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Research 31–60 of 189
- Epidemiology and burden of alopecia areata in Taiwan: a systematic review
- Alopecia Areata Incognita: Current Evidence
- Alopecia areata incognito: an elusive disease
- Alopecia Areata Incognita: A Case Report
- A liquid chromatography/tandem mass spectrometry method for determination of aristolochic acid‐I in rat plasma
- Hudtilstanden alopecia areata, hårtap og dets innvirkning på hverdagsliv
- Female diffuse non‐cicatricial alopecia—The diagnostic value of trichoscopy
- A Case of Cronkhite-Canada Syndrome with Telogen Effluvium and Onycholysis
- The Importance of Myeloid-Derived Suppressor Cells in the Regulation of Autoimmune Effector Cells by a Chronic Contact Eczema
- Activation of Cutaneous Protein Kinase Cα Induces Keratinocyte Apoptosis and Intraepidermal Inflammation by Independent Signaling Pathways
- RANKL Induces Organized Lymph Node Growth by Stromal Cell Proliferation
- MHC Class I-Like MILL Molecules Are β2-Microglobulin-Associated, GPI-Anchored Glycoproteins That Do Not Require TAP for Cell Surface Expression
- Associations Between Skin Microbiome and Metabolome in the Pathogenesis of Atopic Dermatitis Patients With Scalp Involvement
- The investigation of selective sphingosine-1 phosphate receptor 1&4 modulator to treat alopecia areata mouse model
- Increased proliferation of epidermal gamma delta T cells and expression of the transmembrane protein, BST2, in Alopecia areata
- CD4 T cells from mice with alopecia areata express an effector like phenotype and can transfer disease
- Exogenous IL-27 prevents the development of 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
- Generation of autoreactive CD8 T cell in a mouse model of alopecia areata
- Role of <i>foxn1</i> in <i>Xenopus laevis</i> thymopoiesis.
- Helminth TGF-β mimic, TGM, increases leukocyte migration and activation while also enhancing cutaneous wound healing and tissue regeneration.
- 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
- 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)
- 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)
- Treatment and Long-Term Outcome of COVID-19 Disease in Children with Inborn Errors of Immunity (IEI): Does Hematopoietic Stem Cell Transplantation (HSCT) Have a Protective Effect?
- How the Innate Lymphoid Cells Improved Our Understanding of the Mechanisms of Allergic Diseases and Influenced the Standpoint?
- Feronia: A malectin-like domain-containing receptor kinase in Arabidopsis thaliana insights into polarized cell growth, pollen tube - Pistil interactions, and sugar signaling
- Expression, characterization, and structural analysis of human liver delta4-3-ketosteroid 5beta-reductase (AKR1D1) and its disease-related mutant P133R