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Biorxiv : the Preprint Server for Biology|March 11, 2024
The USH3A causative gene clarin1 functions in Müller glia to maintain retinal photoreceptorsHannah J T Nonarath, Samantha L Simpson, Tricia L Slobodianuk, et al.
Plos Genetics|March 11, 2025
The USH3A causative gene clarin1 functions in Müller glia to maintain retinal photoreceptorsHannah J T Nonarath, Samantha L Simpson, Tricia L Slobodianuk, et al.
Human Gene Therapy|June 18, 2005
Adeno-associated virus-vectored gene therapy for retinal diseaseAstra Dinculescu, Lyudmyla Glushakova, Seok-Hong Min, et al.
Molecular Vision|June 25, 2004
The surface of visual arrestin that binds to rhodopsinW Clay Smith, Astra Dinculescu, James J Peterson, et al.
Human Gene Therapy|January 27, 2022
A Modified Arrestin1 Increases Lactate Production in the Retina and Slows Retinal DegenerationTiffany S Nelson, Chiab Simpson, Frank Dyka, et al.
Advances in Experimental Medicine and Biology|March 26, 2014
Gene therapy in the rd6 mouse model of retinal degenerationAstra Dinculescu, Seok-Hong Min, Wen-Tao Deng, et al.
Molecular Vision|December 25, 2013
Review: the history and role of naturally occurring mouse models with Pde6b mutationsJuanjuan Han, Astra Dinculescu, Xufeng Dai, et al.
Molecular Vision|May 10, 2011
Quantifying transduction efficiencies of unmodified and tyrosine capsid mutant AAV vectors in vitro using two ocular cell linesRenee C Ryals, Sanford L Boye, Astra Dinculescu, et al.
Advances in Experimental Medicine and Biology|December 30, 2019
Systemic Delivery of Genes to Retina Using Adeno-Associated VirusesChiab P Simpson, Susan N Bolch, Ping Zhu, et al.
Molecular Vision|October 7, 2008
Intraocular route of AAV2 vector administration defines humoral immune response and therapeutic potentialQiuhong Li, Rehae Miller, Ping-Yang Han, et al.
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