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Toplam kayıt 8, listelenen: 1-8
Gene-environment interaction in molar-incisor hypomineralization
(Public Library of Science, 2021)
Molar incisor hypomineralization (MIH) is an enamel condition characterized by lesions ranging in color from white to brown which present rapid caries progression, and mainly affects permanent first molars and incisors. ...
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 ...
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 ...
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. ...