Genetic and epigenetic contributors to FSHD-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Genetic and epigenetic contributors to FSHD

Published:2015-08 Issue: Volume:33 Page:56-61
ISSN:0959-437X
Container-title:Current Opinion in Genetics & Development
language:en
Short-container-title:Current Opinion in Genetics & Development

Author:

Daxinger Lucia,Tapscott Stephen J,van der Maarel Silvère M

Funder

National Institutes of Health

Prinses Beatrix Spierfonds

Muscular Dystrophy Association

FSHD Global Research Foundation

FSH Society

Spieren voor Spieren

Friends of FSH Research

LUMC

Publisher

Elsevier BV

Subject

Developmental Biology,Genetics

Reference53 articles.

1. Diagnostic criteria for facioscapulohumeral muscular dystrophy;Padberg;Neuromuscul Disord,1991

2. FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2kb tandemly repeated unit;van Deutekom;Hum Mol Genet,1993

3. Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy;Wijmenga;Nat Genet,1992

4. Facioscapulohumeral muscular dystrophy is uniquely associated with one of the two variants of the 4q subtelomere;Lemmers;Nat Genet,2002

5. Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2;Lemmers;Nat Genet,2012

Cited by 73 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. D4Z4 Hypomethylation in Human Germ Cells;Cells;2024-09-06

2. SMCHD1 maintains heterochromatin and genome compartments in human myoblasts;2024-07-10

3. Muscle strength, quantity and quality and muscle fat quantity and their association with oxidative stress in patients with facioscapulohumeral muscular dystrophy: Effect of antioxidant supplementation;Free Radical Biology and Medicine;2024-07

4. Systemic Pharmacotherapeutic Treatment of the ACTA1-MCM/FLExDUX4 Preclinical Mouse Model of FSHD;International Journal of Molecular Sciences;2024-06-26

5. Engineered FSHD mutations results in D4Z4 heterochromatin disruption and feedforward DUX4 network activation;iScience;2024-04

同舟云学术

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