Hippocampal dysfunction in the Euchromatin histone methyltransferase 1 heterozygous knockout mouse model for Kleefstra syndrome. - Wikidata - wikimedia - TriplyDB

Hippocampal dysfunction in the Euchromatin histone methyltransferase 1 heterozygous knockout mouse model for Kleefstra syndrome.

Hippocampal dysfunction in the Euchromatin histone methyltransferase 1 heterozygous knockout mouse model for Kleefstra syndrome.

http://www.wikidata.org/entity/Q42516528

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Haploinsufficiency of EHMT1 improves pattern separation and increases hippocampal cell proliferation Exon resequencing of H3K9 methyltransferase complex genes, EHMT1, EHTM2 and WIZ, in Japanese autism subjects.Input-specific regulation of hippocampal circuit maturation by non-muscle myosin IIB.H3K9me3 Inhibition Improves Memory, Promotes Spine Formation, and Increases BDNF Levels in the Aged Hippocampus.Chromatin modifications associated with DNA double-strand breaks repair as potential targets for neurological diseases.A Novel Kleefstra Syndrome-associated Variant That Affects the Conserved TPLX Motif within the Ankyrin Repeat of EHMT1 Leads to Abnormal Protein Folding.A novel de novo frameshift deletion in EHMT1 in a patient with Kleefstra Syndrome results in decreased H3K9 dimethylation Modelling the genetic contribution to mental illness: a timely end for the psychiatric rodent?Regulation of cell differentiation and function by the euchromatin histone methyltranserfases G9a and GLP.Altered neurite morphology and cholinergic function of induced pluripotent stem cell-derived neurons from a patient with Kleefstra syndrome and autism Reconsolidation and extinction: Using epigenetic signatures to challenge conventional wisdom.Epigenetic Mistakes in Neurodevelopmental Disorders.Euchromatin histone methyltransferase 1 regulates cortical neuronal network development.Histone Lysine Methylation and Neurodevelopmental Disorders.Reversible white matter lesions associated with mutant EHMT1 and Kleefstra syndrome.Genome-wide DNA methylation changes associated with olfactory learning and memory in Apis mellifera.Functional convergence of histone methyltransferases EHMT1 and KMT2C involved in intellectual disability and autism spectrum disorder.Epigenetic Etiology of Intellectual Disability.Increased H3K9 methylation and impaired expression of Protocadherins are associated with the cognitive dysfunctions of the Kleefstra syndrome.Synaptic Disorders Sex-specific Behavioral Features of Rodent Models of Autism Spectrum Disorder

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Hippocampal dysfunction in the Euchromatin histone methyltransferase 1 heterozygous knockout mouse model for Kleefstra syndrome.

http://www.wikidata.org/entity/Q42516528

description

2012 nî lūn-bûn

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2012年の論文

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年學術文章

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Hippocampal dysfunction in the ...... model for Kleefstra syndrome.

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Human Molecular Genetics

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Hippocampal dysfunction in the ...... model for Kleefstra syndrome.

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Andy J Beynon

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Catharina E E M Van der Zee

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Ger Ramakers

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Hans van Bokhoven

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Jorine M Eeftens

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Makoto Tachibana

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Maksym V Kopanitsa

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Marco Benevento

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Monique C M Balemans

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Nael Nadif Kasri

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Anxiety in children and adolescents with autism spectrum disorders

Zinc finger protein Wiz links G9a/GLP histone methyltransferases to the co-repressor molecule CtBP

Epigenetics in the mature mammalian brain: effects on behavior and synaptic transmission

Histone methylation regulates memory formation.

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

Dendritic anomalies in disorders associated with mental retardation

Short-term synaptic plasticity

G9a/GLP histone lysine dimethyltransferase complex activity in the hippocampus and the entorhinal cortex is required for gene activation and silencing during memory consolidation

The Rho-linked mental retardation protein oligophrenin-1 controls synapse maturation and plasticity by stabilizing AMPA receptors

Histone methyltransferases G9a and GLP form heteromeric complexes and are both crucial for methylation of euchromatin at H3-K9

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852-866

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10.1093/HMG/DDS490

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5

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22

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2012-11-21T00:00:00Z

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