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Research 661–690 of 1000+
- Alopecia areata: A multifactorial autoimmune condition
- Tyrosine Kinases in Autoimmune and Inflammatory Skin Diseases
- Role of the Autoimmune Regulator (<i>AIRE</i>) gene in alopecia areata: Strong association of a potentially functional <i>AIRE</i> polymorphism with alopecia universalis
- The Importance of Myeloid-Derived Suppressor Cells in the Regulation of Autoimmune Effector Cells by a Chronic Contact Eczema
- Alopecia areata: Animal models illuminate autoimmune pathogenesis and novel immunotherapeutic strategies
- Autoimmune Disease Induction in a Healthy Human Organ: A Humanized Mouse Model of Alopecia Areata
- Oxidative stress and autoimmune skin disease
- The emerging role of Janus kinase inhibitors in the treatment of autoimmune and inflammatory diseases
- Controlled Delivery of T-box21 Small Interfering RNA Ameliorates Autoimmune Alopecia (Alopecia Areata) in a C3H/HeJ Mouse Model
- The analysis of genetics and associated autoimmune diseases in Chinese vitiligo patients
- T helper 17 cell/regulatory T-cell imbalance in hidradenitis suppurativa/acne inversa: the link to hair follicle dissection, obesity, smoking and autoimmune comorbidities
- Vitiligo: An Autoimmune Skin Disease and its Immunomodulatory Therapeutic Intervention
- Hair follicle is a target of stress hormone and autoimmune reactions
- Resident Memory T Cells in Autoimmune Skin Diseases
- Immunoregulatory Effects of Myeloid-Derived Suppressor Cell Exosomes in Mouse Model of Autoimmune Alopecia Areata
- Autoimmune Disease and Hair Loss
- The Effects of Androgens on T Cells: Clues to Female Predominance in Autoimmune Liver Diseases?
- Autoimmune comorbid diseases associated with lichen planus: a nationwide case–control study
- Alopecia Areata: An Autoimmune Disease of Multiple Players
- Alopecia areata as a model for T cell‐dependent autoimmune diseases
- Nonsegmental Vitiligo and Autoimmune Mechanism
- Breakdown of Immune Tolerance in AIRE-Deficient Rats Induces a Severe Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy–like Autoimmune Disease
- Novel and recurrent mutations in the <i>AIRE</i> gene of autoimmune polyendocrinopathy syndrome type 1 (APS1) patients
- The role of natural killer cells in autoimmune blistering diseases
- 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
- A case of simultaneously occurring lichen sclerosus and segmental vitiligo: connecting the underlying autoimmune pathogenesis
- Case Series: Gene Expression Analysis in Canine Vogt-Koyanagi-Harada/Uveodermatologic Syndrome and Vitiligo Reveals Conserved Immunopathogenesis Pathways Between Dog and Human Autoimmune Pigmentary Disorders
- SOCS3 treatment prevents the development of alopecia areata by inhibiting CD8+ T cell-mediated autoimmune destruction
- Altered expression of keratin 14 in lesional epidermis of autoimmune skin diseases
- Clinical features of vitiligo associated with comorbid autoimmune disease: A prospective survey