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Research 31–60 of 658
- P63 targeted deletion under the FOXN1 promoter disrupts pre-and post-natal thymus development, function and maintenance as well as induces severe hair loss
- Viruses, Variants, and Vaccines: How COVID-19 Has Changed the Way We Look at Skin
- The nude gene and the skin
- Refractory Myasthenia Gravis and Concurrent Alopecia Areata Postthymectomy With Improvements After Cortisone Taper: A Case Report
- Identification of an Intronic Regulatory Element Necessary for Tissue-Specific Expression of <i>Foxn1</i> in Thymic Epithelial Cells
- Minoxidil restores thymic growth in 22q11.2 deletion syndrome by limiting Sox9+ chondrocyte expansion
- Tregs: Where We Are and What Comes Next?
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Biological significance of FoxN1 gain-of-function mutations during T and B lymphopoiesis in juvenile mice
- Acute sensitivity of the oral mucosa to oncogenic <i>K‐ras</i>
- Non-motor Comorbidity of Myasthenia Gravis: Myasthenia Gravis as a Systemic Immunological Disorder Involving Non-motor Systems
- Human Placenta Extract (HPH) Suppresses Inflammatory Responses in TNF-α/IFN-γ-Stimulated HaCaT Cells and a DNCB Atopic Dermatitis (AD)-Like Mouse Model
- The Skin Microenvironment: A Dynamic Regulator of Hair Follicle Development, Cycling and Disease
- Autoimmune alopecia areata due to thymoma without myasthenia gravis: a case report
- Repurposing of Various Current Medicines as Radioprotective Agents
- Author response: Deletion of the MAD2L1 spindle assembly checkpoint gene is tolerated in mouse models of acute T-cell lymphoma and hepatocellular carcinoma
- Tissue Resident Foxp3+ Regulatory T Cells: Sentinels and Saboteurs in Health and Disease
- Chronic inflammatory diseases are stimulated by current lifestyle: how diet, stress levels and medication prevent our body from recovering
- Sexually dimorphic sail feathers in the Mandarin duck as a model for lifelong developmental modulation
- The developing immune network in human prenatal skin
- Cutaneous gain-of-function mutation of LRIG3 leads to alopecia by upregulation of ERBB, PI3K/AKT, NOTCH1 signaling pathways
- Mast cell deficient and neurokinin-1 receptor knockout mice are protected from stress-induced hair growth inhibition
- Assessment of hair loss: clinical relevance of hair growth evaluation methods
- Pax9 is required for filiform papilla development and suppresses skin-specific differentiation of the mammalian tongue epithelium
- Research Relevant Conditions and Pathology in Nonhuman Primates
- DKK1 Mediated Inhibition of Wnt Signaling in Postnatal Mice Leads to Loss of TEC Progenitors and Thymic Degeneration
- Molecular Basis for Hair Loss in Mice Carrying a Novel Nonsense Mutation (<i>Hr<sup>rh-R</sup></i>) in the Hairless Gene (<i>Hr</i>)
- Highly Upregulated Lhx2 in the Foxn1−/− Nude Mouse Phenotype Reflects a Dysregulated and Expanded Epidermal Stem Cell Niche
- Peripherally-Derived Regulatory T Cells in Mouse Autoimmune Diabetes