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Research 991–1000 of 1000+
- Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2
- Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix
- Formation and Structure of Human Hair
- Action of isotretinoin in acne rosacea and gram-negative folliculitis
- Trichothiodystrophy
- Cell-Type-Specific Chromatin States Differentially Prime Squamous Cell Carcinoma Tumor-Initiating Cells for Epithelial to Mesenchymal Transition
- A Hot New Twist to Hair Biology
- Clinical, Hormonal, Behavioral, and Genetic Characteristics of Androgen Insensitivity Syndrome in a Brazilian Cohort: Five Novel Mutations in the Androgen Receptor Gene
- Androgenetic alopecia: pathogenesis and potential for therapy
- Collider bias undermines our understanding of COVID-19 disease risk and severity