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Research 901–930 of 1000+
- An N-Ethyl-N-Nitrosourea Induced Corticotropin-Releasing Hormone Promoter Mutation Provides a Mouse Model for Endogenous Glucocorticoid Excess
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Elevated Dehydroepiandrosterone Sulfate Levels as the Reproductive Phenotype in the Brothers of Women with Polycystic Ovary Syndrome
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- Genetic Hair Disorders: A Review
- Bioengineering the Hair Follicle
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Poster Presentations
- Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles
- The Implication of Neuroactive Steroids in Tourette's Syndrome Pathogenesis: A Role for 5α‐Reductase?
- Frontal Fibrosing Alopecia: A Review
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- The Genetic Architecture of Alopecia Areata
- Female pattern hair loss
- Temporal expression and steroidal regulation of piRNA pathway genes (mael, piwi, vasa) during Silurana (Xenopus) tropicalis embryogenesis and early larval development
- Stem Cell Therapies for Epidermolysis Bullosa Treatment
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- TCF/Lef1-Mediated Control of Lipid Metabolism Regulates Skin Barrier Function
- Alopecia Areata: Pathogenesis, Diagnosis, and Therapies
- Regulatory T cells in skin mediate immune privilege of the hair follicle stem cell niche
- Wanted, dead and alive: Why a multidisciplinary approach is needed to unlock hair treatment potential
- Cronkhite-Canada Syndrome Associated with Serrated Adenoma and Malignant Polyp: A Case Report and a Literature Review of 13 Cronkhite-Canada Syndrome Cases in Korea
- Developmental genetics of color pattern establishment in cats
- Ethnobotanical Survey of Natural Galactagogues Prescribed in Traditional Chinese Medicine Pharmacies in Taiwan
- Polycystic Ovary Syndrome (PCOS) and Fertility
- Symptomatic zinc deficiency in a full-term breast-fed infant
- Atrichia with papular lesions in two Pakistani consanguineous families resulting from mutations in the human hairless gene
- A computational modelling framework to quantify the effects of passaging cell lines
- Systematic analysis of somatic mutations driving cancer: uncovering functional protein regions in disease development