| scholarly article | Q13442814 |
| P50 | author | Anand Swaroop | Q30506132 |
| Jerome Roger | Q57421156 | ||
| P2093 | author name string | Hong Cheng | |
| Naheed W Khan | |||
| P2860 | cites work | Identification of a photoreceptor cell-specific nuclear receptor | Q22009463 |
| Molecular genetics of human color vision: the genes encoding blue, green, and red pigments | Q24294339 | ||
| A conserved retina-specific gene encodes a basic motif/leucine zipper domain | Q24297019 | ||
| Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor | Q24311359 | ||
| The nuclear receptor NR2E3 plays a role in human retinal photoreceptor differentiation and degeneration | Q24531333 | ||
| Recurrent mutation in the first zinc finger of the orphan nuclear receptor NR2E3 causes autosomal dominant retinitis pigmentosa | Q24676600 | ||
| Multiple phosphorylated isoforms of NRL are expressed in rod photoreceptors | Q28209552 | ||
| Crx, a novel Otx-like paired-homeodomain protein, binds to and transactivates photoreceptor cell-specific genes | Q28255968 | ||
| Mutation analysis of NR2E3 and NRL genes in Enhanced S Cone Syndrome | Q28285701 | ||
| Blimp1 suppresses Chx10 expression in differentiating retinal photoreceptor precursors to ensure proper photoreceptor development | Q28507479 | ||
| Retinoid-related orphan nuclear receptor RORbeta is an early-acting factor in rod photoreceptor development | Q28509786 | ||
| The photoreceptor-specific nuclear receptor Nr2e3 interacts with Crx and exerts opposing effects on the transcription of rod versus cone genes | Q28593002 | ||
| Nrl is required for rod photoreceptor development | Q28595099 | ||
| A thyroid hormone receptor that is required for the development of green cone photoreceptors | Q31804576 | ||
| Photoreceptor-specific nuclear receptor NR2E3 functions as a transcriptional activator in rod photoreceptors | Q33203655 | ||
| Mutations in the DNA-binding domain of NR2E3 affect in vivo dimerization and interaction with CRX. | Q33510152 | ||
| Two phases of rod photoreceptor differentiation during rat retinal development | Q57742125 | ||
| Retinal cone differentiation | Q59066947 | ||
| Spectral sensitivity of human cone photoreceptors | Q59080458 | ||
| Rods and cones in the mouse retina. II. Autoradiographic analysis of cell generation using tritiated thymidine | Q66961734 | ||
| Importance of intrinsic mechanisms in cell fate decisions in the developing rat retina | Q79349334 | ||
| Cell fate determination in the vertebrate retina | Q33564487 | ||
| Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate. | Q33888425 | ||
| Human photoreceptor topography | Q34034782 | ||
| Sumoylation of bZIP transcription factor NRL modulates target gene expression during photoreceptor differentiation. | Q34055928 | ||
| Excess cone cell proliferation due to lack of a functional NR2E3 causes retinal dysplasia and degeneration in rd7/rd7 mice | Q34085942 | ||
| Vertebrate neural cell-fate determination: lessons from the retina | Q34185937 | ||
| Shared mutations in NR2E3 in enhanced S-cone syndrome, Goldmann-Favre syndrome, and many cases of clumped pigmentary retinal degeneration | Q34229025 | ||
| Expression of photoreceptor-specific nuclear receptor NR2E3 in rod photoreceptors of fetal human retina | Q34336263 | ||
| The rod photoreceptor-specific nuclear receptor Nr2e3 represses transcription of multiple cone-specific genes. | Q34382038 | ||
| Targeting of GFP to newborn rods by Nrl promoter and temporal expression profiling of flow-sorted photoreceptors | Q34410806 | ||
| Generating neuronal diversity in the retina: one for nearly all. | Q34500852 | ||
| Making the gradient: thyroid hormone regulates cone opsin expression in the developing mouse retina | Q34597372 | ||
| A CTRP5 gene S163R mutation knock-in mouse model for late-onset retinal degeneration | Q34829498 | ||
| In vivo function of the orphan nuclear receptor NR2E3 in establishing photoreceptor identity during mammalian retinal development | Q35070506 | ||
| Transformation of cone precursors to functional rod photoreceptors by bZIP transcription factor NRL. | Q35606996 | ||
| Cone-like morphological, molecular, and electrophysiological features of the photoreceptors of the Nrl knockout mouse | Q35861721 | ||
| Mutations in NR2E3 can cause dominant or recessive retinal degenerations in the same family | Q36856211 | ||
| A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the rd7 mouse | Q36981827 | ||
| Rod differentiation factor NRL activates the expression of nuclear receptor NR2E3 to suppress the development of cone photoreceptors | Q37138691 | ||
| A comprehensive analysis of sequence variants and putative disease-causing mutations in photoreceptor-specific nuclear receptor NR2E3. | Q37412933 | ||
| NR2E3 mutations in enhanced S-cone sensitivity syndrome (ESCS), Goldmann-Favre syndrome (GFS), clumped pigmentary retinal degeneration (CPRD), and retinitis pigmentosa (RP). | Q37589555 | ||
| Transcriptional regulation of photoreceptor development and homeostasis in the mammalian retina | Q37774553 | ||
| Blimp1 controls photoreceptor versus bipolar cell fate choice during retinal development | Q39238722 | ||
| 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 | Q40275731 | ||
| Progressive restriction in fate potential by neural progenitors during cerebral cortical development. | Q41741155 | ||
| Spatial and temporal expression of cone opsins during monkey retinal development | Q42437365 | ||
| Mammalian inscuteable regulates spindle orientation and cell fate in the developing retina | Q42807828 | ||
| Pias3-dependent SUMOylation directs rod photoreceptor development | Q43106810 | ||
| Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degeneration | Q44960254 | ||
| Cell differentiation in the retina of the mouse | Q45193462 | ||
| Phylogenomic analysis and expression patterns of large Maf genes in Xenopus tropicalis provide new insights into the functional evolution of the gene family in osteichthyans | Q46368750 | ||
| Physiological function of S-cone system is not enhanced in rd7 mice | Q46591612 | ||
| Retinoid X receptor (gamma) is necessary to establish the S-opsin gradient in cone photoreceptors of the developing mouse retina | Q46618793 | ||
| The murine cone photoreceptor: a single cone type expresses both S and M opsins with retinal spatial patterning | Q47818507 | ||
| Nr2e3 and Nrl can reprogram retinal precursors to the rod fate in Xenopus retina. | Q51991027 | ||
| The transcription factor Nr2e3 functions in retinal progenitors to suppress cone cell generation. | Q51995718 | ||
| Spatial and temporal expression of short, long/medium, or both opsins in human fetal cones. | Q52165457 | ||
| Retinopathy and attenuated circadian entrainment in Crx-deficient mice. | Q52537179 | ||
| Two of these or two of those? | Q53648171 | ||
| P433 | issue | 21 | |
| P921 | main subject | retinal degeneration | Q3043268 |
| photoreceptor protein | Q7187894 | ||
| P304 | page(s) | 4102-4115 | |
| P577 | publication date | 2011-08-03 | |
| P1433 | published in | Human Molecular Genetics | Q2720965 |
| P1476 | title | 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 | |
| P478 | volume | 20 |
| Q89280626 | An FRMD4B variant suppresses dysplastic photoreceptor lesions in models of enhanced S-cone syndrome and of Nrl deficiency |
| Q28084726 | Biology and therapy of inherited retinal degenerative disease: insights from mouse models |
| Q45845107 | Brief report: self-organizing neuroepithelium from human pluripotent stem cells facilitates derivation of photoreceptors. |
| Q64937510 | Correction of NR2E3 Associated Enhanced S-cone Syndrome Patient-specific iPSCs using CRISPR-Cas9. |
| Q34199858 | Defects in the outer limiting membrane are associated with rosette development in the Nrl-/- retina |
| Q37238631 | Differential dimerization of variants linked to enhanced S-cone sensitivity syndrome (ESCS) located in the NR2E3 ligand-binding domain |
| Q51762764 | Epigenetic control of gene regulation during development and disease: A view from the retina. |
| Q34552542 | Feedback induction of a photoreceptor-specific isoform of retinoid-related orphan nuclear receptor β by the rod transcription factor NRL. |
| Q90567439 | Functional Genomics of the Retina to Elucidate its Construction and Deconstruction |
| Q85951343 | LSD1-Mediated Demethylation of H3K4me2 Is Required for the Transition from Late Progenitor to Differentiated Mouse Rod Photoreceptor |
| Q27014125 | Minireview: the role of nuclear receptors in photoreceptor differentiation and disease |
| Q38848956 | Multimodal Regulation Orchestrates Normal and Complex Disease States in the Retina |
| Q31126223 | Network-based bioinformatics analysis of spatio-temporal RNA-Seq data reveals transcriptional programs underpinning normal and aberrant retinal development |
| Q89983887 | Nr2e3 is a genetic modifier that rescues retinal degeneration and promotes homeostasis in multiple models of retinitis pigmentosa |
| Q34708558 | Overexpression of retinal degeneration slow (RDS) protein adversely affects rods in the rd7 model of enhanced S-cone syndrome |
| Q26786718 | Photoreceptor cell fate specification in vertebrates |
| Q28818084 | Potential of Small Molecule-Mediated Reprogramming of Rod Photoreceptors to Treat Retinitis Pigmentosa |
| Q38124977 | S cones: Evolution, retinal distribution, development, and spectral sensitivity |
| Q46085195 | Small molecule Photoregulin3 prevents retinal degeneration in the RhoP23H mouse model of retinitis pigmentosa. |
| Q57038377 | Swept source optical coherence tomography and optical coherence tomography angiography in pediatric enhanced S-cone syndrome: a case report |
| Q27680068 | The Crystal Structure of the Orphan Nuclear Receptor NR2E3/PNR Ligand Binding Domain Reveals a Dimeric Auto-Repressed Conformation |
| Q50436594 | The nuclear hormone receptor gene Nr2c1 (Tr2) is a critical regulator of early retina cell patterning. |
| Q53165022 | Two-color pupillometry in enhanced S-cone syndrome caused by NR2E3 mutations. |
| Q35470460 | Vision from next generation sequencing: multi-dimensional genome-wide analysis for producing gene regulatory networks underlying retinal development, aging and disease |
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