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Research 331–360 of 371
- Analysis of Vitamin D Receptor (VDR) Gene Polymorphisms in Alopecia Areata
- Skin Commensal Antigens: Taking the Road Less Traveled
- Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations
- High prevalence of chronic thyroiditis in patients with polycystic ovary syndrome
- Regulatory T cells in inflammatory skin disease: from mice to humans
- Cell and Tissue Damage after Skin Exposure to Ionizing Radiation: Short- and Long-Term Effects after a Single and Fractional Doses
- The Intersection of Sleep and Hair Loss: A Systematic Review
- Hashimoto Thyroiditis - A Comprehensive Review
- Regulatory T cells in skin mediate immune privilege of the hair follicle stem cell niche
- Interleukin gene polymorphisms and alopecia areata: A systematic review and meta-analysis
- Celiac disease associated with alopecia areata: A multicenter case-control study
- Association of JAK 1 and JAK 2 gene polymorphism with alopecia areata risk: a case–control genetic study
- 054 Deep Analysis of CD4+ Trm Cells in Normal and Atopic Dermatitis Human Skin
- Author response: scRNA+TCR-seq reveals the proportion and characteristics of dual TCR Treg cells in mouse lymphoid and non-lymphoid tissues
- 0009 Regulatory γδ T cells protect human scalp hair follicles from alopecia areata in vivo and represent potential therapeutic target
- P110 Comparative efficacy of low-dose oral minoxidil, topical minoxidil, and platelet-rich plasma with topical minoxidil in androgenetic alopecia: a randomized controlled trial
- BH06 (P110) Comparative efficacy of low-dose oral minoxidil, topical minoxidil, and platelet-rich plasma with topical minoxidil in androgenetic alopecia: a randomized controlled trial
- Mendelian randomization study highlights hypothyroidism as a causal determinant of alopecia areata
- Desarrollo de una nueva terapia para el tratamiento de lesiones ulcerosas crónicas mediante el trasplante alogénico de una subpoblación de células madre mesenquimales derivadas de cordones umbilicales humanos
- Overview of Alopecia Areata
- Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2
- The Role of Hair Follicle Immune Privilege Collapse in Alopecia Areata: Status and Perspectives
- A transcriptomic map of murine and human alopecia areata
- Association Between Interleukin 18 Polymorphisms and Alopecia Areata in Koreans
- Type 1 Diabetes Mellitus and Autoimmune Diseases: A Critical Review of the Association and the Application of Personalized Medicine
- The association between rs2476601 polymorphism in PTPN22 gene and risk of alopecia areata
- Genetically predicted levels of circulating cytokines and the risk of six immune skin diseases: a two-sample Mendelian randomization study
- Alopecia Areata: Updates from the Mouse Perspective
- Pathophysiology of Alopecia Areata in the Pediatric Patient
- Increased CRHR1 expression on monocytes from patients with AA enables a pro‐inflammatory response to corticotrophin‐releasing hormone