Association study of SHANK3 gene polymorphisms with autism in Chinese Han population. - Wikidata - awgldk - TriplyDB

Association study of SHANK3 gene polymorphisms with autism in Chinese Han population.

Association study of SHANK3 gene polymorphisms with autism in Chinese Han population.

http://www.wikidata.org/entity/Q30157213

about

The 22q13.3 Deletion Syndrome (Phelan-McDermid Syndrome)Prevalence of SHANK3 variants in patients with different subtypes of autism spectrum disorders Sociability and motor functions in Shank1 mutant mice Reduced excitatory neurotransmission and mild autism-relevant phenotypes in adolescent Shank3 null mutant mice Identification of rare X-linked neuroligin variants by massively parallel sequencing in males with autism spectrum disorder [Genetic and brain structure anomalies in autism spectrum disorders. Towards an understanding of the aetiopathogenesis?].Replicable in vivo physiological and behavioral phenotypes of the Shank3B null mutant mouse model of autism.Cell adhesion molecules and their involvement in autism spectrum disorder.Autism spectrum disorders: the quest for genetic syndromes.Modeling of Autism Using Organoid Technology.A double hit implicates DIAPH3 as an autism risk gene.Association study between autistic-like traits and polymorphisms in the autism candidate regions RELN, CNTNAP2, SHANK3, and CDH9/10.A commonly carried genetic variant, rs9616915, in SHANK3 gene is associated with a reduced risk of autism spectrum disorder: replication in a Chinese population.Genetic variability in scaffolding proteins and risk for schizophrenia and autism-spectrum disorders: a systematic review.

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P2860

Association study of SHANK3 gene polymorphisms with autism in Chinese Han population.

http://www.wikidata.org/entity/Q30157213

description

2009 nî lūn-bûn

@nan

2009 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի հունիսին հրատարակված գիտական հոդված

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2009年の論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年论文

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name

Association study of SHANK3 gene polymorphisms with autism in Chinese Han population.

@ast

Association study of SHANK3 gene polymorphisms with autism in Chinese Han population.

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type

label

Association study of SHANK3 gene polymorphisms with autism in Chinese Han population.

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Association study of SHANK3 gene polymorphisms with autism in Chinese Han population.

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prefLabel

Association study of SHANK3 gene polymorphisms with autism in Chinese Han population.

@ast

Association study of SHANK3 gene polymorphisms with autism in Chinese Han population.

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BMC Medical Genetics

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Association study of SHANK3 gene polymorphisms with autism in Chinese Han population.

@en

P2093

Dai Zhang

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Jian Qin

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

Jing Liu

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

Jishui Zhang

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Lifang Wang

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Meixiang Jia

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Tianlan Lu

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Weihua Yue

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

Xiaoling Yang

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Yan Ruan

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P2860

Shank, a novel family of postsynaptic density proteins that binds to the NMDA receptor/PSD-95/GKAP complex and cortactin

Characterization of the Shank family of synaptic proteins. Multiple genes, alternative splicing, and differential expression in brain and development

Advances in autism genetics: on the threshold of a new neurobiology

Searching for ways out of the autism maze: genetic, epigenetic and environmental clues

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

Reduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autism.

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

Disruption of the ProSAP2 gene in a t(12;22)(q24.1;q13.3) is associated with the 22q13.3 deletion syndrome

A neuroligin-3 mutation implicated in autism increases inhibitory synaptic transmission in mice

Contribution of SHANK3 mutations to autism spectrum disorder

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