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Research 601–630 of 1000+
- Hair greying & its palliative management
- Autoimmune Liver Disease In Children
- Autoimmune polyglandular syndrome type 4 – case report
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- Functional mapping of the mouse <i>hairless</i> gene promoter region
- Issue Information
- Oral Presentations
- 138 Characterization of xenobiotic metabolizing enzymes of a reconstructed human epidermal model from adult hair follicles
- Identification of neprilysin as a potential target of arteannuin using computational drug repositioning
- Genetic Defects of Female Sexual Differentiation
- Immunopathogenesis of Primary Cicatricial Alopecia
- Definition criteria and diagnostic assessments
- Australasian Society for Dermatology Research Meeting, May 2007
- Syndromes of Severe Insulin Resistance (SSIRs)
- Cutaneous signals of immune system disease
- Alopecia Areata
- Malignancy and Cancer Treatment-Related Hair and Nail Changes
- Aging and Immortality: Quasi-Programmed Senescence and Its Pharmacologic Inhibition
- Biology of the wool follicle: an excursion into a unique tissue interaction system waiting to be re‐discovered
- The Spectrum of Skin Disease Among Indian Children
- GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk
- Sex steroid synthesis in human skin in situ: The roles of aromatase and steroidogenic acute regulatory protein in the homeostasis of human skin
- Stem cells and aberrant signaling of molecular systems in skin aging
- From gene to therapy in spinal and bulbar muscular atrophy: Are we there yet?
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Androgenic Alopecia Is Associated with Less Dietary Soy, Higher Blood Vanadium and rs1160312 1 Polymorphism in Taiwanese Communities
- Novel Systematics of Nomenclature and Classification of Female Functional Androgenization (Including Polycystic Ovary Syndrome and Non-Classic Congenital Adrenal Hyperplasia)
- Novel <i>ABCD1</i> Gene Mutation in Adrenomyeloneuropathy with Hypoplasia and Agenesis of the Corpus Callosum
- Urticaria, Drug Hypersensitivity Rashes, Nodules and Tumors, and Atrophic Diseases