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- P63 targeted deletion under the FOXN1 promoter disrupts pre-and post-natal thymus development, function and maintenance as well as induces severe hair loss
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- Minoxidil restores thymic growth in 22q11.2 deletion syndrome by limiting Sox9+ chondrocyte expansion
- Low-Dose IL-2 for Treating Moderate to Severe Alopecia Areata: A 52-Week Multicenter Prospective Placebo-Controlled Study Assessing its Impact on T Regulatory Cell and NK Cell Populations
- Fatal autoimmunity results from the conditional deletion of Snai2 and Snai3
- PD-1+CXCR5−CD4+T cells are correlated with the severity of systemic lupus erythematosus
- Cytostatics and immunosuppressive drugs
- HuR ablation destabilizes Foxp3 mRNA and impairs regulatory T cell function, contributing to an autoimmune phenotype
- Tissue resident and follicular Treg cell differentiation is regulated by CRAC channels
- Hair follicle–derived IL-7 and IL-15 mediate skin-resident memory T cell homeostasis and lymphoma
- Aldesleukin
- T-Cell Reconstitution after Thymus Xenotransplantation Induces Hair Depigmentation and Loss
- Cutting Edge: Memory Regulatory T Cells Require IL-7 and Not IL-2 for Their Maintenance in Peripheral Tissues
- Cytotoxicity of bendamustine, alone and in combination with novel agents, toward adult T-cell leukemia cells
- Idiopathic CD4+ T-lymphocytopenia
- Toxicity of the immune suppressant cyclosporin A in the rat
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Folliculotropic Mycosis Fungoides: Update on Diagnosis, Clinicopathological Stage, and Management
- SYK inhibitor entospletinib prevents ocular and skin GVHD in mice
- Developing Human Skin Contains Lymphocytes Demonstrating a Memory Signature
- Immunological challenges associated with artificial skin grafts: available solutions and stem cells in future design of synthetic skin
- FOXN1 deficient nude severe combined immunodeficiency
- Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2
- Decision‐Making Regarding the Administration of Live Vaccines to Patients With a <i>FOXN1</i> Heterozygous Missense Variant
- The JAK/STAT signaling pathway: from bench to clinic
- Targeting host cell proteases as a potential treatment strategy to limit the spread of SARS‐CoV‐2 in the respiratory tract
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- Graft-versus-host disease
- SLE and Serum Complement: Causative, Concomitant or Coincidental?
- Hypersensitivity Reactions to Anticoagulant Drugs