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Comparison of root canal length measurement methods in primary teeth
(University Library System, University of Pittsburgh, 2018)
Objectves: The purpose of this study was to evaluate the accuracy of conven5onal radiography, intraoral digital radi- ovisiography and electronic apex locator in determining the working length of root canals in primary ...
8-12 yaş arası çocuklarda görülen kötü ağız alışkanlıklarının sıklığı
(Istanbul University Press, 2011)
Bu çalışmanın amacı, 8-12 yaşları arasındaki çocuklarda kötü ağız alışkanlıklarının sıklığının değerlendirilmesi ve sonuçlarının yaşa ve ağız sağlığına göre karşılaştırılmasıdır. Yaşları 8 ile 12 arasında değişen 107 çocuk ...
Aquaporin 5 interacts with fluoride and possibly protects against caries
(Public Library of Science, 2015)
Aquaporins (AQP) are water channel proteins and the genes coding for AQP2, AQP5, and AQP6 are clustered in 12q13. Since AQP5 is expressed in serous acinar cells of salivary glands, we investigated its involvement in caries. ...
Rethinking isolated cleft lip and palate as a syndrome
(Elsevier Science Inc, 2018)
Objective. The goal of the present work was to use dental conditions that have been independently associated with cleft lip and palate (CL/P) as a tool to identify a broader collection of individuals to be used for gene ...
Investigation of surface topography of different root-end filling materials: an in vitro study
(University Library System, University of Pittsburgh, 2019)
Aim: Although there are many materials that can be used for retrograde filling in surgical endodontics, none of them can be regarded as an ideal material yet. The purpose of this study was to compare the surface topography ...
Genetic influences on dental enamel that impact caries differ between the primary and permanent dentitions
(Wiley, 2015)
Clinically, primary and permanent teeth are distinct anatomically and the presentation of caries lesions differs between the two dentitions. Hence, the possibility exists that genetic contributions to tooth formation of ...
Mutations in RELT cause autosomal recessive amelogenesis imperfecta
(Wiley, 2019)
Amelogenesis imperfecta (AI) is a collection of isolated (non-syndromic) inherited diseases affecting dental enamel formation or a clinical phenotype in syndromic conditions. We characterized three consanguineous AI families ...
Clinical and oral findings of a patient with Simpson-Golabi-Behmel syndrome
(Springer, 2015)
Background The Simpson-Golabi-Behmel syndrome (SGBS) is an overgrowth condition characterised by macrosomia, mental deficiency, large head, prominent skull sutures, midface deficiency, hypertelorism, broad nose, wide mouth, ...
Role of estrogen related receptor beta (ESRRB) in DFN35B hearing impairment and dental decay
(BMC, 2014)
Background: Congenital forms of hearing impairment can be caused by mutations in the estrogen related receptor beta (ESRRB) gene. Our initial linkage studies suggested the ESRRB locus is linked to high caries experience ...
In vitro acid-mediated initial dental enamel loss is associated with genetic variants previously linked to caries experience
(Frontiers Media S.A., 2017)
We have previously shown that AQP5 and BTF3 genetic variation and expression in whole saliva are associated with caries experience suggesting that these genes may have a functional role in protecting against caries. To ...