Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders
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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 disordersGilles 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 DisorderHeterozygous Missense Variants: Risk Factors for Autism Spectrum Disorder and/or Other Pathologies?
P2860
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P2860
Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders
description
2015 nî lūn-bûn
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2015 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2015年の論文
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2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
name
Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders
@ast
Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders
@en
Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders
@nl
type
label
Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders
@ast
Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders
@en
Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders
@nl
prefLabel
Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders
@ast
Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders
@en
Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders
@nl
P2860
P3181
P356
P1476
Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders
@en
P2093
Martin Poot
P2860
P3181
P356
10.1159/000371594
P407
P577
2015-02-01T00:00:00Z