Behavioral characterization of a mouse model overexpressing DSCR1/ RCAN1.
DSCR1/ RCAN1 is a chromosome 21 gene found to be overexpressed in the brains of Down syndrome (DS) and postulated as a good candidate to contribute to mental disability. However, even though Rcan1 knockout mice have pronounced spatial learning and memory deficits, the possible deleterious effects of...
Guardado en:
Autores principales: | Mara Dierssen, Gloria Arqué, Jerome McDonald, Nuria Andreu, Carmen Martínez-Cué, Jesús Flórez, Cristina Fillat |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Public Library of Science (PLoS)
2011
|
Materias: | |
Acceso en línea: | https://doaj.org/article/9e7ed7bf502a4cbc88351f0f74b27a57 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
NGF upregulates the plasminogen activation inhibitor-1 in neurons via the calcineurin/NFAT pathway and the Down syndrome-related proteins DYRK1A and RCAN1 attenuate this effect.
por: Georgios C Stefos, et al.
Publicado: (2013) -
Dyrk1A is dynamically expressed on subsets of motor neurons and in the neuromuscular junction: possible role in Down syndrome.
por: Gloria Arque, et al.
Publicado: (2013) -
Social Factors Influence Behavior in the Novel Object Recognition Task in a Mouse Model of Down Syndrome
por: Cesar Sierra, et al.
Publicado: (2021) -
Conditional deletion of Rcan1 predisposes to hypertension-mediated intramural hematoma and subsequent aneurysm and aortic rupture
por: Silvia Villahoz, et al.
Publicado: (2018) -
Impaired spatial learning strategies and novel object recognition in mice haploinsufficient for the dual specificity tyrosine-regulated kinase-1A (Dyrk1A).
por: Glòria Arqué, et al.
Publicado: (2008)