457 related articles for article (PubMed ID: 18400900)
1. Trafficking of membrane-associated proteins to cone photoreceptor outer segments requires the chromophore 11-cis-retinal.
Zhang H; Fan J; Li S; Karan S; Rohrer B; Palczewski K; Frederick JM; Crouch RK; Baehr W
J Neurosci; 2008 Apr; 28(15):4008-14. PubMed ID: 18400900
[TBL] [Abstract][Full Text] [Related]
2. Rpe65-/- and Lrat-/- mice: comparable models of leber congenital amaurosis.
Fan J; Rohrer B; Frederick JM; Baehr W; Crouch RK
Invest Ophthalmol Vis Sci; 2008 Jun; 49(6):2384-9. PubMed ID: 18296659
[TBL] [Abstract][Full Text] [Related]
3. Loss of cone photoreceptors caused by chromophore depletion is partially prevented by the artificial chromophore pro-drug, 9-cis-retinyl acetate.
Maeda T; Cideciyan AV; Maeda A; Golczak M; Aleman TS; Jacobson SG; Palczewski K
Hum Mol Genet; 2009 Jun; 18(12):2277-87. PubMed ID: 19339306
[TBL] [Abstract][Full Text] [Related]
4. Ciliary neurotrophic factor (CNTF) protects retinal cone and rod photoreceptors by suppressing excessive formation of the visual pigments.
Li S; Sato K; Gordon WC; Sendtner M; Bazan NG; Jin M
J Biol Chem; 2018 Sep; 293(39):15256-15268. PubMed ID: 30115683
[TBL] [Abstract][Full Text] [Related]
5. Pharmacological Amelioration of Cone Survival and Vision in a Mouse Model for Leber Congenital Amaurosis.
Li S; Samardzija M; Yang Z; Grimm C; Jin M
J Neurosci; 2016 May; 36(21):5808-19. PubMed ID: 27225770
[TBL] [Abstract][Full Text] [Related]
6. Cone opsin mislocalization in Rpe65-/- mice: a defect that can be corrected by 11-cis retinal.
Rohrer B; Lohr HR; Humphries P; Redmond TM; Seeliger MW; Crouch RK
Invest Ophthalmol Vis Sci; 2005 Oct; 46(10):3876-82. PubMed ID: 16186377
[TBL] [Abstract][Full Text] [Related]
7. Nrl-knockout mice deficient in Rpe65 fail to synthesize 11-cis retinal and cone outer segments.
Feathers KL; Lyubarsky AL; Khan NW; Teofilo K; Swaroop A; Williams DS; Pugh EN; Thompson DA
Invest Ophthalmol Vis Sci; 2008 Mar; 49(3):1126-35. PubMed ID: 18326740
[TBL] [Abstract][Full Text] [Related]
8. Cone outer segment morphology and cone function in the Rpe65-/- Nrl-/- mouse retina are amenable to retinoid replacement.
Kunchithapautham K; Coughlin B; Crouch RK; Rohrer B
Invest Ophthalmol Vis Sci; 2009 Oct; 50(10):4858-64. PubMed ID: 19407011
[TBL] [Abstract][Full Text] [Related]
9. Lentiviral gene transfer of RPE65 rescues survival and function of cones in a mouse model of Leber congenital amaurosis.
Bemelmans AP; Kostic C; Crippa SV; Hauswirth WW; Lem J; Munier FL; Seeliger MW; Wenzel A; Arsenijevic Y
PLoS Med; 2006 Oct; 3(10):e347. PubMed ID: 17032058
[TBL] [Abstract][Full Text] [Related]
10. Intraperitoneal chromophore injections delay early-onset and rapid retinal cone degeneration in a mouse model of Leber congenital amaurosis.
Dai X; Jin X; Ye Q; Huang H; Duo L; Lu C; Bao J; Chen H
Exp Eye Res; 2021 Nov; 212():108776. PubMed ID: 34582935
[TBL] [Abstract][Full Text] [Related]
11. Protection of cone photoreceptor M-opsin degradation with 9-cis-β-carotene-rich alga Dunaliella bardawil in Rpe65(-/-) mouse retinal explant culture.
Ozaki T; Nakazawa M; Kudo T; Hirano S; Suzuki K; Ishiguro S
Curr Eye Res; 2014 Dec; 39(12):1221-31. PubMed ID: 25006880
[TBL] [Abstract][Full Text] [Related]
12. Light prevents exogenous 11-cis retinal from maintaining cone photoreceptors in chromophore-deficient mice.
Fan J; Crouch RK; Kono M
Invest Ophthalmol Vis Sci; 2011 Apr; 52(5):2412-6. PubMed ID: 21228385
[TBL] [Abstract][Full Text] [Related]
13. In conditions of limited chromophore supply rods entrap 11-cis-retinal leading to loss of cone function and cell death.
Samardzija M; Tanimoto N; Kostic C; Beck S; Oberhauser V; Joly S; Thiersch M; Fahl E; Arsenijevic Y; von Lintig J; Wenzel A; Seeliger MW; Grimm C
Hum Mol Genet; 2009 Apr; 18(7):1266-75. PubMed ID: 19147682
[TBL] [Abstract][Full Text] [Related]
14. Explant cultures of Rpe65-/- mouse retina: a model to investigate cone opsin trafficking.
Bandyopadhyay M; Kono M; Rohrer B
Mol Vis; 2013; 19():1149-57. PubMed ID: 23734084
[TBL] [Abstract][Full Text] [Related]
15. Pathophysilogical mechanism and treatment strategies for Leber congenital amaurosis.
Fu Y; Zhang T
Adv Exp Med Biol; 2014; 801():791-6. PubMed ID: 24664772
[TBL] [Abstract][Full Text] [Related]
16. Genetic deletion of S-opsin prevents rapid cone degeneration in a mouse model of Leber congenital amaurosis.
Zhang T; Enemchukwu NO; Jones A; Wang S; Dennis E; Watt CB; Pugh EN; Fu Y
Hum Mol Genet; 2015 Mar; 24(6):1755-63. PubMed ID: 25416279
[TBL] [Abstract][Full Text] [Related]
17. A model for transport of membrane-associated phototransduction polypeptides in rod and cone photoreceptor inner segments.
Karan S; Zhang H; Li S; Frederick JM; Baehr W
Vision Res; 2008 Feb; 48(3):442-52. PubMed ID: 17949773
[TBL] [Abstract][Full Text] [Related]
18. Cone opsin determines the time course of cone photoreceptor degeneration in Leber congenital amaurosis.
Zhang T; Zhang N; Baehr W; Fu Y
Proc Natl Acad Sci U S A; 2011 May; 108(21):8879-84. PubMed ID: 21555576
[TBL] [Abstract][Full Text] [Related]
19. Opsin activation of transduction in the rods of dark-reared Rpe65 knockout mice.
Fan J; Woodruff ML; Cilluffo MC; Crouch RK; Fain GL
J Physiol; 2005 Oct; 568(Pt 1):83-95. PubMed ID: 15994181
[TBL] [Abstract][Full Text] [Related]
20. Downregulation of cone-specific gene expression and degeneration of cone photoreceptors in the Rpe65-/- mouse at early ages.
Znoiko SL; Rohrer B; Lu K; Lohr HR; Crouch RK; Ma JX
Invest Ophthalmol Vis Sci; 2005 Apr; 46(4):1473-9. PubMed ID: 15790918
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]