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Research 121–150 of 139
- Genetic Basis of Alopecia Areata
- Canine hair‐follicle keratinocytes enriched with bulge cells have the highly proliferative characteristic of stem cells
- The Effects of Androgens on T Cells: Clues to Female Predominance in Autoimmune Liver Diseases?
- The Genetic Architecture of Alopecia Areata
- p53 Is a Direct Transcriptional Repressor of Keratin 17: Lessons from a Rat Model of Radiation Dermatitis
- Autoantigen Discovery in the Hair Loss Disorder, Alopecia Areata: Implication of Post-Translational Modifications
- What is behind the ‘swarm of bees’ in alopecia areata
- Candidate Gene Analysis Of Alopecia Areata In Jordanian Population Of Arab Descent: A Case–Control Study
- Immune therapies for alopecia areata: evidence and new perspectives
- Alopecia areata
- Skin and Scalp Health Benefits of a Specific Botanical Extract Blend: Results from a Double-Blind Placebo-Controlled Study in Urban Outdoor Workers
- Cuero cabelludo sensible: diagnóstico y manejo práctico
- Claves diagnósticas en displasias pilosas II
- Transcriptomic crossroads: Decoding genes and pathways that connect alopecia areata with chronic inflammatory skin disorders
- Stem cell-based therapies for alopecia areata: a narrative review
- Association of JAK 1 and JAK 2 gene polymorphism with alopecia areata risk: a case–control genetic study
- Clinicopathological Features and Pathogenesis of Thymoma Complicated with Alopecia Areata: A Multicenter, Matched Case Analysis
- ALOPECIA AREATA: ASPECTOS FISIOLÓGICOS E AVANÇOS TERAPÊUTICOS – UMA REVISÃO DE LITERATURA
- Entdeckung von Autoantigenen bei der Haarverluststörung Alopecia areata: Implikation von posttranslationalen Modifikationen
- AIRE Deficiency Leads to the Development of Alopecia Areata‒Like Lesions in Mice
- Breakdown of Immune Tolerance in AIRE-Deficient Rats Induces a Severe Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy–like Autoimmune Disease
- The Role of Interferon-γ in Autoimmune Polyendocrine Syndrome Type 1
- The Autoimmune Regulator (AIRE), Which Is Defective in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Patients, Is Expressed in Human Epidermal and Follicular Keratinocytes and Associates With the Intermediate Filament Protein Cytokeratin 17
- Role of Aire and Notch4 Allelic Mutations in Alopecia Areata in C3H/HeJ Mice
- Dermatologic manifestations of endocrine disorders
- Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports
- Alopecia Areata
- Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- Cutaneous Manifestations in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED): A Comprehensive Review