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AUTS2 isoforms control neuronal differentiation | Molecular Psychiatry
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 the AUTS2 genomic region. Human accelerated sequences are... | Download Scientific Diagram
Analysis of syndrome weakens gene's link to autism | Spectrum | Autism Research News
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
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
Anti-AUTS2 antibody produced in rabbit Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution | Sigma-Aldrich
Schematic of AUTS2 genomic region and the protein structure of AUTS2... | Download Scientific Diagram
Genome-wide distribution of Auts2 binding localizes with active neurodevelopmental genes | Translational Psychiatry
NRF1 Association with AUTS2-Polycomb Mediates Specific Gene Activation in the Brain | bioRxiv
AUTS2 Regulation of Synapses for Proper Synaptic Inputs and Social Communication - ScienceDirect
AUTS2 (autism susceptibility candidate 2)
AUTS2 Gene - GeneCards | AUTS2 Protein | AUTS2 Antibody
Frontiers | Untangle the Multi-Facet Functions of Auts2 as an Entry Point to Understand Neurodevelopmental Disorders
AUTS2 Controls Neuronal Lineage Choice Through a Novel PRC1-Independent Complex and BMP Inhibition | SpringerLink
Schematic of AUTS2 genomic region and the protein structure of AUTS2... | Download Scientific Diagram
AUTS2 Gene - GeneCards | AUTS2 Protein | AUTS2 Antibody
Sebastian's Story: Defining AUTS2
Function and Regulation of AUTS2, a Gene Implicated in Autism and Human Evolution | PLOS Genetics
Auts2 deletion involves in DG hypoplasia and social recognition deficit: The developmental and neural circuit mechanisms | Science Advances
A detailed clinical analysis of 13 patients with AUTS2 syndrome further delineates the phenotypic spectrum and underscores the behavioural phenotype | Journal of Medical Genetics
NRF1 association with AUTS2-Polycomb mediates specific gene activation in the brain
Frontiers | AUTS2 Syndrome: Molecular Mechanisms and Model Systems
AUTS2 Syndrome - Promoting Research | Facebook
Frontiers | AUTS2 Syndrome: Molecular Mechanisms and Model Systems
Cytoskeletal Regulation by AUTS2 in Neuronal Migration and Neuritogenesis - ScienceDirect
Exonic Deletions in AUTS2 Cause a Syndromic Form of Intellectual Disability and Suggest a Critical Role for the C Terminus - ScienceDirect