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Research 61–90 of 1000+
- Loss of epidermal Evi/Wls results in a phenotype resembling psoriasiform dermatitis
- Case Report: PTCH1 splice-site mutation and sonidegib treatment in Gorlin-Goltz syndrome: clinical insights from a family case study
- 136 Physiological function of Krox20 (Egr2) in epithelial stem cells
- Nociceptive and Nonnociceptive Roles of TRPV3 and Its “Druggability”
- TCF/Lef1-Mediated Control of Lipid Metabolism Regulates Skin Barrier Function
- Epidermal PPARγ Is a Key Homeostatic Regulator of Cutaneous Inflammation and Barrier Function in Mouse Skin
- Integration of Biochemical and Mechanical Signals at the Nuclear Periphery: Impacts on Skin Development and Disease
- The Role of Extracellular Vesicles in Cutaneous Remodeling and Hair Follicle Dynamics
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- The acyl-CoA binding protein is required for normal epidermal barrier function in mice
- Autophagy Dysfunction: The Kernel of Hair Loss?
- Malt1 Protease Is Critical in Maintaining Function of Regulatory T Cells and May Be a Therapeutic Target for Antitumor Immunity
- Cell death in skin function, inflammation, and disease
- Alopecia in a Viable Phospholipase C Delta 1 and Phospholipase C Delta 3 Double Mutant
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- Mast cell hyperplasia in the skin of Dsg4-deficient hypotrichosis mice, which are long-living mutants of lupus-prone mice
- Current Progress Regarding Cordyceps militaris, Its Metabolite Function, and Its Production
- Hair, Cutaneous Homeostasis and Stem Cell Functions
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- Forkhead/winged-helix transcription factor whn regulates hair keratin gene expression: Molecular analysis of theNude skin phenotype
- Mdm2-p53 Signaling in Tissue Homeostasis and the DNA Damage Response: A Dissertation
- Faculty Opinions recommendation of Loss of desmocollin 3 in mice leads to epidermal blistering.
- Cyclic Alopecia and Abnormal Epidermal Cornification in Zdhhc13 -Deficient Mice Reveal the Importance of Palmitoylation in Hair and Skin Differentiation
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Role of Stearoyl-CoA Desaturase-1 in Skin Integrity and Whole Body Energy Balance
- Dermatologic Manifestations of Mitochondrial Dysfunction: A Review of the Literature
- Patched1 Functions as a Gatekeeper by Promoting Cell Cycle Progression
- Hair & Cutaneous Development
- Clock genes, hair growth and aging
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype