287 related articles for article (PubMed ID: 21818300)
41. microRNA122-regulated transgene expression increases specificity of cardiac gene transfer upon intravenous delivery of AAV9 vectors.
Geisler A; Jungmann A; Kurreck J; Poller W; Katus HA; Vetter R; Fechner H; Müller OJ
Gene Ther; 2011 Feb; 18(2):199-209. PubMed ID: 21048795
[TBL] [Abstract][Full Text] [Related]
42. 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; 58(14):6429-6439. PubMed ID: 29260200
[TBL] [Abstract][Full Text] [Related]
43. Retinal transduction profiles by high-capacity viral vectors.
Puppo A; Cesi G; Marrocco E; Piccolo P; Jacca S; Shayakhmetov DM; Parks RJ; Davidson BL; Colloca S; Brunetti-Pierri N; Ng P; Donofrio G; Auricchio A
Gene Ther; 2014 Oct; 21(10):855-65. PubMed ID: 24989814
[TBL] [Abstract][Full Text] [Related]
44. Triple Vectors Expand AAV Transfer Capacity in the Retina.
Maddalena A; Tornabene P; Tiberi P; Minopoli R; Manfredi A; Mutarelli M; Rossi S; Simonelli F; Naggert JK; Cacchiarelli D; Auricchio A
Mol Ther; 2018 Feb; 26(2):524-541. PubMed ID: 29292161
[TBL] [Abstract][Full Text] [Related]
45. 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; 29(10):1124-1139. PubMed ID: 29580100
[TBL] [Abstract][Full Text] [Related]
46. Long-term doxycycline-regulated transgene expression in the retina of nonhuman primates following subretinal injection of recombinant AAV vectors.
Stieger K; Le Meur G; Lasne F; Weber M; Deschamps JY; Nivard D; Mendes-Madeira A; Provost N; Martin L; Moullier P; Rolling F
Mol Ther; 2006 May; 13(5):967-75. PubMed ID: 16442848
[TBL] [Abstract][Full Text] [Related]
47. 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
[TBL] [Abstract][Full Text] [Related]
48. Tropisms of AAV for subretinal delivery to the neonatal mouse retina and its application for in vivo rescue of developmental photoreceptor disorders.
Watanabe S; Sanuki R; Ueno S; Koyasu T; Hasegawa T; Furukawa T
PLoS One; 2013; 8(1):e54146. PubMed ID: 23335994
[TBL] [Abstract][Full Text] [Related]
49. Optimized adeno-associated virus (AAV)-protein phosphatase-5 helper viruses for efficient liver transduction by single-stranded AAV vectors: therapeutic expression of factor IX at reduced vector doses.
Jayandharan GR; Zhong L; Sack BK; Rivers AE; Li M; Li B; Herzog RW; Srivastava A
Hum Gene Ther; 2010 Mar; 21(3):271-83. PubMed ID: 19788390
[TBL] [Abstract][Full Text] [Related]
50. Distinct Expression Patterns of AAV8 Vectors with Broadly Active Promoters from Subretinal Injections of Neonatal Mouse Eyes at Two Different Ages.
Xiong W; Cepko C
Adv Exp Med Biol; 2016; 854():501-7. PubMed ID: 26427452
[TBL] [Abstract][Full Text] [Related]
51. Efficient trans-splicing in the retina expands the utility of adeno-associated virus as a vector for gene therapy.
Reich SJ; Auricchio A; Hildinger M; Glover E; Maguire AM; Wilson JM; Bennett J
Hum Gene Ther; 2003 Jan; 14(1):37-44. PubMed ID: 12573057
[TBL] [Abstract][Full Text] [Related]
52. Laser Photocoagulation Induces Transduction of Retinal Pigment Epithelial Cells by Intravitreally Administered Adeno-Associated Viral Vectors.
Lee SH; Kong YJ; Lyu J; Lee H; Park K; Park TK
Hum Gene Ther Methods; 2015 Oct; 26(5):159-61. PubMed ID: 26413863
[TBL] [Abstract][Full Text] [Related]
53. Stable rAAV-mediated transduction of rod and cone photoreceptors in the canine retina.
Bainbridge JW; Mistry A; Schlichtenbrede FC; Smith A; Broderick C; De Alwis M; Georgiadis A; Taylor PM; Squires M; Sethi C; Charteris D; Thrasher AJ; Sargan D; Ali RR
Gene Ther; 2003 Aug; 10(16):1336-44. PubMed ID: 12883530
[TBL] [Abstract][Full Text] [Related]
54. Novel Combinatorial MicroRNA-Binding Sites in AAV Vectors Synergistically Diminish Antigen Presentation and Transgene Immunity for Efficient and Stable Transduction.
Muhuri M; Zhan W; Maeda Y; Li J; Lotun A; Chen J; Sylvia K; Dasgupta I; Arjomandnejad M; Nixon T; Keeler AM; Manokaran S; He R; Su Q; Tai PWL; Gao G
Front Immunol; 2021; 12():674242. PubMed ID: 33995418
[TBL] [Abstract][Full Text] [Related]
55. AAV-Mediated Gene Delivery to 3D Retinal Organoids Derived from Human Induced Pluripotent Stem Cells.
Garita-Hernandez M; Routet F; Guibbal L; Khabou H; Toualbi L; Riancho L; Reichman S; Duebel J; Sahel JA; Goureau O; Dalkara D
Int J Mol Sci; 2020 Feb; 21(3):. PubMed ID: 32028585
[TBL] [Abstract][Full Text] [Related]
56. 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; 17(3):235-247. PubMed ID: 28982327
[TBL] [Abstract][Full Text] [Related]
57. Sustained and Widespread Gene Delivery to the Corneal Epithelium via In Situ Transduction of Limbal Epithelial Stem Cells, Using Lentiviral and Adeno-Associated Viral Vectors.
Basche M; Kampik D; Kawasaki S; Branch MJ; Robinson M; Larkin DF; Smith AJ; Ali RR
Hum Gene Ther; 2018 Oct; 29(10):1140-1152. PubMed ID: 30070149
[TBL] [Abstract][Full Text] [Related]
58. Mir-142-3p target sequences reduce transgene-directed immunogenicity following intramuscular adeno-associated virus 1 vector-mediated gene delivery.
Majowicz A; Maczuga P; Kwikkers KL; van der Marel S; van Logtenstein R; Petry H; van Deventer SJ; Konstantinova P; Ferreira V
J Gene Med; 2013; 15(6-7):219-32. PubMed ID: 23658149
[TBL] [Abstract][Full Text] [Related]
59. Cross-packaging of a single adeno-associated virus (AAV) type 2 vector genome into multiple AAV serotypes enables transduction with broad specificity.
Rabinowitz JE; Rolling F; Li C; Conrath H; Xiao W; Xiao X; Samulski RJ
J Virol; 2002 Jan; 76(2):791-801. PubMed ID: 11752169
[TBL] [Abstract][Full Text] [Related]
60. New MiniPromoter Ple345 (NEFL) Drives Strong and Specific Expression in Retinal Ganglion Cells of Mouse and Primate Retina.
Simpson EM; Korecki AJ; Fornes O; McGill TJ; Cueva-Vargas JL; Agostinone J; Farkas RA; Hickmott JW; Lam SL; Mathelier A; Renner LM; Stoddard J; Zhou M; Di Polo A; Neuringer M; Wasserman WW
Hum Gene Ther; 2019 Mar; 30(3):257-272. PubMed ID: 30062914
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
