From neural development to cognition: unexpected roles for chromatin (Q33567755)

28 July 2017

title

From neural development to cognition: unexpected roles for chromatin (English)

1 reference

28 July 2017

Jehnna L Ronan

1

1 reference

28 July 2017

Wei Wu

series ordinal

2

1 reference

28 July 2017

Gerald R Crabtree

series ordinal

3

1 reference

28 July 2017

language of work or name

1 reference

9 April 2013

1 reference

28 July 2017

published in

Nature Reviews Genetics

1 reference

28 July 2017

volume

14

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28 July 2017

issue

5

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28 July 2017

page(s)

347-359

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The spectrum of SWI/SNF mutations, ubiquitous in human cancers

28 July 2017

cites work

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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Failure of neuronal homeostasis results in common neuropsychiatric phenotypes

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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A recurrent mutation in MED12 leading to R961W causes Opitz-Kaveggia syndrome

21 June 2018

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The ups and downs of Wnt signaling in prevalent neurological disorders

21 June 2018

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BRG1 chromatin remodeling activity is required for efficient chromatin binding by repressor element 1-silencing transcription factor (REST) and facilitates REST-mediated repression

21 June 2018

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Loss-of-function mutations in euchromatin histone methyl transferase 1 (EHMT1) cause the 9q34 subtelomeric deletion syndrome

21 June 2018

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21 June 2018

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Polycomb complexes repress developmental regulators in murine embryonic stem cells

21 June 2018

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Genome-wide analyses identify transcription factors required for proper morphogenesis of Drosophila sensory neuron dendrites.

21 June 2018

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brawn for brains: the role of MEF2 proteins in the developing nervous system

21 June 2018

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Mutations in PHF8 are associated with X linked mental retardation and cleft lip/cleft palate

21 June 2018

1 reference

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Wnt signaling: multiple functions in neural development

21 June 2018

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Genetic heterogeneity in Rubinstein-Taybi syndrome: mutations in both the CBP and EP300 genes cause disease

21 June 2018

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Epigenetic mechanisms in memory formation.

21 June 2018

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Histone demethylation mediated by the nuclear amine oxidase homolog LSD1

21 June 2018

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Mutations in the JARID1C gene, which is involved in transcriptional regulation and chromatin remodeling, cause X-linked mental retardation

21 June 2018

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Mutations in a new member of the chromodomain gene family cause CHARGE syndrome

21 June 2018

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CBP histone acetyltransferase activity is a critical component of memory consolidation

21 June 2018

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Epigenetics in human disease and prospects for epigenetic therapy

21 June 2018

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21 June 2018

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Mental deficiency, alterations in performance, and CNS abnormalities in overgrowth syndromes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4010428

Association of class II histone deacetylases with heterochromatin protein 1: potential role for histone methylation in control of muscle differentiation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4010428

Regulation of cerebral cortical size by control of cell cycle exit in neural precursors

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4010428

Srg3, a mouse homolog of yeast SWI3, is essential for early embryogenesis and involved in brain development

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4010428

The chromatin remodelling factor Brg-1 interacts with beta-catenin to promote target gene activation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4010428

Translating the Histone Code

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4010428

Histone deacetylase 4 possesses intrinsic nuclear import and export signals

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4010428

The polycomb-group gene Ezh2 is required for early mouse development

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4010428

The murine SNF5/INI1 chromatin remodeling factor is essential for embryonic development and tumor suppression

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4010428

Inactivation of the beta-catenin gene by Wnt1-Cre-mediated deletion results in dramatic brain malformation and failure of craniofacial development

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4010428

A Brg1 null mutation in the mouse reveals functional differences among mammalian SWI/SNF complexes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4010428

A novel beta-catenin-binding protein inhibits beta-catenin-dependent Tcf activation and axis formation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4010428

Beta-catenin signaling activity dissected in the early Xenopus embryo: a novel antisense approach

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4010428

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4010428

A mammalian histone deacetylase related to the yeast transcriptional regulator Rpd3p

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4010428

Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4010428

brahma: a regulator of Drosophila homeotic genes structurally related to the yeast transcriptional activator SNF2/SWI2

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4010428

Multiple functions of PBRM-1/Polybromo- and LET-526/Osa-containing chromatin remodeling complexes in C. elegans development

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4010428

Deep sequencing reveals 50 novel genes for recessive cognitive disorders

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4010428

MED23 mutation links intellectual disability to dysregulation of immediate early gene expression

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4010428

Histone modification: cause or cog?

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4010428

Polycomb limits the neurogenic competence of neural precursor cells to promote astrogenic fate transition

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4010428

Polycomb repressive complex 2 is dispensable for maintenance of embryonic stem cell pluripotency

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4010428

The original Lujan syndrome family has a novel missense mutation (p.N1007S) in the MED12 gene

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4010428

Intracellular trafficking of histone deacetylase 4 regulates neuronal cell death.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4010428

Functional characterization of an amino-terminal region of HDAC4 that possesses MEF2 binding and transcriptional repressive activity

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4010428

Integration of long-term-memory-related synaptic plasticity involves bidirectional regulation of gene expression and chromatin structure

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4010428

Components of the SWI/SNF complex are required for asymmetric cell division in C. elegans.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4010428

Brain development, IX: human brain growth

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4010428

Chromatin compaction by a polycomb group protein complex

31 October 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNRG3413

Dose dependent expression of HDAC4 causes variable expressivity in a novel inherited case of brachydactyly mental retardation syndrome

31 March 2020

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNRG3413

31 March 2020

Identifiers

DOI

10.1038/NRG3413

1 reference

Dimensions Publication ID

28 July 2017

0 references

1 reference

28 July 2017

1 reference