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mRNA surveillance in human genetic disease: Molecular determinants of nonsense-mediated mRNA decay

mRNA surveillance in human genetic disease: Molecular determinants of nonsense-mediated mRNA decay
人类遗传疾病中的 mRNA 监测:无义介导的 mRNA 衰变的分子决定因素
批准号:
nhmrc : 1044169
负责人:
A/Pr Shireen Lamande
金额:
$24.76万
依托单位国家:
澳大利亚
项目类别:
Project Grants
财政年份:
2013
资助国家:
澳大利亚
项目状态:
已结题
起止时间:
2013-01-01 至 2015-12-31

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中文摘要
翻译
在大约三分之一的遗传性疾病中,突变会将异常的停止信号引入基因,因此细胞有可能产生截短或错误的蛋白质。为了防止这种情况,细胞已经发展出一种控制监视机制,称为无意义介导的m
英文摘要
In about 1/3 of inherited disorders the mutations introduce an abnormal stop signal into the gene so that cells risk producing truncated or erroneous proteins. To prevent this cells have developed control surveillance mechanisms called Nonsense Mediated m
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  • 项目类别:
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