Functional transcriptome analysis of the postnatal brain of the Ts1Cje mouse model for Down syndrome reveals global disruption of interferon-related molecular networks
Background: The Ts1Cje mouse model of Down syndrome (DS) has partial triplication of mouse chromosome 16 (MMU16), which is partially homologous to human chromosome 21. These mice develop various neuropathological features identified in DS individuals. We analysed the effect of partial triplication o...
Main Authors: | Ling, King Hwa, Hewitt, Chelsee Ann, Tan, Kai Leng, Cheah, Pike See, Vidyadaran, Sharmili, Lai, Mei I., Lee, Han Chung, Simpson, Ken, Hyde, Lavinia, Pritchard, Melanie A., Smyth, Gordon K., Thomas, Tim, Scott, Hamish S. |
---|---|
Format: | Article |
Language: | English |
Published: |
BioMed Central
2014
|
Online Access: | http://psasir.upm.edu.my/id/eprint/37726/1/Functional%20transcriptome%20analysis%20of%20the%20postnatal%20brain%20of%20the%20Ts1Cje%20mouse%20model%20for%20Down%20syndrome%20reveals%20global%20disruption%20of%20interferon.pdf |
Similar Items
-
Transcriptional profiling of the postnatal brain of the Ts1Cje mouse model of Down syndrome
by: Tan, Kai Leng, et al.
Published: (2014) -
Overexpression of interferon alpha or beta receptors in the brain of adult Ts1Cje mouse model of Down syndrome
by: Tan, Kai Leng, et al.
Published: (2015) -
Gene network disruptions and neurogenesis defects in the adult Ts1Cje mouse model of Down syndrome
by: Hewitt, Chelsee Ann, et al.
Published: (2010) -
Disrupted interferon-related molecular networks and the over-expressed Ifnar1 in the brain of adult Ts1Cje mouse model of Down syndrome
by: Tan, Kai Leng, et al.
Published: (2016) -
Gene and protein expression profiles of JAK-STAT signalling pathway in the developing brain of the Ts1Cje down syndrome mouse model
by: Lee, Han Chung, et al.
Published: (2019)