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Research 121–150 of 1000+
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- Serotoninergic and melatoninergic systems are fully expressed in human skin
- Transforming growth factor-β in stem cells and tissue homeostasis
- Cutaneous Androgen Metabolism: Basic Research and Clinical Perspectives
- Human Scalp Hair Follicles Are Both a Target and a Source of Prolactin, which Serves as an Autocrine and/or Paracrine Promoter of Apoptosis-Driven Hair Follicle Regression
- Structure of human type II 5 alpha-reductase gene.
- Extraskeletal actions of vitamin D
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- A Novel Point Mutation in the Ligand-Binding Domain (LBD) of the Human Glucocorticoid Receptor (hGR) Causing Generalized Glucocorticoid Resistance: The Importance of the C Terminus of hGR LBD in Conferring Transactivational Activity
- Recent advances in the molecular mechanisms determining tissue sensitivity to glucocorticoids: novel mutations, circadian rhythm and ligand-induced repression of the human glucocorticoid receptor
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Prolactin: an emerging force along the cutaneous–endocrine axis
- Gender aspects in skin diseases
- Chrousos syndrome: from molecular pathogenesis to therapeutic management
- Loss of Vascular Endothelial Growth Factor in Human Alopecia Hair Follicles
- The Androgen Receptor Antagonizes Wnt/β-Catenin Signaling in Epidermal Stem Cells
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Removing all obstacles: A critical role for p53 in promoting tissue renewal
- What does acne genetics teach us about disease pathogenesis?
- Whole-genome bisulfite sequencing of goat skins identifies signatures associated with hair cycling
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Stem cells and aberrant signaling of molecular systems in skin aging
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- The metabolic syndrome- associated small G protein ARL15 plays a role in adipocyte differentiation and adiponectin secretion
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Epigenetic regulation in adult stem cells and cancers
- Stem cell rejuvenation and the role of autophagy in age retardation by caloric restriction: An update
- Characterization of minoxidil/hydroxypropyl-β-cyclodextrin inclusion complex in aqueous alginate gel useful for alopecia management: Efficacy evaluation in male rat
- The intragenic mRNA-microRNA regulatory network during telogen-anagen hair follicle transition in the cashmere goat
- Vitamin D receptor-mediated control of Soggy, Wise, and Hairless gene expression in keratinocytes