Trinucleotide repeat expansion in neurological disease
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Reference109 articles.
1. Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy
2. Mapping of DNA Instability at the Fragile X to a Trinucleotide Repeat Sequence P(CCG) n
3. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
4. Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member
5. An Unstable Triplet Repeat in a Gene Related to Myotonic Muscular Dystrophy
Cited by 174 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. NMR structures and magnetic force spectroscopy studies of small molecules binding to models of an RNA CAG repeat expansion;2024-08-23
2. PQBP3 prevents senescence by suppressing PSME3-mediated proteasomal Lamin B1 degradation;The EMBO Journal;2024-08-05
3. Gene Therapy for Neurodegeneration in Glaucoma;Essentials in Ophthalmology;2024
4. Revisiting recent unusual drug-DNA complex structures: Implications for cancer and neurological disease diagnostics and therapeutics;Bioorganic & Medicinal Chemistry;2022-12
5. Brain Cell Type-Specific Nuclear Proteomics Is Imperative to Resolve Neurodegenerative Disease Mechanisms;Frontiers in Neuroscience;2022-06-16
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