Cross-platform validation of neurotransmitter release impairments in schizophrenia patient-derived NRXN1-mutant neurons
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
Human Neuropsychiatric Disease Modeling using Conditional Deletion Reveals Synaptic Transmission Defects Caused by Heterozygous
Cross-Platform Validation of Neurotransmitter Release Impairments in Schizophrenia Patient-Derived NRXN1-Mutant Neurons | bioRxiv
Neurexin 1 variants as risk factors for suicide death | Molecular Psychiatry
NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody
NRXN1 Membrane Protein Introduction - Creative Biolabs
Schizophrenia is associated with somatic muta | EurekAlert!
Identification of Nrxn1γ protein as a Nrxn1 gene-derived CA10 receptor.... | Download Scientific Diagram
Neurexin 1 (NRXN1) Deletions in Schizophrenia
Neurexins (such as NRXN1), neuroligins (such as NLGN4) and... | Download Scientific Diagram
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
Table 1 from Resequencing and follow-up of neurexin 1 (NRXN1) in schizophrenia patients | Semantic Scholar
2p16.3 (NRXN1) deletions
A case-control association study of NRXN1 polymorphisms with schizophrenia in Chinese Han population | Behavioral and Brain Functions | Full Text
A deletion of approximately 70 kb encompassing two exons (3,4) from the... | Download Scientific Diagram
Genetic insights and neurobiological implications from NRXN1 in neuropsychiatric disorders | Molecular Psychiatry
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
Human Neuropsychiatric Disease Modeling using Conditional Deletion Reveals Synaptic Transmission Defects Caused by Heterozygous Mutations in NRXN1 - ScienceDirect
JPM | Free Full-Text | Is NRXN1 Gene Expression an Important Marker of Treatment of Depressive Disorders? A Pilot Study
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
Neuronal impact of patient-specific aberrant NRXN1α splicing | Nature Genetics
NRXN1 | Science Over a Cuppa
