<i>RPGR</i>-Related Retinopathy: Clinical Features, Molecular Genetics, and Gene Replacement Therapy-Reference-Cited by-同舟云学术

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RPGR-Related Retinopathy: Clinical Features, Molecular Genetics, and Gene Replacement Therapy

Published:2023-05-15 Issue:11 Volume:13 Page:a041280
ISSN:2157-1422
Container-title:Cold Spring Harbor Perspectives in Medicine
language:en
Short-container-title:Cold Spring Harb Perspect Med

Author:

Awadh Hashem Shaima,Georgiou Michalis,Ali Robin R.,Michaelides Michel

Publisher

Cold Spring Harbor Laboratory

Subject

General Biochemistry, Genetics and Molecular Biology

Reference71 articles.

1. Characterization of Retinal Function Using Microperimetry-Derived Metrics in Both Adults and Children With RPGR-Associated Retinopathy

2. A Frameshift Mutation inRPGRExon ORF15 Causes Photoreceptor Degeneration and Inner Retina Remodeling in a Model of X-Linked Retinitis Pigmentosa

3. Gene therapy rescues photoreceptor blindness in dogs and paves the way for treating human X-linked retinitis pigmentosa

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

5. A Randomized Trial of Vitamin A and Vitamin E Supplementation for Retinitis Pigmentosa

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. From onset to blindness: a comprehensive analysis ofRPGR-associated X-linked retinopathy in a large cohort in China;Journal of Medical Genetics;2024-08-17

2. Gene Therapy for Retinitis Pigmentosa: Current Challenges and New Progress;Biomolecules;2024-07-25

3. Phenotyping and genotyping inherited retinal diseases: Molecular genetics, clinical and imaging features, and therapeutics of macular dystrophies, cone and cone-rod dystrophies, rod-cone dystrophies, Leber congenital amaurosis, and cone dysfunction syndromes;Progress in Retinal and Eye Research;2024-05

4. Quantification of Fundus Autofluorescence Features in a Molecularly Characterized Cohort of More Than 3500 Inherited Retinal Disease Patients from the United Kingdom;2024-03-28

5. AAV-RPGR Gene Therapy Rescues Opsin Mislocalisation in a Human Retinal Organoid Model of RPGR-Associated X-Linked Retinitis Pigmentosa;International Journal of Molecular Sciences;2024-02-02

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