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Research 991–1000 of 1000+
- Characterization of a Cluster of Human High/Ultrahigh Sulfur Keratin-associated Protein Genes Embedded in the Type I Keratin Gene Domain on Chromosome 17q12-21
- Trichoscopy in alopecias: Diagnosis simplified
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Enanthem in Patients With COVID-19 and Skin Rash
- TNF superfamily in skin appendage development
- Mutations in the Desmoglein 4 Gene Are Associated with Monilethrix-like Congenital Hypotrichosis
- Follicular Transplantation
- The RAIG Family Member, GPRC5D, Is Associated with Hard-Keratinized Structures
- Comparison of a gonadotropin-releasing hormone agonist and a low dose oral contraceptive given alone or together in the treatment of hirsutism.
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases