Ara
Toplam kayıt 22, listelenen: 11-20
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 ...
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, ...
Candidate gene studies in hypodontia suggest role for FGF3
(2013)
Introduction The majority of tooth agenesis cases are mild (hypodontia) and typically not associated with the gene mutations linked to oligodontia. From this, we hypothesise that most cases of tooth agenesis fit a polygenic ...
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 ...