Search
for
Sort by
Research 691–720 of 1000+
- Effects of cytokines, anti-cancer agents and cocarcinogen on DNA synthesis in hair bulb cells
- 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
- Frontal fibrosing alopecia and lichen planopilaris in HLA-identical mother and daughter
- 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
- 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
- HLA‐B alleles associated with frontal fibrosing alopecia in Brazil may share similar peptide presentation and T‐cell interaction profiles
- 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
- Linking allergy to mercury to HLA and burning mouth syndrome
- Genome-wide association study in alopecia areata implicates both innate and adaptive immunity
- Alopecia areata update
- Familial aggregation of alopecia areata
- Epidemiology of vitiligo, associated autoimmune diseases and audiological abnormalities: Ankara study of 80 patients in Turkey
- Identification of drug-specific public TCR driving severe cutaneous adverse reactions
- Distribution of major histocompatibility antigens in normal skin
- 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
- 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>
- The aetiology and pathogenesis of alopecia areata
- A comparative analysis of immune privilege in pregnancy and cancer in the context of checkpoint blockade immunotherapy
- The genetics of alopecia areata
- Lepromatous Leprosy in a Renal Transplant Recipient
- Polymorphism of genes in patients with new coronavirus infection COVID-19
- Analysis of DNA in hair fibers.
- Association of lichen planopilaris with hypothyroidism: a systematic review and meta‐analysis
- Frontal fibrosing alopecia: A review of disease pathogenesis
- Healthy individuals genetically at-risk for the development of Pemphigus vulgaris or Alopecia areata share disease-like cytokine dysregulation
- Clinical and Genetic Aspects of Alopecia Areata: A Cutting Edge Review
- Alopecia Areata