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Research 30 of 87
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Phenotypic variability associated with<i>WNT10A</i>nonsense mutations
- The fundamentals of WNT10A
- Biology and Genetics of Hair
- N02. Hair and Nails
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Inherited Disorders of the Hair
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- <i>WNT10A</i> , dermatology and dentistry
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Current Genetics in Hair Diseases
- Wnt Signaling in Skin Development, Homeostasis, and Disease
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Macrophages Contribute to the Cyclic Activation of Adult Hair Follicle Stem Cells
- Role of β-Catenin Activation Levels and Fluctuations in Controlling Cell Fate
- Distinct tooth regeneration systems deploy a conserved battery of genes
- Genetic prediction of male pattern baldness
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- WNT Signaling in Disease
- WNT10A promotes an invasive and self-renewing phenotype in esophageal squamous cell carcinoma
- Distinct tooth regeneration systems deploy a conserved battery of genes
- Using WGCNA (weighted gene co-expression network analysis) to identify the hub genes of skin hair follicle development in fetus stage of Inner Mongolia cashmere goat
- Overactive Wnt5a signaling disrupts hair follicle polarity during mouse skin development
- 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
- Wnt Signaling Across Adult Skin Mini-Organs: Interfollicular Epidermis, Hair Follicle, and Nail—Implications for Disease and Regeneration
- Alopecia in Children
- The Genetics of Acne