| scholarly article | Q13442814 |
| P50 | author | Joseph E O'Tousa | Q45712629 |
| P2093 | author name string | Kurada P | |
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | retinal degeneration | Q3043268 |
| P304 | page(s) | 571-579 | |
| P577 | publication date | 1995-03-01 | |
| P1433 | published in | Neuron | Q3338676 |
| P1476 | title | Retinal degeneration caused by dominant rhodopsin mutations in Drosophila. | |
| P478 | volume | 14 |
| Q37576581 | 4E-BP is a target of the GCN2-ATF4 pathway during Drosophila development and aging |
| Q52584174 | A molecular pathway for light-dependent photoreceptor apoptosis in Drosophila. |
| Q44045954 | A rhodopsin mutant linked to autosomal dominant retinitis pigmentosa is prone to aggregate and interacts with the ubiquitin proteasome system |
| Q42151382 | A role for the cytoplasmic DEAD box helicase Dbp21E2 in rhodopsin maturation and photoreceptor viability |
| Q77874512 | Activation of caspase-3 in the retina of transgenic rats with the rhodopsin mutation s334ter during photoreceptor degeneration |
| Q91890102 | Aging and the clock: Perspective from flies to humans |
| Q47934948 | Anti-apoptosis therapy: a way of treating neural degeneration? |
| Q52561684 | Blocking apoptosis prevents blindness in Drosophila retinal degeneration mutants. |
| Q35870707 | CDK5 and MEKK1 mediate pro-apoptotic signalling following endoplasmic reticulum stress in an autosomal dominant retinitis pigmentosa model |
| Q41872250 | CDK7 regulates the mitochondrial localization of a tail-anchored proapoptotic protein, Hid |
| Q42266704 | Calnexin is essential for rhodopsin maturation, Ca2+ regulation, and photoreceptor cell survival |
| Q36551266 | Candidate genetic modifiers of retinitis pigmentosa identified by exploiting natural variation in Drosophila |
| Q36502943 | Cell-nonautonomous function of ceramidase in photoreceptor homeostasis |
| Q33927508 | Chaperoning G protein-coupled receptors: from cell biology to therapeutics |
| Q36280664 | Characterization of a folding intermediate from HIV-1 ribonuclease H |
| Q35629107 | Characterization of two dominant alleles of the major rhodopsin-encoding gene ninaE in Drosophila |
| Q40620754 | Constitutive and agonist-dependent self-association of the cell surface human lutropin receptor |
| Q41192041 | Drosophila Rhodopsin 7 can partially replace the structural role of Rhodopsin 1, but not its physiological function |
| Q42118593 | Drosophila fatty acid transport protein regulates rhodopsin-1 metabolism and is required for photoreceptor neuron survival. |
| Q37194635 | ER stress protects from retinal degeneration |
| Q95819253 | Examining rhodopsin folding and assembly through expression of polypeptide fragments |
| Q58554380 | Human eye conditions: insights from the fly eye |
| Q24317208 | Identification and characterization of a conserved family of protein serine/threonine phosphatases homologous to Drosophila retinal degeneration C |
| Q47071934 | Identification of a novel Drosophila opsin reveals specific patterning of the R7 and R8 photoreceptor cells. |
| Q24300657 | Identification of new kinase clusters required for neurite outgrowth and retraction by a loss-of-function RNA interference screen |
| Q34333825 | Identification of the Drosophila ortholog of HSPB8: implication of HSPB8 loss of function in protein folding diseases. |
| Q27346679 | Inactivation of VCP/ter94 suppresses retinal pathology caused by misfolded rhodopsin in Drosophila |
| Q24683146 | Interconversion of red opsin isoforms by the cyclophilin-related chaperone protein Ran-binding protein 2 |
| Q36743972 | Ire1 supports normal ER differentiation in developing Drosophila photoreceptors |
| Q30661583 | Isolation of a zebrafish rod opsin promoter to generate a transgenic zebrafish line expressing enhanced green fluorescent protein in rod photoreceptors. |
| Q34019109 | LEDGF(1-326) decreases P23H and wild type rhodopsin aggregates and P23H rhodopsin mediated cell damage in human retinal pigment epithelial cells |
| Q44728734 | Limited role of developmental programmed cell death pathways in Drosophila norpA retinal degeneration. |
| Q45712563 | Loss of the phospholipase C gene product induces massive endocytosis of rhodopsin and arrestin in Drosophila photoreceptors |
| Q48654058 | Mammalian homolog of Drosophila retinal degeneration B rescues the mutant fly phenotype |
| Q33870792 | Modeling human neurodegenerative diseases in Drosophila: on a wing and a prayer. |
| Q34665702 | Molecular aspects of retinal degenerative diseases |
| Q37928310 | Molecular genetics of retinal degeneration: A Drosophila perspective |
| Q41788170 | Mutation of a TADR protein leads to rhodopsin and Gq-dependent retinal degeneration in Drosophila |
| Q36269243 | Neurodegenerative mutants in Drosophila: a means to identify genes and mechanisms involved in human diseases? |
| Q24514484 | Normal light response, photoreceptor integrity, and rhodopsin dephosphorylation in mice lacking both protein phosphatases with EF hands (PPEF-1 and PPEF-2) |
| Q44795507 | Novel dominant rhodopsin mutation triggers two mechanisms of retinal degeneration and photoreceptor desensitization. |
| Q26752261 | Oligomerization of GPCRs involved in endocrine regulation |
| Q54949712 | PCYT1A Regulates Phosphatidylcholine Homeostasis from the Inner Nuclear Membrane in Response to Membrane Stored Curvature Elastic Stress. |
| Q36208331 | PDA (prolonged depolarizing afterpotential)-defective mutants: the story of nina's and ina's--pinta and santa maria, too. |
| Q41524945 | Perspectives on eye development |
| Q36814854 | Phototransduction and retinal degeneration in Drosophila. |
| Q45296540 | Polyglutamine-expanded human huntingtin transgenes induce degeneration of Drosophila photoreceptor neurons. |
| Q27631214 | Proline in α-helical kink is required for folding kinetics but not for kinked structure, function, or stability of heat shock transcription factor |
| Q47761256 | Rab6 regulation of rhodopsin transport in Drosophila |
| Q27015947 | Retinal degeneration in the fly |
| Q38135048 | Rhodopsin homeostasis and retinal degeneration: lessons from the fly. |
| Q73794365 | Role of asparagine-linked oligosaccharides in rhodopsin maturation and association with its molecular chaperone, NinaA |
| Q36197653 | Role of rhodopsin and arrestin phosphorylation in retinal degeneration of Drosophila |
| Q33886329 | Site-directed mutagenesis of highly conserved amino acids in the first cytoplasmic loop of Drosophila Rh1 opsin blocks rhodopsin synthesis in the nascent state |
| Q37359601 | Suppression of retinal degeneration in Drosophila by stimulation of ER-associated degradation |
| Q35918261 | The Drosophila tctex-1 light chain is dispensable for essential cytoplasmic dynein functions but is required during spermatid differentiation |
| Q38360057 | The accessibility of yeast ribosomal protein L1 as probed by proteolysis and site-directed mutagenesis is different in intact 60 and 80 S ribosome |
| Q27315072 | The retromer complex is required for rhodopsin recycling and its loss leads to photoreceptor degeneration |
| Q47111001 | Transcriptome profiling of aging Drosophila photoreceptors reveals gene expression trends that correlate with visual senescence |
| Q35947581 | Transgenic mice carrying the dominant rhodopsin mutation P347S: evidence for defective vectorial transport of rhodopsin to the outer segments |
| Q99557293 | Translational induction of ATF4 during integrated stress response requires noncanonical initiation factors eIF2D and DENR |
| Q24682908 | Unfolded protein response in a Drosophila model for retinal degeneration |
| Q39440497 | XPORT-dependent transport of TRP and rhodopsin. |
| Q50098079 | highroad Is a Carboxypetidase Induced by Retinoids to Clear Mutant Rhodopsin-1 in Drosophila Retinitis Pigmentosa Models |
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