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Journal Abstract Search

346 related items for PubMed ID: 26865709

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  • 2. Heparan Sulfate Binding Promotes Accumulation of Intravitreally Delivered Adeno-associated Viral Vectors at the Retina for Enhanced Transduction but Weakly Influences Tropism.
    Woodard KT, Liang KJ, Bennett WC, Samulski RJ.
    J Virol; 2016 Nov 01; 90(21):9878-9888. PubMed ID: 27558418
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  • 3. 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 Nov 01; 8(4):e62097. PubMed ID: 23637972
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  • 6. SubILM Injection of AAV for Gene Delivery to the Retina.
    Gamlin PD, Alexander JJ, Boye SL, Witherspoon CD, Boye SE.
    Methods Mol Biol; 2019 Nov 01; 1950():249-262. PubMed ID: 30783978
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  • 8. 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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  • 9. Improvement of Photoreceptor Targeting via Intravitreal Delivery in Mouse and Human Retina Using Combinatory rAAV2 Capsid Mutant Vectors.
    Reid CA, Ertel KJ, Lipinski DM.
    Invest Ophthalmol Vis Sci; 2017 Dec 01; 58(14):6429-6439. PubMed ID: 29260200
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  • 11. Focused ultrasound as a novel strategy for noninvasive gene delivery to retinal Müller glia.
    Touahri Y, Dixit R, Kofoed RH, Miloska K, Park E, Raeisossadati R, Markham-Coultes K, David LA, Rijal H, Zhao J, Lynch M, Hynynen K, Aubert I, Schuurmans C.
    Theranostics; 2020 Dec 01; 10(7):2982-2999. PubMed ID: 32194850
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  • 12. Photoreceptor-targeted gene delivery using intravitreally administered AAV vectors in dogs.
    Boyd RF, Sledge DG, Boye SL, Boye SE, Hauswirth WW, Komáromy AM, Petersen-Jones SM, Bartoe JT.
    Gene Ther; 2016 Feb 01; 23(2):223-30. PubMed ID: 26467396
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  • 13. Rationally designed AAV2 and AAVrh8R capsids provide improved transduction in the retina and brain.
    Sullivan JA, Stanek LM, Lukason MJ, Bu J, Osmond SR, Barry EA, O'Riordan CR, Shihabuddin LS, Cheng SH, Scaria A.
    Gene Ther; 2018 Jun 01; 25(3):205-219. PubMed ID: 29785047
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  • 14. Comparative analysis of in vivo and in vitro AAV vector transduction in the neonatal mouse retina: effects of serotype and site of administration.
    Pang JJ, Lauramore A, Deng WT, Li Q, Doyle TJ, Chiodo V, Li J, Hauswirth WW.
    Vision Res; 2008 Feb 01; 48(3):377-85. PubMed ID: 17950399
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  • 16. Inner limiting membrane barriers to AAV-mediated retinal transduction from the vitreous.
    Dalkara D, Kolstad KD, Caporale N, Visel M, Klimczak RR, Schaffer DV, Flannery JG.
    Mol Ther; 2009 Dec 01; 17(12):2096-102. PubMed ID: 19672248
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  • 17. Tropism of engineered and evolved recombinant AAV serotypes in the rd1 mouse and ex vivo primate retina.
    Hickey DG, Edwards TL, Barnard AR, Singh MS, de Silva SR, McClements ME, Flannery JG, Hankins MW, MacLaren RE.
    Gene Ther; 2017 Dec 01; 24(12):787-800. PubMed ID: 28872643
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  • 19. Effects of Altering HSPG Binding and Capsid Hydrophilicity on Retinal Transduction by AAV.
    Crosson SM, Bennett A, Fajardo D, Peterson JJ, Zhang H, Li W, Leahy MT, Jennings CK, Boyd RF, Boye SL, Agbandge-McKenna M, Boye SE.
    J Virol; 2021 Apr 26; 95(10):. PubMed ID: 33658343
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