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Journal Abstract Search

206 related items for PubMed ID: 27367507

  • 21. Recombinant AAV-mediated delivery of a tet-inducible reporter gene to the rat retina.
    McGee Sanftner LH, Rendahl KG, Quiroz D, Coyne M, Ladner M, Manning WC, Flannery JG.
    Mol Ther; 2001 May; 3(5 Pt 1):688-96. PubMed ID: 11356074
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  • 22. Vasoinhibin gene transfer by adenoassociated virus type 2 protects against VEGF- and diabetes-induced retinal vasopermeability.
    Ramírez M, Wu Z, Moreno-Carranza B, Jeziorski MC, Arnold E, Díaz-Lezama N, Martínez de la Escalera G, Colosi P, Clapp C.
    Invest Ophthalmol Vis Sci; 2011 Nov 21; 52(12):8944-50. PubMed ID: 22003113
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  • 23. Characterization of intravitreally delivered capsid mutant AAV2-Cre vector to induce tissue-specific mutations in murine retinal ganglion cells.
    Langouet-Astrie CJ, Yang Z, Polisetti SM, Welsbie DS, Hauswirth WW, Zack DJ, Merbs SL, Enke RA.
    Exp Eye Res; 2016 Oct 21; 151():61-7. PubMed ID: 27481653
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  • 24. Fundus imaging of retinal ganglion cells transduced by retrograde transport of rAAV2-retro.
    Nanjappa R, Dilbeck MD, Economides JR, Horton JC.
    Exp Eye Res; 2022 Jun 21; 219():109084. PubMed ID: 35460667
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  • 28. 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 21; 24(12):787-800. PubMed ID: 28872643
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  • 32. 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 21; 31(13-14):719-729. PubMed ID: 32486858
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  • 35. Vitrectomy Before Intravitreal Injection of AAV2/2 Vector Promotes Efficient Transduction of Retinal Ganglion Cells in Dogs and Nonhuman Primates.
    Tshilenge KT, Ameline B, Weber M, Mendes-Madeira A, Nedellec S, Biget M, Provost N, Libeau L, Blouin V, Deschamps JY, Le Meur G, Colle MA, Moullier P, Pichard V, Rolling F.
    Hum Gene Ther Methods; 2016 Jun 21; 27(3):122-34. PubMed ID: 27229628
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  • 37. Efficient expression of self-complementary AAV in ganglion cells of the ex vivo primate retina.
    Koilkonda RD, Hauswirth WW, Guy J.
    Mol Vis; 2009 Dec 16; 15():2796-802. PubMed ID: 20019878
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  • 38. Comparative Study of Adeno-associated Virus, Adenovirus, Bacu lovirus and Lentivirus Vectors for Gene Therapy of the Eyes.
    Kalesnykas G, Kokki E, Alasaarela L, Lesch HP, Tuulos T, Kinnunen K, Uusitalo H, Airenne K, Yla-Herttuala S.
    Curr Gene Ther; 2017 Dec 16; 17(3):235-247. PubMed ID: 28982327
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  • 40. Highly Efficient Delivery of Adeno-Associated Viral Vectors to the Primate Retina.
    Boye SE, Alexander JJ, Witherspoon CD, Boye SL, Peterson JJ, Clark ME, Sandefer KJ, Girkin CA, Hauswirth WW, Gamlin PD.
    Hum Gene Ther; 2016 Aug 16; 27(8):580-97. PubMed ID: 27439313
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