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Publikováno v:
Autism Research. 13:352-368
Genetic mutations are the major pathogenic factor of Autism Spectrum Disorder (ASD). In recent years, more and more ASD risk genes have been revealed, among which there are a group of transcriptional regulators. Considering the similarity of the core
Publikováno v:
Autism Research. 12:1322-1333
Copy number variations (CNVs) at the 16p11.2 chromosomal region are associated with myriad clinical features including intellectual disability and autism spectrum disorder. The aim of this study is to determine whether 16p11.2 deletion (DEL) and dupl
Autor:
Shlomit Levi, Lubov Nemanov, David Mankuta, Richard P. Ebstein, Maya Yaari, Salomon Israel, Yirmiya Nurit, Elad Lerer
Publikováno v:
Autism Research. 3:293-302
Background: Impairments in social processes characterize one of the core deficits in autism spectrum disorders (ASD) and accumulating evidence suggests that oxytocin neurotransmission is implicated in mediating social adaptation in ASD. Using a mouse