Dyka FM - Search Results

1

Long-term preservation of cone photoreceptors and restoration of cone function by gene therapy in the guanylate cyclase-1 knockout (GC1KO) mouse.

Boye SL, Conlon T, Erger K, Ryals R, Neeley A, Cossette T, Pang J, Dyka FM, Hauswirth WW, Boye SE. Boye SL, et al. Among authors: dyka fm. Invest Ophthalmol Vis Sci. 2011 Sep 9;52(10):7098-108. doi: 10.1167/iovs.11-7867. Invest Ophthalmol Vis Sci. 2011. PMID: 21778276 Free PMC article.

2

AAV-mediated gene therapy in the guanylate cyclase (RetGC1/RetGC2) double knockout mouse model of Leber congenital amaurosis.

Boye SL, Peshenko IV, Huang WC, Min SH, McDoom I, Kay CN, Liu X, Dyka FM, Foster TC, Umino Y, Karan S, Jacobson SG, Baehr W, Dizhoor A, Hauswirth WW, Boye SE. Boye SL, et al. Among authors: dyka fm. Hum Gene Ther. 2013 Feb;24(2):189-202. doi: 10.1089/hum.2012.193. Hum Gene Ther. 2013. PMID: 23210611 Free PMC article.

3

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. Kay CN, et al. Among authors: dyka fm. PLoS One. 2013 Apr 26;8(4):e62097. doi: 10.1371/journal.pone.0062097. Print 2013. PLoS One. 2013. PMID: 23637972 Free PMC article.

4

Cone specific promoter for use in gene therapy of retinal degenerative diseases.

Dyka FM, Boye SL, Ryals RC, Chiodo VA, Boye SE, Hauswirth WW. Dyka FM, et al. Adv Exp Med Biol. 2014;801:695-701. doi: 10.1007/978-1-4614-3209-8_87. Adv Exp Med Biol. 2014. PMID: 24664760 Free PMC article.

5

Gene Therapy in Opn1mw^-/-/Opn1sw^-/- Mice and Implications for Blue Cone Monochromacy Patients with Deletion Mutations.

Ma X, Sechrest ER, Fajardo D, Zhu P, Dyka F, Wang Y, Lobanova E, Boye SE, Baehr W, Deng WT. Ma X, et al. Hum Gene Ther. 2022 Jul;33(13-14):708-718. doi: 10.1089/hum.2021.298. Epub 2022 May 16. Hum Gene Ther. 2022. PMID: 35272502 Free PMC article.

6

Dual ABCA4-AAV Vector Treatment Reduces Pathogenic Retinal A2E Accumulation in a Mouse Model of Autosomal Recessive Stargardt Disease.

Dyka FM, Molday LL, Chiodo VA, Molday RS, Hauswirth WW. Dyka FM, et al. Hum Gene Ther. 2019 Nov;30(11):1361-1370. doi: 10.1089/hum.2019.132. Epub 2019 Sep 30. Hum Gene Ther. 2019. PMID: 31418294 Free PMC article.

7

Dual adeno-associated virus vectors result in efficient in vitro and in vivo expression of an oversized gene, MYO7A.

Dyka FM, Boye SL, Chiodo VA, Hauswirth WW, Boye SE. Dyka FM, et al. Hum Gene Ther Methods. 2014 Apr;25(2):166-77. doi: 10.1089/hgtb.2013.212. Hum Gene Ther Methods. 2014. PMID: 24568220 Free PMC article.

8

Stability and Safety of an AAV Vector for Treating RPGR-ORF15 X-Linked Retinitis Pigmentosa.

Deng WT, Dyka FM, Dinculescu A, Li J, Zhu P, Chiodo VA, Boye SL, Conlon TJ, Erger K, Cossette T, Hauswirth WW. Deng WT, et al. Among authors: dyka fm. Hum Gene Ther. 2015 Sep;26(9):593-602. doi: 10.1089/hum.2015.035. Epub 2015 Jul 29. Hum Gene Ther. 2015. PMID: 26076799 Free PMC article.

9

Intravitreal delivery of a novel AAV vector targets ON bipolar cells and restores visual function in a mouse model of complete congenital stationary night blindness.

Scalabrino ML, Boye SL, Fransen KM, Noel JM, Dyka FM, Min SH, Ruan Q, De Leeuw CN, Simpson EM, Gregg RG, McCall MA, Peachey NS, Boye SE. Scalabrino ML, et al. Among authors: dyka fm. Hum Mol Genet. 2015 Nov 1;24(21):6229-39. doi: 10.1093/hmg/ddv341. Epub 2015 Aug 26. Hum Mol Genet. 2015. PMID: 26310623 Free PMC article.

10

AAV-Mediated Clarin-1 Expression in the Mouse Retina: Implications for USH3A Gene Therapy.

Dinculescu A, Stupay RM, Deng WT, Dyka FM, Min SH, Boye SL, Chiodo VA, Abrahan CE, Zhu P, Li Q, Strettoi E, Novelli E, Nagel-Wolfrum K, Wolfrum U, Smith WC, Hauswirth WW. Dinculescu A, et al. Among authors: dyka fm. PLoS One. 2016 Feb 16;11(2):e0148874. doi: 10.1371/journal.pone.0148874. eCollection 2016. PLoS One. 2016. PMID: 26881841 Free PMC article.

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