These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
220 related articles for article (PubMed ID: 25637522)
1. Glycosylation of rhodopsin is necessary for its stability and incorporation into photoreceptor outer segment discs. Murray AR; Vuong L; Brobst D; Fliesler SJ; Peachey NS; Gorbatyuk MS; Naash MI; Al-Ubaidi MR Hum Mol Genet; 2015 May; 24(10):2709-23. PubMed ID: 25637522 [TBL] [Abstract][Full Text] [Related]
2. Transgenic mice carrying the dominant rhodopsin mutation P347S: evidence for defective vectorial transport of rhodopsin to the outer segments. Li T; Snyder WK; Olsson JE; Dryja TP Proc Natl Acad Sci U S A; 1996 Nov; 93(24):14176-81. PubMed ID: 8943080 [TBL] [Abstract][Full Text] [Related]
4. Photoactivation-induced instability of rhodopsin mutants T4K and T17M in rod outer segments underlies retinal degeneration in X. laevis transgenic models of retinitis pigmentosa. Tam BM; Noorwez SM; Kaushal S; Kono M; Moritz OL J Neurosci; 2014 Oct; 34(40):13336-48. PubMed ID: 25274813 [TBL] [Abstract][Full Text] [Related]
5. Retinal degeneration in humanized mice expressing mutant rhodopsin under the control of the endogenous murine promoter. Liu X; Jia R; Meng X; Li Y; Yang L Exp Eye Res; 2022 Feb; 215():108893. PubMed ID: 34919893 [TBL] [Abstract][Full Text] [Related]
6. Light regulation of rhodopsin distribution during outer segment renewal in murine rod photoreceptors. Rose K; Chen N; Andreev A; Chen J; Kefalov VJ; Chen J Curr Biol; 2024 Apr; 34(7):1492-1505.e6. PubMed ID: 38508186 [TBL] [Abstract][Full Text] [Related]
7. A diffusible factor from normal retinal cells promotes rod photoreceptor survival in an in vitro model of retinitis pigmentosa. Streichert LC; Birnbach CD; Reh TA J Neurobiol; 1999 Jun; 39(4):475-90. PubMed ID: 10380070 [TBL] [Abstract][Full Text] [Related]
8. Rhodopsin gene expression determines rod outer segment size and rod cell resistance to a dominant-negative neurodegeneration mutant. Price BA; Sandoval IM; Chan F; Nichols R; Roman-Sanchez R; Wensel TG; Wilson JH PLoS One; 2012; 7(11):e49889. PubMed ID: 23185477 [TBL] [Abstract][Full Text] [Related]
9. P23H opsin knock-in mice reveal a novel step in retinal rod disc morphogenesis. Sakami S; Kolesnikov AV; Kefalov VJ; Palczewski K Hum Mol Genet; 2014 Apr; 23(7):1723-41. PubMed ID: 24214395 [TBL] [Abstract][Full Text] [Related]
10. A rhodopsin gene mutation responsible for autosomal dominant retinitis pigmentosa results in a protein that is defective in localization to the photoreceptor outer segment. Sung CH; Makino C; Baylor D; Nathans J J Neurosci; 1994 Oct; 14(10):5818-33. PubMed ID: 7523628 [TBL] [Abstract][Full Text] [Related]
11. Opsin localization and rhodopsin photochemistry in a transgenic mouse model of retinitis pigmentosa. Wu TH; Ting TD; Okajima TI; Pepperberg DR; Ho YK; Ripps H; Naash MI Neuroscience; 1998 Dec; 87(3):709-17. PubMed ID: 9758235 [TBL] [Abstract][Full Text] [Related]
12. Retinopathy induced in mice by targeted disruption of the rhodopsin gene. Humphries MM; Rancourt D; Farrar GJ; Kenna P; Hazel M; Bush RA; Sieving PA; Sheils DM; McNally N; Creighton P; Erven A; Boros A; Gulya K; Capecchi MR; Humphries P Nat Genet; 1997 Feb; 15(2):216-9. PubMed ID: 9020854 [TBL] [Abstract][Full Text] [Related]
13. The role of rhodopsin glycosylation in protein folding, trafficking, and light-sensitive retinal degeneration. Tam BM; Moritz OL J Neurosci; 2009 Dec; 29(48):15145-54. PubMed ID: 19955366 [TBL] [Abstract][Full Text] [Related]
14. Increased sensitivity to light-induced damage in a mouse model of autosomal dominant retinal disease. White DA; Fritz JJ; Hauswirth WW; Kaushal S; Lewin AS Invest Ophthalmol Vis Sci; 2007 May; 48(5):1942-51. PubMed ID: 17460245 [TBL] [Abstract][Full Text] [Related]
15. Restoration of photoreceptor ultrastructure and function in retinal degeneration slow mice by gene therapy. Ali RR; Sarra GM; Stephens C; Alwis MD; Bainbridge JW; Munro PM; Fauser S; Reichel MB; Kinnon C; Hunt DM; Bhattacharya SS; Thrasher AJ Nat Genet; 2000 Jul; 25(3):306-10. PubMed ID: 10888879 [TBL] [Abstract][Full Text] [Related]
16. Rhodopsin transgenic pigs as a model for human retinitis pigmentosa. Li ZY; Wong F; Chang JH; Possin DE; Hao Y; Petters RM; Milam AH Invest Ophthalmol Vis Sci; 1998 Apr; 39(5):808-19. PubMed ID: 9538889 [TBL] [Abstract][Full Text] [Related]
17. Autosomal dominant retinitis pigmentosa caused by the threonine-17-methionine rhodopsin mutation: retinal histopathology and immunocytochemistry. Li ZY; Jacobson SG; Milam AH Exp Eye Res; 1994 Apr; 58(4):397-408. PubMed ID: 7925677 [TBL] [Abstract][Full Text] [Related]
18. Effect of vitamin A supplementation on rhodopsin mutants threonine-17 --> methionine and proline-347 --> serine in transgenic mice and in cell cultures. Li T; Sandberg MA; Pawlyk BS; Rosner B; Hayes KC; Dryja TP; Berson EL Proc Natl Acad Sci U S A; 1998 Sep; 95(20):11933-8. PubMed ID: 9751768 [TBL] [Abstract][Full Text] [Related]
19. Mechanisms of neurodegeneration in a preclinical autosomal dominant retinitis pigmentosa knock-in model with a Rho Sancho-Pelluz J; Cui X; Lee W; Tsai YT; Wu WH; Justus S; Washington I; Hsu CW; Park KS; Koch S; Velez G; Bassuk AG; Mahajan VB; Lin CS; Tsang SH Cell Mol Life Sci; 2019 Sep; 76(18):3657-3665. PubMed ID: 30976840 [TBL] [Abstract][Full Text] [Related]
20. ER stress is involved in T17M rhodopsin-induced retinal degeneration. Kunte MM; Choudhury S; Manheim JF; Shinde VM; Miura M; Chiodo VA; Hauswirth WW; Gorbatyuk OS; Gorbatyuk MS Invest Ophthalmol Vis Sci; 2012 Jun; 53(7):3792-800. PubMed ID: 22589437 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]