Cis-silencing of PIP5K1B evidenced in Friedreich's ataxia patient cells results in cytoskeleton anomalies-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Cis-silencing of PIP5K1B evidenced in Friedreich's ataxia patient cells results in cytoskeleton anomalies

Published:2013-04-02 Issue:14 Volume:22 Page:2894-2904
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Bayot Aurélien,Reichman Sacha,Lebon Sophie,Csaba Zsolt,Aubry Laetitia,Sterkers Ghislaine,Husson Isabelle,Rak Malgorzata,Rustin Pierre

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/22/14/2894/17259719/ddt144.pdf

Reference65 articles.

1. Friedreich's ataxia: a clinical and genetic study of 90 families with an analysis of early diagnostic criteria and intrafamilial clustering of clinical features;Harding;Brain,1981

2. Friedreich ataxia: the clinical picture;Pandolfo;J. Neurol.,2009

3. Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion;Campuzano;Science,1996

4. Is Friedreich ataxia an epigenetic disorder?;Kumari;Clin. Epigenetics,2012

5. DNA triplet repeats mediate heterochromatin-protein-1-sensitive variegated gene silencing;Saveliev;Nature,2003

Cited by 28 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. The ataxia-telangiectasia disease protein ATM controls vesicular protein secretion via CHGA and microtubule dynamics via CRMP5;2024-06-26

2. One-to-one Benefit provided by Antioxidants to cultured skin Fibroblasts from Friedreich Ataxia patients;2024-04-28

3. Loss of filamentous actin, tight junction protein expression, and paracellular barrier integrity in frataxin-deficient human brain microvascular endothelial cells—implications for blood-brain barrier physiology in Friedreich’s ataxia;Frontiers in Molecular Biosciences;2024-01-11

4. Lipid Metabolism: Key Determinant in Neurodegenerative Diseases;Altered Metabolism: A Major Contributor of Comorbidities in Neurodegenerative Diseases;2024

5. Genomic Analysis Reveals Candidate Genes Underlying Sex-Linked Eyelid Coloboma, Feather Color Traits, and Climatic Adaptation in Huoyan Geese;Animals;2023-11-22

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