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

Acute retinal injury and the relationship between nerve growth factor, Notch1 transcription and short-lived dedifferentiation transient changes of mammalian Müller cells

Jian, Q., Tao, Z., Li, Y., & Yin, Z. Q. (2015) · Vision Research · doi:10.1016/j.visres.2015.01.030 · Cited by 24

Tracking the fate of her4 expressing cells in the regenerating retina using her4:Kaede zebrafish

Wilson, S. G., Wen, W., Pillai‐Kastoori, L., & Morris, A. C. (2015) · Experimental Eye Research · doi:10.1016/j.exer.2015.11.002 · Cited by 24

Müller stem cell dependent retinal regeneration

Chohan, A., Singh, U., Kumar, A., & Kaur, J. (2016) · Clinica Chimica Acta · doi:10.1016/j.cca.2016.11.030 · Cited by 25

Development and epigenetic plasticity of murine Müller glia

Dvoriantchikova, G., Seemungal, R. J., & Ivanov, D. (2019) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2019.06.019 · Cited by 25

Injury-induced Cavl-expressing cells at lesion rostral side play major roles in spinal cord regeneration

Zeng, C., Kamei, Y., Shigenobu, S., Sheu, J., & Tsai, H. (2021) · Open Biology · doi:10.1098/rsob.200304 · Cited by 24

Light-Induced Photoreceptor Degeneration in the Retina of the Zebrafish

Taylor, S. M., Chen, J., Luo, J., & Hitchcock, P. F. (2012) · Methods in molecular biology · doi:10.1007/978-1-61779-848-1_17 · Cited by 24

Retinal Stem Cell ‘Retirement Plans’: Growth, Regulation and Species Adaptations in the Retinal Ciliary Marginal Zone

Miles, A., & Tropepe, V. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22126528 · Cited by 26

Heparin-binding epidermal growth factor and fibroblast growth factor 2 rescue Müller glia-derived progenitor cell formation in microglia- and macrophage-ablated chick retinas

El‐Hodiri, H. M., Bentley, J. R., Reske, A., Taylor, O. B., Palazzo, I., Campbell, W. A., Halloy, N. R., & Fischer, A. J. (2023) · Development · doi:10.1242/dev.202070 · Cited by 23

Müller glia express rhodopsin in a mouse model of inherited retinal degeneration

Goel, M., & Dhingra, N. K. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.08.066 · Cited by 23

Ontogenic retinal changes in three ecologically distinct elopomorph fishes (Elopomorpha:Teleostei) correlate with light environment and behavior

Taylor, S. M., Loew, E. R., & Grace, M. S. (2015) · Visual Neuroscience · doi:10.1017/s0952523815000024 · Cited by 23

Rewiring the Regenerated Zebrafish Retina: Reemergence of Bipolar Neurons and Cone-Bipolar Circuitry Following an Inner Retinal Lesion

McGinn, T. E., Galicia, C., Leoni, D. C., Partington, N., Mitchell, D. M., & Stenkamp, D. L. (2019) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2019.00095 · Cited by 23

Longitudinal fluorescent observation of retinal degeneration and regeneration in zebrafish using fundus lens imaging.

DuVal, M. G., Chung, H., Lehmann, O. J., & Allison, W. T. (2013) · Europe PMC (PubMed Central) · Cited by 22

Mesenchymal stem cell‐conditioned medium attenuates the retinal pathology in amyloid‐β‐induced rat model of Alzheimer's disease: Underlying mechanisms

Kuo, S., Chio, C., Yeh, C., Ma, J., Liu, W., Lin, M., Lin, K., & Chang, C. (2021) · Aging Cell · doi:10.1111/acel.13340 · Cited by 22

Developing and adult reef fish show rapid light‐induced plasticity in their visual system

Fogg, L. G., Cortesi, F., Gache, C., Lecchini, D., Marshall, N. J., & de Busserolles, F. (2022) · Molecular Ecology · doi:10.1111/mec.16744 · Cited by 23

Correlation between photoreceptor injury-regeneration and behavior in a zebrafish model

Tang, X., Li, Y., Wang, Y., Cai, S., Cui, J., & Chen, Y. (2017) · Neural Regeneration Research · doi:10.4103/1673-5374.206651 · Cited by 22

Nestin expressing progenitor cells during establishment of the neural retina and its vasculature

Lee, J., Park, H.-S., Shin, J. M., Chun, M., & Oh, S.-J. (2012) · Anatomy & Cell Biology · doi:10.5115/acb.2012.45.1.38 · Cited by 22

Müller Glia as a Source of Neuronal Progenitor Cells to Regenerate the Damaged Zebrafish Retina

Nelson, C. M., & Hyde, D. R. (2011) · Advances in experimental medicine and biology · doi:10.1007/978-1-4614-0631-0_54 · Cited by 21

De novo neurogenesis by targeted expression of Atoh7 to Müller glia cells

Lust, K., Sinn, R., Saturnino, A. P., Centanin, L., & Wittbrodt, J. (2016) · Development · doi:10.1242/dev.135905 · Cited by 21

Using neurogenin to Reprogram Chick RPE to Produce Photoreceptor-like Neurons

Li, X., Ma, W., Zhuo, Y., Yan, R., & Wang, S. (2010) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.09-3822 · Cited by 21

Cell lineage tracing in the retina: Could material transfer distort conclusions?

Boudreau‐Pinsonneault, C., & Cayouette, M. (2017) · Developmental Dynamics · doi:10.1002/dvdy.24535 · Cited by 21

Fate bias during neural regeneration adjusts dynamically without recapitulating developmental fate progression

Kei, J. N. C., Currie, P. D., & Jusuf, P. R. (2017) · Neural Development · doi:10.1186/s13064-017-0089-y · Cited by 21

Nrl Is Dispensable for Specification of Rod Photoreceptors in Adult Zebrafish Despite Its Deeply Conserved Requirement Earlier in Ontogeny

Oel, A. P., Neil, G. J., Dong, E. M., Balay, S. D., Collett, K., & Allison, W. T. (2020) · iScience · doi:10.1016/j.isci.2020.101805 · Cited by 21

Retinal Stem/Progenitor Cells Derived From Adult Müller Glia for the Treatment of Retinal Degeneration

Too, L. K., & Simunovic, M. P. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.749131 · Cited by 21

A Comparative Analysis of Gene and Protein Expression Throughout a Full 28-Day Retinal Regeneration Time-Course in Adult Zebrafish

Kramer, A. C., Gurdziel, K., & Thummel, R. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.741514 · Cited by 21

Retinal Stem Cells and Regeneration of Vision System

Yip, H. K.-F. (2013) · The Anatomical Record · doi:10.1002/ar.22800 · Cited by 21

Retinal proliferation response in the buphthalmic zebrafish, bugeye

Lama-Sherpa, T. D., Hunter, S. S., Frey, R. A., Robison, B. D., & Stenkamp, D. L. (2011) · Experimental Eye Research · doi:10.1016/j.exer.2011.06.001 · Cited by 21

6PPD and 6PPDQ embryonic exposure induced distinct developmental neurotoxicity in zebrafish

Yang, L., Lu, X., Pan, D., Zhang, Y., Zheng, Y., He, M., Yang, B., Sun, D., Li, Q., Lin, J., et al. (2025) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2025.118456 · Cited by 20

Granulin 1 Promotes Retinal Regeneration in Zebrafish

Tsuruma, K., Saito, Y., Okuyoshi, H., Yamaguchi, A., Shimazawa, M., Goldman, D. J., & Hara, H. (2018) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.18-24828 · Cited by 20

Pax2 is expressed in a subpopulation of Müller cells in the central chick retina

Boije, H., Ring, H., López‐Gallardo, M., Prada, C., & Hallböök, F. (2010) · Developmental Dynamics · doi:10.1002/dvdy.22309 · Cited by 20

Expression of a 12-kb promoter element derived from the zebrafish enolase-2 gene in the zebrafish visual system

Bai, Q., Wei, X., & Burton, E. A. (2008) · Neuroscience Letters · doi:10.1016/j.neulet.2008.10.101 · Cited by 20

Immunohistochemical localization of mitochondrial fatty acid β-oxidation enzymes in Müller cells of the retina

Atsuzawa, K., Nakazawa, A., Mizutani, K., Fukasawa, M., Yamamoto, N., Hashimoto, T., & Usuda, N. (2010) · Histochemistry and Cell Biology · doi:10.1007/s00418-010-0752-4 · Cited by 20

Restoring vision and rebuilding the retina by Müller glial cell reprogramming

Agarwal, D., Do, H., Mazo, K. W., Chopra, M., & Wahlin, K. J. (2022) · Stem Cell Research · doi:10.1016/j.scr.2022.103006 · Cited by 19

Chromatin access regulates the formation of Müller glia‐derived progenitor cells in the retina

Campbell, W. A., El‐Hodiri, H. M., Torres, D., Hawthorn, E. C., Kelly, L. E., Volkov, L. I., Akanonu, D., & Fischer, A. J. (2023) · Glia · doi:10.1002/glia.24366 · Cited by 19

Müller Glial Cell–Dependent Regeneration of the Retina in Zebrafish and Mice

Jui, J., & Goldman, D. J. (2024) · Annual Review of Genetics · doi:10.1146/annurev-genet-111523-102000 · Cited by 19

Genesis of rods in the zebrafish retina occurs in a microenvironment provided by polysialic acid‐expressing Müller glia

Kustermann, S., Hildebrandt, H., Bolz, S., Dengler, K., & Köhler, K. (2009) · The Journal of Comparative Neurology · doi:10.1002/cne.22232 · Cited by 19

Proteome of brain glia: The molecular basis of diverse glial phenotypes

Jha, M. K., Kim, J., & Suk, K. (2013) · PROTEOMICS · doi:10.1002/pmic.201300236 · Cited by 19

A Novel Light Damage Paradigm for Use in Retinal Regeneration Studies in Adult Zebrafish

Thomas, J. L., & Thummel, R. (2013) · Journal of Visualized Experiments · doi:10.3791/51017 · Cited by 19

Hydroquinone induces oxidative and mitochondrial damage to human retinal Müller cells (MIO-M1)

Ramírez, C., Pham, K., Estrago-Franco, M. F., Chwa, M., Limb, G. A., Kuppermann, B. D., & Kenney, M. C. (2013) · NeuroToxicology · doi:10.1016/j.neuro.2013.08.004 · Cited by 19

Retinal stem cells and potential cell transplantation treatments

Lin, T., Hsu, C., Chien, K., Hung, K.-H., Peng, C., & Chen, S. (2014) · Journal of the Chinese Medical Association · doi:10.1016/j.jcma.2014.08.001 · Cited by 20

Heterogeneity in quiescent Müller glia in the uninjured zebrafish retina drive differential responses following photoreceptor ablation

Krylov, A., Yu, S., Veen, K., Newton, A. H., Ye, A., Qin, H., He, J., & Jusuf, P. R. (2023) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2023.1087136 · Cited by 19

GABA-mediated induction of early neuronal markers expression in postnatal rat progenitor cells in culture

Ramı́rez, M., Hernández-Montoya, J., Sánchez-Serrano, S. L., Ordaz, B., Ferraro, S., Quintero, H., Peña‐Ortega, F., & Lamas, M. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.08.044 · Cited by 19

Extensive growth is followed by neurodegenerative pathology in the continuously expanding adult zebrafish retina

houcke, J. V., Geeraerts, E., Vanhunsel, S., Beckers, A., Noterdaeme, L., Christiaens, M., Bollaerts, I., Groef, L. D., & Moons, L. (2018) · Biogerontology · doi:10.1007/s10522-018-9780-6 · Cited by 20

Survival, excitability, and transfection of retinal neurons in an organotypic culture of mature zebrafish retina

Kustermann, S., Schmid, S., Biehlmaier, O., & Köhler, K. (2008) · Cell and Tissue Research · doi:10.1007/s00441-008-0589-5 · Cited by 19

Retinal Wnt signaling defect in a zebrafish fetal alcohol spectrum disorder model

Muralidharan, P., Sarmah, S., & Marrs, J. A. (2018) · PLoS ONE · doi:10.1371/journal.pone.0201659 · Cited by 18

Development and characterization of a chronic photoreceptor degeneration model in adult zebrafish that does not trigger a regenerative response

Turkalj, B. A., Quallich, D., Bessert, D. A., Kramer, A. C., Cook, T. A., & Thummel, R. (2021) · Experimental Eye Research · doi:10.1016/j.exer.2021.108630 · Cited by 18

Compensatory engulfment and Müller glia reactivity in the absence of microglia

Thiel, W. A., Blume, Z. I., & Mitchell, D. M. (2022) · Glia · doi:10.1002/glia.24182 · Cited by 18

MAP4Ks inhibition promotes retinal neuron regeneration from Müller glia in adult mice

Zhang, H., Guo, Y., Yang, Y., Wang, Y., Zhang, Y., Zhuang, J., Zhang, Y., Shen, M., Zhao, J., Zhang, R., et al. (2023) · npj Regenerative Medicine · doi:10.1038/s41536-023-00310-6 · Cited by 18

Advances in the study of Müller glia reprogramming in mammals

Guo, Y.-M., Jiang, X., Min, J., Huang, J., Huang, X., & Lu, Y. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1305896 · Cited by 18

Inflammation is a critical factor for successful regeneration of the adult zebrafish retina in response to diffuse light lesion

Bludau, O., Weber, A., Bosak, V., Kuscha, V., Dietrich, K., Hans, S., & Brand, M. (2024) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2024.1332347 · Cited by 18

Murine dopaminergic Müller cells restore motor function in a model of Parkinson's disease

Stutz, B., da Conceição, F. S. L., Santos, L. E., Cadilhe, D. V., Fleming, R. L., Acquarone, M., Gardino, P. F., Reis, R. A. D. M., Dickson, P. W., Dunkley, P. R., et al. (2013) · Journal of Neurochemistry · doi:10.1111/jnc.12475 · Cited by 18

The capacity of neural crest‐derived stem cells for ocular repair

Liu, B., Hunter, D. J., Smith, A. A., Chen, S., & Helms, J. A. (2014) · Birth Defects Research Part C Embryo Today Reviews · doi:10.1002/bdrc.21077 · Cited by 18

Reprogramming chick RPE progeny cells to differentiate towards retinal neurons by ash1.

Mao, W., Yan, R., & Wang, S.-Z. (2008) · PubMed Central · Cited by 18

Photoreceptor Structure and Development

Perkins, B. D., & Fadool, J. M. (2010) · Methods in cell biology · doi:10.1016/b978-0-12-384892-5.00007-4 · Cited by 19

Proliferation of the ciliary epithelium with retinal neuronal and photoreceptor cell differentiation in human eyes with retinal detachment and proliferative vitreoretinopathy

Ducournau, Y., Boscher, C., Adelman, R. A., Guillaubey, C., Schmidt-Morand, D., Mosnier, J., & Ducournau, D. H. (2011) · Graefe s Archive for Clinical and Experimental Ophthalmology · doi:10.1007/s00417-011-1797-3 · Cited by 18

Interkinetic Nuclear Migration in the Regenerating Retina

Lahne, M., & Hyde, D. R. (2015) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-17121-0_78 · Cited by 18

Using Electrical Stimulation to Enhance the Efficacy of Cell Transplantation Therapies for Neurodegenerative Retinal Diseases: Concepts, Challenges, and Future Perspectives

Manthey, A. L., Liu, W., Jiang, Z. X., Lee, M. H. K., Ji, J., So, K., Lai, J. S. M., Lee, V. W. H., & Chiu, K. (2017) · Cell Transplantation · doi:10.3727/096368917x694877 · Cited by 18

The Cell Biology of Stem Cells

Meshorer, E., & Plath, K. (2010) · Advances in experimental medicine and biology · doi:10.1007/978-1-4419-7037-4 · Cited by 20

A large-scale CRISPR screen reveals context-specific genetic regulation of retinal ganglion cell regeneration

Emmerich, K., Hageter, J., Hoang, T. V., Lyu, P., Sharrock, A. V., Ceisel, A., Thierer, J. H., Chunawala, Z., Nimmagadda, S., Palazzo, I., et al. (2024) · Development · doi:10.1242/dev.202754 · Cited by 17

Recent Advances towards the Clinical Application of Stem Cells for Retinal Regeneration

Becker, S., Jayaram, H., & Limb, G. A. (2012) · Cells · doi:10.3390/cells1040851 · Cited by 17

Increased Müller Cell De-Differentiation After Grafting of Retinal Stem Cell in the Sub-Retinal Space of Royal College of Surgeons Rats

Tian, C., Zhao, T., Zeng, Y., & Yin, Z. Q. (2011) · Tissue Engineering Part A · doi:10.1089/ten.tea.2010.0649 · Cited by 17

Regulation of genomic output and (pluri)potency in regeneration

Duncan, E. M., & Sánchez Alvarado, A. (2019) · Annual Review of Genetics · doi:10.1146/annurev-genet-112618-043733 · Cited by 17

Pluripotent Stem Cells for the Treatment of Retinal Degeneration: Current Strategies and Future Directions

Ikelle, L., Al‐Ubaidi, M. R., & Naash, M. I. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00743 · Cited by 18

Inhibition of GABAA-ρ receptors induces retina regeneration in zebrafish

Kent, M. R., Kara, N., & Patton, J. G. (2020) · Neural Regeneration Research · doi:10.4103/1673-5374.286972 · Cited by 17

Retinal Glia

Reichenbach, A., & Bringmann, A. (2015) · Colloquium Series on Neuroglia in Biology and Medicine From Physiology to Disease · doi:10.4199/c00122ed1v01y201412ngl003 · Cited by 18

MicroRNA-28 potentially regulates the photoreceptor lineage commitment of Müller glia-derived progenitors

Ji, H., Xiong, Y., Song, W., Zhang, E.-D., Gao, Z., Yao, F., Su, T., Zhou, R., & Xia, X.-B. (2017) · Scientific Reports · doi:10.1038/s41598-017-11112-4 · Cited by 17

Neuroretinal Apoptosis as a Vascular Dysfunction in Diabetic Patients

Mrugacz, M., Bryl, A., & Bossowski, A. T. (2016) · Current Neuropharmacology · doi:10.2174/1570159x14666160523144245 · Cited by 17

Ancient origin of the rod bipolar cell pathway in the vertebrate retinaPreprint

Hellevik, A., Mardoum, P., Hahn, J., Kölsch, Y., D’Orazi, F. D., Suzuki, S. C., Godinho, L., Lawrence, O. T., Rieke, F. M., Shekhar, K., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.09.12.557433 · Cited by 17

Retina regeneration: lessons from vertebrates

Sharma, P., & Ramachandran, R. (2022) · Oxford Open Neuroscience · doi:10.1093/oons/kvac012 · Cited by 16

Characterization of Pax2 Expression in the Goldfish Optic Nerve Head during Retina Regeneration

Parrilla, M., Lillo, C., Herrero-Turrión, M. J., Arévalo, R., Aijón, J., Lara, J. M., & Velasco, A. (2012) · PLoS ONE · doi:10.1371/journal.pone.0032348 · Cited by 16

QDPR homologues in Danio rerio regulate melanin synthesis, early gliogenesis, and glutamine homeostasis

Breuer, M., Guglielmi, L., Zielonka, M., Hemberger, V., Kölker, S., Okun, J. G., Hoffmann, G. F., Carl, M., Sauer, S. W., & Opladen, T. (2019) · PLoS ONE · doi:10.1371/journal.pone.0215162 · Cited by 16

Developmental Regulation of TAC1 in Peptidergic-Induced Human Mesenchymal Stem Cells: Implication for Spinal Cord Injury in Zebrafish

Patel, N., Klassert, T. E., Greco, S. J., Patel, S. A., Munoz, J. L., Reddy, B. Y., Bryan, M., Campbell, N., Kokorina, N. A., Sabaawy, H. E., et al. (2011) · Stem Cells and Development · doi:10.1089/scd.2011.0179 · Cited by 16

Brain derived neurotrophic factor in the retina of the teleost N. furzeri

GATTA, C. L., CASTALDO, L., Cellerino, A., de Girolamo, P., Lucini, C., & D’Angelo, L. (2014) · Annals of Anatomy - Anatomischer Anzeiger · doi:10.1016/j.aanat.2014.01.002 · Cited by 16

Gut-brain axis dysfunction mediates neurotoxicity of embryonic p-phenylenediamine exposure in zebrafish

Xu, M., Pan, D., Yi, J., Zheng, Y., Zeng, G., Lin, J., Song, Y., Sun, D., & Chen, J. (2025) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2025.139650 · Cited by 15

Notch Signaling Induces Retinal Stem-Like Properties in Perinatal Neural Retina Progenitors and Promotes Symmetric Divisions in Adult Retinal Stem Cells

Balenci, L., & van der Kooy, D. (2013) · Stem Cells and Development · doi:10.1089/scd.2013.0177 · Cited by 15

Injury-induced purinergic signalling molecules upregulate pluripotency gene expression and mitotic activity of progenitor cells in the zebrafish retina

Medrano, M. P., Bejarano, C. A., Battista, A. G., Venera, G. D., Bernabeu, R., & Faillace, M. P. (2017) · Purinergic Signalling · doi:10.1007/s11302-017-9572-5 · Cited by 15

Excitatory neurotransmission activates compartmentalized calcium transients in Müller glia without affecting lateral process motility

Tworig, J. M., Coate, C. J., & Feller, M. B. (2021) · eLife · doi:10.7554/elife.73202 · Cited by 15

Disruption of miR-18a Alters Proliferation, Photoreceptor Replacement Kinetics, Inflammatory Signaling, and Microglia/Macrophage Numbers During Retinal Regeneration in Zebrafish

Magner, E. T., Sandoval-Sanchez, P., Kramer, A. C., Thummel, R., Hitchcock, P. F., & Taylor, S. M. (2022) · Molecular Neurobiology · doi:10.1007/s12035-022-02783-w · Cited by 15

Retinal differentiation in an altricial bird species, Taeniopygia guttata: An immunohistochemical study

Álvarez‐Hernán, G., Hernández‐Núñez, I., Rico-Leo, E. M., Marzal, A., de Mera‐Rodríguez, J. A., Rodríguez‐León, J., Martín‐Partido, G., & Francisco‐Morcillo, J. (2019) · Experimental Eye Research · doi:10.1016/j.exer.2019.107869 · Cited by 15

Histone deacetylase inhibition promotes regenerative neurogenesis after stab wound injury in the adult zebrafish optic tectum

Kiyooka, M., Shimizu, Y., & Ohshima, T. (2020) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2020.06.025 · Cited by 15

MACULAR TELANGIECTASIA–CHANGES IN MACULAR PIGMENT OPTICAL DENSITY DURING A 5-YEAR FOLLOW-UP

Zeimer, M. B., Spital, G., Heimes, B., Lommatzsch, A. P., & Pauleikhoff, D. (2013) · Retina · doi:10.1097/iae.0000000000000023 · Cited by 15

Expression of SoxC Transcription Factors during Zebrafish Retinal and Optic Nerve Regeneration

Mu, Z., Zhang, S., He, C., Hou, H., Liu, D., Hu, N., & Xu, H. (2016) · Neuroscience Bulletin · doi:10.1007/s12264-016-0073-2 · Cited by 15

Eyes on CHARGE syndrome: Roles of CHD7 in ocular development

Krueger, L. A., & Morris, A. C. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.994412 · Cited by 14

Intercellular contact and cargo transfer between Müller glia and to microglia precede apoptotic cell clearance in the developing retina

Morales, M., Findley, A. P., & Mitchell, D. M. (2024) · Development · doi:10.1242/dev.202407 · Cited by 14

New Perspectives in Stem Cell Transplantation and Associated Therapies to Treat Retinal Diseases: From Gene Editing to 3D Bioprinting

dos Santos, G. B., de Lima-Vasconcellos, T. H., Móvio, M. I., Birbrair, A., Debbio, C. B. D., & Kihara, A. H. (2024) · Stem Cell Reviews and Reports · doi:10.1007/s12015-024-10689-4 · Cited by 14

Regulating the formation of Müller glia‐derived progenitor cells in the retina

Taylor, O. B., El‐Hodiri, H. M., Palazzo, I., Todd, L. J., & Fischer, A. J. (2024) · Glia · doi:10.1002/glia.24635 · Cited by 14

Ocular Stem Cell Research from Basic Science to Clinical Application: A Report from Zhongshan Ophthalmic Center Ocular Stem Cell Symposium

Ouyang, H. W., Goldberg, J. L., Chen, S., Li, W. S., Xu, G.-T., Li, W. S., Zhang, K., Nussenblatt, R. B., Li, W. S., Xie, T., et al. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17030415 · Cited by 14

Novel Animal Model of Crumbs-Dependent Progressive Retinal Degeneration That Targets Specific Cone Subtypes

Fu, J., Nagashima, M., Guo, C., Raymond, P. A., & Wei, X. (2018) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.17-22572 · Cited by 14

Isolation of photoreceptors from mature, developing, and regenerated zebrafish retinas, and of microglia/macrophages from regenerating zebrafish retinas

Sun, C., Mitchell, D. M., & Stenkamp, D. L. (2018) · Experimental Eye Research · doi:10.1016/j.exer.2018.08.002 · Cited by 14

Sox2 expression in the visual system of two teleost species

DeOliveira‐Mello, L., Lara, J. M., Arévalo, R., Velasco, A., & Mack, A. F. (2019) · Brain Research · doi:10.1016/j.brainres.2019.146350 · Cited by 14

Contribution of platelet-derived growth factor signaling to retina regeneration in zebrafish

Saito, Y., Yamaguchi, A., Nakamura, S., Okuyoshi, H., Shimazawa, M., & Hara, H. (2020) · Neuroscience Letters · doi:10.1016/j.neulet.2020.134930 · Cited by 14

Development and postnatal neurogenesis in the retina: a comparison between altricial and precocial bird species

Francisco‐Morcillo, J., Álvarez‐Hernán, G., de Mera‐Rodríguez, J. A., Gañán, Y., Solana-Fajardo, J., Martín‐Partido, G., & Rodríguez‐León, J. (2020) · Neural Regeneration Research · doi:10.4103/1673-5374.286947 · Cited by 14

Decline in Constitutive Proliferative Activity in the Zebrafish Retina with Ageing

Hernández‐Núñez, I., Quelle‐Regaldie, A., Sanchez, L. E., Adrio, F., Candal, E., & Barreiro‐Iglesias, A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222111715 · Cited by 14

Economic Growth and Unemployment in Algeria: An Econometric Study

Dahmani, M. D. (2013) · An-Najah University Journal for Research - B (Humanities) · doi:10.35552/0247-027-006-006 · Cited by 14

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

Retinal development and function in a ‘blind’ mole

Carmona, F. D., Glösmann, M., Ou, J., Jiménez, R., & Collinson, J. M. (2009) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2009.1744 · Cited by 14

Opportunities for CRISPR/Cas9 Gene Editing in Retinal Regeneration Research

Campbell, L. J., & Hyde, D. R. (2017) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2017.00099 · Cited by 14

Midkine-a functions as a universal regulator of proliferation during epimorphic regeneration in adult zebrafish

Ang, N. B., Saera-Vila, A., Walsh, C. E., Hitchcock, P. F., Kahana, A., Thummel, R., & Nagashima, M. (2020) · PLoS ONE · doi:10.1371/journal.pone.0232308 · Cited by 14

Zebrafish cadherin‐11 participates in retinal differentiation and retinotectal axon projection during visual system development

Clendenon, S. G., Sarmah, S., Shah, B., Liu, Q., & Marrs, J. A. (2012) · Developmental Dynamics · doi:10.1002/dvdy.23729 · Cited by 14

Molecular Factors of the Maintenance and Activation of the Juvenile Phenotype of Cellular Sources for Eye Tissue Regeneration

Grigoryan, E. N. (2018) · Biochemistry (Moscow) · doi:10.1134/s0006297918110032 · Cited by 14

Reactive Muller Glia as Potential Retinal Progenitors

Teri, L. L., Ellen, C. W., Muñoz-Cabrera, J., & Dharmaraj, S. (2013) · InTech eBooks · doi:10.5772/55150 · Cited by 14

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)