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Research 721–750 of 1000+
- Hairless Suppresses Vitamin D Receptor Transactivation in Human Keratinocytes
- Fundamental hair follicle biology and fine fibre production in animals
- The biology and genetics of curly hair
- 17β-estradiol Inhibits the Production of RANTES in Human Keratinocytes
- Inflammatory perspectives of polycystic ovary syndrome: role of specific mediators and markers
- Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds
- Single-cell transcriptomics defines keratinocyte differentiation in avian scutate scales
- Regulation of stem cell fate by HSPGs: implication in hair follicle cycling
- The Role of gp91phox and the Effect of Tranexamic Acid Administration on Hair Color in Mice
- Combined Systemic and Cutaneous Ovalbumin–Aluminum Sensitization Triggers Thermal Hyperalgesia, Spinal Gliosis, and Nociceptive Nerve Fibers Sprouting in Mice
- Xiaozhi Yufa decoction ameliorates androgenetic alopecia through inhibition of MAPK signaling and regulation of lipid metabolism
- In vitro strategies for mimicking dynamic cell–ECM reciprocity in 3D culture models
- Atypical formations of gintonin lysophosphatidic acids as new materials and their beneficial effects on degenerative diseases
- Fibroblasts: Origins, definitions, and functions in health and disease
- Therapeutic strategy for hair regeneration: hair cycle activation, niche environment modulation, wound-induced follicle neogenesis, and stem cell engineering
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Entdeckung von Autoantigenen bei der Haarverluststörung Alopecia areata: Implikation von posttranslationalen Modifikationen
- Revealing biological mechanisms of skin pigment recovery during treatment in vitiligo patients: A proteomic analysis
- Roles of <i>jumonji</i> and <i>jumonji</i> family genes in chromatin regulation and development
- Mutations in Sterol O-Acyltransferase 1 (Soat1) Result in Hair Interior Defects in AKR/J Mice
- Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia
- Cutaneous gain-of-function mutation of LRIG3 leads to alopecia by upregulation of ERBB, PI3K/AKT, NOTCH1 signaling pathways
- 565 Cutaneous delivery of LEKTI via an engineered strain of staphylococcus epidermidis for the treatment of netherton syndrome
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- The relationship between keratin 18 and epithelial-derived tumors: as a diagnostic marker, prognostic marker, and its role in tumorigenesis
- A frameshift mutation in HTRA1 expands CARASIL syndrome and peripheral small arterial disease to the Chinese population
- CPK1 activates CNGCs through phosphorylation for Ca2+ signaling to promote root hair growth in Arabidopsis
- ST14 interacts with TMEFF1 and is a predictor of poor prognosis in ovarian cancer
- Macrophage-Derived Extracellular Vesicle Promotes Hair Growth
- Androgen deprivation therapy may constitute a more effective COVID-19 prophylactic than therapeutic strategy