FOXP2 gene and language impairment in schizophrenia: association and epigenetic studies. - Wikidata - awgldk - TriplyDB

FOXP2 gene and language impairment in schizophrenia: association and epigenetic studies.

FOXP2 gene and language impairment in schizophrenia: association and epigenetic studies.

http://www.wikidata.org/entity/Q30986287

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FOXP2 The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders Functional characterization of rare FOXP2 variants in neurodevelopmental disorder.An informatics approach to integrating genetic and neurological data in speech and language neuroscience.Parental communication and psychosis: a meta-analysis.Epigenetic mechanisms during ageing and neurogenesis as novel therapeutic avenues in human brain disorders.DNA methylation changes in the postmortem dorsolateral prefrontal cortex of patients with schizophrenia.Methylome-wide association study of schizophrenia: identifying blood biomarker signatures of environmental insults Epigenetics of major psychosis: progress, problems and perspectives.DNA methylation patterns of protein-coding genes and long non-coding RNAs in males with schizophrenia.Risperidone and NAP protect cognition and normalize gene expression in a schizophrenia mouse model Epigenetic studies of schizophrenia: progress, predicaments, and promises for the future.DNA methylation in schizophrenia: progress and challenges of epigenetic studies Plasma total homocysteine is associated with DNA methylation in patients with schizophrenia.Psychosis in autism: comparison of the features of both conditions in a dually affected cohort.Formal Thought Disorder and language impairment in schizophrenia.The multidimensional nature of metabolic syndrome in schizophrenia: lessons from studies of one-carbon metabolism and DNA methylation.Genomics and epigenomics in novel schizophrenia drug discovery: translating animal models to clinical research and back.Foxp2 regulates neuronal differentiation and neuronal subtype specification.Deictic and Propositional Meaning-New Perspectives on Language in Schizophrenia.Association between forkhead-box P2 gene polymorphism and clinical symptoms in chronic schizophrenia in a Chinese population.Antipsychotic drugs attenuate aberrant DNA methylation of DTNBP1 (dysbindin) promoter in saliva and post-mortem brain of patients with schizophrenia and Psychotic bipolar disorder.Genome-wide methylome analyses reveal novel epigenetic regulation patterns in schizophrenia and bipolar disorder.Assessing the effects of common variation in the FOXP2 gene on human brain structure.PKNOX2 is associated with formal thought disorder in schizophrenia: a meta-analysis of two genome-wide association studies.Aberrant DNA methylation of blood in schizophrenia by adjusting for estimated cellular proportions.Comprehensive DNA methylation analysis of peripheral blood cells derived from patients with first-episode schizophrenia.Neuroplasticity may play a role in inter-individual difference among neuropsychiatric disease treatment efficacy.Sociability and synapse subtype-specific defects in mice lacking SRPX2, a language-associated gene.Interstitial deletion within 7q31.1q31.3 in a woman with mild intellectual disability and schizophrenia.Positive and balancing selection on gene associated with psychiatric disorders and human-unique personality traits

P2860

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P2860

FOXP2 gene and language impairment in schizophrenia: association and epigenetic studies.

http://www.wikidata.org/entity/Q30986287

description

2010 nî lūn-bûn

@nan

2010 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի հուլիսին 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

FOXP2 gene and language impairment in schizophrenia: association and epigenetic studies.

@ast

FOXP2 gene and language impairment in schizophrenia: association and epigenetic studies.

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type

label

FOXP2 gene and language impairment in schizophrenia: association and epigenetic studies.

@ast

FOXP2 gene and language impairment in schizophrenia: association and epigenetic studies.

@en

prefLabel

FOXP2 gene and language impairment in schizophrenia: association and epigenetic studies.

@ast

FOXP2 gene and language impairment in schizophrenia: association and epigenetic studies.

@en

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1471-2350-11-114

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BMC Medical Genetics

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FOXP2 gene and language impairment in schizophrenia: association and epigenetic studies.

@en

P2093

Adam M Dagnall

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

Amparo Tolosa

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Julio Sanjuán

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María D Moltó

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Neus Herrero

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Rosa de Frutos

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P2860

Molecular evolution of FOXP2, a gene involved in speech and language

The ʻbig bangʼ theory of the origin of psychosis and the faculty of language

Genome-wide detection and characterization of positive selection in human populations

A functional genetic link between distinct developmental language disorders

Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits

High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders

Epigenomic profiling reveals DNA-methylation changes associated with major psychosis

The social brain hypothesis of schizophrenia

cDNAs with long CAG trinucleotide repeats from human brain

A forkhead-domain gene is mutated in a severe speech and language disorder

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