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Research 991–1000 of 1000+
- Activation of Nrf2 in keratinocytes causes chloracne (MADISH)‐like skin disease in mice
- Directed Expression of Keratin 16 to the Progenitor Basal Cells of Transgenic Mouse Skin Delays Skin Maturation
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Structural and Molecular Hair Abnormalities in Trichothiodystrophy
- Edar Signaling in the Control of Hair Follicle Development
- Epidermal Growth Factor Receptor Inhibitors: A Review of Cutaneous Adverse Events and Management
- Dermatoscopy of hair shaft disorders
- Delayed epidermal permeability barrier formation and hair follicle aberrations in Inv-Cldn6 mice
- Research Advances in Electrospun Nanofiber Membranes for Non-Invasive Medical Applications
- Primary Follicular Dystrophy With Scarring Dermatitis in C57BL/6 Mouse Substrains Resembles Central Centrifugal Cicatricial Alopecia in Humans