Home

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
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
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
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
Dysregulation of NRXN1 by mutant MIR8485 leads to calcium overload in pre-synapses inducing neurodegeneration in Multiple sclerosis - ScienceDirect

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

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

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

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

NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody
NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody

PDF] Neurexin 1 (NRXN1) deletions in schizophrenia. | Semantic Scholar
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
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
Neurexins (such as NRXN1), neuroligins (such as NLGN4) and... | Download Scientific Diagram

SAM68 Regulates Neuronal Activity-Dependent Alternative Splicing of  Neurexin-1: Cell
SAM68 Regulates Neuronal Activity-Dependent Alternative Splicing of Neurexin-1: Cell

2p16.3 (NRXN1) deletions
2p16.3 (NRXN1) deletions

Information about each variant of interest in NRXN1. a Diagram of... |  Download Scientific Diagram
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
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
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
Emerging evidence implicating a role for neurexins in neurodegenerative and neuropsychiatric disorders | Open Biology

Nrxn1 (neurexin I) | Gene Report | BioGPS
Nrxn1 (neurexin I) | Gene Report | BioGPS

Cross-Platform Validation of Neurotransmitter Release Impairments in  Schizophrenia Patient-Derived NRXN1-Mutant Neurons | bioRxiv
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
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
Evidence of novel fine-scale structural variation at autism spectrum disorder candidate loci | Molecular Autism | Full Text

NRXN1 (neurexin 1) | Gene Report | BioGPS
NRXN1 (neurexin 1) | Gene Report | BioGPS

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

Molecular characterization of NRXN1 deletions from 19,263 clinical  microarray cases identifies exons important for neurodevelopmental disease  expression | Genetics in Medicine
Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression | Genetics in Medicine