Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia
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Web-based, participant-driven studies yield novel genetic associations for common traitsMacrophages contribute to the cyclic activation of adult hair follicle stem cellsWNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotesWNT10A missense mutation associated with a complete odonto-onycho-dermal dysplasia syndromeWnt modulators in the biotech pipelineWnt/beta-catenin signaling: components, mechanisms, and diseasesCommon variants in the trichohyalin gene are associated with straight hair in EuropeansMolecular basis of hypohidrotic ectodermal dysplasia: an updateTaurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindredsFrizzled6 deficiency disrupts the differentiation process of nail developmentReciprocal requirements for EDA/EDAR/NF-kappaB and Wnt/beta-catenin signaling pathways in hair follicle inductionCandidate gene analysis of tooth agenesis identifies novel mutations in six genes and suggests significant role for WNT and EDA signaling and allele combinations.WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiationExpression of Gpr177, a Wnt trafficking regulator, in mouse embryogenesisWnt activation in nail epithelium couples nail growth to digit regeneration.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).Wnt signaling and the control of human stem cell fate.The molecular basis of hereditary enamel defects in humans.SMAD4-mediated WNT signaling controls the fate of cranial neural crest cells during tooth morphogenesis.Establishment of intestinal identity and epithelial-mesenchymal signaling by Cdx2.Mutations in Frizzled 6 cause isolated autosomal-recessive nail dysplasia.Involvement of and interaction between WNT10A and EDA mutations in tooth agenesis cases in the Chinese populationWnt/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.Polymorphisms in WNT6 and WNT10A and colorectal adenoma risk.A Comprehensive Overview of Skeletal Phenotypes Associated with Alterations in Wnt/β-catenin Signaling in Humans and Mice.Odonto-onycho-dermal dysplasia in a patient homozygous for a WNT10A nonsense mutation and mild manifestations of ectodermal dysplasia in carriers of the mutationMutations in TSPEAR, Encoding a Regulator of Notch Signaling, Affect Tooth and Hair Follicle Morphogenesis.Abnormal primary and permanent dentitions with ectodermal symptoms predict WNT10A deficiency.Genetic prediction of male pattern baldness.Wnt signaling in skin development, homeostasis, and disease.Wnt/β-Catenin Regulates the Activity of Epiprofin/Sp6, SHH, FGF, and BMP to Coordinate the Stages of OdontogenesisTo Control Site-Specific Skin Gene Expression, Autocrine Mimics Paracrine Canonical Wnt Signaling and Is Activated Ectopically in Skin DiseaseEight Mutations of Three Genes (EDA, EDAR, and WNT10A) Identified in Seven Hypohidrotic Ectodermal Dysplasia Patients.Developmental disorders of the dentition: an update.Almost Unilateral Focal Dermal Hypoplasia.To grow or not to grow: hair morphogenesis and human genetic hair disordersWnt and the Wnt signaling pathway in bone development and disease.
P2860
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P2860
Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia
description
2007 nî lūn-bûn
@nan
2007 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Mutation in WNT10A is associat ...... odonto-onycho-dermal dysplasia
@ast
Mutation in WNT10A is associat ...... odonto-onycho-dermal dysplasia
@en
Mutation in WNT10A is associat ...... odonto-onycho-dermal dysplasia
@en-gb
Mutation in WNT10A is associat ...... odonto-onycho-dermal dysplasia
@nl
type
label
Mutation in WNT10A is associat ...... odonto-onycho-dermal dysplasia
@ast
Mutation in WNT10A is associat ...... odonto-onycho-dermal dysplasia
@en
Mutation in WNT10A is associat ...... odonto-onycho-dermal dysplasia
@en-gb
Mutation in WNT10A is associat ...... odonto-onycho-dermal dysplasia
@nl
prefLabel
Mutation in WNT10A is associat ...... odonto-onycho-dermal dysplasia
@ast
Mutation in WNT10A is associat ...... odonto-onycho-dermal dysplasia
@en
Mutation in WNT10A is associat ...... odonto-onycho-dermal dysplasia
@en-gb
Mutation in WNT10A is associat ...... odonto-onycho-dermal dysplasia
@nl
P2093
P2860
P3181
P356
P1476
Mutation in WNT10A is associat ...... odonto-onycho-dermal dysplasia
@en
P2093
Andre Megarbane
Eliane Chouery
Elsa Nicolas
Hala Megarbane
Hanen Belguith
Lynn Adaimy
Philippe de Mazancourt
Salman Mroueh
Valerie Delague
P2860
P3181
P356
10.1086/520064
P407
P577
2007-10-01T00:00:00Z