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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

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

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

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

Gene: Nrxn1 (ENSMUSG00000024109) - Summary - Mus_musculus - Ensembl genome browser 109
Gene: Nrxn1 (ENSMUSG00000024109) - Summary - Mus_musculus - Ensembl genome browser 109

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

Gene: NRXN1 (ENSG00000179915) - Summary - Homo_sapiens - Ensembl genome browser 109
Gene: NRXN1 (ENSG00000179915) - Summary - Homo_sapiens - Ensembl genome browser 109

Further insight into the neurobehavioral pattern of children carrying the 2p16.3 heterozygous deletion involving NRXN1: Report of five new cases - Alfieri - 2020 - Genes, Brain and Behavior - Wiley Online Library
Further insight into the neurobehavioral pattern of children carrying the 2p16.3 heterozygous deletion involving NRXN1: Report of five new cases - Alfieri - 2020 - Genes, Brain and Behavior - Wiley Online Library

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

Genetic insights and neurobiological implications from NRXN1 in neuropsychiatric disorders | Molecular Psychiatry
Genetic insights and neurobiological implications from NRXN1 in neuropsychiatric disorders | Molecular Psychiatry

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

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

NRXN1 Membrane Protein Introduction - Creative Biolabs
NRXN1 Membrane Protein Introduction - Creative Biolabs

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

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

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

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

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

Association of genes with phenotype in autism spectrum disorder | Aging
Association of genes with phenotype in autism spectrum disorder | Aging

Human Neuropsychiatric Disease Modeling using Conditional Deletion Reveals Synaptic Transmission Defects Caused by Heterozygous Mutations in NRXN1 - ScienceDirect
Human Neuropsychiatric Disease Modeling using Conditional Deletion Reveals Synaptic Transmission Defects Caused by Heterozygous Mutations in NRXN1 - ScienceDirect

NRXN1 - Wikipedia
NRXN1 - Wikipedia

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

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

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

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

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