Organization of the human NRXN1 gene as described by Rowen et al... | Download Scientific Diagram
Impairments Found In Neurons Derived From People With Schizophrenia and Genetic Mutation - Neuroscience News
NRXN1 | Science Over a Cuppa
Genes | Free Full-Text | Computational Saturation Mutagenesis to Investigate the Effects of Neurexin-1 Mutations on AlphaFold Structure
NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody
Mutation Screening and Copy Number Detection of NRXN1 in Chinese Han Patients with Autism
Figure 1 from Resequencing and follow-up of neurexin 1 (NRXN1) in schizophrenia patients | Semantic Scholar
Dysregulation of NRXN1 by mutant MIR8485 leads to calcium overload in pre-synapses inducing neurodegeneration in Multiple sclerosis - ScienceDirect
NRXN1 - Wikipedia
Genetic insights and neurobiological implications from NRXN1 in neuropsychiatric disorders | Molecular Psychiatry
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
Neuronal impact of patient-specific aberrant NRXN1α splicing | Nature Genetics
Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopm
Human Neuropsychiatric Disease Modeling using Conditional Deletion Reveals Synaptic Transmission Defects Caused by Heterozygous
2p16.3 (NRXN1) deletions
NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody
NRXN1 - Wikipedia
Identification of Nrxn1γ protein as a Nrxn1 gene-derived CA10 receptor.... | Download Scientific Diagram
Neurexins (such as NRXN1), neuroligins (such as NLGN4) and... | Download Scientific Diagram
Schizophrenia-associated NRXN1 deletions induce developmental-timing- and cell-type-specific vulnerabilities in human brain organoids | bioRxiv
Information about each variant of interest in NRXN1. a Diagram of... | Download Scientific Diagram
NRXN1 (neurexin 1) | Gene Report | BioGPS
Human Neuropsychiatric Disease Modeling using Conditional Deletion Reveals Synaptic Transmission Defects Caused by Heterozygous Mutations in NRXN1 - ScienceDirect
A common cognitive, psychiatric, and dysmorphic phenotype in carriers of NRXN1 deletion - Viñas‐Jornet - 2014 - Molecular Genetics & Genomic Medicine - Wiley Online Library
