Genetic and functional analyses identify DISC1 as a novel callosal agenesis candidate gene. - Wikidata - awgldk - TriplyDB

Genetic and functional analyses identify DISC1 as a novel callosal agenesis candidate gene.

Genetic and functional analyses identify DISC1 as a novel callosal agenesis candidate gene.

http://www.wikidata.org/entity/Q52613482

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The role of corpus callosum development in functional connectivity and cognitive processing A New Outlook on Mental Illnesses: Glial Involvement Beyond the Glue Following the genes: a framework for animal modeling of psychiatric disorders The BTBR T+ tf/J mouse model for autism spectrum disorders-in search of biomarkers.Effects of a Balanced Translocation between Chromosomes 1 and 11 Disrupting the DISC1 Locus on White Matter Integrity.Possible functional links among brain- and skull-related genes selected in modern humans 708 Common and 2010 rare DISC1 locus variants identified in 1542 subjects: analysis for association with psychiatric disorder and cognitive traits.Clinical, genetic and imaging findings identify new causes for corpus callosum development syndromes.DISC1 (disrupted-in-schizophrenia-1) regulates differentiation of oligodendrocytes A 54 Mb 11qter duplication and 0.9 Mb 1q44 deletion in a child with laryngomalacia and agenesis of corpus callosum.Sonic hedgehog functions upstream of disrupted-in-schizophrenia 1 (disc1): implications for mental illness.DISC1 genetics, biology and psychiatric illness Hippocampal commissure defects in crosses of four inbred mouse strains with absent corpus callosum.Bridging the Gap between Genes and Language Deficits in Schizophrenia: An Oscillopathic Approach.DISC1 as a therapeutic target for mental illnesses.DISC1 Pathway in Brain Development: Exploring Therapeutic Targets for Major Psychiatric Disorders.Missense-depleted regions in population exomes implicate ras superfamily nucleotide-binding protein alteration in patients with brain malformation.A prenatal interruption of DISC1 function in the brain exhibits a lasting impact on adult behaviors, brain metabolism, and interneuron development.Synaptic Disorders Toward the Language Oscillogenome

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Genetic and functional analyses identify DISC1 as a novel callosal agenesis candidate gene.

http://www.wikidata.org/entity/Q52613482

description

2011 nî lūn-bûn

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2011年の論文

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年學術文章

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2011年學術文章

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name

Genetic and functional analyse ...... losal agenesis candidate gene.

@en

Genetic and functional analyse ...... losal agenesis candidate gene.

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type

label

Genetic and functional analyse ...... losal agenesis candidate gene.

@en

Genetic and functional analyse ...... losal agenesis candidate gene.

@nl

prefLabel

Genetic and functional analyse ...... losal agenesis candidate gene.

@en

Genetic and functional analyse ...... losal agenesis candidate gene.

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American Journal of Medical Genetics

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Genetic and functional analyse ...... losal agenesis candidate gene.

@en

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Cailyn H Spurrell

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

Elena Boland

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

Elliott H Sherr

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

Eric Rider

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

Jiang Li

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

Len A Pennacchio

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

Mari Wakahiro

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

Mary C O'Driscoll

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

Nathan Osbun

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

Polina Bukshpun

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

P2860

Functional and anatomical cortical underconnectivity in autism: evidence from an FMRI study of an executive function task and corpus callosum morphometry

Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance.

DISC1 (Disrupted-In-Schizophrenia 1) is a centrosome-associated protein that interacts with MAP1A, MIPT3, ATF4/5 and NUDEL: regulation and loss of interaction with mutation

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

Disrupted-in-Schizophrenia-1 (DISC-1): mutant truncation prevents binding to NudE-like (NUDEL) and inhibits neurite outgrowth

Microduplications of 16p11.2 are associated with schizophrenia

DISC1 splice variants are upregulated in schizophrenia and associated with risk polymorphisms

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

Disruption of two novel genes by a translocation co-segregating with schizophrenia

Association between microdeletion and microduplication at 16p11.2 and autism

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1865-1876

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scholarly article

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10.1002/AJMG.A.34081

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8

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155A

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William B. Dobyns

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2011-07-07T00:00:00Z

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21739582

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5544936

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