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Research 541–570 of 558
- Crosslinking Between Trichocyte Keratins and Keratin Associated Proteins
- Solubility of Foreign Molecules in Stratum Corneum Brick and Mortar Structure
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Transcription Regulation and Protein Subcellular Localization of the Truncated Basic Hair Keratin hHb1-ΔN in Human Breast Cancer Cells
- Transcriptional regulation of the thymus master regulator <i>Foxn1</i>
- Sphingolipid metabolism orchestrates establishment of the hair follicle stem cell compartment
- KLHL24-Mediated Hair Follicle Stem Cells Structural Disruption Causes Alopecia
- Fabrication and characterization of epithelial scaffolds for hair follicle regeneration
- A 15% Trichloroacetic Acid + 3% Glycolic Acid Chemical Peel Series Improves Appearance of Hand Lentigines: An Evaluator-Blinded, Split-Hand Prospective Trial
- Vitamin A resolves lineage plasticity to orchestrate stem cell lineage choices
- Keratin Promotes Differentiation of Keratinocytes Seeded on Collagen/Keratin Hydrogels
- The Possible Role of Antibodies in Alopecia: A Narrative Review
- Comparative Skin Transcriptomics Reveals Key Regulators of Cashmere Fiber Production in Inner Mongolian Goats
- Beyond the Epidermal-Melanin-Unit: The Human Scalp Anagen Hair Bulb Is Home to Multiple Melanocyte Subpopulations of Variable Melanogenic Capacity
- Genome-wide detection of RNA editing events during the hair follicles cycle of Tianzhu white yak
- Exosomes for Regeneration, Rejuvenation, and Repair
- Proceedings of the Ninth World Congress for Hair Research (2015)
- Stem Cells in the Skin
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Dysfunction of keratinocyte adhesion
- 875 A novel animal model of Desmoglein 1 (Dsg1) deficiency reveals an essential role for Dsg1 in epidermal barrier formation
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- LB1076 Using the frog embryonic epidermis as a model to study desmosome function during development
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- A desmosomal cadherin controls multipotent hair follicle stem cell quiescence and orchestrates regeneration through adhesion signaling
- Biology and Genetics of Hair
- Stratum corneum dysfunction in dandruff
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- Cutaneous Markers of Disorders Affecting Adult Horses