Cargando…
Allelic contribution of Nrxn1α to autism-relevant behavioral phenotypes in mice
Copy number variations (CNVs) in the Neurexin 1 (NRXN1) gene, which encodes a presynaptic protein involved in neurotransmitter release, are some of the most frequently observed single-gene variants associated with autism spectrum disorder (ASD). To address the functional contribution of NRXN1 CNVs t...
Autores principales: | Xu, Bing, Ho, Yugong, Fasolino, Maria, Medina, Joanna, O’Brien, William Timothy, Lamonica, Janine M., Nugent, Erin, Brodkin, Edward S., Fuccillo, Marc V., Bucan, Maja, Zhou, Zhaolan |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9997995/ https://www.ncbi.nlm.nih.gov/pubmed/36848371 http://dx.doi.org/10.1371/journal.pgen.1010659 |
Ejemplares similares
-
Mutation Analysis of the NRXN1 Gene in Autism Spectrum Disorders
por: Onay, H, et al.
Publicado: (2016) -
Long genes linked to autism spectrum disorders harbor broad enhancer-like chromatin domains
por: Zhao, Ying-Tao, et al.
Publicado: (2018) -
Disruption of Nrxn1α within excitatory forebrain circuits drives value-based dysfunction
por: Alabi, Opeyemi O, et al.
Publicado: (2020) -
NRXN1 deletions identified by array comparative genome hybridisation in a clinical case series – further understanding of the relevance of NRXN1 to neurodevelopmental disorders
por: Curran, Sarah, et al.
Publicado: (2013) -
Functional characterization of rare NRXN1 variants identified in autism spectrum disorders and schizophrenia
por: Ishizuka, Kanako, et al.
Publicado: (2020)