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Research 391–420 of 1000+
- Notch Signaling Regulates Late-Stage Epidermal Differentiation and Maintains Postnatal Hair Cycle Homeostasis
- Expression of Cyclooxygenase Isozymes During Morphogenesis and Cycling of Pelage Hair Follicles in Mouse Skin: Precocious Onset of the First Catagen Phase and Alopecia upon Cyclooxygenase-2 Overexpression
- TCF/Lef1-Mediated Control of Lipid Metabolism Regulates Skin Barrier Function
- Novel D323G mutation of <i>DSG4</i> gene in a girl with localized autosomal recessive hypotrichosis clinically overlapped with monilethrix
- Autophagy-Mediated Cellular Remodeling during Terminal Differentiation of Keratinocytes in the Epidermis and Skin Appendages
- Dermatopathia pigmentosa reticularis: A report of a case with delayed onset alopecia and onychodystrophy
- Abstract 18: Targeted epidermal ablation of EGFR causes local and systemic inflammation
- Selenium in the supplement as the probable cause of hair loss and nail dystrophy
- Constitutive activation of Stat3 in mouse epidermis is linked to hair deficiency and cytoskeletal network damage
- Clinico-epidemiology of Keratosis Pilaris with Histopathologic and Dermoscopic Evaluation – A Cross-sectional Study in a Rural Tertiary Hospital
- A Novel Model System to Identify Cellular and Molecular Defects Underlying Rare Genetic Disorders
- Solitary Nodular Lesion Over Face
- 피부장벽, 이온, 사이토카인
- Disturbed Keratinocyte Differentiation in Transgenic Mice and Organotypic Keratinocyte Cultures as a Result of Spermidine/Spermine N1-Acetyltransferase Overexpression
- Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia
- Impaired wound healing in transgenic mice overexpressing the activin antagonist follistatin in the epidermis
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Wwox Deficiency Causes Downregulation of Prosurvival ERK Signaling and Abnormal Homeostatic Responses in Mouse Skin
- Defective trophoblast function in mice with a targeted mutation of Ets2
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- LPA-producing enzyme PA-PLA<sub>1</sub>α regulates hair follicle development by modulating EGFR signalling
- Dlx3 is a crucial regulator of hair follicle differentiation and cycling
- Epidermal Growth Factor as a Biologic Switch in Hair Growth Cycle
- Folliculin, the Product of the Birt-Hogg-Dube Tumor Suppressor Gene, Interacts with the Adherens Junction Protein p0071 to Regulate Cell-Cell Adhesion
- Mitochondrial Function in Murine Skin Epithelium Is Crucial for Hair Follicle Morphogenesis and Epithelial–Mesenchymal Interactions
- PPAR‐γ signalling as a key mediator of human hair follicle physiology and pathology