Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindreds - Wikidata - awgldk - TriplyDB

Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindreds

Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindreds

http://www.wikidata.org/entity/Q28256055

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Malformations of the tooth root in humans WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation Natural history collections as windows on evolutionary processes.Odonto-onycho-dermal dysplasia in a patient homozygous for a WNT10A nonsense mutation and mild manifestations of ectodermal dysplasia in carriers of the mutation Loss-of-Function Mutations in the WNT Co-receptor LRP6 Cause Autosomal-Dominant Oligodontia.Abnormal primary and permanent dentitions with ectodermal symptoms predict WNT10A deficiency.Root anomalies and dentin dysplasia in autosomal recessive hyperphosphatemic familial tumoral calcinosis (HFTC).Signaling Pathways Critical for Tooth Root Formation.Cellular and molecular mechanisms of tooth root development.Full Spectrum of Postnatal Tooth Phenotypes in a Novel Irf6 Cleft Lip Model.The association between WNT10A variants and dental development in patients with isolated oligodontia.Isolation and Characterization of Human Adult Epithelial Stem Cells from the Periodontal Ligament.Role of WNT10A in failure of tooth development in humans and zebrafish.Gene screening facilitates diagnosis of complicated symptoms: A case report.The Impact of the Eda Pathway on Tooth Root Development.Whole-Exome Sequencing Identifies Novel Variants for Tooth Agenesis.The Biology Underlying Abnormalities of Tooth Number in Humans.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.The Changing Landscape in the Genetic Etiology of Human Tooth Agenesis.Critical in vivo roles of WNT10A in wound healing by regulating collagen expression/synthesis in WNT10A-deficient mice.Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning

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P2860

Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindreds

http://www.wikidata.org/entity/Q28256055

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2015 nî lūn-bûn

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2015 թուականի Յունուարին հրատարակուած գիտական յօդուած

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2015 թվականի հունվարին հրատարակված գիտական հոդված

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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name

Taurodontism, variations in to ...... a null mice and human kindreds

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Taurodontism, variations in to ...... a null mice and human kindreds

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Taurodontism, variations in to ...... a null mice and human kindreds

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Taurodontism, variations in to ...... a null mice and human kindreds

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Taurodontism, variations in to ...... a null mice and human kindreds

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Taurodontism, variations in to ...... a null mice and human kindreds

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Taurodontism, variations in to ...... a null mice and human kindreds

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Taurodontism, variations in to ...... a null mice and human kindreds

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Taurodontism, variations in to ...... a null mice and human kindreds

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Taurodontism, variations in to ...... a null mice and human kindreds

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Bryan M Reid

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Curtis R Herzog

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Hera Kim-Berman

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James P Simmer

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Jan C-C Hu

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Jie Yang

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K C Kent Lloyd

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Moses Lee

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Murim Choi

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Paul J Benke

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P2860

Genetic diagnosis by whole exome capture and massively parallel DNA sequencing

Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia

Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer

WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes

The complete genome sequence of a Neanderthal from the Altai Mountains

LEF1 is a critical epithelial survival factor during tooth morphogenesis

The role of Axin2 in calvarial morphogenesis and craniosynostosis

Reciprocal requirements for EDA/EDAR/NF-kappaB and Wnt/beta-catenin signaling pathways in hair follicle induction

Neural crest deletion of Dlx3 leads to major dentin defects through down-regulation of Dspp

Bone abnormalities in latent TGF-[beta] binding protein (Ltbp)-3-null mice indicate a role for Ltbp-3 in modulating TGF-[beta] bioavailability

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40-58

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10.1002/MGG3.111

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25629078

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4299714

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