Late-stage neuronal progenitors in the retina are radial Müller glia that function as retinal stem cells

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

For the Long Run

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

Methanol Induced Optic Neuropathy: Molecular Mysteries, Public Health Perspective, Clinical Insights and Treatment Strategies

Sobhi, N., Abdollahi, M., Arman, A., Mahmoodpoor, A., & Jafarizadeh, A. (2024) · Seminars in Ophthalmology · doi:10.1080/08820538.2024.2358310 · Cited by 13

Retinal glia in myopia: current understanding and future directions

Chen, P., Ji, J., Chen, X., Zhang, J., Wen, X., & Liu, L. (2024) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2024.1512988 · Cited by 13

Embryonic Stem Cell-Derived Microvesicles: Could They be Used for Retinal Regeneration?

Farber, D. B., & Katsman, D. (2015) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-17121-0_75 · Cited by 13

Retinal morphology in Astyanax mexicanus during eye degeneration

Emam, A., Yoffe, M., Cardona, H., & Soares, D. (2019) · The Journal of Comparative Neurology · doi:10.1002/cne.24835 · Cited by 13

Loss of Active Neurogenesis in the Adult Shark Retina

Hernández‐Núñez, I., Robledo, D., Mayeur, H., Mazan, S., Sanchez, L. E., Adrio, F., Barreiro‐Iglesias, A., & Candal, E. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.628721 · Cited by 13

Glia Regulate the Development, Function, and Plasticity of the Visual System From Retina to Cortex

Benfey, N. J., Foubert, D., & Ruthazer, E. S. (2022) · Frontiers in Neural Circuits · doi:10.3389/fncir.2022.826664 · Cited by 13

Develop an efficient and specific AAV-based labeling system for Muller glia in mice

Gao, Y., Fang, K., Yan, Z., Zhang, H., Geng, G., Wu, W., Ding, X., Zhang, H., Zhong, N., Wang, Q., et al. (2022) · Scientific Reports · doi:10.1038/s41598-022-27013-0 · Cited by 13

Technical brief: Constant intense light exposure to lesion and initiate regeneration in normally pigmented zebrafish.

Rajaram, K., Summerbell, E. R., & Patton, J. G. (2014) · PubMed Central · Cited by 13

Zebrafish Lbh-like Is Required for Otx2-mediated Photoreceptor Differentiation

Li, W., Zhou, L., Li, Z., Wang, Y., Shi, J.-T., Yang, Y., & Gui, J. (2015) · International Journal of Biological Sciences · doi:10.7150/ijbs.11244 · Cited by 13

Reparative neurogenesis in the brain and changes in the optic nerve of adult trout Oncorhynchus mykiss after mechanical damage of the eye

Pushchina, E. V., Alekseevich, V. A., & Obukhov, D. K. (2016) · Russian Journal of Developmental Biology · doi:10.1134/s1062360416010057 · Cited by 13

microRNA expression in the neural retina: Focus on Müller glia

Quintero, H., & Lamas, M. (2017) · Journal of Neuroscience Research · doi:10.1002/jnr.24181 · Cited by 13

Regeneration of zebrafish retina following toxic injury

Pietra, A. L., Bianchi, A. R., Capriello, T., Mobilio, T., Guagliardi, A., Maio, A. D., & Ferrandino, I. (2024) · Environmental Toxicology and Pharmacology · doi:10.1016/j.etap.2024.104582 · Cited by 12

Age- and cell cycle-related expression patterns of transcription factors and cell cycle regulators in Müller glia

Kato, M., Sudou, N., Nomura-Komoike, K., Iida, T., & Fujieda, H. (2022) · Scientific Reports · doi:10.1038/s41598-022-23855-w · Cited by 12

Eyes on DNA methylation: current evidence for DNA methylation in ocular development and disease

Otteson, D. C. (2011) · Journal of ocular biology, diseases, and informatics · doi:10.1007/s12177-012-9078-x · Cited by 12

The Zebrafish Anillin-eGFP Reporter Marks Late Dividing Retinal Precursors and Stem Cells Entering Neuronal Lineages

Malo, M. C., Duchemin, A., Guglielmi, L., Patzel, E., Sel, S., Auffarth, G. U., Carl, M., & Poggi, L. (2017) · PLoS ONE · doi:10.1371/journal.pone.0170356 · Cited by 13

SMAD7 deficiency stimulates Müller progenitor cell proliferation during the development of the mammalian retina

Kugler, M., Schlecht, A., Fuchshofer, R., Schmitt, S. I., Kleiter, I., Aigner, L., Tamm, E. R., & Braunger, B. M. (2017) · Histochemistry and Cell Biology · doi:10.1007/s00418-017-1549-5 · Cited by 12

An insight on established retinal injury mechanisms and prevalent retinal stem cell activation pathways in vertebrate models

Sherpa, R. D., & Hui, S. P. (2021) · Animal Models and Experimental Medicine · doi:10.1002/ame2.12177 · Cited by 12

Effects of the isoflavone genistein in early life stages of the Senegalese sole, Solea senegalensis: role of the Survivin and proliferation versus apoptosis pathways

Sarasquete, C., Úbeda-Manzanaro, M., & Ortiz-Delgado, J. B. (2018) · BMC Veterinary Research · doi:10.1186/s12917-018-1333-3 · Cited by 12

Single-cell RNA-seq analysis maps the development of human fetal retinaPreprint

Lu, Y., Yi, W., Wu, Q., Zhong, S., Zuo, Z., Zhao, F., Zhang, M., Tsai, N. Y., Zhuo, Y., He, S., et al. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/423830 · Cited by 12

Polarized RPE Secretome Preserves Photoreceptors in Retinal Dystrophic RCS Rats

Ahluwalia, K., Martínez-Camarillo, J.-C., Thomas, B. B., Naik, A. A., Gonzalez-Calle, A., Pollalis, D., LEBKOWSKI, J. S., Lee, S. Y., Mitra, D., Louie, S. G., et al. (2023) · Cells · doi:10.3390/cells12131689 · Cited by 11

Spatiotemporal Pattern of Doublecortin Expression in the Retina of the Sea Lamprey

Fernández‐López, B., Romaus‐Sanjurjo, D., Senra-Martínez, P., Anadón, R., Barreiro‐Iglesias, A., & Rodicio, M. C. (2016) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2016.00005 · Cited by 11

Stem Cells for Retinal Repair

Stern, J. H., & Temple, S. (2014) · Developments in ophthalmology · doi:10.1159/000357328 · Cited by 11

The Lineage Before Time: Circadian and Nonclassical Clock Influences on Development

Bedont, J. L., Iascone, D. M., & Sehgal, A. (2020) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-100818-125454 · Cited by 11

Cell-cell interaction in the pathogenesis of inherited retinal diseases

Du, X., Butler, A. G., & Chen, H. Y. (2024) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2024.1332944 · Cited by 12

Microarray-Based Gene Profiling Analysis of Müller Glia-Derived Retinal Stem Cells in Light-Damaged Retinas from Adult Zebrafish

Qin, Z., & Raymond, P. A. (2012) · Methods in molecular biology · doi:10.1007/978-1-61779-848-1_18 · Cited by 11

Neurogenesis

Chapouton, P., & Godinho, L. (2010) · Methods in cell biology · doi:10.1016/b978-0-12-384892-5.00004-9 · Cited by 11

Class I histone deacetylases in retinal progenitors and differentiating ganglion cells

Saha, A., Tiwari, S., Dharmarajan, S., Otteson, D. C., & Belecky‐Adams, T. L. (2018) · Gene Expression Patterns · doi:10.1016/j.gep.2018.08.007 · Cited by 11

Deconstructing Neurogenesis, Transplantation and Genome-Editing as Neural Repair Strategies in Brain Disease

Chohan, M. O. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00116 · Cited by 11

Induction of a proliferative response in the zebrafish retina by injection of extracellular vesicles

Didiano, D., Abner, J. J., Hinger, S. A., Flickinger, Z., Kent, M. R., Clement, M. A., Balaiya, S., Liu, Q., Dai, X., Levine, E. M., et al. (2020) · Experimental Eye Research · doi:10.1016/j.exer.2020.108254 · Cited by 11

Brief Report: Rx1 Defines Retinal Precursor Identity by Repressing Alternative Fates Through the Activation of TLE2 and Hes4

Giannaccini, M., Giudetti, G., Biasci, D., Mariotti, S., Martini, D., Barsacchi, G., & Andreazzoli, M. (2013) · Stem Cells · doi:10.1002/stem.1530 · Cited by 11

Antiviral Drug Ganciclovir Is a Potent Inhibitor of the Proliferation of Müller Glia–Derived Progenitors During Zebrafish Retinal Regeneration

Zhang, S., Mu, Z., He, C., Zhou, M., Liu, D., Zhao, X., Goldman, D. J., & Xu, H. (2016) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.15-18669 · Cited by 11

Directed robust generation of functional retinal ganglion cells from Müller gliaPreprint

Xiao, D., Qiu, S., Huang, X., Zhang, R., Lei, Q., Huang, W., Chen, H., Gou, B., Tie, X., Liu, S., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/735357 · Cited by 11

Restoration of cone-circuit functionality in the regenerating adult zebrafish retina

Abraham, E., Hartmann, H., Yoshimatsu, T., Baden, T., & Brand, M. (2024) · Developmental Cell · doi:10.1016/j.devcel.2024.07.005 · Cited by 10

Forced MyD88 signaling in microglia impacts the production and survival of regenerated retinal neurons

Rumford, J. E., Grieshaber, A., Lewiston, S., Reed, J. L., Long, S. S., & Mitchell, D. M. (2024) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2024.1495586 · Cited by 10

Photobiomodulation therapy activates YAP and triggers proliferation and dedifferentiation of Müller glia in mammalian retina

Kim, S., Song, M.-J., Kim, I., Park, T. K., & Lyu, J. (2023) · BMB Reports · doi:10.5483/bmbrep.2023-0059 · Cited by 10

Intrinsic and Induced Neuronal Regeneration in the Mammalian Retina

Woodworth, M. B., Greig, L. C., & Goldberg, J. L. (2023) · Antioxidants and Redox Signaling · doi:10.1089/ars.2023.0309 · Cited by 10

ID factors regulate the ability of Müller glia to become proliferating neurogenic progenitor‐like cells

Taylor, O. B., Patel, S. P., Hawthorn, E. C., El‐Hodiri, H. M., & Fischer, A. J. (2024) · Glia · doi:10.1002/glia.24523 · Cited by 10

Live-cell imaging: new avenues to investigate retinal regeneration

Hyde, D. R., & Lahne, M. (2017) · Neural Regeneration Research · doi:10.4103/1673-5374.213533 · Cited by 10

Endogenous Cell Sources for Eye Retina Regeneration in Vertebrate Animals and Humans

Grigoryan, E. N. (2018) · Russian Journal of Developmental Biology · doi:10.1134/s106236041901003x · Cited by 10

Human adult retinal pigment epithelial cells as potential cell source for retina recovery

Kuznetsova, A. V., Grigoryan, E. N., & Aleksandrova, M. A. (2011) · Cell and Tissue Biology · doi:10.1134/s1990519x11050075 · Cited by 10

Isolation and characterisation of neural progenitor cells from the adult Chx10orJ/orJ central neural retina

Kokkinopoulos, I., Pearson, R. A., MacNeil, A., Dhomen, N. S., MacLaren, R. E., Ali, R. R., & Sowden, J. C. (2008) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2008.03.008 · Cited by 10

Midkine expression is regulated by the circadian clock in the retina of the zebrafish

Calinescu, A., Raymond, P. A., & Hitchcock, P. F. (2009) · Visual Neuroscience · doi:10.1017/s0952523809990204 · Cited by 10

Müller Glia Cells Activation in Rat Retina After Optic Nerve Injury: Spatiotemporal Correlation with Transcription Initiation Factor IIB

Xu, Y., Chen, C., Jin, N., Zhu, J., Kang, L., Zhou, T., Wang, J., Sheng, A., Shi, J., Gu, Z., et al. (2013) · Journal of Molecular Neuroscience · doi:10.1007/s12031-012-9941-z · Cited by 9

Differential distribution of steroid hormone signaling networks in the human choroid-retinal pigment epithelial complex

Galindez, S. M., Keightley, A., & Koulen, P. (2022) · BMC Ophthalmology · doi:10.1186/s12886-022-02585-7 · Cited by 9

Epigenetic mechanisms of Müller glial reprogramming mediating retinal regeneration

Si, T., Li, Z., Zhang, J., Su, S., Liu, Y., Chen, S., Peng, G.-H., Cao, J., & Zang, W. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1157893 · Cited by 9

Mycb and Mych stimulate Müller glial cell reprogramming and proliferation in the uninjured and injured zebrafish retina

Lee, M., Jui, J., Sahu, A., & Goldman, D. J. (2024) · Development · doi:10.1242/dev.203062 · Cited by 9

New concepts for reconstruction of retinal and pigment epithelial tissues

Layer, P. G., Araki, M., & Vogel‐Höpker, A. (2010) · Expert Review of Ophthalmology · doi:10.1586/eop.10.42 · Cited by 9

Photo-regulation of rod precursor cell proliferation

Lahne, M., Piekos, S. N., O'Neill, J., Ackerman, K. M., & Hyde, D. R. (2018) · Experimental Eye Research · doi:10.1016/j.exer.2018.09.015 · Cited by 9

Hagfish to Illuminate the Developmental and Evolutionary Origins of the Vertebrate Retina

Bradshaw, S. N., & Allison, W. T. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.822358 · Cited by 8

Characteristics of Whale Müller Glia in Primary and Immortalized Cultures

Pereiro, X., Beriain, S., Rodriguez, L., Roiz‐Valle, D., Ruzafa, N., & Vecino, E. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.854278 · Cited by 8

Transcriptomics of CD29+/CD44+ cells isolated from hPSC retinal organoids reveals a single cell population with retinal progenitor and Müller glia characteristics

Eastlake, K., Luis, J., Wang, W., Lamb, W. D. B., Khaw, P. T., & Limb, G. A. (2023) · Scientific Reports · doi:10.1038/s41598-023-32058-w · Cited by 8

Characterization of Macroglia Response during Tissue Repair in a Laser-Induced Model of Retinal Degeneration

Jahnke, L., Zandi, S., Elhelbawi, A., Conedera, F. M., & Enzmann, V. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24119172 · Cited by 8

Plasticity of cell proliferation in the retina of Austrolebias charrua fish under light and darkness conditions

Berrosteguieta, I., Rosillo, J. C., Herrera, M., Olivera‐Bravo, S., Casanova, G., Herranz‐Pérez, V., García‐Verdugo, J. M., & Fernández, A. S. (2022) · Current Research in Neurobiology · doi:10.1016/j.crneur.2022.100042 · Cited by 8

Talkin’ about my (re)generation: The who of intrinsic retinal stem cells

Otteson, D. C. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.01.022 · Cited by 8

bFGF and insulin lead to migration of Müller glia to photoreceptor layer in rd1 mouse retina

Goel, M., & Dhingra, N. K. (2021) · Neuroscience Letters · doi:10.1016/j.neulet.2021.135936 · Cited by 8

Effects of different light conditions on the retinal microstructure and ultrastructure of Dicentrarchus labrax larvae

Yan, H., Liu, Q., Shen, X., Liu, W., Cui, X., Hu, P., Yuan, Z., Zhang, L., Song, C., Liu, L., et al. (2019) · Fish Physiology and Biochemistry · doi:10.1007/s10695-019-00735-1 · Cited by 7

Galectins and their involvement in ocular disease and development

Luis, J., Eastlake, K., Khaw, P. T., & Limb, G. A. (2020) · Experimental Eye Research · doi:10.1016/j.exer.2020.108120 · Cited by 7

Brd activity regulates Müller glia‐dependent retinal regeneration in zebrafish

Lee, J., Lee, B., & Gross, J. M. (2023) · Glia · doi:10.1002/glia.24457 · Cited by 7

Zebrafish

Rihel, J., & Ghosh, M. (2015) · Springer eBooks · doi:10.1007/978-3-319-05392-9_135 · Cited by 8

CD45 in ocular tissues during larval and juvenile stages and early stages of V. anguillarum infection in young lumpfish (Cyclopterus lumpus)

Gendron, R. L., Hyde, T., Paradis, H., Cao, T., Machimbirike, V. I., Segovia, C., Vásquez, I., Ghasemieshkaftaki, M., Scapigliati, G., Boyce, D., et al. (2022) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2022.08.023 · Cited by 7

Effects of retinoic acid exposure during zebrafish retinogenesis

Carreño, H., Santos‐Ledo, A., Velasco, A., Lara, J. M., Aijón, J., & Arévalo, R. (2013) · Neurotoxicology and Teratology · doi:10.1016/j.ntt.2013.06.001 · Cited by 7

Müller Glia, Vision-Guided Ocular Growth, Retinal Stem Cells, and a Little Serendipity

Fischer, A. J. (2011) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.11-8330 · Cited by 7

Culture of Adult Transgenic Zebrafish Retinal Explants for Live-cell Imaging by Multiphoton Microscopy

Lahne, M., Gorsuch, R. A., Nelson, C. M., & Hyde, D. R. (2017) · Journal of Visualized Experiments · doi:10.3791/55335 · Cited by 7

Preparing a Single Cell Suspension from Zebrafish Retinal Tissue for Flow Cytometric Cell Sorting of Müller Glia

Allan, K. M., DiCicco, R. M., Ramos, M. S., Asosingh, K., & Yuan, A. (2019) · Cytometry Part A · doi:10.1002/cyto.a.23936 · Cited by 7

Regeneration of Organs and Appendages in Zebrafish: A Window into Underlying Control Mechanisms

Antos, C. L., Knopf, F., & Brand, M. (2016) · Wiley eBooks · doi:10.1002/9780470015902.a0022101.pub2 · Cited by 7

Retinal Structure of Poecilia sphenops: Photoreceptor Mosaics, Synaptic Ribbon Patterns, and Glial Cell Expressions

Mokhtar, D. M., Albano, M., Alonaizan, R., & Attaai, A. (2024) · Animals · doi:10.3390/ani14060939 · Cited by 6

MSC exosomes and MSC exosomes loaded with LncRNA H19 as nanotherapeutics regulate the neurogenetic potential of Müller Glial Cells in dry age-related macular degeneration

Tang, Y., Cheng, C., Ding, R., Qian, J., Liu, M., Guo, Y., & Li, Q. (2025) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2025.02.039 · Cited by 6

Generating Widespread and Scalable Retinal Lesions in Adult Zebrafish by Intraocular Injection of Ouabain

Mitchell, D. M., & Stenkamp, D. L. (2023) · Methods in molecular biology · doi:10.1007/978-1-0716-3012-9_12 · Cited by 6

PCNA Staining of Retinal Cryosections to Assess Microglial/Macrophage Proliferation

Lovel, A. G., & Mitchell, D. M. (2023) · Methods in molecular biology · doi:10.1007/978-1-0716-3012-9_21 · Cited by 6

The Regenerative Potential of the Vertebrate Retina: Lessons from the Zebrafish

Jeremy, N., Currie, P. D., & Jusuf, P. R. (2014) · Stem cell biology and regenerative medicine · doi:10.1007/978-1-4939-0787-8_3 · Cited by 7

Zebrafish Photoreceptor Degeneration and Regeneration Research to Understand Hereditary Human Blindness

Iribarne, M. (2019) · IntechOpen eBooks · doi:10.5772/intechopen.88758 · Cited by 6

Differential Responses of Neural Retina Progenitor Populations to Chronic Hyperglycemia

Schmitner, N., Recheis, C., Thönig, J., & Kimmel, R. A. (2021) · Cells · doi:10.3390/cells10113265 · Cited by 7

Bioinformatic analysis and functional predictions of selected regeneration-associated transcripts expressed by zebrafish microglia

Salia, O. I., & Mitchell, D. M. (2020) · BMC Genomics · doi:10.1186/s12864-020-07273-8 · Cited by 6

Reprogramming and Stemness

Laplane, L. (2015) · Perspectives in biology and medicine · doi:10.1353/pbm.2015.0022 · Cited by 6

Gliotic Response and Reprogramming Potential of Human Müller Cell Line MIO-M1 Exposed to High Glucose and Glucose Fluctuations

Russo, B., D’Addato, G., Salvatore, G., Menduni, M., Frontoni, S., Carbone, L., Camaioni, A., Klinger, F. G., Felici, M. D., Picconi, F., et al. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252312877 · Cited by 5

The regeneration-responsive element careg monitors activation of Müller glia after MNU-induced damage of photoreceptors in the zebrafish retina

Bise, T., Pfefferli, C., Bonvin, M., Taylor, L., Lischer, H. E. L., Bruggmann, R., & Jaźwińska, A. (2023) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2023.1160707 · Cited by 5

Methylmercury-induced visual deficits involve loss of GABAergic cells in the zebrafish embryo retina

Wang, J., Guo, S., & Yang, L. (2025) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2024.178329 · Cited by 5

Chemical Genetics and Regeneration

Sengupta, S., Zhang, L., & Mumm, J. S. (2015) · Future Medicinal Chemistry · doi:10.4155/fmc.15.137 · Cited by 5

Multipotent stem cell-derived retinal ganglion cells in 3D culture as tools for neurotrophic factor gene delivery system development

Chen, D.-W., Narsineni, L., & Földvári, M. (2019) · Nanomedicine Nanotechnology Biology and Medicine · doi:10.1016/j.nano.2019.102045 · Cited by 5

Retinal Stem Cells

Debbio, C. B. D., Parameswaran, S., Das, A. V., & Ahmad, I. (2012) · Springer eBooks · doi:10.1007/978-1-4614-3801-4_9 · Cited by 5

Nanoplastics amplify 6PPD ocular toxicity in zebrafish

Lin, J., Pan, D., Chen, X., Xu, M., Zhu, Y., Zheng, Y., Song, Y., & Chen, J. (2026) · Environmental Science and Ecotechnology · doi:10.1016/j.ese.2026.100657 · Cited by 4

Applying Protein–Protein Interactions and Complex Networks to Identify Novel Genes in Retinitis Pigmentosa Pathogenesis

Yoon, S.-B., Ma, Y.-C., Venkat, A., Liu, C.-Y., & Zheng, J. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23073962 · Cited by 4

Müller glia in short-term dark adaptation of the Austrolebias charrua retina: Cell proliferation and cytoarchitecture

Herrera-Astorga, L., Silva-Jaureguiberry, S., Berrosteguieta, I., Rosillo, J. C., & Fernández, A. S. (2024) · Experimental Cell Research · doi:10.1016/j.yexcr.2024.114394 · Cited by 4

Notch Is Required for Neural Progenitor Proliferation During Embryonic Eye Regrowth

Guerin, D. J., Gutierrez, B., Zhang, B., & Tseng, K. A.-S. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26062637 · Cited by 4

The neuroimmune interface in retinal regeneration

Bhattacharya, S., Deka, J., Avallone, T., & Todd, L. J. (2025) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2025.101361 · Cited by 4

Innate Immune Pathways Regulating Retinal Cell Development and Regeneration

Ghena, N., López, N. N., Roberts, J. M., Bosco, A., & Vetter, M. L. (2025) · Annual Review of Vision Science · doi:10.1146/annurev-vision-102122-110045 · Cited by 4

Müller glial and microglial responses coupled to recovery of cone photoreceptors following limited cone ablation in zebrafish retina

Weimar, H. V., Farre, A. A., Rumford, J. E., & Mitchell, D. M. (2026) · Scientific Reports · doi:10.1038/s41598-026-40141-1 · Cited by 4

Rod precursors in the adult retina of the Austrolebias charrua annual fish

Herrera, M., Silva, S., Berrosteguieta, I., Casanova, G., Rosillo, J. C., & Fernández, A. S. (2023) · Tissue and Cell · doi:10.1016/j.tice.2023.102150 · Cited by 4

A comparative analysis of gene and protein expression in chronic and acute models of photoreceptor degeneration in adult zebrafish

Kramer, A. C., Carthage, J., Berry, Y., Gurdziel, K., Cook, T. A., & Thummel, R. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1233269 · Cited by 4

Damage-Induced Senescent Immune Cells Regulate Regeneration of the Zebrafish Retina

Patton, J. G., Konar, G. J., Flickinger, Z., Sharma, S., Vallone, K. T., Lyon, C. E., Doshier, C., Lingan, A. L., & Lyon, W. (2024) · doi:10.59368/agingbio.20240021 · Cited by 4

Derivation and Characterization of Murine and Amphibian Müller Glia Cell Lines

Gallo, R. A., Qureshi, F. M., Strong, T. A., Lang, S. H., Pino, K. A., Dvoriantchikova, G., & Pelaez, D. (2022) · Translational Vision Science & Technology · doi:10.1167/tvst.11.4.4 · Cited by 4

Protein phosphatases regulate the formation of Müller glia-derived progenitor cells in the chick retina

Kelly, L. E., El‐Hodiri, H. M., Crider, A., & Fischer, A. J. (2024) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2024.103932 · Cited by 4

The Newt as a Model for Eye Regeneration

Roddy, M., & Tsonis, P. A. (2008) · Elsevier eBooks · doi:10.1016/b978-0-12-374169-1.00007-2 · Cited by 4

Ectopic Proliferation Contributes to Retinal Dysplasia in the Juvenile Zebrafish patched2 Mutant Eye

Bibliowicz, J., & Gross, J. M. (2011) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.11-8033 · Cited by 4

Retinal neural progenitors express topographic map markers

Goolsby, J. E., Atamas, M., Rollor, S. R., Asanuma, D., Schuh, R. A., Makar, T. K., Fishman, P. S., Bever, C. T., & Trisler, D. N. (2012) · Neurochemistry International · doi:10.1016/j.neuint.2012.02.010 · Cited by 4

Photoreceptor ablation following ATP induced injury triggers Müller glia driven regeneration in zebrafish

Brandli, A. A., Dudczig, S., Currie, P. D., & Jusuf, P. R. (2021) · Experimental Eye Research · doi:10.1016/j.exer.2021.108569 · Cited by 3

Assessing Rewiring of the Retinal Circuitry by Electroretinogram (ERG) After Inner Retinal Lesion in Adult Zebrafish

Barrett, L. M., Meighan, P. C., Mitchell, D. M., Varnum, M. D., & Stenkamp, D. L. (2023) · Methods in molecular biology · doi:10.1007/978-1-0716-3012-9_23 · Cited by 3

III-2 : LA NEURORETINE : ASPECTS FONCTIONNELS

Rigaudière, F., & Gargasson, J. L. (2012) · Rigaudiere(Florence) eBooks · doi:10.4267/oeiletphysiologiedelavision.215 · Cited by 3

Promotion on the differentiation of retinal Müller cells into retinal ganglion cells by Brn-3b

Wu, Z., Cao, L., Zhang, X., Song, W., & Xia, X. (2016) · International Journal of Ophthalmology · doi:10.18240/ijo.2016.07.03 · Cited by 3

β-SNAP activity in the outer segment growth period is critical for preventing BNip1-dependent apoptosis in zebrafish photoreceptors

Nishiwaki, Y., & Masai, I. (2020) · Scientific Reports · doi:10.1038/s41598-020-74360-x · Cited by 3

Müller glia: Stem cells for generation and regeneration of retinal neurons in teleost fish

Lenkowski, J. R., & Raymond, P. A. (2014) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2013.12.007 · Cited by 333

Characterization of Müller glia and neuronal progenitors during adult zebrafish retinal regeneration

Thummel, R., Kassen, S. C., Enright, J. M., Nelson, C. M., Montgomery, J. E., & Hyde, D. R. (2008) · Experimental Eye Research · doi:10.1016/j.exer.2008.07.009 · Cited by 203

Müller glial cells induce stem cell properties in retinal progenitors in vitro and promote their further differentiation into photoreceptors

Simón, M. V., Genaro, P. D., Abrahan, C. E., Santos, B. D. L., Rotstein, N. P., & Politi, L. E. (2011) · Journal of Neuroscience Research · doi:10.1002/jnr.22747 · Cited by 14

Zebrafish Müller glia-derived progenitors are multipotent, exhibit proliferative biases and regenerate excess neurons

Powell, C., Cornblath, E. J., Elsaeidi, F., Wan, J., & Goldman, D. J. (2016) · Scientific Reports · doi:10.1038/srep24851 · Cited by 122

Deciphering the transcriptional states of Müller glia and their progeny in the regenerating zebrafish retina

Celotto, L. (2022) · Qucosa (Saxon State and University Library Dresden)