Genetic modifiers of age-at-onset in polyglutamine diseases
Author:
Publisher
Elsevier BV
Subject
Neurology,Molecular Biology,Aging,Biochemistry,Biotechnology
Reference130 articles.
1. Cognitive decline in Parkinson disease;Aarsland;Nat. Rev. Neurol.,2017
2. Proteins containing expanded polyglutamine tracts and neurodegenerative disease;Adegbuyiro;Biochemistry,2017
3. Association between BDNF Val66Met polymorphism and age at onset in Huntington disease;Alberch;Neurology,2005
4. Normal ATXN2 alleles influences on the age at onset in spinocerebellar ataxia type 2;Almaguer-Mederos;Mov. Disord.,2017
5. Replication of twelve association studies for Huntington’s disease residual age of onset in large Venezuelan kindreds;Andresen;J. Med. Genet.,2007
Cited by 22 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. The parkin V380L variant is a genetic modifier of Machado–Joseph disease with impact on mitophagy;Acta Neuropathologica;2024-08-01
2. Progress of Repetitive Transcranial Magnetic Stimulation in the Treatment of Spinocerebellar Ataxia;Advances in Clinical Medicine;2024
3. CAG Repeat Expansion in THAP11 Is Associated with a Novel Spinocerebellar Ataxia;Movement Disorders;2023-05-06
4. Synaptic Loss in Spinocerebellar Ataxia Type 3 Revealed by SV2A Positron Emission Tomography;Movement Disorders;2023-04-06
5. Calpain-mediated proteolysis as driver and modulator of polyglutamine toxicity;Frontiers in Molecular Neuroscience;2022-10-19
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