| Literature DB >> 28167097 |
Abstract
Autism spectrum disorder (ASD) is the most commonly diagnosed neurodevelopmental disorder, with current estimates of more than 1% of affected children across nations. The patients form a highly heterogeneous group with only the behavioral phenotype in common. The genetic heterogeneity is reflected in a plethora of animal models representing multiple mutations found in families of affected children. Despite many years of scientific effort, for the majority of cases the genetic cause remains elusive. It is therefore crucial to include well-validated models of idiopathic autism in studies searching for potential therapeutic agents. One of these models is the BTBR T+Itpr3tf/J mouse. The current review summarizes data gathered in recent research on potential molecular mechanisms responsible for the autism-like behavioral phenotype of this strain.Entities:
Keywords: BTBR; Molecular mechanisms; Neuroanatomy; Pharmacological manipulations; Repetitive behavior; Social behavior
Mesh:
Year: 2017 PMID: 28167097 PMCID: PMC5403558 DOI: 10.1016/j.neubiorev.2016.12.037
Source DB: PubMed Journal: Neurosci Biobehav Rev ISSN: 0149-7634 Impact factor: 8.989