Search filters

List of works by Wen-Tao Deng

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

scientific article published on 16 February 2016

AAV-mediated cone rescue in a naturally occurring mouse model of CNGA3-achromatopsia

scientific article (publication date: 2012)

AAV-mediated lysophosphatidylcholine acyltransferase 1 (Lpcat1) gene replacement therapy rescues retinal degeneration in rd11 mice.

scientific article published on 20 March 2014

Comparative analysis of in vivo and in vitro AAV vector transduction in the neonatal mouse retina: effects of serotype and site of administration.

scientific article published on 22 October 2007

Cone Phosphodiesterase-6γ' Subunit Augments Cone PDE6 Holoenzyme Assembly and Stability in a Mouse Model Lacking Both Rod and Cone PDE6 Catalytic Subunits

scientific article published on 09 July 2018

Cone phosphodiesterase-6α' restores rod function and confers distinct physiological properties in the rod phosphodiesterase-6β-deficient rd10 mouse

scientific article published on July 2013

Correction: AAV-Mediated Cone Rescue in a Naturally Occurring Mouse Model of CNGA3-Achromatopsia.

scientific article published on 6 January 2014

Functional interchangeability of rod and cone transducin alpha-subunits.

scholarly article

Gene Therapy for MERTK-Associated Retinal Degenerations.

scientific article published on January 2016

Gene therapy in the rd6 mouse model of retinal degeneration.

scientific article published on January 2014

Gene-based Therapy in a Mouse Model of Blue Cone Monochromacy.

scientific article published on 27 July 2017

Human L- and M-opsins restore M-cone function in a mouse model for human blue cone monochromacy

scientific article published on 8 January 2018

Molecular characterization of the Arabidopsis 9-cis epoxycarotenoid dioxygenase gene family

scientific article (publication date: July 2003)

Pathological Effects of Mutant C1QTNF5 (S163R) Expression in Murine Retinal Pigment Epithelium

scientific article published on October 2015

Preclinical potency and safety studies of an AAV2-mediated gene therapy vector for the treatment of MERTK associated retinitis pigmentosa.

scientific article published on March 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).

scientific article published on 23 May 2006

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

scientific article

Successful arrest of photoreceptor and vision loss expands the therapeutic window of retinal gene therapy to later stages of disease

scientific article

Toxicology and Pharmacology of an AAV Vector Expressing Codon-optimized RPGR in RPGR-deficient Rd9 Mice

article

Treatment of retinitis pigmentosa due to MERTK mutations by ocular subretinal injection of adeno-associated virus gene vector: results of a phase I trial

scientific article

Tyrosine-mutant AAV8 delivery of human MERTK provides long-term retinal preservation in RCS rats.

scientific article published on 06 April 2012

Vitreal delivery of AAV vectored Cnga3 restores cone function in CNGA3-/-/Nrl-/- mice, an all-cone model of CNGA3 achromatopsia

scientific article published on 8 April 2015

Paulina is supported by:

About Paulina

Help