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Research 301–330 of 1000+
- Skin Manifestations Associated with Autoimmune Liver Diseases: a Systematic Review
- Novel and recurrent mutations in the <i>AIRE</i> gene of autoimmune polyendocrinopathy syndrome type 1 (APS1) patients
- Recombinant human hepatitis B vaccine initiating alopecia areata: testing the hypothesis using the C3H/HeJ mouse model
- Epigallocatechin-3 Gallate Inhibits STAT-1/JAK2/IRF-1/HLA-DR/HLA-B and Reduces CD8 MKG2D Lymphocytes of Alopecia Areata Patients
- Type 1 Diabetes Mellitus and Autoimmune Diseases: A Critical Review of the Association and the Application of Personalized Medicine
- Alopecia areata
- How Our Microbiome Influences the Pathogenesis of Alopecia Areata
- Genetic Polymorphisms of Immunity Regulatory Genes and Alopecia Areata Susceptibility in Jordanian Patients
- Diagnosis of Hair Loss: Clinical features of common causes of hair loss.
- Transcriptomic crossroads: Decoding genes and pathways that connect alopecia areata with chronic inflammatory skin disorders
- Stem Cells Applications in Regenerative Medicine and Disease Therapeutics
- Fibroblast growth factors: key players in regeneration and tissue repair
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- Keratins and disease at a glance
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- The molecular basis of human keratin disorders
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Madarosis: A marker of many Maladies
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Cronkhite–Canada syndrome: from clinical features to treatment
- Molecular pathways involved in hair follicle tumor formation: all about mammalian target of rapamycin?
- Severe Abnormalities in the Oral Mucosa Induced by Suprabasal Expression of Epidermal Keratin K10 in Transgenic Mice
- The Roles of Non-coding RNA in the Development and Regeneration of Hair Follicles: Current Status and Further Perspectives
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Eyebrow and Eyelash Alopecia: A Clinical Review
- P63 targeted deletion under the FOXN1 promoter disrupts pre-and post-natal thymus development, function and maintenance as well as induces severe hair loss