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Research 211–240 of 1000+
- Perspectives in dermatopathology: telomeres and telomerase in ageing and cancer; with emphasis on cutaneous disease
- Development of novel wound dressing based on elastin-like recombinamers for skin regeneration
- Immunopathogenesis of Primary Cicatricial Alopecia
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Physiologic functions of PP2A: Lessons from genetically modified mice
- Sp6 downregulation of follistatin gene expression in ameloblasts
- Chapter 23. Therapeutic Control of Androgen Action
- Extraction and Detection of mRNA from Horsehair
- Discovery of Natural Steroid 5 Alpha-Reductase Inhibitors
- Control of pelage hair follicle development and cycling by complex interactions between follistatin and activin
- Large Scale Gene Expression Profiles of Regenerating Inner Ear Sensory Epithelia
- Chrousos syndrome: from molecular pathogenesis to therapeutic management
- An Ovol2‐Zeb1 transcriptional circuit regulates epithelial directional migration and proliferation
- Crosstalk between androgen and Wnt/β-catenin leads to changes of wool density in FGF5-knockout sheep
- Protein Kinase C<i>ε</i>, Which Is Linked to Ultraviolet Radiation-Induced Development of Squamous Cell Carcinomas, Stimulates Rapid Turnover of Adult Hair Follicle Stem Cells
- Expression of an Olfactomedin-Related Gene in Rat Hair Follicular Papilla Cells
- Functional mapping of the mouse <i>hairless</i> gene promoter region
- Rat steroid 5α-reductase kinetic characteristics: Extreme pH-dependency of the type II isozyme in prostate and epididymis homogenates
- Synthesis and in Vitro Evaluation of 4-Substituted N-(1,1-Dimethylethyl)-3-oxo-4-androstene-17.beta.-carboxamides as 5.alpha.-Reductase Inhibitors and Antiandrogens
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- Transforming growth factor-β in stem cells and tissue homeostasis
- Androgen receptors and their biology
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Suppression of Wnt/β-catenin signaling by EGF receptor is required for hair follicle development
- 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
- INTERFERONS IN DERMATOLOGY
- The crosstalk of monocyte-neutrophil in hair follicles regulates neutrophil transepidermal migration in contact dermatitis
- Pregnancy in postpartum estrus induces inflammatory milk production and catagen specific pup skin inflammation in interleukin-10 deficient mice
- The G1/S transition in mammalian stem cells in vivo is autonomously regulated by cell size