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NRXN3
Synaptic Modulators Nrxn1 and Nrxn3 Are Disregulated in a Disc1 Mouse
ADHD) Gene Networks in Children of Both African American and European American Ancestry
Association of Neurexin 3 Polymorphisms with Smoking Behavior
Transcriptomic Causal Networks Identified Patterns of Differential Gene Regulation in Human Brain from Schizophrenia Cases Versus Controls
Cartography of Neurexin Alternative Splicing Mapped by Single
Widespread Sex Differences in Gene Expression and Splicing in the Adult Human Brain
Peripheral Nerve Single-Cell Analysis Identifies Mesenchymal Ligands That Promote Axonal Growth
Patterns of Sequence Conservation in Presynaptic Neural Genes
Downloaded from 4D Nucleome Portal 1346 (
Significance of Neurexin and Neuroligin Polymorphisms in Regulating Risk of Hirschsprung’S Disease Yanhong Li, Hui Liu, Yubin Dong
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
Specification of Synaptic Connectivity by Cell Surface Interactions
Neuroligin-1 Is Altered in the Hippocampus of Alzheimer's Disease Patients and Mouse Models, and Modulates the Toxicity of Amyloid-Beta Oligomers
Familial Deletion Within NLGN4 Associated with Autism and Tourette Syndrome
The Contribution of Rare and Common Variants in 30 Genes to Risk Nicotine Dependence
Mouse Nrxn3 Conditional Knockout Project (CRISPR/Cas9)
A 14Q31.1-Q32.11 Deletion Case: Genotype – Neurological Phenotype Correlations in 14Q Interstitial Deletion Syndrome
Interstitial 14Q24.3 to Q31.3 Deletion in a 6-Year-Old Boy with a Non-Specific Dysmorphic Phenotype
Top View
Polymorphisms in NRXN3, TFAP2B, MSRA, LYPLAL1, FTO and MC4R and Their Effect on Visceral Fat Area in the Japanese Population
Aerobic Exercise Induces Alternative Splicing of Neurexins in Frontal Cortex
Divergent Roles of ALS-Linked Proteins FUS/TLS and TDP-43 Intersect In
Data-Driven and Knowledge-Driven Computational Models of Angiogenesis in Application to Peripheral Arterial Disease
Modeling the Functional Genomics of Autism Using Human Neurons
Interstitial 14Q24.3 to Q31.3 Deletion in a 6-Year-Old Boy With
2P16.3 (NRXN1) Deletions
Is NRXN1 Gene Expression an Important Marker of Treatment of Depressive Disorders? a Pilot Study
NRXN3 Antibody (RQ6203)
Rare Deletions at the Neurexin 3 Locus in Autism Spectrum Disorder
Principles Governing DNA Methylation During Neuronal Lineage and Subtype Specification
Inbreeding and Inbreeding Depression in Linebred Beef Cattle (PDF)
Human Neurexin-3-Beta / NRXN3 Protein (Fc Tag)
Neurexin 3 Transmembrane and Soluble Isoform Expression And
Supplementary Table 1. a Full List of Cancer Genes
Stem Cells Pinpoint Players in Nerve Cell Development