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Research 391–420 of 1000+
- HOXC8 initiates an ectopic mammary program by regulating Fgf10 and Tbx3 expression, and Wnt/β-catenin signaling
- Update on the pathogenesis, genetics and medical treatment of patterned hair loss.
- Novel <i>KRT83</i> and <i>KRT86</i> mutations associated with monilethrix
- Efficient expansion of human keratinocyte stem/progenitor cells carrying a transgene with lentiviral vector
- Linear Lichen Planopilaris of the Trunk: First Report of a Case
- Enhanced Expansion and Sustained Inductive Function of Skin-Derived Precursor Cells in Computer-Controlled Stirred Suspension Bioreactors
- Keratins: the hair shaft's backbone revealed
- A Two-Stepped Culture Method for Efficient Production of Trichogenic Keratinocytes
- Nanoscale microenvironment engineering for expanding human hair follicle stem cell and revealing their plasticity
- A novel monilethrix mutation in coil 2A of KRT86 causing autosomal dominant monilethrix with incomplete penetrance
- A Comprehensive Review of Platelet-Rich Plasma and Its Emerging Role in Accelerating Bone Healing
- Human epidermal neural crest stem cells as candidates for cell-based therapies, disease modeling, and drug discovery
- Generalized calcinosis cutis associated with probable leptospirosis in a dog
- Single-Administration Long-Acting Microarray Patch with Ultrahigh Loading Capacity and Multiple Releases of Thermally Stable Antibodies
- Generation of trichogenic adipose-derived stem cells by expression of three factors
- Thirty Years of Autologous Platelet Concentrates: From Platelet‐Rich Plasma to Platelet‐Rich Fibrin
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Semidominant Inheritance in Epidermolytic Ichthyosis
- Follicular dysplasia in two cows
- Editorial: Mesenchymal Stromal Cell Therapy for Regenerative Medicine
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Clinical and Genetic Characterization of Tunisian Children with Hereditary 1,25-Dihydroxyvitamin D-Resistant Rickets
- Many Paths to Alopecia via Compromised Regeneration of Hair Follicle Stem Cells
- A novel mutation in the FERMT1 gene in a Spanish family with Kindler’s syndrome
- ATP6AP1‐CDG: Follow‐up and female phenotype
- Mast cell hyperplasia in the skin of Dsg4-deficient hypotrichosis mice, which are long-living mutants of lupus-prone mice
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- Shedding light on the FDA’s 510(k) approvals process: low-level laser therapy devices used in the treatment of androgenetic alopecia
- A translational approach to improve therapeutics in atopic dermatitis and beyond