Impaired protein stability and nuclear localization ofNOBOXvariants associated with premature ovarian insufficiency
出版年份 2016 全文链接
标题
Impaired protein stability and nuclear localization ofNOBOXvariants associated with premature ovarian insufficiency
作者
关键词
-
出版物
HUMAN MOLECULAR GENETICS
Volume -, Issue -, Pages ddw342
出版商
Oxford University Press (OUP)
发表日期
2016-10-11
DOI
10.1093/hmg/ddw342
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- NOBOXis a strong autosomal candidate gene in Tunisian patients with primary ovarian insufficiency
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- Physiological and pathophysiological role of nonsense-mediated mRNA decay
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- Genetics of primary ovarian insufficiency: new developments and opportunities
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- NewNOBOXMutations Identified in a Large Cohort of Women With Primary Ovarian Insufficiency DecreaseKIT-LExpression
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- A mutation in the nucleoporin-107 gene causes XX gonadal dysgenesis
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- NOBOX is a key FOXL2 partner involved in ovarian folliculogenesis
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- Premature ovarian failure in nobox-deficient mice is caused by defects in somatic cell invasion and germ cell cyst breakdown
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- Oogenesis: Transcriptional regulators and mouse models
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- SUMOylation of the Forkhead Transcription Factor FOXL2 Promotes Its Stabilization/Activation through Transient Recruitment to PML Bodies
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