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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

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

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

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

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

PDF] Neurexin 1 (NRXN1) deletions in schizophrenia. | Semantic Scholar
PDF] Neurexin 1 (NRXN1) deletions in schizophrenia. | Semantic Scholar

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

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

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

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

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

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

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

Neurexins (such as NRXN1), neuroligins (such as NLGN4) and... | Download Scientific Diagram
Neurexins (such as NRXN1), neuroligins (such as NLGN4) and... | Download Scientific Diagram

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

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

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

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

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

NRXN1 - Wikipedia
NRXN1 - Wikipedia

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

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

What is NRXN1 Gene Pitt-Hopkins syndrome NGS Genetic DNA Test ?
What is NRXN1 Gene Pitt-Hopkins syndrome NGS Genetic DNA Test ?

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