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Research 451–480 of 1000+
- DNMT1-mediated methylation inhibits microRNA-214-3p and promotes hair follicle stem cell differentiate into adipogenic lineages
- Coexisting trichorrhexis nodosa and pili annulati: a case report of hair shaft abnormalities in a syrian family
- Congenital triangular alopecia: A close mimicker of alopecia areata
- Pharmacotherapy of alopecia areata
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- The Biology and Genomics of Human Hair Follicles: A Focus on Androgenetic Alopecia
- Autistic-undisciplined thinking in the practice of medical trichology
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Self-Amplifying RNA Approach for Protein Replacement Therapy
- Skin applications of cannabidiol: sources, effects, delivery systems, marketed formulations and safety
- Chaperones as thermodynamic sensors
- Trichoscopy in genetic hair shaft abnormalities
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Management of the Female With Non-classical Congenital Adrenal Hyperplasia (NCCAH): A Patient-Oriented Approach
- Engineered Hair Follicle Mesenchymal Stem Cells Overexpressing Controlled-Release Insulin Reverse Hyperglycemia in Mice with Type l Diabetes
- Zinc and Zinc Transporters in Dermatology
- LPA-producing enzyme PA-PLA<sub>1</sub>α regulates hair follicle development by modulating EGFR signalling
- Concomitant immobilization of androgen receptors and 5α- reductase in androgenic alopecia
- An extract of <i>Leontopodium alpinum</i> inhibits catagen development ex vivo and increases hair density in vivo
- A Mouse Model of Androgenetic Alopecia
- Bacteria Display Differential Growth and Adhesion Characteristics on Human Hair Shafts
- Roles of the Hedgehog Signaling Pathway in Cutaneous Physiology and Oncology
- Trichoscopy and Trichogram
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Desmogleins: Hair perspective
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Oral Presentations
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- KCNQ Potassium Channels Modulate Sensitivity of Skin Down-hair (D-hair) Mechanoreceptors