Schizophrenia is associated with somatic muta | EurekAlert!
Human Neuropsychiatric Disease Modeling using Conditional Deletion Reveals Synaptic Transmission Defects Caused by Heterozygous Mutations in NRXN1 - ScienceDirect
Neurexin 1 (NRXN1) Deletions in Schizophrenia
Neurexins (such as NRXN1), neuroligins (such as NLGN4) and... | Download Scientific Diagram
Frontiers | NRXN1 Deletion and Exposure to Methylmercury Increase Astrocyte Differentiation by Different Notch-Dependent Transcriptional Mechanisms
Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression | Genetics in Medicine
Human Neuropsychiatric Disease Modeling using Conditional Deletion Reveals Synaptic Transmission Defects Caused by Heterozygous
Organization of the human NRXN1 gene as described by Rowen et al... | Download Scientific Diagram
Genetic insights and neurobiological implications from NRXN1 in neuropsychiatric disorders | Molecular Psychiatry
Allelic contribution of Nrxn1α to autism-relevant behavioral phenotypes in mice | PLOS Genetics
CNTNAP2 and NRXN1 Are Mutated in Autosomal-Recessive Pitt-Hopkins-like Mental Retardation and Determine the Level of a Common Synaptic Protein in Drosophila - ScienceDirect
NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody
Deletions of NRXN1 (neurexin‐1) predispose to a wide spectrum of developmental disorders - Ching - 2010 - American Journal of Medical Genetics Part B: Neuropsychiatric Genetics - Wiley Online Library
Cross-platform validation of neurotransmitter release impairments in schizophrenia patient-derived NRXN1-mutant neurons
Further insight into the neurobehavioral pattern of children carrying the 2p16.3 heterozygous deletion involving NRXN1: Report of five new cases - Alfieri - 2020 - Genes, Brain and Behavior - Wiley Online Library
Neuronal impact of patient-specific aberrant NRXN1α splicing | Nature Genetics
NRXN1 deletions and the double hit hypothesis of idiopathic epilepsy | Beyond the Ion Channel
A deletion of approximately 70 kb encompassing two exons (3,4) from the... | Download Scientific Diagram
NRXN1 - Wikipedia
Neurexin 1 variants as risk factors for suicide death | Molecular Psychiatry
Dysregulation of NRXN1 by mutant MIR8485 leads to calcium overload in pre-synapses inducing neurodegeneration in Multiple sclerosis - ScienceDirect
Human Neuropsychiatric Disease Modeling using Conditional Deletion Reveals Synaptic Transmission Defects Caused by Heterozygous
JPM | Free Full-Text | Is NRXN1 Gene Expression an Important Marker of Treatment of Depressive Disorders? A Pilot Study
Cross-Platform Validation of Neurotransmitter Release Impairments in Schizophrenia Patient-Derived NRXN1-Mutant Neurons | bioRxiv
