The loss of methyl-CpG binding protein 1 leads to autism-like behavioral deficits. - Wikidata - awgldk - TriplyDB

The loss of methyl-CpG binding protein 1 leads to autism-like behavioral deficits.

The loss of methyl-CpG binding protein 1 leads to autism-like behavioral deficits.

http://www.wikidata.org/entity/Q30488542

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Epigenetic choreographers of neurogenesis in the adult mammalian brain Epigenetic regulation of miR-184 by MBD1 governs neural stem cell proliferation and differentiation Epigenetics in the mature mammalian brain: effects on behavior and synaptic transmission Emerging Molecular and Biological Functions of MBD2, a Reader of DNA Methylation Transcriptional co-repressors and memory storage Neuroprotective role of a brain-enriched tyrosine phosphatase, STEP, in focal cerebral ischemia Epigenetic regulation of the stem cell mitogen Fgf-2 by Mbd1 in adult neural stem/progenitor cells Genetic models of sensorimotor gating: relevance to neuropsychiatric disorders.Epigenetics, hippocampal neurogenesis, and neuropsychiatric disorders: unraveling the genome to understand the mind.High Resolution Imaging of DNA Methylation Dynamics using a Zebrafish Reporter A functional polymorphism in the reduced folate carrier gene and DNA hypomethylation in mothers of children with autism Novel variants identified in methyl-CpG-binding domain genes in autistic individuals.New approaches to manipulating the epigenome.An epigenetic feedback regulatory loop involving microRNA-195 and MBD1 governs neural stem cell differentiation Epigenetic programming of hypoxic-ischemic encephalopathy in response to fetal hypoxia.Ablation of Fmrp in adult neural stem cells disrupts hippocampus-dependent learning Epigenetic approaches to psychiatric disorders.Assessment of 2q23.1 microdeletion syndrome implicates MBD5 as a single causal locus of intellectual disability, epilepsy, and autism spectrum disorder.An epigenetic regulator: methyl-CpG-binding domain protein 1 (MBD1).Epigenetic (de)regulation of adult hippocampal neurogenesis: implications for depression Social Behavioral Deficits Coincide with the Onset of Seizure Susceptibility in Mice Lacking Serotonin Receptor 2c.Basic concepts of epigenetics: impact of environmental signals on gene expression.Metabolic imbalance associated with methylation dysregulation and oxidative damage in children with autism.Perinatal exposure to 50 ppb sodium arsenate induces hypothalamic-pituitary-adrenal axis dysregulation in male C57BL/6 mice The expanding role of MBD genes in autism: identification of a MECP2 duplication and novel alterations in MBD5, MBD6, and SETDB1.Tagging methyl-CpG-binding domain proteins reveals different spatiotemporal expression and supports distinct functions.Gene-environment interactions affect long-term depression (LTD) through changes in dopamine receptor affinity in Snap25 deficient mice.Suppression and epigenetic regulation of MiR-9 contributes to ethanol teratology: evidence from zebrafish and murine fetal neural stem cell models Epigenetics, autism spectrum, and neurodevelopmental disorders.Neonatal maternal separation alters the capacity of adult neural precursor cells to differentiate into neurons via methylation of retinoic acid receptor gene promoter Methyl-CpG-Binding Protein MBD1 Regulates Neuronal Lineage Commitment through Maintaining Adult Neural Stem Cell Identity MicroRNA regulation of neural stem cells and neurogenesis.Epigenetic impacts on neurodevelopment: pathophysiological mechanisms and genetic modes of action.Genetic variation in the epigenetic machinery and mental health.Crosstalk among Epigenetic Pathways Regulates Neurogenesis The endogenous regenerative capacity of the damaged newborn brain: boosting neurogenesis with mesenchymal stem cell treatment.Impaired one carbon metabolism and DNA methylation in alcohol toxicity.DNA methylation: dynamic and stable regulation of memory.Methyl-CpG-Binding Protein (MBD) Family: Epigenomic Read-Outs Functions and Roles in Tumorigenesis and Psychiatric Diseases.Genetics and Epigenetics in Adult Neurogenesis.

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The loss of methyl-CpG binding protein 1 leads to autism-like behavioral deficits.

http://www.wikidata.org/entity/Q30488542

description

2008 nî lūn-bûn

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2008 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2008 թվականի ապրիլին հրատարակված գիտական հոդված

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2008年の論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年论文

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name

The loss of methyl-CpG binding protein 1 leads to autism-like behavioral deficits.

@ast

The loss of methyl-CpG binding protein 1 leads to autism-like behavioral deficits.

@en

type

label

The loss of methyl-CpG binding protein 1 leads to autism-like behavioral deficits.

@ast

The loss of methyl-CpG binding protein 1 leads to autism-like behavioral deficits.

@en

prefLabel

The loss of methyl-CpG binding protein 1 leads to autism-like behavioral deficits.

@ast

The loss of methyl-CpG binding protein 1 leads to autism-like behavioral deficits.

@en

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Human Molecular Genetics

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The loss of methyl-CpG binding protein 1 leads to autism-like behavioral deficits

@en

P2093

Changhui Pak

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

Dahua Chen

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

Keith E Szulwach

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

Peng Jin

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

Xiaomin Liang

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

Xinyu Zhao

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

Xuekun Li

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

Yuping Luo

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

P2860

DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development

Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene

DNA methylation patterns and epigenetic memory

Mutations in ATRX, encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation

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

MCAF mediates MBD1-dependent transcriptional repression

Methyl-CpG binding domain 1 (MBD1) interacts with the Suv39h1-HP1 heterochromatic complex for DNA methylation-based transcriptional repression

Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors

A genomewide screen of 345 families for autism-susceptibility loci.

Mbd1 is recruited to both methylated and nonmethylated CpGs via distinct DNA binding domains

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2047-2057

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scholarly article

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10.1093/HMG/DDN102

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13

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17

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2008-04-01T00:00:00Z

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5467766

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18385101

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2700628

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