Extensive characterization of a Williams syndrome murine model shows Gtf2ird1-mediated rescue of select sensorimotor tasks, but no effect on enhanced social behavior

Nygaard, K. R., Maloney, S. E., Swift, R. G., McCullough, K. B., Wagner, R. E., Fass, S. B., Garbett, K., Mirnics, K., Veenstra‐VanderWeele, J., & Dougherty, J. D. (2023). Extensive characterization of a Williams syndrome murine model shows Gtf2ird1‐mediated rescue of select sensorimotor tasks, but no effect on enhanced social behavior. Genes, Brain and Behavior, 22(4). Portico. https://doi.org/10.1111/gbb.12853
Authors:
Kayla R Nygaard
Susan E Maloney
Raylynn G Swift
Katherine B McCullough
Rachael E Wagner
Stuart B Fass
Krassimira Garbett
Karoly Mirnics
Jeremy Veenstra-VanderWeele
Joseph D Dougherty
Affiliated Authors:
Jeremy Veenstra-VanderWeele
Columbia Affiliation:
Subjects:
Williams Syndrome (MeSH)
Author Keywords:
gtf2ird1
williams syndrome
anxiety
motor function
mouse model
sociability
elink
Publication Type:
Article
Unique ID:
10.1111/gbb.12853
PMID:
37370259
DOI:
10.1111/gbb.12853
Journal:
Genes, Brain and Behavior
Publication Date:
Data Source:
PubMed
Source Link:
View PubMed Record

Record Created: