Dosage of the Abcg1-U2af1 region modifies locomotor and cognitive deficits observed in the Tc1 mouse model of Down syndrome.
Down syndrome (DS) results from one extra copy of human chromosome 21 and leads to several alterations including intellectual disabilities and locomotor defects. The transchromosomic Tc1 mouse model carrying an extra freely-segregating copy of human chromosome 21 was developed to better characterize...
Saved in:
| Main Authors: | Damien Marechal, Patricia Lopes Pereira, Arnaud Duchon, Yann Herault |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Public Library of Science (PLoS)
2015-01-01
|
| Series: | PLoS ONE |
| Online Access: | https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0115302&type=printable |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Fully-Automated μMRI Morphometric Phenotyping of the Tc1 Mouse Model of Down Syndrome.
by: Nick M Powell, et al.
Published: (2016-01-01) -
ABCG1 and ABCG4 Suppress γ-Secretase Activity and Amyloid β Production.
by: Osamu Sano, et al.
Published: (2016-01-01) -
Alterations to dendritic spine morphology, but not dendrite patterning, of cortical projection neurons in Tc1 and Ts1Rhr mouse models of Down syndrome.
by: Matilda A Haas, et al.
Published: (2013-01-01) -
Massively parallel sequencing reveals the complex structure of an irradiated human chromosome on a mouse background in the Tc1 model of Down syndrome.
by: Susan M Gribble, et al.
Published: (2013-01-01) -
Auditory function in the Tc1 mouse model of down syndrome suggests a limited region of human chromosome 21 involved in otitis media.
by: Stephanie Kuhn, et al.
Published: (2012-01-01)