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Research 241–270 of 386
- Pink scaling papules and plaques on the palms, soles, chest, abdomen, and extremities
- Faculty Opinions recommendation of Loss of desmocollin 3 in mice leads to epidermal blistering.
- Cell death by cornification
- Mucocutaneous reactions to chemotherapy
- 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
- WNT Signaling in Disease
- British Association of Dermatologists guidelines on the efficacy and use of acitretin in dermatology
- TRP Channels in Skin Biology and Pathophysiology
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity
- Unraveling the ECM-Immune Cell Crosstalk in Skin Diseases
- Regulation of Keratin 9 in Nonpalmoplantar Keratinocytes by Palmoplantar Fibroblasts Through Epithelial–Mesenchymal Interactions
- 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
- 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