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Research 211–240 of 662
- Therapeutic Use of Botulinum Neurotoxins in Dermatology: Systematic Review
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion
- Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Keratins 6, 16, and 17 in Health and Disease: A Summary of Recent Findings
- Regionalisation of the skin
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- The expanding significance of keratin intermediate filaments in normal and diseased epithelia
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- TRP Channels in Skin Biology and Pathophysiology
- Unraveling the ECM-Immune Cell Crosstalk in Skin Diseases
- 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
- Prevention and management of dermatological toxicities related to anticancer agents: ESMO Clinical Practice Guidelines☆
- 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
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- A new mutation Rim3 resembling Re den is mapped close to retinoic acid receptor alpha (Rara) gene on mouse Chromosome 11
- Keratins and skin disease
- New clinico‐genetic classification of trichothiodystrophy
- Genetics of Inherited Ichthyoses and Related Diseases
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- 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
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis