نتایج جستجو برای: dentinogenesis

تعداد نتایج: 320  

Journal: :European journal of medical genetics 2008
Isabelle Bailleul-Forestier Ariane Berdal Frans Vinckier Thomy de Ravel Jean Pierre Fryns Alain Verloes

Teeth are specialized structural components of the craniofacial skeleton. Developmental defects occur either alone or in combination with other birth defects. In this paper, we review the dental anomalies in several multiple congenital anomaly (MCA) syndromes, in which the dental component is pivotal in the recognition of the phenotype and/or the molecular basis of the disorder is known. We wil...

Journal: :Journal of dental research 1997
K L Hirst K Ibaraki-O'Connor M F Young M J Dixon

The dentin matrix acidic phosphoprotein gene has been mapped to human chromosome 4q21 and mouse chromosome 5q21. Expression studies have implicated a role for this gene in the mineralization of dentin. In the current investigation, a cDNA encoding bovine dentin matrix acidic phosphoprotein has been cloned and sequenced. A comparison of the bovine gene with its rat counterpart has indicated that...

Journal: :Molecular genetics & genomic medicine 2016
Jie Yang Kazuhiko Kawasaki Moses Lee Bryan M Reid Stephanie M Nunez Murim Choi Figen Seymen Mine Koruyucu Yelda Kasimoglu Ninna Estrella-Yuson Brent P J Lin James P Simmer Jan C-C Hu

Nonsyndromic dentin defects classified as type II dentin dysplasia and types II and III dentinogenesis imperfecta are caused by mutations in DSPP (dentin sialophosphoprotein). Most reported disease-causing DSPP mutations occur within the repetitive DPP (dentin phosphoprotein) coding sequence. We characterized the DPP sequences of five probands with inherited dentin defects using single molecule...

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