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Research 841–870 of 1000+
- Hypoxia enhances the hair growth-promoting effects of embryonic stem cell-derived mesenchymal stem cells via NADPH oxidase 4
- Editor's evaluation: Involvement of ILC1-like innate lymphocytes in human autoimmunity, lessons from alopecia areata
- Meeting Report: 68th Montagna Symposium on the Biology of Skin “Decoding Complex Skin Diseases: Integrating Genetics, Genomics, and Disease Biology”
- Autoimmune associations of alopecia areata in pediatric population - A study in tertiary care centre
- Tratamiento de la alopecia areata, un recorrido desde las opciones terapéuticas clásicas hasta los nuevos fármacos aparecidos en los últimos años
- Protein profiling of forehead epidermal corneocytes distinguishes frontal fibrosing from androgenetic alopecia
- Investigation of hub genes and immune infiltration in androgenetic alopecia using bioinformatics analysis
- Genome-wide association study in frontal fibrosing alopecia identifies four susceptibility loci including HLA-B*07:02
- Adrenal 21-hydroxylase gene mutations in Slovenian hyperandrogenic women: evaluation of corticotrophin stimulation and HLA polymorphisms in screening for carrier status
- Joint study of the associations of HLA‐B and the transmembrane short tandem repeat polymorphism of MICA protein with alopecia areata shows independent associations of both with the disease
- Changes in Populations of HLA- DR+CD3+ Cells and CD57–CD16+ Cells in Alopecia areata after Corticosteroid Therapy
- [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
- Immunogenetic and metabolic risk factors in male androgenetic alopecia: the role of HLA-DRB1 alleles and vitamin D3 deficiency
- Alopecia areata update
- Familial aggregation of alopecia areata
- Identification of drug-specific public TCR driving severe cutaneous adverse reactions
- Genetic association of <i>HLA‐DQB1</i> and <i>HLA‐DRB1</i> polymorphisms with alopecia areata in the Italian population
- 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
- The aetiology and pathogenesis of alopecia areata
- The genetics of alopecia areata
- RETRACTED: Causal role of immune cells in alopecia areata: A two‐sample Mendelian randomization study
- Lepromatous Leprosy in a Renal Transplant Recipient
- Exacerbation of alopecia areata during pegylated interferon alpha-2b and ribavirin therapy, possibly due to the collapse of hair follicle immune privilege
- Polymorphism of genes in patients with new coronavirus infection COVID-19
- Hypertrichosis lanuginosa acquisita following cytotoxic chemotherapy
- Association of lichen planopilaris with hypothyroidism: a systematic review and meta‐analysis
- Healthy individuals genetically at-risk for the development of Pemphigus vulgaris or Alopecia areata share disease-like cytokine dysregulation
- Frontal Fibrosing Alopecia