Frontiers | NRXN1 Deletion and Exposure to Methylmercury Increase Astrocyte Differentiation by Different Notch-Dependent Transcriptional Mechanisms
Phenotypic spectrum and genotype–phenotype correlations of NRXN1 exon deletions | European Journal of Human Genetics
A common cognitive, psychiatric, and dysmorphic phenotype in carriers of NRXN1 deletion - Viñas‐Jornet - 2014 - Molecular Genetics & Genomic Medicine - Wiley Online Library
Neurexin 1 (NRXN1) Deletions in Schizophrenia
Organization of the human NRXN1 gene as described by Rowen et al... | Download Scientific Diagram
Neurexin 1 variants as risk factors for suicide death | Molecular Psychiatry
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
NRXN1 | Science Over a Cuppa
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
2p16.3 (NRXN1) deletions
NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody
JPM | Free Full-Text | Is NRXN1 Gene Expression an Important Marker of Treatment of Depressive Disorders? A Pilot Study
NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody
Identification of Nrxn1γ protein as a Nrxn1 gene-derived CA10 receptor.... | Download Scientific Diagram
NRXN1 Membrane Protein Introduction - Creative Biolabs
Phenotypic spectrum of NRXN1 mono‐ and bi‐allelic deficiency: A systematic review - Castronovo - 2020 - Clinical Genetics - Wiley Online Library
Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression | Genetics in Medicine
Neurexins (such as NRXN1), neuroligins (such as NLGN4) and... | Download Scientific Diagram
A deletion of approximately 70 kb encompassing two exons (3,4) from the... | Download Scientific Diagram
Cross-platform validation of neurotransmitter release impairments in schizophrenia patient-derived NRXN1-mutant neurons
Allelic contribution of Nrxn1α to autism-relevant behavioral phenotypes in mice | PLOS Genetics
A case-control association study of NRXN1 polymorphisms with schizophrenia in Chinese Han population | Behavioral and Brain Functions | Full Text
NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody
