Transcriptional regulation of photoreceptor development and homeostasis in the mammalian retina

Human photoreceptor topography

Curcio, C. A., Sloan, K. R., Kalina, R. E., & Hendrickson, A. E. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.902920402 · Cited by 2,792 · see citing works

Exome sequencing identifies the cause of a mendelian disorder

Ng, S. B., Buckingham, K. J., Lee, C., Bigham, A. W., Tabor, H. K., Dent, K. M., Huff, C. D., Shannon, P. T., Jabs, E. W., Nickerson, D. A., et al. (2010) · Nature Genetics · doi:10.1038/ng.499 · Cited by 1,957 · see citing works

Molecular Genetics of Human Color Vision: The Genes Encoding Blue, Green, and Red Pigments

Nathans, J., Thomas, D., & Hogness, D. S. (1986) · Science · doi:10.1126/science.2937147 · Cited by 1,732 · see citing works

Parallel processing in the mammalian retina

Wässle, H. (2004) · Nature reviews. Neuroscience · doi:10.1038/nrn1497 · Cited by 1,253 · see citing works

The fundamental plan of the retina

Masland, R. H. (2001) · Nature Neuroscience · doi:10.1038/nn0901-877 · Cited by 1,247 · see citing works

The Retina: An Approachable Part of the Brain

(1989) · Archives of Ophthalmology · doi:10.1001/archopht.1989.01070020357018 · Cited by 1,124 · see citing works

Retinal repair by transplantation of photoreceptor precursors

MacLaren, R. E., Pearson, R. A., MacNeil, A., Douglas, R. H., Salt, T. E., Akimoto, M., Swaroop, A., Sowden, J. C., & Ali, R. R. (2006) · Nature · doi:10.1038/nature05161 · Cited by 1,099 · see citing works

Cell differentiation in the retina of the mouse

Young, R. W. (1985) · The Anatomical Record · doi:10.1002/ar.1092120215 · Cited by 1,079 · see citing works

Cell fate determination in the vertebrate retina.

Cepko, C. L., Austin, C. P., Yang, X.-J., Alexiades, M. R., & Ezzeddine, D. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.2.589 · Cited by 989 · see citing works

The arrangement of the three cone classes in the living human eye

Roorda, A., & Williams, D. R. (1999) · Nature · doi:10.1038/17383 · Cited by 986 · see citing works

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 · see citing works

Nrl is required for rod photoreceptor development

Mears, A. J., Kondo, M., Swain, P. K., Takada, Y., Bush, R. A., Saunders, T. L., Sieving, P. A., & Swaroop, A. (2001) · Nature Genetics · doi:10.1038/ng774 · Cited by 912 · see citing works

Crx, a Novel otx-like Homeobox Gene, Shows Photoreceptor-Specific Expression and Regulates Photoreceptor Differentiation

Furukawa, T., Morrow, E. M., & Cepko, C. L. (1997) · Cell · doi:10.1016/s0092-8674(00)80439-0 · Cited by 901 · see citing works

Gene regulatory networks for development

Levine, M., & Davidson, E. H. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0408031102 · Cited by 796 · see citing works

Crx, a Novel Otx-like Paired-Homeodomain Protein, Binds to and Transactivates Photoreceptor Cell-Specific Genes

Chen, S., Wang, Q., Nie, Z., Sun, H., Lennon, G. G., Copeland, N. G., Gilbert, D. J., Jenkins, N. A., & Zack, D. J. (1997) · Neuron · doi:10.1016/s0896-6273(00)80394-3 · Cited by 712 · see citing works

The Rx homeobox gene is essential for vertebrate eye development

Mathers, P. H., Grinberg, A., Mahon, K. A., & Jamrich, M. (1997) · Nature · doi:10.1038/42475 · Cited by 712 · see citing works

Rods and cones in the mouse retina. I. Structural analysis using light and electron microscopy

Carter‐Dawson, L. D., & LaVail, M. M. (1979) · The Journal of Comparative Neurology · doi:10.1002/cne.901880204 · Cited by 695 · see citing works

Six3 , a murine homologue of the sine oculis gene, demarcates the most anterior border of the developing neural plate and is expressed during eye development

Oliver, G. C., Mailhos, A., Wehr, R., Copeland, N. G., Jenkins, N. A., & Gruß, P. (1995) · Development · doi:10.1242/dev.121.12.4045 · Cited by 674 · see citing works

Controlled expression of transgenes introduced by in vivo electroporation

Matsuda, T., & Cepko, C. L. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0610155104 · Cited by 666 · see citing works

Lineage-independent determination of cell type in the embryonic mouse retina

Turner, D. L., Snyder, E. Y., & Cepko, C. L. (1990) · Neuron · doi:10.1016/0896-6273(90)90136-4 · Cited by 662 · see citing works

Cellular determination in the xenopus retina is independent of lineage and birth date

Holt, C. E., Bertsch, T. W., Ellis, H. M., & Harris, W. A. (1988) · Neuron · doi:10.1016/0896-6273(88)90205-x · Cited by 648 · see citing works

Photoreceptor degeneration: genetic and mechanistic dissection of a complex trait

Wright, A. F., Chakarova, C. F., El-Aziz, M. M. A., & Bhattacharya, S. S. (2010) · Nature Reviews Genetics · doi:10.1038/nrg2717 · Cited by 632 · see citing works

Toward the generation of rod and cone photoreceptors from mouse, monkey and human embryonic stem cells

Osakada, F., Ikeda, H. O., Mandai, M., Wataya, T., Watanabe, K., Yoshimura, N., Akaike, A., Sasai, Y., & Takahashi, M. (2008) · Nature Biotechnology · doi:10.1038/nbt1384 · Cited by 629 · see citing works

Modeling early retinal development with human embryonic and induced pluripotent stem cells

Meyer, J. S., Shearer, R., Capowski, E., Wright, L., Wallace, K., Mcmillan, E., Zhang, S.-C., & Gamm, D. (2009) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.0905245106 · Cited by 609 · see citing works

Otx2 homeobox gene controls retinal photoreceptor cell fate and pineal gland development

Nishida, A., Furukawa, A., Koike, C., Tano, Y., Aizawa, S., Matsuo, I., & Furukawa, T. (2003) · Nature Neuroscience · doi:10.1038/nn1155 · Cited by 607 · see citing works

Transplantation of Human Embryonic Stem Cell-Derived Photoreceptors Restores Some Visual Function in Crx-Deficient Mice

Lamba, D. A., Gust, J., & Reh, T. A. (2009) · Cell stem cell · doi:10.1016/j.stem.2008.10.015 · Cited by 604 · see citing works

The First Steps in Seeing

Rodieck, R. W. (1998) · Optometry and Vision Science · doi:10.1097/00006324-199812000-00004 · Cited by 602 · see citing works

The Murine Cone Photoreceptor

Applebury, M. L., Antoch, M. P., Baxter, L. C., Chun, L. L. Y., Falk, J. D., Farhangfar, F., Kage, K., Krzystolik, M. G., Lyass, L., & Robbins, J. T. (2000) · Neuron · doi:10.1016/s0896-6273(00)00062-3 · Cited by 566 · see citing works

Cone-Rod Dystrophy Due to Mutations in a Novel Photoreceptor-Specific Homeobox Gene () Essential for Maintenance of the Photoreceptor

Freund, C. L., Gregory, C. Y., Furukawa, T., Papaioannou, M. G., Looser, J., Ploder, L., Bellingham, J., Ng, D., Herbrick, J.-A., Duncan, A. M. V., et al. (1997) · Cell · doi:10.1016/s0092-8674(00)80440-7 · Cited by 564 · see citing works

A thyroid hormone receptor that is required for the development of green cone photoreceptors

Ng, L., Hurley, J. B., Dierks, B. D., Srinivas, M., Saltó, C., Vennström, B., Reh, T. A., & Forrest, D. (2001) · Nature Genetics · doi:10.1038/83829 · Cited by 561 · see citing works

Specification of the vertebrate eye by a network of eye field transcription factors

Zuber, M. E., Gestri, G., Viczian, A. S., Barsacchi, G., & Harris, W. A. (2003) · Development · doi:10.1242/dev.00723 · Cited by 541 · see citing works

Retinopathy and attenuated circadian entrainment in Crx-deficient mice

Furukawa, T., Morrow, E. M., Li, T., Davis, F. C., & Cepko, C. L. (1999) · Nature Genetics · doi:10.1038/70591 · Cited by 534 · see citing works

Cell death during differentiation of the retina in the mouse

Young, R. W. (1984) · The Journal of Comparative Neurology · doi:10.1002/cne.902290307 · Cited by 532 · see citing works

Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate

Haider, N. B., Jacobson, S. G., Cideciyan, A. V., Swiderski, R., Streb, L. M., Searby, C., Beck, G., Hockey, R., Hanna, D. B., Gorman, S., et al. (2000) · Nature Genetics · doi:10.1038/72777 · Cited by 507 · see citing works

Protection of mouse photoreceptors by survival factors in retinal degenerations.

LaVail, M. M., Yasumura, D., Matthes, M. T., Lau-Villacorta, C., Unoki, K., Sung, C. –., & Steinberg, R. H. (1998) · PubMed · Cited by 493 · see citing works

Evolution of vertebrate visual pigments

Bowmaker, J. K. (2008) · Vision Research · doi:10.1016/j.visres.2008.03.025 · Cited by 454 · see citing works

A locus control region adjacent to the human red and green visual pigment genes

Wang, Y., Macke, J. P., Merbs, S. L., Zack, D. J., Klaunberg, B. A., Bennett, J., Gearhart, J. D., & Nathans, J. (1992) · Neuron · doi:10.1016/0896-6273(92)90181-c · Cited by 414 · see citing works

Rods and cones in the mouse retina. II. Autoradiographic analysis of cell generation using tritiated thymidine

Carter‐Dawson, L. D., & LaVail, M. M. (1979) · The Journal of Comparative Neurology · doi:10.1002/cne.901880205 · Cited by 404 · see citing works

Massively Parallel Sequencing: The Next Big Thing in Genetic Medicine

Tucker, T., Marra, M. A., & Friedman, J. M. (2009) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2009.06.022 · Cited by 384 · see citing works

Timing and topography of cell genesis in the rat retina

Rapaport, D. H., Wong, L., Wood, E. D., Yasumura, D., & LaVail, M. M. (2004) · The Journal of Comparative Neurology · doi:10.1002/cne.20134 · Cited by 376 · see citing works

Surface mechanics mediate pattern formation in the developing retina

Hayashi, T., & Carthew, R. W. (2004) · Nature · doi:10.1038/nature02952 · Cited by 366 · see citing works

Generating neuronal diversity in the retina: one for nearly all

Marquardt, T., & Gruß, P. (2002) · Trends in Neurosciences · doi:10.1016/s0166-2236(00)02028-2 · Cited by 361 · see citing works

The Evolution and Physiology of Human Color Vision

Nathans, J. (1999) · Neuron · doi:10.1016/s0896-6273(00)80845-4 · Cited by 347 · see citing works

Targeting of GFP to newborn rods by Nrl promoter and temporal expression profiling of flow-sorted photoreceptors

Akimoto, M., Cheng, H., Zhu, D., Brzezinski, J. A., Khanna, R., Filippova, E. V., Oh, E. C. T., Jing, Y., Linares, J., Brooks, M., et al. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0508214103 · Cited by 314 · see citing works

A conserved retina-specific gene encodes a basic motif/leucine zipper domain.

Swaroop, A., Xu, J. Z., Pawar, H., Jackson, A., Skolnick, C., & Agarwal, N. A. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.1.266 · Cited by 305 · see citing works

Physiological Features of the S- and M-cone Photoreceptors of Wild-type Mice from Single-cell Recordings

Nikonov, S. S., Kholodenko, R. V., Lem, J., & Pugh, E. N. (2006) · The Journal of General Physiology · doi:10.1085/jgp.200609490 · Cited by 298 · see citing works

The Rod Photoreceptor-Specific Nuclear Receptor Nr2e3 Represses Transcription of Multiple Cone-Specific Genes

Chen, J., Rattner, A., & Nathans, J. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.3571-04.2005 · Cited by 286 · see citing works

A Range of Clinical Phenotypes Associated with Mutations in CRX, a Photoreceptor Transcription-Factor Gene

Sohocki, M. M., Sullivan, L. S., Mintz-Hittner, H. A., Birch, D. G., Heckenlively, J. R., Freund, C. L., McInnes, R. R., & Daiger, S. P. (1998) · The American Journal of Human Genetics · doi:10.1086/302101 · Cited by 283 · see citing works

Cell-specific effects of RB or RB/p107 loss on retinal development implicate an intrinsically death-resistant cell-of-origin in retinoblastoma

Chen, D., Livne-bar, I., Vanderluit, J. L., Slack, R. S., Agochiya, M., & Bremner, R. (2004) · Cancer Cell · doi:10.1016/j.ccr.2004.05.025 · Cited by 281 · see citing works

Making the gradient: Thyroid hormone regulates cone opsin expression in the developing mouse retina

Roberts, M. R., Srinivas, M., Forrest, D., de Escobar, G. M., & Reh, T. A. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0509981103 · Cited by 274 · see citing works

The photoreceptor-specific nuclear receptor Nr2e3 interacts with Crx and exerts opposing effects on the transcription of rod versus cone genes

Peng, G.-H., Ahmad, O. R., Ahmad, F., Liu, J., & Chen, S. (2005) · Human Molecular Genetics · doi:10.1093/hmg/ddi070 · Cited by 271 · see citing works

Retinal cell fate determination and bHLH factors

Hatakeyama, J., & Kageyama, R. (2004) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2003.09.005 · Cited by 269 · see citing works

Photoreceptor-specific nuclear receptor NR2E3 functions as a transcriptional activator in rod photoreceptors

Cheng, H. (2004) · Human Molecular Genetics · doi:10.1093/hmg/ddh173 · Cited by 268 · see citing works

The Retina: An Approachable Part of the Brain

COGAN, D. G. (1988) · Archives of Ophthalmology · doi:10.1001/archopht.1988.01060130648016 · Cited by 252 · see citing works

Notch 1 inhibits photoreceptor production in the developing mammalian retina

Jadhav, A. P., Mason, H. A., & Cepko, C. L. (2006) · Development · doi:10.1242/dev.02245 · Cited by 248 · see citing works

Properties of developmental gene regulatory networks

Davidson, E. H., & Levine, M. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0806007105 · Cited by 247 · see citing works

Retinoblastoma Has Properties of a Cone Precursor Tumor and Depends Upon Cone-Specific MDM2 Signaling

Xu, X. L., Fang, Y., Lee, T. C., Forrest, D., Gregory, C. Y., Almeida, D., Liu, A., Jhanwar, S. C., Abramson, D. H., & Cobrinik, D. E. (2009) · Cell · doi:10.1016/j.cell.2009.03.051 · Cited by 246 · see citing works

From Progenitors to Differentiated Cells in the Vertebrate Retina

Agathocleous, M., & Harris, W. A. (2009) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.042308.113259 · Cited by 240 · see citing works

Plasticity and Differentiation of Embryonic Retinal Cells After Terminal Mitosis

Adler, R., & Hatlee, M. (1989) · Science · doi:10.1126/science.2911751 · Cited by 228 · see citing works

Postmitotic cells fated to become rod photoreceptors can be respecified by CNTF treatment of the retina

Ezzedine, Z. D., Yang, X.-J., DeChiara, T. M., Yancopoulos, G. D., & Cepko, C. L. (1997) · Development · doi:10.1242/dev.124.5.1055 · Cited by 226 · see citing works

The Leucine Zipper of NRL Interacts with the CRX Homeodomain

Mitton, K. P., Swain, P. K., Chen, S., Xu, S., Zack, D. J., & Swaroop, A. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m003658200 · Cited by 226 · see citing works

A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the <i>rd7</i> mouse

Akhmedov, N. B., Piriev, N. I., Chang, B., Rapoport, A. L., Hawes, N. L., Nishina, P. M., Nusinowitz, S., Heckenlively, J. R., Roderick, T. H., Kozak, C. A., et al. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.10.5551 · Cited by 221 · see citing works

Identification of a photoreceptor cell-specific nuclear receptor

Kobayashi, M., Takezawa, S., Hara, K., Yu, R. T., Umesono, Y., Agata, K., Taniwaki, M., Yasuda, K., & Umesono, K. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.9.4814 · Cited by 215 · see citing works

Regulation of photoreceptor gene expression by Crx-associated transcription factor network

Hennig, A. K., Peng, G.-H., & Chen, S. (2008) · Brain Research · doi:10.1016/j.brainres.2007.06.036 · Cited by 214 · see citing works

Disruption of retinoid‐related orphan receptor β changes circadian behavior, causes retinal degeneration and leads to vacillans phenotype in mice

André, É., Conquet, F., Steinmayr, M., Stratton, S. C., Porciatti, V., & Becker-André, M. (1998) · The EMBO Journal · doi:10.1093/emboj/17.14.3867 · Cited by 214 · see citing works

Progenitor cell proliferation in the retina is dependent on Notch-independent Sonic hedgehog/Hes1 activity

Wall, D. S., Mears, A. J., McNeill, B., Mazerolle, C. J., Thurig, S., Wang, Y., Kageyama, R., & Wallace, V. A. (2009) · The Journal of Cell Biology · doi:10.1083/jcb.200805155 · Cited by 208 · see citing works

Leber congenital amaurosis caused by a homozygous mutation (R90W) in the homeodomain of the retinal transcription factor CRX: direct evidence for the involvement of CRX in the development of photoreceptor function

Swaroop, A. (1999) · Human Molecular Genetics · doi:10.1093/hmg/8.2.299 · Cited by 203 · see citing works

Retinoid X Receptor γ Is Necessary to Establish the S-opsin Gradient in Cone Photoreceptors of the Developing Mouse Retina

Roberts, M. R., Hendrickson, A. E., McGuire, C. R., & Reh, T. A. (2005) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.05-0093 · Cited by 202 · see citing works

Sonic Hedgehog Promotes Rod Photoreceptor Differentiation in Mammalian Retinal CellsIn Vitro

Levine, E. M., Roelink, H., Turner, J. K., & Reh, T. A. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-16-06277.1997 · Cited by 196 · see citing works

Notch1 functions to suppress cone-photoreceptor fate specification in the developing mouse retina

Yaron, O., Farhy, C., Marquardt, T., Applebury, M., & Ashery‐Padan, R. (2006) · Development · doi:10.1242/dev.02311 · Cited by 193 · see citing works

Functional Roles of Otx2 Transcription Factor in Postnatal Mouse Retinal Development

Koike, C., Nishida, A., Ueno, S., Saito, H., Sanuki, R., Sato, S., Furukawa, A., Aizawa, S., Matsuo, I., 昇, 鈴., et al. (2007) · Molecular and Cellular Biology · doi:10.1128/mcb.01209-07 · Cited by 192 · see citing works

Rb regulates proliferation and rod photoreceptor development in the mouse retina

Zhang, J., Gray, J., Wu, L., Leone, G., Rowan, S., Cepko, C. L., Zhu, X., Craft, C. M., & Dyer, M. A. (2004) · Nature Genetics · doi:10.1038/ng1318 · Cited by 190 · see citing works

Retinoic acid alters photoreceptor development in vivo

Hyatt, G. A., Schmitt, E. A., Fadool, J. M., & Dowling, J. E. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.23.13298 · Cited by 189 · see citing works

How vision begins: An odyssey

Luo, D.-G., Xue, T., & Yau, K. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0708405105 · Cited by 186 · see citing works

Expression profiling of the developing and mature Nrl −/− mouse retina: identification of retinal disease candidates and transcriptional regulatory targets of Nrl

Yoshida, S., Mears, A. J., Friedman, J. S., Carter, T., He, S., Oh, E. C. T., Jing, Y., Farjo, R. A., Fleury, G. A., Barlow, C., et al. (2004) · Human Molecular Genetics · doi:10.1093/hmg/ddh160 · Cited by 182 · see citing works

Shared Mutations in NR2E3 in Enhanced S-cone Syndrome, Goldmann-Favre Syndrome, and Many Cases of Clumped Pigmentary Retinal Degeneration

Sharon, D. (2003) · Archives of Ophthalmology · doi:10.1001/archopht.121.9.1316 · Cited by 179 · see citing works

A Hybrid Photoreceptor Expressing Both Rod and Cone Genes in a Mouse Model of Enhanced S-Cone Syndrome

Corbo, J. C., & Cepko, C. L. (2005) · PLoS Genetics · doi:10.1371/journal.pgen.0010011 · Cited by 174 · see citing works

Spatial and temporal expression of short, long/medium, or both opsins in human fetal cones

Xiao, M., & Hendrickson, A. E. (2000) · The Journal of Comparative Neurology · doi:10.1002/1096-9861(20001002)425:4 · Cited by 165 · see citing works

Blimp1 controls photoreceptor versus bipolar cell fate choice during retinal development

Brzezinski, J. A., Lamba, D. A., & Reh, T. A. (2010) · Development · doi:10.1242/dev.043968 · Cited by 163 · see citing works

Transformation of cone precursors to functional rod photoreceptors by bZIP transcription factor NRL

Oh, E. C. T., Khan, N. W., Novelli, E., Khanna, H., Strettoi, E., & Swaroop, A. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0605934104 · Cited by 163 · see citing works

Role of a locus control region in the mutually exclusive expression of human red and green cone pigment genes

Smallwood, P. M., Wang, Y., & Nathans, J. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.022629799 · Cited by 162 · see citing works

The spatial arrangement of cones in the primate fovea

Mollon, J. D., & Bowmaker, J. K. (1992) · Nature · doi:10.1038/360677a0 · Cited by 159 · see citing works

Thyroid hormone receptors in chick retinal development: differential expression of mRNAs for α and N-terminal variant β receptors

Sjöberg, M., Vennström, B., & Forrest, D. (1992) · Development · doi:10.1242/dev.114.1.39 · Cited by 155 · see citing works

Two Phases of Rod Photoreceptor Differentiation during Rat Retinal Development

Morrow, E. M., Belliveau, M. J., & Cepko, C. L. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-10-03738.1998 · Cited by 151 · see citing works

Nuclear receptor TLX prevents retinal dystrophy and recruits the corepressor atrophin1Preprint

Zhang, C., Zou, Y., Yu, R. T., Gage, F. H., & Evans, R. M. (2006) · Genes & Development · doi:10.1101/gad.1413606 · Cited by 143 · see citing works

The Cis-regulatory Logic of the Mammalian Photoreceptor Transcriptional Network

Hsiau, T. H.-C., Diaconu, C. I., Myers, C. A., Lee, J., Cepko, C. L., & Corbo, J. C. (2007) · PLoS ONE · doi:10.1371/journal.pone.0000643 · Cited by 141 · see citing works

Retinoid-related orphan nuclear receptor RORβ is an early-acting factor in rod photoreceptor development

Li, J., Oh, E. C. T., Ng, L., Srinivas, M., Brooks, M., Swaroop, A., & Forrest, D. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0902425106 · Cited by 140 · see citing works

Lineage in the vertebrate retina

Cayouette, M., Poggi, L., & Harris, W. A. (2006) · Trends in Neurosciences · doi:10.1016/j.tins.2006.08.003 · Cited by 138 · see citing works

A Role for Ligand-Gated Ion Channels in Rod Photoreceptor Development

Young‐Pearse, T. L., & Cepko, C. L. (2004) · Neuron · doi:10.1016/s0896-6273(04)00141-2 · Cited by 137 · see citing works

Eye, Retina, and Visual System of the Mouse

Chalupa, L. M., & Williams, R. W. (2008) · The MIT Press eBooks · doi:10.7551/mitpress/7578.001.0001 · Cited by 137 · see citing works

Rod differentiation factor NRL activates the expression of nuclear receptor NR2E3 to suppress the development of cone photoreceptors

Oh, E. C. T., Cheng, H., Hong, H., Jia, L., Khan, N. W., & Swaroop, A. (2008) · Brain Research · doi:10.1016/j.brainres.2008.01.028 · Cited by 132 · see citing works

Pias3-Dependent SUMOylation Directs Rod Photoreceptor Development

Onishi, A., Peng, G.-H., Hsu, C., Alexis, U., Chen, S., & Blackshaw, S. (2009) · Neuron · doi:10.1016/j.neuron.2008.12.006 · Cited by 129 · see citing works

Retinal degenerations with truncation mutations in the cone-rod homeobox (CRX) gene.

Jacobson, S. G., Cideciyan, A. V., Huang, Y., Hanna, D. B., Freund, C. L., Affatigato, L. M., Carr, R. E., Zack, D. J., Stone, E. M., & McInnes, R. R. (1998) · PubMed · Cited by 126 · see citing works

In vivo function of the orphan nuclear receptor NR2E3 in establishing photoreceptor identity during mammalian retinal development

Cheng, H., Alemán, T. S., Cideciyan, A. V., Khanna, R., Jacobson, S. G., & Swaroop, A. (2006) · Human Molecular Genetics · doi:10.1093/hmg/ddl185 · Cited by 126 · see citing works

X‐ray structure of the orphan nuclear receptor RORβ ligand‐binding domain in the active conformation

Stehlin, C., Wurtz, J., Steinmetz, A. C. U., Greiner, E. F., Schüle, R., Moras, D., & Renaud, J. (2001) · The EMBO Journal · doi:10.1093/emboj/20.21.5822 · Cited by 125 · see citing works

The orphan nuclear receptor Tlx regulates Pax2 and is essential for vision

Yu, R. T., Chiang, M.-Y., Tanabe, T., Kobayashi, M., Yasuda, K., Evans, R. M., & Umesono, K. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.050566897 · Cited by 124 · see citing works

Multiple Phosphorylated Isoforms of NRL Are Expressed in Rod Photoreceptors

Swain, P. K., Hicks, D., Mears, A. J., Apel, I. J., Smith, J. E., John, S. K., Hendrickson, A. E., Milam, A. H., & Swaroop, A. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m105855200 · Cited by 122 · see citing works

Blimp1 Suppresses Chx10 Expression in Differentiating Retinal Photoreceptor Precursors to Ensure Proper Photoreceptor Development

Katoh, K., Omori, Y., Onishi, A., Sato, S., Kondo, M., & Furukawa, T. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.0771-10.2010 · Cited by 120 · see citing works

Rod photoreceptor differentiation in fetal and infant human retina

Hendrickson, A. E., O’Brien, K. M. B., Natoli, R., Ramamurthy, V., Possin, D. E., & Provis, J. M. (2008) · Experimental Eye Research · doi:10.1016/j.exer.2008.07.016 · Cited by 115 · see citing works

Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degeneration

Jacobson, S. G. (2004) · Human Molecular Genetics · doi:10.1093/hmg/ddh198 · Cited by 115 · see citing works

Chx10 is required to block photoreceptor differentiation but is dispensable for progenitor proliferation in the postnatal retina

Livne-Bar, I., Pacal, M., Cheung, M., Hankin, M., Trogadis, J. E., Chen, D., Dorval, K. M., & Bremner, R. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0600083103 · Cited by 112 · see citing works

Math5 is required for both early retinal neuron differentiation and cell cycle progression

Le, T. T., Wroblewski, E. E., Patel, S., Riesenberg, A. N., & Brown, N. L. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2006.03.055 · Cited by 110 · see citing works

Mutation analysis ofNR2E3 andNRL genes in Enhanced S Cone Syndrome

Wright, A. F., Reddick, A. C., Schwartz, S., Ferguson, J. S., Alemán, T. S., Kellner, U., Jurklies, B., Schuster, A., Zrenner, E., Wissinger, B., et al. (2004) · Human Mutation · doi:10.1002/humu.9285 · Cited by 108 · see citing works

Activation of the Blue Opsin Gene in Cone Photoreceptor Development by Retinoid-Related Orphan Receptor β

Srinivas, M., Ng, L., Liu, H., Li, J., & Forrest, D. (2006) · Molecular Endocrinology · doi:10.1210/me.2005-0505 · Cited by 107 · see citing works

Recessive NRL mutations in patients with clumped pigmentary retinal degeneration and relative preservation of blue cone function

Nishiguchi, K. M., Friedman, J. S., Sandberg, M. A., Swaroop, A., Berson, E. L., & Dryja, T. P. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0408183101 · Cited by 106 · see citing works

Mutually exclusive expression of human red and green visual pigment-reporter transgenes occurs at high frequency in murine cone photoreceptors

Wang, Y., Smallwood, P. M., Cowan, M., Blesh, D., Lawler, A. M., & Nathans, J. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.9.5251 · Cited by 105 · see citing works

Spatial and temporal differences between the expression of short‐ and middle‐wave sensitive cone pigments in the mouse retina: A developmental study

Szél, Á., Röhlich, P., Mieziewska, K., Aguirre, G. K., & Veen, T. V. (1993) · The Journal of Comparative Neurology · doi:10.1002/cne.903310411 · Cited by 104 · see citing works

The LIM homeobox transcription factor Lhx2 is required to specify the retina field and synergistically cooperates with Pax6 for Six6 trans-activation

Tétreault, N., Champagne, M.-P., & Bernier, G. (2008) · Developmental Biology · doi:10.1016/j.ydbio.2008.12.022 · Cited by 101 · see citing works

The Teleost Retina as a Model for Developmental and Regeneration Biology

Hitchcock, P. F., & Raymond, P. A. (2004) · Zebrafish · doi:10.1089/zeb.2004.1.257 · Cited by 101 · see citing works

Expression of Photoreceptor-Specific Nuclear Receptor NR2E3 in Rod Photoreceptors of Fetal Human Retina

O’Brien, K. M. B., Cheng, H., Jiang, Y., Schulte, D., Swaroop, A., & Hendrickson, A. E. (2004) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.03-1317 · Cited by 101 · see citing works

Photoreceptor distribution in the retinas of subprimate mammals

Szél, Á., Lukáts, Á., Fekete, T., Szepessy, Z., & Röhlich, P. (2000) · Journal of the Optical Society of America A · doi:10.1364/josaa.17.000568 · Cited by 99 · see citing works

Retinal cone differentiation

Szél, Á., van Veen, T., & Röhlich, P. (1994) · Nature · doi:10.1038/370336a0 · Cited by 98 · see citing works

A typology of photoreceptor gene expression patterns in the mouse

Corbo, J. C., Myers, C. A., Lawrence, K. A., Jadhav, A. P., & Cepko, C. L. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0705465104 · Cited by 97 · see citing works

Retinoic acid receptor‐related orphan receptor α regulates a subset of cone genes during mouse retinal development

Fujieda, H., Bremner, R., Mears, A. J., & Sasaki, H. (2008) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2008.05739.x · Cited by 90 · see citing works

Tbx2b is required for ultraviolet photoreceptor cell specification during zebrafish retinal development

Álvarez-Delfín, K., Morris, A. C., Snelson, C. D., Gamse, J. T., Gupta, T., Marlow, F. L., Mullins, M. C., Burgess, H. A., Granato, M., & Fadool, J. M. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0809439106 · Cited by 89 · see citing works

NeuroD1 Regulates Expression of Thyroid Hormone Receptor β2 and Cone Opsins in the Developing Mouse Retina

Liu, H., Etter, P., Hayes, S., Jones, I., Nelson, B. R., Hartman, B. H., Forrest, D., & Reh, T. A. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.4832-07.2008 · Cited by 87 · see citing works

CD73, a Novel Cell Surface Antigen That Characterizes Retinal Photoreceptor Precursor Cells

Koso, H., Minami, C., Tabata, Y., Inoue, M., Sasaki, E., Satoh, S., & Watanabe, S. (2009) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.08-3246 · Cited by 78 · see citing works

A role for the fibroblast growth factor receptor in cell fate decisions in the developing vertebrate retina

McFarlane, S., Zuber, M. E., & Holt, C. E. (1998) · Development · doi:10.1242/dev.125.20.3967 · Cited by 78 · see citing works

Cytokine-Induced Activation of Signal Transducer and Activator of Transcription in Photoreceptor Precursors Regulates Rod Differentiation in the Developing Mouse Retina

Rhee, K. D., Goureau, O., Chen, S., & Yang, X.-J. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.1785-04.2004 · Cited by 75 · see citing works

Activin A Promotes Progenitor Differentiation into Photoreceptors in Rodent Retina

Davis, A. A., Matzuk, M. M., & Reh, T. A. (2000) · Molecular and Cellular Neuroscience · doi:10.1006/mcne.1999.0806 · Cited by 75 · see citing works

Genetics of variation in human color vision and the retinal cone mosaic

Deeb, S. S. (2006) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2006.04.002 · Cited by 75 · see citing works

Retinal regeneration in the Xenopus laevis tadpole: a new model system.

(2009) · PubMed Central · Cited by 73 · see citing works

The Spatial Patterning of Mouse Cone Opsin Expression Is Regulated by Bone Morphogenetic Protein Signaling through Downstream Effector COUP-TF Nuclear Receptors

Satoh, S., Tang, K., Iida, A., Inoue, M., Kodama, T., Tsai, M., Tsai, M., Furuta, Y., & Watanabe, S. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.0951-09.2009 · Cited by 73 · see citing works

Effects of L1 retrotransposon insertion on transcript processing, localization and accumulation: lessons from the retinal degeneration 7 mouse and implications for the genomic ecology of L1 elements

Chen, J., Rattner, A., & Nathans, J. (2006) · Human Molecular Genetics · doi:10.1093/hmg/ddl138 · Cited by 73 · see citing works

Retinoic Acid Regulates the Expression of Photoreceptor Transcription Factor NRL

Khanna, H., Akimoto, M., Siffroi‐Fernandez, S., Friedman, J. S., Hicks, D., & Swaroop, A. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m605500200 · Cited by 69 · see citing works

Developmental expression of thyroid hormone receptor β2 protein in cone photoreceptors in the mouse

Ng, L., Ma, M., Curran, T., & Forrest, D. (2009) · Neuroreport · doi:10.1097/wnr.0b013e32832a2c63 · Cited by 69 · see citing works

Nrl and Sp Nuclear Proteins Mediate Transcription of Rod-specific cGMP-phosphodiesterase β-Subunit Gene

Lerner, L. E., Gribanova, Y. E., Ji, M. H., Knox, B. E., & Farber, D. B. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m103301200 · Cited by 69 · see citing works

Identification of a locus control region for quadruplicated green-sensitive opsin genes in zebrafish

Tsujimura, T., Chinen, A., & Kawamura, S. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0704061104 · Cited by 67 · see citing works

Cell fate decisions and patterning in the vertebrate retina: the importance of timing, asymmetry, polarity and waves

Malicki, J. J. (2004) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2004.01.015 · Cited by 64 · see citing works

Thyroid Hormone Action Is Required for Normal Cone Opsin Expression during Mouse Retinal Development

a, C. N. P., Santiago, L. A., Santiago, D. A., Machado, D. S., Rocha, F. A. D. F., Ventura, D. F., Hokoç, J. N., Pazos-Moura, C. C., Wondisford, F. E., Gardino, P. F., et al. (2008) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.07-0908 · Cited by 63 · see citing works

An Intron Control Region Differentially Regulates Expression of Thyroid Hormone Receptor β2 in the Cochlea, Pituitary, and Cone Photoreceptors

Jones, I., Ng, L., Liu, H., & Forrest, D. (2007) · Molecular Endocrinology · doi:10.1210/me.2007-0037 · Cited by 62 · see citing works

Retarded Developmental Expression and Patterning of Retinal Cone Opsins in Hypothyroid Mice

Lu, A., Ng, L., Ma, M., Kefas, B. A., Davies, T. F., Hernández, A., Chan, C., & Forrest, D. (2008) · Endocrinology · doi:10.1210/en.2008-1092 · Cited by 62 · see citing works

Identification of regulatory targets of tissue-specific transcription factors: application to retina-specific gene regulation

Qian, J. (2005) · Nucleic Acids Research · doi:10.1093/nar/gki658 · Cited by 62 · see citing works

Functional Analysis of the Rod Photoreceptor cGMP Phosphodiesterase α-Subunit Gene Promoter

Pittler, S. J., Zhang, Y., Chen, S., Mears, A. J., Zack, D. J., Ren, Z. J., Swain, P. K., Yao, S., Swaroop, A., & White, B. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m401864200 · Cited by 61 · see citing works

Retinoic acid promotes rod photoreceptor differentiation in rat retina in vivo

Kelley, M. W., Williams, R. C., Turner, J. K., Kraft, J. C., & Reh, T. A. (1999) · Neuroreport · doi:10.1097/00001756-199908020-00031 · Cited by 59 · see citing works

Retinopathy mutations in the bZIP protein NRL alter phosphorylation and transcriptional activity

Kanda, A., Friedman, J. S., Nishiguchi, K. M., & Swaroop, A. (2007) · Human Mutation · doi:10.1002/humu.20488 · Cited by 57 · see citing works

Development of the Cone ERG in Infants

Hansen, R. M., & Fulton, A. B. (2005) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.05-0382 · Cited by 55 · see citing works

Quantification of Normal Cell Death in the Rat Retina: Implications for Clone Composition in Cell Lineage Analysis

Voyvodic, J. T., Burne, J. F., & RAFF, M. C. (1995) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1995.tb01045.x · Cited by 52 · see citing works

Distribution of short-wavelength-sensitive cones in human fetal and postnatal retina: early development of spatial order and density profiles

Cornish, E. E., Hendrickson, A. E., & Provis, J. M. (2004) · Vision Research · doi:10.1016/j.visres.2004.03.030 · Cited by 51 · see citing works

The Minimal Transactivation Domain of the Basic Motif-Leucine Zipper Transcription Factor NRL Interacts with TATA-binding Protein

Friedman, J. S., Khanna, H., Swain, P. K., DeNicola, R., Cheng, H., Mitton, K. P., Weber, C. H., Hicks, D., & Swaroop, A. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m408298200 · Cited by 44 · see citing works

Sumoylation of bZIP Transcription Factor NRL Modulates Target Gene Expression during Photoreceptor Differentiation

Roger, J. E., Nellissery, J. K., Kim, D. S., & Swaroop, A. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.142810 · Cited by 44 · see citing works

The nuclear receptor transcription factor, retinoid-related orphan receptor β, regulates retinal progenitor proliferation

Chow, L., Levine, E. M., & Reh, T. A. (1998) · Mechanisms of Development · doi:10.1016/s0925-4773(98)00135-x · Cited by 44 · see citing works

Spatiotemporal gradients of cell genesis in the primate retina.

Rapaport, D. H., RAKIC, P. T., & Mm, L. (1996) · PubMed · Cited by 43 · see citing works

Putting neurons in the right places: local interactions in the genesis of retinal architecture

Galli‐Resta, L. (2002) · Trends in Neurosciences · doi:10.1016/s0166-2236(02)02279-8 · Cited by 43 · see citing works

Have we achieved a unified model of photoreceptor cell fate specification in vertebrates?

Adler, R., & Raymond, P. A. (2007) · Brain Research · doi:10.1016/j.brainres.2007.03.044 · Cited by 42 · see citing works

Intrinsic and extrinsic signals in the developing vertebrate and fly eyes: viewing vertebrate and invertebrate eyes in the same light.

Reh, T. A., & Cagan, R. L. (1994) · PubMed · Cited by 39 · see citing works

Leukemia Inhibitory Factor Blocks Expression of Crx and Nrl Transcription Factors to Inhibit Photoreceptor Differentiation

Graham, D. R., Overbeek, P. A., & Ash, J. D. (2005) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.05-0129 · Cited by 35 · see citing works

Identification of potent agonists of photoreceptor-specific nuclear receptor (NR2E3) and preparation of a radioligand

Wolkenberg, S. E., Zhao, Z., Kapitskaya, M. Z., Webber, A. L., Petrukhin, K. E., Tang, Y. S., Dean, D. C., Hartman, G. D., & Lindsley, C. W. (2006) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2006.07.056 · Cited by 32 · see citing works

A comprehensive analysis of sequence variants and putative disease-causing mutations in photoreceptor-specific nuclear receptor NR2E3.

Kanda, A., & Swaroop, A. (2009) · PubMed Central · Cited by 31 · see citing works

The course of maturation of rod-mediated visual thresholds in infants.

Hansen, R., & Fulton, A. B. (1999) · PubMed · Cited by 29 · see citing works

FGF19 Exhibits Neuroprotective Effects on Adult Mammalian Photoreceptors In Vitro

Siffroi‐Fernandez, S., Felder‐Schmittbuhl, M., Khanna, H., Swaroop, A., & Hicks, D. (2008) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.07-1272 · Cited by 22 · see citing works

From Disease Genes to Cellular Pathways: A Progress Report

Yu, J., Mears, A. J., Yoshida, S., Farjo, R. A., Carter, T., Ghosh, D., Hero, A. O., Barlow, C., & Swaroop, A. (2003) · Novartis Foundation symposium · doi:10.1002/0470092645.ch11 · Cited by 11 · see citing works

Mutually exclusive expression of the L and M pigment genes in the human retinoblastoma cell line WERI: Resetting by cell division

Deeb, S. S., Liu, Y., & Hayashi, T. (2006) · Visual Neuroscience · doi:10.1017/s0952523806233030 · Cited by 9 · see citing works

Characterization of the retinal proteome during rod photoreceptor genesis

Barnhill, A. E., Hecker, L. A., Kohutyuk, O., Buss, J. E., Honavar, V., & Greenlee, H. (2010) · BMC Research Notes · doi:10.1186/1756-0500-3-25 · Cited by 9 · see citing works

Evolution of Gene Regulatory Networks Controlling Body Plan Development

Peter, I. S., & Davidson, E. H. (2011) · Cell · doi:10.1016/j.cell.2011.02.017 · Cited by 417 · see citing works

Evolution of phototransduction, vertebrate photoreceptors and retina

Lamb, T. D. (2013) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2013.06.001 · Cited by 387 · see citing works

Chemistry of the Retinoid (Visual) Cycle

Kiser, P. D., Golczak, M., & Palczewski, K. (2014) · Chemical Reviews · doi:10.1021/cr400107q · Cited by 353 · see citing works

Mouse Retinal Cell Atlas: Molecular Identification of over Sixty Amacrine Cell Types

Yan, W., Laboulaye, M. A., Tran, N. M., Whitney, I. E., Benhar, I., & Sanes, J. R. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.0471-20.2020 · Cited by 329 · see citing works

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 322 · see citing works

Cell fate determination in the vertebrate retina

Bassett, E. A., & Wallace, V. A. (2012) · Trends in Neurosciences · doi:10.1016/j.tins.2012.05.004 · Cited by 300 · see citing works

Nrl knockdown by AAV-delivered CRISPR/Cas9 prevents retinal degeneration in mice

Yu, W., Mookherjee, S., Chaitankar, V., Hiriyanna, S., Kim, J.-W., Brooks, M., Ataeijannati, Y., Sun, X., Dong, L., Li, T., et al. (2017) · Nature Communications · doi:10.1038/ncomms14716 · Cited by 271 · see citing works

The Dynamic Epigenetic Landscape of the Retina During Development, Reprogramming, and Tumorigenesis

Aldiri, I., Xu, B., Wang, L., Chen, X. '., Hiler, D. J., Griffiths, L. M., Valentine, M. B., Shirinifard, A., Thiagarajan, S., Sablauer, A., et al. (2017) · Neuron · doi:10.1016/j.neuron.2017.04.022 · Cited by 249 · see citing works

Biology and therapy of inherited retinal degenerative disease: insights from mouse models

Veleri, S., Lazar, C. H., Chang, B., Sieving, P. A., Banin, E., & Swaroop, A. (2015) · Disease Models & Mechanisms · doi:10.1242/dmm.017913 · Cited by 232 · see citing works

Cone photoreceptor types in zebrafish are generated by symmetric terminal divisions of dedicated precursors

Suzuki, S. C., Bleckert, A., Williams, P. R., Takechi, M., Kawamura, S., & Wong, R. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1303551110 · Cited by 226 · see citing works

Thyroid hormone receptors, cell growth and differentiation

Pascual, A., & Aranda, A. (2012) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2012.03.012 · Cited by 207 · see citing works

Regulation of Terminal Differentiation Programs in the Nervous System

Hobert, O. (2011) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-092910-154226 · Cited by 198 · see citing works

Accelerated and Improved Differentiation of Retinal Organoids from Pluripotent Stem Cells in Rotating-Wall Vessel Bioreactors

DiStefano, T. J., Chen, H. Y., Panebianco, C. J., Kaya, K. D., Brooks, M. J., Gieser, L. M., Morgan, N. Y., Pohida, T., & Swaroop, A. (2017) · Stem Cell Reports · doi:10.1016/j.stemcr.2017.11.001 · Cited by 195 · see citing works

Retinitis Pigmentosa: Progress in Molecular Pathology and Biotherapeutical Strategies

Liu, W., Liu, S., Li, P., & Yao, K. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23094883 · Cited by 183 · see citing works

Molecular basis for photoreceptor outer segment architecture

Goldberg, A. F. X., Moritz, O. L., & Williams, D. S. (2016) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2016.05.003 · Cited by 180 · see citing works

Generation, transcriptome profiling, and functional validation of cone-rich human retinal organoids

Kim, S., Lowe, A., Dharmat, R., Lee, S., Owen, L. A., Wang, J., Shakoor, A., Li, Y., Morgan, D. J., Hejazi, A. A., et al. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1901572116 · Cited by 174 · see citing works

Photoreceptor cell fate specification in vertebrates

Brzezinski, J. A., & Reh, T. A. (2015) · Development · doi:10.1242/dev.127043 · Cited by 160 · see citing works

Onecut1 and Onecut2 redundantly regulate early retinal cell fates during development

Sapkota, D., Chintala, H., Wu, F., Fliesler, S. J., Hu, Z., & Mu, X. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1405354111 · Cited by 159 · see citing works

Epigenomic landscapes of retinal rods and cones

Mo, A., Luo, C., Davis, F. P., Mukamel, E. A., Henry, G. L., Nery, J. R., Urich, M. A., Picard, S., Lister, R., Eddy, S. R., et al. (2016) · eLife · doi:10.7554/elife.11613 · Cited by 158 · see citing works

Transcriptome Dynamics of Developing Photoreceptors in Three-Dimensional Retina Cultures Recapitulates Temporal Sequence of Human Cone and Rod Differentiation Revealing Cell Surface Markers and Gene Networks

Kaewkhaw, R., Kaya, K. D., Brooks, M., Homma, K., Zou, J., Chaitankar, V., Rao, M. S., & Swaroop, A. (2015) · Stem Cells · doi:10.1002/stem.2122 · Cited by 154 · see citing works

Function of human pluripotent stem cell-derived photoreceptor progenitors in blind mice

Barnea-Cramer, A. O., Wang, W., Lu, S., Singh, M. S., Luo, C., Huo, H., McClements, M. E., Barnard, A. R., MacLaren, R. E., & Lanza, R. (2016) · Scientific Reports · doi:10.1038/srep29784 · Cited by 151 · see citing works

Organoid technology for retinal repair

Llonch, S., Carido, M., & Ader, M. (2017) · Developmental Biology · doi:10.1016/j.ydbio.2017.09.028 · Cited by 151 · see citing works

Pluripotent stem cell-derived retinal organoids for disease modeling and development of therapies

Kruczek, K., & Swaroop, A. (2020) · Stem Cells · doi:10.1002/stem.3239 · Cited by 148 · see citing works

Deletion of a remote enhancer near ATOH7 disrupts retinal neurogenesis, causing NCRNA disease

Ghiasvand, N. M., Rudolph, D. D., Mashayekhi, M., Brzezinski, J. A., Goldman, D. J., & Glaser, T. M. (2011) · Nature Neuroscience · doi:10.1038/nn.2798 · Cited by 147 · see citing works

Role of the type 2 iodothyronine deiodinase (D2) in the control of thyroid hormone signaling

Drigo, R. A. E., Fonseca, T. L., Werneck‐de‐Castro, J. P., & Bianco, A. C. (2012) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2012.08.019 · Cited by 146 · see citing works

Rapid Sequential in Situ Multiplexing with DNA Exchange Imaging in Neuronal Cells and Tissues

Wang, Y., Woehrstein, J. B., Donoghue, N. D., Dai, M., Avendaño, M. S., Schackmann, R. C. J., Zoeller, J. J., Wang, S. S. H., Tillberg, P. W., Park, D., et al. (2017) · Nano Letters · doi:10.1021/acs.nanolett.7b02716 · Cited by 146 · see citing works

Otx2 and Onecut1 Promote the Fates of Cone Photoreceptors and Horizontal Cells and Repress Rod Photoreceptors

Emerson, M. M., Surzenko, N., Goetz, J. J., Trimarchi, J. M., & Cepko, C. L. (2013) · Developmental Cell · doi:10.1016/j.devcel.2013.06.005 · Cited by 144 · see citing works

NRL-Regulated Transcriptome Dynamics of Developing Rod Photoreceptors

Kim, J.-W., Yang, H., Brooks, M. J., Zelinger, L., Karakülah, G., Gotoh, N., Boleda, A., Gieser, L. M., Giuste, F., Whitaker, D. T., et al. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.10.074 · Cited by 142 · see citing works

Photoreceptor cell replacement in macular degeneration and retinitis pigmentosa: A pluripotent stem cell-based approach

Gagliardi, G., M’Barek, K. B., & Goureau, O. (2019) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2019.03.001 · Cited by 139 · see citing works

Human Embryonic Stem Cell-Derived Organoid Retinoblastoma Reveals a Cancerous Origin

Liu, H., Zhang, Y., Zhang, Y.-Y., Li, Y.-P., Hua, Z.-Q., Zhang, C.-J., Jin, S., Zhang, C.-J., Wu, K.-C., Su, J., et al. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2011780117 · Cited by 136 · see citing works

Multimodal spatiotemporal phenotyping of human retinal organoid development

Wahle, P., Brancati, G., Harmel, C., He, Z., Gut, G., del Castillo, J. S., dos Santos, A. X. D. S., Yu, Q., Noser, P., Fleck, J. S., et al. (2023) · Nature Biotechnology · doi:10.1038/s41587-023-01747-2 · Cited by 136 · see citing works

Recruitment of Rod Photoreceptors from Short-Wavelength-Sensitive Cones during the Evolution of Nocturnal Vision in Mammals

Kim, J.-W., Yang, H., Oel, A. P., Brooks, M. J., Li, J., Plachetzki, D. C., Li, W., Allison, W. T., & Swaroop, A. (2016) · Developmental Cell · doi:10.1016/j.devcel.2016.05.023 · Cited by 133 · see citing works

Epigenetic control of gene regulation during development and disease: A view from the retina

Corso‐Díaz, X., Jaeger, C., Chaitankar, V., & Swaroop, A. (2018) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2018.03.002 · Cited by 129 · see citing works

Cellular strategies for retinal repair by photoreceptor replacement

Jayakody, S. A., Gonzalez-Cordero, A., Ali, R. R., & Pearson, R. A. (2015) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2015.01.003 · Cited by 126 · see citing works

Development of the Vertebrate Eye and Retina

Stenkamp, D. L. (2015) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2015.06.006 · Cited by 125 · see citing works

Massively parallel cis-regulatory analysis in the mammalian central nervous systemPreprint

Shen, S. Q., Myers, C. A., Hughes, A. E. O., Byrne, L. C., Flannery, J. G., & Corbo, J. C. (2015) · Genome Research · doi:10.1101/gr.193789.115 · Cited by 123 · see citing works

Transcriptional Regulation of Rod Photoreceptor Homeostasis Revealed by In Vivo NRL Targetome Analysis

Hao, H., Kim, D. S., Klocke, B., Johnson, K. R., Cui, K., Gotoh, N., Zang, C., Gregorski, J., Gieser, L. M., Peng, W., et al. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1002649 · Cited by 121 · see citing works

Functional diversity of melanopsins and their global expression in the teleost retina

Davies, W. I. L., Zheng, L., Hughes, S., Tamai, K., Turton, M., Halford, S., Foster, F., Whitmore, D., & Hankins, M. W. (2011) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-011-0785-4 · Cited by 120 · see citing works

Single-nuclei RNA-seq on human retinal tissue provides improved transcriptome profiling

Liang, Q., Dharmat, R., Owen, L. A., Shakoor, A., Li, Y., Kim, S., Vitale, A. T., Kim, I. K., Morgan, D. J., Liang, S., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-12917-9 · Cited by 120 · see citing works

Eyes underground: Regression of visual protein networks in subterranean mammals

Emerling, C. A., & Springer, M. S. (2014) · Molecular Phylogenetics and Evolution · doi:10.1016/j.ympev.2014.05.016 · Cited by 119 · see citing works

cGMP production of patient-specific iPSCs and photoreceptor precursor cells to treat retinal degenerative blindness

Wiley, L. A., Burnight, E. R., DeLuca, A. P., Anfinson, K. R., Cranston, C. M., Kaalberg, E. E., Penticoff, J. A., Affatigato, L. M., Mullins, R. F., Stone, E. M., et al. (2016) · Scientific Reports · doi:10.1038/srep30742 · Cited by 117 · see citing works

Two transcription factors, Pou4f2 and Isl1, are sufficient to specify the retinal ganglion cell fate

Wu, F., Kaczynski, T. J., Sethuramanujam, S., Li, R., Jain, V., Slaughter, M. M., & Mu, X. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1421535112 · Cited by 115 · see citing works

COCO enhances the efficiency of photoreceptor precursor differentiation in early human embryonic stem cell-derived retinal organoids

Pan, D., Xia, X.-X., Zhou, H., Jin, S., Lu, Y.-Y., Liu, H., Gao, M.-L., & Jin, Z. (2020) · Stem Cell Research & Therapy · doi:10.1186/s13287-020-01883-5 · Cited by 112 · see citing works

An epigenetic mechanism for cavefish eye degeneration

Gore, A. V., Tomins, K. A., Iben, J., Ma, L., Castranova, D., Davis, A. E. M., Parkhurst, A., Jeffery, W. R., & Weinstein, B. M. (2018) · Nature Ecology & Evolution · doi:10.1038/s41559-018-0569-4 · Cited by 111 · see citing works

Differentiation of human embryonic stem cells into cone photoreceptors through simultaneous inhibition of BMP, TGFβ and Wnt signaling

Zhou, S., Flamier, A., Abdouh, M., Tétreault, N., Barabino, A., Wadhwa, S., & Bernier, G. (2015) · Development · doi:10.1242/dev.125385 · Cited by 110 · see citing works

Pharmacologic fibroblast reprogramming into photoreceptors restores vision

Mahato, B., Kaya, K. D., Fan, Y., Sumien, N., Shetty, R. A., Zhang, W., Davis, D., Mock, T., Batabyal, S., Ni, A., et al. (2020) · Nature · doi:10.1038/s41586-020-2201-4 · Cited by 107 · see citing works

Improved Retinal Organoid Differentiation by Modulating Signaling Pathways Revealed by Comparative Transcriptome Analyses with Development In Vivo

Brooks, M. J., Chen, H. Y., Kelley, R. A., Mondal, A. K., Nagashima, K., de Val, N., Li, T., Chaitankar, V., & Swaroop, A. (2019) · Stem Cell Reports · doi:10.1016/j.stemcr.2019.09.009 · Cited by 105 · see citing works

S cones: Evolution, retinal distribution, development, and spectral sensitivity

HUNT, D. M., & Peichl, L. (2013) · Visual Neuroscience · doi:10.1017/s0952523813000242 · Cited by 103 · see citing works

Eye organogenesis: A hierarchical view of ocular development

Miesfeld, J. B., & Brown, N. L. (2019) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2018.12.008 · Cited by 102 · see citing works

Transplantation of Photoreceptors Derived From Human Müller Glia Restore Rod Function in the P23H Rat

Jayaram, H., Jones, M. F., Eastlake, K., Cottrill, P. B., Becker, S., Wiseman, J., Khaw, P. T., & Limb, G. A. (2014) · Stem Cells Translational Medicine · doi:10.5966/sctm.2013-0112 · Cited by 101 · see citing works

Hierarchies in Visual Pathway: Functions and Inspired Artificial Vision

Zhu, S., Xie, T., Lv, Z., Leng, Y., Zhang, Y., Xu, R., Qin, J., Zhou, Y., Roy, V. A. L., & Han, S. (2023) · Advanced Materials · doi:10.1002/adma.202301986 · Cited by 101 · see citing works

Developing Rods Transplanted into the Degenerating Retina of Crx-Knockout Mice Exhibit Neural Activity Similar to Native Photoreceptors

Homma, K., Okamoto, S., Mandai, M., Gotoh, N., Rajasimha, H. K., Chang, Y.-S., Chen, S., Li, W., Cogliati, T., Swaroop, A., et al. (2013) · Stem Cells · doi:10.1002/stem.1372 · Cited by 99 · see citing works

Retinal regeneration in adult zebrafish requires regulation of TGFβ signaling

Lenkowski, J. R., Qin, Z., Sifuentes, C. J., Thummel, R., Soto, C. M., Moens, C. B., & Raymond, P. A. (2013) · Glia · doi:10.1002/glia.22549 · Cited by 99 · see citing works

Regulated Reprogramming in the Regeneration of Sensory Receptor Cells

Bermingham‐McDonogh, O., & Reh, T. A. (2011) · Neuron · doi:10.1016/j.neuron.2011.07.015 · Cited by 98 · see citing works

Homeobox genes and the specification of neuronal identity

Hobert, O. (2021) · Nature reviews. Neuroscience · doi:10.1038/s41583-021-00497-x · Cited by 98 · see citing works

Differentiation and Transplantation of Embryonic Stem Cell-Derived Cone Photoreceptors into a Mouse Model of End-Stage Retinal Degeneration

Kruczek, K., Gonzalez-Cordero, A., Goh, D., Naeem, A., Jonikas, M., Blackford, S. J. I., Kloc, M., Durán, Y., Georgiadis, A., Sampson, R. D., et al. (2017) · Stem Cell Reports · doi:10.1016/j.stemcr.2017.04.030 · Cited by 97 · see citing works

Two Transcription Factors Can Direct Three Photoreceptor Outcomes from Rod Precursor Cells in Mouse Retinal Development

Ng, L., Lu, A., Swaroop, A., Sharlin, D. S., Swaroop, A., & Forrest, D. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.1709-11.2011 · Cited by 97 · see citing works

Hypoxia induces cell damage via oxidative stress in retinal epithelial cells

Cervellati, F., Cervellati, C., Romani, A., Cremonini, E., Sticozzi, C., Belmonte, G., Pessina, F., & Valacchi, G. (2013) · Free Radical Research · doi:10.3109/10715762.2013.867484 · Cited by 95 · see citing works

Investigating cone photoreceptor development using patient-derived NRL null retinal organoids

Kallman, A., Capowski, E. E., Wang, J., Kaushik, A. M., Jansen, A. D., Edwards, K. L., Chen, L., Berlinicke, C. A., Phillips, M. J., Pierce, E. A., et al. (2020) · Communications Biology · doi:10.1038/s42003-020-0808-5 · Cited by 94 · see citing works

Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell Loss

Collin, G. B., Gogna, N., Chang, B., Damkham, N., Pinkney, J., Hyde, L. F., Stone, L. V., Naggert, J. Κ., Nishina, P. M., & Krebs, M. P. (2020) · Cells · doi:10.3390/cells9040931 · Cited by 94 · see citing works

Transphyletic conservation of developmental regulatory state in animal evolution

Royo, J. L., Maeso, I., Irimia, M., Gao, F., Peter, I. S., Lopes, C. S., D'Aniello, S., Casares, F., Davidson, E. H., Garcia-Fernández, J., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1109037108 · Cited by 93 · see citing works

An integrated transcriptional analysis of the developing human retina

Mellough, C., Bauer, R., Collin, J., Dorgau, B., Zerti, D., Dolan, D., Jones, C. M., Izuogu, O. G., Yu, M., Hallam, D., et al. (2019) · Development · doi:10.1242/dev.169474 · Cited by 93 · see citing works

Developmental and genetic mechanisms of neural circuit evolution

Tosches, M. A. (2017) · Developmental Biology · doi:10.1016/j.ydbio.2017.06.016 · Cited by 91 · see citing works

Conditional knockdown of DNA methyltransferase 1 reveals a key role of retinal pigment epithelium integrity in photoreceptor outer segment morphogenesis

Nasonkin, I. O., Merbs, S. L., Lazo, K., Oliver, V. F., Brooks, M., Patel, K., Enke, R. A., Nellissery, J. K., Jamrich, M., Le, Y. Z., et al. (2013) · Development · doi:10.1242/dev.086603 · Cited by 90 · see citing works

Relating enhancer genetic variation across mammals to complex phenotypes using machine learning

Kaplow, I. M., Lawler, A. J., Schäffer, D. E., Srinivasan, C., Sestili, H. H., Wirthlin, M. E., Phan, B. N., Prasad, K., Brown, A. R., Zhang, X., et al. (2023) · Science · doi:10.1126/science.abm7993 · Cited by 90 · see citing works

Opposite Feedbacks in the Hippo Pathway for Growth Control and Neural Fate

Jukam, D., Xie, B., Rister, J., Terrell, D., Charlton-Perkins, M. A., Pistillo, D., Gebelein, B. A., Desplan, C., & Cook, T. A. (2013) · Science · doi:10.1126/science.1238016 · Cited by 88 · see citing works

Halting progressive neurodegeneration in advanced retinitis pigmentosa

Koch, S., Tsai, Y.-T., Duong, J., Wu, W.-H., Hsu, C., Wu, W., Bonet‐Ponce, L., Lin, C., & Tsang, S. H. (2015) · Journal of Clinical Investigation · doi:10.1172/jci82462 · Cited by 85 · see citing works

One‐Phototransistor–One‐Memristor Array with High‐Linearity Light‐Tunable Weight for Optic Neuromorphic Computing

Dang, B., Liu, K., Wu, X., Yang, Z., Xu, L., Yang, Y., & Huang, R. (2022) · Advanced Materials · doi:10.1002/adma.202204844 · Cited by 84 · see citing works

Evolution of the Eye Transcriptome under Constant Darkness in Sinocyclocheilus Cavefish

Meng, F., Braasch, I., Phillips, J. B., Lin, X., Titus, T. A., Zhang, C., & Postlethwait, J. H. (2013) · Molecular Biology and Evolution · doi:10.1093/molbev/mst079 · Cited by 83 · see citing works

Defective photoreceptor phagocytosis in a mouse model of enhanced S‐cone syndrome causes progressive retinal degeneration

Mustafi, D., Kevany, B. M., Genoud, C., Okano, K., Cideciyan, A. V., Sumaroka, A., Román, A. J., Jacobson, S. G., Engel, A. H., Adams, M. D., et al. (2011) · The FASEB Journal · doi:10.1096/fj.11-186767 · Cited by 81 · see citing works

Three-dimensional retinal organoids from mouse pluripotent stem cells mimic in vivo development with enhanced stratification and rod photoreceptor differentiation.

Chen, H. Y., Kaya, K. D., Dong, L., & Swaroop, A. (2016) · Europe PMC (PubMed Central) · Cited by 80 · see citing works

OTX2 loss causes rod differentiation defect in CRX-associated congenital blindness

Roger, J. E., Hiriyanna, A., Gotoh, N., Hong, H., Cheng, D. F., Ratnapriya, R., Kautzmann, M.-A. I., Chang, B., & Swaroop, A. (2014) · Journal of Clinical Investigation · doi:10.1172/jci72722 · Cited by 79 · see citing works

The Musashi 1 Controls the Splicing of Photoreceptor-Specific Exons in the Vertebrate Retina

Murphy, D., Cieply, B. W., Carstens, R. P., Ramamurthy, V., & Stoilov, P. (2016) · PLoS Genetics · doi:10.1371/journal.pgen.1006256 · Cited by 78 · see citing works

Blood-retina barrier failure and vision loss in neuron-specific degeneration

Ivanova, E., Alam, N. M., Prusky, G. T., & Sagdullaev, B. T. (2019) · JCI Insight · doi:10.1172/jci.insight.126747 · Cited by 77 · see citing works

Cell Type-Specific Epigenomic Analysis Reveals a Uniquely Closed Chromatin Architecture in Mouse Rod Photoreceptors

Hughes, A. E. O., Enright, J. M., Myers, C. A., Shen, S. Q., & Corbo, J. C. (2017) · Scientific Reports · doi:10.1038/srep43184 · Cited by 76 · see citing works

Stem cell-based retina models

Achberger, K., Haderspeck, J. C., Kleger, A., & Liebau, S. (2019) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2018.05.005 · Cited by 75 · see citing works

NRL and CRX Define Photoreceptor Identity and Reveal Subgroup-Specific Dependencies in Medulloblastoma

Garancher, A., Lin, C. Y., Morabito, M., Richer, W., Rocques, N., Larcher, M., Bihannic, L., Smith, K. S., Miquel, C., Leboucher, S., et al. (2018) · Cancer Cell · doi:10.1016/j.ccell.2018.02.006 · Cited by 72 · see citing works

An isoform of retinoid-related orphan receptor β directs differentiation of retinal amacrine and horizontal interneurons

Liu, H., Kim, S., Fu, Y., Wu, X., Ng, L., Swaroop, A., & Forrest, D. (2013) · Nature Communications · doi:10.1038/ncomms2793 · Cited by 71 · see citing works

Post-translational regulation of RORγt—A therapeutic target for the modulation of interleukin-17-mediated responses in autoimmune diseases

Rutz, S., Eidenschenk, C., Kiefer, J. R., & Ouyang, W. (2016) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2016.07.004 · Cited by 69 · see citing works

Limitations and Promise of Retinal Tissue From Human Pluripotent Stem Cells for Developing Therapies of Blindness

Singh, R. K., & Nasonkin, I. O. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00179 · Cited by 66 · see citing works

Cell-Specific DNA Methylation Patterns of Retina-Specific Genes

Merbs, S. L., Khan, M. A., Hackler, L., Oliver, V. F., Wan, J., Qian, J. X., & Zack, D. J. (2012) · PLoS ONE · doi:10.1371/journal.pone.0032602 · Cited by 66 · see citing works

Neurogenesis and Specification of Retinal Ganglion Cells

Nguyen-Ba-Charvet, K. T., & Rebsam, A. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21020451 · Cited by 66 · see citing works

The transcription-splicing protein NonO/p54nrb and three NonO-interacting proteins bind to distal enhancer region and augment rhodopsin expression

Yadav, S. P., Hao, H., Yang, H., Kautzmann, M.-A. I., Brooks, M., Nellissery, J. K., Klocke, B., Seifert, M., & Swaroop, A. (2013) · Human Molecular Genetics · doi:10.1093/hmg/ddt609 · Cited by 65 · see citing works

The role of homeobox genes in retinal development and disease

Zagozewski, J. L., Zhang, Q., Pinto, V. I., Wigle, J. T., & Eisenstat, D. D. (2014) · Developmental Biology · doi:10.1016/j.ydbio.2014.07.004 · Cited by 65 · see citing works

Single cell transcriptomics reveals lineage trajectory of retinal ganglion cells in wild-type and Atoh7-null retinas

Wu, F., Bard, J., Kann, J., Yergeau, D. A., Sapkota, D., Ge, Y., Hu, Z., Wang, J., Liu, T., & Mu, X. (2021) · Nature Communications · doi:10.1038/s41467-021-21704-4 · Cited by 64 · see citing works

Retinoic Acid Signaling Regulates Differential Expression of the Tandemly-Duplicated Long Wavelength-Sensitive Cone Opsin Genes in Zebrafish

Mitchell, D. M., Stevens, C. B., Frey, R. A., Hunter, S. S., Ashino, R., Kawamura, S., & Stenkamp, D. L. (2015) · PLoS Genetics · doi:10.1371/journal.pgen.1005483 · Cited by 64 · see citing works

Animal modelling for inherited central vision loss

Kostic, C., & Arsenijévic, Y. (2015) · The Journal of Pathology · doi:10.1002/path.4641 · Cited by 64 · see citing works

Pluripotent Stem Cells for Retinal Tissue Engineering: Current Status and Future Prospects

Singh, R. K., Cuzzani, O., Binette, F., Sternberg, H., West, M. D., & Nasonkin, I. O. (2018) · Stem Cell Reviews and Reports · doi:10.1007/s12015-018-9802-4 · Cited by 63 · see citing works

The retinal mosaics of opsin expression in invertebrates and vertebrates

Rister, J., & Desplan, C. (2011) · Developmental Neurobiology · doi:10.1002/dneu.20905 · Cited by 62 · see citing works

Onecut 1 and Onecut 2 are potential regulators of mouse retinal development

Wu, F., Sapkota, D., Li, R., & Mu, X. (2011) · The Journal of Comparative Neurology · doi:10.1002/cne.22741 · Cited by 62 · see citing works

Hydrogel-based milliwell arrays for standardized and scalable retinal organoid cultures

Decembrini, S., Hoehnel, S., Brandenberg, N., Arsenijévic, Y., & Lütolf, M. P. (2020) · Scientific Reports · doi:10.1038/s41598-020-67012-7 · Cited by 61 · see citing works

Standardization and clinical applications of retinal imaging biomarkers for cardiovascular disease: a Roadmap from an NHLBI workshop

Chew, E. Y., Burns, S. A., Abraham, A. G., Bakhoum, M. F., Beckman, J. A., Chui, T. Y. P., Finger, R. P., Frangi, A. F., Gottesman, R. F., Grant, M. B., et al. (2024) · Nature Reviews Cardiology · doi:10.1038/s41569-024-01060-8 · Cited by 61 · see citing works

The Hippo Pathway Controls a Switch between Retinal Progenitor Cell Proliferation and Photoreceptor Cell Differentiation in Zebrafish

Asaoka, Y., Hata, S., Namae, M., Furutani‐Seiki, M., & Nishina, H. (2014) · PLoS ONE · doi:10.1371/journal.pone.0097365 · Cited by 60 · see citing works

Minireview: The Role of Nuclear Receptors in Photoreceptor Differentiation and Disease

Forrest, D., & Swaroop, A. (2012) · Molecular Endocrinology · doi:10.1210/me.2012-1010 · Cited by 60 · see citing works

Excess cones in the retinal degeneration rd7 mouse, caused by the loss of function of orphan nuclear receptor Nr2e3, originate from early-born photoreceptor precursors

Cheng, H., Khan, N. W., Roger, J. E., & Swaroop, A. (2011) · Human Molecular Genetics · doi:10.1093/hmg/ddr334 · Cited by 60 · see citing works

Pet-1 Switches Transcriptional Targets Postnatally to Regulate Maturation of Serotonin Neuron Excitability

Wyler, S. C., Spencer, W. C., Green, N. H., Rood, B. D., Crawford, L. K., Craige, C. P., Gresch, P. J., McMahon, D. G., Beck, S. G., & Deneris, E. S. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.3798-15.2016 · Cited by 60 · see citing works

Insights into photoreceptor ciliogenesis revealed by animal models

Baehr, W., Hanke‐Gogokhia, C., Sharif, A. S., Reed, M., Dahl, T. M., Frederick, J. M., & Ying, G. (2018) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2018.12.004 · Cited by 60 · see citing works

Characterization of Three-Dimensional Retinal Tissue Derived from Human Embryonic Stem Cells in Adherent Monolayer Cultures

Singh, R. K., Mallela, R. K., Cornuet, P. K., Reifler, A. N., Chervenak, A. P., West, M. D., Wong, K. Y., & Nasonkin, I. O. (2015) · Stem Cells and Development · doi:10.1089/scd.2015.0144 · Cited by 59 · see citing works

Genetic regulation of vertebrate eye development

Zagozewski, J. L., Zhang, Q., & Eisenstat, D. D. (2014) · Clinical Genetics · doi:10.1111/cge.12493 · Cited by 58 · see citing works

Maturation arrest in early postnatal sensory receptors by deletion of the miR-183/96/182 cluster in mouse

Fan, J., Li, J., Li, Y., Ebrahim, S., May‐Simera, H., Wood, A. N., Morell, R. J., Liu, P., Lei, J., Kachar, B., et al. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1619442114 · Cited by 58 · see citing works

Photoreceptor cell fate specification in vertebrates

Brzezinski, J. A., & Reh, T. A. (2015) · Development · doi:10.1242/dev.127043 · Cited by 160 · see citing works

Regulation of photoreceptor gene expression by Crx-associated transcription factor network

Hennig, A. K., Peng, G.-H., & Chen, S. (2008) · Brain Research · doi:10.1016/j.brainres.2007.06.036 · Cited by 214 · see citing works

Transcriptional regulation of the developing retina

Goodson, N. (2020) · doi:10.25677/9kgz-6d81

Excess cones in the retinal degeneration rd7 mouse, caused by the loss of function of orphan nuclear receptor Nr2e3, originate from early-born photoreceptor precursors

Cheng, H., Khan, N. W., Roger, J. E., & Swaroop, A. (2011) · Human Molecular Genetics · doi:10.1093/hmg/ddr334 · Cited by 60 · see citing works

NRL-Regulated Transcriptome Dynamics of Developing Rod Photoreceptors

Kim, J.-W., Yang, H., Brooks, M. J., Zelinger, L., Karakülah, G., Gotoh, N., Boleda, A., Gieser, L. M., Giuste, F., Whitaker, D. T., et al. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.10.074 · Cited by 142 · see citing works