WordNet

coat, inlay, or surface with enamel
a colored glassy compound (opaque or partially opaque) that is fused to the surface of metal or glass or pottery for decoration or protection
a paint that dries to a hard glossy finish
any smooth glossy coating that resembles ceramic glaze
hard white substance covering the crown of a tooth (同)tooth enamel

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〈U〉〈C〉エナメル,ほうろう / 〈C〉ほうろう細工,ほうろう鉄器 / 〈U〉〈C〉エナメル,光沢塗料 / 〈U〉(歯の)ほうろう質 / …‘に'エナメルをかける,ほうろう引きする;〈皮・布など〉‘に'つや出しする

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1. 歯の発達障害 developmental defects of the teeth
2. 小児におけるセリアック病の臨床症状および診断 clinical manifestations and diagnosis of celiac disease in children
3. 左心低形成症候群 hypoplastic left heart syndrome
4. 歯の解剖学的構造および発達 anatomy and development of the teeth
5. 新生児におけるチアノーゼの心臓の原因 cardiac causes of cyanosis in the newborn

Bmp2 deletion causes an amelogenesis imperfecta phenotype via regulating enamel gene expression.

Guo F1, Feng J, Wang F, Li W, Gao Q, Chen Z, Shoff L, Donly KJ, Gluhak-Heinrich J, Chun YH, Harris SE, MacDougall M, Chen S.
Journal of cellular physiology.J Cell Physiol.2015 Aug;230(8):1871-82. doi: 10.1002/jcp.24915.
Although Bmp2 is essential for tooth formation, the role of Bmp2 during enamel formation remains unknown in vivo. In this study, the role of Bmp2 in regulation of enamel formation was investigated by the Bmp2 conditional knock out (Bmp2 cKO) mice. Teeth of Bmp2 cKO mice displayed severe and profound
PMID 25545831

"Missing perikymata"-fact or fiction? A study on chimpanzee (Pan troglodytes verus) canines.

Kierdorf H1, Witzel C1, Kierdorf U1, Skinner MM2,3, Skinner MF4.
American journal of physical anthropology.Am J Phys Anthropol.2015 Jun;157(2):276-83. doi: 10.1002/ajpa.22720. Epub 2015 Feb 18.
Recently, a lower than expected number of perikymata between repetitive furrow-type hypoplastic defects has been reported in chimpanzee canines from the Fongoli site, Senegal (Skinner and Pruetz: Am J Phys Anthropol 149 (2012) 468-482). Based on an observation in a localized enamel fracture surface
PMID 25693508

Volodarsky M1, Zilberman U2, Birk OS3.
Archives of oral biology.Arch Oral Biol.2015 Jun;60(6):919-22. doi: 10.1016/j.archoralbio.2015.02.018. Epub 2015 Feb 28.
OBJECTIVE: To relate the peculiar phenotype of amelogenesis imperfecta in a large Bedouin family to the genotype determined by whole genome linkage analysis.DESIGN: Amelogenesis imperfecta (AI) is a broad group of inherited pathologies affecting enamel formation, characterized by variability in phen
PMID 25827751