells are formed by self-duplication rather than stem-cell differentiation

Dor, Y., Brown, J., Martinez, O. I., & Melton, D. A. (2004) · Nature · doi:10.1038/nature02520 · Cited by 2,219 · see citing works

Crypt stem cells as the cells-of-origin of intestinal cancer

Barker, N., Ridgway, R. A., van Es, J. H., van de Wetering, M., Begthel, H., van den Born, M., Danenberg, E., Clarke, A. R., Sansom, O. J., & Clevers, H. C. (2008) · Nature · doi:10.1038/nature07602 · Cited by 2,159 · see citing works

Generation of a functional mammary gland from a single stem cell

Shackleton, M., Vaillant, F., Simpson, K. J., Stingl, J., Smyth, G. K., Asselin-Labat, M.-L., Wu, L., Lindeman, G. J., & Visvader, J. E. (2006) · Nature · doi:10.1038/nature04372 · Cited by 2,005 · see citing works

Intestinal crypt homeostasis results from neutral competition between symmetrically dividing Lgr5 stem cells

Snippert, H. J., van der Flier, L. G., Sato, T., van Es, J. H., van den Born, M., Kroon-Veenboer, C., Barker, N., Klein, A. M., van Rheenen, J., Simons, B. D., et al. (2010) · Cell · doi:10.1016/j.cell.2010.09.016 · Cited by 1,951 · see citing works

Purification and unique properties of mammary epithelial stem cells

Stingl, J., Eirew, P. D., Ricketson, I., Shackleton, M. J., Vaillant, F., Choi, D., Li, H. I., & Eaves, C. J. (2006) · Nature · doi:10.1038/nature04496 · Cited by 1,562 · see citing works

Lgr5+ve Stem Cells Drive Self-Renewal in the Stomach and Build Long-Lived Gastric Units In Vitro

Barker, N., Huch, M., Kujala, P., van de Wetering, M., Snippert, H. J., van Es, J. H., Sato, T., Stange, D. E., Begthel, H., van den Born, M., et al. (2010) · Cell Stem Cell · doi:10.1016/j.stem.2009.11.013 · Cited by 1,547 · see citing works

Coexistence of Quiescent and Active Adult Stem Cells in Mammals

Li, L., & Clevers, H. (2010) · Science · doi:10.1126/science.1180794 · Cited by 1,247 · see citing works

A reserve stem cell population in small intestine renders Lgr5-positive cells dispensable

Tian, H., Biehs, B., Warming, S., Leong, K. G., Rangell, L. K., Klein, O. D., & de Sauvage, F. J. (2011) · Nature · doi:10.1038/nature10408 · Cited by 1,194 · see citing works

β Cells Can Be Generated from Endogenous Progenitors in Injured Adult Mouse Pancreas

Xu, X., D’Hoker, J., Stangé, G. M., Bonné, S., Leu, N. D., Xiao, X., de Casteele, M. V., Mellitzer, G., Ling, Z., Pipeleers, D., et al. (2008) · Cell · doi:10.1016/j.cell.2007.12.015 · Cited by 989 · see citing works

Stem and progenitor cells: origins, phenotypes, lineage commitments, and transdifferentiations

Weissman, I. L., Anderson, D. J., & Gage, F. (2001) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.17.1.387 · Cited by 948 · see citing works

Continuous cell supply from a Sox9-expressing progenitor zone in adult liver, exocrine pancreas and intestine

Furuyama, K., Kawaguchi, Y., Akiyama, H., Horiguchi, M., Kodama, S., Kuhara, T., Hosokawa, S., Elbahrawy, A., Soeda, T., Koizumi, M., et al. (2011) · Nature Genetics · doi:10.1038/ng.722 · Cited by 830 · see citing works

The intestinal stem cell markers Bmi1 and Lgr5 identify two functionally distinct populations

Yan, K. S., Chia, L. A., Li, X., Ootani, A., Su, J., Lee, J. Y., Su, N. Y., Luo, Y., Heilshorn, S. C., Amieva, M. R., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1118857109 · Cited by 817 · see citing works

<i>Lgr6</i> Marks Stem Cells in the Hair Follicle That Generate All Cell Lineages of the Skin

Snippert, H. J., Haegebarth, A., Kasper, M., Jaks, V., van Es, J. H., Barker, N., van de Wetering, M., van den Born, M., Begthel, H., Vries, R. G., et al. (2010) · Science · doi:10.1126/science.1184733 · Cited by 751 · see citing works

Interconversion Between Intestinal Stem Cell Populations in Distinct Niches

Takeda, N., Jain, R., LeBoeuf, M. R., Wang, Q., Lu, M. M., & Epstein, J. A. (2011) · Science · doi:10.1126/science.1213214 · Cited by 742 · see citing works

A luminal epithelial stem cell that is a cell of origin for prostate cancer

Wang, X., Julio, M. K., Economides, K. D., Walker, D., Yu, H., Halili, M. V., Hu, Y.-P., Price, S. M., Abate-Shen, C. T., & Shen, M. M. (2009) · Nature · doi:10.1038/nature08361 · Cited by 734 · see citing works

Lineage Tracing

Kretzschmar, K., & Watt, F. M. (2012) · Cell · doi:10.1016/j.cell.2012.01.002 · Cited by 719 · see citing works

Liver Regeneration after Partial Hepatectomy

Michalopoulos, G. K. (2010) · The American Journal of Pathology · doi:10.2353/ajpath.2010.090675 · Cited by 713 · 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

Stem Cells and Liver Regeneration

Duncan, A. W., Dorrell, C., & Grompe, M. (2009) · Gastroenterology · doi:10.1053/j.gastro.2009.05.044 · Cited by 547 · see citing works

Sox9+ ductal cells are multipotent progenitors throughout development but do not produce new endocrine cells in the normal or injured adult pancreas

Kopp, J. L., Dubois, C. L., Schaffer, A., Hao, E., Shih, H., Seymour, P. A., Ma, J., & Sander, M. (2011) · Development · doi:10.1242/dev.056499 · Cited by 472 · 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

Fate tracing of mature hepatocytes in mouse liver homeostasis and regeneration

Malato, Y., Naqvi, S., Schürmann, N., Ng, R., Wang, B., Zape, J., Kay, M. A., Grimm, D., & Willenbring, H. (2011) · Journal of Clinical Investigation · doi:10.1172/jci59261 · Cited by 434 · see citing works

Isolation and functional characterization of murine prostate stem cells

Lawson, D. A., Xin, L., Lukacs, R. U., Cheng, D., & Witte, O. N. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0609684104 · Cited by 399 · see citing works

Wnt Signaling, Lgr5, and Stem Cells in the Intestine and Skin

Haegebarth, A., & Clevers, H. C. (2009) · American Journal Of Pathology · doi:10.2353/ajpath.2009.080758 · Cited by 360 · see citing works

Long-term renewal of hair follicles from clonogenic multipotent stem cells

Claudinot, S., Nicolas, M., Oshima, H., Rochat, A., & Barrandon, Y. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0507250102 · Cited by 308 · see citing works

Why Stem Cells?

van der Kooy, D., & Weiss, S. (2000) · Science · doi:10.1126/science.287.5457.1439 · Cited by 275 · see citing works

The cancer stem cell niche—there goes the neighborhood?

Cabarcas‐Petroski, S., Mathews, L., & Farrar, W. L. (2011) · International Journal of Cancer · doi:10.1002/ijc.26312 · Cited by 264 · see citing works

Prospective isolation of a bipotential clonogenic liver progenitor cell in adult micePreprint

Dorrell, C., Erker, L. R., Schug, J., Kopp, J. L., Canaday, P. S., Fox, A. J., Smirnova, O., Duncan, A. W., Finegold, M. J., Sander, M., et al. (2011) · Genes & Development · doi:10.1101/gad.2029411 · Cited by 236 · see citing works

A role for microRNAs in maintenance of mouse mammary epithelial progenitor cellsPreprint

Ibarra, I., Erlich, Y., Muthuswamy, S. K., Sachidanandam, R., & Hannon, G. J. (2007) · Genes & Development · doi:10.1101/gad.1616307 · Cited by 218 · see citing works

Slowly cycling (label‐retaining) epidermal cells behave like clonogenic stem cells <i>in vitro</i>

Morris, R. J., & Potten, C. S. (1994) · Cell Proliferation · doi:10.1111/j.1365-2184.1994.tb01425.x · Cited by 207 · see citing works

Specific MicroRNAs Are Preferentially Expressed by Skin Stem Cells To Balance Self-Renewal and Early Lineage Commitment

Zhang, L., Stokes, N., Polak, L., & Fuchs, E. V. (2011) · Cell stem cell · doi:10.1016/j.stem.2011.01.014 · Cited by 187 · 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

What does the concept of the stem cell niche really mean today?

Lander, A. D., Kimble, J. E., Clevers, H. C., Fuchs, E. V., Montarras, D., BUCKINGHAM, M. E., Calof, A. L., Trumpp, A., & Óskarsson, T. (2012) · BMC Biology · doi:10.1186/1741-7007-10-19 · Cited by 175 · see citing works

A microRNA-21 surge facilitates rapid cyclin D1 translation and cell cycle progression in mouse liver regeneration

Ng, R., Song, G., Roll, G. R., Frandsen, N. M., & Willenbring, H. (2012) · Journal of Clinical Investigation · doi:10.1172/jci46039 · Cited by 164 · see citing works

The hair follicle—a stem cell zoo

Jaks, V., Kasper, M., & Toftgård, R. (2010) · Experimental Cell Research · doi:10.1016/j.yexcr.2010.03.014 · Cited by 156 · see citing works

Foxl1-Cre-marked adult hepatic progenitors have clonogenic and bilineage differentiation potentialPreprint

Shin, S., Walton, G., Aoki, R., Brondell, K., Schug, J., Fox, A., Smirnova, O., Dorrell, C., Erker, L. R., Chu, A. S., et al. (2011) · Genes & Development · doi:10.1101/gad.2027811 · Cited by 153 · see citing works

Duct Cells Contribute to Regeneration of Endocrine and Acinar Cells Following Pancreatic Damage in Adult Mice

Criscimanna, A., Speicher, J. A., Houshmand, G., Shiota, C., Prasadan, K. L., Ji, B., Logsdon, C. D., Gittes, G. K., & Esni, F. (2011) · Gastroenterology · doi:10.1053/j.gastro.2011.07.003 · Cited by 149 · see citing works

Human prostate sphere‐forming cells represent a subset of basal epithelial cells capable of glandular regeneration in vivo

Garraway, I. P., Sun, W., Tran, C. P., Perner, S., Zhang, B., Goldstein, A. S., Hahm, S. A., Haider, M. A., Head, C. S., Reiter, R. E., et al. (2009) · The Prostate · doi:10.1002/pros.21083 · Cited by 145 · see citing works

Regulation of human breast epithelial stem cells

Clarke, R. B., Anderson, E. L., Howell, A., & Potten, C. S. (2003) · Cell Proliferation · doi:10.1046/j.1365-2184.36.s.1.5.x · Cited by 124 · see citing works

MicroRNAs and their roles in mammalian stem cells

Yi, R., & Fuchs, E. V. (2011) · Journal of Cell Science · doi:10.1242/jcs.069104 · Cited by 97 · see citing works

Label-retaining keratinocytes and Langerhans cells in mouse epithelia

Mackenzie, I. C., & Bickenbach, J. R. (1985) · Cell and Tissue Research · doi:10.1007/bf00225420 · Cited by 97 · see citing works

Differential Regeneration of Intestinal Proliferative Cells and Cryptogenic Cells after Irradiation

Potten, C. A., & Hendry, J. H. (1975) · International Journal of Radiation Biology and Related Studies in Physics Chemistry and Medicine · doi:10.1080/09553007514550411 · Cited by 90 · see citing works

Progenitor cell domains in the developing and adult pancreas

Kopp, J. L., Dubois, C. L., Hao, E., Thorel, F., Herrera, P. L., & Sander, M. (2011) · Cell Cycle · doi:10.4161/cc.10.12.16010 · Cited by 85 · see citing works

The ups and downs of miR-205: Identifying the roles of miR-205 in mammary gland development and breast cancer

Greene, S. B., Herschkowitz, J. I., & Rosen, J. M. (2010) · RNA Biology · doi:10.4161/rna.7.3.11837 · Cited by 83 · see citing works

Label-Retaining Cells in the Rat Pancreas

Duvillié, B., Attali, M., Aïello, V., Quéméneur, É., & Scharfmann, R. (2003) · Diabetes · doi:10.2337/diabetes.52.8.2035 · Cited by 75 · see citing works

The stem cell niche in health and malignancy

Burness, M. L., & Sipkins, D. A. (2010) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2010.05.006 · Cited by 48 · see citing works

Contributions of new hepatocyte lineages to liver growth, maintenance, and regeneration in mice

Iverson, S. V., Comstock, K. M., Kundert, J. A., & Schmidt, E. E. (2011) · Hepatology · doi:10.1002/hep.24398 · Cited by 43 · see citing works

What Signals Operate in the Mammary Niche?

Tanos, T., & Brisken, C. (2008) · Breast Disease · doi:10.3233/bd-2008-29108 · Cited by 34 · see citing works

An Overview of MicroRNA Methods: Expression Profiling and Target Identification

Smith, S. M., & Murray, D. W. (2011) · Methods in molecular biology · doi:10.1007/978-1-60327-216-2_9 · Cited by 30 · see citing works

Label Retaining Cells and Cutaneous Stem Cells

Terskikh, V. V., Vasiliev, A. V., & Vorotelyak, E. A. (2011) · Stem Cell Reviews and Reports · doi:10.1007/s12015-011-9299-6 · Cited by 24 · see citing works

In Vitro and In Vivo Gene Silencing by TransKingdom RNAi (tkRNAi)

Xiang, S., Keates, A. C., Fruehauf, J. H., Yang, Y., Guo, H., Nguyen, T. A., & Li, C. J. (2008) · Methods in molecular biology · doi:10.1007/978-1-60327-547-7_7 · Cited by 19 · 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

Developmental Relationships of Four Exhausted CD8+ T Cell Subsets Reveals Underlying Transcriptional and Epigenetic Landscape Control Mechanisms

Beltra, J., Manne, S., Abdel-Hakeem, M. S., Kurachi, M., Giles, J. R., Chen, Z., Casella, V., Ngiow, S. F., Khan, O., Huang, Y., et al. (2020) · Immunity · doi:10.1016/j.immuni.2020.04.014 · Cited by 1,091 · see citing works

Secretion of Shh by a Neurovascular Bundle Niche Supports Mesenchymal Stem Cell Homeostasis in the Adult Mouse Incisor

Zhao, H., Feng, J., Seidel, K., Shi, S., Klein, O. D., Sharpe, P. T., & Chai, Y. (2014) · Cell stem cell · doi:10.1016/j.stem.2013.12.013 · Cited by 464 · see citing works

Spermatogonial stem cells†

Kubota, H., & Brinster, R. L. (2018) · Biology of Reproduction · doi:10.1093/biolre/ioy077 · Cited by 235 · see citing works

Mobilized Adult Pituitary Stem Cells Contribute to Endocrine Regeneration in Response to Physiological Demand

Rizzoti, K., Akiyama, H., & Lovell-Badge, R. H. (2013) · Cell stem cell · doi:10.1016/j.stem.2013.07.006 · Cited by 187 · see citing works

The Conserved Misshapen-Warts-Yorkie Pathway Acts in Enteroblasts to Regulate Intestinal Stem Cells in Drosophila

Li, Q., Li, S., Mana‐Capelli, S., Flach, R. J. R., Danai, L. V., Amcheslavsky, A., Nie, Y., Kaneko, S., Yao, X., Chen, X., et al. (2014) · Developmental Cell · doi:10.1016/j.devcel.2014.09.012 · Cited by 142 · see citing works

Transcription factor p63 controls the reserve status but not the stemness of horizontal basal cells in the olfactory epithelium

Schnittke, N., Herrick, D. B., Lin, B., Peterson, J. N., Coleman, J. H., Packard, A. I., Jang, W., & Schwob, J. E. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1512272112 · Cited by 100 · see citing works

Differentiation-based model of hematopoietic stem cell functions and lineage pathways

Höfer, T., & Rodewald, H.-R. (2018) · Blood · doi:10.1182/blood-2018-03-791517 · Cited by 94 · see citing works

Reactive Oxygen Species Are Required for Human Mesenchymal Stem Cells to Initiate Proliferation after the Quiescence Exit

Lyublinskaya, O. G., Borisov, Y. G., Pugovkina, N. A., Smirnova, I. S., Obidina, J. V., Ivanova, J. S., Zenin, V. V., Shatrova, A. N., Borodkina, A. V., Aksenov, N., et al. (2015) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2015/502105 · Cited by 78 · see citing works

Stacking the DEK: From chromatin topology to cancer stem cells

Vinnedge, L. M. P., Kappes, F., Nassar, N. N., & Wells, S. I. (2012) · Cell Cycle · doi:10.4161/cc.23121 · Cited by 70 · see citing works

Cellular Mechanisms of Somatic Stem Cell Aging

Jung, Y., & Brack, A. S. (2014) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/b978-0-12-416022-4.00014-7 · Cited by 60 · see citing works

Stem cell therapy: an exercise in patience and prudence

Lin, H.-T., Otsu, M., & Nakauchi, H. (2013) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2011.0334 · Cited by 15 · see citing works

Rejuvenation of mesenchymal stem cells by extracellular vesicles inhibits the elevation of reactive oxygen species

Khánh, V. C., Yamashita, T., Ohneda, K., Tokunaga, C., Kato, H., Osaka, M., Hiramatsu, Y., & Ohneda, O. (2020) · Scientific Reports · doi:10.1038/s41598-020-74444-8 · Cited by 56 · see citing works

Chromosomal Abnormalities in Embryonic and Somatic Stem Cells

Rebuzzini, P., Zuccotti, M., Redi, C. A., & Garagna, S. (2015) · Cytogenetic and Genome Research · doi:10.1159/000441645 · Cited by 48 · see citing works

Anatomy of the olfactory mucosa

Salazar, I., Sánchez‐Quinteiro, P., Barrios, A. W., Amado, M. L., & Vega, J. A. (2019) · Handbook of clinical neurology · doi:10.1016/b978-0-444-63855-7.00004-6 · Cited by 47 · see citing works

Ionizing radiation induces stem cell-like properties in a caspase-dependent manner in Drosophila

Verghese, S., & Su, T. T. (2018) · PLoS Genetics · doi:10.1371/journal.pgen.1007659 · Cited by 37 · see citing works

Runx2 contributes to the regenerative potential of the mammary epithelium

Ferrari, N., Riggio, A. I., Mason, S. M., McDonald, L., King, A., Higgins, T., Rosewell, I. R., Neil, J. C., Smalley, M. J., Sansom, O. J., et al. (2015) · Scientific Reports · doi:10.1038/srep15658 · Cited by 36 · see citing works

Cancer cells and adaptive explanations

Germain, P. (2012) · Biology & Philosophy · doi:10.1007/s10539-012-9334-2 · Cited by 36 · see citing works

Aminoglycoside Damage and Hair Cell Regeneration in the Chicken Utricle

Scheibinger, M., Ellwanger, D. C., Corrales, C. E., Stone, J. S., & Heller, S. (2017) · Journal of the Association for Research in Otolaryngology · doi:10.1007/s10162-017-0646-4 · Cited by 33 · see citing works

Dynamic stem cell selection safeguards the genomic integrity of the epidermis

Kato, T., Liu, N., Morinaga, H., Asakawa, K., Muraguchi, T., Muroyama, Y., Shimokawa, M., Matsumura, H., Nishimori, Y., Tan, L. J., et al. (2021) · Developmental Cell · doi:10.1016/j.devcel.2021.11.018 · Cited by 32 · see citing works

Stem Cells and the Bird Cochlea—Where Is Everybody?Preprint

Janesick, A., & Heller, S. (2018) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a033183 · Cited by 33 · see citing works

Nanotechnology to Drive Stem Cell Commitment

Bressan, E. A., Carraro, A., Ferroni, L., Gardin, C., Sbricoli, L., Guazzo, R., Stellini, E., Roman, M., Pinton, P., Sivolella, S., et al. (2013) · Nanomedicine · doi:10.2217/nnm.13.12 · Cited by 32 · see citing works

Endometrial Stem Cells in Farm Animals: Potential Role in Uterine Physiology and Pathology

Lara, E., Rivera, N., Cabezas, J. G., Navarrete, F., Saravia, F., Rodriguez-Alvarez, L., & Castro, F. O. (2018) · Bioengineering · doi:10.3390/bioengineering5030075 · Cited by 22 · see citing works

Proliferation-related changes in K+ content in human mesenchymal stem cells

Marakhova, I. I., Domnina, A. P., Shatrova, A. N., Borodkina, A. V., Burova, E., Pugovkina, N. A., Zemelko, V. I., & Nikolsky, N. N. (2019) · Scientific Reports · doi:10.1038/s41598-018-36922-y · Cited by 20 · see citing works

Concise Review: A Critical Evaluation of Criteria Used to Define Salivary Gland Stem Cells

Weng, P., Aure, M. H., & Ovitt, C. E. (2019) · Stem Cells · doi:10.1002/stem.3046 · Cited by 18 · see citing works

PDGF, NT-3 and IGF-2 in Combination Induced Transdifferentiation of Muscle-Derived Stem Cells into Schwann Cell-Like Cells

Tang, Y., He, H., Cheng, N., Yan-ling, S., Ding, W., Zhang, Y., Zhang, W., Zhang, J., Peng, H., & Jiang, H. (2014) · PLoS ONE · doi:10.1371/journal.pone.0073402 · Cited by 17 · see citing works

Antioxidants Attenuate Heat Shock Induced Premature Senescence of Bovine Mesenchymal Stem Cells

Nir, D., Ribarski-Chorev, I., Shimoni, C., Strauss, C., Frank, J., & Schlesinger, S. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23105750 · Cited by 16 · see citing works

Future application of hair follicle stem cells: capable in differentiation into sweat gland cells

Wang, Y., Liu, Z., Zhao, Q., Sun, T.-Z., Ma, K., & Fu, X. (2013) · Chinese Medical Journal · doi:10.3760/cma.j.issn.0366-6999.20130931 · Cited by 16 · see citing works

Effect of Biopsy Location and Size on Proliferative Capacity of Ex Vivo Expanded Conjunctival Tissue

Eidet, J. R., Fostad, I. G., Shatos, M. A., Utheim, T. P., Utheim, Ø. A., Ræder, S., & Dartt, D. A. (2012) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.11-8269 · Cited by 15 · see citing works

Chromatin remodeling in tissue stem cell fate determination

Li, X., Zhu, G., & Zhao, B. T. (2024) · Cell Regeneration · doi:10.1186/s13619-024-00203-z · Cited by 15 · see citing works

Functional Modification of Drosophila Intestinal Stem Cells by Ionizing Radiation

Pyo, J.-H., Park, J., Na, H., Jeon, H.-J., Lee, S., Kim, J., Park, S., Jin, Y.-W., Kim, Y.-S., & Yoo, M. (2014) · Radiation Research · doi:10.1667/rr13545.1 · Cited by 14 · see citing works

Nanoparticle labeling identifies slow cycling human endometrial stromal cells

Xiang, L., Chan, R., Ng, E. H. Y., & Yeung, W. S. B. (2014) · Stem Cell Research & Therapy · doi:10.1186/scrt473 · Cited by 13 · see citing works

S100A6 as a Constituent and Potential Marker of Adult and Cancer Stem Cells

Leśniak, W., & Filipek, A. (2022) · Stem Cell Reviews and Reports · doi:10.1007/s12015-022-10403-2 · Cited by 13 · see citing works

Advanced Biotechnologies Toward Engineering a Cell Home for Stem Cell Accommodation

Tian, B., He, X., Xu, X., Li, X., Wu, R., & Chen, F. (2017) · Advanced Materials Technologies · doi:10.1002/admt.201700022 · Cited by 11 · see citing works

Macrophage precursor cells from the left atrial appendage of the heart spontaneously reprogram into a C-kit+/CD45− stem cell-like phenotype

Leinonen, J., Emanuelov, A. K., Wolf, Y., Milgrom-Hoffman, M., Lichtstein, D., Hoss, S., Lotan, C., Tzahor, E., Jung, S., & Beeri, R. (2016) · International Journal of Cardiology · doi:10.1016/j.ijcard.2016.02.040 · Cited by 11 · see citing works

Cellular plasticity, caspases and autophagy; that which does not kill us, well, makes us different

Su, T. T. (2018) · Open Biology · doi:10.1098/rsob.180157 · Cited by 9 · see citing works

The role of long-term label-retaining cells in the regeneration of adult mouse kidney after ischemia/reperfusion injury

Liu, X., Liu, H., Sun, L., Chen, Z., Nie, H., Sun, A., Liu, G., & Guan, G. (2016) · Stem Cell Research & Therapy · doi:10.1186/s13287-016-0324-1 · Cited by 7 · see citing works

Transplantation and Culture of Spermatogonial Stem Cells

Kubota, H., & Brinster, R. L. (2017) · Springer eBooks · doi:10.1007/978-1-4939-7505-1_11 · Cited by 7 · see citing works

Stem Cell Differentiation and Therapeutic Use

Alexander, M. S., Casar, J. C., & Motohashi, N. (2015) · Stem Cells International · doi:10.1155/2015/308128 · Cited by 5 · see citing works

Methods to identify epithelial stem cells

Jeong, Y. (2022) · Organoid · doi:10.51335/organoid.2022.2.e24 · Cited by 5 · see citing works

Suppressing Pitx2 inhibits proliferation and promotes differentiation of iHepSCs

Chen, F., Yao, H., Wang, M., Yu, B., Liu, Q., Li, J., He, Z., & Hu, Y. (2016) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2016.09.024 · Cited by 5 · see citing works

Stem and Progenitor Cells of the Trachea and Proximal Airways

Hegab, A. E., Betsuyaku, T., & Gomperts, B. N. (2015) · Stem cell biology and regenerative medicine · doi:10.1007/978-3-319-21082-7_6 · Cited by 4 · see citing works

Cutting-edge therapies in the treatment of surgical wounds

Zepeda, J. M., Contreras-Cárdenas, J., Gutiérrez, F. O., Jimenez, M., & Murrieta, A. (2021) · International Surgery Journal · doi:10.18203/2349-2902.isj20214821 · Cited by 2 · see citing works

Ion Homeostasis during the Growth of Human Mesenchymal Stem Culture. I. Density-Dependent Changes of Intracellular K+ and Na+ Content and K+ Influxes

Shatrova, A. N., Виноградова, Т. А., Domnina, A. P., Zemelko, V. I., Pugovkina, N. A., Nikolsky, N. N., & Marakhova, I. I. (2019) · Cell and Tissue Biology · doi:10.1134/s1990519x19020111 · Cited by 1 · see citing works

Cardiovascular Stem Cell Niche

Leri, A., Rota, M., Goichberg, P., Hosoda, T., Moccetti, T., & Anversa, P. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-802734-9.00007-x · Cited by 1 · see citing works

Produção de suportes poliméricos para o crescimento de células-tronco mesenquimais e sua aplicação em regeneração óssea

Bentini, R. (2013) · doi:10.11606/t.46.2013.tde-15012014-094457

Optimización de los cultivos de epitelio limbar humano para su posterior trasplante a la superficie ocular "Optimization of human limbal epithelial cultures for clinical transplantation"

López‐Paniagua, M. (2013) · doi:10.35376/10324/4391

Chromosome Instability in Stem Cells

Rebuzzini, P., Zuccotti, M., Redi, C. A., & Garagna, S. (2017) · doi:10.1002/9781118647110.ch3

Stem Cell Transplantation in Diabetes Mellitus Type I and Type II

Tu, S., & Tu, J. (2017) · Stem cells in clinical applications · doi:10.1007/978-3-319-55687-1_1

The many fates of tissue regeneration

Abdullah, C., & Duronio, R. J. (2018) · PLoS Genetics · doi:10.1371/journal.pgen.1007728

CANCER STEM CELL BIOLOGY

Göktuna, S. İ., Chau, T. L., & Xhafa, E. (2019) · Trakya University Journal of Natural Sciences · doi:10.23902/trkjnat.483577

Regulation for regenerative medicine-based therapies

Migliaccio, G. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-814831-0.00035-x

Cytogenetic studies of mesenchymal stem cells in rabbit: a mini-review.

Čurlej, J., Tomková, M., Vašíček, J., & Chrenek, P. (2018) · Slovak Journal of Animal Science

СОМАТИКАЛЫҚ БАҒАНАЛЫ ЖАСУШАЛАРДЫҢ ҚАРТАЮ

Umbayev, B. A., & Сафарова, Ю. И. (2022) · Vestnik · doi:10.53065/kaznmu.2022.16.11.012

Where new approaches can stem from: Focus on stem cell identification

Adams, V., Challen, G. A., Zuba‐Surma, E. K., Ulrich, H., Vereb, G., & Tárnok, A. (2008) · Cytometry Part A · doi:10.1002/cyto.a.20695 · Cited by 17 · see citing works

Analyzing stem cell dynamics: use of cutting edge genetic approaches in model organisms

Hime, G. R., Siddall, N. A., Horvay, K., & Abud, H. E. (2015) · Frontiers in Biology · doi:10.1007/s11515-015-1347-1

Concise Review: Quiescence in Adult Stem Cells: Biological Significance and Relevance to Tissue Regeneration

Rumman, M., Dhawan, J., & Kassem, M. S. (2015) · Stem Cells · doi:10.1002/stem.2056 · Cited by 169 · see citing works

Adult stem cell lineage tracing and deep tissue imaging

Fink, J., Andersson-Rolf, A., & Koo, B. (2015) · BMB Reports · doi:10.5483/bmbrep.2015.48.12.249 · Cited by 19 · see citing works

Definitions for adult stem cells debated

Muñoz‐Cánoves, P., & Huch, M. (2018) · Nature · doi:10.1038/d41586-018-07175-6 · Cited by 15 · see citing works