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Research 31–60 of 164
- Alopecia Areata
- Alopecia areata: An update
- Alopecia areata: a review on diagnosis, immunological etiopathogenesis and treatment options
- The Molecular Mechanism Underlying the Proliferating and Preconditioning Effect of Vitamin C on Adipose-Derived Stem Cells
- Alopecia Areata. Current situation and perspectives
- iNKT cells ameliorate human autoimmunity: Lessons from alopecia areata
- Genome-wide association study of skin complex diseases
- The Genetics of Human Skin Disease
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
- Peripheral blood gene expression in alopecia areata reveals molecular pathways distinguishing heritability, disease and severity
- Alopecia Areata is Associated with Increased Expression of Heart Disease Biomarker Cardiac Troponin I
- Identification of ultraviolet B radiation-induced microRNAs in normal human dermal papilla cells
- Novel therapies for alopecia areata: The era of rational drug development
- Discovery of genes and proteins possibly regulating mean wool fibre diameter using cDNA microarray and proteomic approaches
- Generalized hypertrichosis due to secukinumab in a patient with moderate psoriasis: A case of serendipity or zemblanity?
- Identification of differentially expressed genes in actinic keratosis samples treated with ingenol mebutate gel
- Construction of regulatory network for alopecia areata progression and identification of immune monitoring genes based on multiple machine-learning algorithms
- ESGCT and FSGT Collaborative Congress Helsinki, Finland September 17–20, 2015 Abstracts
- Etiopathogenesis of Alopecia Areata
- Inherited Disorders of the Hair
- HuR ablation destabilizes Foxp3 mRNA and impairs regulatory T cell function, contributing to an autoimmune phenotype
- Genome-Wide Association Study of Alopecia Areata in Taiwan: The Conflict Between Individuals and Hair Follicles
- Lentiginous melanoma. A clinically malignant entity that histopathologically seems benign. Case study harbouring BRAF V 600R mutation
- Gli2-serpinh1 drives fibroblast state transition during skin wound healing
- Regenerative potential of CD200- subpopulations of hair follicle bulge
- A novel hairless highly immunodeficient mice model optimized for in vivo imaging
- Risk Factors for Pediatric Alopecia Areata: Clinical and Biochemical Findings from a Case – Control Study
- The Intersection of Sleep and Hair Loss: A Systematic Review
- Precision therapeutics in non-scarring alopecia: a systemic genomic and pathway-based framework for targeted interventions
- Alopecia areata: from immunopathogenesis to emerging therapeutic approaches