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T-genes and limb bud development.

机译:T基因和肢芽发育。

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摘要

The T-box family of transcriptional factors is ancient and highly conserved among most species of animals. Haploinsufficiency of multiple T-box proteins results in severe human congenital malformation syndromes, involving craniofacial, cardiovascular, and skeletal structures. These genes have major roles in embryogenesis, including the development of the limbs. Formation of the limbs begins with a limb bud and its morphogenesis requires complex epithelial-mesenchymal interactions. Recent studies have shown that T, Tbx2, Tbx3, Tbx4, Tbx5, Tbx15, and Tbx18 are all expressed in the limb buds, and many have developmental functions. The study of these genes is clinically relevant as mutations in several of them cause human congenital malformation syndromes. Furthermore, understanding the function and biology of these genes is important in understanding normal embryogenesis.
机译:T-box转录因子家族是古老的,在大多数动物中都高度保守。多种T-box蛋白的单倍剂量不足会导致严重的人类先天性畸形综合症,涉及颅面,心血管和骨骼结构。这些基因在包括四肢发育在内的胚胎发生中起主要作用。四肢的形成始于四肢芽,其形态发生需要复杂的上皮-间质相互作用。最近的研究表明,T,Tbx2,Tbx3,Tbx4,Tbx5,Tbx15和Tbx18都在肢芽中表达,并且许多具有发育功能。这些基因的研究与临床相关,因为其中一些突变会导致人类先天性畸形综合症。此外,了解这些基因的功能和生物学对于了解正常胚胎发生很重要。

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