AAV Delivery of Wild-Type Rhodopsin Preserves Retinal Function in a Mouse Model of Autosomal Dominant Retinitis Pigmentosa-Reference-Cited by-同舟云学术

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AAV Delivery of Wild-Type Rhodopsin Preserves Retinal Function in a Mouse Model of Autosomal Dominant Retinitis Pigmentosa

Published:2011-05 Issue:5 Volume:22 Page:567-575
ISSN:1043-0342
Container-title:Human Gene Therapy
language:en
Short-container-title:Human Gene Therapy

Author:

Mao Haoyu¹,James Thomas¹,Schwein Alison¹,Shabashvili Arseniy E.¹,Hauswirth William W.¹²,Gorbatyuk Marina S.¹³,Lewin Alfred S.¹

Affiliation:

1. Department of Molecular Genetics and Microbiology, University of Florida, Gainesville, FL 32610.

2. Department of Ophthalmology, University of Florida, Gainesville, FL 32610.

3. Current address: Department of Cell Biology and Anatomy, University of North Texas Health Science Center, Ft. Worth, TX 76107.

Publisher

Mary Ann Liebert Inc

Subject

Genetics,Molecular Biology,Molecular Medicine

Link

http://www.liebertpub.com/doi/pdf/10.1089/hum.2010.140

Reference48 articles.

1. Effect of Gene Therapy on Visual Function in Leber's Congenital Amaurosis

2. Contributions of Genetics to Our Understanding of Inherited Monogenic Retinal Diseases and Age-Related Macular Degeneration

3. Towards mutation-independent silencing of genes involved in retinal degeneration by RNA interference

4. HumanRPE65Gene Therapy for Leber Congenital Amaurosis: Persistence of Early Visual Improvements and Safety at 1 Year

5. Perspective on Genes and Mutations Causing Retinitis Pigmentosa

Cited by 107 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. Autosomal dominant Retinitis Pigmentosa caused by the rhodopsin isoleucine 255 deletion features rapid neuroretinal degeneration, decreased synaptic connectivity, and neuroinflammation;2024-08-30

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

3. The double whammy of ER-retention and dominant-negative effects in numerous autosomal dominant diseases: significance in disease mechanisms and therapy;Journal of Biomedical Science;2024-06-27

4. Gene Therapy Trial on X-Linked Retinitis Pigmentosa Caused by Mutations in RPGR;Essentials in Ophthalmology;2024

5. Gene Supplementation in Mice Heterozygous for the D477G RPE65 Variant Implicated in Autosomal Dominant Retinitis Pigmentosa;Human Gene Therapy;2023-07-01

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