AUTS2 Monoclonal Antibody (CL7067) (MA5-31446)
Frontiers | AUTS2 Syndrome: Molecular Mechanisms and Model Systems
Frontiers | AUTS2 Syndrome: Molecular Mechanisms and Model Systems
A detailed clinical analysis of 13 patients with AUTS2 syndrome further delineates the phenotypic spectrum and underscores the behavioural phenotype | Journal of Medical Genetics
Schematic of AUTS2 genomic region and the protein structure of AUTS2... | Download Scientific Diagram
NRF1 association with AUTS2-Polycomb mediates specific gene activation in the brain
Cytoskeletal Regulation by AUTS2 in Neuronal Migration and Neuritogenesis - ScienceDirect
AUTS2 Gene - GeneCards | AUTS2 Protein | AUTS2 Antibody
AUTS2 (autism susceptibility candidate 2)
Sebastian's Story: Defining AUTS2
Function and Regulation of AUTS2, a Gene Implicated in Autism and Human Evolution | PLOS Genetics
AUTS2 isoforms control neuronal differentiation | Molecular Psychiatry
AUTS2 transcripts and protein isoforms. (A) The full-length AUTS2... | Download Scientific Diagram
NRF1 Association with AUTS2-Polycomb Mediates Specific Gene Activation in the Brain | bioRxiv
Auts2 deletion involves in DG hypoplasia and social recognition deficit: The developmental and neural circuit mechanisms | Science Advances
Autism Susceptibility Gene 2 Protein (AUTS2) Antibody | Abbexa Ltd
Exonic Deletions in AUTS2 Cause a Syndromic Form of Intellectual Disability and Suggest a Critical Role for the C Terminus - ScienceDirect
AUTS2 Regulation of Synapses for Proper Synaptic Inputs and Social Communication - ScienceDirect
Cells | Free Full-Text | AUTS2 Gene: Keys to Understanding the Pathogenesis of Neurodevelopmental Disorders
AUTS2 Controls Neuronal Lineage Choice Through a Novel PRC1-Independent Complex and BMP Inhibition | SpringerLink
A case of autism spectrum disorder with cleft lip and palate carrying a mutation in exon 8 of AUTS2 - Saeki - 2019 - Clinical Case Reports - Wiley Online Library
Two male adults with pathogenic AUTS2 variants, including a two-base pair deletion, further delineate the AUTS2 syndrome | European Journal of Human Genetics
Frontiers | AUTS2 Syndrome: Molecular Mechanisms and Model Systems
A detailed clinical analysis of 13 patients with AUTS2 syndrome further delineates the phenotypic spectrum and underscores the behavioural phenotype | Journal of Medical Genetics
AUTS2 Gene - GeneCards | AUTS2 Protein | AUTS2 Antibody
