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Research 481–510 of 1000+
- Skin Pigmentation Types, Causes and Treatment—A Review
- Epithelial Integrity Is Maintained by a Matriptase-Dependent Proteolytic Pathway
- FGF5 is a crucial regulator of hair length in humans
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- The Distribution of Estrogen Receptor β Is Distinct to That of Estrogen Receptor α and the Androgen Receptor in Human Skin and the Pilosebaceous Unit
- Small extracellular vesicles from menstrual blood-derived mesenchymal stem cells (MenSCs) as a novel therapeutic impetus in regenerative medicine
- Cytochrome P450: A Target for Drug Development for Skin Diseases
- Hedgehog signaling is essential for normal wound healing
- Overexpression of Smad7 results in severe pathological alterations in multiple epithelial tissues
- The sensory innervation of primate facial skin. II. Vermilion border and mucosa of lip
- A slow-cycling LGR5 tumour population mediates basal cell carcinoma relapse after therapy
- Overexpression of Hedgehog Signaling Is Associated with Epidermal Tumor Formation in Vitamin D Receptor–Null Mice
- Delineation of Matriptase Protein Expression by Enzymatic Gene Trapping Suggests Diverging Roles in Barrier Function, Hair Formation, and Squamous Cell Carcinogenesis
- Microneedles as transdermal drug delivery system for enhancing skin disease treatment
- Thou shall not heal: Overcoming the non-healing behaviour of diabetic foot ulcers by engineering the inflammatory microenvironment
- Human Female Hair Follicles Are a Direct, Nonclassical Target for Thyroid-Stimulating Hormone
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Dissecting the bulge in hair regeneration
- Evidence of Heterogeneity and Quantitative Differences of the Type 1 5α-Reductase Expression in Cultured Human Skin Cells – Evidence of its Presence in Melanocytes
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Hairless Suppresses Vitamin D Receptor Transactivation in Human Keratinocytes
- Improved health-span and lifespan in mtDNA mutator mice treated with the mitochondrially targeted antioxidant SkQ1
- Local and systemic mechanisms that control the hair follicle stem cell niche
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses
- Expression of Desmoglein 1 Compensates for Genetic Loss of Desmoglein 3 in Keratinocyte Adhesion
- Variables affecting the potential efficacy of PRP in providing chronic pain relief
- mTOR signaling promotes stem cell activation via counterbalancing BMP-mediated suppression during hair regeneration
- Direct conversion of mouse and human fibroblasts to functional melanocytes by defined factors