Wen-Tao Deng
Wen-Tao Deng
Assistant Professor, West Virginia University
Verified email at
Cited by
Cited by
Molecular characterization of the Arabidopsis 9‐cis epoxycarotenoid dioxygenase gene family
BC Tan, LM Joseph, WT Deng, L Liu, QB Li, K Cline, DR McCarty
The Plant Journal 35 (1), 44-56, 2003
Gene therapy rescues photoreceptor blindness in dogs and paves the way for treating human X-linked retinitis pigmentosa
WA Beltran, AV Cideciyan, AS Lewin, S Iwabe, H Khanna, A Sumaroka, ...
Proceedings of the National Academy of Sciences 109 (6), 2132-2137, 2012
Novel properties of tyrosine-mutant AAV2 vectors in the mouse retina
H Petrs-Silva, A Dinculescu, Q Li, WT Deng, J Pang, SH Min, V Chiodo, ...
Molecular Therapy 19 (2), 293-301, 2011
Treatment of retinitis pigmentosa due to MERTK mutations by ocular subretinal injection of adeno-associated virus gene vector: results of a phase I trial
NG Ghazi, EB Abboud, SR Nowilaty, H Alkuraya, A Alhommadi, H Cai, ...
Human genetics 135, 327-343, 2016
AAV-mediated gene therapy for retinal degeneration in the rd10 mouse containing a recessive PDEβ mutation
J Pang, SL Boye, A Kumar, A Dinculescu, W Deng, J Li, Q Li, A Rani, ...
Investigative ophthalmology & visual science 49 (10), 4278-4283, 2008
AAV-mediated cone rescue in a naturally occurring mouse model of CNGA3-achromatopsia
J Pang, WT Deng, X Dai, B Lei, D Everhart, Y Umino, J Li, K Zhang, S Mao, ...
PloS one 7 (4), e35250, 2012
AAV-mediated cone rescue in a naturally occurring mouse model of CNGA3-achromatopsia
J Pang, WT Deng, X Dai, B Lei, D Everhart, Y Umino, J Li, K Zhang, S Mao, ...
PloS one 7 (4), e35250, 2012
Comparative analysis of in vivo and in vitro AAV vector transduction in the neonatal mouse retina: effects of serotype and site of administration
J Pang, A Lauramore, W Deng, Q Li, TJ Doyle, V Chiodo, J Li, ...
Vision research 48 (3), 377-385, 2008
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
Proceedings of the Third International Symposium on Retinopathy of Prematurity: an update on ROP from the lab to the nursery (November 2003, Anaheim, California)
G Lutty, T Chan-Ling, D Phelps, A Adamis, K Berns, C Chan, C Cole, ...
Molecular vision 12 (63), 532-580, 2006
Successful arrest of photoreceptor and vision loss expands the therapeutic window of retinal gene therapy to later stages of disease
WA Beltran, AV Cideciyan, S Iwabe, M Swider, MS Kosyk, K McDaid, ...
Proceedings of the National Academy of Sciences 112 (43), E5844-E5853, 2015
Tyrosine-mutant AAV8 delivery of human MERTK provides long-term retinal preservation in RCS rats
WT Deng, A Dinculescu, Q Li, SL Boye, J Li, MS Gorbatyuk, J Pang, ...
Investigative ophthalmology & visual science 53 (4), 1895-1904, 2012
Mechanistic basis for the failure of cone transducin to translocate: why cones are never blinded by light
ES Lobanova, R Herrmann, S Finkelstein, B Reidel, NP Skiba, WT Deng, ...
Journal of Neuroscience 30 (20), 6815-6824, 2010
Achromatopsia as a potential candidate for gene therapy
JJ Pang, J Alexander, B Lei, W Deng, K Zhang, Q Li, B Chang, ...
Retinal Degenerative Diseases: Laboratory and Therapeutic Investigations …, 2010
Stability and Safety of an AAV Vector for Treating RPGR-ORF15 X-Linked Retinitis Pigmentosa
WT Deng, FM Dyka, A Dinculescu, J Li, P Zhu, VA Chiodo, SL Boye, ...
Human gene therapy 26 (9), 593-602, 2015
Functional interchangeability of rod and cone transducin α-subunits
WT Deng, K Sakurai, J Liu, A Dinculescu, J Li, J Pang, SH Min, VA Chiodo, ...
Proceedings of the National Academy of Sciences 106 (42), 17681-17686, 2009
Gene Therapy for Retinitis Pigmentosa Caused by MFRP Mutations: Human Phenotype and Preliminary Proof of Concept
A Dinculescu, J Estreicher, JC Zenteno, TS Aleman, SB Schwartz, ...
Human gene therapy 23 (4), 367-376, 2012
Gene Therapy for MERTK-Associated Retinal Degenerations
MM LaVail, D Yasumura, MT Matthes, H Yang, WW Hauswirth, WT Deng, ...
Retinal Degenerative Diseases: Mechanisms and Experimental Therapy, 487-493, 2016
Gene-based therapy in a mouse model of blue cone monochromacy
Y Zhang, WT Deng, W Du, P Zhu, J Li, F Xu, J Sun, CD Gerstner, W Baehr, ...
Scientific reports 7 (1), 6690, 2017
AAV-mediated lysophosphatidylcholine acyltransferase 1 (Lpcat1) gene replacement therapy rescues retinal degeneration in rd11 mice
X Dai, J Han, Y Qi, H Zhang, L Xiang, J Lv, J Li, WT Deng, B Chang, ...
Investigative ophthalmology & visual science 55 (3), 1724-1734, 2014
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