The role of PAX3 mutant on chromatin changing in Waardenburg syndrome
碩士 === 國立中興大學 === 分子生物學研究所 === 100 === PAX3, a transcription factor, regulates many development-related gene expression to affect vertebrate development. When PAX3 protein is mutated, a differentiation disease, called Waardenburg syndrome happen. From previous study in Waardenburg syndrome, resear...
Main Authors: | Yi-Ping Kuo, 郭依萍 |
---|---|
Other Authors: | Wen-Ming Yang |
Format: | Others |
Language: | zh-TW |
Published: |
2012
|
Online Access: | http://ndltd.ncl.edu.tw/handle/51582082529038690237 |
Similar Items
-
Study of PAX3 Waardenburg syndrome mutants, SUMOylation and PARylation in replication foci
by: Yi-Chia Chiu, et al.
Published: (2019) -
Case Report: A Novel PAX3 Mutation Associated With Waardenburg Syndrome Type 1
by: Qiuming Hu, et al.
Published: (2021-03-01) -
Waardenburg Syndrome: description of two novel mutations in the PAX3 gene, one of which incompletely penetrant
by: Eliete Pardono, et al.
Published: (2006-01-01) -
Two novel mutations of PAX3 and SOX10 were characterized as genetic causes of Waardenburg Syndrome
by: Yongbo Yu, et al.
Published: (2020-05-01) -
A novel mutation of the PAX3 gene in a Chinese family with Waardenburg syndrome type I
by: Jing Ma, et al.
Published: (2019-07-01)