Natural History and Retinal Structure in Patients with Usher Syndrome Type 1 Owing to MYO7A Mutation
Author:
Publisher
Elsevier BV
Subject
Ophthalmology
Reference46 articles.
1. Clinical utility gene card for: Usher syndrome;Bolz;Eur J Hum Genet,2011
2. Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48;Riazuddin;Nat Genet,2012
3. Genetics and pathological mechanisms of Usher syndrome;Yan;J Hum Genet,2010
4. Molecular basis of human Usher syndrome: deciphering the meshes of the Usher protein network provides insights into the pathomechanisms of the Usher disease;Reiners;Exp Eye Res,2006
5. A novel Usher protein network at the periciliary reloading point between molecular transport machineries in vertebrate photoreceptor cells;Maerker;Hum Mol Genet,2008
Cited by 30 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. Neural (Sensory) Retina;Ocular Pathology;2025
2. Characterizing Retinal Sensitivity and Structure in Congenital Stationary Night Blindness: A Combined Microperimetry and OCT Study;Investigative Ophthalmology & Visual Science;2024-06-25
3. Sema4D Knockout Attenuates Choroidal Neovascularization by Inhibiting M2 Macrophage Polarization Via Regulation of the RhoA/ROCK Pathway;Investigative Ophthalmology & Visual Science;2024-06-24
4. Multicentric Longitudinal Prospective Study in a European Cohort of MYO7A Patients: Disease Course and Implications for Gene Therapy;Investigative Ophthalmology & Visual Science;2024-06-17
5. Optical coherence tomography in children with inherited retinal disease;Clinical and Experimental Optometry;2024-01-22
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3