AUTS2 isoforms control neuronal differentiation | Molecular Psychiatry
Auts2 deletion involves in DG hypoplasia and social recognition deficit: The developmental and neural circuit mechanisms | Science Advances
Frontiers | AUTS2 Syndrome: Molecular Mechanisms and Model Systems
AUTS2 (autism susceptibility candidate 2)
Frontiers | AUTS2 Syndrome: Molecular Mechanisms and Model Systems
NRF1 Association with AUTS2-Polycomb Mediates Specific Gene Activation in the Brain | bioRxiv
AUTS2 transcripts and protein isoforms. (A) The full-length AUTS2... | Download Scientific Diagram
Cells | Free Full-Text | AUTS2 Gene: Keys to Understanding the Pathogenesis of Neurodevelopmental Disorders
Cytoskeletal Regulation by AUTS2 in Neuronal Migration and Neuritogenesis - ScienceDirect
Auts2 deletion involves in DG hypoplasia and social recognition deficit: The developmental and neural circuit mechanisms | Science Advances
Mutations in Auts2 cause increased cell death during in vitro... | Download Scientific Diagram
AUTS2 Gene - GeneCards | AUTS2 Protein | AUTS2 Antibody
AUTS2 Gene - GeneCards | AUTS2 Protein | AUTS2 Antibody
Function and Regulation of AUTS2, a Gene Implicated in Autism and Human Evolution | PLOS Genetics
Cells | Free Full-Text | AUTS2 Gene: Keys to Understanding the Pathogenesis of Neurodevelopmental Disorders
AUTS2 Syndrome - Promoting Research | Facebook
Large study catalogs effects of autism candidate gene's loss | Spectrum | Autism Research News
NRF1 Association with AUTS2-Polycomb Mediates Specific Gene Activation in the Brain | bioRxiv
NRF1 association with AUTS2-Polycomb mediates specific gene activation in the brain - ScienceDirect
AUTS2 Controls Neuronal Lineage Choice Through a Novel PRC1-Independent Complex and BMP Inhibition | SpringerLink
Genes | Free Full-Text | Whole Exome Sequencing Reveals a Novel AUTS2 In-Frame Deletion in a Boy with Global Developmental Delay, Absent Speech, Dysmorphic Features, and Cerebral Anomalies
Exonic Deletions in AUTS2 Cause a Syndromic Form of Intellectual Disability and Suggest a Critical Role for the C Terminus - ScienceDirect
AUTS2 (autism susceptibility candidate 2)
De novo small deletion affecting transcription start site of short isoform of AUTS2 gene in a patient with syndromic neurodevelopmental defects - Martinez‐Delgado - 2021 - American Journal of Medical Genetics Part
Modeling AUTS2 syndrome using cerebral organoids. (A) AUTS2 mutant... | Download Scientific Diagram
