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Journal Abstract Search

593 related items for PubMed ID: 15326152

  • 1. RS-1 Gene Delivery to an Adult Rs1h Knockout Mouse Model Restores ERG b-Wave with Reversal of the Electronegative Waveform of X-Linked Retinoschisis.
    Zeng Y, Takada Y, Kjellstrom S, Hiriyanna K, Tanikawa A, Wawrousek E, Smaoui N, Caruso R, Bush RA, Sieving PA.
    Invest Ophthalmol Vis Sci; 2004 Sep; 45(9):3279-85. PubMed ID: 15326152
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  • 2. Retinoschisin gene therapy and natural history in the Rs1h-KO mouse: long-term rescue from retinal degeneration.
    Kjellstrom S, Bush RA, Zeng Y, Takada Y, Sieving PA.
    Invest Ophthalmol Vis Sci; 2007 Aug; 48(8):3837-45. PubMed ID: 17652759
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  • 3. Prolonged recovery of retinal structure/function after gene therapy in an Rs1h-deficient mouse model of x-linked juvenile retinoschisis.
    Min SH, Molday LL, Seeliger MW, Dinculescu A, Timmers AM, Janssen A, Tonagel F, Tanimoto N, Weber BH, Molday RS, Hauswirth WW.
    Mol Ther; 2005 Oct; 12(4):644-51. PubMed ID: 16027044
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  • 4. Reduced synaptic vesicle density and aberrant synaptic localization caused by a splice site mutation in the Rs1h gene.
    Johnson BA, Ikeda S, Pinto LH, Ikeda A.
    Vis Neurosci; 2006 Oct; 23(6):887-98. PubMed ID: 17266781
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  • 5. An ENU-induced mutation in Rs1h causes disruption of retinal structure and function.
    Jablonski MM, Dalke C, Wang X, Lu L, Manly KF, Pretsch W, Favor J, Pardue MT, Rinchik EM, Williams RW, Goldowitz D, Graw J.
    Mol Vis; 2005 Jul 27; 11():569-81. PubMed ID: 16088326
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  • 9. Juvenile X-linked retinoschisis with normal scotopic b-wave in the electroretinogram at an early stage of the disease.
    Eksandh L, Andréasson S, Abrahamson M.
    Ophthalmic Genet; 2005 Sep 27; 26(3):111-7. PubMed ID: 16272055
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  • 11. Preclinical Dose-Escalation Study of Intravitreal AAV-RS1 Gene Therapy in a Mouse Model of X-linked Retinoschisis: Dose-Dependent Expression and Improved Retinal Structure and Function.
    Bush RA, Zeng Y, Colosi P, Kjellstrom S, Hiriyanna S, Vijayasarathy C, Santos M, Li J, Wu Z, Sieving PA.
    Hum Gene Ther; 2016 May 27; 27(5):376-89. PubMed ID: 27036983
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  • 12. Solid lipid nanoparticle-based vectors intended for the treatment of X-linked juvenile retinoschisis by gene therapy: In vivo approaches in Rs1h-deficient mouse model.
    Apaolaza PS, Del Pozo-Rodríguez A, Torrecilla J, Rodríguez-Gascón A, Rodríguez JM, Friedrich U, Weber BH, Solinís MA.
    J Control Release; 2015 Nov 10; 217():273-83. PubMed ID: 26400864
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  • 15. Structural recovery of the retina in a retinoschisin-deficient mouse after gene replacement therapy by solid lipid nanoparticles.
    Apaolaza PS, Del Pozo-Rodríguez A, Solinís MA, Rodríguez JM, Friedrich U, Torrecilla J, Weber BH, Rodríguez-Gascón A.
    Biomaterials; 2016 Jun 10; 90():40-9. PubMed ID: 26986855
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  • 19. The X-linked juvenile retinoschisis protein retinoschisin is a novel regulator of mitogen-activated protein kinase signalling and apoptosis in the retina.
    Plössl K, Weber BH, Friedrich U.
    J Cell Mol Med; 2017 Apr 10; 21(4):768-780. PubMed ID: 27995734
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  • 20. Synaptic pathology and therapeutic repair in adult retinoschisis mouse by AAV-RS1 transfer.
    Ou J, Vijayasarathy C, Ziccardi L, Chen S, Zeng Y, Marangoni D, Pope JG, Bush RA, Wu Z, Li W, Sieving PA.
    J Clin Invest; 2015 Jul 01; 125(7):2891-903. PubMed ID: 26098217
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