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Items: 1 to 20 of 101

1.

Helper-Dependent Adenovirus Transduces the Human and Rat Retina but Elicits an Inflammatory Reaction When Delivered Subretinally in Rats.

Han IC, Burnight E, Ulferts MJ, Worthington KS, Russell SR, Sohn EH, Mullins RF, Stone E, Tucker BA, Wiley LA.

Hum Gene Ther. 2019 Aug 28. doi: 10.1089/hum.2019.159. [Epub ahead of print]

PMID:
31456426
2.

Adeno-associated virus serotype-9 efficiently transduces the retinal outer plexiform layer.

Lei B, Zhang K, Yue Y, Ghosh A, Duan D.

Mol Vis. 2009 Jul 17;15:1374-82.

3.

Rod Outer Segment Development Influences AAV-Mediated Photoreceptor Transduction After Subretinal Injection.

Petit L, Ma S, Cheng SY, Gao G, Punzo C.

Hum Gene Ther. 2017 Jun;28(6):464-481. doi: 10.1089/hum.2017.020.

4.

Does recombinant adeno-associated virus-vectored proximal region of mouse rhodopsin promoter support only rod-type specific expression in vivo?

Glushakova LG, Timmers AM, Issa TM, Cortez NG, Pang J, Teusner JT, Hauswirth WW.

Mol Vis. 2006 Apr 7;12:298-309.

5.

Adeno-associated virus serotype-9 mediated retinal outer plexiform layer transduction is mainly through the photoreceptors.

Lei B, Zhang K, Yue Y, Ghosh A, Duan D.

Adv Exp Med Biol. 2010;664:671-8. doi: 10.1007/978-1-4419-1399-9_77.

PMID:
20238072
6.

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. doi: 10.1371/journal.pone.0054146. Epub 2013 Jan 15.

7.

The human rhodopsin kinase promoter in an AAV5 vector confers rod- and cone-specific expression in the primate retina.

Boye SE, Alexander JJ, Boye SL, Witherspoon CD, Sandefer KJ, Conlon TJ, Erger K, Sun J, Ryals R, Chiodo VA, Clark ME, Girkin CA, Hauswirth WW, Gamlin PD.

Hum Gene Ther. 2012 Oct;23(10):1101-15. doi: 10.1089/hum.2012.125. Epub 2012 Sep 20.

8.

Human blue-opsin promoter preferentially targets reporter gene expression to rat s-cone photoreceptors.

Glushakova LG, Timmers AM, Pang J, Teusner JT, Hauswirth WW.

Invest Ophthalmol Vis Sci. 2006 Aug;47(8):3505-13.

PMID:
16877422
9.

Evaluation of lateral spread of transgene expression following subretinal AAV-mediated gene delivery in dogs.

Bruewer AR, Mowat FM, Bartoe JT, Boye SL, Hauswirth WW, Petersen-Jones SM.

PLoS One. 2013;8(4):e60218. doi: 10.1371/journal.pone.0060218. Epub 2013 Apr 3.

10.

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;21(1):96-105. doi: 10.1038/gt.2013.64. Epub 2013 Nov 14.

11.
12.

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 Oct 14;90(21):9878-9888. doi: 10.1128/JVI.01568-16. Print 2016 Nov 1.

13.

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;15:267-75. Epub 2009 Feb 6.

14.

SubILM Injection of AAV for Gene Delivery to the Retina.

Gamlin PD, Alexander JJ, Boye SL, Witherspoon CD, Boye SE.

Methods Mol Biol. 2019;1950:249-262. doi: 10.1007/978-1-4939-9139-6_14.

15.

Retinal degeneration is slowed in transgenic rats by AAV-mediated delivery of FGF-2.

Lau D, McGee LH, Zhou S, Rendahl KG, Manning WC, Escobedo JA, Flannery JG.

Invest Ophthalmol Vis Sci. 2000 Oct;41(11):3622-33.

PMID:
11006261
16.

Transplantation of human bone marrow mesenchymal stem cells as a thin subretinal layer ameliorates retinal degeneration in a rat model of retinal dystrophy.

Tzameret A, Sher I, Belkin M, Treves AJ, Meir A, Nagler A, Levkovitch-Verbin H, Barshack I, Rosner M, Rotenstreich Y.

Exp Eye Res. 2014 Jan;118:135-44. doi: 10.1016/j.exer.2013.10.023. Epub 2013 Nov 13.

PMID:
24239509
17.

Avian Adeno-Associated Viral Transduction of the Postembryonic Chicken Retina.

Waldner DM, Visser F, Fischer AJ, Bech-Hansen NT, Stell WK.

Transl Vis Sci Technol. 2019 Jul 1;8(4):1. doi: 10.1167/tvst.8.4.1. eCollection 2019 Jul.

18.

Outer Plexiform Layer Structures Are Not Altered Following AAV-Mediated Gene Transfer in Healthy Rat Retina.

Giers BC, Klein D, Mendes-Madeira A, Isiegas C, Lorenz B, Haverkamp S, Stieger K.

Front Neurol. 2017 Feb 23;8:59. doi: 10.3389/fneur.2017.00059. eCollection 2017.

19.

Highly efficient retinal gene delivery with helper-dependent adenoviral vectors.

Lam S, Cao H, Wu J, Duan R, Hu J.

Genes Dis. 2014 Dec;1(2):227-237. doi: 10.1016/j.gendis.2014.09.002.

20.

AAV-mediated photoreceptor transduction of the pig cone-enriched retina.

Mussolino C, della Corte M, Rossi S, Viola F, Di Vicino U, Marrocco E, Neglia S, Doria M, Testa F, Giovannoni R, Crasta M, Giunti M, Villani E, Lavitrano M, Bacci ML, Ratiglia R, Simonelli F, Auricchio A, Surace EM.

Gene Ther. 2011 Jul;18(7):637-45. doi: 10.1038/gt.2011.3. Epub 2011 Mar 17.

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