Triplet Repeat Mutations in Human Disease
Author:
Affiliation:
1. nstitute for Molecular Genetics, Baylor College of Medicine, Houston, TX 77030.
Publisher
American Association for the Advancement of Science (AAAS)
Subject
Multidisciplinary
Reference56 articles.
1. ASLANIDIS, C, CLONING OF THE ESSENTIAL MYOTONIC-DYSTROPHY REGION AND MAPPING OF THE PUTATIVE DEFECT, NATURE 355: 548 (1992).
2. BALLABIO, A, CURR OPIN GENE DEV 1: 25 (1991).
3. BELL, M.V., PHYSICAL MAPPING ACROSS THE FRAGILE-X - HYPERMETHYLATION AND CLINICAL EXPRESSION OF THE FRAGILE-X SYNDROME, CELL 64: 861 (1991).
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. A Receptor-Mediated Pathway for Cholesterol Homeostasis
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. Comprehensive Analysis of Fragile X Syndrome: Full Characterization of the FMR1 Locus by Long-Read Sequencing;Clinical Chemistry;2022-09-29
2. C. Thomas Caskey (1938–2022);Genome Research;2022-02-17
3. BigFiRSt: A Software Program Using Big Data Technique for Mining Simple Sequence Repeats From Large-Scale Sequencing Data;Frontiers in Big Data;2022-01-18
4. Advancing genomic technologies and clinical awareness accelerates discovery of disease-associated tandem repeat sequences;Genome Research;2021-12-29
5. FMRP binding to a ranked subset of long genes is revealed by coupled CLIP and TRAP in specific neuronal cell types;2019-09-09
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