标题
The 22q11 deletion: DiGeorge and velocardiofacial syndromes and the role of TBX1
作者
关键词
-
出版物
Wiley Interdisciplinary Reviews-Developmental Biology
Volume 2, Issue 3, Pages 393-403
出版商
Wiley
发表日期
2012-06-20
DOI
10.1002/wdev.75
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- Her9 represses neurogenic fate downstream of Tbx1 and retinoic acid signaling in the inner ear
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- Ripply3, a Tbx1 repressor, is required for development of the pharyngeal apparatus and its derivatives in mice
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- Hes1 expression is reduced in Tbx1 null cells and is required for the development of structures affected in 22q11 deletion syndrome
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- Tbx1 Regulates Proliferation and Differentiation of Multipotent Heart Progenitors
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