394 related articles for article (PubMed ID: 21715356)
1. Altered expression of the transcription factor Mef2c during retinal degeneration in Rpe65-/- mice.
Escher P; Schorderet DF; Cottet S
Invest Ophthalmol Vis Sci; 2011 Jul; 52(8):5933-40. PubMed ID: 21715356
[TBL] [Abstract][Full Text] [Related]
2. Retinal disease in Rpe65-deficient mice: comparison to human leber congenital amaurosis due to RPE65 mutations.
Caruso RC; Aleman TS; Cideciyan AV; Roman AJ; Sumaroka A; Mullins CL; Boye SL; Hauswirth WW; Jacobson SG
Invest Ophthalmol Vis Sci; 2010 Oct; 51(10):5304-13. PubMed ID: 20484585
[TBL] [Abstract][Full Text] [Related]
3. Retinal degeneration 12 (rd12): a new, spontaneously arising mouse model for human Leber congenital amaurosis (LCA).
Pang JJ; Chang B; Hawes NL; Hurd RE; Davisson MT; Li J; Noorwez SM; Malhotra R; McDowell JH; Kaushal S; Hauswirth WW; Nusinowitz S; Thompson DA; Heckenlively JR
Mol Vis; 2005 Feb; 11():152-62. PubMed ID: 15765048
[TBL] [Abstract][Full Text] [Related]
4. Different effects of valproic acid on photoreceptor loss in Rd1 and Rd10 retinal degeneration mice.
Mitton KP; Guzman AE; Deshpande M; Byrd D; DeLooff C; Mkoyan K; Zlojutro P; Wallace A; Metcalf B; Laux K; Sotzen J; Tran T
Mol Vis; 2014; 20():1527-44. PubMed ID: 25489226
[TBL] [Abstract][Full Text] [Related]
5. Altered expression of β-galactosidase-1-like protein 3 (Glb1l3) in the retinal pigment epithelium (RPE)-specific 65-kDa protein knock-out mouse model of Leber's congenital amaurosis.
Le Carré J; Schorderet DF; Cottet S
Mol Vis; 2011; 17():1287-97. PubMed ID: 21633714
[TBL] [Abstract][Full Text] [Related]
6. Early apoptosis of rod photoreceptors in Rpe65(-/-) mice is associated with the upregulated expression of lysosomal-mediated autophagic genes.
Métrailler S; Schorderet DF; Cottet S
Exp Eye Res; 2012 Mar; 96(1):70-81. PubMed ID: 22227450
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Expression profiling of the developing and mature Nrl-/- mouse retina: identification of retinal disease candidates and transcriptional regulatory targets of Nrl.
Yoshida S; Mears AJ; Friedman JS; Carter T; He S; Oh E; Jing Y; Farjo R; Fleury G; Barlow C; Hero AO; Swaroop A
Hum Mol Genet; 2004 Jul; 13(14):1487-503. PubMed ID: 15163632
[TBL] [Abstract][Full Text] [Related]
9. The transcription factor neural retina leucine zipper (NRL) controls photoreceptor-specific expression of myocyte enhancer factor Mef2c from an alternative promoter.
Hao H; Tummala P; Guzman E; Mali RS; Gregorski J; Swaroop A; Mitton KP
J Biol Chem; 2011 Oct; 286(40):34893-902. PubMed ID: 21849497
[TBL] [Abstract][Full Text] [Related]
10. Bax-induced apoptosis in Leber's congenital amaurosis: a dual role in rod and cone degeneration.
Hamann S; Schorderet DF; Cottet S
PLoS One; 2009 Aug; 4(8):e6616. PubMed ID: 19672311
[TBL] [Abstract][Full Text] [Related]
11. RPE65 is essential for the function of cone photoreceptors in NRL-deficient mice.
Wenzel A; von Lintig J; Oberhauser V; Tanimoto N; Grimm C; Seeliger MW
Invest Ophthalmol Vis Sci; 2007 Feb; 48(2):534-42. PubMed ID: 17251447
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Gene therapy restores vision-dependent behavior as well as retinal structure and function in a mouse model of RPE65 Leber congenital amaurosis.
Pang JJ; Chang B; Kumar A; Nusinowitz S; Noorwez SM; Li J; Rani A; Foster TC; Chiodo VA; Doyle T; Li H; Malhotra R; Teusner JT; McDowell JH; Min SH; Li Q; Kaushal S; Hauswirth WW
Mol Ther; 2006 Mar; 13(3):565-72. PubMed ID: 16223604
[TBL] [Abstract][Full Text] [Related]
14. The Consequences of Hypomorphic RPE65 for Rod and Cone Photoreceptors.
Samardzija M; Barben M; Geiger P; Grimm C
Adv Exp Med Biol; 2016; 854():341-6. PubMed ID: 26427430
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. Rpe65 as a modifier gene for inherited retinal degeneration.
Samardzija M; Wenzel A; Naash M; Remé CE; Grimm C
Eur J Neurosci; 2006 Feb; 23(4):1028-34. PubMed ID: 16519667
[TBL] [Abstract][Full Text] [Related]
18. Retinopathy mutations in the bZIP protein NRL alter phosphorylation and transcriptional activity.
Kanda A; Friedman JS; Nishiguchi KM; Swaroop A
Hum Mutat; 2007 Jun; 28(6):589-98. PubMed ID: 17335001
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Electroretinographic analyses of Rpe65-mutant rd12 mice: developing an in vivo bioassay for human gene therapy trials of Leber congenital amaurosis.
Roman AJ; Boye SL; Aleman TS; Pang JJ; McDowell JH; Boye SE; Cideciyan AV; Jacobson SG; Hauswirth WW
Mol Vis; 2007 Sep; 13():1701-10. PubMed ID: 17960108
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
