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Journal Abstract Search

342 related items for PubMed ID: 33752467

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  • 3. Tropism of AAV Vectors in Photoreceptor-Like Cells of Human iPSC-Derived Retinal Organoids.
    McClements ME, Steward H, Atkin W, Goode EA, Gándara C, Chichagova V, MacLaren RE.
    Transl Vis Sci Technol; 2022 Apr 01; 11(4):3. PubMed ID: 35377942
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  • 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
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  • 6. 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
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  • 7. 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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  • 9. 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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  • 12. 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 15; 21(10):913-20. PubMed ID: 25056608
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  • 14. Assessment of AAV Vector Tropisms for Mouse and Human Pluripotent Stem Cell-Derived RPE and Photoreceptor Cells.
    Gonzalez-Cordero A, Goh D, Kruczek K, Naeem A, Fernando M, Kleine Holthaus SM, Takaaki M, Blackford SJI, Kloc M, Agundez L, Sampson RD, Borooah S, Ovando-Roche P, Mehat MS, West EL, Smith AJ, Pearson RA, Ali RR.
    Hum Gene Ther; 2018 Oct 15; 29(10):1124-1139. PubMed ID: 29580100
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  • 16. Pseudotyped adeno-associated viral vectors for gene transfer in dermal fibroblasts: implications for wound-healing applications.
    Balaji S, King A, Dhamija Y, Le LD, Shaaban AF, Crombleholme TM, Keswani SG.
    J Surg Res; 2013 Sep 15; 184(1):691-8. PubMed ID: 23590866
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  • 18. Self-complementary and tyrosine-mutant rAAV vectors enhance transduction in cystic fibrosis bronchial epithelial cells.
    Lopes-Pacheco M, Kitoko JZ, Morales MM, Petrs-Silva H, Rocco PRM.
    Exp Cell Res; 2018 Nov 15; 372(2):99-107. PubMed ID: 30244179
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  • 19. 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 15; 21(1):96-105. PubMed ID: 24225638
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  • 20. SubILM Injection of AAV for Gene Delivery to the Retina.
    Gamlin PD, Alexander JJ, Boye SL, Witherspoon CD, Boye SE.
    Methods Mol Biol; 2019 Jan 15; 1950():249-262. PubMed ID: 30783978
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