T-box genes and congenital heart/limb malformations

被引:11
|
作者
Isphording, D [1 ]
Leylek, AM [1 ]
Yeung, J [1 ]
Mischel, A [1 ]
Simon, HG [1 ]
机构
[1] Northwestern Univ, Feinberg Sch Med, Dept Pediat, Childrens Mem Inst Educ & Res, Chicago, IL 60614 USA
关键词
ACTH deficiency; CPX; DGS; HOS; SPS; Tbx1; Tbx19; Tbx22; Tbx3; Tbx4; Tbx5; UMS;
D O I
10.1111/j.1399-0004.2004.00314.x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Congenital malformations cause significant morbidity and mortality; however, the underlying basis for many of these developmental defects is not well understood. Over the past years, a new family of genes called T-box genes has been identified that play essential roles during the development of various tissues and organs. A number of developmental syndromes have recently been shown to be linked to mutations in T-box genes, and brought direct medical relevance to their study. This review emphasizes emerging data on the molecular, cell, and disease levels, which establish a basis for parallel events in limb and heart development, and suggests that common regulatory pathways are crucial for proper differentiation and growth of these embryonic structures.
引用
收藏
页码:253 / 264
页数:12
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