NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody
Human Neuropsychiatric Disease Modeling using Conditional Deletion Reveals Synaptic Transmission Defects Caused by Heterozygous
Identification of Nrxn1γ protein as a Nrxn1 gene-derived CA10 receptor.... | Download Scientific Diagram
Dysregulation of NRXN1 by mutant MIR8485 leads to calcium overload in pre-synapses inducing neurodegeneration in Multiple sclerosis - ScienceDirect
Human Neuropsychiatric Disease Modeling using Conditional Deletion Reveals Synaptic Transmission Defects Caused by Heterozygous
Neurexins (such as NRXN1), neuroligins (such as NLGN4) and... | Download Scientific Diagram
NRXN1 | Science Over a Cuppa
Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression | Genetics in Medicine
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
Neurexin 1 variants as risk factors for suicide death | Molecular Psychiatry
Information about each variant of interest in NRXN1. a Diagram of... | Download Scientific Diagram
NRXN1 - Wikipedia
Organization of the human NRXN1 gene as described by Rowen et al... | Download Scientific Diagram
Human Neuropsychiatric Disease Modeling using Conditional Deletion Reveals Synaptic Transmission Defects Caused by Heterozygous Mutations in NRXN1 - ScienceDirect
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
Phenotypic spectrum and genotype–phenotype correlations of NRXN1 exon deletions | European Journal of Human Genetics
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
Allelic contribution of Nrxn1α to autism-relevant behavioral phenotypes in mice | PLOS Genetics
Neurexin 1 (NRXN1) Deletions in Schizophrenia
2p16.3 (NRXN1) deletions
Cross-Platform Validation of Neurotransmitter Release Impairments in Schizophrenia Patient-Derived NRXN1-Mutant Neurons | bioRxiv
A deletion of approximately 70 kb encompassing two exons (3,4) from the... | Download Scientific Diagram
NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody
NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody
Schizophrenia is associated with somatic muta | EurekAlert!
