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Behavioral profiles of mouse models for autism spectrum disorders.

Behavioral profiles of mouse models for autism spectrum disorders.

http://www.wikidata.org/entity/Q37844007

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Behavioral phenotypes of genetic mouse models of autism.Understanding the molecular basis of autism in a dish using hiPSCs-derived neurons from ASD patients Hippocampal neuroligin-2 overexpression leads to reduced aggression and inhibited novelty reactivity in rats Mice with Dab1 or Vldlr insufficiency exhibit abnormal neonatal vocalization patterns Complete or partial reduction of the Met receptor tyrosine kinase in distinct circuits differentially impacts mouse behavior Gender Dependent Evaluation of Autism like Behavior in Mice Exposed to Prenatal Zinc Deficiency Negative allosteric modulation of the mGluR5 receptor reduces repetitive behaviors and rescues social deficits in mouse models of autism.Autistic-like behaviours and hyperactivity in mice lacking ProSAP1/Shank2 Letting a typical mouse judge whether mouse social interactions are atypical Tipping the balance of autism risk: potential mechanisms linking pesticides and autism Histopathologic characterization of the BTBR mouse model of autistic-like behavior reveals selective changes in neurodevelopmental proteins and adult hippocampal neurogenesis Translational Mouse Models of Autism: Advancing Toward Pharmacological Therapeutics.Neuronal connectivity as a convergent target of gene × environment interactions that confer risk for Autism Spectrum Disorders Recording Mouse Ultrasonic Vocalizations to Evaluate Social Communication.Altered social behavior and ultrasonic communication in the dystrophin-deficient mdx mouse model of Duchenne muscular dystrophy.Genetic targeting of NRXN2 in mice unveils role in excitatory cortical synapse function and social behaviors Limited impact of Cntn4 mutation on autism-related traits in developing and adult C57BL/6J mice.Comprehensive behavioral analysis of RNG105 (Caprin1) heterozygous mice: Reduced social interaction and attenuated response to novelty Lack of parvalbumin in mice leads to behavioral deficits relevant to all human autism core symptoms and related neural morphofunctional abnormalities.Pre-clinical models of neurodevelopmental disorders: focus on the cerebellum PTEN regulation of local and long-range connections in mouse auditory cortex.Translational animal models of autism and neurodevelopmental disorders.Are Sema5a mutant mice a good model of autism? A behavioral analysis of sensory systems, emotionality and cognition.Adult male mice emit context-specific ultrasonic vocalizations that are modulated by prior isolation or group rearing environment.Mouse model of Timothy syndrome recapitulates triad of autistic traits.Acute alcohol exposure during neurulation: Behavioral and brain structural consequences in adolescent C57BL/6J mice.Neurexins.RECENT DEVELOPMENTS IN NEUROPATHOLOGY OF AUTISM SPECTRUM DISORDERS.The hunt for gene effects pertinent to behavioral traits and psychiatric disorders: from mouse to human.The BTBR mouse model of autism spectrum disorders has learning and attentional impairments and alterations in acetylcholine and kynurenic acid in prefrontal cortex.Genetic effects on cerebellar structure across mouse models of autism using a magnetic resonance imaging atlas Clustering autism: using neuroanatomical differences in 26 mouse models to gain insight into the heterogeneity.Therapeutic strategies in fragile X syndrome: dysregulated mGluR signaling and beyond.Exogenous and evoked oxytocin restores social behavior in the Cntnap2 mouse model of autism.A Case of Autism with Ring Chromosome 14.Oxytocin receptor and Mecp2 308/Y knockout mice exhibit altered expression of autism-related social behaviors.The E3 ubiquitin ligase protein associated with Myc (Pam) regulates mammalian/mechanistic target of rapamycin complex 1 (mTORC1) signaling in vivo through N- and C-terminal domains.Hippocampal Transcriptomic and Proteomic Alterations in the BTBR Mouse Model of Autism Spectrum Disorder.Alterations in intrinsic membrane properties and the axon initial segment in a mouse model of Angelman syndrome The oxytocin system in drug discovery for autism: animal models and novel therapeutic strategies

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Behavioral profiles of mouse models for autism spectrum disorders.

http://www.wikidata.org/entity/Q37844007

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article científic

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bilimsel makale

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scientific article published on 05 January 2011

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vedecký článok

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vetenskaplig artikel

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vědecký článek

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Behavioral profiles of mouse models for autism spectrum disorders.

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Behavioral profiles of mouse models for autism spectrum disorders.

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Behavioral profiles of mouse models for autism spectrum disorders.

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Behavioral profiles of mouse models for autism spectrum disorders.

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Behavioral profiles of mouse models for autism spectrum disorders.

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Behavioral profiles of mouse models for autism spectrum disorders.

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Autism Research

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Behavioral profiles of mouse models for autism spectrum disorders.

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Claire S Leblond

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Elodie Ey

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P2860

Annotation: What do we know about sensory dysfunction in autism? A critical review of the empirical evidence

The genetics of autistic disorders and its clinical relevance: a review of the literature

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

The Autistic Neuron: Troubled Translation?

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

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

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

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

Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation

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

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5-16

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scholarly article

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10.1002/AUR.175

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1

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4

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Thomas Bourgeron

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2011-01-05T00:00:00Z

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49843105

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21328568

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Autism spectrum