| scholarly article | Q13442814 |
| P819 | ADS bibcode | 2009PNAS..10618728L |
| P356 | DOI | 10.1073/PNAS.0902593106 |
| P932 | PMC publication ID | 2765920 |
| P698 | PubMed publication ID | 19850870 |
| P5875 | ResearchGate publication ID | 38030440 |
| P50 | author | John Greenwood | Q48240403 |
| Juan Pedro Martinez-Barbera | Q50630645 | ||
| Marcus Fruttiger | Q56697566 | ||
| P2093 | author name string | Stephen E Moss | |
| Rebecca Longbottom | |||
| Ron H Douglas | |||
| P2860 | cites work | Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophy | Q24317514 |
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| Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa | Q28142917 | ||
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| Leber congenital amaurosis: comprehensive survey of the genetic heterogeneity, refinement of the clinical definition, and genotype-phenotype correlations as a strategy for molecular diagnosis | Q28250847 | ||
| Monocarboxylate transporter MCT1 is located in the apical membrane and MCT3 in the basal membrane of rat RPE | Q28572521 | ||
| An efficient recombination system for chromosome engineering in Escherichia coli | Q29615038 | ||
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| The retinal pigment epithelium in visual function | Q36178984 | ||
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| Regulation of Cre recombinase activity by mutated estrogen receptor ligand-binding domains | Q38343320 | ||
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| RPE destruction causes choriocapillary atrophy. | Q42458037 | ||
| Mouse MCT3 gene is expressed preferentially in retinal pigment and choroid plexus epithelia | Q43565203 | ||
| An epithelial cell destined for apoptosis signals its neighbors to extrude it by an actin- and myosin-dependent mechanism | Q43812071 | ||
| Morphologic characteristics of retinal degeneration induced by sodium iodate in mice | Q44467504 | ||
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| Drusen are associated with local and distant disruptions to human retinal pigment epithelium cells | Q46258004 | ||
| Stabilization of the retinal vascular network by reciprocal feedback between blood vessels and astrocytes. | Q46404558 | ||
| Efficient, inducible Cre-recombinase activation in vascular endothelium. | Q46767104 | ||
| A subset of oligodendrocytes generated from radial glia in the dorsal spinal cord. | Q52054114 | ||
| Débridement of the Pig Retinal Pigment Epithelium In Vivo | Q52508547 | ||
| Cell loss in the aging retina. Relationship to lipofuscin accumulation and macular degeneration. | Q52525243 | ||
| Aging of the human retina. Differential loss of neurons and retinal pigment epithelial cells | Q53709826 | ||
| Cellular and subcellular expression of monocarboxylate transporters in the pigment epithelium and retina of the rat | Q57612087 | ||
| The onset of pigment epithelial proliferation after retinal detachment | Q70828830 | ||
| The effects of iodate and iodoacetate on the retinal adhesion | Q71399650 | ||
| Clinicopathologic correlation of localized retinal pigment epithelium debridement | Q73341486 | ||
| Surgically induced degeneration and regeneration of the choriocapillaris in rabbit | Q78164834 | ||
| Age-related changes in human RPE cell density and apoptosis proportion in situ | Q78305675 | ||
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P433 | issue | 44 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | photoreceptor protein | Q7187894 |
| P1104 | number of pages | 6 | |
| P304 | page(s) | 18728-18733 | |
| P577 | publication date | 2009-10-22 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | Genetic ablation of retinal pigment epithelial cells reveals the adaptive response of the epithelium and impact on photoreceptors | |
| P478 | volume | 106 |
| Q33708713 | Age- and gene-dosage-dependent cre-induced abnormalities in the retinal pigment epithelium |
| Q55314451 | Amyloid beta deposition related retinal pigment epithelium cell impairment and subretinal microglia activation in aged APPswePS1 transgenic mice. |
| Q28589357 | Ascl1 (Mash1) knockout perturbs differentiation of nonneuronal cells in olfactory epithelium |
| Q38767261 | Cell-based therapeutic strategies for replacement and preservation in retinal degenerative diseases |
| Q36301644 | Characterization of Three-Dimensional Retinal Tissue Derived from Human Embryonic Stem Cells in Adherent Monolayer Cultures. |
| Q36648662 | Conditional knockdown of DNA methyltransferase 1 reveals a key role of retinal pigment epithelium integrity in photoreceptor outer segment morphogenesis |
| Q42693296 | Early stages of retinal development depend on Sec13 function |
| Q35646014 | Enhanced retinal pigment epithelium regeneration after injury in MRL/MpJ mice |
| Q35951856 | Evidence for baseline retinal pigment epithelium pathology in the Trp1-Cre mouse |
| Q35005840 | Generation of Cre transgenic mice with postnatal RPE-specific ocular expression |
| Q59804481 | Generation of an inducible RPE-specific Cre transgenic-mouse line |
| Q39762044 | Human induced pluripotent stem-derived retinal pigment epithelium (RPE) cells exhibit ion transport, membrane potential, polarized vascular endothelial growth factor secretion, and gene expression pattern similar to native RPE. |
| Q45875257 | In situ regeneration of retinal pigment epithelium by gene transfer of E2F2: a potential strategy for treatment of macular degenerations |
| Q50333811 | Iron Overload Accelerates the Progression of Diabetic Retinopathy in Association with Increased Retinal Renin Expression |
| Q47152861 | Loss of Extracellular Signal-Regulated Kinase 1/2 in the Retinal Pigment Epithelium Leads to RPE65 Decrease and Retinal Degeneration |
| Q64093656 | Macular hyperpigmentary changes in -Stargardt disease |
| Q35883310 | Microarray analysis of gene expression in West Nile virus-infected human retinal pigment epithelium |
| Q51846846 | Microphthalmia-associated transcription factor acts through PEDF to regulate RPE cell migration. |
| Q35962348 | Mouse slc9a8 mutants exhibit retinal defects due to retinal pigmented epithelium dysfunction |
| Q33558461 | Multimodal Fundus Imaging of Sodium Iodate-Treated Mice Informs RPE Susceptibility and Origins of Increased Fundus Autofluorescence |
| Q36676410 | Mutations in CTNNA1 cause butterfly-shaped pigment dystrophy and perturbed retinal pigment epithelium integrity |
| Q36996228 | Nanofiber Scaffold-Based Tissue-Engineered Retinal Pigment Epithelium to Treat Degenerative Eye Diseases. |
| Q51139789 | Optimal control in the treatment of retinitis pigmentosa. |
| Q21562190 | Otx2 gene deletion in adult mouse retina induces rapid RPE dystrophy and slow photoreceptor degeneration |
| Q34082626 | PALS1 is essential for retinal pigment epithelium structure and neural retina stratification. |
| Q61795965 | Photoreceptor degeneration in microphthalmia () mice: partial rescue by pigment epithelium-derived factor |
| Q52314577 | Pluripotent Stem Cells for Retinal Tissue Engineering: Current Status and Future Prospects. |
| Q27329045 | Protection of retina by αB crystallin in sodium iodate induced retinal degeneration |
| Q39494352 | Quantifying the metabolic contribution to photoreceptor death in retinitis pigmentosa via a mathematical model |
| Q37623614 | R9AP overexpression alters phototransduction kinetics in iCre75 mice. |
| Q64234640 | Regeneration of the zebrafish retinal pigment epithelium after widespread genetic ablation |
| Q41295415 | Retinal changes precede visual dysfunction in the complement factor H knockout mouse |
| Q35456717 | Retinal pigment epithelial expression of complement regulator CD46 is altered early in the course of geographic atrophy |
| Q38141303 | Retinal pigment epithelium development, plasticity, and tissue homeostasis |
| Q34396844 | Selective impairment of a subset of Ran-GTP-binding domains of ran-binding protein 2 (Ranbp2) suffices to recapitulate the degeneration of the retinal pigment epithelium (RPE) triggered by Ranbp2 ablation. |
| Q34494259 | The new paradigm: retinal pigment epithelium cells generated from embryonic or induced pluripotent stem cells |
| Q36727830 | Transcriptional Reactivation of OTX2, RX1 and SIX3 during Reprogramming Contributes to the Generation of RPE Cells from Human iPSCs |
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