Top View
- Regulated Dynamic Trafficking of Neurexins Inside and Outside of Synaptic Terminals
- An Exploration of the FOXP2 Gene, Songbird Development, Human Language, and Autism
- Astrocytic Neurexin-1 Orchestrates Functional Synapse Assembly
- 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
- The Structure of Neurexin 1Α (N1α) and Its Role As Synaptic Organizer
- Neurexins and New Synapses
- Scientists Finger Neurexin 1 Defects in Autism
- Diversity and Specificity of Actions of Slit2 Proteolytic Fragments in Axon
- The Structures of Synaptic Cell Adhesion Proteins Neuroligin-1 In
- Autism Spectrum Disorder Susan L
- Autistic Phenotypes and Genetic Testing: State-Of-The- Art for the Clinical Geneticist C Lintas, a M Persico
- Autism Spectrum Disorders: Etiology and Pathology
- Foxp2 and Vocalization
- Neurexin Is Expressed on Nerves, but Not at Nerve Terminals, in the Electric Organ
- The Beta-Neurexin-Neuroligin Link
- Craig M. Powell, MD, Ph.D
- Molecular Characterization of NRXN1 Deletions from 19,263 Clinical Microarray Cases Identifies Exons Important for Neurodevelopmental Disease Expression
- The Soluble Neurexin-1Β Ectodomain Causes Calcium Influx And
- Phenotype Correlations of NRXN1 Exon Deletions
- Genetic Testing for Autism Predisposition: Ethical, Legal, And
- 2P16.3 (NRXN1) Deletions
- Synaptic Proteins and Receptors Defects in Autism Spectrum Disorders
- An Autism-Associated Mutation Impairs Neuroligin-4 Glycosylation and Enhances Excitatory Synaptic Transmission in Human Neurons
- Is NRXN1 Gene Expression an Important Marker of Treatment of Depressive Disorders? a Pilot Study
- The Role of Epilepsy and Epileptiform Eegs in Autism Spectrum Disorders
- A Parent's Guide to Autism Spectrum Disorder
- FOXP2 and Language Alterations in Psychiatric Pathology
- Rare Deletions at the Neurexin 3 Locus in Autism Spectrum Disorder
- Recent Update of Autism Spectrum Disorders
- Neuroligin-Deficient Mutants of C. Elegans Have Sensory Processing Deficits and Are Hypersensitive to Oxidative Stress and Mercury Toxicity
- Foxp2 in Songbirds
- The Neurexin Superfamily of Caenorhabditis Elegans
- Candidate Genes for Inherited Autism Susceptibility in the Lebanese Population Received: 11 November 2016 Silva Kourtian1,2,*, Jihane Soueid1,*, Nadine J
- Snapshot: Neuroligin-Neurexin Complexes Stéphane Baudouin and Peter Scheiffele Biozentrum of the University of Basel, 4056 Basel, Switzerland
- FOXP2 and Language Alterations in Psychiatric Pathology