DOCSLIB.ORG
Explore
Sign Up
Log In
Upload
Search
Home
» Tags
» NLGN2
NLGN2
PSD-95 Binding Dynamically Regulates NLGN1 Trafficking and Function
Gabaergic Deficits and Schizophrenia-Like Behaviors in A
Neuroligin 2 Deletion Alters Inhibitory Synapse Function and Anxiety-Associated Neuronal Activation in the Amygdala
A Causal Gene Network with Genetic Variations Incorporating Biological Knowledge and Latent Variables
Orbitofrontal Neuroadaptations and Cross-Species Synaptic Biomarkers in Heavy-Drinking Macaques
1 a Novel Function for Neurexin and Neuroligin
An Automated Functional Annotation Pipeline That Rapidly Prioritizes Clinically Relevant Genes for Autism Spectrum Disorder
Neuroligin 1, 2, and 3 Regulation at the Synapse: FMRP-Dependent Translation and Activity-Induced Proteolytic Cleavage
Characterization of the Caspr2 and NLGN2 Ligands: a Proteomic and Biochemical Approach
Distinct Roles for Extracellular and Intracellular Domains in Neuroligin Function at Inhibitory Synapses Quynh-Anh Nguyen1,2, Meryl E Horn1,2, Roger a Nicoll1,3*
Neuronal Connectivity As a Convergent Target of Gene × Environment Interactions That Confer Risk for Autism Spectrum Disorders
Using Gene Ontology to Describe the Role of the Neurexin-Neuroligin-SHANK Complex in Human, Mouse and Rat and Its Relevance to Autism Patel Et Al
UNIVERSITY of CALIFORNIA RIVERSIDE a Comparison of Gene
Familial Deletion Within NLGN4 Associated with Autism and Tourette Syndrome
Three Classes of Recurrent DNA Break Clusters in Brain Progenitors Identified by 3D Proximity-Based Break Joining Assay
Autistic Phenotypes and Genetic Testing: State-Of-The- Art for the Clinical Geneticist C Lintas, a M Persico
Identification and Mechanistic Investigation of Recurrent Functional Genomic and Transcriptional Alterations in Advanced Prostat
Mutational Analysis of the Neurexin/Neuroligin Complex Reveals Essential and Regulatory Components
Top View
Circdym Prevents Chronic Neuropathic Pain by Competitive Inhibition of Nlgn2 Mrna Transport in Neurites
Unbalance Between Excitation and Inhibition in Phenylketonuria, a Genetic Metabolic Disease Associated with Autism
Distinct Transcriptomic Profiles in the Dorsal Hippocampus and Prelimbic
Trans Effects of Chromosome Aneuploidies on DNA Methylation
Structure-Function Relationships of Rna and Protein in Synaptic Plasticity
3-O-Sulfated Heparan Sulfate Interactors Target Synaptic Adhesion Molecules from Neonatal Mouse Brain and Inhibit Neural Activit
In Silico Insight Into Nucleosome Repositioning Via Oxygen Delivery and Extracellular Movement
Identification of Gene Ontologies Linked to Prefrontal–Hippocampal
Whole-Genome Deep Learning Analysis Reveals Causal Role of Noncoding Mutations in Autism
Trans Effects of Chromosome Aneuploidies on DNA Methylation Patterns in Human Down Syndrome and Mouse Models
Autism Genetics
ASTN2 Modulates Synaptic Strength by Trafficking and Degradation of Surface Proteins
Integrative Analysis Identified Key Schizophrenia Risk Factors from An
Open Chicheng Sun Thesis.Pdf
Three Classes of Recurrent DNA Break Clusters in Brain Progenitors Identified by 3D Proximity-Based Break Joining Assay
Cell-Type-Specific Role for Nucleus Accumbens Neuroligin-2 in Depression and Stress Susceptibility
1 a Gene Ontology Approach to Autism Spectrum Disorders
Anti-NLGN2 (RABBIT) Antibody - 600-401-DC7
1 Abnormal Social Behaviors and Dysfunction of Autism-Related Genes
Comparative Analysis of Autosomal and X-Linked Genes Involved in Nonspecific Cognitive Impairment