关注
Shannon Boye
Shannon Boye
Associate Professor, University of Florida
在 ufl.edu 的电子邮件经过验证
标题
引用次数
引用次数
年份
Current clinical applications of in vivo gene therapy with AAVs
JR Mendell, SA Al-Zaidy, LR Rodino-Klapac, K Goodspeed, SJ Gray, ...
Molecular Therapy 29 (2), 464-488, 2021
5152021
A comprehensive review of retinal gene therapy
SE Boye, SL Boye, AS Lewin, WW Hauswirth
Molecular therapy 21 (3), 509-519, 2013
3442013
Virally delivered channelrhodopsin-2 safely and effectively restores visual function in multiple mouse models of blindness
MM Doroudchi, KP Greenberg, J Liu, KA Silka, ES Boyden, JA Lockridge, ...
Molecular Therapy 19 (7), 1220-1229, 2011
3432011
Targeting photoreceptors via intravitreal delivery using novel, capsid-mutated AAV vectors
CN Kay, RC Ryals, GV Aslanidi, SH Min, Q Ruan, J Sun, FM Dyka, ...
PloS one 8 (4), e62097, 2013
2012013
Gene delivery to mitochondria by targeting modified adenoassociated virus suppresses Leber’s hereditary optic neuropathy in a mouse model
H Yu, RD Koilkonda, TH Chou, V Porciatti, SS Ozdemir, V Chiodo, ...
Proceedings of the National Academy of Sciences 109 (20), E1238-E1247, 2012
1842012
Long-term retinal function and structure rescue using capsid mutant AAV8 vector in the rd10 mouse, a model of recessive retinitis pigmentosa
J Pang, X Dai, SE Boye, I Barone, SL Boye, S Mao, D Everhart, ...
Molecular therapy 19 (2), 234-242, 2011
1822011
Retinal gene therapy with a large MYO7A cDNA using adeno-associated virus
VS Lopes, SE Boye, CM Louie, S Boye, F Dyka, V Chiodo, H Fofo, ...
Gene therapy 20 (8), 824-833, 2013
1632013
The human rhodopsin kinase promoter in an AAV5 vector confers rod-and cone-specific expression in the primate retina
SE Boye, JJ Alexander, SL Boye, CD Witherspoon, KJ Sandefer, ...
Human gene therapy 23 (10), 1101-1115, 2012
1362012
Dual Adeno-Associated Virus Vectors Result in Efficient In Vitro and In Vivo Expression of an Oversized Gene, MYO7A
FM Dyka, SL Boye, VA Chiodo, WW Hauswirth, SE Boye
Human gene therapy methods 25 (2), 166-177, 2014
1312014
Functional and behavioral restoration of vision by gene therapy in the guanylate cyclase-1 (GC1) knockout mouse
SE Boye, SL Boye, J Pang, R Ryals, D Everhart, Y Umino, AW Neeley, ...
PloS one 5 (6), e11306, 2010
1192010
Preclinical potency and safety studies of an AAV2-mediated gene therapy vector for the treatment of MERTK associated retinitis pigmentosa
TJ Conlon, WT Deng, K Erger, T Cossette, J Pang, R Ryals, N Clément, ...
Human gene therapy Clinical development 24 (1), 23-28, 2013
1062013
rAAV2/5 gene-targeting to rods: dose-dependent efficiency and complications associated with different promoters
WA Beltran, SL Boye, SE Boye, VA Chiodo, AS Lewin, WW Hauswirth, ...
Gene therapy 17 (9), 1162-1174, 2010
932010
Light-driven cone arrestin translocation in cones of postnatal guanylate cyclase-1 knockout mouse retina treated with AAV-GC1
SE Haire, J Pang, SL Boye, I Sokal, CM Craft, K Palczewski, ...
Investigative ophthalmology & visual science 47 (9), 3745-3753, 2006
902006
Somatic Gene Editing of GUCY2D by AAV-CRISPR/Cas9 Alters Retinal Structure and Function in Mouse and Macaque
KT McCullough, SL Boye, D Fajardo, K Calabro, JJ Peterson, CE Strang, ...
Human gene therapy 30 (5), 571-589, 2019
872019
Highly efficient delivery of adeno-associated viral vectors to the primate retina
SE Boye, JJ Alexander, CD Witherspoon, SL Boye, JJ Peterson, ME Clark, ...
Human gene therapy 27 (8), 580-597, 2016
852016
Optimization of retinal gene therapy for X-linked retinitis pigmentosa due to RPGR mutations
WA Beltran, AV Cideciyan, SE Boye, GJ Ye, S Iwabe, VL Dufour, ...
Molecular Therapy 25 (8), 1866-1880, 2017
822017
Impact of heparan sulfate binding on transduction of retina by recombinant adeno-associated virus vectors
SL Boye, A Bennett, ML Scalabrino, KT McCullough, K Van Vliet, ...
Journal of virology 90 (8), 4215-4231, 2016
822016
Self-complementary AAV-mediated gene therapy restores cone function and prevents cone degeneration in two models of Rpe65 deficiency
J Pang, SE Boye, B Lei, SL Boye, D Everhart, R Ryals, Y Umino, B Rohrer, ...
Gene therapy 17 (7), 815-826, 2010
812010
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
ML Scalabrino, SL Boye, KMH Fransen, JM Noel, FM Dyka, SH Min, ...
Human molecular genetics 24 (21), 6229-6239, 2015
802015
Lentiviral expression of retinal guanylate cyclase-1 (RetGC1) restores vision in an avian model of childhood blindness
ML Williams, JE Coleman, SE Haire, TS Aleman, AV Cideciyan, I Sokal, ...
PLoS medicine 3 (6), e201, 2006
802006
系统目前无法执行此操作,请稍后再试。
文章 1–20