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Research 481–510 of 1000+
- Distribution and Localization of Hydrophobic and Ionic Chemical Groups at the Surface of Bleached Human Hair Fibers
- Human TSC2-null fibroblast-like cells induce hair follicle neogenesis and hamartoma morphogenesis
- The balance of Bmp6 and Wnt10b regulates the telogen-anagen transition of hair follicles
- Enzyme Treatment of Wool and Specialty Hair Fibers
- Relative Influence of Ethanol and Propylene Glycol Cosolvents on Deposition of Minoxidil into the Skin
- Hair-Thread Tourniquet Syndrome: A Case Report and Literature Review
- Skin manifestations among<i>GATA2</i>-deficient patients
- [4-t-Butylphenyl]-N-(4-imidazol-1-yl phenyl)sulfonamide (ISCK03) inhibits SCF/c-kit signaling in 501mel human melanoma cells and abolishes melanin production in mice and brownish guinea pigs
- Dapsone Therapy for Pustular Psoriasis: Case Series and Review of the Literature
- Combination of media, biomaterials and extracellular matrix proteins to enhance the differentiation of neural stem/precursor cells into neurons
- Aesthetic Facial Surgery for the Asian Male
- Hair regrowth in 2 patients with recalcitrant central centrifugal cicatricial alopecia after use of topical metformin
- PTCH1 Germline Mutations and the Basaloid Follicular Hamartoma Values in the Tumor Spectrum of Basal Cell Carcinoma Syndrome (NBCCS)
- Polycystic Ovary Syndrome: A Common Reproductive and Metabolic Disorder Necessitating Early Recognition and Treatment
- Review paper The use of reflectance confocal microscopy in selected inflammatory skin diseases
- Female Adolescent Hair Disorders
- Patient Selection, Hair Transplant Design, and Hairstyle
- DERMATOLOGIC DISEASES AND PROBLEMS OF WOMEN THROUGHOUT THE LIFE CYCLE
- Aesthetic Strategies for the Aging Asian Face
- Basal Cell Carcinoma, Hedgehog Signaling, and Targeted Therapeutics: The Long and Winding Road
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Stem Cell Competition for Niche Occupancy: Emerging Themes and Mechanisms
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Protein and amino acid composition of hair from mice carrying the naked (<i>N</i>) gene
- Metabolic dysfunction in female mice with disruption of 5α-reductase 1
- Congenital atrichia and hypotrichosis
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Alopecia - the search for novel agents continues
- Guía clínica chilena para el estudio y tratamiento de hidradenitis supurativa. Resumen ejecutivo
- Efficacy and Safety of Long-Pulsed 755-nm Alexandrite Laser for Keratosis Pilaris: A Split-Body Randomized Clinical Trial