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Research 91–120 of 181
- Nanoparticles for Topical Application in the Treatment of Skin Dysfunctions—An Overview of Dermo-Cosmetic and Dermatological Products
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Quality of life in children with scalp hair loss: a Clinico-epidemiological study
- TONGUE, RED
- Targeting the Complexity of In Vitro Skin Models: A Review of Cutting-Edge Developments
- Genetically modified laboratory mice with sebaceous glands abnormalities
- Steatocystoma Multiplex
- The successful treatment of nephrogenic fibrosing dermopathy (NFD) with mycophenolate mofetil (MMF)
- The prevalence of itch and pain and its characteristics in patients with mild to moderate insufficiency and its relationship to the degree of venous insufficiency
- Cannabinoid Signaling in the Skin: Therapeutic Potential of the “C(ut)annabinoid” System
- TCF/Lef1 activity controls establishment of diverse stem and progenitor cell compartments in mouse epidermis
- From structural resilience to cell specification — Intermediate filaments as regulators of cell fate
- 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
- Aberrant Wnt Signaling Induces Comedo-Like Changes in the Murine Upper Hair Follicle
- Generalized multiple eruptive milia in an infant – An unusual presentation
- Keratins: the hair shaft's backbone revealed
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Planar cell polarity effector gene Intu regulates cell fate-specific differentiation of keratinocytes through the primary cilia
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Novel <i>KRT83</i> and <i>KRT86</i> mutations associated with monilethrix
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- The Autoimmune Regulator (AIRE), Which Is Defective in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Patients, Is Expressed in Human Epidermal and Follicular Keratinocytes and Associates With the Intermediate Filament Protein Cytokeratin 17
- Development of Hair Fibres
- Frizzled Receptors in Development and Disease
- A novel control of human keratin expression: cannabinoid receptor 1-mediated signaling down-regulates the expression of keratins K6 and K16 in human keratinocytes<i>in vitro</i>and<i>in situ</i>
- Update on hidradenitis suppurativa: connecting the tracts
- cDNA Cloning, Expression, and Assembly Characteristics of Mouse Keratin 16
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Molecular pathology of skin adnexal tumours
- Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa