Identification of Nrxn1γ protein as a Nrxn1 gene-derived CA10 receptor.... | Download Scientific Diagram
Cross-platform validation of neurotransmitter release impairments in schizophrenia patient-derived NRXN1-mutant neurons
Organization of the human NRXN1 gene as described by Rowen et al... | Download Scientific Diagram
Allelic contribution of Nrxn1α to autism-relevant behavioral phenotypes in mice | PLOS Genetics
NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody
NRXN1 deletions and the double hit hypothesis of idiopathic epilepsy | Beyond the Ion Channel
Human Neuropsychiatric Disease Modeling using Conditional Deletion Reveals Synaptic Transmission Defects Caused by Heterozygous Mutations in NRXN1 - ScienceDirect
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
Schizophrenia is associated with somatic muta | EurekAlert!
Dysregulation of NRXN1 by mutant MIR8485 leads to calcium overload in pre-synapses inducing neurodegeneration in Multiple sclerosis - ScienceDirect
Disruption of Neurexin 1 Associated with Autism Spectrum Disorder - ScienceDirect
Information about each variant of interest in NRXN1. a Diagram of... | Download Scientific Diagram
A case-control association study of NRXN1 polymorphisms with schizophrenia in Chinese Han population | Behavioral and Brain Functions | Full Text
NRXN1 | Science Over a Cuppa
Neurexins (such as NRXN1), neuroligins (such as NLGN4) and... | Download Scientific Diagram
Phenotypic spectrum and genotype–phenotype correlations of NRXN1 exon deletions | European Journal of Human Genetics
NRXN1 - Wikipedia
Phenotypic spectrum of NRXN1 mono‐ and bi‐allelic deficiency: A systematic review - Castronovo - 2020 - Clinical Genetics - Wiley Online Library
Frontiers | NRXN1 Deletion and Exposure to Methylmercury Increase Astrocyte Differentiation by Different Notch-Dependent Transcriptional Mechanisms
Human Neuropsychiatric Disease Modeling using Conditional Deletion Reveals Synaptic Transmission Defects Caused by Heterozygous
Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression | Genetics in Medicine
Neurexin 1 (NRXN1) Deletions in Schizophrenia
Genetic insights and neurobiological implications from NRXN1 in neuropsychiatric disorders | Molecular Psychiatry
NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody
Neuronal impact of patient-specific aberrant NRXN1α splicing | Nature Genetics
