A rhodopsin gene mutation responsible for autosomal dominant retinitis pigmentosa results in a protein that is defective in localization to the photoreceptor outer segment-Reference-Cited by-同舟云学术

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A rhodopsin gene mutation responsible for autosomal dominant retinitis pigmentosa results in a protein that is defective in localization to the photoreceptor outer segment

Published:1994-10-01 Issue:10 Volume:14 Page:5818-5833
ISSN:0270-6474
Container-title:The Journal of Neuroscience
language:en
Short-container-title:J. Neurosci.

Author:

Sung CH,Makino C,Baylor D,Nathans J

Publisher

Society for Neuroscience

Subject

General Neuroscience

Cited by 237 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. Role of endosomal pathway in the ciliary transport and the membrane organization of outer segment disc membrane in photoreceptors;Folia Pharmacologica Japonica;2024-07-01

2. Downregulation of rhodopsin is an effective therapeutic strategy in ameliorating peripherin-2-associated inherited retinal disorders;Nature Communications;2024-06-04

3. Disease modeling and pharmacological rescue of autosomal dominant retinitis pigmentosa associated with RHO copy number variation;eLife;2024-04-25

4. Rhodopsin mislocalization drives ciliary dysregulation in a novel autosomal dominant retinitis pigmentosa knock‐in mouse model;The FASEB Journal;2024-04-22

5. The Logistical Backbone of Photoreceptor Cell Function: Complementary Mechanisms of Dietary Vitamin A Receptors and Rhodopsin Transporters;International Journal of Molecular Sciences;2024-04-12

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