Mutant prominin 1 found in patients with macular degeneration disrupts photoreceptor disk morphogenesis in mice-Reference-Cited by-同舟云学术

Mutant prominin 1 found in patients with macular degeneration disrupts photoreceptor disk morphogenesis in mice

Published:2008-07-01 Issue: Volume: Page:
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

Yang Zhenglin,Chen Yali,Lillo Concepcion,Chien Jeremy,Yu Zhengya,Michaelides Michel,Klein Martin,Howes Kim A.,Li Yang,Kaminoh Yuuki,Chen Haoyu,Zhao Chao,Chen Yuhong,Al-Sheikh Youssef Tawfik,Karan Goutam,Corbeil Denis,Escher Pascal,Kamaya Shin,Li Chunmei,Johnson Samantha,Frederick Jeanne M.,Zhao Yu,Wang Changguan,Cameron D. Joshua,Huttner Wieland B.,Schorderet Daniel F.,Munier Frances L.,Moore Anthony T.,Birch David G.,Baehr Wolfgang,Hunt David M.,Williams David S.,Zhang Kang

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference44 articles.

1. THE RENEWAL OF PHOTORECEPTOR CELL OUTER SEGMENTS

2. Identification of a photoreceptor-specific mRNA encoded by the gene responsible for retinal degeneration slow (rds)

3. Photoreceptor peripherin is the normal product of the gene responsible for retinal degeneration in the rds mouse.

4. Mutation of the Stargardt Disease Gene ( ABCR ) in Age-Related Macular Degeneration

5. Insights into the Function of Rim Protein in Photoreceptors and Etiology of Stargardt's Disease from the Phenotype in abcr Knockout Mice

Cited by 217 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. Inpp5e is a Critical Regulator of Protein Transport to Photoreceptor Outer Segments;2024-08-28

2. Cdhr1a and pcdh15b link photoreceptor outer segments with inner segment calyceal processes revealing a potential mechanism for cone-rod dystrophy;2024-07-26

3. Clinical exome analysis and targeted gene repair of the c.1354dupT variant in iPSC lines from patients with PROM1-related retinopathies exhibiting diverse phenotypes;Stem Cell Research & Therapy;2024-07-02

4. Next-generation sequencing to genetically diagnose a diverse range of inherited eye disorders in 15 consanguineous families from Pakistan;Experimental Eye Research;2024-07

5. Prominin-1 null Xenopus laevis develop subretinal drusenoid-like deposits, cone-rod dystrophy, and RPE atrophy;2024-06-03