| scholarly article | Q13442814 |
| P50 | author | Theodore G. Wensel | Q42403865 |
| P2093 | author name string | John H Wilson | |
| Samuel M Wu | |||
| Fung Chan | |||
| Brandee A Price | |||
| Ivette M Sandoval | |||
| David L Simons | |||
| P2860 | cites work | Rhodopsin accumulation at abnormal sites in retinas of mice with a human P23H rhodopsin transgene | Q72805174 |
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| Transgenic mice with a rhodopsin mutation (Pro23His): a mouse model of autosomal dominant retinitis pigmentosa | Q28115055 | ||
| Engineering mouse chromosomes with Cre-loxP: range, efficiency, and somatic applications | Q28141304 | ||
| IRE1 signaling affects cell fate during the unfolded protein response | Q29615502 | ||
| Retinitis pigmentosa | Q29616538 | ||
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| Probing mechanisms of photoreceptor degeneration in a new mouse model of the common form of autosomal dominant retinitis pigmentosa due to P23H opsin mutations | Q34695879 | ||
| Preparation and properties of phospholipid bilayers containing rhodopsin | Q34729108 | ||
| Knock-in human rhodopsin-GFP fusions as mouse models for human disease and targets for gene therapy | Q34836312 | ||
| Morphological, physiological, and biochemical changes in rhodopsin knockout mice | Q34853562 | ||
| Functional heterogeneity of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa | Q34951881 | ||
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| The nature of dominant mutations of rhodopsin and implications for gene therapy | Q35566986 | ||
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| Characterization of rhodopsin P23H-induced retinal degeneration in a Xenopus laevis model of retinitis pigmentosa | Q40249918 | ||
| Structure and function in rhodopsin. 7. Point mutations associated with autosomal dominant retinitis pigmentosa | Q41467175 | ||
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| A rhodopsin mutant linked to autosomal dominant retinitis pigmentosa is prone to aggregate and interacts with the ubiquitin proteasome system | Q44045954 | ||
| Retinoids assist the cellular folding of the autosomal dominant retinitis pigmentosa opsin mutant P23H. | Q44760460 | ||
| Differential oocyte-specific expression of Cre recombinase activity in GDF-9-iCre, Zp3cre, and Msx2Cre transgenic mice. | Q44950379 | ||
| Mouse opsin. Gene structure and molecular basis of multiple transcripts | Q48247850 | ||
| Defective development of photoreceptor membranes in a mouse model of recessive retinal degeneration. | Q50715249 | ||
| Structural and functional rescue of murine rod photoreceptors by human rhodopsin transgene. | Q52535368 | ||
| Light-induced acceleration of photoreceptor degeneration in transgenic mice expressing mutant rhodopsin | Q71007252 | ||
| Functional abnormalities in transgenic mice expressing a mutant rhodopsin gene | Q72410745 | ||
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P433 | issue | 13 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | retinitis pigmentosa | Q847057 |
| P304 | page(s) | 9728-9736 | |
| P577 | publication date | 2011-12-28 | |
| P1433 | published in | Investigative Ophthalmology Visual Science | Q6060707 |
| P1476 | title | Mislocalization and degradation of human P23H-rhodopsin-GFP in a knockin mouse model of retinitis pigmentosa | |
| P478 | volume | 52 |
| Q91866889 | A Novel Mouse Model of MYO7A USH1B Reveals Auditory and Visual System Haploinsufficiencies |
| Q39052548 | A Pro23His mutation alters prenatal rod photoreceptor morphology in a transgenic swine model of retinitis pigmentosa. |
| Q59330365 | ADP-Ribosylation Factor-Like 2 (ARL2) regulates cilia stability and development of outer segments in rod photoreceptor neurons |
| Q34267941 | Abrupt onset of mutations in a developmentally regulated gene during terminal differentiation of post-mitotic photoreceptor neurons in mice |
| Q41941697 | Assessing the correlation between mutant rhodopsin stability and the severity of retinitis pigmentosa |
| Q43116400 | Can fly photoreceptors lead to treatments for rho ((P23H)) -linked retinitis pigmentosa? |
| Q89723035 | Conformational perturbation, allosteric modulation of cellular signaling pathways, and disease in P23H rhodopsin |
| Q35970716 | Determining Membrane Protein Topology Using Fluorescence Protease Protection (FPP). |
| Q53611722 | Dominant and recessive mutations in rhodopsin activate different cell death pathways. |
| Q42141681 | Endoplasmic reticulum stress in vertebrate mutant rhodopsin models of retinal degeneration |
| Q37662833 | Fluorescence spectroscopy of rhodopsins: insights and approaches |
| Q38327842 | Fluorescent knock-in mice to decipher the physiopathological role of G protein-coupled receptors |
| Q35968065 | Mfsd2a Is a Transporter for the Essential ω-3 Fatty Acid Docosahexaenoic Acid (DHA) in Eye and Is Important for Photoreceptor Cell Development |
| Q36271072 | Misfolded opsin mutants display elevated β-sheet structure |
| Q89064003 | Misfolded rhodopsin mutants display variable aggregation properties |
| Q38853535 | Molecular basis for photoreceptor outer segment architecture |
| Q36794716 | Molecular studies of phenotype variation in canine RPGR-XLPRA1. |
| Q37619284 | P23H opsin knock-in mice reveal a novel step in retinal rod disc morphogenesis |
| Q47364210 | Phenotypic characterization of P23H and S334ter rhodopsin transgenic rat models of inherited retinal degeneration |
| Q34268949 | Photoactivation-induced instability of rhodopsin mutants T4K and T17M in rod outer segments underlies retinal degeneration in X. laevis transgenic models of retinitis pigmentosa |
| Q40511870 | Prenatal Exposure to Curcumin Protects Rod Photoreceptors in a Transgenic Pro23His Swine Model of Retinitis Pigmentosa |
| Q37705588 | Progression of Pro23His Retinopathy in a Miniature Swine Model of Retinitis Pigmentosa |
| Q41214333 | Protective effect of clusterin on rod photoreceptor in rat model of retinitis pigmentosa |
| Q41583879 | Restoration of Cone Photoreceptor Function in Retinitis Pigmentosa |
| Q52930035 | Retinitis pigmentosa: impact of different Pde6a point mutations on the disease phenotype. |
| Q34490664 | Rhodopsin gene expression determines rod outer segment size and rod cell resistance to a dominant-negative neurodegeneration mutant |
| Q58700462 | Targeted disruption of the endogenous zebrafish locus as models of rapid rod photoreceptor degeneration |
| Q45873271 | The molecular and cellular basis of rhodopsin retinitis pigmentosa reveals potential strategies for therapy |
| Q37213895 | The severe autosomal dominant retinitis pigmentosa rhodopsin mutant Ter349Glu mislocalizes and induces rapid rod cell death |
| Q55333805 | Tissue inhibitor of metalloproteinases 1 enhances rod survival in the rd1 mouse retina. |
| Q37732157 | Translational and posttranslational regulation of XIAP by eIF2α and ATF4 promotes ER stress-induced cell death during the unfolded protein response |
| Q36803227 | Two-Step Reactivation of Dormant Cones in Retinitis Pigmentosa |
| Q41881511 | Wild-type opsin does not aggregate with a misfolded opsin mutant |
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