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Research 31–60 of 55
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity
- Delayed epidermal permeability barrier formation and hair follicle aberrations in Inv-Cldn6 mice
- Macrophage ferroportin is essential for stromal cell proliferation in wound healing
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- Hair Follicular Expression and Function of Group X Secreted Phospholipase A2 in Mouse Skin
- Nagashima-Type Palmoplantar Keratosis: A Common Asian Type Caused by SERPINB7 Protease Inhibitor Deficiency
- New developments in the molecular treatment of ichthyosis: review of the literature
- Notch signaling is significantly suppressed in basal cell carcinomas and activation induces basal cell carcinoma cell apoptosis
- The secret identities of TMPRSS2: Fertility factor, virus trafficker, inflammation moderator, prostate protector and tumor suppressor
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Hair follicles modulate skin barrier function
- Impact of androgen deprivation therapy on mortality of prostate cancer patients with COVID-19: a propensity score-based analysis
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Pica for Uncooked Basmati Rice in Two Women with Iron Deficiency and a Review of Ryzophagia
- Growth retardation and hair loss in transgenic mice overexpressing human H-ferritin gene
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Steroidogenic Factor-1 Lineage Origin of Skin Lesions in Carney Complex Syndrome
- Research Techniques Made Simple: Zebrafish Models for Human Dermatologic Disease
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions
- Current Genetics in Hair Diseases
- Iron Deficiency-Induced Hair Loss Is Associated with ROS-Mediated Disruption of Wnt/β-Catenin Signaling
- Iron–Skin Axis: Exploring the Interplay between Iron Homeostasis and Skin Disorders
- ST14 interacts with TMEFF1 and is a predictor of poor prognosis in ovarian cancer
- Identification of SLC40A1, LCN2, CREB5, and SLC7A11 as ferroptosis-related biomarkers in alopecia areata through machine learning
- Imbalanced redox dynamics induce fibroblast senescence leading to impaired stem cell pools and skin aging
- Matriptase/MT-SP1 is required for postnatal survival, epidermal barrier function, hair follicle development, and thymic homeostasis
- Matriptase: Potent Proteolysis on the Cell Surface
- Epithelial Integrity Is Maintained by a Matriptase-Dependent Proteolytic Pathway
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Delineation of Matriptase Protein Expression by Enzymatic Gene Trapping Suggests Diverging Roles in Barrier Function, Hair Formation, and Squamous Cell Carcinogenesis