Search
for
Sort by
Research 30 of 1000+
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome with Concomitant Lymphopenia: A Novel TP63 Mutation
- Compound Heterozygous Mutations in <i>Forkhead Box N1</i> (<i>FOXN1</i>) Lead to a Severe Immunodeficiency but Normal Hair and Nail Development in Patients
- P63 targeted deletion under the FOXN1 promoter disrupts pre-and post-natal thymus development, function and maintenance as well as induces severe hair loss
- 036 Expanded T cells under lymphopenic condition exhibit memory phenotype and infiltrate around hair follicle
- Patients with Compound Heterozygous Mutations in Forkhead Box N1 have a Severe Immunodeficiency while Maintaining Normal Skin and Hair Development
- Fatal autoimmunity results from the conditional deletion of Snai2 and Snai3
- Minoxidil restores thymic growth in 22q11.2 deletion syndrome by limiting Sox9+ chondrocyte expansion
- HuR ablation destabilizes Foxp3 mRNA and impairs regulatory T cell function, contributing to an autoimmune phenotype
- T-Cell Reconstitution after Thymus Xenotransplantation Induces Hair Depigmentation and Loss
- Hair follicle–derived IL-7 and IL-15 mediate skin-resident memory T cell homeostasis and lymphoma
- A rare primary subcutaneous panniculitis-like T-cell lymphoma with scalp involvement associated with lupus panniculitis
- Tissue resident and follicular Treg cell differentiation is regulated by CRAC channels
- 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
- Human FOXN1-Deficiency Is Associated with αβ Double-Negative and FoxP3+ T-Cell Expansions That Are Distinctly Modulated upon Thymic Transplantation
- Cytotoxicity of bendamustine, alone and in combination with novel agents, toward adult T-cell leukemia cells
- ASSOCIATION OF SYSTEMIC LUPUS ERYTHEMATOSUS AND CHRONIC GRANULOMATOUS DISEASE IN ADULTS: REPORT OF 2 CASES
- Aldesleukin
- Idiopathic CD4+ T-lymphocytopenia
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- SYK inhibitor entospletinib prevents ocular and skin GVHD in mice
- Toxicity of the immune suppressant cyclosporin A in the rat
- Folliculotropic Mycosis Fungoides: Update on Diagnosis, Clinicopathological Stage, and Management
- PD-1+CXCR5−CD4+T cells are correlated with the severity of systemic lupus erythematosus
- 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
- Remission of Alopecia Universalis Following Successful Clinical Islet Transplantation
- FOXN1 deficient nude severe combined immunodeficiency
- MCMV Infection Lowers the Threshold for the Development of Clinical GvHD after Allogeneic Bone Marrow Transplantation.
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association