Search
for
Sort by
Research 91–120 of 197
- The importance of biomedical engineers in the health system
- Transgenic Kallikrein 14 Mice Display Major Hair Shaft Defects Associated with Desmoglein 3 and 4 Degradation, Abnormal Epidermal Differentiation, and IL-36 Signature
- Netherton syndrome subtypes share IL-17/IL-36 signature with distinct IFN-α and allergic responses
- Netherton Syndrome: A Case-Based Review of Diagnosis, Management, and Emerging Treatments.
- Hair shaft disorders in children – An update
- Cell death by cornification
- The Immunological Impact of IL-1 Family Cytokines on the Epidermal Barrier
- 513 Demonstration of hair health benefits using an oral supplement
- Saw Palmetto Extract Inhibits Metastasis and Antiangiogenesis through STAT3 Signal Pathway in Glioma Cell
- Botulinum Toxins in Medical and Cosmetic Dermatology
- MicroRNA-148a Controls Epidermal and Hair Follicle Stem/Progenitor Cells by Modulating the Activities of ROCK1 and ELF5
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- Hair follicles modulate skin barrier function
- First Symposium of Ichthyosis Experts
- Current Genetics in Hair Diseases
- Targeting Cutaneous Cannabinoid Signaling in Inflammation - A “High”-way to Heal?
- Amphiregulin in Fibrotic Diseases and Cancer
- Knockout of integrin β1 in induced pluripotent stem cells accelerates skin-wound healing by promoting cell migration in extracellular matrix
- Amphiregulin in Fibrotic Diseases and Cancer
- Genome-Wide Association Study and Transcriptome Differential Expression Analysis of the Feather Rate in Shouguang Chickens
- Profibrotic Molecules Are Reduced in CRISPR-Edited Emery–Dreifuss Muscular Dystrophy Fibroblasts
- New Plant Extracts Exert Complementary Anti‐Hair Loss Properties in Human In Vitro and Ex Vivo Models
- Hair microscopy: an easy adjunct to diagnosis of systemic diseases in children
- Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivity
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Dupilumab in Inflammatory Skin Diseases: A Systematic Review
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- Targeting the Complexity of In Vitro Skin Models: A Review of Cutting-Edge Developments