Subtle neurological and metabolic abnormalities in an Opa1 mouse model of autosomal dominant optic atrophy
Author:
Publisher
Elsevier BV
Subject
Developmental Neuroscience,Neurology
Reference44 articles.
1. A splice site mutation in the murine Opa1 gene features pathology of autosomal dominant optic atrophy;Alavi;Brain,2007
2. OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28;Alexander;Nat. Genet.,2000
3. OPA1 mutations induce mitochondrial DNA instability and optic atrophy ‘plus’ phenotypes;Amati-Bonneau;Brain,2008
4. A third locus for dominant optic atrophy on chromosome 22q;Barbet;J. Med. Genet.,2005
5. OPA1, associated with autosomal dominant optic atrophy, is widely expressed in the human brain;Bette;Acta Neuropathol. (Berl.),2005
Cited by 45 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. Establishing induced pluripotent stem cell lines from two dominant optic atrophy patients with distinct OPA1 mutations and clinical pathologies;Frontiers in Genetics;2023-09-04
2. OPA1 deficiency impairs oxidative metabolism in cycling cells, underlining a translational approach for degenerative diseases;Disease Models & Mechanisms;2023-09-01
3. Latest advances in the regulatory genes of adipocyte thermogenesis;Frontiers in Endocrinology;2023-08-23
4. In Vivo Efficacy and Safety Evaluations of Therapeutic Splicing Correction Using U1 snRNA in the Mouse Retina;Cells;2023-03-21
5. The status and trends of mitochondrial dynamics research: A global bibliometric and visualized analysis;Journal of Bioenergetics and Biomembranes;2023-02
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