Autism gene variant causes hyperserotonemia, serotonin receptor hypersensitivity, social impairment and repetitive behavior. - Wikidata - wikimedia - TriplyDB

Autism gene variant causes hyperserotonemia, serotonin receptor hypersensitivity, social impairment and repetitive behavior.

Autism gene variant causes hyperserotonemia, serotonin receptor hypersensitivity, social impairment and repetitive behavior.

http://www.wikidata.org/entity/Q30462749

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Monoamine oxidase A and A/B knockout mice display autistic-like features.Behavioral phenotypes of genetic mouse models of autism.The SLC6 transporters: perspectives on structure, functions, regulation, and models for transporter dysfunction From psychiatric disorders to animal models: a bidirectional and dimensional approach Targeted pharmacological treatment of autism spectrum disorders: fragile X and Rett syndromes Seizure-dependent mTOR activation in 5-HT neurons promotes autism-like behaviors in mice Serotonin transporter variant drives preventable gastrointestinal abnormalities in development and function.The bowel and beyond: the enteric nervous system in neurological disorders Neuronal mechanisms and circuits underlying repetitive behaviors in mouse models of autism spectrum disorder Letting a typical mouse judge whether mouse social interactions are atypical Acute dietary tryptophan manipulation differentially alters social behavior, brain serotonin and plasma corticosterone in three inbred mouse strains Mice genetically depleted of brain serotonin display social impairments, communication deficits and repetitive behaviors: possible relevance to autism The serotonin system in autism spectrum disorder: From biomarker to animal models Risperidone and the 5-HT2A receptor antagonist M100907 improve probabilistic reversal learning in BTBR T + tf/J mice The disruption of Celf6, a gene identified by translational profiling of serotonergic neurons, results in autism-related behaviors.Current progress and challenges in the search for autism biomarkers Of mice and monkeys: using non-human primate models to bridge mouse- and human-based investigations of autism spectrum disorders 5HT2A receptor blockade in dorsomedial striatum reduces repetitive behaviors in BTBR mice Behavioral, perceptual, and neural alterations in sensory and multisensory function in autism spectrum disorder Does Prenatal Valproate Interact with a Genetic Reduction in the Serotonin Transporter? A Rat Study on Anxiety and Cognition.The rare DAT coding variant Val559 perturbs DA neuron function, changes behavior, and alters in vivo responses to psychostimulants.Reduced isolation-induced pup ultrasonic communication in mouse pups lacking brain serotonin.Towards identification of individual etiologies by resolving genomic and biological conundrums in patients with autism spectrum disorders.Autism-relevant social abnormalities and cognitive deficits in engrailed-2 knockout mice Genetic background modulates phenotypes of serotonin transporter Ala56 knock-in mice Allergic fetal priming leads to developmental, behavioral and neurobiological changes in mice Modeling environmental risk factors of autism in mice induces IBD-related gut microbial dysbiosis and hyperserotonemia.An autism-associated serotonin transporter variant disrupts multisensory processing.The Gut Microbiota and Autism Spectrum Disorders.Serotonin-prefrontal cortical circuitry in anxiety and depression phenotypes: pivotal role of pre- and post-synaptic 5-HT1A receptor expression Largely typical patterns of resting-state functional connectivity in high-functioning adults with autism Intrainsular connectivity and somatosensory responsiveness in young children with ASD.Neuronal ablation of p-Akt at Ser473 leads to altered 5-HT1A/2A receptor function Effects of a social stimulus on gene expression in a mouse model of fragile X syndrome Serotonergic Mechanisms Regulating the GI Tract: Experimental Evidence and Therapeutic Relevance 5-HT7 receptors as modulators of neuronal excitability, synaptic transmission and plasticity: physiological role and possible implications in autism spectrum disorders.Kinase-dependent Regulation of Monoamine Neurotransmitter Transporters.Altered serotonin, dopamine and norepinepherine levels in 15q duplication and Angelman syndrome mouse models Drosophila melanogaster as a genetic model system to study neurotransmitter transporters.Neuroimaging endophenotypes in animal models of autism spectrum disorders: lost or found in translation?

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P2860

Autism gene variant causes hyperserotonemia, serotonin receptor hypersensitivity, social impairment and repetitive behavior.

http://www.wikidata.org/entity/Q30462749

description

2012 nî lūn-bûn

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2012 թուականի Մարտին հրատարակուած գիտական յօդուած

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2012 թվականի մարտին հրատարակված գիտական հոդված

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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Autism gene variant causes hyp ...... rment and repetitive behavior.

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Autism gene variant causes hyp ...... rment and repetitive behavior.

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Proceedings of the National Academy of Sciences of the United States of America

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Lynette C Daws

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Padmanabhan Mannangatti

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P2860

Subcellular redistribution of the serotonin transporter by secretory carrier membrane protein 2

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

Antidepressant- and cocaine-sensitive human serotonin transporter: molecular cloning, expression, and chromosomal localization

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

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

Shank3 mutant mice display autistic-like behaviours and striatal dysfunction

Marble burying reflects a repetitive and perseverative behavior more than novelty-induced anxiety

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

Autism and the serotonin transporter: the long and short of it

Broad and narrow heritabilities of quantitative traits in a founder population.

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