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Research 601–630 of 1000+
- The developmental basis of fingerprint pattern formation and variation
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Keratin intermediate filaments in the colon: guardians of epithelial homeostasis
- Molecular Genetics of the PI3K-AKT-mTOR Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities
- Ichthyosis with confetti: clinics, molecular genetics and management
- Demodicosis in Different Age Groups and Alternative Treatment Options—A Review
- S100A4/Nonmuscle Myosin IIA/p53 Axis Contributes to Aggressive Features in Ovarian High-Grade Serous Carcinoma
- FOXN1 deficient nude severe combined immunodeficiency
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- The Role of Sex and Gender in Dermatology - From Pathogenesis to Clinical Implications
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i>
- Fibrodysplasia Ossificans Progressiva (FOP): A Segmental Progeroid Syndrome
- Developing stratified epithelia: lessons from the epidermis and thymus
- SOCS1 and SOCS3 as key checkpoint molecules in the immune responses associated to skin inflammation and malignant transformation
- Genetic Hair Disorders: A Review
- Identification of the keratin-associated protein 13-3 (KAP13-3) gene in sheep
- Poster Presentations
- Venus trap in the mouse embryo reveals distinct molecular dynamics underlying specification of first embryonic lineages
- Innate type 2 immunity controls hair follicle commensalism by Demodex mites
- The Immunological Impact of IL-1 Family Cytokines on the Epidermal Barrier
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- 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
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- Colchicine in Managing Skin Conditions: A Systematic Review
- Thiopurines: Recent Topics and Their Role in the Treatment of Inflammatory Bowel Diseases
- Real-world single-center experience with 10 cases of generalized pustular psoriasis successfully treated with ixekizumab
- Developmental genetics of color pattern establishment in cats
- Deletion of the epidermis derived laminin γ1 chain leads to defects in the regulation of late hair morphogenesis
- Biochemical and Structural Characteristics, Gene Regulation, Physiological, Pathological and Clinical Features of Lipocalin-Type Prostaglandin D2 Synthase as a Multifunctional Lipocalin