Histological and molecular characterisation of hypotonia in adult Ts1Cje mouse model for down syndrome
Down syndrome (DS) is a genetic disorder caused by presence of extra copy of human chromosome 21 (Hsa21), a condition termed as trisomy 21. It is characterised by several number of clinical phenotypes such as intellectual disability, characteristic sets of facial features, cardiac defects and differ...
Saved in:
主要作者: | Bala, Usman |
---|---|
格式: | Thesis |
語言: | English |
出版: |
2016
|
主題: | |
在線閱讀: | http://psasir.upm.edu.my/id/eprint/66388/1/FPSK%202016%201%20IR.pdf |
標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|
相似書籍
-
Metabolic and functional characterisation of adult skeletal muscle in down syndrome mouse model (Ts1CJe) for insights into hypotonia in human condition
由: Lim, Chai Ling
出版: (2017) -
Metabolic profiling of neurospheres derived from embryonic cerebral cortex Ts1Cje mouse model for down syndrome
由: Mohamed Seth, Eryse Amira
出版: (2019) -
Expression of gamma secretase and notch signalling pathway in TS1CJE mouse model of down syndrome
由: Md Yusof, Hadri Hadi
出版: (2017) -
Transcriptomic and protein expression analyses of skeletal muscles isolated from Ts1cje mouse model for Down syndrome
由: Leong, Melody Pui Yee
出版: (2017) -
Identification of disrupted molecular networks involved in brain maturation and function in the TS1CJE mouse model of down syndrome
由: Tan, Kai Leng
出版: (2016)