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Research 631–660 of 845
- The regulation of skin homeostasis, repair and the pathogenesis of skin diseases by spatiotemporal activation of epidermal mTOR signaling
- Hair Follicular Expression and Function of Group X Secreted Phospholipase A2 in Mouse Skin
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Loss of Keratin K2 Expression Causes Aberrant Aggregation of K10, Hyperkeratosis, and Inflammation
- Chronic graft versus host disease and skin
- Transglutaminase-3 Enzyme: A Putative Actor in Human Hair Shaft Scaffolding?
- Eyebrow Loss
- Distinct Developmental Functions of Prostasin (CAP1/PRSS8) Zymogen and Activated Prostasin
- Novel Therapeutic Hybrid Systems Using Hydrogels and Nanotechnology: A Focus on Nanoemulgels for the Treatment of Skin Diseases
- Genetic Hair Disorders: A Review
- Dermatologic adverse events in pediatric patients receiving targeted anticancer therapies: A pooled analysis
- [Trichothiodystrophy: a morphological and biochemical study].
- Poster Presentations
- Phospholipase A2 in skin biology: new insights from gene-manipulated mice and lipidomics
- The Genetics of Human Skin Disease
- Nagashima-Type Palmoplantar Keratosis: A Common Asian Type Caused by SERPINB7 Protease Inhibitor Deficiency
- A randomized placebo-controlled study on the effects of pioglitazone on cortisol metabolism in polycystic ovary syndrome
- The Immunological Impact of IL-1 Family Cytokines on the Epidermal Barrier
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Management of the psychological comorbidities of dermatological conditions: practitioners' guidelines
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- Taiwanese Dermatological Association consensus for the prevention and management of epidermal growth factor receptor tyrosine kinase inhibitor-related skin toxicities
- Genetically modified laboratory mice with sebaceous glands abnormalities
- Stem Cells behind the Barrier
- A descriptive study of alopecia patterns and their relation to thyroid dysfunction
- TCF/Lef1-Mediated Control of Lipid Metabolism Regulates Skin Barrier Function
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- A Monoallelic Two-Hit Mechanism in PLCD1 Explains the Genetic Pathogenesis of Hereditary Trichilemmal Cyst Formation
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Expression Profiling Reveals Genes Involved in the Regulation of Wool Follicle Bulb Regression and Regeneration in Sheep