1655 related articles for article (PubMed ID: 15765048)
1. 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]
2. 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]
3. 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]
4. Retinal degeneration 6 (rd6): a new mouse model for human retinitis punctata albescens.
Hawes NL; Chang B; Hageman GS; Nusinowitz S; Nishina PM; Schneider BS; Smith RS; Roderick TH; Davisson MT; Heckenlively JR
Invest Ophthalmol Vis Sci; 2000 Sep; 41(10):3149-57. PubMed ID: 10967077
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Predominant rod photoreceptor degeneration in Leber congenital amaurosis.
van der Spuy J; Munro PM; Luthert PJ; Preising MN; Bek T; Heegaard S; Cheetham ME
Mol Vis; 2005 Jul; 11():542-53. PubMed ID: 16052170
[TBL] [Abstract][Full Text] [Related]
7. Gene replacement therapy rescues photoreceptor degeneration in a murine model of Leber congenital amaurosis lacking RPGRIP.
Pawlyk BS; Smith AJ; Buch PK; Adamian M; Hong DH; Sandberg MA; Ali RR; Li T
Invest Ophthalmol Vis Sci; 2005 Sep; 46(9):3039-45. PubMed ID: 16123399
[TBL] [Abstract][Full Text] [Related]
8. Morphological characterization of the retinal degeneration in three strains of mice carrying the rd-3 mutation.
Linberg KA; Fariss RN; Heckenlively JR; Farber DB; Fisher SK
Vis Neurosci; 2005; 22(6):721-34. PubMed ID: 16469183
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophy.
Gu SM; Thompson DA; Srikumari CR; Lorenz B; Finckh U; Nicoletti A; Murthy KR; Rathmann M; Kumaramanickavel G; Denton MJ; Gal A
Nat Genet; 1997 Oct; 17(2):194-7. PubMed ID: 9326941
[TBL] [Abstract][Full Text] [Related]
11. Early-onset severe rod-cone dystrophy in young children with RPE65 mutations.
Lorenz B; Gyürüs P; Preising M; Bremser D; Gu S; Andrassi M; Gerth C; Gal A
Invest Ophthalmol Vis Sci; 2000 Aug; 41(9):2735-42. PubMed ID: 10937591
[TBL] [Abstract][Full Text] [Related]
12. Genetics and phenotypes of RPE65 mutations in inherited retinal degeneration.
Thompson DA; Gyürüs P; Fleischer LL; Bingham EL; McHenry CL; Apfelstedt-Sylla E; Zrenner E; Lorenz B; Richards JE; Jacobson SG; Sieving PA; Gal A
Invest Ophthalmol Vis Sci; 2000 Dec; 41(13):4293-9. PubMed ID: 11095629
[TBL] [Abstract][Full Text] [Related]
13. Novel TULP1 mutation causing leber congenital amaurosis or early onset retinal degeneration.
Mataftsi A; Schorderet DF; Chachoua L; Boussalah M; Nouri MT; Barthelmes D; Borruat FX; Munier FL
Invest Ophthalmol Vis Sci; 2007 Nov; 48(11):5160-7. PubMed ID: 17962469
[TBL] [Abstract][Full Text] [Related]
14. Clinicopathologic effects of mutant GUCY2D in Leber congenital amaurosis.
Milam AH; Barakat MR; Gupta N; Rose L; Aleman TS; Pianta MJ; Cideciyan AV; Sheffield VC; Stone EM; Jacobson SG
Ophthalmology; 2003 Mar; 110(3):549-58. PubMed ID: 12623820
[TBL] [Abstract][Full Text] [Related]
15. New views on RPE65 deficiency: the rod system is the source of vision in a mouse model of Leber congenital amaurosis.
Seeliger MW; Grimm C; Ståhlberg F; Friedburg C; Jaissle G; Zrenner E; Guo H; Remé CE; Humphries P; Hofmann F; Biel M; Fariss RN; Redmond TM; Wenzel A
Nat Genet; 2001 Sep; 29(1):70-4. PubMed ID: 11528395
[TBL] [Abstract][Full Text] [Related]
16. Fundus albipunctatus associated with compound heterozygous mutations in RPE65.
Schatz P; Preising M; Lorenz B; Sander B; Larsen M; Rosenberg T
Ophthalmology; 2011 May; 118(5):888-94. PubMed ID: 21211845
[TBL] [Abstract][Full Text] [Related]
17. Detailed histopathologic characterization of the retinopathy, globe enlarged (rge) chick phenotype.
Montiani-Ferreira F; Fischer A; Cernuda-Cernuda R; Kiupel M; DeGrip WJ; Sherry D; Cho SS; Shaw GC; Evans MG; Hocking PM; Petersen-Jones SM
Mol Vis; 2005 Jan; 11():11-27. PubMed ID: 15660021
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. The findings of optical coherence tomography of retinal degeneration in relation to the morphological and electroretinographic features in RPE65-/- mice.
Tanabu R; Sato K; Monai N; Yamauchi K; Gonome T; Xie Y; Takahashi S; Ishiguro SI; Nakazawa M
PLoS One; 2019; 14(1):e0210439. PubMed ID: 30695025
[TBL] [Abstract][Full Text] [Related]
20. R91W mutation in Rpe65 leads to milder early-onset retinal dystrophy due to the generation of low levels of 11-cis-retinal.
Samardzija M; von Lintig J; Tanimoto N; Oberhauser V; Thiersch M; Remé CE; Seeliger M; Grimm C; Wenzel A
Hum Mol Genet; 2008 Jan; 17(2):281-92. PubMed ID: 17933883
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]