Search
for
Sort by
Research 541–570 of 679
- 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
- 308-nm excimer laser therapy in alopecia areata
- RASopathic Skin Eruptions during Vemurafenib Therapy
- 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
- The Two Functional Keratin 6 Genes of Mouse Are Differentially Regulated and Evolved Independently from Their Human Orthologs
- Directed Expression of Keratin 16 to the Progenitor Basal Cells of Transgenic Mouse Skin Delays Skin Maturation
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Rapidly progressing mycosis fungoides presenting as follicular mucinosis
- A new mutation Rim3 resembling Re den is mapped close to retinoic acid receptor alpha (Rara) gene on mouse Chromosome 11
- Environmental Air Pollutants Affecting Skin Functions with Systemic Implications
- Keratins and skin disease
- New clinico‐genetic classification of trichothiodystrophy
- Alteration of Skin Properties with Autologous Dermal Fibroblasts
- Genetics of Inherited Ichthyoses and Related Diseases
- Phototherapy in Childhood
- The genetics of alopecia areata: New approaches, new findings, new treatments
- Cylindroma as Tumor of Hair Follicle Origin
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- Significance of stress keratin expression in normal and diseased epithelia
- Dynamic expression of Runx1 in skin affects hair structure
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Complete Structure of an Epithelial Keratin Dimer: Implications for Intermediate Filament Assembly
- The Role of Nutrition in Immune-Mediated, Inflammatory Skin Disease: A Narrative Review
- 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
- Reconstitution of full-thickness skin by microcolumn grafting
- Ichthyosis with confetti: clinics, molecular genetics and management
- The extraction and characterization of human nail keratin