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Journal Abstract Search

312 related items for PubMed ID: 27481653

  • 21. rAAV-compatible human mini promoters enhance transgene expression in rat retinal ganglion cells.
    Araujo VG, Dias MS, Hauswirth WW, Linden R, Petrs-Silva H.
    Exp Eye Res; 2024 Feb; 239():109758. PubMed ID: 38123011
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  • 26. Gene therapy and transplantation in the retinofugal pathway.
    Harvey AR, Hellström M, Rodger J.
    Prog Brain Res; 2009 Feb; 175():151-61. PubMed ID: 19660654
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  • 28. Sphingosine 1-phosphate receptor 1 is required for retinal ganglion cell survival after optic nerve trauma.
    Joly S, Pernet V.
    J Neurochem; 2016 Aug; 138(4):571-86. PubMed ID: 27309795
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  • 29. Exchange of surface proteins impacts on viral vector cellular specificity and transduction characteristics: the retina as a model.
    Auricchio A, Kobinger G, Anand V, Hildinger M, O'Connor E, Maguire AM, Wilson JM, Bennett J.
    Hum Mol Genet; 2001 Dec 15; 10(26):3075-81. PubMed ID: 11751689
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  • 31. Evaluation of Photoreceptor Transduction Efficacy of Capsid-Modified Adeno-Associated Viral Vectors Following Intravitreal and Subretinal Delivery in Sheep.
    Ross M, Obolensky A, Averbukh E, Ezra-Elia R, Yamin E, Honig H, Dvir H, Rosov A, Hauswirth WW, Gootwine E, Banin E, Ofri R.
    Hum Gene Ther; 2020 Jul 15; 31(13-14):719-729. PubMed ID: 32486858
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  • 32. Targeting photoreceptors via intravitreal delivery using novel, capsid-mutated AAV vectors.
    Kay CN, Ryals RC, Aslanidi GV, Min SH, Ruan Q, Sun J, Dyka FM, Kasuga D, Ayala AE, Van Vliet K, Agbandje-McKenna M, Hauswirth WW, Boye SL, Boye SE.
    PLoS One; 2013 Jul 15; 8(4):e62097. PubMed ID: 23637972
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  • 34. AAV2-mediated GRP78 Transfer Alleviates Retinal Neuronal Injury by Downregulating ER Stress and Tau Oligomer Formation.
    Ha Y, Liu W, Liu H, Zhu S, Xia F, Gerson JE, Azhar NA, Tilton RG, Motamedi M, Kayed R, Zhang W.
    Invest Ophthalmol Vis Sci; 2018 Sep 04; 59(11):4670-4682. PubMed ID: 30267089
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  • 35. AAV2-Mediated Expression of HspB1 in RGCs Prevents Somal Damage and Axonal Transport Deficits in a Mouse Model of Ocular Hypertension.
    Nam MH, Nahomi RB, Pantcheva MB, Dhillon A, Chiodo VA, Smith WC, Nagaraj RH.
    Transl Vis Sci Technol; 2022 Nov 01; 11(11):8. PubMed ID: 36355386
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  • 36. In Vivo Fluorescence Retinal Imaging Following AAV2-Mediated Gene Delivery in the Rat Retina.
    Lee JY, Hwang Y, Kim JH, Kim YS, Jung BK, Kim P, Lee H.
    Invest Ophthalmol Vis Sci; 2016 Jun 01; 57(7):3390-6. PubMed ID: 27367507
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  • 37. Laser photocoagulation enhances adeno-associated viral vector transduction of mouse retina.
    Lee SH, Colosi P, Lee H, Ohn YH, Kim SW, Kwak HW, Park TK.
    Hum Gene Ther Methods; 2014 Feb 01; 25(1):83-91. PubMed ID: 24191872
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  • 38. Neural stem cell-based intraocular administration of ciliary neurotrophic factor attenuates the loss of axotomized ganglion cells in adult mice.
    Flachsbarth K, Kruszewski K, Jung G, Jankowiak W, Riecken K, Wagenfeld L, Richard G, Fehse B, Bartsch U.
    Invest Ophthalmol Vis Sci; 2014 Sep 30; 55(11):7029-39. PubMed ID: 25270193
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  • 39. Baculoviral IAP repeat-containing-4 protects optic nerve axons in a rat glaucoma model.
    McKinnon SJ, Lehman DM, Tahzib NG, Ransom NL, Reitsamer HA, Liston P, LaCasse E, Li Q, Korneluk RG, Hauswirth WW.
    Mol Ther; 2002 Jun 30; 5(6):780-7. PubMed ID: 12027563
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  • 40. Safety and effects of the vector for the Leber hereditary optic neuropathy gene therapy clinical trial.
    Koilkonda RD, Yu H, Chou TH, Feuer WJ, Ruggeri M, Porciatti V, Tse D, Hauswirth WW, Chiodo V, Boye SL, Lewin AS, Neuringer M, Renner L, Guy J.
    JAMA Ophthalmol; 2014 Apr 01; 132(4):409-20. PubMed ID: 24457989
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