The DOI matches its Crossref record; 60 of the 60 references it cites were found in a registry or an index.
Late-stage neuronal progenitors in the retina are radial Müller glia that function as retinal stem cells
Open accessAbstract
Neuronal progenitors in the mammalian brain derive from radial glia or specialized astrocytes. In developing neural retina, radial glia-like Müller cells are generated late in neurogenesis and are not considered to be neuronal progenitors, but they do proliferate after injury and can express neuronal markers, suggesting a latent neurogenic capacity. To examine the neurogenic capacity of retinal glial cells, we used lineage tracing in transgenic zebrafish with a glial-specific promoter (gfap, for glial fibrillary acid protein) driving green fluorescent protein in differentiated Müller glia. We found that all Müller glia in the zebrafish retina express low levels of the multipotent progenitor marker Pax6 (paired box gene 6), and they proliferate at a low frequency in the intact, uninjured retina. Müller glia-derived progenitors express Crx (cone rod homeobox) and are late retinal progenitors that generate the rod photoreceptor lineage in the postembryonic retina. These Müller glia-derived progenitors also remain competent to produce earlier neuronal lineages, in that they respond to loss of cone photoreceptors by specifically regenerating the missing neurons. We conclude that zebrafish Müller glia function as multipotent retinal stem cells that generate retinal neurons by homeostatic and regenerative developmental mechanisms.
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?
In the citing paper
“The zebrafish retina is an important model for revealing these mechanisms since the retina is able to mount a robust regenerative response following injury and this response is dependent on the dedifferentiation of Müller glia (MG)”
From HB-EGF is Necessary and Sufficient for Müller Glia Dedifferentiation and Retina Regeneration (2012) · cites this paper as Bernardos et al., 2007
In the citing paper
“Key to successful retina regeneration are Müller glia (MG), the major glial cell-type in the retina (Bernardos et al., 2007; Fausett and Goldman, 2006; Fimbel et al., 2007).”
From Retinal injury, growth factors, and cytokines converge on β-catenin and pStat3 signaling to stimulate retina regeneration (2014) · cites this paper as Bernardos et al., 2007
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
The zebrafish book : a guide for the laboratory use of zebrafish (Danio rerio)
Westerfield, M. (1995) · Medical Entomology and Zoology · Cited by 6,813
Mode of cell migration to the superficial layers of fetal monkey neocortex
Rakic, P. (1972) · Journal of Comparative Neurology · doi:10.1002/cne.901450105 · Cited by 2,170
The cell biology of neurogenesis
Götz, M., & Huttner, W. B. (2005) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1739 · Cited by 2,130
Neurons derived from radial glial cells establish radial units in neocortex
Noctor, S. C., Flint, A. C., Weissman, T. A., Dammerman, R. S., & Kriegstein, A. R. (2001) · Nature · doi:10.1038/35055553 · Cited by 2,016
Müller cells in the healthy and diseased retina
Bringmann, A., Pannicke, T., Grosche, J., Francke, M., Wiedemann, P., Skatchkov, S. N., Osborne, N. N., & Reichenbach, A. (2006) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2006.05.003 · Cited by 1,967
A common progenitor for neurons and glia persists in rat retina late in development
Turner, D. L., & Cepko, C. L. (1987) · Nature · doi:10.1038/328131a0 · Cited by 1,430
Álvarez-Buylla, A., & Lim, D. A. (2004) · Neuron · doi:10.1016/s0896-6273(04)00111-4 · Cited by 1,348
Vertebrate neural cell-fate determination: Lessons from the retina
Livesey, F. J., & Cepko, C. L. (2001) · Nature reviews. Neuroscience · doi:10.1038/35053522 · Cited by 948
Pax6 Is Required for the Multipotent State of Retinal Progenitor Cells
Marquardt, T., Ashery‐Padan, R., Andrejewski, N., Scardigli, R., Guillemot, F., & Gruß, P. (2001) · Cell · doi:10.1016/s0092-8674(01)00295-1 · Cited by 926
Radial Glia Serve as Neuronal Progenitors in All Regions of the Central Nervous System
Anthony, T. E., Klein, C., Fishell, G., & Heintz, N. (2004) · Neuron · doi:10.1016/s0896-6273(04)00140-0 · Cited by 852
Cited by
Sorted by citations
Items 501–600 of 637
Freude, K., Saruhanian, S., McCauley, A., Paterson, C., Odette, M. M., Oostenink, A., Hyttel, P., Gillies, M. C., Haukedal, H., & Kolko, M. (2020) · World Journal of Stem Cells · doi:10.4252/wjsc.v12.i10.1171 · Cited by 3
Incomplete Recovery of Zebrafish Retina Following Cryoinjury
Džulová, D., Lawless, D., Pinton, G., Renner, N. A., & Schorderet, D. F. (2022) · Cells · doi:10.3390/cells11081373 · Cited by 3
Müller Glial Kir4.1 Channel Dysfunction in APOE4 ‐ KI Model of Alzheimer's Disease
Abhyankar, S. D., Xiao, Y., Mahajan, N. S., Luo, Q., Cummins, T., Oblak, A. L., Lamb, B. T., Corson, T. W., & Bhatwadekar, A. D. (2026) · Glia · doi:10.1002/glia.70119 · Cited by 3
Her6 and Prox1a are novel regulators of photoreceptor regeneration in the zebrafish retina
Veen, K., Krylov, A., Yu, S., He, J., Boyd, P., Hyde, D. R., Mantamadiotis, T., Cheng, L. Y., & Jusuf, P. R. (2023) · PLoS Genetics · doi:10.1371/journal.pgen.1011010 · Cited by 3
Stem Cell Based Therapies for Glaucoma
Jayaram, H., Becker, S., & Limb, G. A. (2011) · InTech eBooks · doi:10.5772/21726 · Cited by 3
Cell Death, Apoptosis, and Autophagy in Retinal Injury
Boulton, M. E., Mitter, S. K., Rao, H. V., & Dunn, W. A. (2012) · Elsevier eBooks · doi:10.1016/b978-1-4557-0737-9.00024-2 · Cited by 3
Stulberg, J., & Tropepe, V. (2022) · Methods in molecular biology · doi:10.1007/978-1-0716-1979-7_22 · Cited by 3
Hussein, M. N. A., Cao, X., Elokil, A., & Huang, S. (2019) · Journal of Fish Biology · doi:10.1111/jfb.14189 · Cited by 3
The development of seahorse vision: morphological and behavioural aspects
Lee, H. R. (2014) · ANU Open Research (Australian National University) · doi:10.25911/5d738fcd6306d · Cited by 3
Palazzo, I., Todd, L. J., Hoang, T. V., Reh, T. A., Blackshaw, S., & Fischer, A. J. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.10.05.463152 · Cited by 3
Regeneration of Organs and Appendages in Zebrafish: A Window into Underlying Control Mechanisms
Antos, C. L., & Brand, M. (2010) · Wiley eBooks · doi:10.1002/9780470015902.a0022101 · Cited by 3
The rod synapse in aging wildtype and Dscaml1 mutant mice
Clemons, M. R., Dimico, R. H., Black, C. X., Schlussler, M. K., Camerino, M. J., Aldinger-Gibson, K., Bartle, A., Reynolds, N., Eisenbrandt, D., Rogers, A., et al. (2023) · PLoS ONE · doi:10.1371/journal.pone.0290257 · Cited by 2
Advancements in Müller Glia Reprogramming: Pioneering Approaches for Retinal Neuron Regeneration
Zhou, Y., Qin, S., & Wu, J. (2025) · Neuroglia · doi:10.3390/neuroglia6020020 · Cited by 2
Nguyen, L., Vallejos, C. A., Mill, P., & Megaw, R. D. (2025) · Genes · doi:10.3390/genes16091088 · Cited by 2
Microglia response and function in a chronic model of photoreceptor damage
Raghavan, D., Jeakle, O., Berry, Y., Victor, M., & Thummel, R. (2025) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2025.1699271 · Cited by 2
Babiloni-Chust, I., Donato, L., Sartori, S., Carl, M., Zerti, D., Rinaldi, C., Flati, V., Feligioni, M., D’Angelo, R., Maccarone, R., et al. (2026) · Antioxidants · doi:10.3390/antiox15030348 · Cited by 3
Mitra, S., Devi, S., Lee, M., Sahu, A., Jui, J., Kriukov, E., Baranov, P. Y., & Goldman, D. J. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2535044123 · Cited by 2
Sarusie, M. V., Rönnbäck, C., Jespersgaard, C., Baungaard, S., Ali, Y., Kessel, L., Christensen, S. T., Brøndum‐Nielsen, K., Møllgård, K., Rosenberg, T., et al. (2024) · Human Molecular Genetics · doi:10.1093/hmg/ddae134 · Cited by 2
Konar, G. J., Lingan, A. L., Vallone, K. T., Nguyen, T. D., Flickinger, Z., & Patton, J. G. (2025) · Experimental Eye Research · doi:10.1016/j.exer.2025.110420 · Cited by 2
Genotoxicity Induced by Cypermethrin in the Zebrafish Retina
Paravani, E. V., & Casco, V. H. (2018) · InTech eBooks · doi:10.5772/intechopen.72434 · Cited by 2
Age-related degeneration leads to gliosis but not regeneration in the zebrafish retina
Martins, R. R., Zamzam, M. E., Moosajee, M., Thummel, R., Henriques, C. M., & MacDonald, R. B. (2020) · White Rose Research Online (University of Leeds, The University of Sheffield, University of York) · Cited by 2
New pathways to neurogenesis: Insights from injury‐induced retinal regeneration
Blackshaw, S., Qian, J. X., & Hyde, D. R. (2024) · BioEssays · doi:10.1002/bies.202400133 · Cited by 2
Liu, K., Kang, Z., Yang, M., Chen, F., Xia, M., Dai, W., Zheng, S., Chen, H., Lu, Q. R., Zhou, W., et al. (2024) · Glia · doi:10.1002/glia.24625 · Cited by 2
Marx, M., Lebuhotel, C., Laugier, D., Chapelle, A., Calothy, G., & Saule, S. (2010) · Experimental Eye Research · doi:10.1016/j.exer.2010.03.015 · Cited by 2
Santacroce, M. P. (2014) · Journal of Bioprocessing & Biotechniques · doi:10.4172/2155-9821.1000186 · Cited by 2
Regenerative Medicine for Diseases of the Retina
Lamba, D. A., & Reh, T. A. (2010) · Elsevier eBooks · doi:10.1016/b978-0-12-381422-7.10024-0 · Cited by 2
Rihel, J., & Ghosh, M. (2015) · Springer eBooks · doi:10.1007/978-3-642-27728-3_135-1 · Cited by 2
Neuron-Astroglial Interactions in Cell Fate Commitment in the Central Nervous System
Stipursky, J., Spohr, T. C. L. D. S. E., Romão, L. F., & Gomes, F. C. A. (2009) · Springer eBooks · doi:10.1007/978-90-481-3375-8_11 · Cited by 2
The Function of Stem Cells in Ocular Homeostasis
Riazuddin, S., Khan, S. Y., & Ali, M. (2022) · Springer eBooks · doi:10.1007/978-981-19-2655-6_32 · Cited by 2
The Potential of Stem Cells in Ocular Treatments
Riazuddin, S. A., Khan, S. Y., & Ali, M. (2022) · Springer eBooks · doi:10.1007/978-981-19-2655-6_33 · Cited by 2
Celotto, L., Rost, F., Machate, A., Bläsche, J., Dahl, A., Weber, A., Hans, S., & Brand, M. (2023) · eLife · doi:10.7554/elife.86507.1 · Cited by 2
Ancient origin of the rod bipolar cell pathway in the vertebrate retinaPreprint
Yoshimatsu, T., Hellevik1, A., Mardoum, P., Hahn, J., Kölsch, Y., D’Orazi1, F., Suzuki, S. C., Godinho, L., Lawrence, O. T., Rieke, F. M., et al. (2023) · Research Square · doi:10.21203/rs.3.rs-3411693/v1 · Cited by 2
Tropism of the AAV6.2 Vector in the Murine Retina
Suzuki, R., Katada, Y., Fujii, M., Serizawa, N., Negishi, K., & Kurihara, T. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26041580 · Cited by 1
Rumford, J. E., Farre, A. A., Mai, J., Weimar, H. V., Shelton, C. D., Morales, M. C., & Mitchell, D. M. (2026) · PLoS ONE · doi:10.1371/journal.pone.0344737 · Cited by 1
Yasuda, T., Nakazawa, T., Hirakawa, K., Matsumoto, I., Nagata, K., Mori, S., Igarashi, K., Sagara, H., Oda, S., & Mitani, H. (2023) · International Journal of Radiation Biology · doi:10.1080/09553002.2023.2242932 · Cited by 1
Dicer is essential for proper maturation, composition, and function in the postnatal retina
Kang, S., Larbi, D., Bruns, E., Hahne, K., Khodadadi‐Jamayran, A., Sreenivasaiah, C., Carneiro, M. L., Andrade, M., Batsuuri, K., Chen, S., et al. (2025) · iScience · doi:10.1016/j.isci.2025.113794 · Cited by 1
Microglia maintain retinal redox homeostasis following ablation of rod photoreceptors in zebrafish
Morales, M., & Mitchell, D. M. (2026) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2026.113169 · Cited by 1
Pidishetty, D., Damera, S. K., Murugavel, M., Susaimanickam, P. J., Chittajallu, S. N. S. H., Kushawah, G., Sarkar, P., Bharadwaj, S. R., Mishra, R. K., & Mariappan, I. (2025) · Scientific Reports · doi:10.1038/s41598-025-28951-1 · Cited by 1
Storey, S. S., Hehr, C. L., Standing, S., & McFarlane, S. (2026) · Glia · doi:10.1002/glia.70220 · Cited by 1
Dedifferentiation and Organ Regeneration
Fu, X., Zhao, A., & Hu, T. H. (2018) · Springer eBooks · doi:10.1007/978-3-662-56179-9_10 · Cited by 1
Live Cell Imaging of Dynamic Processes in Adult Zebrafish Retinal Cross-Section Cultures
Lahne, M., & Hyde, D. R. (2023) · Methods in molecular biology · doi:10.1007/978-1-0716-3012-9_20 · Cited by 1
Tochman-Kanty, K., Jasielska, M., & Mackiewicz, J. (2024) · Ophthalmology · doi:10.5114/oku/187930 · Cited by 1
Isolation and Characterization of Extracellular Vesicles to Activate Retina Regeneration
Nelson, H. M., Konar, G. J., & Patton, J. G. (2024) · Methods in molecular biology · doi:10.1007/978-1-0716-4087-6_9 · Cited by 1
Berry, Y., Kramer, A. C., Carthage, J., & Thummel, R. (2025) · Experimental Eye Research · doi:10.1016/j.exer.2025.110532 · Cited by 1
Biomaterials for repair and regeneration of the neural retina
Limb, G. A., Jones, M. F., Eastlake, K., & Becker, S. (2016) · Elsevier eBooks · doi:10.1016/b978-0-08-100147-9.00010-9 · Cited by 1
Sensory Epithelium of the Eye and Ear
Cepko, C. L., & Fekete, D. M. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-409503-8.00014-7 · Cited by 1
Mobilizing Endogenous Stem Cells for Retinal Repair
Yu, H., Talib, M., Vu, T. H. K., Cho, K., Guo, C., & Chen, D. F. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-800548-4.00020-6 · Cited by 1
Eymann, J., & Di‐Poï, N. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00406 · Cited by 1
Chapter 5 - Restoring Vision to the Blind: Endogenous Regeneration
Science, T. L. I. I. F. I. I. V. S. T. L. I. I. F. I. I. V. (2014) · Translational Vision Science & Technology · doi:10.1167/tvst.3.7.7 · Cited by 1
MicroRNAs in the Retina and in Visual Connectivity
Maiorano, N. A., & Hindges, R. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-405544-5.00019-8 · Cited by 1
Zebrafish: Retinal Development and Regeneration
Bailey, T. J., & Hyde, D. R. (2010) · Elsevier eBooks · doi:10.1016/b978-0-12-374203-2.00166-4 · Cited by 1
Editorial: Accessory Cells of Sensory Systems and Their Functional Roles
Ackerman, S. D., Singhvi, A., & Bianchi, L. K. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.965580 · Cited by 1
Shihabeddin, E., Santhanam, A., Tetenborg, S., Aronowitz, A. L., Wei, H., Qin, G., Cai, C., Wu, J., & O’Brien, J. (2025) · eLife · doi:10.7554/elife.105965 · Cited by 1
CERKL, generació d’un model knockout de retinosi pigmentària i estudis funcionals
Garanto, A. (2011) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas) · Cited by 1
Nagashima, M., Awad, S., Jiang, L., Santos, L. R. D. C., Flickinger, Z., Hitchcock, P. F., & Hoang, T. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.03.15.711785 · Cited by 1
Storey, S. S., Hehr, C. L., Standing, S., & McFarlane, S. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.03.22.713558 · Cited by 1
Westphal, M., Branch, R., Docampo-Seara, A., Coşacak, M. İ., Logvinova, E., Bellia, M., Cheng, S., Tsarouchas, T. M., Bretschneider, A., Zoeller, D., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.06.25.734505 · Cited by 1
Sensory Epithelium of the Eye and Ear
Cepko, C. L., & Fekete, D. M. (2009) · Elsevier eBooks · doi:10.1016/b978-0-12-374729-7.00021-4
Animal Models of Inherited Retinal Degenerations
Stone, J., & Heckenlively, J. R. (2009) · Elsevier eBooks · doi:10.1016/b978-008045046-9.00902-5
Molecular Mechanisms of Zebrafish Photoreceptor Regeneration.
Qin, Z. (2010) · Deep Blue (University of Michigan)
Batts, S. A. (2009) · Deep Blue (University of Michigan)
Degeneration and Regeneration in the Vertebrate Retina
Colozza, G., Mazabraud, A., & Perro, M. (2011) · InTech eBooks · doi:10.5772/25843
Flores, A. I. (2015) · Tesis Doctorals en Xarxa (Consorci de Serveis Universitaris de Catalunya)
Polo, A. D. (2009) · Future Neurology · doi:10.2217/fnl.09.45
Development of Methods for Retinal Ganglion Cell Replacement in Glaucoma
Jones, M. F. (2013) · UCL Discovery (University College London)
Mechanisms of Telomere Protection and Deprotection in Human Cells
Sarthy, J. F. (2011) · KU ScholarWorks (The University of Kansas)
A novel role for the «Ostm1» Osteopetrotic gene in neuronal homeostasis
Griffiths, A. (2010) · eScholarship@McGill (McGill) · doi:10.82308/30322
Doh, S. T. (2010) · Rutgers University Community Repository (Rutgers University) · doi:10.7282/t3wd40b9
Retinal Repair Using Stem Cells
Gutierrez, M. A., & Lamba, D. A. (2015) · Springer eBooks · doi:10.1007/978-3-7091-1232-8_15
The Role of Signaling Pathway Integration in Neurogenesis
Ringuette, R. (2016) · uO Research (University of Ottawa) · doi:10.20381/ruor-5369
The role of Diencephalon/Mesencephalon Homeobox 1 (Dmbx1) in Zebrafish Visual System Development
Wong, L. (2013) · TSpace (University of Toronto)
The Role of Stat3 in Mouse Models of Inherited Photoreceptor Degeneration
Jiang, K. (2013) · TSpace (University of Toronto)
Graca, A. B. (2017) · UCL Discovery (University College London)
Characterizing the role of ice1 in maintaining zebrafish neural stem cells
D’Amata, C. (2017) · TSpace (University of Toronto)
The Progress of Research on the WNT/β-Catenin Pathway in Regeneration
谢, 成. (2017) · Advances in Marine Sciences · doi:10.12677/ams.2017.44016
Dedifferentiation and Vision System
Fu, X., Zhao, A., & Hu, T. H. (2018) · Springer eBooks · doi:10.1007/978-3-662-56179-9_7
Chen, D.-W. (2018) · UWSpace (University of Waterloo)
Zebrafish in Biomedical Research
Cleghorn, W. M., & Brockerhoff, S. E. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-812431-4.00021-x · Cited by 1
Inverted Internal Limiting Membrane Flap for Full-Thickness Macular Hole
Nawrocki, J., Nawrocka, Z., & Michalewska, Z. (2020) · Springer eBooks · doi:10.1007/978-981-15-7644-7_19
Sabry, D. A., & El-Badry, D. A. (2020) · Zoologia (Curitiba) · doi:10.3897/zoologia.37.e51603
Saito, Y., Okuyoshi, H., Nakamura, S., Otsu, W., Yamaguchi, A., Hitchcock, P. F., Nagashima, M., Shimazawa, M., & Hara, H. (2020) · BPB Reports · doi:10.1248/bpbreports.3.3_92
Investigating Disease Presentation and Mechanism in RP1L1-Associated Photoreceptor Degeneration
Noel, N. C. L. (2021) · ERA: Education and Research Archive (University of Alberta) · doi:10.7939/r3-6bg3-1e79
The erotics of citizenship: Derek Jarman's Jubilee and Isaac Julien's Young Soul Rebels
Ellis, J. (2001) · The Southern Quarterly
Histologic manifestations of retinal disease
Bruce Grahn DVM, D. A. C. O. V. O. A. T. A. B. O. V. P., Peiffer, R. L., & Wilcock, B. P. (2018) · Wiley eBooks · doi:10.1002/9781119108603.ch12
Magner, E. T., Sandoval-Sanchez, P., Kramer, A. C., Thummel, R., Hitchcock, P. F., & Taylor, S. M. (2021) · Research Square · doi:10.21203/rs.3.rs-465951/v2
Mira, H., Díez del Corral, R., & Morales, A. V. (2020) · Frontiers research topics · doi:10.3389/978-2-88963-988-5
Fain, G. (2018) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.733813829.793550038
Functions of Rx in early vertebrate ocular development
Zamora, B. G. (2009) · doi:10.33915/etd.4554
Sampath, A. P. (2018) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.733813829.793552305
Recent Papers on Zebrafish and Other Aquarium Fish Models
(2007) · Zebrafish · doi:10.1089/zeb.2007.9983
The Potential of Stem Cells in Ocular Treatments
Riazuddin, S. A., Khan, S. Y., & Ali, M. (2022) · Springer eBooks · doi:10.1007/978-981-16-6016-0_33-1
The Function of Stem Cells in Ocular Homeostasis
Riazuddin, S., Khan, S. Y., & Ali, M. (2022) · Springer eBooks · doi:10.1007/978-981-16-6016-0_32-1
Cellular and molecular mechanisms of retinal regeneration in the axolotl salamander
Yandulskaya, A. S. (2022) · Digital Repository Service (Northeastern University) · doi:10.17760/d20439213
Loss of GFAP causes optico-retinal dysplasia and vision impairmentPreprint
Sarusie, M. V., Rönnbäck, C., Jespersgaard, C., Baungaard, S., Ali, Y., Kessel, L., Christensen, S. T., Brøndum‐Nielsen, K., Møllgård, K., Rosenberg, T., et al. (2022) · medRxiv · doi:10.1101/2022.11.09.22282105
Neuro-regeneration and stem-cell therapies
Zhang, J.-X., Wu, S., Jin, Z., & Wang, N. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-88442-6.00006-6
Metadata
- Authors
- Bernardos, R. L., Barthel, L. K., Meyers, J. R., & Raymond, P. A.
- Affiliations
- University of Michigan (US)
- Venue
- Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2007-06-27
- Volume
- 27
- Issue
- 26
- Pages
- 7028-7040
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6672216
- OpenAlex
- W2016508121
- Cited by
- 647
- References
- 60
- Citations by year
- 2026: 28 · 2025: 22 · 2024: 32 · 2023: 40 · 2022: 39 · 2021: 38 · 2020: 38 · 2019: 33 · 2018: 31 · 2017: 27 · 2016: 36 · 2015: 32 · 2014: 33 · 2013: 45 · 2012: 33
- FWCI
- 13.23
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Neuroscience (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health
- National Eye Institute (R01EY004318, F32EY017251)
- National Institute of Neurological Disorders and Stroke (F31NS047909)
- Topics
- Health Sciences › Medicine › Ophthalmology › Retinal Development and Disorders
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Keywords
- Müller cells, retinal stem cells, neuronal precursors, retinal neurogenesis, zebrafish retina, Pax6, CRX, rod photoreceptors, photoreceptor regeneration, glial fibrillary acidic protein, lineage tracing, retinal homeostasis, multipotent progenitors
- MeSH terms
- Aging, Animals, Cell Differentiation, Homeostasis, Neuroglia, Neurons, Regeneration, Retina, Species Specificity, Stem Cells, Zebrafish, Cell Lineage
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