Dysregulation of BRD4 Function Underlies the Functional Abnormalities of MeCP2 Mutant Neurons-Reference-Cited by-同舟云学术

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Dysregulation of BRD4 Function Underlies the Functional Abnormalities of MeCP2 Mutant Neurons

Published:2020-07 Issue:1 Volume:79 Page:84-98.e9
ISSN:1097-2765
Container-title:Molecular Cell
language:en
Short-container-title:Molecular Cell

Author:

Xiang Yangfei,Tanaka Yoshiaki,Patterson Benjamin,Hwang Sung-Min,Hysolli Eriona,Cakir Bilal,Kim Kun-Yong,Wang Wanshan,Kang Young-Jin,Clement Ethan M.,Zhong Mei,Lee Sang-Hun,Cho Yee Sook,Patra Prabir,Sullivan Gareth J.,Weissman Sherman M.,Park In-Hyun^ORCID

Funder

NIH

CSCRF

Kavli Foundation

Simons Foundation

Nomis Foundation

KRIBB/KRCF Research Initiative Program

College of Medicine

University of Arkansas for Medical Sciences

Core Facilities of the Center for Translational Neuroscience

IDeA Program

NIGMS

Norwegian Research Council

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology

Reference62 articles.

1. MeCP2-mediated transcription repression in the basolateral amygdala may underlie heightened anxiety in a mouse model of Rett syndrome;Adachi;J. Neurosci.,2009

2. HiCPlotter integrates genomic data with interaction matrices;Akdemir;Genome Biol.,2015

3. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat. Genet.,1999

4. Petilla terminology: nomenclature of features of GABAergic interneurons of the cerebral cortex;Ascoli;Nat. Rev. Neurosci.,2008

5. Identification of astrocyte-expressed factors that modulate neural stem/progenitor cell differentiation;Barkho;Stem Cells Dev.,2006

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