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Disruption of Neurexin 1 Associated with Autism Spectrum Disorder -  ScienceDirect
Disruption of Neurexin 1 Associated with Autism Spectrum Disorder - ScienceDirect

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

JPM | Free Full-Text | Is NRXN1 Gene Expression an Important Marker of  Treatment of Depressive Disorders? A Pilot Study
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
NRXN1 Membrane Protein Introduction - Creative Biolabs

Identification of Nrxn1γ protein as a Nrxn1 gene-derived CA10 receptor....  | Download Scientific Diagram
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
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
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
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
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
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
A deletion of approximately 70 kb encompassing two exons (3,4) from the... | Download Scientific Diagram

NRXN1 | Science Over a Cuppa
NRXN1 | Science Over a Cuppa

Frontiers | NRXN1 Deletion and Exposure to Methylmercury Increase Astrocyte  Differentiation by Different Notch-Dependent Transcriptional Mechanisms
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
Neurexins (such as NRXN1), neuroligins (such as NLGN4) and... | Download Scientific Diagram

Neurexin 1 variants as risk factors for suicide death | Molecular Psychiatry
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
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
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
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
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
Phenotypic spectrum and genotype–phenotype correlations of NRXN1 exon deletions | European Journal of Human Genetics