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Research 121–150 of 1000+
- 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
- Hair Loss Caused by Gain-of-Function Mutant TRPV3 Is Associated with Premature Differentiation of Follicular Keratinocytes
- VEGF165 modulates proliferation, adhesion, migration and differentiation of cultured human outer root sheath cells from central hair follicle epithelium through VEGFR-2 activation in vitro
- Genome wide association analysis of root hair traits in rice reveals novel genomic regions controlling epidermal cell differentiation
- Delayed epidermal permeability barrier formation and hair follicle aberrations in Inv-Cldn6 mice
- Overexpression of hepatoma-derived growth factor in melanocytes does not lead to oncogenic transformation
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Topographical and developmental studies on target sites of 1,25 (OH2) vitamin D3 in skin
- Netherton syndrome subtypes share IL-17/IL-36 signature with distinct IFN-α and allergic responses
- TGFβ signaling regulates lipogenesis in human sebaceous glands cells
- TCF/Lef1-Mediated Control of Lipid Metabolism Regulates Skin Barrier Function
- A Systematic Review of Keratinocyte Secretions: A Regenerative Perspective
- Orchestration of tissue‐scale mechanics and fate decisions by polarity signalling
- Author response: NuMA-microtubule interactions are critical for spindle orientation and the morphogenesis of diverse epidermal structures
- Decision letter: NuMA-microtubule interactions are critical for spindle orientation and the morphogenesis of diverse epidermal structures
- Impaired Notch‐MKP‐1 signalling in hidradenitis suppurativa: an approach to pathogenesis by evidence from translational biology
- KGF and EGF signalling block hair follicle induction and promote interfollicular epidermal fate in developing mouse skin
- The nude gene and the skin
- The mineralocorticoid receptor plays a transient role in mouse skin development
- Wwox Deficiency Causes Downregulation of Prosurvival ERK Signaling and Abnormal Homeostatic Responses in Mouse Skin
- Coactivator MED1 Ablation in Keratinocytes Results in Hair-Cycling Defects and Epidermal Alterations
- The Catalog of Human Hair Keratins
- HOXC13 Is Involved in the Regulation of Human Hair Keratin Gene Expression
- Phospholipase C 1 is required for skin stem cell lineage commitment
- Mutations in γ-secretase subunit–encoding PSENEN underlie Dowling-Degos disease associated with acne inversa
- A Novel Epithelial Keratin, hK6irs1, is Expressed Differentially in All Layers of the Inner Root Sheath, Including Specialized Huxley Cells (Flügelzellen) of the Human Hair Follicle
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Alarmin Cytokines as Central Regulators of Cutaneous Immunity
- BLIMP1 Is Required for Postnatal Epidermal Homeostasis but Does Not Define a Sebaceous Gland Progenitor under Steady-State Conditions
- Glucocorticoids Influencing Wnt/β-Catenin Pathway; Multiple Sites, Heterogeneous Effects