Dupa nume cerni eșarfă gene nrxn1 balet Pungă reforma
A common cognitive, psychiatric, and dysmorphic phenotype in carriers of NRXN1 deletion - Viñas‐Jornet - 2014 - Molecular Genetics & Genomic Medicine - Wiley Online Library
Cross-platform validation of neurotransmitter release impairments in schizophrenia patient-derived NRXN1-mutant neurons | PNAS
Association of genes with phenotype in autism spectrum disorder | Aging
Dysregulation of NRXN1 by mutant MIR8485 leads to calcium overload in pre-synapses inducing neurodegeneration in Multiple sclerosis - ScienceDirect
NRXN1 | Science Over a Cuppa
JPM | Free Full-Text | Is NRXN1 Gene Expression an Important Marker of Treatment of Depressive Disorders? A Pilot Study
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
NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody
PDF] Neurexin 1 (NRXN1) deletions in schizophrenia. | Semantic Scholar
Genes | Free Full-Text | Computational Saturation Mutagenesis to Investigate the Effects of Neurexin-1 Mutations on AlphaFold Structure
Neurexins (such as NRXN1), neuroligins (such as NLGN4) and... | Download Scientific Diagram
SAM68 Regulates Neuronal Activity-Dependent Alternative Splicing of Neurexin-1: Cell
2p16.3 (NRXN1) deletions
Information about each variant of interest in NRXN1. a Diagram of... | Download Scientific Diagram
Figure 1 from Resequencing and follow-up of neurexin 1 (NRXN1) in schizophrenia patients | Semantic Scholar
A case-control association study of NRXN1 polymorphisms with schizophrenia in Chinese Han population | Behavioral and Brain Functions | Full Text
Emerging evidence implicating a role for neurexins in neurodegenerative and neuropsychiatric disorders | Open Biology
Nrxn1 (neurexin I) | Gene Report | BioGPS
Cross-Platform Validation of Neurotransmitter Release Impairments in Schizophrenia Patient-Derived NRXN1-Mutant Neurons | bioRxiv
Organization of the human NRXN1 gene as described by Rowen et al... | Download Scientific Diagram
Evidence of novel fine-scale structural variation at autism spectrum disorder candidate loci | Molecular Autism | Full Text
NRXN1 (neurexin 1) | Gene Report | BioGPS
Allelic contribution of Nrxn1α to autism-relevant behavioral phenotypes in mice | PLOS Genetics
Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression | Genetics in Medicine