MECP2 mutations affect ciliogenesis: a novel perspective for Rett syndrome and related disorders-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

MECP2 mutations affect ciliogenesis: a novel perspective for Rett syndrome and related disorders

Published:2020-05-08 Issue:6 Volume:12 Page:
ISSN:1757-4676
Container-title:EMBO Molecular Medicine
language:en
Short-container-title:EMBO Mol Med

Author:

Frasca Angelisa¹^ORCID,Spiombi Eleonora¹,Palmieri Michela²,Albizzati Elena¹,Valente Maria Maddalena³,Bergo Anna³,Leva Barbara³,Kilstrup‐Nielsen Charlotte³,Bianchi Federico⁴,Di Carlo Valerio¹,Di Cunto Ferdinando⁴⁵^ORCID,Landsberger Nicoletta¹²^ORCID

Affiliation:

1. Department of Medical Biotechnology and Translational Medicine University of Milan Milan Italy

2. Neuroscience Division IRCCS San Raffaele Scientific Institute Milan Italy

3. Department of Biotechnology and Life Sciences Centre of Neuroscience University of Insubria Busto Arsizio Italy

4. Neuroscience Institute Cavalieri Ottolenghi Orbassano Italy

5. Department of Neuroscience University of Torino Torino Italy

Publisher

EMBO

Subject

Molecular Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.15252/emmm.201910270

Reference66 articles.

1. Neuroanatomy in mouse models of Rett syndrome is related to the severity of Mecp2 mutation and behavioral phenotypes

2. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

3. Stages of ciliogenesis and regulation of ciliary length

4. Rett syndrome and the urge of novel approaches to study MeCP2 functions and mechanisms of action

5. Defects DuringMecp2Null Embryonic Cortex Development Precede the Onset of Overt Neurological Symptoms

Cited by 25 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. Ciliary biology intersects autism and congenital heart disease;2024-07-31

2. MECP2 directly interacts with RNA polymerase II to modulate transcription in human neurons;Neuron;2024-06

3. GDF15 controls primary cilia morphology and function thereby affecting progenitor proliferation;Life Science Alliance;2024-05-07

4. Mecp2 knock-out astrocytes affect synaptogenesis by interleukin 6 dependent mechanisms;iScience;2024-03

5. Rett Syndrome and the Role of MECP2: Signaling to Clinical Trials;Brain Sciences;2024-01-24

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