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Confirmed rare copy number variants implicate novel genes in schizophrenia

Confirmed rare copy number variants implicate novel genes in schizophrenia

http://www.wikidata.org/entity/Q28276679

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Understanding the impact of 1q21.1 copy number variant Small molecule inhibitors of zinc-dependent histone deacetylases The FMRP regulon: from targets to disease convergence Restoration of Sp4 in Forebrain GABAergic Neurons Rescues Hypersensitivity to Ketamine in Sp4 Hypomorphic Mice.Haploinsufficiency of Cyfip1 produces fragile X-like phenotypes in mice The microRNA cluster miR-183/96/182 contributes to long-term memory in a protein phosphatase 1-dependent manner.KCNQ1, KCNE2, and Na+-coupled solute transporters form reciprocally regulating complexes that affect neuronal excitability KCNE2 forms potassium channels with KCNA3 and KCNQ1 in the choroid plexus epithelium Autism As a Disorder of High Intelligence Cyfip1 Regulates Presynaptic Activity during Development The autism and schizophrenia associated gene CYFIP1 is critical for the maintenance of dendritic complexity and the stabilization of mature spines Up-regulated cytoplasmic FMRP-interacting protein 1 in intractable temporal lobe epilepsy patients and a rat model CYFIP1 coordinates mRNA translation and cytoskeleton remodeling to ensure proper dendritic spine formation Prolonged Ketamine Effects in Sp4 Hypomorphic Mice: Mimicking Phenotypes of Schizophrenia.Ion channels and schizophrenia: a gene set-based analytic approach to GWAS data for biological hypothesis testing.Store-operated calcium entry promotes the degradation of the transcription factor Sp4 in resting neurons.GlyT-1 Inhibition Attenuates Attentional But Not Learning or Motivational Deficits of the Sp4 Hypomorphic Mouse Model Relevant to Psychiatric Disorders Clinical and molecular cytogenetic analyses of four families with 1q21.1 microdeletion or microduplication.Behavioral characterization of a mouse model overexpressing DSCR1/ RCAN1.Copy number variants in extended autism spectrum disorder families reveal candidates potentially involved in autism risk.Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders.A novel method to identify high order gene-gene interactions in genome-wide association studies: gene-based MDR.Modeling a genetic risk for schizophrenia in iPSCs and mice reveals neural stem cell deficits associated with adherens junctions and polarity.Transcription factor Sp4 regulates expression of nervous wreck 2 to control NMDAR1 levels and dendrite patterning.The genetics of cognitive impairment in schizophrenia: a phenomic perspective.The transcription factor SP4 is reduced in postmortem cerebellum of bipolar disorder subjects: control by depolarization and lithium.Phosphorylation of transcription factor specificity protein 4 is increased in peripheral blood mononuclear cells of first-episode psychosis The neurobiology of mouse models syntenic to human chromosome 15q.Association study of the KCNJ3 gene as a susceptibility candidate for schizophrenia in the Chinese population.The role of protein intrinsic disorder in major psychiatric disorders.Expression of the G72/G30 gene in transgenic mice induces behavioral changes.HDAC9 is implicated in schizophrenia and expressed specifically in post-mitotic neurons but not in adult neural stem cells.Increased abundance of translation machinery in stem cell-derived neural progenitor cells from four schizophrenia patients.Methylomic changes during conversion to psychosis.Therapeutic potential of isoform selective HDAC inhibitors for the treatment of schizophrenia.Natural products as zinc-dependent histone deacetylase inhibitors.miR-124, -128, and -137 Orchestrate Neural Differentiation by Acting on Overlapping Gene Sets Containing a Highly Connected Transcription Factor Network.Phosphorylation of the transcription factor Sp4 is reduced by NMDA receptor signaling.Application of induced pluripotent stem cells to understand neurobiological basis of bipolar disorder and schizophrenia.Genomics of Lithium Action and Response.

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P2860

Confirmed rare copy number variants implicate novel genes in schizophrenia

http://www.wikidata.org/entity/Q28276679

description

2010 nî lūn-bûn

@nan

2010 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի ապրիլին հրատարակված գիտական հոդված

@hy

2010年の論文

@ja

2010年論文

@yue

2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

@zh-mo

2010年論文

@zh-tw

2010年论文

@wuu

name

Confirmed rare copy number variants implicate novel genes in schizophrenia

@ast

Confirmed rare copy number variants implicate novel genes in schizophrenia

@en

Confirmed rare copy number variants implicate novel genes in schizophrenia

@nl

type

label

Confirmed rare copy number variants implicate novel genes in schizophrenia

@ast

Confirmed rare copy number variants implicate novel genes in schizophrenia

@en

Confirmed rare copy number variants implicate novel genes in schizophrenia

@nl

prefLabel

Confirmed rare copy number variants implicate novel genes in schizophrenia

@ast

Confirmed rare copy number variants implicate novel genes in schizophrenia

@en

Confirmed rare copy number variants implicate novel genes in schizophrenia

@nl

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Biochemical Society Transactions

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Confirmed rare copy number variants implicate novel genes in schizophrenia

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P2093

Douglas H R Blackwood

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

Gloria W C Tam

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

Karen E Strathdee

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Louie N van de Lagemaat

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Mary P Malloy

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Mike D R Croning

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

Nigel P Carter

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Walter J Muir

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445-451

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scholarly article

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379839

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10.1042/BST0380445

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2

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38

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Benjamin S Pickard

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2010-04-01T00:00:00Z

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20298200

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