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Research 421–450 of 1000+
- Female pattern hair loss: current treatment concepts.
- Enhanced cutaneous wound healing by functional injectable thermo-sensitive chitosan-based hydrogel encapsulated human umbilical cord-mesenchymal stem cells
- Polymorphisms in the Human High Sulfur Hair Keratin-associated Protein 1, KAP1, Gene Family
- Hair: What is New in Diagnosis and Management?
- Repairing the lungs one breath at a time: How dedicated or facultative are you?
- Systematic approach to hair loss in women
- Vibrissa hair bulge houses two populations of skin epithelial stem cells distinct by their keratin profile
- The developmental basis of fingerprint pattern formation and variation
- Acquired scalp alopecia. Part I: A review
- An unexpected role for keratin 10 end domains in susceptibility to skin cancer
- Congenital hair loss disorders: Rare, but not too rare
- Conversion of the Nipple to Hair-Bearing Epithelia by Lowering Bone Morphogenetic Protein Pathway Activity at the Dermal-Epidermal Interface
- Evaluation of the predictive capacity of DNA variants associated with straight hair in Europeans
- Ageing processes influence keratin and KAP expression in human hair follicles
- Exogen hair characterization in human scalp
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Stem cells and alopecia: a review of pathogenesis
- Human Hair Follicle Stem/Progenitor Cells Express Hypoxia Markers
- cDNA Cloning, Expression, and Assembly Characteristics of Mouse Keratin 16
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Oxidative stress management in the hair follicle: Could targeting NRF2 counter age‐related hair disorders and beyond?
- Non-scarring patchy alopecia in patients with systemic lupus erythematosus differs from that of alopecia areata
- Damage of hair follicle stem cells and alteration of keratin expression in external radiation-induced acute alopecia
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Biomechanical properties of scalp flaps and their correlations to reconstructive and aesthetic surgery procedures
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Thyroxine (T4) may promote re-epithelialisation and angiogenesis in wounded human skin ex vivo
- Recombinant human hair keratin proteins for halting bleeding
- Biochemistry of epidermal stem cells
- Identification of the keratin-associated protein 13-3 (KAP13-3) gene in sheep