Lack of RAB39B mutations in early-onset and familial Parkinson's disease in a Taiwanese cohort
Author:
Funder
National Ministry of Science and Technology
Publisher
Elsevier BV
Subject
Geriatrics and Gerontology,Developmental Biology,Neurology (clinical),Aging,General Neuroscience
Reference19 articles.
1. Mutational analysis of SYNJ1 gene (PARK20) in Parkinson's disease in a Taiwanese population;Chen;Neurobiol. Aging,2015
2. Isolation and characterization of a human novel RAB (RAB39B) gene;Cheng;Cytogenet. Genome Res.,2002
3. Projected number of people with Parkinson disease in the most populous nations, 2005 through 2030;Dorsey;Neurology,2007
4. Lack of CHCHD2 mutations in Parkinson's disease in a Taiwanese population;Fan;Neurobiol. Aging,2016
5. Genetics in Parkinson disease: Mendelian versus non-Mendelian inheritance;Hernandez;J. Neurochem.,2016
Cited by 8 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. Loss of RAB39B does not alter MPTP-induced Parkinson’s disease-like phenotypes in mice;Frontiers in Aging Neuroscience;2023-01-25
2. Dysfunction of RAB39B‐ Mediated Vesicular Trafficking in Lewy Body Diseases;Movement Disorders;2021-05-03
3. RAB39B's role in membrane traffic, autophagy, and associated neuropathology;Journal of Cellular Physiology;2020-08-06
4. Genetic Analysis of RAB39B in an Early-Onset Parkinson's Disease Cohort;Frontiers in Neurology;2020-06-26
5. Genetic analysis of PODXL gene in patients with familial and young-onset Parkinson's disease in a Taiwanese population;Neurobiology of Aging;2019-12
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