WNT10A missense mutation associated with a complete odonto-onycho-dermal dysplasia syndrome
about
Macrophages contribute to the cyclic activation of adult hair follicle stem cellsMolecular basis of hypohidrotic ectodermal dysplasia: an updateFrizzled6 deficiency disrupts the differentiation process of nail developmentCircadian disruption accelerates tumor growth and angio/stromagenesis through a Wnt signaling pathway.Variability in dentofacial phenotypes in four families with WNT10A mutationsNovel missense mutation in the RSPO4 gene in congenital hyponychia and evidence for a polymorphic initiation codon (p.M1I).Mutations in Frizzled 6 cause isolated autosomal-recessive nail dysplasia.Wnt/beta-catenin signaling in oral tissue development and disease.WNT10A promotes an invasive and self-renewing phenotype in esophageal squamous cell carcinoma.Topical application of lithium chloride on the pulp induces dentin regeneration.A Novel AXIN2 Missense Mutation Is Associated with Non-Syndromic Oligodontia.Odonto-onycho-dermal dysplasia in a patient homozygous for a WNT10A nonsense mutation and mild manifestations of ectodermal dysplasia in carriers of the mutationAbnormal primary and permanent dentitions with ectodermal symptoms predict WNT10A deficiency.Wnt signaling in skin development, homeostasis, and disease.Hear the Wnt Ror: how melanoma cells adjust to changes in Wnt.Genetic pathways in disorders of epidermal differentiation.The association between WNT10A variants and dental development in patients with isolated oligodontia.WNT10A exonic variant increases the risk of keratoconus by decreasing corneal thickness.Roles of heparan sulfate sulfation in dentinogenesisWNT10A variants are associated with non-syndromic tooth agenesis in the general population.Nucleotide variants of genes encoding components of the Wnt signalling pathway and the risk of non-syndromic tooth agenesis.Dental and extra-oral clinical features in 41 patients with WNT10A gene mutations: A multicentric genotype-phenotype study.Case report of Schöpf-Schulz-Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in WNT10A.Impacted Lower Second Permanent Molars at the Ramus and Coronoid Process: A New Clinical Symptom of the WNT10A Mutation in Ectodermal Dysplasia.Common polymorphisms in WNT10A affect tooth morphology as well as hair shape.The Changing Landscape in the Genetic Etiology of Human Tooth Agenesis.WNT10A mutations account for ¼ of population-based isolated oligodontia and show phenotypic correlations.Mutations in WNT10A are frequently involved in oligodontia associated with minor signs of ectodermal dysplasia
P2860
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P2860
WNT10A missense mutation associated with a complete odonto-onycho-dermal dysplasia syndrome
description
2009 nî lūn-bûn
@nan
2009 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
WNT10A missense mutation assoc ...... ycho-dermal dysplasia syndrome
@ast
WNT10A missense mutation assoc ...... ycho-dermal dysplasia syndrome
@en
WNT10A missense mutation assoc ...... ycho-dermal dysplasia syndrome
@nl
type
label
WNT10A missense mutation assoc ...... ycho-dermal dysplasia syndrome
@ast
WNT10A missense mutation assoc ...... ycho-dermal dysplasia syndrome
@en
WNT10A missense mutation assoc ...... ycho-dermal dysplasia syndrome
@nl
prefLabel
WNT10A missense mutation assoc ...... ycho-dermal dysplasia syndrome
@ast
WNT10A missense mutation assoc ...... ycho-dermal dysplasia syndrome
@en
WNT10A missense mutation assoc ...... ycho-dermal dysplasia syndrome
@nl
P2093
P2860
P356
P1476
WNT10A missense mutation assoc ...... ycho-dermal dysplasia syndrome
@en
P2093
Jens Schuster
Joakim Klar
Muhammad Aslam
Muhammad Tariq
Muhammad Wajid
Niklas Dahl
Sadia Nawaz
Shahid Mahmood Baig
P2860
P2888
P304
P356
10.1038/EJHG.2009.81
P407
P577
2009-12-01T00:00:00Z
P5875
P6179
1050755052