Results 81 to 90 of about 7,348,517 (171)

Effects of PAX9 and MSX1 gene variants to hypodontia, tooth size and the type of congenitally missing teeth

open access: yesCellular and Molecular Biology, 2016
ooth agenesis, affecting up to 20% of human population, is one of the most common congenital disorder. The most frequent form of tooth agenesis is known as hypodontia, which is characterized by the absence of one to five permanent teeth excluding third molars.
D, Kirac   +8 more
openaire   +4 more sources

A periodic pattern generator for dental diversity

open access: yesBMC Biology, 2008
Background Periodic patterning of iterative structures is a fundamental process during embryonic organization and development. Studies have shown how gene networks are employed to pattern butterfly eyespots, fly bristles and vertebrate epithelial ...
Streelman J Todd   +2 more
doaj   +1 more source

Characterization of pax1, pax9, and uncx sclerotomal genes during Xenopus laevis embryogenesis

open access: yesDevelopmental Dynamics, 2013
Background: The axial skeleton develops from the sclerotome, a mesenchymal cell population derived from somites. Sclerotomal cells migrate from somites to the perinotochordal and perineural space where they differentiate into chondrocytes to form cartilage and bone.
Sanchez, Romel Sebastian   +1 more
openaire   +3 more sources

Genetic factors define CPO and CLO subtypes of nonsyndromicorofacial cleft.

open access: yesPLoS Genetics, 2019
Nonsyndromic orofacial cleft (NSOFC) is a severe birth defect that occurs early in embryonic development and includes the subtypes cleft palate only (CPO), cleft lip only (CLO) and cleft lip with cleft palate (CLP).
Lulin Huang   +26 more
doaj   +1 more source

Genetic Variants of MSX1, PAX9, and AXIN2 in Mayan Probands with Dental Agenesis from Yucatan, Mexico

open access: yesOdovtos - International Journal of Dental Sciences
The present study aimed to determine the genetic variants of PAX9, MSX1, and AXIN2 in Mayan probands with non-syndromic dental agenesis (NSDA) from Yucatan, Mexico. We sequenced DNA of specific exons of the PAX9, MSX1, and AXIN2 genes by using the Sanger
Nayelli A. González-Pérez   +9 more
semanticscholar   +1 more source

Characterization of novel MSX1 mutations identified in Japanese patients with nonsyndromic tooth agenesis.

open access: yesPLoS ONE, 2014
Since MSX1 and PAX9 are linked to the pathogenesis of nonsyndromic tooth agenesis, we performed detailed mutational analysis of these two genes sampled from Japanese patients.
Seishi Yamaguchi   +11 more
doaj   +1 more source

Diagnostic and prognostic biomarkers associated with histotype in advanced epithelial ovarian cancer

open access: yesScientific Reports
Despite advances in cancer treatments, epithelial ovarian cancer (EOC) remains the leading cause of death among gynecologic cancers. EOC is stratified into five main histopathological subtypes: high-grade serous carcinoma (HGSC), low-grade serous ...
Ella Ittner   +10 more
doaj   +1 more source

MSX1 and PAX9 Polymorphisms and Their Association With Lateral Incisor Morphology in Patients With Maxillary Canine Impaction. [PDF]

open access: yesMed Sci Monit
Todorović A   +8 more
europepmc   +1 more source

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