Results 101 to 110 of about 207,903 (181)
The phenotype and genotype of PAX9 mutations causing tooth agenesis
Objectives: The purpose of this study was to identify associations between PAX9 mutations and clinical features of non-syndromic tooth agenesis patients.
Feng Wang +11 more
core +1 more source
Association between agenesis and root morphology of anterior teeth
Introduction Tooth agenesis is likely to affect the root teeth and should be considerated in orthodontic tratament. Objective The aim of this study was to assess the association between agenesis and root morphology of anterior teeth.
Rodrigo BORALI +4 more
doaj +1 more source
Third molar agenesis in modern humans with and without agenesis of other teeth. [PDF]
Background The number of teeth in the human dentition is of interest both from developmental and evolutionary aspects. The present case-control study focused on the formation of third molars in modern humans aiming to shed more light on the most ...
Scheiwiller, Maya +2 more
core +2 more sources
Novel frameshift variant of WNT10A in a Japanese patient with hypodontia
Congenital tooth agenesis is caused by the impairment of crucial genes related to tooth development, such as Wnt signaling pathway genes. Here, we investigated the genetic causes of sporadic congenital tooth agenesis. Exome sequencing, followed by Sanger
Michiyo Ando +11 more
doaj +1 more source
Association of tooth agenesis with dental anomalies in young subjects
Aim: The aim of the current study is to correlate the presence of tooth agenesis with other dental anomalies in 7- to 15-year-old patients. Materials and methods: After evaluating 4000 panoramic radiographs of young subjects, 430 revealed the presence of
Marra P. M. +3 more
core +1 more source
Genetic polymorphism in esr2 and risk of tooth agenesis
Introduction: Tooth agenesis (TA) is the congenital absence of teeth. Several studies have proposed a strong genetic background for this condition. Aim: The present cross-sectional study aimed to evaluate whether genetic polymorphisms in the genes that code for estrogen receptors (ESR1 and ESR2) are associated with the presence of isolated TA in a ...
Marañón-Vásquez, Guido Artemio +7 more
openaire +2 more sources
Association of AXIN2 gene polymorphisms with nonsyndromic oligodontia in Turkish families
Tooth agenesis is the most common developmental abnormality of the human dentition characterized by the congenital absence of one or more permanent teeth.
Nuriye Dinckan +3 more
doaj +1 more source
Molecular genetics of tooth agenesis [PDF]
Congenital missing of teeth, tooth agenesis or hypodontia, is one of the most common developmental anomalies in man. The common forms in which one or a few teeth are absent, may cause occlusal or cosmetic harm, while severe forms which are relatively ...
Nieminen, Pekka
core
Is Third-Molar Agenesis Related to the Incidence of Other Missing Teeth?
Objective:The aim of this study was to investigate whether third-molar agenesis is related to agenesis of other missing teeth (incisor-premolar hypodontia [IPH]).Materials and Method:A sample of 94 Turkish patients with agenesis of upper lateral incisors
A. Burcu Altan, Ali Altuğ Bıçakçı
doaj +1 more source

