A neuronal enhancer network upstream of MEF2C is compromised in patients with Rett-like characteristics-Reference-Cited by-同舟云学术

A neuronal enhancer network upstream of MEF2C is compromised in patients with Rett-like characteristics

Published:2018-11-15 Issue:5 Volume:28 Page:818-827
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

D’haene Eva¹^ORCID,Bar-Yaacov Reut²³,Bariah Inbar²³,Vantomme Lies¹,Van Loo Sien¹,Cobos Francisco Avila¹⁴⁵,Verboom Karen¹⁴,Eshel Reut²³,Alatawna Rawan²³,Menten Björn¹,Birnbaum Ramon Y²³^ORCID,Vergult Sarah¹

Affiliation:

1. Center for Medical Genetics, Ghent University, 9000 Ghent, Belgium

2. Department of Life Sciences, Faculty of Natural Sciences, The Ben-Gurion University of the Negev, Beersheba, Israel

3. Center of Evolutionary Genomics and Medicine, The Ben-Gurion University of the Negev, Beersheba, Israel

4. Cancer Research Institute Ghent (CRIG), 9000 Ghent, Belgium

5. Bioinformatics Institute Ghent from Nucleotides to Networks (BIG N2N), Ghent, Belgium

Funder

Research Foundation Flanders

National Science Foundation

Brain and Behavior Research Foundation

Marie Curie integration

doctoral and postdoctoral fellowship

Special Research Fund

Ghent University

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/28/5/818/27894943/ddy393.pdf

Reference52 articles.

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2. Mef2 gene expression marks the cardiac and skeletal muscle lineages during mouse embryogenesis;Edmondson;Development,1994

3. Control of mouse cardiac morphogenesis and myogenesis by transcription factor MEF2C;Lin;Science,1997

4. MEF2C, a transcription factor that facilitates learning and memory by negative regulation of synapse numbers and function;Barbosa;Proc. Natl. Acad. Sci. U. S. A.,2008

5. Mutations in MEF2C from the 5q14.3q15 microdeletion syndrome region are a frequent cause of severe mental retardation and diminish MECP2 and CDKL5 expression;Zweier;Hum. Mutat.,2010

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