Results 1 to 10 of about 12,299 (233)
Continuously growing mouse incisors are widely used to study amelogenesis, since all stages of this process (i.e., secretory, transition and maturation) are present in a spatially determined sequence at any given time.
Ai Thu Bui+13 more
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Gingival inflammation, enamel defects, and tooth sensitivity in children with amelogenesis imperfecta: a case-control study [PDF]
Gingival conditions and tooth sensitivity of young patients with amelogenesis imperfecta lack in depth studies. This case-control study aimed to compare (1) the gingival inflammation, the presence of enamel defects, and tooth sensitivity in young ...
Camille QUANDALLE+5 more
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Management guidelines for amelogenesis imperfecta: a case report and review of the literature
Background Rehabilitation of the entire dentition with amelogenesis imperfecta (AI) tends to pose a great challenge to the clinician. Most of the cases of amelogenesis imperfecta are reported to be associated with skeletal and dental deformities which ...
M. Roma+3 more
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The role of the TGF-β1 signaling pathway in the process of amelogenesis [PDF]
Amelogenesis is a highly regulated process involving multiple signaling pathways, among which the transforming growth factor-β1 (TGF-β1) signaling pathway plays a pivotal role in enamel formation.
Xiaoxue Ma+3 more
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Amelogenesis Imperfecta; Genes, Proteins, and Pathways
Amelogenesis imperfecta (AI) is the name given to a heterogeneous group of conditions characterized by inherited developmental enamel defects. AI enamel is abnormally thin, soft, fragile, pitted and/or badly discolored, with poor function and aesthetics,
Claire E. L. Smith+8 more
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Amelogenesis Imperfecta - An account of Three Generations affected in a Family
Amelogenesis Imperfecta is a hereditary condition affecting dental enamel without any systemic manifestation. This condition can be inherited as either Autosomal or X-linked.
G Sarat+3 more
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Transcriptional factor DLX3 promotes the gene expression of enamel matrix proteins during amelogenesis. [PDF]
Mutation of distal-less homeobox 3 (DLX3) is responsible for human tricho-dento-osseous syndrome (TDO) with amelogenesis imperfecta, indicating a crucial role of DLX3 in amelogenesis.
Zhichun Zhang+7 more
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MAST4 regulates stem cell maintenance with DLX3 for epithelial development and amelogenesis [PDF]
The 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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The circadian clock in enamel development [PDF]
Circadian rhythms are self-sustaining oscillations within biological systems that play key roles in a diverse multitude of physiological processes.
Ke Wu+5 more
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Enamel Research: Priorities and Future Directions [PDF]
Jennifer Kirkham+5 more
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