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Research 511–540 of 1000+
- Dietary Supplements in Chemotherapy-Induced Peripheral Neuropathy: A New Hope?
- Gene-knockout mice with abnormal epidermal and hair follicular development
- Expression profile analysis of dermal papilla cells mRNA in response to WNT10B treatment
- Amphiregulin in Fibrotic Diseases and Cancer
- Hair Follicle-Related MicroRNA-34a Serum Expression and rs2666433A/G Variant in Patients with Alopecia: A Cross-Sectional Analysis
- Aging skin and non-surgical procedures: a basic science overview
- Amphiregulin in Fibrotic Diseases and Cancer
- Porokeratotic Eccrine Ostial and Dermal Duct Nevus: A Report of Rare Late-Onset Solitary Lesion
- Anti-Aging Potential of Platelet Rich Plasma (PRP): Evidence from Osteoarthritis (OA) and Applications in Senescence and Inflammaging
- Wnt Signaling Across Adult Skin Mini-Organs: Interfollicular Epidermis, Hair Follicle, and Nail—Implications for Disease and Regeneration
- Poster Presentations at the 28th Joint Meeting of the International Society of Dermatopathology, March 5–6, 2025, Orlando, Florida, USA
- Intraoperative Iris Behavior during Phacoemulsification Maneuvers in Rabbits Treated with Selective α1-Blocker, 5α-Reductase Inhibitor, or Anxiolytic Medication
- Reprogramming adult dermis to a neonatal state through epidermal activation of β-catenin
- Activated Kras Alters Epidermal Homeostasis of Mouse Skin, Resulting in Redundant Skin and Defective Hair Cycling
- A comprehensive genome-wide analysis for signatures of selection in goat (genus Capra) revealed new candidate genes for environmental adaptation and productive traits
- Genome-Wide Associations with Body and Fleece Weight in United States Sheep
- Pathological sequelae of long-haul COVID
- Cutaneous scarring: Pathophysiology, molecular mechanisms, and scar reduction therapeutics
- Independent genomewide screens identify the tumor suppressor VTRNA2-1 as a human epiallele responsive to periconceptional environment
- Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load
- PolyQ length co-evolution in neural proteins
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- Endocrine Functions of the Testes
- Polycystic Ovary Syndrome in the Context of Pituitary Adenomas: Prevalence, Pathophysiology and Clinical Management
- A young male with kidney damage from genetic mitochondrial disease: case report and literature review
- Potential of Natural Products in Hangeshashinto Water Extract on the Direct Suppression of Stomatitis Induced by Intra-/Extracellular Advanced Glycation End-Products
- Pilomatricoma in Syndromic Contexts: A Literature Review and a Report of a Case in Apert Syndrome
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Dynamics and Epigenetics of the Epidermal Differentiation Complex
- E-Poster