Setdb1 histone methyltransferase regulates mood-related behaviors and expression of the NMDA receptor subunit NR2B. - Wikidata - wikimedia - TriplyDB

Setdb1 histone methyltransferase regulates mood-related behaviors and expression of the NMDA receptor subunit NR2B.

Setdb1 histone methyltransferase regulates mood-related behaviors and expression of the NMDA receptor subunit NR2B.

http://www.wikidata.org/entity/Q30495175

about

Epigenetic mechanisms in experience-driven memory formation and behavior "Seq-ing" insights into the epigenetics of neuronal gene regulation Transcriptional co-repressors and memory storage Epigenetics of the depressed brain: role of histone acetylation and methylation ACF chromatin-remodeling complex mediates stress-induced depressive-like behavior Nuclear organization and 3D chromatin architecture in cognition and neuropsychiatric disorders Maternal immune activation alters behavior in adult offspring, with subtle changes in the cortical transcriptome and epigenome Memory enhancement by targeting Cdk5 regulation of NR2B.Dynorphin up-regulation in the dentate granule cell mossy fiber pathway following chronic inhibition of GluN2B-containing NMDAR is associated with increased CREB (Ser 133) phosphorylation, but is independent of BDNF/TrkB signaling pathways Epigenetic mechanisms of depression Epigenetic mechanisms of depression and antidepressant action Epigenetic memory: the Lamarckian brain Reduced ceramide synthase 2 activity causes progressive myoclonic epilepsy Setdb1-mediated histone H3K9 hypermethylation in neurons worsens the neurological phenotype of Mecp2-deficient mice.Individual differences in the effect of social defeat on anhedonia and histone acetylation in the rat hippocampus Conserved higher-order chromatin regulates NMDA receptor gene expression and cognition.AGO2 and SETDB1 cooperate in promoter-targeted transcriptional silencing of the androgen receptor gene.Balancing histone methylation activities in psychiatric disorders.Cognition and mood-related behaviors in L3mbtl1 null mutant mice.Transgenerational Epigenetic Contributions to Stress Responses: Fact or Fiction?Prenatal antidepressant exposure associated with CYP2E1 DNA methylation change in neonates.Phosphorylation of MeCP2 at Ser421 contributes to chronic antidepressant action.Epigenetics in the human brain The expanding role of MBD genes in autism: identification of a MECP2 duplication and novel alterations in MBD5, MBD6, and SETDB1.NMDA hypofunction as a convergence point for progression and symptoms of schizophrenia BAZ1B in Nucleus Accumbens Regulates Reward-Related Behaviors in Response to Distinct Emotional Stimuli.Conserved chromosome 2q31 conformations are associated with transcriptional regulation of GAD1 GABA synthesis enzyme and altered in prefrontal cortex of subjects with schizophrenia.Individual differences in novelty seeking predict subsequent vulnerability to social defeat through a differential epigenetic regulation of brain-derived neurotrophic factor expression.Longitudinal assessment of neuronal 3D genomes in mouse prefrontal cortex.The brain reward circuitry in mood disorders.The genome in three dimensions: a new frontier in human brain research.Epigenetic determinants of healthy and diseased brain aging and cognition.Chromosomal microarray analysis in clinical evaluation of neurodevelopmental disorders-reporting a novel deletion of SETDB1 and illustration of counseling challenge Functional genomics of the brain: uncovering networks in the CNS using a systems approach.Signaling from the cytoplasm to the nucleus in striatal medium-sized spiny neurons Heterochromatin as an incubator for pathology and treatment non-response: implication for neuropsychiatric illness Histone methylation in the nervous system: functions and dysfunctions.Tipping the lysine methylation balance in disease Matters of life and death: the role of chromatin remodeling proteins in retinal neuron survival Epigenetics components of aging in the central nervous system.

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Setdb1 histone methyltransferase regulates mood-related behaviors and expression of the NMDA receptor subunit NR2B.

http://www.wikidata.org/entity/Q30495175

description

2010 nî lūn-bûn

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2010 թուականի Մայիսին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի մայիսին հրատարակված գիտական հոդված

@hy

2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

Setdb1 histone methyltransfera ...... he NMDA receptor subunit NR2B.

@ast

Setdb1 histone methyltransfera ...... he NMDA receptor subunit NR2B.

@en

type

label

Setdb1 histone methyltransfera ...... he NMDA receptor subunit NR2B.

@ast

Setdb1 histone methyltransfera ...... he NMDA receptor subunit NR2B.

@en

prefLabel

Setdb1 histone methyltransfera ...... he NMDA receptor subunit NR2B.

@ast

Setdb1 histone methyltransfera ...... he NMDA receptor subunit NR2B.

@en

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JNEUROSCI.1314-10.2010

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Journal of Neuroscience

P1476

Setdb1 histone methyltransfera ...... the NMDA receptor subunit NR2B

@en

P2093

Caroline Connor

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

Cong L Lin

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

Frederick A Schroeder

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Gilles Martin

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Juerg Straubhaar

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Rahul Bharadwaj

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Schahram Akbarian

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Yan Jiang

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P2860

Model-based analysis of ChIP-Seq (MACS)

Initial sequencing and comparative analysis of the mouse genome

The HP1alpha-CAF1-SetDB1-containing complex provides H3K9me1 for Suv39-mediated K9me3 in pericentric heterochromatin

The histone methyltransferase SETDB1 and the DNA methyltransferase DNMT3A interact directly and localize to promoters silenced in cancer cells

An ERG (ets-related gene)-associated histone methyltransferase interacts with histone deacetylases 1/2 and transcription co-repressors mSin3A/B

Bipolar I disorder and schizophrenia: a 440-single-nucleotide polymorphism screen of 64 candidate genes among Ashkenazi Jewish case-parent trios

Maternal care effects on the hippocampal transcriptome and anxiety-mediated behaviors in the offspring that are reversible in adulthood

Histone methylation regulates memory formation.

Combinatorial patterns of histone acetylations and methylations in the human genome

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

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7152-7167

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scholarly article

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10.1523/JNEUROSCI.1314-10.2010

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P433

21

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30

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Mira Jakovcevski

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2010-05-01T00:00:00Z

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20505083

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2893142

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