Cargando…
Genetic targeting of NRXN2 in mice unveils role in excitatory cortical synapse function and social behaviors
Human genetics has identified rare copy number variations and deleterious mutations for all neurexin genes (NRXN1-3) in patients with neurodevelopmental diseases, and electrophysiological recordings in animal brains have shown that Nrxns are important for synaptic transmission. While several mouse m...
Autores principales: | Born, Gesche, Grayton, Hannah M., Langhorst, Hanna, Dudanova, Irina, Rohlmann, Astrid, Woodward, Benjamin W., Collier, David A., Fernandes, Cathy, Missler, Markus |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4333794/ https://www.ncbi.nlm.nih.gov/pubmed/25745399 http://dx.doi.org/10.3389/fnsyn.2015.00003 |
Ejemplares similares
-
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) -
Altered Social Behaviours in Neurexin 1α Knockout Mice Resemble Core Symptoms in Neurodevelopmental Disorders
por: Grayton, Hannah Mary, et al.
Publicado: (2013) -
Dendritic spine formation and synaptic function require neurobeachin
por: Niesmann, Katharina, et al.
Publicado: (2011) -
Molecular Dissection of Neurobeachin Function at Excitatory Synapses
por: Repetto, Daniele, et al.
Publicado: (2018) -
Disruption of Nrxn1α within excitatory forebrain circuits drives value-based dysfunction
por: Alabi, Opeyemi O, et al.
Publicado: (2020)