| scholarly article | Q13442814 |
| P819 | ADS bibcode | 1998PNAS...95.7103C |
| P356 | DOI | 10.1073/PNAS.95.12.7103 |
| P932 | PMC publication ID | 22754 |
| P698 | PubMed publication ID | 9618546 |
| P5875 | ResearchGate publication ID | 235609307 |
| P2093 | author name string | Y Huang | |
| A H Milam | |||
| S G Jacobson | |||
| Z Y Li | |||
| E Banin | |||
| E M Stone | |||
| D C Hood | |||
| A V Cideciyan | |||
| P2860 | cites work | Light-induced acceleration of photoreceptor degeneration in transgenic mice expressing mutant rhodopsin | Q71007252 |
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| Rhodopsin mutations in autosomal dominant retinitis pigmentosa | Q24564252 | ||
| Identification of novel rhodopsin mutations responsible for retinitis pigmentosa: implications for the structure and function of rhodopsin | Q30445562 | ||
| Human photoreceptor topography | Q34034782 | ||
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| Phenotypes of stop codon and splice site rhodopsin mutations causing retinitis pigmentosa. | Q34339881 | ||
| Defective intracellular transport is the molecular basis of rhodopsin-dependent dominant retinal degeneration | Q34535642 | ||
| Retinal function and rhodopsin levels in autosomal dominant retinitis pigmentosa with rhodopsin mutations | Q34842125 | ||
| Functional heterogeneity of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa | Q34951881 | ||
| Autosomal dominant sectoral retinitis pigmentosa. Two families with transversion mutation in codon 23 of rhodopsin | Q35010653 | ||
| Null mutation in the rhodopsin kinase gene slows recovery kinetics of rod and cone phototransduction in man | Q35678097 | ||
| Cellular interactions implicated in the mechanism of photoreceptor degeneration in transgenic mice expressing a mutant rhodopsin gene | Q36535541 | ||
| Drosophila in vision research. The Friedenwald Lecture | Q38574728 | ||
| A molecular view of vertebrate retinal development | Q39581663 | ||
| Survival factors in retinal degenerations | Q40563558 | ||
| Expanding horizons for receptors coupled to G proteins: diversity and disease | Q40668287 | ||
| Strategies for rescue of retinal photoreceptor cells | Q40790332 | ||
| Mechanisms of photoreceptor death in retinal degenerations. From the cell biology of the 1990s to the ophthalmology of the 21st century? | Q40934393 | ||
| Beta wave of the scotopic (rod) electroretinogram as a measure of the activity of human on-bipolar cells | Q40984973 | ||
| Lineage study of degenerating photoreceptor cells in the rd mouse retina | Q41102330 | ||
| Mutations and diseases of G protein coupled receptors | Q41198838 | ||
| Structure and function in rhodopsin. 7. Point mutations associated with autosomal dominant retinitis pigmentosa | Q41467175 | ||
| Inborn errors of signal transduction: Mutations in G proteins and G protein‐coupled receptors as a cause of disease | Q41521363 | ||
| Characterization of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa. Mutations on the cytoplasmic surface affect transducin activation. | Q41554234 | ||
| Identification of genes causing photoreceptor degenerations leading to blindness | Q41652312 | ||
| Defective phototransductive disk membrane morphogenesis in transgenic mice expressing opsin with a mutated N-terminal domain. | Q42447195 | ||
| Rod bipolar cells in the macaque monkey retina: immunoreactivity and connectivity | Q43536224 | ||
| Genetically engineered large animal model for studying cone photoreceptor survival and degeneration in retinitis pigmentosa | Q44868831 | ||
| Variability in rate of cone degeneration in the retinal degeneration (rd/rd) mouse | Q45882878 | ||
| Tissue-specific and developmental regulation of rod opsin chimeric genes in transgenic mice | Q45967554 | ||
| Rod phototransduction in retinitis pigmentosa: estimation and interpretation of parameters derived from the rod a-wave. | Q50771772 | ||
| An alternative phototransduction model for human rod and cone ERG a-waves: normal parameters and variation with age. | Q52299670 | ||
| Rod phototransduction in retinitis pigmentosa. Distinguishing alternative mechanisms of degeneration. | Q52342400 | ||
| Understanding changes in the b-wave of the ERG caused by heterogeneous receptor damage. | Q52378969 | ||
| Retinal degeneration in transgenic mice with photoreceptor-specific expression of a dominant-negative fibroblast growth factor receptor. | Q52520863 | ||
| Unusual topography of bovine rhodopsin promoter-lacZ fusion gene expression in transgenic mouse retinas. | Q54701113 | ||
| Autosomal dominant retinitis pigmentosa in a large family: a clinical and molecular genetic study | Q57222639 | ||
| Abnormal rod dark adaptation in autosomal dominant retinitis pigmentosa with proline-23-histidine rhodopsin mutation | Q57223613 | ||
| Autosomal Dominant Retinitis Pigmentosa Caused by the Threonine-17-Methionine Rhodopsin Mutation: Retinal Histopathology and Immunocytochemistry | Q58378357 | ||
| Influence of eye pigmentation and light deprivation on inherited retinal dystrophy in the rat | Q67273988 | ||
| Retinal genetics: a nullifying effect for rhodopsin | Q67482918 | ||
| A quantitative account of the activation steps involved in phototransduction in amphibian photoreceptors | Q67503550 | ||
| Morphological findings in retinitis pigmentosa with early diffuse rod dysfunction | Q68096611 | ||
| X-linked recessive retinitis pigmentosa. Clinical characteristics of carriers | Q69608946 | ||
| Autosomal dominant retinitis pigmentosa. A method of classification | Q70069057 | ||
| Molecular genetics of retinitis pigmentosa | Q70838272 | ||
| Clinicopathologic effects of the Q64ter rhodopsin mutation in retinitis pigmentosa | Q71007245 | ||
| P433 | issue | 12 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | photoreceptor protein | Q7187894 |
| P304 | page(s) | 7103-7108 | |
| P577 | publication date | 1998-06-01 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | Disease sequence from mutant rhodopsin allele to rod and cone photoreceptor degeneration in man. | |
| P478 | volume | 95 |
| Q46852193 | A mutation in the cone-specific pde6 gene causes rapid cone photoreceptor degeneration in zebrafish. |
| Q34387798 | A novel locus (RP24) for X-linked retinitis pigmentosa maps to Xq26-27. |
| Q43722371 | AP-1 mediated retinal photoreceptor apoptosis is independent of N-terminal phosphorylation of c-Jun |
| Q33778139 | Acute and Protracted Cell Death in Light-Induced Retinal Degeneration in the Canine Model of Rhodopsin Autosomal Dominant Retinitis Pigmentosa. |
| Q37427526 | Advances in gene therapy technologies to treat retinitis pigmentosa. |
| Q41941697 | Assessing the correlation between mutant rhodopsin stability and the severity of retinitis pigmentosa |
| Q37217166 | Assessment of visual function and retinal structure following acute light exposure in the light sensitive T4R rhodopsin mutant dog |
| Q44023000 | Attenuation of retinal photooxidative damage in thioredoxin transgenic mice. |
| Q43757186 | Augmented rod bipolar cell function in partial receptor loss: an ERG study in P23H rhodopsin transgenic and aging normal rats |
| Q35682509 | Autofluorescence imaging with near-infrared excitation:normalization by reflectance to reduce signal from choroidal fluorophores. |
| Q93034373 | Autophagy in Xenopus laevis rod photoreceptors is independently regulated by phototransduction and misfolded RHOP23H |
| Q35925194 | Autosomal recessive retinitis pigmentosa caused by mutations in the MAK gene |
| Q33853152 | Caenorhabditis elegans TRPV channels function in a modality-specific pathway to regulate response to aberrant sensory signaling |
| Q36648600 | Clinical light exposure, photoreceptor degeneration, and AP-1 activation: a cell death or cell survival signal in the rhodopsin mutant retina? |
| Q59342182 | Clinically Relevant Outcome Measures for the I307N Rhodopsin Mouse: A Model of Inducible Autosomal Dominant Retinitis Pigmentosa |
| Q44353664 | Clinicopathologic effects of mutant GUCY2D in Leber congenital amaurosis |
| Q37275303 | Complexity of the Class B Phenotype in Autosomal Dominant Retinitis Pigmentosa Due to Rhodopsin Mutations. |
| Q89510723 | Comprehensive Geno- and Phenotyping in a Complex Pedigree Including Four Different Inherited Retinal Dystrophies |
| Q42574125 | Concepts and Strategies in Retinal Gene Therapy. |
| Q33605009 | Cone survival despite rod degeneration in XOPS-mCFP transgenic zebrafish |
| Q51062868 | Congenital Achromatopsia and Macular Atrophy Caused by a Novel Recessive PDE6C Mutation (p.E591K). |
| Q34090917 | Constitutive overexpression of human erythropoietin protects the mouse retina against induced but not inherited retinal degeneration |
| Q44780613 | Contribution of cone photoreceptors and post-receptoral mechanisms to the human photopic electroretinogram |
| Q90258074 | Coupling of Human Rhodopsin to a Yeast Signaling Pathway Enables Characterization of Mutations Associated with Retinal Disease |
| Q40451095 | Cytoprotective effects of geranylgeranylacetone against retinal photooxidative damage. |
| Q40090254 | Dark rearing rescues P23H rhodopsin-induced retinal degeneration in a transgenic Xenopus laevis model of retinitis pigmentosa: a chromophore-dependent mechanism characterized by production of N-terminally truncated mutant rhodopsin. |
| Q41327038 | Dark-Adapted Chromatic Perimetry for Measuring Rod Visual Fields in Patients with Retinitis Pigmentosa |
| Q34789382 | Distinct and atypical intrinsic and extrinsic cell death pathways between photoreceptor cell types upon specific ablation of Ranbp2 in cone photoreceptors. |
| Q37612350 | Does apoptosis regulate the function of retinal photoreceptors? |
| Q92715720 | Down-regulation of Fra-2 alleviates light-induced retina damage by inhibiting the PARP-1/AIF pathway |
| Q34548710 | EnRICH: Extraction and Ranking using Integration and Criteria Heuristics |
| Q35103311 | Exclusion of the unfolded protein response in light-induced retinal degeneration in the canine T4R RHO model of autosomal dominant retinitis pigmentosa. |
| Q73766109 | For want of a disc, the cell was lost.... |
| Q36674599 | From vivarium to bedside: lessons learned from animal models. |
| Q34321474 | Functional photoreceptor loss revealed with adaptive optics: an alternate cause of color blindness |
| Q30936163 | Fundus autofluorescence in carriers of X-linked recessive retinitis pigmentosa associated with mutations in RPGR, and correlation with electrophysiological and psychophysical data |
| Q34083185 | Gene augmentation for adRP mutations in RHO. |
| Q34084443 | Gene therapy and retinitis pigmentosa: advances and future challenges |
| Q34533601 | Genetics of photoreceptor degeneration and regeneration in zebrafish |
| Q46379155 | Genetics of retinitis pigmentosa: metabolic classification and phenotype/genotype correlations |
| Q24649299 | Haploinsufficiency of RanBP2 is neuroprotective against light-elicited and age-dependent degeneration of photoreceptor neurons |
| Q37151815 | High levels of retinal membrane docosahexaenoic acid increase susceptibility to stress-induced degeneration |
| Q36499614 | Identification of two mutations of the RHO gene in two Chinese families with retinitis pigmentosa: correlation between genotype and phenotype. |
| Q30856833 | In vivo dynamics of retinal injury and repair in the rhodopsin mutant dog model of human retinitis pigmentosa |
| Q28576663 | Increased light damage susceptibility at night does not correlate with RPE65 levels and rhodopsin regeneration in rats |
| Q37671070 | Inner and outer retinal changes in retinal degenerations associated with ABCA4 mutations |
| Q91771366 | Inner retinal preservation in the photoinducible I307N rhodopsin mutant mouse, a model of autosomal dominant retinitis pigmentosa |
| Q28577902 | Intraperitoneal injection of Ginkgo biloba extract enhances antioxidation ability of retina and protects photoreceptors after light-induced retinal damage in rats |
| Q90152961 | Leber Congenital Amaurosis (LCA): Potential for Improvement of Vision |
| Q33992484 | Leber congenital amaurosis due to RPE65 mutations and its treatment with gene therapy |
| Q27307727 | Lentiviral expression of retinal guanylate cyclase-1 (RetGC1) restores vision in an avian model of childhood blindness |
| Q35933054 | Lifespan and mitochondrial control of neurodegeneration |
| Q36481342 | Light and inherited retinal degeneration |
| Q37680148 | Light damage in Abca4 and Rpe65rd12 mice |
| Q28360305 | Light induced apoptosis is accelerated in transgenic retina overexpressing human EAT/mcl-1, an anti-apoptotic bcl-2 related gene |
| Q37987979 | Light might directly affect retinal ganglion cell mitochondria to potentially influence function. |
| Q89975685 | Metabolic and Redox Signaling of the Nucleoredoxin-Like-1 Gene for the Treatment of Genetic Retinal Diseases |
| Q36098417 | Molecular Heterogeneity Within the Clinical Diagnosis of Pericentral Retinal Degeneration. |
| Q73082838 | Molecular analysis of the rhodopsin gene in southern France: identification of the first duplication responsible for retinitis pigmentosa, c.998999ins4 |
| Q41577738 | Mouse models of human ocular disease for translational research |
| Q59354224 | Mutation-independent rhodopsin gene therapy by knockdown and replacement with a single AAV vector |
| Q51786028 | Mutational Analysis of the Rhodopsin Gene in Sector Retinitis Pigmentosa. |
| Q40539527 | Mutations in ABCA4 result in accumulation of lipofuscin before slowing of the retinoid cycle: a reappraisal of the human disease sequence |
| Q50336767 | Mutations in RGR, encoding a light-sensitive opsin homologue, in patients with retinitis pigmentosa |
| Q33825000 | Mutations of the opsin gene (Y102H and I307N) lead to light-induced degeneration of photoreceptors and constitutive activation of phototransduction in mice |
| Q34029081 | Naturally occurring rhodopsin mutation in the dog causes retinal dysfunction and degeneration mimicking human dominant retinitis pigmentosa |
| Q36804427 | New therapeutic targets in atrophic age-related macular degeneration |
| Q36731022 | Nonsense mutations in the rhodopsin gene that give rise to mild phenotypes trigger mRNA degradation in human cells by nonsense-mediated decay |
| Q35593740 | Novel rhodopsin mutations and genotype-phenotype correlation in patients with autosomal dominant retinitis pigmentosa |
| Q33334037 | Operating in the dark: a night-vision system for surgery in retinas susceptible to light damage |
| Q48163206 | Opposing Effects of Valproic Acid Treatment Mediated by Histone Deacetylase Inhibitor Activity in Four Transgenic X. laevis Models of Retinitis Pigmentosa. |
| Q41051547 | Pattern of retinal morphological and functional decay in a light-inducible, rhodopsin mutant mouse |
| Q39957785 | Pharmacological dissection of multifocal electroretinograms of rabbits with Pro347Leu rhodopsin mutation |
| Q28818673 | Potential implication of the chemical properties and bioactivity of nitrone spin traps for therapeutics |
| Q33715782 | Prevalence and novelty of PRPF31 mutations in French autosomal dominant rod-cone dystrophy patients and a review of published reports |
| Q34695879 | Probing mechanisms of photoreceptor degeneration in a new mouse model of the common form of autosomal dominant retinitis pigmentosa due to P23H opsin mutations |
| Q36108106 | Prospectives for gene therapy of retinal degenerations |
| Q56873521 | Protection of Rpe65-deficient mice identifies rhodopsin as a mediator of light-induced retinal degeneration |
| Q37602649 | Rearrangement of the cone mosaic in the retina of the rat model of retinitis pigmentosa |
| Q64079162 | Regional Variations and Intra-/Intersession Repeatability for Scotopic Sensitivity in Normal Controls and Patients With Inherited Retinal Degenerations |
| Q35687907 | Retinal disease course in Usher syndrome 1B due to MYO7A mutations |
| Q35229775 | Retinal laminar architecture in human retinitis pigmentosa caused by Rhodopsin gene mutations |
| Q52175364 | Retinal rod photoreceptor-specific gene mutation perturbs cone pathway development. |
| Q79172589 | Retinitis pigmentosa associated with rhodopsin mutations: Correlation between phenotypic variability and molecular effects |
| Q27330479 | Retinotopic Distribution of Structural and Functional Damages following Bright Light Exposure of Juvenile Rats |
| Q37149399 | Rhodopsin F45L Allele Does Not Cause Autosomal Dominant Retinitis Pigmentosa in a Large Caucasian Family |
| Q37074555 | Rod and rod-driven function in achromatopsia and blue cone monochromatism |
| Q98158710 | Rod function deficit in retained photoreceptors of patients with class B Rhodopsin mutations |
| Q37012770 | Rod photoreceptors protect from cone degeneration-induced retinal remodeling and restore visual responses in zebrafish |
| Q39259487 | Rod-cone interactions: developmental and clinical significance |
| Q33662583 | Rpe65 as a modifier gene for inherited retinal degeneration |
| Q44260720 | SOD2 knockdown mouse model of early AMD. |
| Q92134388 | SRD005825 Acts as a Pharmacologic Chaperone of Opsin and Promotes Survival of Photoreceptors in an Animal Model of Autosomal Dominant Retinitis Pigmentosa |
| Q92460496 | Sector retinitis pigmentosa: Report of ten cases and a review of the literature |
| Q100526014 | Sectoral activation of glia in an inducible mouse model of autosomal dominant retinitis pigmentosa |
| Q35007950 | Spectrum of rhodopsin mutations in French autosomal dominant rod-cone dystrophy patients |
| Q37344299 | Steroids do not prevent photoreceptor degeneration in the light-exposed T4R rhodopsin mutant dog retina irrespective of AP-1 inhibition |
| Q34302617 | Substitution of isoleucine for threonine at position 190 of S-opsin causes S-cone-function abnormalities. |
| Q34497784 | Successful arrest of photoreceptor and vision loss expands the therapeutic window of retinal gene therapy to later stages of disease |
| Q58700462 | Targeted disruption of the endogenous zebrafish locus as models of rapid rod photoreceptor degeneration |
| Q43517437 | The Rpe65 Leu450Met variation increases retinal resistance against light-induced degeneration by slowing rhodopsin regeneration. |
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| Q46314250 | The cytoplasmic tail of rhodopsin triggers rapid rod degeneration in kinesin-2 mutants |
| Q45873271 | The molecular and cellular basis of rhodopsin retinitis pigmentosa reveals potential strategies for therapy |
| Q36328538 | The retinal phenotype of Grk1-/- is compromised by a Crb1 rd8 mutation |
| Q36388888 | The temporal topography of the N-Methyl- N-nitrosourea induced photoreceptor degeneration in mouse retina |
| Q37458980 | The use of canine models of inherited retinal degeneration to test novel therapeutic approaches |
| Q35092187 | Therapeutic challenges to retinitis pigmentosa: from neuroprotection to gene therapy. |
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| Q34024392 | Xenopus laevis P23H rhodopsin transgene causes rod photoreceptor degeneration that is more severe in the ventral retina and is modulated by light |
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