Distinct impacts of bi-allelic WNT10A mutations on the permanent and primary dentitions in odonto-onycho-dermal dysplasia
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Title
Distinct impacts of bi-allelic WNT10A
mutations on the permanent and primary dentitions in odonto-onycho-dermal dysplasia
Authors
Keywords
-
Journal
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
Volume -, Issue -, Pages -
Publisher
Wiley
Online
2018-12-20
DOI
10.1002/ajmg.a.60682
References
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Related references
Note: Only part of the references are listed.- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- (2017) Mingang Xu et al. Nature Communications
- Abnormal primary and permanent dentitions with ectodermal symptoms predict WNT10A deficiency
- (2016) Birgitta Bergendal et al. BMC Medical Genetics
- Tricho-odonto-onycho-dermal dysplasia andWNT10Amutations
- (2014) P. Kantaputra et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- The WNT10A gene in ectodermal dysplasias and selective tooth agenesis
- (2014) Gabriele Mues et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Novel missense mutations in the AXIN2 gene associated with non-syndromic oligodontia
- (2014) Singwai Wong et al. ARCHIVES OF ORAL BIOLOGY
- Variability in dentofacial phenotypes in four families with WNT10A mutations
- (2014) Christian P Vink et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Taurodontism, variations in tooth number, and misshapened crowns inWnt10anull mice and human kindreds
- (2014) Jie Yang et al. Molecular Genetics & Genomic Medicine
- Mutations inWNT10Aare frequently involved in oligodontia associated with minor signs of ectodermal dysplasia
- (2013) Julie Plaisancié et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- WNT10Amutations account for ¼ of population-based isolated oligodontia and show phenotypic correlations
- (2013) Pakeeza Shaiq Arzoo et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- WNT10Amutations also associated with agenesis of the maxillary permanent canines, a separate entity
- (2013) P. Kantaputra et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Down-regulation of Wnt10a affects odontogenesis and proliferation in mesenchymal cells
- (2013) Yang Liu et al. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
- WNT10A variants are associated with non-syndromic tooth agenesis in the general population
- (2013) Shujuan Song et al. HUMAN GENETICS
- Involvement of and Interaction between WNT10A and EDA Mutations in Tooth Agenesis Cases in the Chinese Population
- (2013) Huiying He et al. PLoS One
- Mutations inWNT10Aare present in more than half of isolated hypodontia cases
- (2012) Marie-José van den Boogaard et al. JOURNAL OF MEDICAL GENETICS
- Intra-familial Variability of Ectodermal Defects Associated with WNT10A Mutations
- (2011) JA McGrath et al. ACTA DERMATO-VENEREOLOGICA
- WNT10A and isolated hypodontia
- (2011) Piranit Kantaputra et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Schöpf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation, p.Cys107X, in WNT10A
- (2011) Gabriela Petrof et al. AUSTRALASIAN JOURNAL OF DERMATOLOGY
- Phenotypic variability associated with WNT10A nonsense mutations
- (2010) M. Van Geel et al. BRITISH JOURNAL OF DERMATOLOGY
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- (2009) Axel Bohring et al. AMERICAN JOURNAL OF HUMAN GENETICS
- WNT10A missense mutation associated with a complete Odonto-Onycho-Dermal Dysplasia syndrome
- (2009) Sadia Nawaz et al. EUROPEAN JOURNAL OF HUMAN GENETICS
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