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Research 211–240 of 732
- SYK inhibitor entospletinib prevents ocular and skin GVHD in mice
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- CAQ Corner: Basic concepts of transplant immunology
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Editor's evaluation: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Alopecia areata: What’s new in epidemiology, pathogenesis, diagnosis, and therapeutic options?
- Thymic Stromal Lymphopoietin in Cutaneous Immune-Mediated Diseases
- Frontal fibrosing alopecia: An update on the hypothesis of pathogenesis and treatment
- Alopecia Areata. Current situation and perspectives
- IL-17a induces age-related olfactory dysfunction by impairing regeneration and promoting respiratory metaplasia in mice
- Mechanism of PPARα agonist in alopecia areata
- Keep quiet—how stress regulates hair follicle stem cells
- Mediator 1 ablation induces enamel-to-hair lineage conversion in mice through enhancer dynamics
- Loss of Msx2 Function Down-Regulates the FoxE3 Expression and Results in Anterior Segment Dysgenesis Resembling Peters Anomaly
- Immunological challenges associated with artificial skin grafts: available solutions and stem cells in future design of synthetic skin
- The mechanisms of MicroRNA 21 in premature ovarian insufficiency mice with mesenchymal stem cells transplantation
- Intravenous Transplantation of Human Hair Follicle-Derived Mesenchymal Stem Cells Ameliorates Trabecular Bone Loss in Osteoporotic Mice
- Epigallocatechin-3 Gallate Inhibits STAT-1/JAK2/IRF-1/HLA-DR/HLA-B and Reduces CD8 MKG2D Lymphocytes of Alopecia Areata Patients
- JAK-STAT1 as therapeutic target for EGFR deficiency-associated inflammation and scarring alopecia
- MicroRNA in skin diseases
- FOXN1 deficient nude severe combined immunodeficiency
- A comparison of transcriptomic patterns measured in the skin of Chinese fine and coarse wool sheep breeds
- ASH2L mediates epidermal differentiation and hair follicle morphogenesis via H3K4me3 modification
- Transcriptomic Analysis Reveals AKT1 Upregulation in Inner Mongolian Cashmere Goats at 12 and 15 Months of Age
- Physiologic functions of PP2A: Lessons from genetically modified mice
- The inconsistent regulation of HOXC13 on different keratins and the regulation mechanism on HOXC13 in cashmere goat (Capra hircus)
- Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2
- Malnutrition and Allergies: Tipping the Immune Balance towards Health
- Rejuvenation by Design: Building Cosmetic Products with Extracellular Vesicle Technology, the Example of Exo.Reset®
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association