Search
for
Sort by
Research 391–420 of 1000+
- Acne Vulgaris
- Oral Presentations
- 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
- 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
- Laminin 332 Is Indispensable for Homeostatic Epidermal Differentiation Programs
- Iron Metabolism of the Skin: Recycling versus Release
- <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
- Autophagy-Mediated Cellular Remodeling during Terminal Differentiation of Keratinocytes in the Epidermis and Skin Appendages
- Cannabinoid Signaling in the Skin: Therapeutic Potential of the “C(ut)annabinoid” System
- Nanoparticles for Topical Application in the Treatment of Skin Dysfunctions—An Overview of Dermo-Cosmetic and Dermatological Products
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Significance of stress keratin expression in normal and diseased epithelia
- Hidradenitis Suppurativa as a Potential Subtype of Autoinflammatory Keratinization Disease
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Chronic graft versus host disease and skin
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Novel <i>KRT83</i> and <i>KRT86</i> mutations associated with monilethrix
- RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development
- Cannabinoid Compounds as a Pharmacotherapeutic Option for the Treatment of Non-Cancer Skin Diseases
- Steatocystoma Multiplex
- Recessive Epidermolysis Bullosa Simplex Phenotype Reproduced in Vitro
- Putting the Human Hair Follicle Cycle on the Map
- Congenital Adrenal Hyperplasia-Current Insights in Pathophysiology, Diagnostics, and Management.
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor