| scholarly article | Q13442814 |
| P356 | DOI | 10.1167/TVST.4.5.5 |
| P8608 | Fatcat ID | release_y2csu6hq2vflthgx74nj5jusk4 |
| P932 | PMC publication ID | 4572939 |
| P698 | PubMed publication ID | 26396931 |
| P2093 | author name string | Maureen A McCall | |
| Henry J Kaplan | |||
| Patrick A Scott | |||
| P2860 | cites work | Gene therapy for Leber's congenital amaurosis is safe and effective through 1.5 years after vector administration | Q24627838 |
| Safranal, a saffron constituent, attenuates retinal degeneration in P23H rats | Q27323948 | ||
| Functional cone rescue by RdCVF protein in a dominant model of retinitis pigmentosa | Q33713504 | ||
| Rescue of photoreceptor degeneration by curcumin in transgenic rats with P23H rhodopsin mutation. | Q33954730 | ||
| Rod-derived cone viability factor for treating blinding diseases: from clinic to redox signaling | Q33960294 | ||
| Identification and characterization of rod-derived cone viability factor | Q33979422 | ||
| Activation of mislocalized opsin kills rod cells: a novel mechanism for rod cell death in retinal disease | Q34025929 | ||
| A point mutation of the rhodopsin gene in one form of retinitis pigmentosa | Q34168407 | ||
| Tauroursodeoxycholic acid prevents retinal degeneration in transgenic P23H rats. | Q34179718 | ||
| Inhibitory peptide of mitochondrial μ-calpain protects against photoreceptor degeneration in rhodopsin transgenic S334ter and P23H rats | Q34950176 | ||
| Viral-mediated RdCVF and RdCVFL expression protects cone and rod photoreceptors in retinal degeneration | Q35242633 | ||
| Gene therapy using stem cells | Q35245259 | ||
| Generation of an inbred miniature pig model of retinitis pigmentosa. | Q35797314 | ||
| Mislocalization and degradation of human P23H-rhodopsin-GFP in a knockin mouse model of retinitis pigmentosa | Q35925204 | ||
| Mislocalized opsin and cAMP signaling: a mechanism for sprouting by rod cells in retinal degeneration | Q36299882 | ||
| Proinsulin slows retinal degeneration and vision loss in the P23H rat model of retinitis pigmentosa | Q36469478 | ||
| Human retinal gene therapy for Leber congenital amaurosis shows advancing retinal degeneration despite enduring visual improvement | Q36598421 | ||
| Advances in gene therapy technologies to treat retinitis pigmentosa. | Q37427526 | ||
| Artificial vision: needs, functioning, and testing of a retinal electronic prosthesis | Q37574446 | ||
| Animal models and different therapies for treatment of retinitis pigmentosa. | Q37581508 | ||
| Cone photoreceptors develop normally in the absence of functional rod photoreceptors in a transgenic swine model of retinitis pigmentosa | Q37714131 | ||
| Optogenetics, visual prosthesis and electrostimulation for retinal dystrophies | Q38116908 | ||
| Recent advances of stem cell therapy for retinitis pigmentosa | Q38241625 | ||
| Recent advances in treatment of retinitis pigmentosa | Q38262801 | ||
| Patient-specific induced pluripotent stem cells (iPSCs) for the study and treatment of retinal degenerative diseases | Q38275478 | ||
| Thioredoxin rod-derived cone viability factor protects against photooxidative retinal damage | Q38990569 | ||
| The heat-shock response co-inducer arimoclomol protects against retinal degeneration in rhodopsin retinitis pigmentosa. | Q38992661 | ||
| A Pro23His mutation alters prenatal rod photoreceptor morphology in a transgenic swine model of retinitis pigmentosa. | Q39052548 | ||
| Characterization of rhodopsin P23H-induced retinal degeneration in a Xenopus laevis model of retinitis pigmentosa | Q40249918 | ||
| Retinitis pigmentosa. The Friedenwald Lecture | Q40896642 | ||
| Expression of opsin and IRBP genes in mutant RCS rats | Q41094539 | ||
| Dominant retinitis pigmentosa with reduced penetrance. Further studies of the electroretinogram | Q41667247 | ||
| Neuroprotective effects of the cannabinoid agonist HU210 on retinal degeneration. | Q45746761 | ||
| The Argus II Retinal Prosthesis: 12-month outcomes from a single-study center. | Q53615341 | ||
| A rhodopsin gene mutation responsible for autosomal dominant retinitis pigmentosa results in a protein that is defective in localization to the photoreceptor outer segment | Q71651373 | ||
| Rod Responses in Retinitis Pigmentosa, Dominantly Inherited | Q72067408 | ||
| Rod and cone responses in sex-linked retinitis pigmentosa | Q72337820 | ||
| Rhodopsin accumulation at abnormal sites in retinas of mice with a human P23H rhodopsin transgene | Q72805174 | ||
| Rhodopsin transgenic pigs as a model for human retinitis pigmentosa | Q74432045 | ||
| Histopathology of the human retina in retinitis pigmentosa | Q77057686 | ||
| Immunocytochemical localization of opsin in degenerating photoreceptors of RCS rats and rd and rds mice | Q93531433 | ||
| P433 | issue | 5 | |
| P921 | main subject | curcumin | Q312266 |
| photoreceptor protein | Q7187894 | ||
| P304 | page(s) | 5 | |
| P577 | publication date | 2015-09-16 | |
| P1433 | published in | Translational vision science & technology | Q27724547 |
| P1476 | title | Prenatal Exposure to Curcumin Protects Rod Photoreceptors in a Transgenic Pro23His Swine Model of Retinitis Pigmentosa | |
| P478 | volume | 4 |
| Q56978275 | Anatomic Studies of the Miniature Swine Cornea |
| Q92629828 | Curcumin as a Therapeutic Option in Retinal Diseases |
| Q37705588 | Progression of Pro23His Retinopathy in a Miniature Swine Model of Retinitis Pigmentosa |
| Q47412922 | Swine models, genomic tools and services to enhance our understanding of human health and diseases |
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