(Q42164701)

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Spatiotemporal 16p11.2 protein network implicates cortical late mid-fetal brain development and KCTD13-Cul3-RhoA pathway in psychiatric diseases

scientific article published on February 2015

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Europe PubMed Central

PMC publication ID

17 October 2017

Spatiotemporal 16p11.2 protein network implicates cortical late mid-fetal brain development and KCTD13-Cul3-RhoA pathway in psychiatric diseases (English)

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17 October 2017

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Lilia M. Iakoucheva

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Roser Corominas

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1 February 2015

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17 October 2017

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3 June 2020

A proteome-scale map of the human interactome network

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1 reference

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Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism

1 reference

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Spatial and temporal mapping of de novo mutations in schizophrenia to a fetal prefrontal cortical network

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Reciprocal duplication of the Williams-Beuren syndrome deletion on chromosome 7q11.23 is associated with schizophrenia

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Timothy syndrome is associated with activity-dependent dendritic retraction in rodent and human neurons

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Intra-axonal translation of RhoA promotes axon growth inhibition by CSPG.

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Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disorders.

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26 October 2017

KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant

1 reference

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De Novo Gene Disruptions in Children on the Autistic Spectrum

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Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations

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Dosage-dependent phenotypes in models of 16p11.2 lesions found in autism

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1 reference

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1 reference

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17 August 2018

Identifiers

10.1016/J.NEURON.2015.01.010

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3 June 2020

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3 June 2020

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3 June 2020

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