An MLPA-based approach for high-resolution genotyping of disease-related multi-allelic CNVs
Author:
Funder
National Science Centre
Publisher
Elsevier BV
Subject
Genetics,General Medicine
Reference51 articles.
1. High proportion of large genomic STK11 deletions in Peutz–Jeghers syndrome;Aretz;Hum. Mutat.,2005
2. Accurate, high-throughput typing of copy number variation using paralogue ratios from dispersed repeats;Armour;Nucleic Acids Res.,2007
3. Association of higher DEFB4 genomic copy number with Crohn's disease;Bentley;Am. J. Gastroenterol.,2010
4. CCL3L1 and HIV/AIDS susceptibility;Bhattacharya;Nat. Med.,2009
5. Simultaneous MLPA-based multiplex point mutation and deletion analysis of the dystrophin gene;Bunyan;Mol. Biotechnol.,2007
Cited by 13 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. Development and validation of a TTR-specific copy number screening tool, and application to potentially relevant patient cohorts;Molecular and Cellular Probes;2018-10
2. qEva-CRISPR: a method for quantitative evaluation of CRISPR/Cas-mediated genome editing in target and off-target sites;Nucleic Acids Research;2018-06-07
3. Quantitative Methods to Monitor RNA Biomarkers in Myotonic Dystrophy;Scientific Reports;2018-04-12
4. The 30 kb deletion in the APOBEC3 cluster decreases APOBEC3A and APOBEC3B expression and creates a transcriptionally active hybrid gene but does not associate with breast cancer in the European population;Oncotarget;2017-07-19
5. MLPA-Based Analysis of Copy Number Variation in Plant Populations;Frontiers in Plant Science;2017-02-21
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