Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism - Test2 - elhamkhani - TriplyDB

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

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

http://www.wikidata.org/entity/Q24299042

about

Bridging the synaptic gap: neuroligins and neurexin I in Apis mellifera Why are autism spectrum conditions more prevalent in males?Mutation screening of melatonin-related genes in patients with autism spectrum disorders Association of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a candidate gene analysis Neuropathology and animal models of autism: genetic and environmental factors Alterations of GABAergic signaling in autism spectrum disorders Autistic phenotypes and genetic testing: state-of-the-art for the clinical geneticist The genetics of autistic disorders and its clinical relevance: a review of the literature Genetics of autism spectrum disorder Advances in autism genetics: on the threshold of a new neurobiology Neuroligins and neurexins link synaptic function to cognitive disease Autism and brain development Convulsing toward the pathophysiology of autism The role of immune dysfunction in the pathophysiology of autism Unraveling autism Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments Disorder-associated mutations lead to functional inactivation of neuroligins Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia Dissection of synapse induction by neuroligins: effect of a neuroligin mutation associated with autism Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability Rare deletions at the neurexin 3 locus in autism spectrum disorder Neuroligin-1-dependent competition regulates cortical synaptogenesis and synapse number Structural analysis of the synaptic protein neuroligin and its beta-neurexin complex: determinants for folding and cell adhesion Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders Reduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autism.A neuroligin-4 missense mutation associated with autism impairs neuroligin-4 folding and endoplasmic reticulum export Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation SHANK1 Deletions in Males with Autism Spectrum Disorder Structural insights into the exquisite selectivity of neurexin/neuroligin synaptic interactions.The association of GPR85 with PSD-95-neuroligin complex and autism spectrum disorder: a molecular analysis Synapse formation regulated by protein tyrosine phosphatase receptor T through interaction with cell adhesion molecules and Fyn CASK Functions as a Mg2+-independent neurexin kinase Neurexins induce differentiation of GABA and glutamate postsynaptic specializations via neuroligins Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders Investigating synapse formation and function using human pluripotent stem cell-derived neurons X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family Functional impact of global rare copy number variation in autism spectrum disorders Shank3 mutant mice display autistic-like behaviours and striatal dysfunction Autism risk factors: genes, environment, and gene-environment interactions

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

http://www.wikidata.org/entity/Q24299042

description

2003 nî lūn-bûn

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2003 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2003 թվականի մայիսին հրատարակված գիտական հոդված

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2003年の論文

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Mutations of the X-linked gene ...... GN4 are associated with autism

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Mutations of the X-linked gene ...... GN4 are associated with autism

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Mutations of the X-linked gene ...... GN4 are associated with autism

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Mutations of the X-linked gene ...... GN4 are associated with autism

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Mutations of the X-linked gene ...... GN4 are associated with autism

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Mutations of the X-linked gene ...... GN4 are associated with autism

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Mutations of the X-linked gene ...... GN4 are associated with autism

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Mutations of the X-linked gene ...... GN4 are associated with autism

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Mutations of the X-linked gene ...... GN4 are associated with autism

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Mutations of the X-linked gene ...... GN4 are associated with autism

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Mutations of the X-linked gene ...... GN4 are associated with autism

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Mutations of the X-linked gene ...... GN4 are associated with autism

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Catherine Colineaux

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Henrik Soderstrom

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Hélène Quach

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I Carina Gillberg

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Maria Råstam

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P2860

Genetics of austim: complex aetiology for a heterogeneous disorder

Neuroligin expressed in nonneuronal cells triggers presynaptic development in contacting axons

Identification of a novel neuroligin in humans which binds to PSD-95 and has a widespread expression

A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27

Common EF-hand motifs in cholinesterases and neuroligins suggest a role for Ca2+ binding in cell surface associations

Neuroligin 1 is a postsynaptic cell-adhesion molecule of excitatory synapses

The structure and expression of the human neuroligin-3 gene

Binding properties of neuroligin 1 and neurexin 1beta reveal function as heterophilic cell adhesion molecules

Structures, alternative splicing, and neurexin binding of multiple neuroligins

Neuroligin 1: a splice site-specific ligand for beta-neurexins

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10.1038/NG1136

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1

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Christopher Gillberg

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Catalina Betancur

Stéphane Jamain

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232794714

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vocalization behavior

Neuroligin 4 X-linked

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1925054

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