30051304 27052928 33531684 36261499 32072884 33830174 32486858 26751519 26865709 29367457 31147753 28939376 30447199 31150809 31562387 33510064 31499165 33930398 33815052 29234687 28925755 27052802 36503723 - Search Results

Year	Number of Results
2016	4
2017	3
2018	5
2019	5
2020	3
2021	5
2022	2
2023	0

1

Phenotypic characterization of complete CSNB in the inbred research beagle: how common is CSNB in research and companion dogs?

Oh A, Loew ER, Foster ML, Davidson MG, English RV, Gervais KJ, Herring IP, Mowat FM. Oh A, et al. Doc Ophthalmol. 2018 Oct;137(2):87-101. doi: 10.1007/s10633-018-9653-y. Epub 2018 Jul 26. Doc Ophthalmol. 2018. PMID: 30051304

2

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. Boyd RF, et al. Gene Ther. 2016 Apr;23(4):400. doi: 10.1038/gt.2016.10. Gene Ther. 2016. PMID: 27052928 No abstract available.

3

Human MiniPromoters for ocular-rAAV expression in ON bipolar, cone, corneal, endothelial, Müller glial, and PAX6 cells.

Korecki AJ, Cueva-Vargas JL, Fornes O, Agostinone J, Farkas RA, Hickmott JW, Lam SL, Mathelier A, Zhou M, Wasserman WW, Di Polo A, Simpson EM. Korecki AJ, et al. Gene Ther. 2021 Jun;28(6):351-372. doi: 10.1038/s41434-021-00227-z. Epub 2021 Feb 2. Gene Ther. 2021. PMID: 33531684 Free PMC article.

4

Serotype-specific transduction of canine joint tissue explants and cultured monolayers by self-complementary adeno-associated viral vectors.

Kim AY, Duerr FM, Phillips JN, Samulski RJ, Grieger JC, Goodrich LR. Kim AY, et al. Gene Ther. 2022 Oct 20. doi: 10.1038/s41434-022-00366-x. Online ahead of print. Gene Ther. 2022. PMID: 36261499

5

Effect of Proteasome Inhibitors on the AAV-Mediated Transduction Efficiency in Retinal Bipolar Cells.

Cui S, Ganjawala TH, Abrams GW, Pan ZH. Cui S, et al. Curr Gene Ther. 2020;19(6):404-412. doi: 10.2174/1566523220666200211111326. Curr Gene Ther. 2020. PMID: 32072884

6

Subretinal Rather Than Intravitreal Adeno-Associated Virus-Mediated Delivery of a Complement Alternative Pathway Inhibitor Is Effective in a Mouse Model of RPE Damage.

Annamalai B, Parsons N, Nicholson C, Obert E, Jones B, Rohrer B. Annamalai B, et al. Invest Ophthalmol Vis Sci. 2021 Apr 1;62(4):11. doi: 10.1167/iovs.62.4.11. Invest Ophthalmol Vis Sci. 2021. PMID: 33830174 Free PMC article.

7

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. Ross M, et al. Hum Gene Ther. 2020 Jul;31(13-14):719-729. doi: 10.1089/hum.2020.023. Epub 2020 Jul 6. Hum Gene Ther. 2020. PMID: 32486858

8

Let There Be Light: Gene and Cell Therapy for Blindness.

Dalkara D, Goureau O, Marazova K, Sahel JA. Dalkara D, et al. Hum Gene Ther. 2016 Feb;27(2):134-47. doi: 10.1089/hum.2015.147. Hum Gene Ther. 2016. PMID: 26751519 Free PMC article. Review.

9

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. Boye SL, et al. J Virol. 2016 Mar 28;90(8):4215-4231. doi: 10.1128/JVI.00200-16. Print 2016 Apr. J Virol. 2016. PMID: 26865709 Free PMC article.

10

Noninvasive gene delivery to foveal cones for vision restoration.

Khabou H, Garita-Hernandez M, Chaffiol A, Reichman S, Jaillard C, Brazhnikova E, Bertin S, Forster V, Desrosiers M, Winckler C, Goureau O, Picaud S, Duebel J, Sahel JA, Dalkara D. Khabou H, et al. JCI Insight. 2018 Jan 25;3(2):e96029. doi: 10.1172/jci.insight.96029. eCollection 2018 Jan 25. JCI Insight. 2018. PMID: 29367457 Free PMC article.

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