Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders - Test2 - elhamkhani - TriplyDB

Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders

Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders

http://www.wikidata.org/entity/Q28086930

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Genetic Syndromes, Maternal Diseases and Antenatal Factors Associated with Autism Spectrum Disorders (ASD)CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders Gilles de la Tourette syndrome is not linked to contactin-associated protein receptor 2 antibodies.Characterization of molecular and cellular phenotypes associated with a heterozygous CNTNAP2 deletion using patient-derived hiPSC neural cells.Molecular characterization of a rare analphoid supernumerary marker chromosome derived from 7q35 → qter: a case report.An update on the comorbidity of ADHD and ASD: a focus on clinical management.Intragenic CNTNAP2 Deletions: A Bridge Too Far?Persistent microglial activation and synaptic loss with behavioral abnormalities in mouse offspring exposed to CASPR2-antibodies in utero.Genetic modulation of oxytocin's effects in social functioning.SHANK Mutations May Disorder Brain Development.Disconnecting CNTNAP2.Mouse Cntnap2 and Human CNTNAP2 ASD Alleles Cell Autonomously Regulate PV+ Cortical Interneurons.Cntnap2 Knockout Rats and Mice Exhibit Epileptiform Activity and Abnormal Sleep-Wake Physiology.Loss of Cntnap2 Causes Axonal Excitability Deficits, Developmental Delay in Cortical Myelination, and Abnormal Stereotyped Motor Behavior.Identification of candidate genes involved in the etiology of sporadic Tourette syndrome by exome sequencing.Evaluation of CNTNAP2 gene rs2107856 polymorphism in Turkish population with pseudoexfoliation syndrome.Rodent models of genetic and chromosomal variations in psychiatric disorders.Pitt-Hopkins Syndrome: A Review of Current Literature, Clinical Approach, and 23-Patient Case Series.Eight further individuals with intellectual disability and epilepsy carrying bi-allelic CNTNAP2 aberrations allow delineation of the mutational and phenotypic spectrum.The Mechanism of Cortico-Striato-Thalamo-Cortical Neurocircuitry in Response Inhibition and Emotional Responding in Attention Deficit Hyperactivity Disorder with Comorbid Disruptive Behavior Disorder.Dysregulation of Parvalbumin Expression in the Mouse Model of Autism Spectrum Disorder Heterozygous Missense Variants: Risk Factors for Autism Spectrum Disorder and/or Other Pathologies?

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Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders

http://www.wikidata.org/entity/Q28086930

description

2015 nî lūn-bûn

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2015 թուականի Փետրուարին հրատարակուած գիտական յօդուած

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2015 թվականի փետրվարին հրատարակված գիտական հոդված

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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name

Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders

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Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders

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Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders

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Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders

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Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders

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Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders

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Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders

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Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders

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Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders

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Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders

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P2860

Transcriptional and functional complexity of Shank3 provides a molecular framework to understand the phenotypic heterogeneity of SHANK3 causing autism and Shank3 mutant mice

Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.

Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1

Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS

Caspr2, a new member of the neurexin superfamily, is localized at the juxtaparanodes of myelinated axons and associates with K+ channels

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

A functional genetic link between distinct developmental language disorders

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

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

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neurodevelopmental disorders

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