Search
for
Sort by
Research 841–870 of 857
- Peptidylarginine Deiminase Isoforms Are Differentially Expressed in the Anagen Hair Follicles and Other Human Skin Appendages
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- An unexpected role for keratin 10 end domains in susceptibility to skin cancer
- cDNA Cloning, Expression, and Assembly Characteristics of Mouse Keratin 16
- Ingestion of a dietary supplement resulting in selenium toxicity
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- Recessive Epidermolysis Bullosa Simplex Phenotype Reproduced in Vitro
- Cyclic Alopecia and Abnormal Epidermal Cornification in Zdhhc13 -Deficient Mice Reveal the Importance of Palmitoylation in Hair and Skin Differentiation
- Laminin 332 Is Indispensable for Homeostatic Epidermal Differentiation Programs
- Iron Metabolism of the Skin: Recycling versus Release
- Medical Dermatology
- <i>In vivo</i> response of GsdmA3<sup>Dfl</sup>/+ mice to topically applied fish oil – effects on cellular markers and macrophages
- JAK-Inhibitors Beyond the Label: Emerging Applications in Dermatology
- Uncommon Presentation of Pityriasis Rubra Pilaris of the Scalp: Clinical, Trichoscopic, and Histopathologic Features and Review of the Literature
- Keratosis Pilaris-like Eruption during Treatment of Chronic Myeloid Leukemia with Tyrosine Kinase Inhibitors: Literature Review and Report of a Case Related to Imatinib
- The Ichthyoses: A Guide to Clinical Diagnosis, Genetic Counseling and Therapy
- Ichthyosis
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Genetics of Inherited Ichthyoses and Related Diseases
- Care of the newborn with ichthyosis
- Ichthyosis with confetti: clinics, molecular genetics and management
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- New developments in the molecular treatment of ichthyosis: review of the literature
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Recent advances in congenital ichthyoses
- Ichthyosis linearis circumflexa in a child. Response to narrowband UVB therapy.
- Ichthyosis with confetti: a rare diagnosis and treatment plan