The DOI matches its Crossref record; 123 of the 124 references it cites were found in a registry or an index.
Adult cell plasticity in vivo: de-differentiation and transdifferentiation are back in style
Open accessAbstract
Biologists have long been intrigued by the possibility that cells can change their identity, a phenomenon known as cellular plasticity. The discovery that terminally differentiated cells can be experimentally coaxed to become pluripotent has invigorated the field, and recent studies have demonstrated that changes in cell identity are not limited to the laboratory. Specifically, certain adult cells retain the capacity to de-differentiate or transdifferentiate under physiological conditions, as part of an organ's normal injury response. Recent studies have highlighted the extent to which cell plasticity contributes to tissue homeostasis, findings that have implications for cell-based therapy.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“In addition, cell reprogramming often occurs in highly specialized regions of injured tissues.11”
From Kupffer-cell-derived IL-6 is repurposed for hepatocyte dedifferentiation via activating progenitor genes from injury-specific enhancers (2023) · cites this paper as [11]
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
1 retracted
Baeyens, L., Lemper, M., Leuckx, G., Groef, S. D., Bonfanti, P., Stangé, G. M., Shemer, R., Nord, C., Scheel, D. W., Pan, F. C., et al. (2013) · Nature Biotechnology · doi:10.1038/nbt.2747 · Cited by 179
RetractedTakahashi, K., & Yamanaka, S. (2006) · Cell · doi:10.1016/j.cell.2006.07.024 · Cited by 26,673
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
Expression of a single transfected cDNA converts fibroblasts to myoblasts
Davis, R. L., Weintraub, H. M., & Lassar, A. B. (1987) · Cell · doi:10.1016/0092-8674(87)90585-x · Cited by 3,388
Direct conversion of fibroblasts to functional neurons by defined factors
Vierbuchen, T., Ostermeier, A., Pang, Z. P., Kokubu, Y., Südhof, T. C., & Wernig, M. (2010) · Nature · doi:10.1038/nature08797 · Cited by 3,017
Direct reprogramming of fibroblasts into functional cardiomyocytes by defined factors
Ieda, M., Fu, J.-D., Delgado-Olguin, P., Vedantham, V., Hayashi, Y., Bruneau, B. G., & Srivastava, D. (2010) · Cell · doi:10.1016/j.cell.2010.07.002 · Cited by 2,454
Bone Marrow as a Potential Source of Hepatic Oval Cells
Petersen, B. E., Bowen, W. C., Patrene, K. D., Mars, W. M., Sullivan, A. K., Murase, N., Boggs, S. S., Greenberger, J. S., & Goff, J. P. (1999) · Science · doi:10.1126/science.284.5417.1168 · Cited by 2,377
In vivo reprogramming of adult pancreatic exocrine cells to β-cells
Zhou, Q., Brown, J., Kanarek, A., Rajagopal, J., & Melton, D. A. (2008) · Nature · doi:10.1038/nature07314 · Cited by 2,010
Heart Regeneration in Zebrafish
Poss, K. D., Wilson, L. G., & Keating, M. T. (2002) · Science · doi:10.1126/science.1077857 · Cited by 1,938
Basal cells as stem cells of the mouse trachea and human airway epithelium
Rock, J. R., Onaitis, M. W., Rawlins, E. L., Lu, Y., Clark, C. P., Xue, Y., Randell, S. H., & Hogan, B. L. M. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0906850106 · Cited by 1,591
Flagged first, then by citations
1 of the 124 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
Hallmarks of Cancer: New Dimensions
Hanahan, D. (2022) · Cancer Discovery · doi:10.1158/2159-8290.cd-21-1059 · Cited by 9,887
Yuan, S., Norgard, R. J., & Stanger, B. Z. (2019) · Cancer Discovery · doi:10.1158/2159-8290.cd-19-0015 · Cited by 491
Self-citationJun, J.-I., & Lau, L. F. (2018) · Journal of Clinical Investigation · doi:10.1172/jci93563 · Cited by 358
Clements, M., Byrne, E., Guerrero, C., Cattin, A.-L., Zakka, L., Ashraf, A., Burden, J. J., Khadayate, S. P., Lloyd, A. C., Marguerat, S., et al. (2017) · Neuron · doi:10.1016/j.neuron.2017.09.008 · Cited by 328
De novo formation of the biliary system by TGFβ-mediated hepatocyte transdifferentiation
Schaub, J. R., Huppert, K. A., Kurial, S. N. T., Hsu, B. Y., Cast, A. E., Donnelly, B., Karns, R. A., Chen, F., Rezvani, M., Luu, H. Y., et al. (2018) · Nature · doi:10.1038/s41586-018-0075-5 · Cited by 289
Emerging role of tumor cell plasticity in modifying therapeutic response
Qin, S., Jiang, J., Lü, Y., Nice, E. C., Huang, C., Zhang, J., & He, W. (2020) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-020-00313-5 · Cited by 289
Proliferation tracing reveals regional hepatocyte generation in liver homeostasis and repair
He, L., Pu, W., Liu, X., Zhang, Z., Han, M., Li, Y., Huang, X., Han, X., Li, Y., Liu, K., et al. (2021) · Science · doi:10.1126/science.abc4346 · Cited by 261
Tumor cell plasticity in targeted therapy-induced resistance: Mechanisms and new strategies
Shi, Z.-D., Pang, K., Wu, Z.-X., Dong, Y., Hao, L., Qin, J.-X., Wang, W., Chen, Z.-S., & Han, C.-H. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01383-x · Cited by 256
Haseeb, A., Kc, R., Angelozzi, M., de Charleroy, C., Rux, D. R., Tower, R. J., Yao, L., da Silva, R. P., Pacifici, M., Qin, L., et al. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2019152118 · Cited by 244
Age-dependent instability of mature neuronal fate in induced neurons from Alzheimer’s patients
Mertens, J., Herdy, J. R., Traxler, L., Schafer, S. T., Schlachetzki, J. C. M., Böhnke, L., Reid, D. A., Lee, H., Zangwill, D., Fernandes, D. P., et al. (2021) · Cell Stem Cell · doi:10.1016/j.stem.2021.04.004 · Cited by 240
Rare Pulmonary Neuroendocrine Cells Are Stem Cells Regulated by Rb, p53, and Notch
Ouadah, Y., Rojas, E., Riordan, D. P., Capostagno, S., Kuo, C. S., & Krasnow, M. A. (2019) · Cell · doi:10.1016/j.cell.2019.09.010 · Cited by 223
Shah, P. T., Stratton, J. A., Stykel, M. G., Abbasi, S., Sharma, S., Mayr, K. A., Koblinger, K., Whelan, P. J., & Biernaskie, J. (2018) · Cell · doi:10.1016/j.cell.2018.03.063 · Cited by 221
Cell plasticity in epithelial homeostasis and tumorigenesis
Varga, J., & Greten, F. R. (2017) · Nature Cell Biology · doi:10.1038/ncb3611 · Cited by 209
Cancer cell plasticity: Impact on tumor progression and therapy response
da Silva-Diz, V., Lorenzo-Sanz, L., Bernat‐Peguera, A., Lopez-Cerda, M., & Muñoz, P. (2018) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2018.08.009 · Cited by 217
Diverse mechanisms for endogenous regeneration and repair in mammalian organs
Wells, J. M., & Watt, F. M. (2018) · Nature · doi:10.1038/s41586-018-0073-7 · Cited by 169
Recording development with single cell dynamic lineage tracing
McKenna, A., & Gagnon, J. A. (2019) · Development · doi:10.1242/dev.169730 · Cited by 169
Sharma, A., Cao, E. Y., Kumar, V., Zhang, X., Leong, H. S., Wong, A. M. L., Ramakrishnan, N., Hakimullah, M., Teo, H. M. V., Chong, F. T., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-07261-3 · Cited by 159
Epithelial–mesenchymal transition in tissue repair and degeneration
Youssef, K. K., & Nieto, M. A. (2024) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-024-00733-z · Cited by 165
Tata, A., Kobayashi, Y., Chow, R. D.-W., Tran, J., Desai, A. P., Massri, A. J., McCord, T. J., Gunn, M. D., & Tata, P. R. (2018) · Cell stem cell · doi:10.1016/j.stem.2018.03.018 · Cited by 156
Cellular plasticity in kidney injury and repair
Chang-Panesso, M., & Humphreys, B. D. (2016) · Nature Reviews Nephrology · doi:10.1038/nrneph.2016.169 · Cited by 151
Dissecting Tumor Growth: The Role of Cancer Stem Cells in Drug Resistance and Recurrence
Aramini, B., Masciale, V., Grisendi, G., Bertolini, F., Maur, M., Guaitoli, G., Isca, C., Morandi, U., Stella, F., Dominici, M., et al. (2022) · Cancers · doi:10.3390/cancers14040976 · Cited by 154
Extracellular Matrix Cues Regulate Mechanosensing and Mechanotransduction of Cancer Cells
Mierke, C. T. (2024) · Cells · doi:10.3390/cells13010096 · Cited by 146
Acid and the basis for cellular plasticity and reprogramming in gastric repair and cancer
Sáenz, J. B., & Mills, J. C. (2018) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2018.5 · Cited by 138
Li, L., Cui, L., Lin, P., Liu, Z., Bao, S., Ma, X., Nan, H., Zhu, W., Cen, J., Mao, Y., et al. (2023) · Cell Stem Cell · doi:10.1016/j.stem.2023.01.009 · Cited by 134
Limited Regeneration of Adult Salivary Glands after Severe Injury Involves Cellular Plasticity
Weng, P., Aure, M. H., Maruyama, T., & Ovitt, C. E. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.07.016 · Cited by 114
Notch2 controls hepatocyte-derived cholangiocarcinoma formation in mice
Wang, J., Dong, M., Xu, Z., Song, X., Zhang, S., Qiao, Y., Che, L., Gordan, J. D., Hu, K., Liu, Y., et al. (2018) · Oncogene · doi:10.1038/s41388-018-0188-1 · Cited by 114
Lineage Plasticity in Cancer Progression and Treatment
Magnen, C. L., Shen, M. M., & Abate-Shen, C. T. (2017) · Annual Review of Cancer Biology · doi:10.1146/annurev-cancerbio-030617-050224 · Cited by 105
The role of biomineralization in disorders of skeletal development and tooth formation
Kovács, C. S., Chaussain, C., Osdoby, P., Brandi, M. L., Clarke, B. L., & Thakker, R. V. (2021) · Nature Reviews Endocrinology · doi:10.1038/s41574-021-00488-z · Cited by 112
Direct cell reprogramming for tissue engineering and regenerative medicine
Grath, A., & Dai, G. (2019) · Journal of Biological Engineering · doi:10.1186/s13036-019-0144-9 · Cited by 109
Compression-induced dedifferentiation of adipocytes promotes tumor progression
Li, Y., Mao, A. S., Seo, B. R., Zhao, X., Gupta, S. K., Chen, M., Han, Y., Shih, T., Mooney, D. J., & Guo, M. (2020) · Science Advances · doi:10.1126/sciadv.aax5611 · Cited by 103
Therapeutic Plasticity of Neural Stem Cells
Ottoboni, L., von Wunster, B., & Martino, G. (2020) · Frontiers in Neurology · doi:10.3389/fneur.2020.00148 · Cited by 105
Dedifferentiation: inspiration for devising engineering strategies for regenerative medicine
Yao, Y., & Wang, C. (2020) · npj Regenerative Medicine · doi:10.1038/s41536-020-00099-8 · Cited by 96
Transcriptional Maintenance of Pancreatic Acinar Identity, Differentiation, and Homeostasis by PTF1A
Hoàng, C., Hale, M. A., Azevedo-Pouly, A., Elsässer, H., Deering, T. G., Willet, S. G., Pan, F. C., Magnuson, M., Wright, C., Swift, G. H., et al. (2016) · Molecular and Cellular Biology · doi:10.1128/mcb.00358-16 · Cited by 87
Filling the Gap: Neural Stem Cells as A Promising Therapy for Spinal Cord Injury
Pereira, I. M., Marote, A., Salgado, A. J., & Silva, N. A. (2019) · Pharmaceuticals · doi:10.3390/ph12020065 · Cited by 91
The stem cell division theory of cancer
López‐Lázaro, M. (2018) · Critical Reviews in Oncology/Hematology · doi:10.1016/j.critrevonc.2018.01.010 · Cited by 91
Ortega, Á., Vera, I., Díaz, M. I., Navarro, C., Rojas, M., Torres, W., Parra, H., Salazar, J. J., Sanctis, J. B. D., & Bermúdez, V. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms23010430 · Cited by 87
Skeletal Stem Cells for Bone Development and Repair: Diversity Matters
Matsushita, Y., Ono, W., & Ono, N. (2020) · Current Osteoporosis Reports · doi:10.1007/s11914-020-00572-9 · Cited by 79
Lorenzo-Sanz, L., & Muñoz, P. (2019) · Cancer Microenvironment · doi:10.1007/s12307-019-00232-2 · Cited by 76
Chen, Y., Yu, Y., Wen, Y., Chen, J., Lin, J., Sheng, Z., Zhou, W., Sun, H., An, C., Chen, J., et al. (2022) · Bone Research · doi:10.1038/s41413-022-00209-w · Cited by 76
Stem cell division theory of cancer
López‐Lázaro, M. (2015) · Cell Cycle · doi:10.1080/15384101.2015.1062330 · Cited by 70
Fate plasticity and reprogramming in genetically distinct populations of Danio leucophores
Lewis, V. M., Saunders, L. M., Larson, T. A., Bain, E. J., Sturiale, S. L., Gur, D., Chowdhury, S., Flynn, J. D., Allen, M. C., Deheyn, D. D., et al. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1901021116 · Cited by 69
High-throughput physical phenotyping of cell differentiation
Lin, J., Kim, D., Tse, H. T. K., Tseng, P., Peng, L. T., Dhar, M., Karumbayaram, S., & Carlo, D. D. (2017) · Microsystems & Nanoengineering · doi:10.1038/micronano.2017.13 · Cited by 69
The Fire within: Cell-Autonomous Mechanisms in Inflammation-Driven Cancer
Todoric, J., & Karin, M. (2019) · Cancer Cell · doi:10.1016/j.ccell.2019.04.001 · Cited by 69
Nomenclature for cellular plasticity: are the terms as plastic as the cells themselves?
Mills, J. C., Stanger, B. Z., & Sander, M. (2019) · The EMBO Journal · doi:10.15252/embj.2019103148 · Cited by 67
Self-citationGauthier, B. R., & Comaills, V. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22147281 · Cited by 68
Targeting of cancer stem cells by differentiation therapy
Arima, Y., Nobusue, H., & Saya, H. (2020) · Cancer Science · doi:10.1111/cas.14504 · Cited by 67
Control of Cell Identity by the Nuclear Receptor HNF4 in Organ Pathophysiology
Dubois, V., Staels, B., Lefebvre, P., Verzi, M., & Eeckhoute, J. (2020) · Cells · doi:10.3390/cells9102185 · Cited by 63
Epithelial–mesenchymal plasticity in kidney fibrosis
Hadpech, S., & Thongboonkerd, V. (2023) · genesis · doi:10.1002/dvg.23529 · Cited by 62
Ring, N., Valdivieso, K., Grillari, J., Redl, H. R., & Ogrodnik, M. B. (2022) · Developmental Cell · doi:10.1016/j.devcel.2022.04.005 · Cited by 59
Transcriptional Control of Peripheral Nerve Regeneration
Zhang, Y., Zhao, Q., Chen, Q., Xu, L., & Yi, S. (2022) · Molecular Neurobiology · doi:10.1007/s12035-022-03090-0 · Cited by 58
Expansion of functional personalized cells with specific transgene combinations
Lipps, C., Klein, F., Wahlicht, T., Seiffert, V., Butueva, M., Zauers, J., Truschel, T., Luckner, M., Köster, M., MacLeod, R. A. F., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-03408-4 · Cited by 63
Somerville, T. D. D., Xu, Y., Wu, X., Maia-Silva, D., Hur, S. K., de Almeida, L. M. N., Preall, J. B., Koo, P. K., & Vakoc, C. R. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1921484117 · Cited by 60
Manufacturing Cell Therapies Using Engineered Biomaterials
Abdeen, A. A., & Saha, K. (2017) · Trends in biotechnology · doi:10.1016/j.tibtech.2017.06.008 · Cited by 55
Tumor Heterogeneity and Consequences for Bladder Cancer Treatment
Lavallée, É., Sfakianos, J. P., & Mulholland, D. J. (2021) · Cancers · doi:10.3390/cancers13215297 · Cited by 60
Ledo, A. M., Vining, K. H., Alonso, M. J., García-Fuentes, M., & Mooney, D. J. (2020) · Acta Biomaterialia · doi:10.1016/j.actbio.2020.04.027 · Cited by 60
Ninche, N., Kwak, M., & Ghazizadeh, S. (2020) · Development · doi:10.1242/dev.192807 · Cited by 54
Single-cell manifold-preserving feature selection for detecting rare cell populations
Liang, S., Mohanty, V., Dou, J., Miao, Q., Huang, Y., Müftüoğlu, M., Ding, L., Peng, W., & Chen, K. (2021) · Nature Computational Science · doi:10.1038/s43588-021-00070-7 · Cited by 53
Lineage Plasticity: The New Cancer Hallmark on the Block
Mehta, A., & Stanger, B. Z. (2023) · Cancer Research · doi:10.1158/0008-5472.can-23-1067 · Cited by 54
Self-citationReversible, tunable epigenetic silencing of TCF1 generates flexibility in the T cell memory decision
Abadie, K., Clark, E. C., Valanparambil, R. M., Ukogu, O., Yang, W., Daza, R. M., Ng, K. K. H., Fathima, J., Wang, A. L., Lee, J., et al. (2024) · Immunity · doi:10.1016/j.immuni.2023.12.006 · Cited by 53
Fanelli, G. N., Naccarato, A. G., & Scatena, C. (2020) · Frontiers in Oncology · doi:10.3389/fonc.2020.00569 · Cited by 53
How Tumor Cell Dedifferentiation Drives Immune Evasion and Resistance to Immunotherapy
Li, J., & Stanger, B. Z. (2020) · Cancer Research · doi:10.1158/0008-5472.can-20-1420 · Cited by 54
Self-citationCREB1 contributes colorectal cancer cell plasticity by regulating lncRNA CCAT1 and NF-κB pathways
Li, B., Zheng, L., Ye, J., Zhang, C., Zhou, J. H. S., Huang, Q.-J., Guo, Y., Wang, L., Yu, P., Liu, S., et al. (2022) · Science China Life Sciences · doi:10.1007/s11427-022-2108-x · Cited by 52
Kim, T., Kim, H., Joo, I., & Lee, J. M. (2020) · Korean Journal of Radiology · doi:10.3348/kjr.2020.0091 · Cited by 48
A pan‐metazoan concept for adult stem cells: the wobbling Penrose landscape
Rinkevich, B., Ballarin, L., Martı́nez, P., Somorjai, I., Ben-Hamo, O., Borisenko, I., Berezikov, E., Ereskovsky, A. V., Gazave, E., Khnykin, D., et al. (2021) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/brv.12801 · Cited by 52
Tasca, A., Helmstädter, M., Brislinger-Engelhardt, M. M., Haas, M., Mitchell, B. J., & Walentek, P. (2021) · Developmental Cell · doi:10.1016/j.devcel.2020.12.005 · Cited by 48
Appendage Regeneration in Vertebrates: What Makes This Possible?
Daponte, V., Tylżanowski, P., & Forlino, A. (2021) · Cells · doi:10.3390/cells10020242 · Cited by 48
Herrera, S. C., & Bach, E. A. (2018) · eLife · doi:10.7554/elife.36095 · Cited by 45
Triboelectric Nanogenerators for Cellular Bioelectrical Stimulation
Zhang, W., Li, G., Wang, B., Zhu, Q., Zeng, L., Wen, Z., Cao, Y., & Pan, Y. (2022) · Advanced Functional Materials · doi:10.1002/adfm.202203029 · Cited by 47
The RSPO‐LGR4/5‐ZNRF3/RNF43 module in liver homeostasis, regeneration, and disease
Annunziato, S., Sun, T., & Tchorz, J. S. (2022) · Hepatology · doi:10.1002/hep.32328 · Cited by 45
Insulin is expressed by enteroendocrine cells during human fetal development
Egozi, A., Llivichuzhca-Loja, D., McCourt, B. T., Halpern, K. B., Farack, L., An, X., Wang, F., Chen, K., Konnikova, L., & Itzkovitz, S. (2021) · Nature Medicine · doi:10.1038/s41591-021-01586-1 · Cited by 44
Recent advances of cellular stimulation with triboelectric nanogenerators
Zhou, X., Li, G., Wu, D., Liang, H., Zhang, W., Zeng, L., Zhu, Q., Lai, P., Wen, Z., Cao, Y., et al. (2023) · Exploration · doi:10.1002/exp.20220090 · Cited by 45
Terminal Schwann Cell Aging: Implications for Age-Associated Neuromuscular Dysfunction
Fuertes-Álvarez, S., & Izeta, A. (2021) · Aging and Disease · doi:10.14336/ad.2020.0708 · Cited by 46
A multistate stem cell dynamics maintains homeostasis in mouse spermatogenesis
Nakagawa, T., Jörg, D. J., Watanabe, H., Mizuno, S., Han, S., Ikeda, T., Omatsu, Y., Nishimura, K., Fujita, M., Takahashi, S., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109875 · Cited by 37
White Adipocyte Plasticity in Physiology and Disease
Bielczyk-Maczyńska, E. (2019) · Cells · doi:10.3390/cells8121507 · Cited by 44
Dynamic Transcriptional and Epigenetic Changes Drive Cellular Plasticity in the Liver
Merrell, A. J., Peng, T., Li, J., Sun, K., Li, B., Katsuda, T., Grompe, M., Tan, K., & Stanger, B. Z. (2021) · Hepatology · doi:10.1002/hep.31704 · Cited by 42
Self-citationFerrario, C., Sugni, M., Somorjai, I., & Ballarin, L. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.587320 · Cited by 41
Schreiner, T., Allnoch, L., Beythien, G., Marek, K., Becker, K., Schaudien, D., Stanelle‐Bertram, S., Schaumburg, B., Kouassi, N. M., Beck, S., et al. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23095124 · Cited by 41
Namoto, K., Baader, C., Orsini, V., Landshammer, A., Breuer, E., Dinh, K. T., Ungricht, R., Pikiolek, M., Laurent, S., Lu, B., et al. (2024) · Cell stem cell · doi:10.1016/j.stem.2024.03.003 · Cited by 42
Wound infiltrating adipocytes are not myofibroblasts
Gopal, S. K., Dai, R., Stefańska, A., Ansari, M., Zhao, J., Ramesh, P., Bagnoli, J., Correa‐Gallegos, D., Lin, Y., Christ, S., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-38591-6 · Cited by 39
Cells of origin of pancreatic neoplasms
Yamaguchi, J., Yokoyama, Y., Kokuryo, T., Ebata, T., & Nagino, M. (2017) · Surgery Today · doi:10.1007/s00595-017-1501-2 · Cited by 40
Reconstructing axial progenitor field dynamics in mouse stem cell-derived embryoids
Bolondi, A., Law, B. K., Kretzmer, H., Gassaloglu, S. I., Buschow, R., Riemenschneider, C., Yang, D., Walther, M., Veenvliet, J. V., Meissner, A., et al. (2024) · Developmental Cell · doi:10.1016/j.devcel.2024.03.024 · Cited by 38
Biology of Cancer; From Cellular Cancerogenesis to Supracellular Evolution of Malignant Phenotype
Motofei, I. G. (2018) · Cancer Investigation · doi:10.1080/07357907.2018.1477955 · Cited by 39
Tanaka, H. Y., Nakazawa, T., Enomoto, A., Masamune, A., & Kano, M. R. (2023) · Cancers · doi:10.3390/cancers15030724 · Cited by 42
Carlessi, R., Köhn‐Gaone, J., Olynyk, J. K., & Tirnitz‐Parker, J. E. E. (2019) · Codon Publications eBooks · doi:10.15586/hepatocellularcarcinoma.2019 · Cited by 39
Zfp281 orchestrates interconversion of pluripotent states by engaging Ehmt1 and Zic2
Mayer, D., Stadler, M. B., Rittirsch, M., Heß, D., Lukonin, I., Winzi, M., Smith, A. G., Buchholz, F., & Betschinger, J. (2019) · The EMBO Journal · doi:10.15252/embj.2019102591 · Cited by 31
Drubbel, A. V., Pirard, S., Kin, S., Dassy, B., Lefort, A., Libert, F., Nomura, S., & Beck, B. (2021) · Cell stem cell · doi:10.1016/j.stem.2021.03.019 · Cited by 33
The versatile plasmacytoid dendritic cell: Function, heterogeneity, and plasticity
(2019) · International Review of Cell and Molecular Biology · doi:10.1016/bs.ircmb.2019.10.002 · Cited by 35
Evolutionary origin of endochondral ossification: the transdifferentiation hypothesis
Cervantes‐Díaz, F., Contreras, P., & Marcellini, S. (2016) · Development Genes and Evolution · doi:10.1007/s00427-016-0567-y · Cited by 34
The phenotype of gingival fibroblasts and their potential use in advanced therapies
García, S. L. A., Parada-Sánchez, M. T., & Toro, D. A. (2020) · European Journal of Cell Biology · doi:10.1016/j.ejcb.2020.151123 · Cited by 34
AXL Is a Driver of Stemness in Normal Mammary Gland and Breast Cancer
Engelsen, A. S. T., Wnuk-Lipińska, K., Bougnaud, S., Vatter, F. A. P., Tiron, C. E., Villadsen, R., Miyano, M., Lotsberg, M. L., Madeleine, N., Panahandeh, P., et al. (2020) · iScience · doi:10.1016/j.isci.2020.101649 · Cited by 34
Epigenetic and Immunological Features of Bladder Cancer
Gilyazova, I. R., Enikeeva, K., Альбертовна, Р. Г., Марсельевна, К. Э., Вакилевна, Ш. Ю., Динаровна, А. Д., & Павлов, В. Н. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24129854 · Cited by 34
Cellular reprogramming in vivo initiated by SOX4 pioneer factor activity
Katsuda, T., Sussman, J. H., Ito, K., Katznelson, A., Yuan, S., Takenaka, N., Li, J., Merrell, A. J., Cure, H., Li, Q., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-45939-z · Cited by 33
Self-citationPapagiannouli, F., Berry, C. W., & Fuller, M. T. (2019) · Stem Cell Reports · doi:10.1016/j.stemcr.2019.03.008 · Cited by 31
Functional analysis of cell plasticity using single-cell technologies
Qin, X., & Tape, C. J. (2024) · Trends in Cell Biology · doi:10.1016/j.tcb.2024.01.006 · Cited by 32
Thong, T., Wang, Y., Brooks, M. D., Lee, C. T.-Y., Scott, C. D., Balzano, L., Wicha, M. S., & Colacino, J. A. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00288 · Cited by 32
Characterisation of Cultured Mesothelial Cells Derived from the Murine Adult Omentum
Dauleh, S., Santeramo, I., Fielding, C., Ward, K., Herrmann, A., Murray, P. A., & Wilm, B. (2016) · PLoS ONE · doi:10.1371/journal.pone.0158997 · Cited by 31
Wnt-β-catenin in hepatobiliary homeostasis, injury, and repair
Nejak‐Bowen, K. N., & Monga, S. P. (2023) · Hepatology · doi:10.1097/hep.0000000000000495 · Cited by 31
FAM3C in Cancer-Associated Adipocytes Promotes Breast Cancer Cell Survival and Metastasis
Kim, S., Oh, J., Park, C., Kim, M., Jo, W., Kim, C.-S., Cho, S. W., & Park, J. (2023) · Cancer Research · doi:10.1158/0008-5472.can-23-1641 · Cited by 32
Long-Term Maintenance of Acinar Cells in Human Submandibular Glands After Radiation Therapy
Luitje, M. E., Israel, A., Cummings, M. A., Giampoli, E. J., Allen, P. D., Newlands, S. D., & Ovitt, C. E. (2020) · International Journal of Radiation Oncology*Biology*Physics · doi:10.1016/j.ijrobp.2020.10.037 · Cited by 30
Clabaut, A., Grare, C., Rolland-Valognes, G., Letarouilly, J.-G., Bourrier, C., Andersen, T. L., Sikjær, T., Rejnmark, L., Ejersted, C., Pastoureau, P., et al. (2021) · PLoS ONE · doi:10.1371/journal.pone.0245014 · Cited by 29
Metadata
- Authors
- Merrell, A. J., & Stanger, B. Z.
- Affiliations
- University of Pennsylvania (US)
- Corresponding author
- Stanger, Ben Z.
- Venue
- Nature Reviews Molecular Cell Biology
- Published
- 2016-03-16
- Volume
- 17
- Issue
- 7
- Pages
- 413-425
- ISSN
- 1471-0072 (ISSN-L)
- 1471-0080
- PMC
- PMC5818993
- OpenAlex
- W2300048866
- Cited by
- 369
- References
- 124
- Citations by year
- 2026: 21 · 2025: 35 · 2024: 45 · 2023: 42 · 2022: 45 · 2021: 49 · 2020: 40 · 2019: 39 · 2018: 26 · 2017: 19 · 2016: 7
- FWCI
- 2.75
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nature Reviews Molecular Cell Biology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Zenodo (CERN European Organization for Nuclear Research) (submittedVersion, other-oa)
- Funders
- National Cancer Institute (R01CA169123)
- National Institute of Diabetes and Digestive and Kidney Diseases (UC4DK104196)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Pluripotent Stem Cells Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Mesenchymal stem cell research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Congenital heart defects research
- Keywords
- cellular plasticity, dedifferentiation, transdifferentiation, terminally differentiated cells, tissue homeostasis, cell therapy, pluripotency
- MeSH terms
- Animals, Cell Transformation, Neoplastic, Humans, Neoplasms, Regeneration, Signal Transduction, Adult Stem Cells, Cell Dedifferentiation, Cell Transdifferentiation
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