Gene network disruptions and neurogenesis defects in the adult Ts1Cje mouse model of Down syndrome
Background: Down syndrome (DS) individuals suffer mental retardation with further cognitive decline and early onset Alzheimer's disease. Methodology/Principal Findings: To understand how trisomy 21 causes these neurological abnormalities we investigated changes in gene expression networ...
Главные авторы: | Hewitt, Chelsee Ann, Ling, King Hwa, Merson, Tobias D., Simpson, Ken M., Ritchie, Matthew E., King, Sarah L., Pritchard, Melanie A., Smyth, Gordon K., Thomas, Tim, Scott, Hamish S., Voss, Anne K. |
---|---|
Формат: | Статья |
Язык: | English |
Опубликовано: |
Public Library of Science
2010
|
Online-ссылка: | http://psasir.upm.edu.my/id/eprint/14865/1/14865.PDF |
Схожие документы
-
Transcriptional profiling of the postnatal brain of the Ts1Cje mouse model of Down syndrome
по: Tan, Kai Leng, и др.
Опубликовано: (2014) -
Functional transcriptome analysis of the postnatal brain of the Ts1Cje mouse model for Down syndrome reveals global disruption of interferon-related molecular networks
по: Ling, King Hwa, и др.
Опубликовано: (2014) -
Ts1Cje mouse model for Down syndrome research
по: Ling, King Hwa
Опубликовано: (2015) -
Overexpression of interferon alpha or beta receptors in the brain of adult Ts1Cje mouse model of Down syndrome
по: Tan, Kai Leng, и др.
Опубликовано: (2015) -
Expression profiling of notch signalling pathway and gamma-secretase activity in the brain of Ts1Cje mouse model of down syndrome
по: Md Yusof, Hadri Hadi, и др.
Опубликовано: (2019)