Background Autism spectrum disorders affect more than one percent of the population, impairing social communication and increasing stereotyped behaviours. A micro-deletion of the 16p11.2 BP4-BP5 chromosomic region has been identified in one percent of patients also displaying intellectual disabilities. In mouse models generated to understand the mechanisms of this deletion, learning and memory deficits were pervasive in most genetic backgrounds, while social communication deficits were only detected in some models. Based on previous study (Arbogast et al. 2016 PLoS genetics), we selected the mouse model of 16p11.2 deletion on a hybrid C57BL/6NxC3B genetic background to itemize the social deficits. We examined whether behavioural deficits ob...
Background Quantitative genetic analysis of basic mouse behaviors is a powerful tool to identify nov...
Profound impairment in social interaction is a core symptom of autism, a severe neurodevelopmental d...
The Potocki-Lupski syndrome (PTLS) is associated with a microduplication of 17p11.2. Clinical featur...
International audienceAutism spectrum disorder (ASD) is a neurodevelopmental condition primarily cha...
Autism spectrum disorder (ASD) is a neurodevelopmental condition primarily characterised by alterati...
Autism spectrum disorder (ASD) is a neurodevelopmental condition primarily characterised by alterati...
International audienceMutations in NLGN4X have been identified in individuals with autism spectrum d...
<p>Intriguingly, two of the key behavioral phenotypes (social interaction and social preference) of ...
There are no current treatments for autism, despite its high prevalence. Deletions of chromosome 16p...
Autism spectrum disorders (ASD) are marked by impairments in social interactions, including reduced ...
There are no current treatments for autism, despite its high prevalence. Deletions of chromosome 16p...
BACKGROUND: Quantitative genetic analysis of basic mouse behaviors is a powerful tool to identify no...
Autism is a severe neurodevelopmental disorder, which typically emerges early in childhood. The core...
Autism spectrum disorder (ASD) is a neurodevelopmental disorder typified by impaired social communic...
The Potocki-Lupski syndrome (PTLS) is associated with a microduplication of 17p11.2. Clinical featur...
Background Quantitative genetic analysis of basic mouse behaviors is a powerful tool to identify nov...
Profound impairment in social interaction is a core symptom of autism, a severe neurodevelopmental d...
The Potocki-Lupski syndrome (PTLS) is associated with a microduplication of 17p11.2. Clinical featur...
International audienceAutism spectrum disorder (ASD) is a neurodevelopmental condition primarily cha...
Autism spectrum disorder (ASD) is a neurodevelopmental condition primarily characterised by alterati...
Autism spectrum disorder (ASD) is a neurodevelopmental condition primarily characterised by alterati...
International audienceMutations in NLGN4X have been identified in individuals with autism spectrum d...
<p>Intriguingly, two of the key behavioral phenotypes (social interaction and social preference) of ...
There are no current treatments for autism, despite its high prevalence. Deletions of chromosome 16p...
Autism spectrum disorders (ASD) are marked by impairments in social interactions, including reduced ...
There are no current treatments for autism, despite its high prevalence. Deletions of chromosome 16p...
BACKGROUND: Quantitative genetic analysis of basic mouse behaviors is a powerful tool to identify no...
Autism is a severe neurodevelopmental disorder, which typically emerges early in childhood. The core...
Autism spectrum disorder (ASD) is a neurodevelopmental disorder typified by impaired social communic...
The Potocki-Lupski syndrome (PTLS) is associated with a microduplication of 17p11.2. Clinical featur...
Background Quantitative genetic analysis of basic mouse behaviors is a powerful tool to identify nov...
Profound impairment in social interaction is a core symptom of autism, a severe neurodevelopmental d...
The Potocki-Lupski syndrome (PTLS) is associated with a microduplication of 17p11.2. Clinical featur...