Analysis of the neuroligin 4Y gene in patients with autism
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Why are autism spectrum conditions more prevalent in males?Neurexin 1 (NRXN1) deletions in schizophreniaOxytocin: the great facilitator of life.Neuroligin-1 deletion results in impaired spatial memory and increased repetitive behavior.Proteins that promote filopodia stability, but not number, lead to more axonal-dendritic contactsThe interplay between synaptic activity and neuroligin function in the CNSUsing Gene Ontology to describe the role of the neurexin-neuroligin-SHANK complex in human, mouse and rat and its relevance to autismRecent advances in the genetics of language impairmentIdentification of rare X-linked neuroligin variants by massively parallel sequencing in males with autism spectrum disorderThe Role of the Y Chromosome in Brain Function.Communication, interventions, and scientific advances in autism: a commentary.Developmental regulation and individual differences of neuronal H3K4me3 epigenomes in the prefrontal cortex.Decreased GABA(B) receptors in the cingulate cortex and fusiform gyrus in autismNeurexins, neuroligins and LRRTMs: synaptic adhesion getting fishyEvidence of novel fine-scale structural variation at autism spectrum disorder candidate lociBehavioral and social phenotypes in boys with 47,XYY syndrome or 47,XXY Klinefelter syndromeBehavioral phenotypes in males with XYY and possible role of increased NLGN4Y expression in autism features.Pharmacology and genetics of autism: implications for diagnosis and treatment.Linkage analysis of schizophrenia in African-American familiesUsing C. elegans to decipher the cellular and molecular mechanisms underlying neurodevelopmental disorders.Molecular basis for prospective pharmacological treatment strategies in intellectual disability syndromes.Autism spectrum disorders in XYY syndrome: two new cases and systematic review of the literature.The complex genetics in autism spectrum disorders.Synaptic alterations associated with depression and schizophrenia: potential as a therapeutic target.Autism genetics - an overview.Not all neuroligin 3 and 4X missense variants lead to significant functional inactivation.Autism Spectrum Disorder in Males with Sex Chromosome Aneuploidy: XXY/Klinefelter Syndrome, XYY, and XXYY.Variations analysis of NLGN3 and NLGN4X gene in Chinese autism patients.Array comparative genomic hybridization findings in a cohort referred for an autism evaluation.Association of Y chromosome haplotypes with autism.Stage 1 Registered Report: Variation in neurodevelopmental outcomes in children with sex chromosome trisomies: protocol for a test of the double hit hypothesis.Stage 2 Registered Report: Variation in neurodevelopmental outcomes in children with sex chromosome trisomies: testing the double hit hypothesisRegulation and postsynaptic binding of neurexins — drug targets for neurodevelopmental and neuropsychiatric disorders
P2860
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P2860
Analysis of the neuroligin 4Y gene in patients with autism
description
2008 nî lūn-bûn
@nan
2008 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Analysis of the neuroligin 4Y gene in patients with autism
@ast
Analysis of the neuroligin 4Y gene in patients with autism
@en
Analysis of the neuroligin 4Y gene in patients with autism
@en-gb
Analysis of the neuroligin 4Y gene in patients with autism
@nl
type
label
Analysis of the neuroligin 4Y gene in patients with autism
@ast
Analysis of the neuroligin 4Y gene in patients with autism
@en
Analysis of the neuroligin 4Y gene in patients with autism
@en-gb
Analysis of the neuroligin 4Y gene in patients with autism
@nl
prefLabel
Analysis of the neuroligin 4Y gene in patients with autism
@ast
Analysis of the neuroligin 4Y gene in patients with autism
@en
Analysis of the neuroligin 4Y gene in patients with autism
@en-gb
Analysis of the neuroligin 4Y gene in patients with autism
@nl
P2093
P921
P1433
P1476
Analysis of the neuroligin 4Y gene in patients with autism
@en
P2093
Charles E Schwartz
Cindy Skinner
Jinong Feng
Richard Schroer
Steve S Sommer
P356
10.1097/YPG.0B013E3282FB7FE6
P407
P50
P577
2008-08-01T00:00:00Z