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Research 10 of 929
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Targeting Wnt/β-Catenin Pathway for Developing Therapies for Hair Loss
- Adenovirus-Mediated Wnt10b Overexpression Induces Hair Follicle Regeneration
- Treatment of MSCs with Wnt1a-conditioned medium activates DP cells and promotes hair follicle regrowth
- WNT10A promotes an invasive and self-renewing phenotype in esophageal squamous cell carcinoma
- The balance of Bmp6 and Wnt10b regulates the telogen-anagen transition of hair follicles
- Wnt10b Promotes Differentiation of Mouse Hair Follicle Melanocytes
- The role of WNT10B in physiology and disease: A 10-year update
- Wnt1a maintains characteristics of dermal papilla cells that induce mouse hair regeneration in a 3D preculture system
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