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Journal Abstract Search

321 related items for PubMed ID: 18515598

  • 1.
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  • 2. 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 28; 11():152-62. PubMed ID: 15765048
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  • 3. 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 28; 13(3):565-72. PubMed ID: 16223604
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  • 4. 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 28; 51(10):5304-13. PubMed ID: 20484585
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  • 6. Studies of visual function and its decay in mice with hereditary retinal degeneration.
    Dräger UC, Hubel DH.
    J Comp Neurol; 1978 Jul 01; 180(1):85-114. PubMed ID: 649791
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  • 7. 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 18; 13():1701-10. PubMed ID: 17960108
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  • 8. 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 18; 41(9):2735-42. PubMed ID: 10937591
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  • 9. Retinal degeneration in the rd mouse in the absence of c-fos.
    Hafezi F, Abegg M, Grimm C, Wenzel A, Munz K, Stürmer J, Farber DB, Remé CE.
    Invest Ophthalmol Vis Sci; 1998 Nov 18; 39(12):2239-44. PubMed ID: 9804131
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  • 11. 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 29; 52(8):5933-40. PubMed ID: 21715356
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  • 18. Rpe65 is necessary for production of 11-cis-vitamin A in the retinal visual cycle.
    Redmond TM, Yu S, Lee E, Bok D, Hamasaki D, Chen N, Goletz P, Ma JX, Crouch RK, Pfeifer K.
    Nat Genet; 1998 Dec 29; 20(4):344-51. PubMed ID: 9843205
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  • 20. 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 29; 41(13):4293-9. PubMed ID: 11095629
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