Results 71 to 80 of about 12,368 (291)
Trio exome sequencing allowed the identification of two novel compound heterozygous variants in PIK3C2A, defining the fifth family presenting a PIK3C2A‐related syndrome characterized by pulverulent cataracts and deafness. Functional testing revealed impaired PI metabolism and primary dysfunction phenotype.
Adella Karam+9 more
wiley +1 more source
Experimental Combat-Stress Model in Rats: Histological Examination of Effects of Amelogenesis-A Possible Measure of Diminished Vagal Tone Episodes [PDF]
Developmental defects of enamel-stress histomarker rings (accentuated striae) may be a potential measure of diminished vagal tone in research on extreme stress such as exposure to combat.
Blanchard, Dr. D. Caroline+4 more
core
Deletion of Slc26a1 and Slc26a7 Delays Enamel Mineralization in Mice
Amelogenesis features two major developmental stages—secretory and maturation. During maturation stage, hydroxyapatite deposition and matrix turnover require delicate pH regulatory mechanisms mediated by multiple ion transporters.
Kaifeng Yin+6 more
doaj +1 more source
Molecular and circadian controls of ameloblasts [PDF]
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/90102/1/j.1600-0722.2011.00918.x ...
Atanasov+32 more
core +1 more source
ABSTRACT Background Luxation injuries to the predecessors can cause sequelae in the permanent successors. Aim To describe and analyze sequelae in permanent successors according to the child's age at the time of different luxation traumas (concussion, subluxation, extrusion, lateral luxation, intrusion and avulsion) in the primary dentition compared ...
Anne‐Marie Folmer+3 more
wiley +1 more source
Endocytosis and Enamel Formation
Enamel formation requires consecutive stages of development to achieve its characteristic extreme mineral hardness. Mineralization depends on the initial presence then removal of degraded enamel proteins from the matrix via endocytosis.
Cong-Dat Pham+7 more
doaj +1 more source
Background Amelogenesis imperfecta (AI) is a type of hereditary diseases that manifest defects in the formation or mineralization of enamel. Recently, it is reported that inactivation of FAM20C, a well-known Golgi casein kinase, caused AI.
Jing Liu+4 more
semanticscholar +1 more source
ABSTRACT Background Molar incisor hypomineralization (MIH) is associated with enamel's existing qualitative developmental defects. Aim This study aimed to assess the cortical and trabecular mandibular bone morphology in pediatric patients with MIH using fractal analysis (FA) and digital panoramic radiography (DPR) with various radiomorphometric indices.
Asli Soğukpinar Önsüren+1 more
wiley +1 more source
The Specific Role of FAM20C in Amelogenesis [PDF]
Previously, we showed that Sox2- Cre;Fam20Cfl/fl mice in which Fam20C was ubiquitously inactivated had severe defects in dentin, enamel, and bone, along with hypophosphatemia. It remains to be determined if the enamel defects in the mice with universal inactivation of Family with sequence similarity 20-C (FAM20C) were associated with the dentin ...
Baozhi Yuan+6 more
openaire +3 more sources
Enhancing Esthetics With Digital Dentistry: A 2‐Year Follow‐Up of 3D‐Printed Restorations
ABSTRACT Esthetics are a common motivation for dental treatments, with veneers, both direct and indirect, being popular restorative options. Technological advancements, particularly in additive manufacturing (3D printing), have streamlined results. In dentistry, 3D printing is used to fabricate restorations ranging from simple inlays to complex crowns ...
Cristian Higashi+4 more
wiley +1 more source