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Research 31–60 of 318
- Increased risk of chronic fatigue and hair loss following COVID-19 in individuals with hypohidrotic ectodermal dysplasia
- Lgr5 Stem Cells and Potential Treatments for Hair Loss
- miR-29a-5p Inhibits Prenatal Hair Placode Formation Through Targeting EDAR by ceRNA Regulatory Network
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- The biology of hair diversity
- Hair Follicle Morphogenesis During Embryogenesis, Neogenesis, and Organogenesis
- The Roles of EDA2R in Ageing and Disease
- Identification of Ectodysplasin Target Genes Reveals the Involvement of Chemokines in Hair Development
- Mesenchymal–epithelial interactions during hair follicle morphogenesis and cycling
- Novel<i>PAX</i><i>9</i>mutation associated with syndromic tooth agenesis
- A new mutation resulting in the truncation of the TRAF6-interacting domain of XEDAR: a possible novel cause of hypohidrotic ectodermal dysplasia: Figure 1
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- dsRNA Released by Tissue Damage Activates TLR3 to Drive Skin Regeneration
- Keratinocyte-specific ablation of the NF-κB regulatory protein A20 (TNFAIP3) reveals a role in the control of epidermal homeostasis
- Androgens and hair loss
- Asian Hair: A Review of Structures, Properties, and Distinctive Disorders
- Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss
- Evidence for two independent functional variants for androgenetic alopecia around the androgen receptor gene
- Characterization of X‐linked hypohidrotic ectodermal dysplasia (XL‐HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Androgenetska alopecija u žena
- Abstracts
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- Adenomatous Polyposis Coli (APC) Is Required for Normal Development of Skin and Thymus
- The Dermal Papilla: An Instructive Niche for Epithelial Stem and Progenitor Cells in Development and Regeneration of the Hair Follicle
- MicroRNA-214 controls skin and hair follicle development by modulating the activity of the Wnt pathway
- Regeneration of skin appendages and nerves: current status and further challenges
- Factors Associated with Severity of Alopecia Areata
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations