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Disruption of Neurexin 1 Associated with Autism Spectrum Disorder - 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
NRXN1 Membrane Protein Introduction - Creative Biolabs
Identification of Nrxn1γ protein as a Nrxn1 gene-derived CA10 receptor.... | Download Scientific Diagram
Allelic contribution of Nrxn1α to autism-relevant behavioral phenotypes in mice | PLOS Genetics
NRXN1 deletions and the double hit hypothesis of idiopathic epilepsy | Beyond the Ion Channel
Table 1 from Resequencing and follow-up of neurexin 1 (NRXN1) in schizophrenia patients | Semantic Scholar
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
Dysregulation of NRXN1 by mutant MIR8485 leads to calcium overload in pre-synapses inducing neurodegeneration in Multiple sclerosis - ScienceDirect
A deletion of approximately 70 kb encompassing two exons (3,4) from the... | Download Scientific Diagram
NRXN1 | Science Over a Cuppa
Frontiers | NRXN1 Deletion and Exposure to Methylmercury Increase Astrocyte Differentiation by Different Notch-Dependent Transcriptional Mechanisms
Neurexins (such as NRXN1), neuroligins (such as NLGN4) and... | Download Scientific Diagram
Neurexin 1 variants as risk factors for suicide death | Molecular Psychiatry
Phenotypic spectrum of NRXN1 mono‐ and bi‐allelic deficiency: A systematic review - Castronovo - 2020 - Clinical Genetics - Wiley Online Library
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
NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody
A common cognitive, psychiatric, and dysmorphic phenotype in carriers of NRXN1 deletion - Viñas‐Jornet - 2014 - Molecular Genetics & Genomic Medicine - Wiley Online Library
Phenotypic spectrum and genotype–phenotype correlations of NRXN1 exon deletions | European Journal of Human Genetics