Les phosphoprotéines sécrétées liant le calcium (SCPP) impliquées dans la formation de l'émail dentaire : expression chez le lézard Anolis carolinensis et évolution chez les amniotes [PDF]
, 2015 Enamel formation requires the involvement of secretory calcium-binding phosphoproteins. Three of them, amelogenin (AMEL), ameloblastin (AMBN) and enamelin (ENAM), have been extensively studied in mammals.
Gasse, Barbara
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Altered Amelogenin Self-assembly Based on Mutations Observed in Human X-linked Amelogenesis Imperfecta (AIH1) [PDF]
, 2002 Michael L. Paine +3 more
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MAST4 regulates stem cell maintenance with DLX3 for epithelial development and amelogenesis
Experimental and Molecular MedicineThe asymmetric division of stem cells permits the maintenance of the cell population and differentiation for harmonious progress. Developing mouse incisors allows inspection of the role of the stem cell niche to provide specific insights into essential ...
Dong-Joon Lee +12 more
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, 2003 Amelogenesis imperfecta causes defects in the tooth enamel. These defects can appear as small pits or dents in the tooth or can be so widespread as to make the entire tooth small in size and/or mis-shaped.
SAITO,Takashi/IBARAKI,Yuji/IZUMIKAWA,Masanobu/KAWAKAMI,Tomofumi/MATSUDA,Koichi
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Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects [PDF]
, 2003 Thomas C. Hart
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Regional odontodysplasia of the deciduous and permanent teeth associated with eruption disorders : a case report [PDF]
, 2008 Regional odontodysplasia (RO) is an unusual, non-hereditary anomaly of the dental hard tissues with characteristic clinical, radiographic and histological findings.
Gunhan, Omer +5 more
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A Transgenic Animal Model Resembling Amelogenesis Imperfecta Related to Ameloblastin Overexpression [PDF]
, 2003 Michael L. Paine +4 more
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Nature Communications, 2018 The majority of skeletal dysplasia are caused by pathogenic variants in genes required for glycosaminoglycan (GAG) metabolism. Here, Dubail et al. identify genetic variants in the solute carrier family protein SLC10A7 in families with skeletal dysplasia ...
Johanne Dubail +23 more
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Amelogenesis Imperfecta: A Case Report
Clinical Dentistry, 2020 Amelogenesis imperfecta is a structural-developmental defect involving enamel. It may be hypoplastic, hypomaturation, or hypocalcified. Genetic mutation of enamel coding proteins noted in this heterogeneous group of hereditary disorder affecting both primary and permanent dentitions.
openaire +2 more sources
MMP20 Active-site Mutation in Hypomaturation Amelogenesis Imperfecta [PDF]
, 2005 Didem Özdemır +7 more
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