386 related articles for article (PubMed ID: 17108167)
1. Stable rhodopsin/arrestin complex leads to retinal degeneration in a transgenic mouse model of autosomal dominant retinitis pigmentosa.
Chen J; Shi G; Concepcion FA; Xie G; Oprian D; Chen J
J Neurosci; 2006 Nov; 26(46):11929-37. PubMed ID: 17108167
[TBL] [Abstract][Full Text] [Related]
2. Constitutive activation of phototransduction by K296E opsin is not a cause of photoreceptor degeneration.
Li T; Franson WK; Gordon JW; Berson EL; Dryja TP
Proc Natl Acad Sci U S A; 1995 Apr; 92(8):3551-5. PubMed ID: 7724596
[TBL] [Abstract][Full Text] [Related]
3. Rhodopsin signaling mediates light-induced photoreceptor cell death in rd10 mice through a transducin-independent mechanism.
Sundar JC; Munezero D; Bryan-Haring C; Saravanan T; Jacques A; Ramamurthy V
Hum Mol Genet; 2020 Feb; 29(3):394-406. PubMed ID: 31925423
[TBL] [Abstract][Full Text] [Related]
4. Mice with a D190N mutation in the gene encoding rhodopsin: a model for human autosomal-dominant retinitis pigmentosa.
Sancho-Pelluz J; Tosi J; Hsu CW; Lee F; Wolpert K; Tabacaru MR; Greenberg JP; Tsang SH; Lin CS
Mol Med; 2012 May; 18(1):549-55. PubMed ID: 22252712
[TBL] [Abstract][Full Text] [Related]
5. The severe autosomal dominant retinitis pigmentosa rhodopsin mutant Ter349Glu mislocalizes and induces rapid rod cell death.
Hollingsworth TJ; Gross AK
J Biol Chem; 2013 Oct; 288(40):29047-55. PubMed ID: 23940033
[TBL] [Abstract][Full Text] [Related]
6. A novel form of transducin-dependent retinal degeneration: accelerated retinal degeneration in the absence of rod transducin.
Brill E; Malanson KM; Radu RA; Boukharov NV; Wang Z; Chung HY; Lloyd MB; Bok D; Travis GH; Obin M; Lem J
Invest Ophthalmol Vis Sci; 2007 Dec; 48(12):5445-53. PubMed ID: 18055791
[TBL] [Abstract][Full Text] [Related]
7. Light-dependent translocation of arrestin in the absence of rhodopsin phosphorylation and transducin signaling.
Mendez A; Lem J; Simon M; Chen J
J Neurosci; 2003 Apr; 23(8):3124-9. PubMed ID: 12716919
[TBL] [Abstract][Full Text] [Related]
8. Novel dominant rhodopsin mutation triggers two mechanisms of retinal degeneration and photoreceptor desensitization.
Iakhine R; Chorna-Ornan I; Zars T; Elia N; Cheng Y; Selinger Z; Minke B; Hyde DR
J Neurosci; 2004 Mar; 24(10):2516-26. PubMed ID: 15014127
[TBL] [Abstract][Full Text] [Related]
9. Wheel running exercise protects against retinal degeneration in the I307N rhodopsin mouse model of inducible autosomal dominant retinitis pigmentosa.
Zhang X; Girardot PE; Sellers JT; Li Y; Wang J; Chrenek MA; Wu W; Skelton H; Nickerson JM; Pardue MT; Boatright JH
Mol Vis; 2019; 25():462-476. PubMed ID: 31523123
[TBL] [Abstract][Full Text] [Related]
10. Retinal histopathology in eyes from patients with autosomal dominant retinitis pigmentosa caused by rhodopsin mutations.
Bonilha VL; Rayborn ME; Bell BA; Marino MJ; Beight CD; Pauer GJ; Traboulsi EI; Hollyfield JG; Hagstrom SA
Graefes Arch Clin Exp Ophthalmol; 2015 Dec; 253(12):2161-9. PubMed ID: 26202387
[TBL] [Abstract][Full Text] [Related]
11. Limited ATF4 Expression in Degenerating Retinas with Ongoing ER Stress Promotes Photoreceptor Survival in a Mouse Model of Autosomal Dominant Retinitis Pigmentosa.
Bhootada Y; Kotla P; Zolotukhin S; Gorbatyuk O; Bebok Z; Athar M; Gorbatyuk M
PLoS One; 2016; 11(5):e0154779. PubMed ID: 27144303
[TBL] [Abstract][Full Text] [Related]
12. Characterization of rhodopsin P23H-induced retinal degeneration in a Xenopus laevis model of retinitis pigmentosa.
Tam BM; Moritz OL
Invest Ophthalmol Vis Sci; 2006 Aug; 47(8):3234-41. PubMed ID: 16877386
[TBL] [Abstract][Full Text] [Related]
13. Xenopus laevis P23H rhodopsin transgene causes rod photoreceptor degeneration that is more severe in the ventral retina and is modulated by light.
Zhang R; Oglesby E; Marsh-Armstrong N
Exp Eye Res; 2008 Apr; 86(4):612-21. PubMed ID: 18291367
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Rhodopsin mislocalization drives ciliary dysregulation in a novel autosomal dominant retinitis pigmentosa knock-in mouse model.
Takita S; Jahan S; S Imanishi S; Harikrishnan H; LePage D; Mann RJ; Conlon RA; Miyagi M; Imanishi Y
FASEB J; 2024 Apr; 38(8):e23606. PubMed ID: 38648465
[TBL] [Abstract][Full Text] [Related]
16. The role of mislocalized phototransduction in photoreceptor cell death of retinitis pigmentosa.
Nakao T; Tsujikawa M; Notomi S; Ikeda Y; Nishida K
PLoS One; 2012; 7(4):e32472. PubMed ID: 22485131
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Autophagy in
Wen RH; Stanar P; Tam B; Moritz OL
Autophagy; 2019 Nov; 15(11):1970-1989. PubMed ID: 30975014
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Effect of AAV-Mediated Rhodopsin Gene Augmentation on Retinal Degeneration Caused by the Dominant P23H Rhodopsin Mutation in a Knock-In Murine Model.
Orlans HO; Barnard AR; PatrĂcio MI; McClements ME; MacLaren RE
Hum Gene Ther; 2020 Jul; 31(13-14):730-742. PubMed ID: 32394751
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]