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Journal Abstract Search

280 related items for PubMed ID: 10869443

  • 1. Rapid restoration of visual pigment and function with oral retinoid in a mouse model of childhood blindness.
    Van Hooser JP, Aleman TS, He YG, Cideciyan AV, Kuksa V, Pittler SJ, Stone EM, Jacobson SG, Palczewski K.
    Proc Natl Acad Sci U S A; 2000 Jul 18; 97(15):8623-8. PubMed ID: 10869443
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  • 2. Recovery of visual functions in a mouse model of Leber congenital amaurosis.
    Van Hooser JP, Liang Y, Maeda T, Kuksa V, Jang GF, He YG, Rieke F, Fong HK, Detwiler PB, Palczewski K.
    J Biol Chem; 2002 May 24; 277(21):19173-82. PubMed ID: 11897783
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  • 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 28; 11():152-62. PubMed ID: 15765048
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  • 4. 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 28; 49(6):2384-9. PubMed ID: 18296659
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  • 5. Human gene therapy for RPE65 isomerase deficiency activates the retinoid cycle of vision but with slow rod kinetics.
    Cideciyan AV, Aleman TS, Boye SL, Schwartz SB, Kaushal S, Roman AJ, Pang JJ, Sumaroka A, Windsor EA, Wilson JM, Flotte TR, Fishman GA, Heon E, Stone EM, Byrne BJ, Jacobson SG, Hauswirth WW.
    Proc Natl Acad Sci U S A; 2008 Sep 30; 105(39):15112-7. PubMed ID: 18809924
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  • 6. Identifying photoreceptors in blind eyes caused by RPE65 mutations: Prerequisite for human gene therapy success.
    Jacobson SG, Aleman TS, Cideciyan AV, Sumaroka A, Schwartz SB, Windsor EA, Traboulsi EI, Heon E, Pittler SJ, Milam AH, Maguire AM, Palczewski K, Stone EM, Bennett J.
    Proc Natl Acad Sci U S A; 2005 Apr 26; 102(17):6177-82. PubMed ID: 15837919
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  • 7. Evaluation of 9-cis-retinyl acetate therapy in Rpe65-/- mice.
    Maeda T, Maeda A, Casadesus G, Palczewski K, Margaron P.
    Invest Ophthalmol Vis Sci; 2009 Sep 26; 50(9):4368-78. PubMed ID: 19407008
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  • 11. 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 26; 29(1):70-4. PubMed ID: 11528395
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  • 13. Canine and human visual cortex intact and responsive despite early retinal blindness from RPE65 mutation.
    Aguirre GK, Komáromy AM, Cideciyan AV, Brainard DH, Aleman TS, Roman AJ, Avants BB, Gee JC, Korczykowski M, Hauswirth WW, Acland GM, Aguirre GD, Jacobson SG.
    PLoS Med; 2007 Jun 26; 4(6):e230. PubMed ID: 17594175
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