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Research 181–210 of 1000+
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Sprouty/FGF signaling regulates the proximal–distal feather morphology and the size of dermal papillae
- Dermal White Adipose Tissue: A Newly Recognized Layer of Skin Innate Defense
- The role of activins and follistatins in skin and hair follicle development and function
- D’orenone blocks polarized tip growth of root hairs by interfering with the PIN2‐mediated auxin transport network in the root apex
- Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia
- Whole-Cell Bioprocessing of Human Fetal Cells for Tissue Engineering of Skin
- A Review of Barbed Sutures—Evolution, Applications and Clinical Significance
- A novel mutation in the connexin 26 gene (<i>GJB2</i>) in a child with clinical and histological features of keratitis–ichthyosis–deafness (KID) syndrome
- Contact Dermatitis Associated With Nail Care Products: Retrospective Analysis of North American Contact Dermatitis Group Data, 2001–2016
- Yellow facial papules associated with frontal fibrosing alopecia: A distinct histologic pattern and response to isotretinoin
- The scope of the dermoscope
- Basonuclin as a cell marker in the formation and cycling of the murine hair follicle
- From good to bad: Intravital imaging of the hijack of physiological processes by cancer cells
- Combinatorial Biosynthesis of Sulfated Benzenediol Lactones with a Phenolic Sulfotransferase from Fusarium graminearum PH-1
- Graham Little-Piccardi-Lassueur syndrome associated with androgen insensitivity syndrome (testicular feminization)
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability
- 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
- A Two-Stepped Culture Method for Efficient Production of Trichogenic Keratinocytes
- 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
- Banding Pattern on Polarized Hair Microscopic Examination and Unilateral Polymicrogyria in a Patient With Steroid Sulfatase Deficiency