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Journal Abstract Search

201 related items for PubMed ID: 26467396

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  • 2. 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; 8(4):e62097. PubMed ID: 23637972
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  • 3. 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; 31(13-14):719-729. PubMed ID: 32486858
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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 Jul; 1950():249-262. PubMed ID: 30783978
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  • 8. Gene therapy following subretinal AAV5 vector delivery is not affected by a previous intravitreal AAV5 vector administration in the partner eye.
    Li W, Kong F, Li X, Dai X, Liu X, Zheng Q, Wu R, Zhou X, Lü F, Chang B, Li Q, Hauswirth WW, Qu J, Pang JJ.
    Mol Vis; 2009 Jul; 15():267-75. PubMed ID: 19190735
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  • 10. 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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  • 12. AAV-mediated expression targeting of rod and cone photoreceptors with a human rhodopsin kinase promoter.
    Khani SC, Pawlyk BS, Bulgakov OV, Kasperek E, Young JE, Adamian M, Sun X, Smith AJ, Ali RR, Li T.
    Invest Ophthalmol Vis Sci; 2007 Sep 01; 48(9):3954-61. PubMed ID: 17724172
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  • 15. 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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  • 16. Quantifying transduction efficiencies of unmodified and tyrosine capsid mutant AAV vectors in vitro using two ocular cell lines.
    Ryals RC, Boye SL, Dinculescu A, Hauswirth WW, Boye SE.
    Mol Vis; 2011 Apr 29; 17():1090-102. PubMed ID: 21552473
    [Abstract] [Full Text] [Related]

  • 17. 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 Apr 29; 10(7):2982-2999. PubMed ID: 32194850
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  • 20. Self-complementary AAV5 vector facilitates quicker transgene expression in photoreceptor and retinal pigment epithelial cells of normal mouse.
    Kong F, Li W, Li X, Zheng Q, Dai X, Zhou X, Boye SL, Hauswirth WW, Qu J, Pang JJ.
    Exp Eye Res; 2010 May 29; 90(5):546-54. PubMed ID: 20138034
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