The NuRD complex and macrocephaly associated neurodevelopmental disorders
Published 2019 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
The NuRD complex and macrocephaly associated neurodevelopmental disorders
Authors
Keywords
-
Journal
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS
Volume 181, Issue 4, Pages 548-556
Publisher
Wiley
Online
2019-11-18
DOI
10.1002/ajmg.c.31752
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- The stoichiometry and interactome of the Nucleosome Remodeling and Deacetylase (NuRD) complex are conserved across multiple cell lines
- (2019) Mehdi Sharifi Tabar et al. FEBS Journal
- The clinical presentation caused by truncating CHD8 variants
- (2019) Sofia Douzgou et al. CLINICAL GENETICS
- Disruption of the MBD2-NuRD complex but not MBD3-NuRD induces high level HbF expression in human erythroid cells
- (2019) Xiaofei Yu et al. HAEMATOLOGICA
- Quality and quantity control of gene expression by nonsense-mediated mRNA decay
- (2019) Tatsuaki Kurosaki et al. NATURE REVIEWS MOLECULAR CELL BIOLOGY
- Rational targeting of a NuRD subcomplex guided by comprehensive in situ mutagenesis
- (2019) Falak Sher et al. NATURE GENETICS
- The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype–phenotype correlations, and molecular basis
- (2019) Karin Weiss et al. GENETICS IN MEDICINE
- The CHD8 overgrowth syndrome: A detailed evaluation of an emerging overgrowth phenotype in 27 patients
- (2019) Philip J. Ostrowski et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS
- A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development
- (2018) Else Eising et al. MOLECULAR PSYCHIATRY
- Tumour-associated missense mutations in the dMi-2 ATPase alters nucleosome remodelling properties in a mutation-specific manner
- (2018) Kristina Kovač et al. Nature Communications
- Chromatin Remodeling Proteins in Epilepsy: Lessons From CHD2-Associated Epilepsy
- (2018) Kay-Marie J. Lamar et al. Frontiers in Molecular Neuroscience
- Neutralizing Gatad2a-Chd4-Mbd3/NuRD Complex Facilitates Deterministic Induction of Naive Pluripotency
- (2018) Nofar Mor et al. Cell Stem Cell
- Intellectual disability due to monoallelic variant in GATAD2B and mosaicism in unaffected parent
- (2018) Rachel Rabin et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- A novel mutation in the GATAD2B gene associated with severe intellectual disability
- (2018) Kimiko Ueda et al. BRAIN & DEVELOPMENT
- CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language
- (2018) Lot Snijders Blok et al. Nature Communications
- Refinement of the subunit interaction network within the nucleosome remodelling and deacetylase (NuRD) complex
- (2017) Mario Torrado et al. FEBS Journal
- Novel GATAD2B loss-of-function mutations cause intellectual disability in two unrelated cases
- (2017) Xiaomei Luo et al. JOURNAL OF HUMAN GENETICS
- CHD3 and CHD4 form distinct NuRD complexes with different yet overlapping functionality
- (2017) Helen Hoffmeister et al. NUCLEIC ACIDS RESEARCH
- Covalent Modifications of Histone H3K9 Promote Binding of CHD3
- (2017) Adam H. Tencer et al. Cell Reports
- Mice lacking the chromodomain helicase DNA-binding 5 chromatin remodeler display autism-like characteristics
- (2017) M T Pisansky et al. Translational Psychiatry
- De Novo Mutations in CHD4 , an ATP-Dependent Chromatin Remodeler Gene, Cause an Intellectual Disability Syndrome with Distinctive Dysmorphisms
- (2016) Karin Weiss et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Dysregulation of select ATP-dependent chromatin remodeling factors in high trait anxiety
- (2016) Alexandra Wille et al. BEHAVIOURAL BRAIN RESEARCH
- The Nucleosome Remodeling and Deacetylase Complex NuRD Is Built from Preformed Catalytically Active Sub-modules
- (2016) W. Zhang et al. JOURNAL OF MOLECULAR BIOLOGY
- Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing
- (2016) Alejandro Sifrim et al. NATURE GENETICS
- A Functional Switch of NuRD Chromatin Remodeling Complex Subunits Regulates Mouse Cortical Development
- (2016) Justyna Nitarska et al. Cell Reports
- The language-related transcription factor FOXP2 is post-translationally modified with small ubiquitin-like modifiers
- (2016) Sara B. Estruch et al. Scientific Reports
- Structure and function insights into the NuRD chromatin remodeling complex
- (2015) Morgan P. Torchy et al. CELLULAR AND MOLECULAR LIFE SCIENCES
- The N-terminal Region of Chromodomain Helicase DNA-binding Protein 4 (CHD4) Is Essential for Activity and Contains a High Mobility Group (HMG) Box-like-domain That Can Bind Poly(ADP-ribose)
- (2015) Ana P. G. Silva et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- The nucleosome remodeling and deacetylase complex in development and disease
- (2015) Jeannine Basta et al. Translational Research
- Role of CHD5 in Human Cancers: 10 Years Later
- (2014) V. Kolla et al. CANCER RESEARCH
- MBD3/NuRD Facilitates Induction of Pluripotency in a Context-Dependent Manner
- (2014) Rodrigo L. dos Santos et al. Cell Stem Cell
- Towards elucidating the stability, dynamics and architecture of the nucleosome remodeling and deacetylase complex by using quantitative interaction proteomics
- (2014) Susan L. Kloet et al. FEBS Journal
- Promoter Decommissioning by the NuRD Chromatin Remodeling Complex Triggers Synaptic Connectivity in the Mammalian Brain
- (2014) Tomoko Yamada et al. NEURON
- Differential Expression and Sex Chromosome Association of CHD3/4 and CHD5 during Spermatogenesis
- (2014) Judith W. Bergs et al. PLoS One
- De Novo Mutations in Moderate or Severe Intellectual Disability
- (2014) Fadi F. Hamdan et al. PLoS Genetics
- FOXP1mutations cause intellectual disability and a recognizable phenotype
- (2013) Anna K. Le Fevre et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- GATAD2Bloss-of-function mutations cause a recognisable syndrome with intellectual disability and are associated with learning deficits and synaptic undergrowth inDrosophila
- (2013) Marjolein H Willemsen et al. JOURNAL OF MEDICAL GENETICS
- Analysis of the Human Tissue-specific Expression by Genome-wide Integration of Transcriptomics and Antibody-based Proteomics
- (2013) Linn Fagerberg et al. MOLECULAR & CELLULAR PROTEOMICS
- Differential roles for MBD2 and MBD3 at methylated CpG islands, active promoters and binding to exon sequences
- (2013) Katharina Günther et al. NUCLEIC ACIDS RESEARCH
- Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations
- (2012) Brian J. O’Roak et al. NATURE
- Bivalent recognition of nucleosomes by the tandem PHD fingers of the CHD4 ATPase is required for CHD4-mediated repression
- (2012) C. A. Musselman et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- p66 -MBD2 coiled-coil interaction and recruitment of Mi-2 are critical for globin gene silencing by the MBD2-NuRD complex
- (2011) M. N. Gnanapragasam et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- De Novo Mutations in FOXP1 in Cases with Intellectual Disability, Autism, and Language Impairment
- (2010) Fadi F. Hamdan et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Foxp1/2/4-NuRD Interactions Regulate Gene Expression and Epithelial Injury Response in the Lung via Regulation of Interleukin-6
- (2010) Ann L. Chokas et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Histone deacetylases 1 and 2 control the progression of neural precursors to neurons during brain development
- (2009) R. L. Montgomery et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Inactivation of NuRD Component Mta2 Causes Abnormal T Cell Activation and Lupus-like Autoimmune Disease in Mice
- (2008) Xiangdong Lu et al. JOURNAL OF BIOLOGICAL CHEMISTRY
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started