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Research 751–780 of 1000+
- A humanized IL-2 fusion protein enhances T regulatory cells in vivo and restrains disease in a murine model of Alopecia Areata 4760
- Serum level of calprotectin as a new inflammatory marker in patients with alopacia areata
- Immune and Non-immune Interactions in the Pathogenesis of Androgenetic Alopecia
- ANAPHYLAXIS: A NOVEL TRIGGER OF TELOGEN EFFLUVIUM IN A CHILD WITH COW'S MILK ALLERGY
- Alopecia Universalis after COVID-19 Vaccination: Case Report and Literature Review
- The vitamin B5/coenzyme A axis: A target for immunomodulation?
- Exogenous IL-27 prevents the development of alopecia areata
- The emergence of Alopecia Areata is not dependent on perforin-mediated cytolysis
- Noval advance of histone modification in inflammatory skin diseases and related treatment methods
- How the Innate Lymphoid Cells Improved Our Understanding of the Mechanisms of Allergic Diseases and Influenced the Standpoint?
- The potential of regulatory T cell-based therapies for alopecia areata
- Identification of BST2 as a biomarker for alopecia areata in both mice and humans
- CD4+ Treg expansion arrests disease progression in a pre-clinical model of alopecia areata
- In vitro expansion of human mesenchymal stem cells and hepatocytes using purified platelet derived growth factors, a potential therapeutic modality for liver fibrosis
- Alopecia areata
- Case Report: Successful Treatment of Alopecia Universalis With Tofacitinib and Increased Cytokine Levels: Normal Therapeutic Reaction or Danger Signal?
- Inflammatory tinea capitis due to <i>Microsporum canis</i> transmitted from asymptomatic domestic cats
- Helminth TGF-β mimic, TGM, increases leukocyte migration and activation while also enhancing cutaneous wound healing and tissue regeneration.
- Thyroidism Effect on Alopecia Patients In Pakistan
- A Fatal Case of Systemic Lupus Erythematosus Complicated with Diffuse Alveolar Hemorrhage
- A(1-7) reduces pathologies associated with SLE in MRL-<i>lpr</i> mice
- 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
- Skin Commensal Antigens: Taking the Road Less Traveled
- Patients with Compound Heterozygous Mutations in Forkhead Box N1 have a Severe Immunodeficiency while Maintaining Normal Skin and Hair Development
- Over-, ectopic-expression of FoxN1 at early life adversely influences lymphopoiesis (HEM3P.280)
- Penilaian Teknis dan Ekonomi Unit Penangkapan Jaring Cumi di PPP Bajomulyo Pati, Jawa Tengah.
- Allergen of the Month—Witch Hazel
- FoxN1 in K14 promoter-driven epithelium is required for generation and maintenance of 3D-thymus medulla and preventing nude phenotype in the skin (36.33)
- A case of systemic lupus erythematosus complicated with aortic regurgitation due to bacterial endocarditis
- A Case of Systemic Lupus Erythematosus with Cutaneous Leukocytoclastic Vasculitis