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Research 511–540 of 1000+
- The role of lymphocytes in the development and treatment of alopecia areata
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- Antiandrogen therapy for androgenetic alopecia
- Mutations in the Serum/Glucocorticoid Regulated Kinase 3 (Sgk3) Are Responsible for the Mouse Fuzzy (fz) Hair Phenotype
- Experimental cutaneous Bacillus anthracis infections in hairless HRS/J mice
- An update on diagnosis and treatment of female pattern hair loss
- The Distribution of Estrogen Receptor β Is Distinct to That of Estrogen Receptor α and the Androgen Receptor in Human Skin and the Pilosebaceous Unit
- Lymphocytes, neuropeptides, and genes involved in alopecia areata
- Cutaneous Androgen Metabolism: Basic Research and Clinical Perspectives
- An unexpected role for keratin 10 end domains in susceptibility to skin cancer
- The New Keratin Nomenclature
- CD34 Expression by Hair Follicle Stem Cells Is Required for Skin Tumor Development in Mice
- Genetically Altered Expression of Spermidine/Spermine N1-Acetyltransferase Affects Fat Metabolism in Mice via Acetyl-CoA
- Dynamic expression of Runx1 in skin affects hair structure
- De Novo Production of Dermal Papilla Cells during the Anagen Phase of the Hair Cycle
- Morphological Approach to Hair Disorders
- What does acne genetics teach us about disease pathogenesis?
- Breakdown of Immune Tolerance in AIRE-Deficient Rats Induces a Severe Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy–like Autoimmune Disease
- Establishment of type II 5α-reductase over-expressing cell line as an inhibitor screening model
- A Transition State Analogue of 5′-Methylthioadenosine Phosphorylase Induces Apoptosis in Head and Neck Cancers
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- Ku80 as a Novel Receptor for Thymosin β4 That Mediates Its Intracellular Activity Different from G-actin Sequestering
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Pitfalls of PCR-Based Strategy for Genotyping <i>Cre-Loxp</i> Mice
- Characterization of a 300 kbp Region of Human DNA Containing the Type II Hair Keratin Gene Domain
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Generalised Glucocorticoid Resistance
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Dermoscopy: A rapid bedside tool to assess monilethrix