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Research 181–210 of 1000+
- Deciphering the Complex Immunopathogenesis of Alopecia Areata
- Genetic Basis of Alopecia Areata
- Human Leukocyte Antigen Class II Alleles Are Associated with Risk of Alopecia Areata
- The Genetic Architecture of Alopecia Areata
- Association between genetically predicted leukocyte telomere length and non-scarring alopecia: A two-sample Mendelian randomization study
- RETRACTED: Gut microbiota, skin microbiota, and alopecia areata: A Mendelian randomization study
- Study of the Thyroid Profile of Patients with Alopecia
- AIRE Deficiency Leads to the Development of Alopecia Areata‒Like Lesions in Mice
- Genome-wide association study of atopic and autoimmune comorbidities in alopecia areata
- T <sub>H</sub> 1 effector CD4 T cells rely on IFN-γ production to induce alopecia areata
- Genetic Insights into Acne, Androgenetic Alopecia, and Alopecia Areata: Implications for Mechanisms and Precision Dermatology
- Elucidating causal relationships of diet-derived circulating antioxidants and the risk of non-scarring alopecia: A Mendelian randomization study
- Recent advances in the genetics of alopecia areata
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Role of Aire and Notch4 Allelic Mutations in Alopecia Areata in C3H/HeJ Mice
- The genetics of alopecia areata: New approaches, new findings, new treatments
- Alopecia areata: What’s new in epidemiology, pathogenesis, diagnosis, and therapeutic options?
- Exploring the Association Between Multidimensional Dietary Patterns and Non-Scarring Hair Loss Using Mendelian Randomization
- Enhanced therapeutic effects of all-trans retinoic acid nanostructured lipid carrier composite gel drug delivery system for alopecia areata
- The Many Faces of Calcineurin Inhibitor Toxicity—What the FK?
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- The Mean Staple Length of Wool Fibre Is Associated with Variation in the Ovine Keratin-Associated Protein 21-2 Gene
- Single nucleotide polymorphisms associated with elevated alanine aminotransferase in patients receiving asunaprevir plus daclatasvir combination therapy for chronic hepatitis C
- Glutathione S-transferase gene polymorphism, total antioxidant status, and blood pressure changes in androgenic alopecia
- Association between PITX2 polymorphism and androgenetic alopecia in the Indian population
- NFATc1 Balances Quiescence and Proliferation of Skin Stem Cells
- Gsdma3 Mutation Causes Bulge Stem Cell Depletion and Alopecia Mediated by Skin Inflammation
- Conditional Activin Receptor Type 1B (Acvr1b) Knockout Mice Reveal Hair Loss Abnormality