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Nerve dependence in tissue, organ, and appendage regeneration
Open accessAbstract
Many regeneration contexts require the presence of regenerating nerves as a transient component of the progenitor cell niche. Here we review nerve involvement in regeneration of various structures in vertebrates and invertebrates. Nerves are also implicated as persistent determinants in the niche of certain stem cells in mammals, as well as in Drosophila. We consider our present understanding of the cellular and molecular mechanisms underlying nerve dependence, including evidence of critical interactions with glia and non-neural cell types. The example of the salamander aneurogenic limb illustrates that developmental interactions between the limb bud and its innervation can be determinative for adult regeneration. These phenomena provide a different perspective on nerve cells to that based on chemical and electrical excitability.
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“Without this initial nerve signal, the wound stump heals, but no limb grows back in newts.”
From Wound repair and regeneration: Mechanisms, signaling, and translation (2014) · cites this paper as [131]
In the citing paper
“The release of nAG from nerves appears to kick-start expression of nAG in the wound epithelium (131).”
From Wound repair and regeneration: Mechanisms, signaling, and translation (2014) · cites this paper as [131]
Citations
Cites
Nonmyelinating Schwann Cells Maintain Hematopoietic Stem Cell Hibernation in the Bone Marrow Niche
Yamazaki, S., Ema, H., Karlsson, G., Yamaguchi, T., Miyoshi, H., Shioda, S., Taketo, M. M., Karlsson, S., Iwama, A., & Nakauchi, H. (2011) · Cell · doi:10.1016/j.cell.2011.09.053 · Cited by 797
Control of acetylcholine receptors in skeletal muscle
Fambrough, D. M. (1979) · Physiological Reviews · doi:10.1152/physrev.1979.59.1.165 · Cited by 775
The bone marrow stem cell niche grows up: mesenchymal stem cells and macrophages move in
Ehninger, A., & Trumpp, A. (2011) · The Journal of Experimental Medicine · doi:10.1084/jem.20110132 · Cited by 586
Comparative Aspects of Animal Regeneration
Brockes, J. P., & Kumar, A. (2008) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.24.110707.175336 · Cited by 491
Self-citationMolecular Basis for the Nerve Dependence of Limb Regeneration in an Adult Vertebrate
Kumar, A., Godwin, J. W., Gates, P. B., Garza-Garcı́a, A., & Brockes, J. P. (2007) · Science · doi:10.1126/science.1147710 · Cited by 487
Self-citationBrownell, I., Guevara, E., Bai, C. B., Loomis, C. A., & Joyner, A. L. (2011) · Cell stem cell · doi:10.1016/j.stem.2011.02.021 · Cited by 451
A New Murine Model for Mammalian Wound Repair and Regeneration
Clark, L. D., Clark, R. K., & Heber‐Katz, E. (1998) · Clinical Immunology and Immunopathology · doi:10.1006/clin.1998.4519 · Cited by 342
A stepwise model system for limb regeneration
Endo, T., Bryant, S. V., & Gardiner, D. M. (2004) · Developmental Biology · doi:10.1016/j.ydbio.2004.02.016 · Cited by 318
Progressive determination during formation of the anteroposterior axis in Xenopus laevis
Sive, H. L., Hattori, K., & Weintraub, H. M. (1989) · Cell · doi:10.1016/0092-8674(89)90413-3 · Cited by 296
Mullen, L., Bryant, S. V., Torok, M. A., Blumberg, B., & Gardiner, D. M. (1996) · Development · doi:10.1242/dev.122.11.3487 · Cited by 251
Flagged first, then by citations
Research works printed but not linked: 4
- Todd, 1823, On the process of reproduction of the members of the aquatic salamander, Q. J. Sci. Lit. Arts, 16, 84
- Huet, 1975, Role of the nervous system during the regeneration of an arm in a starfish: Asterina gibbosa Penn. (Echinodermata, Asteriidae), J. Embryol. Exp. Morphol., 33, 535
- Boilly-Marer, 1971, Role du systéme nerveux parapodial dans l’induction de parapodes supernumeraries par greffes hétérologues chez Nereis pelagica, C. R. Acad. Sci., 272, 261
- Guyenot, 1948, L’exploration du territoire de la patte antérieure du Triton, Rev. Suisse Zool., 55, 1
Cited by
Sorted by citations
Items 101–200 of 289
Li, J., Zhang, S., & Amaya, E. (2016) · Regeneration · doi:10.1002/reg2.69 · Cited by 37
Herrera‐Rincon, C., Golding, A. S., Moran, K. M., Harrison, C., Martyniuk, C. J., Guay, J. A., Zaltsman, J. B., Carabello, H., Kaplan, D. L., & Levin, M. G. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.10.010 · Cited by 37
Injury and stress responses of adult neural crest-derived cells
Parfejevs, V., Antunes, A. T., & Sommer, L. (2018) · Developmental Biology · doi:10.1016/j.ydbio.2018.05.011 · Cited by 35
Mechanisms of Neonatal Heart Regeneration
Cardoso, A. C., Pereira, A. H. M., & Sadek, H. A. (2020) · Current Cardiology Reports · doi:10.1007/s11886-020-01282-5 · Cited by 39
Su, Y., Zeng, L., Deng, R., Ye, B., Tang, S., Xiong, Z., Sun, T., Ding, Q., Su, W., Jing, X., et al. (2023) · Advanced Healthcare Materials · doi:10.1002/adhm.202203027 · Cited by 35
A Stable Thoracic Hox Code and Epimorphosis Characterize Posterior Regeneration in Capitella teleta
de Jong, D. M., & Seaver, E. C. (2016) · PLoS ONE · doi:10.1371/journal.pone.0149724 · Cited by 35
Busse, S. M., McMillen, P. T., & Levin, M. G. (2018) · Development · doi:10.1242/dev.164210 · Cited by 36
Axonal regrowth is impaired during digit tip regeneration in mice
Dolan, C. P., Yan, M., Zimmel, K. N., Yang, T., Leininger, E., Dawson, L., & Muneoka, K. (2018) · Developmental Biology · doi:10.1016/j.ydbio.2018.11.010 · Cited by 34
Wnt/β-Catenin Signaling Pathway in Skin Carcinogenesis and Therapy
Li, J., Ji, L., Chen, J., Zhang, W., & Ye, Z. (2015) · BioMed Research International · doi:10.1155/2015/964842 · Cited by 35
Axo‐glial interaction in the injured PNS
Stassart, R. M., & Woodhoo, A. (2020) · Developmental Neurobiology · doi:10.1002/dneu.22771 · Cited by 30
A Paradigm Shift in Tissue Engineering: From a Top–Down to a Bottom–Up Strategy
Schmidt, T., Yu, X., Bao, X., & Sun, T. (2021) · Processes · doi:10.3390/pr9060935 · Cited by 34
Rubin, N., Harrison, M. R., Krainock, M. R., Kim, R., & Lien, C. (2016) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2016.04.011 · Cited by 33
Pi, W., Chen, H., Liu, Y., Xiang, J., Zhang, H., Yang, X., Zhang, M., Cao, J., Chang, T., Zheng, Y., et al. (2024) · ACS Nano · doi:10.1021/acsnano.4c03974 · Cited by 33
Cellular and molecular mechanisms that regulate mammalian digit tip regeneration
Storer, M. A., & Miller, F. D. (2020) · Open Biology · doi:10.1098/rsob.200194 · Cited by 35
Schwann Cells as Orchestrators of Nerve Repair: Implications for Tissue Regeneration and PathologiesPreprint
Stassart, R. M., Gomez-Sanchez, J. A., & Lloyd, A. C. (2024) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a041363 · Cited by 32
Ong, T., Romanova, E. V., Roberts-Galbraith, R. H., Yang, N., Zimmerman, T. A., Collins, J. J., Lee, J. E., Kelleher, N. L., Newmark, P. A., & Sweedler, J. V. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.709196 · Cited by 30
Somatic multicellularity as a satisficing solution to the prediction-error minimization problem
Fields, C., & Levin, M. G. (2019) · Communicative & Integrative Biology · doi:10.1080/19420889.2019.1643666 · Cited by 29
Hyperinnervation improves Xenopus laevis limb regeneration
Mitogawa, K., Makanae, A., & Satoh, A. (2017) · Developmental Biology · doi:10.1016/j.ydbio.2017.10.007 · Cited by 29
Entangled cellular and molecular relationships at the sensory neuron-cancer interface
Sur, D., Zeng, Y., Kobayashi, H. H., Zhi, X., Goetz, M. R., Müller, C., Zavitsanou, A., Picoli, C. C., Matos, A. A. M., Pareja, J. R., et al. (2025) · Neuron · doi:10.1016/j.neuron.2025.07.017 · Cited by 31
The multifaceted role of nerves in animal regeneration
Sinigaglia, C., & Averof, M. (2019) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2019.07.020 · Cited by 28
Venkataramani, V., Yang, Y., Ille, S., Suchorska, B., Loges, S., Tost, H., Sahm, F., Pfister, S. M., Trumpp, A., Krieg, S. M., et al. (2025) · Cancer Discovery · doi:10.1158/2159-8290.cd-24-0194 · Cited by 33
Whole-Body Regeneration in the Lobate Ctenophore Mnemiopsis leidyi
Edgar, A., Mitchell, D. G., & Martindale, M. Q. (2021) · Genes · doi:10.3390/genes12060867 · Cited by 27
A comparative perspective on lung and gill regeneration
Cádiz, L., & Jonz, M. G. (2020) · Journal of Experimental Biology · doi:10.1242/jeb.226076 · Cited by 27
Bioengineered Lacrimal Gland Organ Regeneration in Vivo
Hirayama, M., Tsubota, K., & Tsuji, T. (2015) · Journal of Functional Biomaterials · doi:10.3390/jfb6030634 · Cited by 25
Khyeam, S., Lee, S., & Huang, G. N. (2021) · Advanced Genetics · doi:10.1002/ggn2.10042 · Cited by 25
Franklin, B. M., Voss, S. R., & Osborn, J. L. (2017) · Mechanisms of Development · doi:10.1016/j.mod.2017.06.001 · Cited by 25
Transcriptomic responses to wounding: meta-analysis of gene expression microarray data
Sass, P., Dąbrowski, M., Charzyńska, A., & Sachadyn, P. (2017) · BMC Genomics · doi:10.1186/s12864-017-4202-8 · Cited by 25
Enduring questions in regenerative biology and the search for answers
Seifert, A. W., Duncan, E. M., & Zayas, R. M. (2023) · Communications Biology · doi:10.1038/s42003-023-05505-7 · Cited by 26
Chang, J. C., Durinck, S., Chen, M. Z., Martinez-Martín, N., Zhang, J. A., Lehoux, I. E., Li, H., Lin, M. H., Wu, J., Bainbridge, T. W., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-45354-1 · Cited by 24
The salamander blastema within the broader context of metazoan regeneration
Tajer, B. J., Savage, A. M., & Whited, J. L. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1206157 · Cited by 25
Tumor-nerve interactions in cancer regulation and progression
Zhao, J., Cheng, L., Yang, J., Xu, F., Qi, W., Liao, K., Zhou, L., Cao, L., Chen, J., & Lin, Y. (2025) · Cancer Letters · doi:10.1016/j.canlet.2025.217483 · Cited by 24
Boilly, B., Boilly‐Marer, Y., & Bely, A. E. (2017) · Regeneration · doi:10.1002/reg2.78 · Cited by 23
Interrupting Neuron—Tumor Interactions to Overcome Treatment Resistance
Hunt, P. J., Kabotyanski, K. E., Călin, G. A., Xie, T., Myers, J. N., & Amit, M. (2020) · Cancers · doi:10.3390/cancers12123741 · Cited by 22
Salamon, R. J., Halbe, P., Kasberg, W., Bae, J., Audhya, A., & Mahmoud, A. I. (2023) · iScience · doi:10.1016/j.isci.2023.107709 · Cited by 22
Nerves, H2O2 and Shh: Three players in the game of regeneration
Meda, F., Rampon, C., Dupont, E., Gauron, C., Mourton, A., Quéguiner, I., Thauvin, M., Volovitch, M., Joliot, A., & Vriz, S. (2017) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2017.08.015 · Cited by 22
Liu, A., Zhang, L., Fei, D., Guo, H., Wu, M., Liu, J., He, X., Zhang, Y., Xuan, K., & Li, B. (2020) · Cell Proliferation · doi:10.1111/cpr.12803 · Cited by 22
Heart Regeneration in Adult Mammals after Myocardial Damage.
Cui, B., Zheng, Y., Sun, L., Shi, T., Shi, Z., Wang, L., Huang, G., & Sun, N. (2018) · PubMed Central · doi:10.6515/acs.201803_34(2).20171206a · Cited by 21
Xu, C., Hutchins, E. D., Tokuyama, M. A., Wilson‐Rawls, J., & Kusumi, K. (2019) · Journal of Immunology and Regenerative Medicine · doi:10.1016/j.regen.2019.100025 · Cited by 22
Neural regulation in tooth regeneration of Ambystoma mexicanum
Makanae, A., Tajika, Y., Nishimura, K., Saito, N., Tanaka, J.-I., & Satoh, A. (2020) · Scientific Reports · doi:10.1038/s41598-020-66142-2 · Cited by 21
Selective promotion of sensory innervation–mediated immunoregulation for tissue repair
Xu, K., Wu, K.-L., Chen, L., Zhao, Y., Li, H., Lin, N., Ye, Z., Xu, J., Huang, D., & Huang, X. (2025) · Science Advances · doi:10.1126/sciadv.ads9581 · Cited by 19
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Dromard, C., Rabiller, L., Jourdan, G., Cousin, B., Pénicaud, L., Casteilla, L., & Lorsignol, A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22147336 · Cited by 19
Neuroregulation during Bone Formation and Regeneration: Mechanisms and Strategies
Zhao, X., Yao, M., Wang, Y., Feng, C., Yang, Y., Tian, L., Bao, C., Li, X., Zhu, X., & Zhang, X. (2025) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.4c16786 · Cited by 20
Ivermectin Promotes Peripheral Nerve Regeneration during Wound Healing
Cairns, D. M., Giordano, J. E. M., Conte, S., Levin, M. G., & Kaplan, D. L. (2018) · ACS Omega · doi:10.1021/acsomega.8b01451 · Cited by 18
Tooth, hair and claw: Comparing epithelial stem cell niches of ectodermal appendages
Naveau, A., Seidel, K., & Klein, O. D. (2014) · Experimental Cell Research · doi:10.1016/j.yexcr.2014.02.003 · Cited by 19
Martinez, V. G., Arellano‐Carbajal, F., Gillen, K. M., Tweeten, K. A., & Zattara, E. E. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.780422 · Cited by 17
Brenneis, G., Frankowski, K., Maaß, L., & Scholtz, G. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2217272120 · Cited by 17
Zhan, C., Huang, M., Chen, J., Lu, Y., Yang, X., & Hou, J. L. (2023) · International Endodontic Journal · doi:10.1111/iej.13989 · Cited by 17
de Franchis, V., Petrungaro, S., Pizzichini, E., Camerini, S., Casella, M., Somma, F., Mandolini, E., Carpino, G., Overi, D., Cardinale, V., et al. (2024) · Cells · doi:10.3390/cells13050366 · Cited by 17
Injuries to appendage extremities and digit tips: A clinical and cellular update
Rinkevich, Y., Maan, Z. N., Walmsley, G. G., & Sen, S. K. (2015) · Developmental Dynamics · doi:10.1002/dvdy.24265 · Cited by 17
Gray, T. A., Alsamman, K., Murray, E., Sims, A. H., & Hupp, T. R. (2014) · Molecular BioSystems · doi:10.1039/c4mb00113c · Cited by 17
Quo vadis: tracing the fate of neural crest cells
Zurkirchen, L., & Sommer, L. (2017) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2017.07.001 · Cited by 17
Fatka, O., Budil, P., & Zicha, O. (2021) · International Journal of Paleopathology · doi:10.1016/j.ijpp.2021.05.011 · Cited by 17
The Contribution of Innervation to Tissue Repair and RegenerationPreprint
Johnston, A. P. W., & Miller, F. D. (2022) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a041233 · Cited by 18
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Stocum, D. L. (2018) · Developmental Neurobiology · doi:10.1002/dneu.22643 · Cited by 16
Pericytes in Cutaneous Wound Healing
Morikawa, S., Iribar, H., Gutiérrez‐Rivera, A., Ezaki, T., & Izeta, A. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-16908-4_1 · Cited by 17
Endocrine regulation of regeneration: Linking global signals to local processes
Easterling, M. R., Engbrecht, K. M., & Crespi, E. J. (2019) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2019.113220 · Cited by 16
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Podolak-Popinigis, J., Ronowicz, A., Dmochowska, M., Jakubiak, A. A., & Sachadyn, P. (2016) · Epigenomics · doi:10.2217/epi-2016-0068 · Cited by 16
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Noble, A., Qubrosi, R., Cariba, S., Favaro, K. J., & Payne, S. L. (2023) · Developmental Dynamics · doi:10.1002/dvdy.650 · Cited by 18
Tomasso, A., Disela, V., Longaker, M. T., & Bartscherer, K. (2024) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2024.102228 · Cited by 19
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Gracià, F., Sánchez‐Laorden, B. L., & Gomez-Sanchez, J. A. (2025) · Open Biology · doi:10.1098/rsob.240337 · Cited by 16
Imperadore, P., Uckermann, O., Galli, R., Steiner, G. R., Kirsch, M., & Fiorito, G. (2018) · Journal of The Royal Society Interface · doi:10.1098/rsif.2017.0889 · Cited by 15
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Jafari, P., Müller, C. T., Grognuz, A., Applegate, L. A., Raffoul, W., di Summa, P. G., & Durand, S. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18051054 · Cited by 15
Digit Tip Injuries: Current Treatment and Future Regenerative Paradigms
Miller, T. J., Deptula, P. L., Buncke, G. M., & Maan, Z. N. (2019) · Stem Cells International · doi:10.1155/2019/9619080 · Cited by 15
Stimulating ideas for heart regeneration: the future of nerve-directed heart therapy
Brandt, E. B., Bashar, S. J., & Mahmoud, A. I. (2019) · Bioelectronic Medicine · doi:10.1186/s42234-019-0024-0 · Cited by 16
Tossas, K., Qi‐Huang, S., Cuyar, E., & García‐Arrarás, J. E. (2014) · Regeneration · doi:10.1002/reg2.15 · Cited by 15
Rampon, C., Gauron, C., Meda, F., Volovitch, M., & Vriz, S. (2014) · Purinergic Signalling · doi:10.1007/s11302-014-9420-9 · Cited by 15
A system for bioelectronic delivery of treatment directed toward wound healing
Baniya, P., Tebyani, M., Asefifeyzabadi, N., Nguyen, T., Hernandez, C., Zhu, K., Li, H., Selberg, J. A., Hsieh, H., Pansodtee, P., et al. (2023) · Scientific Reports · doi:10.1038/s41598-023-41572-w · Cited by 14
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Su, Y., Zhang, M., Yu, B., Feng, T., Zhu, D., Guo, X., Wang, Y., Ding, L., Li, Z., Kong, Y., et al. (2025) · Small · doi:10.1002/smll.202501491 · Cited by 11
Intersection between lung cancer and neuroscience: Opportunities and challenges
Xiao, X., Huang, L., Li, M., & Zhang, Q. (2025) · Cancer Letters · doi:10.1016/j.canlet.2025.217701 · Cited by 12
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Xiang, M. S. W., & Kikuchi, K. (2016) · International review of cytology · doi:10.1016/bs.ircmb.2016.04.002 · Cited by 11
Dlamini, Z., Mathabe, K., Padayachy, L. C., Marima, R. M., Evangelou, G., Syrigos, K. N., Bianchi, A., Lolas, G., & Hull, R. (2021) · Cancers · doi:10.3390/cancers13092138 · Cited by 11
Fields, C., & Levin, M. G. (2020) · Communicative & Integrative Biology · doi:10.1080/19420889.2020.1729601 · Cited by 11
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Unsworth, S. P., Brownell, I., & Wong, S. Y. (2016) · Journal of Visualized Experiments · doi:10.3791/54050 · Cited by 11
Mini-review: Trophic interactions between cancer cells and primary afferent neurons
Hunt, P. J., Andújar, F. N., Silverman, D. A., & Amit, M. (2021) · Neuroscience Letters · doi:10.1016/j.neulet.2021.135658 · Cited by 10
Ivanova, A. S., Tereshina, M. B., Araslanova, K. R., Martynova, N. Y., & Zaraisky, A. G. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.738940 · Cited by 10
Jagadeeshaprasad, M. G., Govindappa, P. K., Nelson, A. M., & Elfar, J. C. (2022) · Journal of Visualized Experiments · doi:10.3791/63776 · Cited by 10
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Wang, Y.-H., Xuan, Y., Liu, C., Wang, X., & Yu, K. (2025) · Cancer Letters · doi:10.1016/j.canlet.2025.217451 · Cited by 9
Preventing Ethanol-Induced Brain and Eye Morphology Defects Using Optogenetics
Pai, V. P., & Adams, D. S. (2019) · Bioelectricity · doi:10.1089/bioe.2019.0008 · Cited by 9
Xu, H., Zhang, H., Fang, Y., Yang, H., Chen, Y., Zhang, C., & Lin, G. (2021) · Cell Regeneration · doi:10.1186/s13619-021-00081-9 · Cited by 9
Osorio-Méndez, D., Miller, A. H., Begeman, I. J., Kurth, A., Hagle, R., Rolph, D., Dickson, A. L., Chen, C., Halloran, M. C., Poss, K. D., et al. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2200342119 · Cited by 9
Czarkwiani, A., Taylor, J. A., & Oliveri, P. (2022) · Biology · doi:10.3390/biology11091360 · Cited by 8
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Metadata
- Authors
- Kumar, A., & Brockes, J. P.
- Affiliations
- Institute of Structural and Molecular Biology (GB)
- Corresponding author
- Brockes, Jeremy P.
- ORCID
- Brockes, Jeremy P.
- Venue
- Trends in Neurosciences
- Publisher
- Elsevier BV
- Published
- 2012-11
- Volume
- 35
- Issue
- 11
- Pages
- 691-699
- ISSN
- 0166-2236 (ISSN-L)
- OpenAlex
- W2048672935
- Cited by
- 290
- References
- 72
- Citations by year
- 2026: 11 · 2025: 26 · 2024: 19 · 2023: 21 · 2022: 14 · 2021: 23 · 2020: 22 · 2019: 21 · 2018: 18 · 2017: 25 · 2016: 33 · 2015: 26 · 2014: 24 · 2013: 7
- FWCI
- 1.93
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Trends in Neurosciences (publishedVersion, cc-by)
- PubMed (publishedVersion)
- UCL Discovery (University College London) (submittedVersion)
- Funders
- Medical Research Council
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Nerve injury and regeneration
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Planarian Biology and Electrostimulation
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- tissue regeneration, organ regeneration, appendage regeneration, stem cell niche, glial interactions, salamander regeneration, vertebrate regeneration
- MeSH terms
- Animals, Axons, Denervation, Drosophila melanogaster, Ear, External, Extremities, Fishes, Hydra, Invertebrates, Mice, Inbred Strains, Organ Specificity, Peripheral Nerves, Planarians, Regeneration, Schwann Cells, Species Specificity, Tail, Caudata, Urodela, Vertebrates, Xenopus laevis, Axotomy, Mice
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