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WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-medi...

WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-medi...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_155ddb06076c415fa01075d340f6d738

WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation

About this item

Full title

WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation

Publisher

London: Nature Publishing Group UK

Journal title

Nature communications, 2017-06, Vol.8 (1), p.15397-15397, Article 15397

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Human
WNT10A
mutations are associated with developmental tooth abnormalities and adolescent onset of a broad range of ectodermal defects. Here we show that β-catenin pathway activity and adult epithelial progenitor proliferation are reduced in the absence of WNT10A, and identify Wnt-active self-renewing stem cells in affected tissues includin...

Alternative Titles

Full title

WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_155ddb06076c415fa01075d340f6d738

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_155ddb06076c415fa01075d340f6d738

Other Identifiers

ISSN

2041-1723

E-ISSN

2041-1723

DOI

10.1038/ncomms15397

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