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Brain-specific epigenetic markers of schizophrenia.

Brain-specific epigenetic markers of schizophrenia.

http://www.wikidata.org/entity/Q37347673

about

Rethinking the Epigenetic Framework to Unravel the Molecular Pathology of Schizophrenia.REC8 functions as a tumor suppressor and is epigenetically downregulated in gastric cancer, especially in EBV-positive subtype.Epigenome-wide association study of DNA methylation in panic disorder.In utero exposure to maternal smoking is associated with DNA methylation alterations and reduced neuronal content in the developing fetal brain.Differential DNA methylation at birth associated with mental disorder in individuals with 22q11.2 deletion syndrome mRNA Expression and DNA Methylation Analysis of Serotonin Receptor 2A (HTR2A) in the Human Schizophrenic Brain.Expression and methylation of BDNF in the human brain in schizophrenia.New Targets for Schizophrenia Treatment beyond the Dopamine Hypothesis Genome-wide DNA methylation profiling in whole blood reveals epigenetic signatures associated with migraine.Genetic vulnerability to DUSP22 promoter hypermethylation is involved in the relation between in utero famine exposure and schizophrenia

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Brain-specific epigenetic markers of schizophrenia.

http://www.wikidata.org/entity/Q37347673

description

2015 nî lūn-bûn

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2015年の論文

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年學術文章

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2015年學術文章

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2015年學術文章

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name

Brain-specific epigenetic markers of schizophrenia.

@en

Brain-specific epigenetic markers of schizophrenia.

@nl

type

label

Brain-specific epigenetic markers of schizophrenia.

@en

Brain-specific epigenetic markers of schizophrenia.

@nl

prefLabel

Brain-specific epigenetic markers of schizophrenia.

@en

Brain-specific epigenetic markers of schizophrenia.

@nl

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Translational Psychiatry

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Brain-specific epigenetic markers of schizophrenia

@en

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B R Lawford

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C P Morris

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E P Noble

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R M Young

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V L J Whitehall

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Rec8p, a meiotic recombination and sister chromatid cohesion phosphoprotein of the Rad21p family conserved from fission yeast to humans

Mutations in CERS3 cause autosomal recessive congenital ichthyosis in humans

2-Hydroxy-ceramide synthesis by ceramide synthase family: enzymatic basis for the preference of FA chain length

SWAN: Subset-quantile within array normalization for illumina infinium HumanMethylation450 BeadChips

Prdm9 controls activation of mammalian recombination hotspots

Male germ cells require polyenoic sphingolipids with complex glycosylation for completion of meiosis: a link to ceramide synthase-3

Epigenetic programming by maternal behavior

Identification of eight members of the Argonaute family in the human genome

Schizophrenia as a complex trait: evidence from a meta-analysis of twin studies

The contribution of de novo coding mutations to autism spectrum disorder

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10.1038/TP.2015.177

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5

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Leesa F. Wockner

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