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Research 31–60 of 159
- Complete Pseudo-Anodontia in an Adult Woman with Pseudo-Hypoparathyroidism Type 1a: A New Additional Nonclassical Feature?
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Genetic Hair Disorders: A Review
- The Roles of EDA2R in Ageing and Disease
- Pathophysiological mechanisms of hair follicle regeneration and potential therapeutic strategies
- Real-world safety of Tepotinib: Insights from the Food and Drug Administration Adverse Event Reporting System
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Wnt Signaling Across Adult Skin Mini-Organs: Interfollicular Epidermis, Hair Follicle, and Nail—Implications for Disease and Regeneration
- Gene network analysis reveals candidate genes related with the hair follicle development in sheep
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Evolution, classification, structure, and functional diversification of steroid 5α-reductase family in eukaryotes
- Multi-omics and AI-driven advances in miRNA-mediated hair follicle regulation in cashmere goats
- Obesity in Adults: Position Statement of Polish Association for the Study on Obesity, Polish Association of Endocrinology, Polish Association of Cardiodiabetology, Polish Psychiatric Association, Section of Metabolic and Bariatric Surgery of the Association of Polish Surgeons, and the College of Family Physicians in Poland
- Trichoscopy in Hair Shaft Disorders
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Sebaceous carcinoma arising at a chronic candidiasis skin lesion of a patient with keratitis-ichthyosis-deafness (KID) syndrome
- Hidradenitis Suppurativa/Acne Inversa/Dissecting Terminal Hair Folliculitis
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Congenital hair loss disorders: Rare, but not too rare
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Genetics of Structural Hair Disorders
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- Two females with hair loss
- Management of congenital ichthyoses: European guidelines of care, part two
- Computational derivation of a molecular framework for hair follicle biology from disease genes
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Regulation of VDR by ΔNp63α is associated with inhibition of cell invasion