about
Clarin-1, encoded by the Usher Syndrome III causative gene, forms a membranous microdomain: possible role of clarin-1 in organizing the actin cytoskeletonAlternative splice variants of the USH3A gene Clarin 1 (CLRN1)Review: the history and role of naturally occurring mouse models with Pde6b mutationsIntraocular route of AAV2 vector administration defines humoral immune response and therapeutic potentialHigh-efficiency transduction of the mouse retina by tyrosine-mutant AAV serotype vectorsArrestin translocation in rod photoreceptors.Adeno-associated virus-vectored gene therapy for retinal disease.Novel properties of tyrosine-mutant AAV2 vectors in the mouse retinaGene therapy for retinitis pigmentosa caused by MFRP mutations: human phenotype and preliminary proof of concept.AAV-mediated gene therapy for retinal degeneration in the rd10 mouse containing a recessive PDEbeta mutation.Downregulation of p22phox in retinal pigment epithelial cells inhibits choroidal neovascularization in miceCone phosphodiesterase-6α' restores rod function and confers distinct physiological properties in the rod phosphodiesterase-6β-deficient rd10 mouseQuantifying transduction efficiencies of unmodified and tyrosine capsid mutant AAV vectors in vitro using two ocular cell lines.Gene Therapy in a Large Animal Model of PDE6A-Retinitis Pigmentosa.Prolonged recovery of retinal structure/function after gene therapy in an Rs1h-deficient mouse model of x-linked juvenile retinoschisis.The surface of visual arrestin that binds to rhodopsin.Adeno-associated virus-mediated expression of vascular endothelial growth factor peptides inhibits retinal neovascularization in a mouse model of oxygen-induced retinopathy.Disease mechanisms and gene therapy in a mouse model for X-linked retinoschisis.
P50
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P50
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Astra Dinculescu
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Astra Dinculescu
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Astra Dinculescu
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Astra Dinculescu
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Astra Dinculescu
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Astra Dinculescu
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Astra Dinculescu
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Astra Dinculescu
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Astra Dinculescu
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Astra Dinculescu
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Astra Dinculescu
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Astra Dinculescu
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