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- HLA‐B alleles associated with frontal fibrosing alopecia in Brazil may share similar peptide presentation and T‐cell interaction profiles
- Psoriasis patients demonstrate HLA-Cw*06:02 allele dosage-dependent T cell proliferation when treated with hair follicle-derived keratin 17 protein
- In response to the letter to the editor by Soha Ghanian et al. re our publication “Shorter androgen receptor polyQ alleles protect against life-threatening COVID-19 disease in European males”
- Investigation of Vaspin and Visfatin -4689G/T Gene Polymorphisms in Alopecia Areata Patients
- Methylenetetrahydrofolate reductase C677T mutation in patients with alopecia areata in Turkish population
- Effect of PTPN22, FAS/FASL, IL2RA and CTLA4 genetic polymorphisms on the risk of developing alopecia areata: A systematic review of the literature and meta-analysis
- Gene polymorphisms and serum levels of BDNF and CRH in vitiligo patients
- Lab Quality Management and Methodology
- Autoimmunity: Alopecia Areata
- The spectrum of hair loss in patients with mycosis fungoides and Sézary syndrome
- MTHFR C677T Polymorphism and Serum Homocysteine Level as Risk Factors of Coronary Heart Disease in Patients with Androgenetic Alopecia: A Case Control Study
- Identification of drug-specific public TCR driving severe cutaneous adverse reactions
- Alopecia Areata
- Alopecia Areata
- Genetically separable determinants of hair keratin gene expression
- Clinical Manifestations of Hyperandrogenism and Ovulatory Dysfunction Are Not Associated with His1058 C/T SNP (rs1799817) Polymorphism of Insulin Receptor Gene Tyrosine Kinase Domain in Kashmiri Women with PCOS
- Osteopontin Gene Polymorphisms rs1126616 C>T and rs1126772 A>G are Associated with Atopic Dermatitis in Polish Population
- The VEGF +405 G>C 5' untranslated region polymorphism and risk of PCOS: a study in the South Indian Women
- Alopecia Areata: A tissue specific autoimmune disease of the hair follicle
- Understanding autoimmunity of vitiligo and alopecia areata
- Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses
- The mouse frizzy (<i>fr</i>) and rat ‘hairless’ (<i>fr</i><sup><i>CR</i></sup>) mutations are natural variants of protease serine S1 family member 8 (<i>Prss8</i>)
- Recent Advances in the Pathogenesis of Autoimmune Hair Loss Disease Alopecia Areata
- COVID-19: Understanding Inter-Individual Variability and Implications for Precision Medicine
- Updates from the British Association of Dermatologists 91st Annual Meeting, 5-7 July 2011, London, U.K.
- Clinical Snippets
- Clinical Snippets
- 9. Immunology and Genetics
- Genetic Association Between Polycystic Ovary Syndrome and the <i>APOA5</i> rs662799 and <i>PLIN1</i> rs894160 Metabolic Variants in the Western Saudi Population: A Case-Control Study
- Research Snippets