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Research 12
- Monilethrix: a keratin hHb6 mutation is co‐dominant with variable expression
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- Wnt/β-catenin signalling: function, biological mechanisms, and therapeutic opportunities
- Androgen receptor gene polymorphism and biological age markers in men
- The orchestrated network of skin photoaging: From intercellular crosstalk to molecular signaling
- The role of platelet-rich plasma in biomedicine: A comprehensive overview
- Frontal Fibrosing Alopecia in Men: A Review of the Literature
- A Bibliometric Analysis of Alopecia Areata Literature over the Past 50 Years.
- Metabolic Syndrome and Skin Diseases
- Musculoskeletal and body composition response to high-dose testosterone with finasteride after chronic incomplete spinal cord injury—a randomized, double-blind, and placebo-controlled pilot study