Study of Ube3a knockdown and expression in the in vitro system.
Angelman syndrome (AS) is a neurological disorder which is caused by loss of maternally expressed genes on the human chromosome 15q11-q13 in the brain. AS patients show signs of mental retardation, seizures, lack of speech and ataxic gait. In this study, we would like to look into Ube3a, whose mutat...
Saved in:
主要作者: | Ng, Xiang Wen. |
---|---|
其他作者: | Chen Ken-Shiung |
格式: | Final Year Project |
語言: | English |
出版: |
2009
|
主題: | |
在線閱讀: | http://hdl.handle.net/10356/16321 |
標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|
機構: | Nanyang Technological University |
語言: | English |
相似書籍
-
UBE3A regulates MC1R expression : a link to hypopigmentation in Angelman Syndrome
由: Low, Daren., et al.
出版: (2011) -
Genome-wide gene expression profiling of the Angelman syndrome mice with Ube3a mutation
由: Low, Daren., et al.
出版: (2011) -
Proteomics analysis of an UBE3A knockout mouse modelling Angelman syndrome
由: Low, Hai Loon
出版: (2014) -
Genome-wide gene expression profiling of the Angelman syndrome mouse with Ube3a mutation : from genotype to phenotype
由: Low, Daren Juan Hsuen
出版: (2012) -
Effect of ube3c polymorphisms on intramuscular fat content and fatty acid composition in duroc pigs
由: P. Supakankul
出版: (2018)