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Research 931–960 of 1000+
- The E211 G>A Androgen Receptor Polymorphism Is Associated with a Decreased Risk of Metastatic Prostate Cancer and Androgenetic Alopecia
- A new path in defining light parameters for hair growth: Discovery and modulation of photoreceptors in human hair follicle
- Beyond Expectations
- The role of lymphocytes in the development and treatment of alopecia areata
- Dissociated Human Dermal Papilla Cells Induce Hair Follicle Neogenesis in Grafted Dermal–Epidermal Composites
- Oral Manifestations of Hematologic and Nutritional Diseases
- Alopecia areata update
- JunB defines functional and structural integrity of the epidermo-pilosebaceous unit in the skin
- Expression and roles of steroidogenic acute regulatory (StAR) protein in ‘non-classical’, extra-adrenal and extra-gonadal cells and tissues
- Hair: What is New in Diagnosis and Management?
- Spinal and bulbar muscular atrophy: pathogenesis and clinical management
- Cushing Syndrome from Percutaneous Absorption of 1% Hydrocortisone Ointment in Netherton Syndrome
- Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss
- Toxic shock syndrome: Recent developments in pathogenesis
- Variation in the caprine keratin-associated protein 15-1 (KAP15-1) gene affects cashmere fibre diameter
- Genome-wide meta-analysis identifies novel loci conferring risk of acne vulgaris
- Sp6 downregulation of follistatin gene expression in ameloblasts
- Evidence for two independent functional variants for androgenetic alopecia around the androgen receptor gene
- Graham Little-Piccardi-Lassueur syndrome associated with androgen insensitivity syndrome (testicular feminization)
- A curated catalog of canine and equine keratin genes
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Cutaneous features of myotonic dystrophy types 1 and 2: Implication of premature aging and vitamin D homeostasis
- Synchronous profiling and analysis of mRNAs and ncRNAs in the dermal papilla cells from cashmere goats
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Analysis of changes in microRNA expression profiles in response to the troxerutin-mediated antioxidant effect in human dermal papilla cells
- Androgen Receptor in Human Health: A Potential Therapeutic Target
- Hair Loss in Autoimmune Cutaneous Bullous Disorders
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- Perspectives in dermatopathology: telomeres and telomerase in ageing and cancer; with emphasis on cutaneous disease
- Androgenetic Alopecia