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NRXN1
Synaptic Modulators Nrxn1 and Nrxn3 Are Disregulated in a Disc1 Mouse
Genome-Wide Copy Number Variation Analysis in a Chinese Autism
Mycobacterium Tuberculosis-Induced Maternal Immune Activation Promotes Autism-Like Phenotype in Infected Mice Offspring
Cartography of Neurexin Alternative Splicing Mapped by Single
Molecular Mechanisms: Researchers Light up Interactions Between Neurons
Investigation of NRXN1 Deletions: Clinical and Molecular Characterization Mindy Preston Dabell,1 Jill A
Khdrbs1 Mouse Shrna Plasmid (Locus ID 20218) Product Data
Significance of Neurexin and Neuroligin Polymorphisms in Regulating Risk of Hirschsprung’S Disease Yanhong Li, Hui Liu, Yubin Dong
Mutations in NRXN1 and NRXN2 in a Patient with Early-Onset Epileptic Encephalopathy and Respiratory Depression
Astrocytic Neurexin-1 Orchestrates Functional Synapse Assembly
Topoisomerase 1 Inhibition Reversibly Impairs Synaptic Function
Neurexin1 – Nrxn1 Knockout Rat
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
Proteolytic Processing of Neurexins by Presenilins Sustains Synaptic Vesicle Release
Scientists Finger Neurexin 1 Defects in Autism
Anti-KHDRBS1 (Aa 331-348) Polyclonal Antibody (CABT-B1716) This Product Is for Research Use Only and Is Not Intended for Diagnostic Use
Aerobic Exercise Induces Alternative Splicing of Neurexins in Frontal Cortex
Functional Characterization of Rare NRXN1 Variants Identified in Autism
Top View
CNTNAP2 and NRXN1 Are Mutated in Autosomal-Recessive Pitt-Hopkins-Like Mental Retardation and Determine the Level of a Common Synaptic Protein in Drosophila
Investigation of Copy Number Variation by Arraycgh in Turkish Children and Adolescents Diagnosed with Autism Spectrum Disorders
Molecular Characterization of NRXN1 Deletions from 19,263 Clinical Microarray Cases Identifies Exons Important for Neurodevelopmental Disease Expression
Phenotype Correlations of NRXN1 Exon Deletions
Deletions of NRXN1 (Neurexin?1) Predispose to a Wide Spectrum Of
Sam68 Promotes Self-Renewal and Glycolytic Metabolism in Mouse Neural Progenitor Cells By
Mouse Khdrbs1 Antibody (C-Term) Affinity Purified Rabbit Polyclonal Antibody (Pab) Catalog # Ap19343b
2016 17-22 Mutation Analysis of the Nrxn1 Gene in Autism
2P16.3 (NRXN1) Deletions
Is NRXN1 Gene Expression an Important Marker of Treatment of Depressive Disorders? a Pilot Study
Rare Structural Variation of Synapse and Neurotransmission Genes In
Rare Deletions at the Neurexin 3 Locus in Autism Spectrum Disorder
Khdrbs1 (NM 011317) Mouse Untagged Clone Product Data
Transcription Factor Expression Defines Subclasses of Developing Projection Neurons Highly Similar to Single-Cell RNA-Seq Subtypes
Snapshot: Neuroligin-Neurexin Complexes Stéphane Baudouin and Peter Scheiffele Biozentrum of the University of Basel, 4056 Basel, Switzerland
LAR-Rptps Directly Interact with Neurexins to Coordinate Bidirectional Assembly of Molecular Machineries
Supplementary Methods Functional Characterization of Rare NRXN1