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Research 30 of 742
- 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
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Phenotypic variability associated with<i>WNT10A</i>nonsense mutations
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Short anagen hair syndrome is caused by mutations in the <i>WNT10A</i> gene and has a genetic overlap with male pattern hair loss
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association
- <i>WNT10A</i> gene variants at the root of short anagen hair syndrome
- Alopecia areata in a patient with WNT10A heterozygous ectodermal dysplasia
- Current Genetics in Hair Diseases
- RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development
- Roles of GasderminA3 in Catagen–Telogen Transition During Hair Cycling
- The fundamentals of WNT10A
- <i>WNT10A</i> , dermatology and dentistry
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- Biology and Genetics of Hair
- Inherited Disorders of the Hair
- Advances in the genetic understanding of hypohidrotic ectodermal dysplasia
- Crosstalk between androgen and Wnt/β-catenin leads to changes of wool density in FGF5-knockout sheep
- WNT10B (wingless-type MMTV integration site family)
- Narrowband UVB treatment induces expression of WNT7B, WNT10B and TCF7L2 in psoriasis skin
- Coordinated Activation of Wnt in Epithelial and Melanocyte Stem Cells Initiates Pigmented Hair Regeneration
- Wnt signaling in skin organogenesis
- Identifying novel strategies for treating human hair loss disorders: Cyclosporine A suppresses the Wnt inhibitor, SFRP1, in the dermal papilla of human scalp hair follicles
- Wnt10b Promotes Differentiation of Mouse Hair Follicle Melanocytes
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- WNT10A promotes an invasive and self-renewing phenotype in esophageal squamous cell carcinoma
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- The role of WNT10B in physiology and disease: A 10-year update