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Research 511–540 of 650
- 308-nm excimer laser therapy in alopecia areata
- RASopathic Skin Eruptions during Vemurafenib Therapy
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- 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
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Keratins and skin disease
- New clinico‐genetic classification of trichothiodystrophy
- Genetics of Inherited Ichthyoses and Related Diseases
- The genetics of alopecia areata: New approaches, new findings, new treatments
- Cylindroma as Tumor of Hair Follicle Origin
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- Skin Structure, Physiology, and Pathology in Topical and Transdermal Drug Delivery
- 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
- Plasma Dermatology: Skin Therapy Using Cold Atmospheric Plasma
- Dynamic expression of Runx1 in skin affects hair structure
- Hair Shaft Abnormalities – Clues to Diagnosis and Treatment
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- A Scarless Healing Tale: Comparing Homeostasis and Wound Healing of Oral Mucosa With Skin and Oesophagus
- Complete Structure of an Epithelial Keratin Dimer: Implications for Intermediate Filament Assembly
- 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