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Research 841–870 of 1000+
- Nonalcoholic fatty liver disease and polycystic ovary syndrome
- TCF/Lef1 activity controls establishment of diverse stem and progenitor cell compartments in mouse epidermis
- Biology and Genetics of Hair
- SOX11 and SOX4 drive the reactivation of an embryonic gene program during murine wound repair
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Learning from nudity: lessons from the nude phenotype
- Valproic Acid Induces Hair Regeneration in Murine Model and Activates Alkaline Phosphatase Activity in Human Dermal Papilla Cells
- What causes hidradenitis suppurativa ?—15 years after
- Nonclassic adrenal hyperplasia
- Dissociated Human Dermal Papilla Cells Induce Hair Follicle Neogenesis in Grafted Dermal–Epidermal Composites
- Synergistic Antibacterial Activity and Wound Healing Properties of Selenium-Chitosan-Mupirocin Nanohybrid System: An in Vivo Study on Rat Diabetic Staphylococcus aureus Wound Infection Model
- Hyperandrogenism in polycystic ovarian syndrome and role of CYP gene variants: a review
- Hair growth-promoting effect of Aconiti Ciliare Tuber extract mediated by the activation of Wnt/β-catenin signaling
- The nude gene and the skin
- Asian Hair: A Review of Structures, Properties, and Distinctive Disorders
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- TCL1 transgenic mouse model as a tool for the study of therapeutic targets and microenvironment in human B-cell chronic lymphocytic leukemia
- Adult epidermal Notch activity induces dermal accumulation of T cells and neural crest derivatives through upregulation of jagged 1
- CBL1‐CIPK26‐mediated phosphorylation enhances activity of the NADPH oxidase RBOHC, but is dispensable for root hair growth
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Lack of androgen receptor transcriptional activity in human keratinocytes
- CAG Repeat Testing of Androgen Receptor Polymorphism: Is This Necessary for the Best Clinical Management of Hypogonadism?
- The VEGF +405 G>C 5' untranslated region polymorphism and risk of PCOS: a study in the South Indian Women
- Interaction between stem cell factor and endothelin-1: effects on melanogenesis in human skin xenografts
- Whole Genome Scan and Selection Signatures for Climate Adaption in Yanbian Cattle
- Anti-aging Properties of Conditioned Media of Epidermal Progenitor Cells Derived from Mesenchymal Stem Cells
- [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
- Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets
- Alopecia Areata