Gene Therapy for Rhodopsin-associated Autosomal Dominant Retinitis Pigmentosa
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Ophthalmology
Reference134 articles.
1. Genes and mutations causing autosomal dominant retinitis pigmentosa;Daiger;Cold Spring Harb Perspect Med,2014
2. The supramolecular structure of the GPCR rhodopsin in solution and native disc membranes;Suda;Mol Membr Biol,2004
3. High-resolution homozygosity mapping is a powerful tool to detect novel mutations causative of autosomal recessive RP in the Dutch population;Collin;Invest Ophthalmol Vis Sci,2011
4. Autosomal recessive retinitis pigmentosa with homozygous rhodopsin mutation E150K and non-coding cis-regulatory variants in CRX-binding regions of SAMD7;Van Schil;Sci Rep,2016
5. Gene therapy in animal models of autosomal dominant retinitis pigmentosa;Rossmiller;Mol Vis,2012
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1. Disease modeling and pharmacological rescue of autosomal dominant retinitis pigmentosa associated with RHO copy number variation;eLife;2024-04-25
2. Adeno-associated virus as a delivery vector for gene therapy of human diseases;Signal Transduction and Targeted Therapy;2024-04-03
3. Disease modeling and pharmacological rescue of autosomal dominant Retinitis Pigmentosa associated with RHO copy number variation;ELIFE;2023-10-23
4. Retinitis Pigmentosa: Novel Therapeutic Targets and Drug Development;Pharmaceutics;2023-02-17
5. Genetic treatment for autosomal dominant inherited retinal dystrophies: approaches, challenges and targeted genotypes;British Journal of Ophthalmology;2022-08-29
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