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Research 391–420 of 1000+
- Exosomes derived from umbilical cord mesenchymal stem cells promote healing of complex perianal fistulas in rats
- Antigen presenting cells in the skin of a patient with hair loss and systemic lupus erythematosus.
- No. 350-Hirsutism: Evaluation and Treatment
- Evo Devo of the Vertebrates Integument
- Performance and Tolerance of a Protocol for Idiopathic Chronic Greasy Seborrhea in 18 Dogs Using a Shampoo and Mousse Containing Plant Extracts
- Retinoic Acid-Induced Epidermal Transdifferentiation in Skin
- Polygenic risk score predicting susceptibility and outcome of benign prostatic hyperplasia in the Han Chinese
- Iron–Skin Axis: Exploring the Interplay between Iron Homeostasis and Skin Disorders
- Molecular mechanism for transcriptional regulation of the parathyroid hormone gene by Epiprofin
- Supraphysiological Dose of Testosterone Impairs the Expression and Distribution of Sex Steroid Receptors during Endometrial Receptivity Development in Female Sprague–Dawley Rats
- Wnt Signaling Across Adult Skin Mini-Organs: Interfollicular Epidermis, Hair Follicle, and Nail—Implications for Disease and Regeneration
- Erythroderma, Alopecia, Anhidrosis, and Vitiligo as Complications of a Red Ink Tattoo—A Case Report
- Effectiveness of the Optimal Pulse Technology in a Novel Technique for Treating Nasal Blackheads in Asians: A Clinical Study
- The Potential Application of Nanocarriers in Delivering Topical Antioxidants
- Pancreatic cancer
- Cell death by cornification
- Activating an adaptive immune response from a hydrogel scaffold imparts regenerative wound healing
- Cutaneous and Mucosal Lichen Planus: A Comprehensive Review of Clinical Subtypes, Risk Factors, Diagnosis, and Prognosis
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Bone morphogenetic protein-2 (BMP-2) transactivates Dlx3 through Smad1 and Smad4: alternative mode for Dlx3 induction in mouse keratinocytes
- The Skin and Inflamm-Aging
- Netherton syndrome subtypes share IL-17/IL-36 signature with distinct IFN-α and allergic responses
- In Search of New Therapeutics—Molecular Aspects of the PCOS Pathophysiology: Genetics, Hormones, Metabolism and Beyond
- 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
- Normal Fur Development and Sebum Production Depends on Fatty Acid 2-Hydroxylase Expression in Sebaceous Glands
- Exploiting Unique Features of Microneedles to Modulate Immunity
- Neuregulin3 alters cell fate in the epidermis and mammary gland
- Hair Follicular Expression and Function of Group X Secreted Phospholipase A2 in Mouse Skin
- Identification and dissection of an enhancer controlling epithelial gene expression in skin