نتایج جستجو برای: amelogenesis

تعداد نتایج: 1829  

Journal: :The journal of medical investigation : JMI 2008
Keiko Miyoshi Hideya Nagata Taigo Horiguchi Kaori Abe Ivan Arie Wahyudi Yoshinobu Baba Hidemitsu Harada Takafumi Noma

Tooth development is regulated by epithelial-mesenchymal interactions and their reciprocal molecular signaling. Bone morphogenetic protein 2 (BMP2) is known as one of the inducers for tooth development. To analyze the molecular mechanisms of BMP2 on ameloblast differentiation (amelogenesis), we performed microarray analyses using rat dental epithelial cell line, HAT-7. After confirming that BMP...

2014
Muriel de la Dure-Molla Mickael Quentric Paulo Marcio Yamaguti Ana-Carolina Acevedo Alan J Mighell Miikka Vikkula Mathilde Huckert Ariane Berdal Agnes Bloch-Zupan

Amelogenesis imperfecta (AI) is a genetically and clinically heterogeneous group of inherited dental enamel defects. Commonly described as an isolated trait, it may be observed concomitantly with other orodental and/or systemic features such as nephrocalcinosis in Enamel Renal Syndrome (ERS, MIM#204690), or gingival hyperplasia in Amelogenesis Imperfecta and Gingival Fibromatosis Syndrome (AIGF...

Journal: :Journal of dental education 2001
J P Simmer J C Hu

The nature of tooth enamel is of inherent interest to dental professionals. The current-day clinical practice of dentistry involves the prevention of enamel demineralization, the promotion of enamel remineralization, the restoration of cavitated enamel where demineralization has become irreversible, the vital bleaching of dental enamel that has become discolored, and the diagnosis and treatment...

2015
James A Poulter Claire E L Smith Gina Murrillo Sandra Silva Sally Feather Marianella Howell Laura Crinnion David T Bonthron Ian M Carr Christopher M Watson Chris F Inglehearn Alan J Mighell

Biallelic FAM20A mutations cause two conditions where Amelogenesis Imperfecta (AI) is the presenting feature: Amelogenesis Imperfecta and Gingival Fibromatosis Syndrome; and Enamel Renal Syndrome. A distinctive oral phenotype is shared in both conditions. On Sanger sequencing of FAM20A in cases with that phenotype, we identified two probands with single, likely pathogenic heterozygous mutations...

Journal: :THE JOURNAL OF THE KOREAN ACADEMY OF PEDTATRIC DENTISTRY 2021

The aim of this study was to determine the prevalence and incidence evaluate current status dental treatment Amelogenesis imperfecta (AI) Dentinogenesis (DI) in South Korea. data based on National Health Insurance Service (NHIS)-National Sample Cohort Database (2002 - 2015) Jeonbuk University (JBNU) Dental Hospital (2011 2020). NHIS analysis showed AI DI were 11.6 2.4 per 100,000 people, respec...

Journal: :Journal of Indian Academy of Oral Medicine and Radiology 2012

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