Ara
Toplam kayıt 22, listelenen: 11-20
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 ...
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 ...
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 ...
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 ...
Genetic mapping of high caries experience on human chromosome 13
(BMC, 2013)
Background: Our previous genome-wide linkage scan mapped five loci for caries experience. The purpose of this study was to fine map one of these loci, the locus 13q31.1, in order to identify genetic contributors to caries. ...