Results 91 to 100 of about 3,804 (207)

MAST4 regulates stem cell maintenance with DLX3 for epithelial development and amelogenesis

Experimental and Molecular Medicine
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, Pyunggang Kim, Hyun-Yi Kim, Jinah Park, Seung-Jun Lee, Haein An, Jin Sun Heo, Min-Jung Lee, Hayato Ohshima, Seiya Mizuno, Satoru Takahashi, Han-Sung Jung, Seong-Jin Kim   +12 more
doaj   +1 more source

Amelogenesis imperfecta with gingival calcification: a rare presentation

, 2005
The purpose of this article is to highlight the rare presence of gingival calcification with Amelogenesis Imperfecta. A case is presented of a 12-year-old girl with a defect of enamel in deciduous as well as permanent dentition with moderate amount of
Sunitha Carnelio
core   +1 more source

The metal ion binding protein Cnnm4 is mutated in rod-cone dystrophy/amelogenesis imperfecta syndrome

, 2009
Purpose:To identify the gene causing rod-cone dystrophy/amelogenesis imperfecta Methods:Homozygosity mapping was performed using the Affymetrix 50K XbaI array in one family and candidate genes in the linked interval were sequenced with ABI Dye ...
Polok, B., Mégarbane, A., Favez, T., Hamel, C., Ambresin, A., Munier, F.L., Voirol, N., Escher, Pascal, Bolay, S., Schorderet, D.F.   +9 more
core  

Intracanal pain remission in child with amelogenesis imperfecta. Case report

Revista Dor
BACKGROUND AND OBJECTIVES:Amelogenesis imperfecta is characterized by enamel structural defects, which may severely affect dental structure in both dentitions.
Armiliana Soares Nascimento, Criseuda Maria Benício Barros, Renata de Souza Coelho Soares, Luciana de Barros Correia Fontes, Rodivan Braz   +4 more
doaj   +1 more source

Amelogenesis Imperfecta and Gingival Hyperplasia in a 21-Year-Old Female Patient: A Case Report

, 2023
Enamel Renal Syndrome (ERS), is a rare genetic condition that is characterized by hypoplastic amelogenesis imperfecta, failed tooth eruption, intra-pulpal calcifications, gingival enlargement, and in some patients, nephrocalcinosis. Patients with ERS are
Fatma Fathy, Hala Elkammar
core  

ACP4 Variants In Hypoplastic Amelogenesis Imperfecta [PDF]

Calcif Tissue Int
Liu L, Au CW, Hany U, Rigby AL, Chauhan A, Brown C, Sims J, Murillo G, de Carmargo MGA, Inglehearn CF, Watson CM, Mighell AJ, Smith CEL.   +12 more
europepmc   +2 more sources

Amelogenesis imperfecta: diagnosis and rehabilitation [PDF]

, 2017
Rezumat Amelogeneza imperfectă (abr. AI) afectează smalţul atât a dinţilor de lapte, cât și a celor permanenţi. Această tulburare ereditară se caracterizează prin pierderea smalţului, esteticul deficitar și hipersensibilitatea dentinară.
Nicolau, Gheorghe, Terehov, Alexei, Năstase, Corneliu, Gnatiuc, Pavel, Burlacu, Valeriu   +4 more
core  

Immunolocalization of gene products responsible for Amelogenesis Imperfecta and Dentinogenesis Imperfecta in mice [PDF]

, 2016
Healthy tooth formation is crucially dependent on normal development of enamel and dentin. Any deviation from norm could lead to serious effects on the teeth function.
Alkhouly, Waddah Mohammed
core  

Oral rehabilitation of a patient with amelogenesis imperfecta

, 2009
Amelogenesis imperfecta is a hereditary disorder that causes defective enamel development in the primary and permanent teeth. Clinical treatment is important to address the esthetic appearance of affected teeth, reduce dentinal sensitivity, preserve ...
Becerik S., Hart T.C., Cogulu D., Emingil G., Hart P.S.   +4 more
core  

Interdisciplinary full mouth rehabilitation of a patient with amelogenesis imperfecta from childhood to young adult‐hood: A 12‐year case report

Clinical Case Reports
Key Clinical Message Treatment of patients with amelogenesis imperfecta extends over many years, from childhood to early adulthood. Their management at any age is complex and has to be adapted in relation to therapies validated in the general population.
Élisa Caussin, Frédéric Courson, Elisabeth Dursun, Yohann Brukarz, Daniel Dot, Catherine Chaussain, Jean‐Pierre Attal, Philippe François   +7 more
doaj   +1 more source