Cargando…
Linking spatial gene expression patterns to sex-specific brain structural changes on a mouse model of 16p11.2 hemideletion
Neurodevelopmental disorders, such as ASD and ADHD, affect males about three to four times more often than females. 16p11.2 hemideletion is a copy number variation that is highly associated with neurodevelopmental disorders. Previous work from our lab has shown that a mouse model of 16p11.2 hemidele...
Autores principales: | Kumar, Vinod Jangir, Grissom, Nicola M., McKee, Sarah E., Schoch, Hannah, Bowman, Nicole, Havekes, Robbert, Kumar, Manoj, Pickup, Stephen, Poptani, Harish, Reyes, Teresa M., Hawrylycz, Mike, Abel, Ted, Nickl-Jockschat, Thomas |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974415/ https://www.ncbi.nlm.nih.gov/pubmed/29844452 http://dx.doi.org/10.1038/s41398-018-0157-z |
Ejemplares similares
-
Male-specific deficits in natural reward learning in a mouse model of neurodevelopmental disorders
por: Grissom, N M, et al.
Publicado: (2018) -
Dissecting 16p11.2 hemi-deletion to study sex-specific striatal phenotypes of neurodevelopmental disorders
por: Abel, Ted, et al.
Publicado: (2023) -
High Resolution Magnetic Resonance Imaging for Characterization of the Neuroligin-3 Knock-in Mouse Model Associated with Autism Spectrum Disorder
por: Kumar, Manoj, et al.
Publicado: (2014) -
Dorsal visual stream and LIMK1: hemideletion, haplotype, and enduring effects in children with Williams syndrome
por: Kippenhan, J. Shane, et al.
Publicado: (2023) -
BDNF Serum Levels are Associated With White Matter Microstructure in Schizophrenia - A Pilot Study
por: Hammans, Christine, et al.
Publicado: (2020)