From neural development to cognition: unexpected roles for chromatin. - Test2 - elhamkhani - TriplyDB

From neural development to cognition: unexpected roles for chromatin.

From neural development to cognition: unexpected roles for chromatin.

http://www.wikidata.org/entity/Q33567755

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Genetics of cognition in epilepsy CHD8 regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP Current Evidence for Developmental, Structural, and Functional Brain Defects following Prenatal Radiation Exposure Mutations and Modeling of the Chromatin Remodeler CHD8 Define an Emerging Autism Etiology Mendelian disorders of the epigenetic machinery: tipping the balance of chromatin states HDAC signaling in neuronal development and axon regeneration mSWI/SNF (BAF) Complexes Are Indispensable for the Neurogenesis and Development of Embryonic Olfactory Epithelium ACF chromatin-remodeling complex mediates stress-induced depressive-like behavior Heterochromatin remodeling by CDK12 contributes to learning in Drosophila.Aberrant Expression of Histone Deacetylases 4 in Cognitive Disorders: Molecular Mechanisms and a Potential Target Advancing the understanding of autism disease mechanisms through genetics Akirin2 is essential for the formation of the cerebral cortex REST and stress resistance in ageing and Alzheimer's disease De novo SOX11 mutations cause Coffin-Siris syndrome The BRAF oncoprotein functions through the transcriptional repressor MAFG to mediate the CpG Island Methylator phenotype Synaptic, transcriptional and chromatin genes disrupted in autism Redox/methylation mediated abnormal DNA methylation as regulators of ambient fine particulate matter-induced neurodevelopment related impairment in human neuronal cells Differential epigenetic effects of chlorpyrifos and arsenic in proliferating and differentiating human neural progenitor cells Essential Roles for ARID1B in Dendritic Arborization and Spine Morphology of Developing Pyramidal Neurons Promoter decommissioning by the NuRD chromatin remodeling complex triggers synaptic connectivity in the mammalian brain Kinetic analysis of npBAF to nBAF switching reveals exchange of SS18 with CREST and integration with neural developmental pathways Association of new deletion/duplication region at chromosome 1p21 with intellectual disability, severe speech deficit and autism spectrum disorder-like behavior: an all-in approach to solving the DPYD enigma Coffin–Siris Syndrome with obesity, macrocephaly, hepatomegaly and hyperinsulinism caused by a mutation in the ARID1B gene Genetics and Genomics of Congenital Heart Disease.Calbindin Knockout Alters Sex-Specific Regulation of Behavior and Gene Expression in Amygdala and Prefrontal Cortex.A multidisciplinary approach unravels early and persistent effects of X-ray exposure at the onset of prenatal neurogenesis An integer programming framework for inferring disease complexes from network data.MCPH1: a window into brain development and evolution.Testicular sex cord-stromal tumor in a boy with 2q37 deletion syndrome.Exome sequencing for bipolar disorder points to roles of de novo loss-of-function and protein-altering mutations.De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability Prioritization of neurodevelopmental disease genes by discovery of new mutations.Arid1b haploinsufficient mice reveal neuropsychiatric phenotypes and reversible causes of growth impairment.Maintaining genome stability in the nervous system.Transcriptional consequences of 16p11.2 deletion and duplication in mouse cortex and multiplex autism families Regulation of histone H3K4 methylation in brain development and disease.The transcriptional regulator ADNP links the BAF (SWI/SNF) complexes with autism.DNA methylation analysis of the autistic brain reveals multiple dysregulated biological pathways.Looping back to leap forward: transcription enters a new era

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From neural development to cognition: unexpected roles for chromatin.

http://www.wikidata.org/entity/Q33567755

description

2013 nî lūn-bûn

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2013 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2013 թվականի ապրիլին հրատարակված գիտական հոդված

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

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From neural development to cognition: unexpected roles for chromatin.

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From neural development to cognition: unexpected roles for chromatin.

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From neural development to cognition: unexpected roles for chromatin.

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From neural development to cognition: unexpected roles for chromatin.

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From neural development to cognition: unexpected roles for chromatin.

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From neural development to cognition: unexpected roles for chromatin.

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From neural development to cognition: unexpected roles for chromatin.

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From neural development to cognition: unexpected roles for chromatin.

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From neural development to cognition: unexpected roles for chromatin.

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Nature Reviews Genetics

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From neural development to cognition: unexpected roles for chromatin.

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Gerald R Crabtree

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Jehnna L Ronan

http://www.w3.org/2001/XMLSchema#string

Wei Wu

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P2860

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

Translating the Histone Code

An integrated encyclopedia of DNA elements in the human genome

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

Genetic disorders associated with macrocephaly

Histone H1 recruitment by CHD8 is essential for suppression of the Wnt-β-catenin signaling pathway

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

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

CHD8 is an ATP-dependent chromatin remodeling factor that regulates beta-catenin target genes

CHD8 suppresses p53-mediated apoptosis through histone H1 recruitment during early embryogenesis

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10.1038/NRG3413

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