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Research 451–480 of 649
- 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
- Dupilumab in Inflammatory Skin Diseases: A Systematic Review
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- 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
- Therapeutic Use of Botulinum Neurotoxins in Dermatology: Systematic Review
- 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
- A clinical study of cutaneous changes in pregnancy
- 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
- Avaliação dos efeitos adversos clínicos e alterações laboratoriais em pacientes com acne vulgar tratados com isotretinoína oral
- 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