(Q37844007)

24 August 2017

title

Behavioral profiles of mouse models for autism spectrum disorders (English)

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24 August 2017

main subject

autism spectrum disorder

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24 August 2017

Claire S Leblond

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24 August 2017

Elodie Ey

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24 August 2017

publication date

5 January 2011

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24 August 2017

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24 August 2017

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24 August 2017

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24 August 2017

page(s)

5-16

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

24 August 2017

cites work

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Fmr1 KO mice as a possible model of autistic features

21 January 2018

1 reference

Increased anxiety-like behavior in mice lacking the inhibitory synapse cell adhesion molecule neuroligin 2

21 January 2018

1 reference

Neuroligin-1 deletion results in impaired spatial memory and increased repetitive behavior

21 January 2018

1 reference

A synaptic trek to autism

21 January 2018

1 reference

The mouse light/dark box test

21 January 2018

1 reference

Mammalian social odours: attraction and individual recognition

21 January 2018

1 reference

Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations

21 January 2018

1 reference

Minimal aberrant behavioral phenotypes of neuroligin-3 R451C knockin mice

21 January 2018

1 reference

Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice

21 January 2018

1 reference

Mild overexpression of MeCP2 causes a progressive neurological disorder in mice.

21 January 2018

1 reference

Learning deficits, but normal development and tumor predisposition, in mice lacking exon 23a of Nf1

21 January 2018

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Altered neuroligin expression is involved in social deficits in a mouse model of the fragile X syndrome

21 January 2018

1 reference

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

21 January 2018

1 reference

Fmr1 knockout mice show reduced anxiety and alterations in neurogenesis that are specific to the ventral dentate gyrus.

21 January 2018

1 reference

Increased levels of anxiety-related behaviors in a Tsc2 dominant negative transgenic mouse model of tuberous sclerosis

21 January 2018

1 reference

Reversal of learning deficits in a Tsc2+/- mouse model of tuberous sclerosis

21 January 2018

1 reference

Reversing neurodevelopmental disorders in adults

21 January 2018

1 reference

From mTOR to cognition: molecular and cellular mechanisms of cognitive impairments in tuberous sclerosis

21 January 2018

1 reference

A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice

21 January 2018

1 reference

The natural history and treatment of epilepsy in a murine model of tuberous sclerosis.

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Disruption of Contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome

21 January 2018

1 reference

Autism spectrum disorder diagnoses in Stockholm preschoolers

21 January 2018

1 reference

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

21 January 2018

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Deletion of Mecp2 in Sim1-expressing neurons reveals a critical role for MeCP2 in feeding behavior, aggression, and the response to stress.

21 January 2018

1 reference

21 January 2018

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De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia

21 January 2018

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Postnatal loss of methyl-CpG binding protein 2 in the forebrain is sufficient to mediate behavioral aspects of Rett syndrome in mice

21 January 2018

1 reference

The paradox of cognitive flexibility in autism

21 January 2018

1 reference

Anxiety in high-functioning children with autism

21 January 2018

1 reference

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

21 January 2018

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Cognitive deficits in Tsc1+/- mice in the absence of cerebral lesions and seizures.

21 January 2018

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A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome

21 January 2018

1 reference

Reversal of neurological defects in a mouse model of Rett syndrome

21 January 2018

1 reference

The mouse light-dark paradigm: a review

21 January 2018

1 reference

Analysis of cerebellar function in Ube3a-deficient mice reveals novel genotype-specific behaviors

21 January 2018

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Synaptic imbalance, stereotypies, and impaired social interactions in mice with altered neuroligin 2 expression

21 January 2018

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Smaller dendritic spines, weaker synaptic transmission, but enhanced spatial learning in mice lacking Shank1.

21 January 2018

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

21 January 2018

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

21 January 2018

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Mutation of the Angelman ubiquitin ligase in mice causes increased cytoplasmic p53 and deficits of contextual learning and long-term potentiation.

21 January 2018

1 reference

Altered ultrasonic vocalization and impaired learning and memory in Angelman syndrome mouse model with a large maternal deletion from Ube3a to Gabrb3.

21 January 2018

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Production of ultrasonic vocalizations by Peromyscus mice in the wild

21 January 2018

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Differences in ultrasonic vocalizations between wild and laboratory California mice (Peromyscus californicus)

21 January 2018

1 reference

The Autistic Neuron: Troubled Translation?

21 January 2018

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Defective body-weight regulation, motor control and abnormal social interactions in Mecp2 hypomorphic mice

21 January 2018

1 reference

Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia

21 January 2018

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Pten regulates neuronal arborization and social interaction in mice

21 January 2018

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X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family

21 January 2018

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Ube3a mRNA and protein expression are not decreased in Mecp2R168X mutant mice

21 January 2018

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Familial deletion within NLGN4 associated with autism and Tourette syndrome

21 January 2018

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Aberrant responses to acoustic stimuli in mice deficient for neural recognition molecule NB-2

21 January 2018

1 reference

The HMG-CoA reductase inhibitor lovastatin reverses the learning and attention deficits in a mouse model of neurofibromatosis type 1

21 January 2018

1 reference

The use of a plus-maze to measure anxiety in the mouse

21 January 2018

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Structural variation of chromosomes in autism spectrum disorder

21 January 2018

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Enhanced anxiety and stress-induced corticosterone release are associated with increased Crh expression in a mouse model of Rett syndrome

21 January 2018

1 reference

A mouse model of tuberous sclerosis: neuronal loss of Tsc1 causes dysplastic and ectopic neurons, reduced myelination, seizure activity, and limited survival

21 January 2018

1 reference

Contribution of SHANK3 mutations to autism spectrum disorder

21 January 2018

1 reference

Abnormalities of social interactions and home-cage behavior in a mouse model of Rett syndrome

21 January 2018

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Learning and memory and synaptic plasticity are impaired in a mouse model of Rett syndrome

21 January 2018

1 reference

Identifying autism loci and genes by tracing recent shared ancestry

21 January 2018

1 reference

Abnormal behavior in a chromosome-engineered mouse model for human 15q11-13 duplication seen in autism

21 January 2018

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A seizure-prone phenotype is associated with altered free-running rhythm in Pten mutant mice

21 January 2018

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Haploinsufficiency for Pten and Serotonin transporter cooperatively influences brain size and social behavior

21 January 2018

1 reference

Reversal of sensorimotor gating abnormalities in Fmr1 knockout mice carrying a human Fmr1 transgene

21 January 2018

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Mecp2 deficiency is associated with learning and cognitive deficits and altered gene activity in the hippocampal region of mice

21 January 2018

1 reference

An altered neonatal behavioral phenotype in Mecp2 mutant mice

21 January 2018

1 reference

Functional impact of global rare copy number variation in autism spectrum disorders

21 January 2018

1 reference

Neuroligin-3-deficient mice: model of a monogenic heritable form of autism with an olfactory deficit.

21 January 2018

1 reference

Enriched environment promotes behavioral and morphological recovery in a mouse model for the fragile X syndrome.

21 January 2018

1 reference

Mouse models of Rett syndrome: from behavioural phenotyping to preclinical evaluation of new therapeutic approaches

21 January 2018

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

21 January 2018

1 reference

Disruption of contactin 4 in three subjects with autism spectrum disorder

21 January 2018

1 reference

Neurocognitive dysfunction in children with neurofibromatosis type 1.

21 January 2018

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A partial loss of function allele of methyl-CpG-binding protein 2 predicts a human neurodevelopmental syndrome

21 January 2018

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Evidence for abnormal early development in a mouse model of Rett syndrome.

21 January 2018

1 reference

Unusual repertoire of vocalizations in the BTBR T+tf/J mouse model of autism

21 January 2018

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Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3

21 January 2018

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Adult reversal of cognitive phenotypes in neurodevelopmental disorders

21 January 2018

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A mouse model for the learning and memory deficits associated with neurofibromatosis type I

21 January 2018

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Behavioural phenotyping assays for mouse models of autism

21 January 2018

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Exaggerated behavioral phenotypes in Fmr1/Fxr2 double knockout mice reveal a functional genetic interaction between Fragile X-related proteins

21 January 2018

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Social behavior in Fmr1 knockout mice carrying a human FMR1 transgene

21 January 2018

1 reference

Behavioral and anatomical abnormalities in Mecp2 mutant mice: a model for Rett syndrome.

21 January 2018

1 reference

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

21 January 2018

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

21 January 2018

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Impaired motor coordination in mice lacking neural recognition molecule NB-3 of the contactin/F3 subgroup

21 January 2018

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Key role for gene dosage and synaptic homeostasis in autism spectrum disorders

21 January 2018

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Astrocyte-specific TSC1 conditional knockout mice exhibit abnormal neuronal organization and seizures

21 January 2018

1 reference

Rescue of neurological deficits in a mouse model for Angelman syndrome by reduction of alphaCaMKII inhibitory phosphorylation.

21 January 2018

1 reference

Analysis of four neuroligin genes as candidates for autism.

21 January 2018

1 reference

Altered ultrasonic vocalizations in a tuberous sclerosis mouse model of autism

21 January 2018

1 reference

A mouse model of the human Fragile X syndrome I304N mutation

21 January 2018

1 reference

Pharmacological inhibition of mTORC1 suppresses anatomical, cellular, and behavioral abnormalities in neural-specific Pten knock-out mice

21 January 2018

1 reference

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

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/AUR.175

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24 August 2017

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