Rett syndrome: Genetic clues based on mitochondrial changes in muscle
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference15 articles.
1. The genetics of rett syndrome: The consequences of a disorder where every case is a new mutation
2. Abnormal mitochondria in the Rett syndrome
3. A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: Report of 35 cases
4. Rett syndrome: Epidemiology and nosology — progress in knowledge 1986 — A conference communication
5. Rett syndrome-search for genetic markers
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. Possibility that the Onset of Autism Spectrum Disorder is Induced by Failure of the Glutamine-Glutamate Cycle;Current Molecular Pharmacology;2020-12-31
2. Transcriptome level analysis in Rett syndrome using human samples from different tissues;Orphanet Journal of Rare Diseases;2018-07-11
3. 4-hydroxynonenal protein adducts: Key mediator in Rett syndrome oxinflammation;Free Radical Biology and Medicine;2017-10
4. Dysregulation of Glutamine Transporter SNAT1 in Rett Syndrome Microglia: A Mechanism for Mitochondrial Dysfunction and Neurotoxicity;Journal of Neuroscience;2015-02-11
5. Anaplerotic Triheptanoin Diet Enhances Mitochondrial Substrate Use to Remodel the Metabolome and Improve Lifespan, Motor Function, and Sociability in MeCP2-Null Mice;PLoS ONE;2014-10-09
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