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Research 391–420 of 804
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Targeting Superficial or Nodular Basal Cell Carcinoma with Topically Formulated Small Molecule Inhibitor of Smoothened
- WNT10A promotes an invasive and self-renewing phenotype in esophageal squamous cell carcinoma
- When whorls collide: the development of hair patterns in frizzled 6 mutant mice
- Clinical biochemistry of dihydrotestosterone
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- 5-α-Reductase type 2 deficiency: is there a genotype-phenotype correlation? A review
- Recently Identified Forms of Epidermolysis Bullosa
- Glucocorticoids Influencing Wnt/β-Catenin Pathway; Multiple Sites, Heterogeneous Effects
- Madarosis: A marker of many Maladies
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Hedgehog Signaling, Keratin 6 Induction, and Sebaceous Gland Morphogenesis
- Identification of the Key Genes Associated with Different Hair Types in the Inner Mongolia Cashmere Goat
- Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds
- Rare and common genetic determinants of metabolic individuality and their effects on human health
- Pleiotropic Role of Notch Signaling in Human Skin Diseases
- Genetic Variants Associated with Hyperandrogenemia in PCOS Pathophysiology
- The role of WNT10B in physiology and disease: A 10-year update
- Developing stratified epithelia: lessons from the epidermis and thymus
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- Poster Presentations
- Keratin expression by corneal and limbal stem cells during development
- Two-ligand priming mechanism for potentiated phosphoinositide synthesis is an evolutionarily conserved feature of Sec14-like phosphatidylinositol and phosphatidylcholine exchange proteins
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Molecular determinants for the chemical activation of the warmth-sensitive TRPV3 channel by the natural monoterpenoid carvacrol
- Regulation of Receptor Binding Specificity of FGF9 by an Autoinhibitory Homodimerization
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)