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:
Main Author: | Ng, Xiang Wen. |
---|---|
Other Authors: | Chen Ken-Shiung |
Format: | Final Year Project |
Language: | English |
Published: |
2009
|
Subjects: | |
Online Access: | http://hdl.handle.net/10356/16321 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Nanyang Technological University |
Language: | English |
Similar Items
-
UBE3A regulates MC1R expression : a link to hypopigmentation in Angelman Syndrome
by: Low, Daren., et al.
Published: (2011) -
Genome-wide gene expression profiling of the Angelman syndrome mice with Ube3a mutation
by: Low, Daren., et al.
Published: (2011) -
Proteomics analysis of an UBE3A knockout mouse modelling Angelman syndrome
by: Low, Hai Loon
Published: (2014) -
Genome-wide gene expression profiling of the Angelman syndrome mouse with Ube3a mutation : from genotype to phenotype
by: Low, Daren Juan Hsuen
Published: (2012) -
Effect of ube3c polymorphisms on intramuscular fat content and fatty acid composition in duroc pigs
by: P. Supakankul
Published: (2018)