273 related articles for article (PubMed ID: 26247368)
21. Vitreal delivery of AAV vectored Cnga3 restores cone function in CNGA3-/-/Nrl-/- mice, an all-cone model of CNGA3 achromatopsia.
Du W; Tao Y; Deng WT; Zhu P; Li J; Dai X; Zhang Y; Shi W; Liu X; Chiodo VA; Ding XQ; Zhao C; Michalakis S; Biel M; Zhang Z; Qu J; Hauswirth WW; Pang JJ
Hum Mol Genet; 2015 Jul; 24(13):3699-707. PubMed ID: 25855802
[TBL] [Abstract][Full Text] [Related]
22. Natural history of cone disease in the murine model of Leber congenital amaurosis due to CEP290 mutation: determining the timing and expectation of therapy.
Boye SE; Huang WC; Roman AJ; Sumaroka A; Boye SL; Ryals RC; Olivares MB; Ruan Q; Tucker BA; Stone EM; Swaroop A; Cideciyan AV; Hauswirth WW; Jacobson SG
PLoS One; 2014; 9(3):e92928. PubMed ID: 24671090
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. 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]
25. Gene therapy rescues cone structure and function in the 3-month-old rd12 mouse: a model for midcourse RPE65 leber congenital amaurosis.
Li X; Li W; Dai X; Kong F; Zheng Q; Zhou X; Lü F; Chang B; Rohrer B; Hauswirth WW; Qu J; Pang JJ
Invest Ophthalmol Vis Sci; 2011 Jan; 52(1):7-15. PubMed ID: 21169527
[TBL] [Abstract][Full Text] [Related]
26. Gucy2f zebrafish knockdown--a model for Gucy2d-related leber congenital amaurosis.
Stiebel-Kalish H; Reich E; Rainy N; Vatine G; Nisgav Y; Tovar A; Gothilf Y; Bach M
Eur J Hum Genet; 2012 Aug; 20(8):884-9. PubMed ID: 22378290
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. NRL
Cuevas E; Holder DL; Alshehri AH; Tréguier J; Lakowski J; Sowden JC
Stem Cells; 2021 Apr; 39(4):414-428. PubMed ID: 33400844
[TBL] [Abstract][Full Text] [Related]
29. Defining Outcomes for Clinical Trials of Leber Congenital Amaurosis Caused by GUCY2D Mutations.
Jacobson SG; Cideciyan AV; Sumaroka A; Roman AJ; Charng J; Lu M; Choudhury S; Schwartz SB; Heon E; Fishman GA; Boye SE
Am J Ophthalmol; 2017 May; 177():44-57. PubMed ID: 28212877
[TBL] [Abstract][Full Text] [Related]
30. Impaired association of retinal degeneration-3 with guanylate cyclase-1 and guanylate cyclase-activating protein-1 leads to leber congenital amaurosis-1.
Zulliger R; Naash MI; Rajala RV; Molday RS; Azadi S
J Biol Chem; 2015 Feb; 290(6):3488-99. PubMed ID: 25477517
[TBL] [Abstract][Full Text] [Related]
31. A mouse model of cone photoreceptor function loss
Naggert ASEN; Collin GB; Wang J; Krebs MP; Chang B
Front Mol Neurosci; 2022; 15():1080136. PubMed ID: 36698779
[TBL] [Abstract][Full Text] [Related]
32. Leber Congenital Amaurosis Due to
Jacobson SG; Cideciyan AV; Sumaroka A; Roman AJ; Wu V; Swider M; Sheplock R; Krishnan AK; Garafalo AV
Int J Mol Sci; 2021 Feb; 22(4):. PubMed ID: 33670772
[TBL] [Abstract][Full Text] [Related]
33. Genotype-functional-phenotype correlations in photoreceptor guanylate cyclase (GC-E) encoded by GUCY2D.
Sharon D; Wimberg H; Kinarty Y; Koch KW
Prog Retin Eye Res; 2018 Mar; 63():69-91. PubMed ID: 29061346
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. Novel GUCY2D mutation causes phenotypic variability of Leber congenital amaurosis in a large kindred.
Gradstein L; Zolotushko J; Sergeev YV; Lavy I; Narkis G; Perez Y; Guigui S; Sharon D; Banin E; Walter E; Lifshitz T; Birk OS
BMC Med Genet; 2016 Jul; 17(1):52. PubMed ID: 27475985
[TBL] [Abstract][Full Text] [Related]
36. Feedback induction of a photoreceptor-specific isoform of retinoid-related orphan nuclear receptor β by the rod transcription factor NRL.
Fu Y; Liu H; Ng L; Kim JW; Hao H; Swaroop A; Forrest D
J Biol Chem; 2014 Nov; 289(47):32469-80. PubMed ID: 25296752
[TBL] [Abstract][Full Text] [Related]
37. Combined rod and cone transduction by adeno-associated virus 2/8.
Manfredi A; Marrocco E; Puppo A; Cesi G; Sommella A; Della Corte M; Rossi S; Giunti M; Craft CM; Bacci ML; Simonelli F; Surace EM; Auricchio A
Hum Gene Ther; 2013 Dec; 24(12):982-92. PubMed ID: 24067103
[TBL] [Abstract][Full Text] [Related]
38. Outcome measure for the treatment of cone photoreceptor diseases: orientation to a scene with cone-only contrast.
Roman AJ; Cideciyan AV; Matsui R; Sheplock R; Schwartz SB; Jacobson SG
BMC Ophthalmol; 2015 Aug; 15():98. PubMed ID: 26253563
[TBL] [Abstract][Full Text] [Related]
39. Cone photoreceptors are the main targets for gene therapy of NPHP5 (IQCB1) or NPHP6 (CEP290) blindness: generation of an all-cone Nphp6 hypomorph mouse that mimics the human retinal ciliopathy.
Cideciyan AV; Rachel RA; Aleman TS; Swider M; Schwartz SB; Sumaroka A; Roman AJ; Stone EM; Jacobson SG; Swaroop A
Hum Mol Genet; 2011 Apr; 20(7):1411-23. PubMed ID: 21245082
[TBL] [Abstract][Full Text] [Related]
40. Photoreceptors of Nrl -/- mice coexpress functional S- and M-cone opsins having distinct inactivation mechanisms.
Nikonov SS; Daniele LL; Zhu X; Craft CM; Swaroop A; Pugh EN
J Gen Physiol; 2005 Mar; 125(3):287-304. PubMed ID: 15738050
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
