WNT10A mutations causing oligodontia
Author:
Funder
SNUDH Research Fund
Publisher
Elsevier BV
Subject
Cell Biology,General Dentistry,General Medicine,Otorhinolaryngology
Reference29 articles.
1. Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: The odonto-onycho-dermal dysplasia;Adaimy;American Journal of Human Genetics,2007
2. WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes;Bohring;American Journal of Human Genetics,2009
3. Involvement of and interaction between WNT10A and EDA mutations in tooth agenesis cases in the Chinese population;He;PloS One,2013
4. Continuous tooth generation in mouse is induced by activated epithelial Wnt/beta-catenin signaling;Jarvinen;Proceedings of the National Academy of Sciences of the United States of America,2006
5. The impact of tooth agenesis on oral health-related quality of life in children;Kotecha;Journal of Orthodontics,2013
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2. Identification of novel candidate genes associated with non-syndromic tooth agenesis in Mongolian families;Clinical Oral Investigations;2023-12-29
3. Phenotypic characteristics of taurodontism and a novel WNT10A variant in non-syndromic oligodontia family;Archives of Oral Biology;2023-10
4. Identification of potential key variants in mandibular premolar hypodontia through whole-exome sequencing;Frontiers in Genetics;2023-09-08
5. Effect of Wnt10a/β-catenin signaling pathway on promoting the repair of different types of dentin-pulp injury;In Vitro Cellular & Developmental Biology - Animal;2023-08
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