Mechanistic characterisation of the epigenetic modifier Smchd1
Mechanistic characterisation of the epigenetic modifier Smchd1
批准号:
nhmrc : GNT1098290
负责人:
A/Pr James Murphy
金额:
$119.71万
依托单位国家:
澳大利亚
项目类别:
Project Grants
财政年份:
2016
资助国家:
澳大利亚
项目状态:
已结题
起止时间:
2016-01-01 至 --
中文摘要
FSHD是一种进行性肌营养不良症,目前还没有治疗或治愈的方法。众所周知,Smchd1在FSHD中扮演着重要的角色,在FSHD中,它通常关闭基因的功能是不完善的,从而导致疾病。在这个项目中,我们将在分子水平上确定Smchd1是如何关闭基因的以及Smchd1是什么样子的,以便我们能够阐明如何增强Smchd1在FSHD治疗中的功能。
英文摘要
FSHD is a progressive muscular dystrophy that currently has no treatment or cure. SMCHD1 is known to play an important role in FSHD, where its usual function in switching genes off is imperfect, contributing to disease. In this project we will determine how SMCHD1 switches genes off and what SMCHD1 looks like at the molecular level, so that we can elucidate how to boost SMCHD1 function for FSHD therapy.
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