(Q37826622)

23 August 2017

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title

Cell adhesion molecules and their involvement in autism spectrum disorder (English)

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23 August 2017

autism spectrum disorder

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Haihong Ye

1

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PubMed ID

21212702

23 August 2017

Jianghong Liu

series ordinal

2

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PubMed ID

21212702

23 August 2017

Jane Y Wu

series ordinal

3

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23 August 2017

1 January 2010

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23 August 2017

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23 August 2017

18

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23 August 2017

2

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23 August 2017

62-71

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Autism spectrum disorders

23 August 2017

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

21 January 2018

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Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

21 January 2018

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Common genetic variants on 5p14.1 associate with autism spectrum disorders

21 January 2018

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Regional differences in synaptogenesis in human cerebral cortex

21 January 2018

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Autism and brain development

21 January 2018

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Cell adhesion molecules: signalling functions at the synapse

21 January 2018

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The emerging role of synaptic cell-adhesion pathways in the pathogenesis of autism spectrum disorders

21 January 2018

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Neurexins induce differentiation of GABA and glutamate postsynaptic specializations via neuroligins

21 January 2018

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Neuroligin expressed in nonneuronal cells triggers presynaptic development in contacting axons

21 January 2018

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Neurexin mediates the assembly of presynaptic terminals

21 January 2018

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Structure and evolution of neurexin genes: insight into the mechanism of alternative splicing

21 January 2018

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Oligonucleotide microarray analysis of genomic imbalance in children with mental retardation

21 January 2018

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A patient with vertebral, cognitive and behavioural abnormalities and a de novo deletion of NRXN1alpha

21 January 2018

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High frequency of neurexin 1beta signal peptide structural variants in patients with autism

21 January 2018

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Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes

21 January 2018

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Mapping autism risk loci using genetic linkage and chromosomal rearrangements

21 January 2018

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Disruption of neurexin 1 associated with autism spectrum disorder

21 January 2018

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CNTNAP2 and NRXN1 are mutated in autosomal-recessive Pitt-Hopkins-like mental retardation and determine the level of a common synaptic protein in Drosophila

21 January 2018

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Mouse neurexin-1alpha deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments

21 January 2018

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Neurexin 1 (NRXN1) deletions in schizophrenia

21 January 2018

1 reference

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

21 January 2018

1 reference

Molecular cytogenetic analysis of a familial interstitial deletion Xp22.2-22.3 with a highly variable phenotype in female carriers.

21 January 2018

1 reference

Autism and nonsyndromic mental retardation associated with a de novo mutation in the NLGN4X gene promoter causing an increased expression level.

21 January 2018

1 reference

X-linked ichthyosis (steroid sulfatase deficiency) is associated with increased risk of attention deficit hyperactivity disorder, autism and social communication deficits.

21 January 2018

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X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family

21 January 2018

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Familial deletion within NLGN4 associated with autism and Tourette syndrome

21 January 2018

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Deletions of VCX-A and NLGN4: a variable phenotype including normal intellect.

21 January 2018

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Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric patients

21 January 2018

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The Arg451Cys-neuroligin-3 mutation associated with autism reveals a defect in protein processing

21 January 2018

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A neuroligin-4 missense mutation associated with autism impairs neuroligin-4 folding and endoplasmic reticulum export

21 January 2018

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

21 January 2018

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Neuroligin-3-deficient mice: model of a monogenic heritable form of autism with an olfactory deficit.

21 January 2018

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

21 January 2018

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Neuroligin-1 deletion results in impaired spatial memory and increased repetitive behavior

21 January 2018

1 reference

ProSAP/Shank proteins - a family of higher order organizing molecules of the postsynaptic density with an emerging role in human neurological disease

21 January 2018

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

21 January 2018

1 reference

Molecular and phenotypic characterization of ring chromosome 22

21 January 2018

1 reference

Terminal 22q deletion syndrome: a newly recognized cause of speech and language disability in the autism spectrum

21 January 2018

1 reference

Contribution of SHANK3 mutations to autism spectrum disorder

21 January 2018

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Novel de novo SHANK3 mutation in autistic patients

21 January 2018

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

21 January 2018

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Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection

21 January 2018

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Activity-dependent validation of excitatory versus inhibitory synapses by neuroligin-1 versus neuroligin-2

21 January 2018

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Thrombospondin 1 accelerates synaptogenesis in hippocampal neurons through neuroligin 1.

21 January 2018

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Regulation of dendritic spine morphology and synaptic function by Shank and Homer

21 January 2018

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Shank expression is sufficient to induce functional dendritic spine synapses in aspiny neurons.

21 January 2018

1 reference

Genome-wide association study identifies ITGB3 as a QTL for whole blood serotonin

21 January 2018

1 reference

Studies on 5-hydroxyindole metabolism in autistic and other mentally retarded children.

21 January 2018

1 reference

Variation in ITGB3 is associated with whole-blood serotonin level and autism susceptibility.

21 January 2018

1 reference

Evidence for epistasis between SLC6A4 and ITGB3 in autism etiology and in the determination of platelet serotonin levels.

21 January 2018

1 reference

Multifactor dimensionality reduction-phenomics: a novel method to capture genetic heterogeneity with use of phenotypic variables

21 January 2018

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ITGB3 shows genetic and expression interaction with SLC6A4.

21 January 2018

1 reference

Evidence of linkage between the serotonin transporter and autistic disorder.

21 January 2018

1 reference

A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.

21 January 2018

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A genomewide screen of 345 families for autism-susceptibility loci

21 January 2018

1 reference

Linkage and association analysis at the serotonin transporter (SLC6A4) locus in a rigid-compulsive subset of autism

21 January 2018

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Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors

21 January 2018

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Modeling rare gene variation to gain insight into the oldest biomarker in autism: construction of the serotonin transporter Gly56Ala knock-in mouse

21 January 2018

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Interactions between integrin alphaIIbbeta3 and the serotonin transporter regulate serotonin transport and platelet aggregation in mice and humans

21 January 2018

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Ligand-induced changes in integrin expression regulate neuronal adhesion and neurite outgrowth.

21 January 2018

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Integrins mediate functional pre- and postsynaptic maturation at a hippocampal synapse

21 January 2018

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Examination of NRCAM, LRRN3, KIAA0716, and LAMB1 as autism candidate genes

21 January 2018

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Association of the alpha4 integrin subunit gene (ITGA4) with autism.

21 January 2018

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Disruption of contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome

21 January 2018

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Disruption of Contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome.

21 January 2018

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Disruption of contactin 4 in three subjects with autism spectrum disorder

21 January 2018

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Identifying autism loci and genes by tracing recent shared ancestry

21 January 2018

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Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene

21 January 2018

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Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2

21 January 2018

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A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism

21 January 2018

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Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders

21 January 2018

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Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia

21 January 2018

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F3/contactin acts as a functional ligand for Notch during oligodendrocyte maturation

21 January 2018

1 reference

Neural recognition molecules CHL1 and NB-3 regulate apical dendrite orientation in the neocortex via PTP alpha

21 January 2018

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Contribution of the neural cell recognition molecule NB-3 to synapse formation between parallel fibers and Purkinje cells in mouse.

21 January 2018

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Juxtaparanodal clustering of Shaker-like K+ channels in myelinated axons depends on Caspr2 and TAG-1

21 January 2018

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Normal variation in fronto-occipital circuitry and cerebellar structure with an autism-associated polymorphism of CNTNAP2

21 January 2018

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Altered functional connectivity in frontal lobe circuits is associated with variation in the autism risk gene CNTNAP2

21 January 2018

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Genetic analyses of roundabout (ROBO) axon guidance receptors in autism.

21 January 2018

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Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesis

21 January 2018

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The serotonin system in autism

21 January 2018

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21 January 2018

Identifiers

DOI

10.1159/000322543

1 reference

23 August 2017

1 reference

PubMed ID

21212702