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Research 361–390 of 1000+
- Recent Advances in Understanding of the Etiopathogenesis, Diagnosis, and Management of Hair Loss Diseases
- SnapshotDx Quiz: January 2021
- Author Index
- Frontal fibrosing alopecia and lichen planopilaris in HLA-identical mother and daughter
- Human Adipose-Derived Mesenchymal Stromal Cells Exhibit High HLA-DR Levels and Altered Cellular Characteristics under a Xeno-free and Serum-free Condition
- Study of Human Leukocyte Antigen ( HLA ) in 13 cases of familial frontal fibrosing alopecia: CYP 21A2 gene p.V281L mutation from congenital adrenal hyperplasia linked to HLA class I haplotype HLA ‐ A*33:01 ; B*14:02; C*08:02 as a genetic marker
- HLA-B27 Antigen in Women With Ankylosing Spondylitis
- Changes in Populations of HLA- DR+CD3+ Cells and CD57–CD16+ Cells in Alopecia areata after Corticosteroid Therapy
- Alopecia areata after HLA-identical BMT from an affected, sibling donor
- [Significance of HLA-DR+ T cells and natural killer (NK) cells in the peripheral blood lymphocytes of alopecia areata (AA)].
- HLA‐B alleles associated with frontal fibrosing alopecia in Brazil may share similar peptide presentation and T‐cell interaction profiles
- Alopecia Areata is associated with MICA and an extended HLA haplotype
- Human Adipose-derived Mesenchymal Stromal Cells Exhibit High HLA-DR Levels and Altered Cellular Characteristics under a Xeno-free and Serum-free Condition
- Linking allergy to mercury to HLA and burning mouth syndrome
- Alopecia areata update
- Familial aggregation of alopecia areata
- Autoimmunity: Alopecia Areata
- Skin manifestations of celiac disease
- THE PATHOGENESIS OF ALOPECIA AREATA
- Epidemiology of vitiligo, associated autoimmune diseases and audiological abnormalities: Ankara study of 80 patients in Turkey
- Distribution of major histocompatibility antigens in normal skin
- Alopecia Areata
- The spectrum of hair loss in patients with mycosis fungoides and Sézary syndrome
- FOXN1 deficient nude severe combined immunodeficiency
- Human FOXN1-Deficiency Is Associated with αβ Double-Negative and FoxP3+ T-Cell Expansions That Are Distinctly Modulated upon Thymic Transplantation
- Alopecia areata patients show deficiency of FOXP3+CD39+ T regulatory cells and clonotypic restriction of Treg TCRβ-chain, which highlights the immunopathological aspect of the disease
- Pemphigus vulgaris in only one of two monozygotic twins
- hMSCs possess the potential to differentiate into DP cells<i>in vivo</i>and<i>in vitro</i>
- A comparative analysis of immune privilege in pregnancy and cancer in the context of checkpoint blockade immunotherapy
- The genetics of alopecia areata