SummaryMutations in the Autism susceptibility candidate 2 gene (AUTS2), whose protein is believed to act in neuronal cell nuclei, have been associated with multiple psychiatric illnesses, including autism spectrum disorders, intellectual disability, and schizophrenia. Here we show that cytoplasmic AUTS2 is involved in the regulation of the cytoskeleton and neural development. Immunohistochemistry and fractionation studies show that AUTS2 localizes not only in nuclei, but also in the cytoplasm, including in the growth cones in the developing brain. AUTS2 activates Rac1 to induce lamellipodia but downregulates Cdc42 to suppress filopodia. Our loss-of-function and rescue experiments show that a cytoplasmic AUTS2-Rac1 pathway is involved in cor...
The autism susceptibility candidate 2 (AUTS2) gene is associated with multiple neurological diseases...
The development of neuronal connectivity requires the careful orchestration of multiple cellular pro...
AUTS2 was originally discovered as the gene disrupted by a translocation in human twins with Autism ...
Mutations in the Autism susceptibility candidate 2 gene (AUTS2), whose protein is believed to act in...
SummaryMutations in the Autism susceptibility candidate 2 gene (AUTS2), whose protein is believed to...
Neuronal migration is one of the pivotal steps to form a functional brain, and disorganization of th...
Neurodevelopmental disorders (NDDs), including autism spectrum disorders (ASD) and intellectual disa...
Autism susceptibility candidate 2 (Auts2) is a gene associated with autism and mental retardation, w...
AUTS2 syndrome is a genetic disorder that causes intellectual disability, microcephaly, and other ph...
Thesis (Ph.D.)--University of Washington, 2018Variants in the gene Autism Susceptibility Candidate 2...
Autism spectrum disorder is a heterogeneous disease, and numerous alterations of gene expression com...
Naturally occurring variations of Polycomb Repressive Complex 1 (PRC1) comprise a core assembly of P...
The Autism Susceptibility Candidate 2 (AUTS2) gene is a critical neuronal gene that is involved in s...
The autism susceptibility candidate 2 (AUTS2) gene is associated with multiple neurological diseases...
Autism susceptibility candidate 2 (AUTS2), a risk gene for autism spectrum disorders (ASDs), is impl...
The autism susceptibility candidate 2 (AUTS2) gene is associated with multiple neurological diseases...
The development of neuronal connectivity requires the careful orchestration of multiple cellular pro...
AUTS2 was originally discovered as the gene disrupted by a translocation in human twins with Autism ...
Mutations in the Autism susceptibility candidate 2 gene (AUTS2), whose protein is believed to act in...
SummaryMutations in the Autism susceptibility candidate 2 gene (AUTS2), whose protein is believed to...
Neuronal migration is one of the pivotal steps to form a functional brain, and disorganization of th...
Neurodevelopmental disorders (NDDs), including autism spectrum disorders (ASD) and intellectual disa...
Autism susceptibility candidate 2 (Auts2) is a gene associated with autism and mental retardation, w...
AUTS2 syndrome is a genetic disorder that causes intellectual disability, microcephaly, and other ph...
Thesis (Ph.D.)--University of Washington, 2018Variants in the gene Autism Susceptibility Candidate 2...
Autism spectrum disorder is a heterogeneous disease, and numerous alterations of gene expression com...
Naturally occurring variations of Polycomb Repressive Complex 1 (PRC1) comprise a core assembly of P...
The Autism Susceptibility Candidate 2 (AUTS2) gene is a critical neuronal gene that is involved in s...
The autism susceptibility candidate 2 (AUTS2) gene is associated with multiple neurological diseases...
Autism susceptibility candidate 2 (AUTS2), a risk gene for autism spectrum disorders (ASDs), is impl...
The autism susceptibility candidate 2 (AUTS2) gene is associated with multiple neurological diseases...
The development of neuronal connectivity requires the careful orchestration of multiple cellular pro...
AUTS2 was originally discovered as the gene disrupted by a translocation in human twins with Autism ...