Ara
Toplam kayıt 26, listelenen: 11-20
Role of TRAV locus in low caries experience
(Springer, 2013)
Caries is the most common chronic, multifactorial disease in the world today; and little is still known about the genetic factors influencing susceptibility. Our previous genome-wide linkage scan has identified five loci ...
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 ...
Enamel formation genes influence enamel microhardness before and after cariogenic challenge
(Public Library Science, 2012)
There is evidence for a genetic component in caries susceptibility, and studies in humans have suggested that variation in enamel formation genes may contribute to caries. For the present study, we used DNA samples collected ...
Genetic polymorphisms influence shear bond resistance of orthodontic brackets
(Elsevier, 2020)
Objectives: The purpose of this study was to determine if shear bond resistance of orthodontic brackets bonded to enamel is associated with genes implicated in the enamel mineralization process.Methods: Ninety-two permanent, ...
Fine mapping of locus Xq25.1-27-2 for a low caries experience phenotype
(Pergamon-Elsevier Science Ltd., 2014)
Objective: The purpose of this study was to fine map the locus Xq25.1-27-2 in order to identify genetic contributors involved in low caries experience. Design: Seventy-two families from the Philippines were studied. Caries ...
Fine-Mapping of 5q12.1-13.3 unveils new genetic contributors to caries
(Karger, 2013)
Caries is a multifactorial disease and little is still known about the host genetic factors influencing susceptibility. Our previous genome-wide linkage scan has identified the interval 5q12.1-5q13.3 as linked to low caries ...
Alteration of exon definition causes amelogenesis imperfecta
(SAGE Publications Inc., 2020)
Amelogenesis imperfecta (AI) is a collection of genetic disorders affecting the quality and/or quantity of tooth enamel. More than 20 genes are, so far, known to be responsible for this condition. In this study, we recruited ...
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 ...
Investigating the level of knowledge of the community about oral and dental health
(Georg Thieme Verlag, 2021)
Objectives This study aimed to determine the knowledge and approaches of the participants about oral and dental health. Materials and Methods This was a questionnaire-based cross-sectional survey. Participants' demographic ...