Mouse models of tooth abnormalities

被引:58
作者
Fleischmannova, Jana [1 ,2 ]
Matalova, Eva [3 ]
Tucker, Abigail S. [2 ,4 ]
Sharpe, Paul T. [4 ]
机构
[1] Univ S Bohemia, Fac Sci, Dept Anim Physiol, Ceske Budejovice 37005, Czech Republic
[2] Acad Sci Czech Republ, Inst Anim Physiol & Genet, Lab Anim Embryol, Brno, Czech Republic
[3] Univ Vet & Pharmaceut Sci, Dept Physiol & Pathophysiol, Brno, Czech Republic
[4] Kings Coll London, Guys Hosp, Inst Dent, Dept Craniofacial Dev, London WC2R 2LS, England
基金
英国医学研究理事会;
关键词
amelogenesis; dental defects; dentinogenesis; ectodermal dysplasia; hypodontia;
D O I
10.1111/j.1600-0722.2007.00504.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Tooth number is abnormal in about 20% of the human population. The most common defect is agenesis of the third molars, followed by loss of the lateral incisors and loss of the second premolars. Tooth loss appears as both a feature of multi-organ syndromes and as a non-syndromic isolated character. Apart from tooth number, abnormalities are also observed in tooth size, shape, and structure. Many of the genes that underlie dental defects have been identified, and several mouse models have been created to allow functional studies to understand, in greater detail, the role of particular genes in tooth development. The ability to manipulate the mouse embryo using explant culture and genome targeting provides a wealth of information that ultimately may pave the way for better diagnostics, treatment or even cures for human dental disorders. This review aims to summarize recent knowledge obtained in mouse models, which can be used to gain a better understanding of the molecular basis of human dental abnormalities.
引用
收藏
页码:1 / 10
页数:10
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