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Journal Abstract Search
730 related items for PubMed ID: 29260200
1. 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 [Abstract] [Full Text] [Related]
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 Dec 01; 8(4):e62097. PubMed ID: 23637972 [Abstract] [Full Text] [Related]
3. Cellular tropism and transduction properties of seven adeno-associated viral vector serotypes in adult retina after intravitreal injection. Hellström M, Ruitenberg MJ, Pollett MA, Ehlert EM, Twisk J, Verhaagen J, Harvey AR. Gene Ther; 2009 Apr 01; 16(4):521-32. PubMed ID: 19092858 [Abstract] [Full Text] [Related]
4. 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 01; 31(13-14):719-729. PubMed ID: 32486858 [Abstract] [Full Text] [Related]
5. 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 [Abstract] [Full Text] [Related]
6. Tyrosine capsid-mutant AAV vectors for gene delivery to the canine retina from a subretinal or intravitreal approach. Mowat FM, Gornik KR, Dinculescu A, Boye SL, Hauswirth WW, Petersen-Jones SM, Bartoe JT. Gene Ther; 2014 Jan 01; 21(1):96-105. PubMed ID: 24225638 [Abstract] [Full Text] [Related]
7. 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 Jan 01; 15():267-75. PubMed ID: 19190735 [Abstract] [Full Text] [Related]
8. Differential targeting of feline photoreceptors by recombinant adeno-associated viral vectors: implications for preclinical gene therapy trials. Minella AL, Mowat FM, Willett KL, Sledge D, Bartoe JT, Bennett J, Petersen-Jones SM. Gene Ther; 2014 Oct 01; 21(10):913-20. PubMed ID: 25056608 [Abstract] [Full Text] [Related]
9. Single residue AAV capsid mutation improves transduction of photoreceptors in the Abca4-/- mouse and bipolar cells in the rd1 mouse and human retina ex vivo. De Silva SR, Charbel Issa P, Singh MS, Lipinski DM, Barnea-Cramer AO, Walker NJ, Barnard AR, Hankins MW, MacLaren RE. Gene Ther; 2016 Nov 01; 23(11):767-774. PubMed ID: 27416076 [Abstract] [Full Text] [Related]
10. Impact of Heparan Sulfate Binding on Transduction of Retina by Recombinant Adeno-Associated Virus Vectors. Boye SL, Bennett A, Scalabrino ML, McCullough KT, Van Vliet K, Choudhury S, Ruan Q, Peterson J, Agbandje-McKenna M, Boye SE. J Virol; 2016 Apr 01; 90(8):4215-4231. PubMed ID: 26865709 [Abstract] [Full Text] [Related]
11. Gene delivery to cone photoreceptors by subretinal injection of rAAV2/6 in the mouse retina. Hori T, Fukutome M, Maejima C, Matsushima H, Kobayashi K, Kitazawa S, Kitahara R, Kitano K, Kobayashi K, Moritoh S, Koike C. Biochem Biophys Res Commun; 2019 Jul 12; 515(1):222-227. PubMed ID: 31146917 [Abstract] [Full Text] [Related]
12. 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 [Abstract] [Full Text] [Related]
13. Recombinant AAV viral vectors pseudotyped with viral capsids from serotypes 1, 2, and 5 display differential efficiency and cell tropism after delivery to different regions of the central nervous system. Burger C, Gorbatyuk OS, Velardo MJ, Peden CS, Williams P, Zolotukhin S, Reier PJ, Mandel RJ, Muzyczka N. Mol Ther; 2004 Aug 01; 10(2):302-17. PubMed ID: 15294177 [Abstract] [Full Text] [Related]
15. 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 Aug 01; 10(7):2982-2999. PubMed ID: 32194850 [Abstract] [Full Text] [Related]
16. Utilizing minimally purified secreted rAAV for rapid and cost-effective manipulation of gene expression in the CNS. Goodwin MS, Croft CL, Futch HS, Ryu D, Ceballos-Diaz C, Liu X, Paterno G, Mejia C, Deng D, Menezes K, Londono L, Arjona K, Parianos M, Truong V, Rostonics E, Hernandez A, Boye SL, Boye SE, Levites Y, Cruz PE, Golde TE. Mol Neurodegener; 2020 Mar 02; 15(1):15. PubMed ID: 32122372 [Abstract] [Full Text] [Related]
17. 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 02; 23(2):223-30. PubMed ID: 26467396 [Abstract] [Full Text] [Related]