Literature DB >> 11144868

Genetic basis of tooth development and dental defects.

I Thesleff1.   

Abstract

Tooth development is under strict genetic control, and during recent years an increasing number of genes have been identified that are involved in the regulation of tooth morphogenesis. One of the organs in which development is now beginning to be understood at the gene level, the tooth is an example of a typical vertebrate organ starting as an epithelial bud and undergoing complex morphogenesis, regulated by interactions between epithelial and mesenchymal tissue layers. It has become evident that developmental regulatory genes have been conserved to a high degree during evolution and that similar gene networks regulate the development of teeth as of other vertebrate organs. So far, all genes that have been linked with early tooth morphogenesis have developmental regulatory functions in other organs, too. The majority of these genes are associated with the signaling pathways transmitting interactions between cells and tissues. They include genes encoding the actual signals as well as their receptors, mediators of signaling in the cytoplasm and transcription factors regulating gene expression in the nucleus. Deletion of the function of many of these genes in transgenic mice results in arrested tooth development, but all these mutants also show defects in many other tissues. Mutations in several of these genes in humans have been identified as causes of dental defects, mainly hypodontia.

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Year:  2000        PMID: 11144868     DOI: 10.1080/000163500750051728

Source DB:  PubMed          Journal:  Acta Odontol Scand        ISSN: 0001-6357            Impact factor:   2.331


  26 in total

1.  Case report: identical twins revealing discordant hypodontia. The rationale of dental arch differences in monozygotic twins.

Authors:  M Varela; M J Trujillo-Tiebas; P Garcia-Camba
Journal:  Eur Arch Paediatr Dent       Date:  2011-12

2.  Non syndromic bilateral microdontia of maxillary second molars: a very rare finding.

Authors:  Manoj Kumar Hans; Subhash Chander; Amrit Singh Ahluwalia; Harleen Chinna
Journal:  J Clin Diagn Res       Date:  2015-04-01

3.  A novel missense mutation in MSX1 underlies autosomal recessive oligodontia with associated dental anomalies in Pakistani families.

Authors:  Muhammad S Chishti; Dost Muhammad; Mahmud Haider; Wasim Ahmad
Journal:  J Hum Genet       Date:  2006-08-24       Impact factor: 3.172

4.  Hyaluronan and hyaluronan synthases expression and localization in embryonic mouse molars.

Authors:  Guofeng Yang; Beizhan Jiang; Wenping Cai; Shangfeng Liu; Shouliang Zhao
Journal:  J Mol Histol       Date:  2016-06-18       Impact factor: 2.611

5.  The restorative management of microdontia.

Authors:  D P Laverty; M B M Thomas
Journal:  Br Dent J       Date:  2016-08-26       Impact factor: 1.626

6.  From the transcription of genes involved in ectodermal dysplasias to the understanding of associated dental anomalies.

Authors:  V Laugel-Haushalter; A Langer; J Marrie; V Fraulob; B Schuhbaur; M Koch-Phillips; P Dollé; A Bloch-Zupan
Journal:  Mol Syndromol       Date:  2012-09-27

7.  Immunolocalization of fibroblast growth factor-2 (FGF-2) in the developing root and supporting structures of the murine tooth.

Authors:  A K Madan; Beverley Kramer
Journal:  J Mol Histol       Date:  2005-03       Impact factor: 2.611

8.  Novel missense mutations and a 288-bp exonic insertion in PAX9 in families with autosomal dominant hypodontia.

Authors:  Parimal Das; Mehreen Hai; Claire Elcock; Suzanne M Leal; Donald T Brown; Alan H Brook; Pragna I Patel
Journal:  Am J Med Genet A       Date:  2003-04-01       Impact factor: 2.802

9.  Genome-wide association study reveals multiple loci associated with primary tooth development during infancy.

Authors:  Demetris Pillas; Clive J Hoggart; David M Evans; Paul F O'Reilly; Kirsi Sipilä; Raija Lähdesmäki; Iona Y Millwood; Marika Kaakinen; Gopalakrishnan Netuveli; David Blane; Pimphen Charoen; Ulla Sovio; Anneli Pouta; Nelson Freimer; Anna-Liisa Hartikainen; Jaana Laitinen; Sarianna Vaara; Beate Glaser; Peter Crawford; Nicholas J Timpson; Susan M Ring; Guohong Deng; Weihua Zhang; Mark I McCarthy; Panos Deloukas; Leena Peltonen; Paul Elliott; Lachlan J M Coin; George Davey Smith; Marjo-Riitta Jarvelin
Journal:  PLoS Genet       Date:  2010-02-26       Impact factor: 5.917

10.  Case report: Macrodont mandibular second premolars, a hereditary dental anomaly.

Authors:  A Kyriazidou; D Haider; C Mason; S Parekh; A Bloch-Zupan
Journal:  Eur Arch Paediatr Dent       Date:  2013-06-05
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