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颅面及牙齿异常的遗传基础。

The genetic basis of craniofacial and dental abnormalities.

作者信息

Kouskoura Thaleia, Fragou Natassa, Alexiou Maria, John Nessy, Sommer Lukas, Graf Daniel, Katsaros Christos, Mitsiadis Thimios A

机构信息

University of Zurich, Institute of Oral Biology, Zurich, Switzerland.

出版信息

Schweiz Monatsschr Zahnmed. 2011;121(7-8):636-46.

Abstract

The embryonic head development, including the formation of dental structures, is a complex and delicate process guided by specific genetic programs. Genetic changes and environmental factors can disturb the execution of these programs and result in abnormalities in orofacial and dental structures. Orofacial clefts and hypodontia/ oligodontia are examples of such abnormalities frequently seen in dental clinics. An insight into the mechanisms and genes involved in the formation of orofacial and dental structures has been gradually gained by genetic analysis of families and by the use of experimental vertebrate models such as the mouse and chick models. The development of novel clinical therapies for orofacial and dental pathological conditions depends very much on a detailed knowledge of the molecular and cellular processes that are involved in head formation.

摘要

胚胎头部发育,包括牙齿结构的形成,是一个由特定基因程序引导的复杂而精细的过程。基因变化和环境因素会干扰这些程序的执行,导致口面部和牙齿结构异常。口腔颌面部裂隙和牙齿发育不全/少牙症是牙科诊所中常见的此类异常的例子。通过对家族的基因分析以及使用小鼠和鸡等实验性脊椎动物模型,人们逐渐深入了解了参与口面部和牙齿结构形成的机制和基因。针对口面部和牙齿病理状况的新型临床治疗方法的开发在很大程度上依赖于对头部形成过程中涉及的分子和细胞过程的详细了解。

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