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Research 31–60 of 1000+
- SLE classification criteria item relationships: implications on SLE as a disease entity
- 801 TEC family kinase inhibitors as a novel class of therapeutics in alopecia areata
- Platelet-derived bio-products: Classification update, applications, concerns and new perspectives
- hMSCs possess the potential to differentiate into DP cells<i>in vivo</i>and<i>in vitro</i>
- Immunology of the Human Nail Apparatus: The Nail Matrix Is a Site of Relative Immune Privilege
- Genome-Wide Association Study of Alopecia Areata in Taiwan: The Conflict Between Individuals and Hair Follicles
- Can the Hair Follicle Become a Model for Studying Selected Aspects of Human Ocular Immune Privilege?
- Controlled Delivery of T-box21 Small Interfering RNA Ameliorates Autoimmune Alopecia (Alopecia Areata) in a C3H/HeJ Mouse Model
- Lichen Planopilaris
- Characterization of Hair Follicle Antigens Targeted by the Anti-Hair Follicle Immune Response
- Human FOXN1-Deficiency Is Associated with αβ Double-Negative and FoxP3+ T-Cell Expansions That Are Distinctly Modulated upon Thymic Transplantation
- Exomic Sequencing of Immune-Related Genes Reveals Novel Candidate Variants Associated with Alopecia Universalis
- Probing the Effects of Stress Mediators on the Human Hair Follicle
- Genome-wide association study in alopecia areata implicates both innate and adaptive immunity
- Maintenance of Hair Follicle Immune Privilege Is Linked to Prevention of NK Cell Attack
- What’s Sex Got to Do With COVID-19? Gender-Based Differences in the Host Immune Response to Coronaviruses
- Human Adipose-derived Mesenchymal Stromal Cells Exhibit High HLA-DR Levels and Altered Cellular Characteristics under a Xeno-free and Serum-free Condition
- Lymphocytes, neuropeptides, and genes involved in alopecia areata
- THE PATHOGENESIS OF ALOPECIA AREATA
- Identification of drug-specific public TCR driving severe cutaneous adverse reactions
- Alopecia Areata: A tissue specific autoimmune disease of the hair follicle
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- FOXN1 deficient nude severe combined immunodeficiency
- Epidermolysis Bullosa Acquisita Occuring In A Patient With Systemic Lupus Erythematosus
- Skin
- Congenital adrenal hyperplasia
- Cutaneous Reactions to Drugs
- Frontal fibrosing alopecia: A review of disease pathogenesis
- Autoimmunity: Alopecia Areata
- Genotyping of the rs1800440 Polymorphism in CYP1B1 Gene and the rs9258883 Polymorphism in HLA-B Gene in a Spanish Cohort of 223 Patients with Frontal Fibrosing Alopecia