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Research 331–360 of 1000+
- TONGUE, RED
- Infections, Infestations and Neoplasms of the Scalp
- Pathology of Mouse Models of Accelerated Aging
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Update on Melasma—Part I: Pathogenesis
- Confluent and Reticulated Papillomatosis Associated with Polycystic Ovarian Syndrome
- DSP c.6310delA p.(Thr2104Glnfs*12) associates with arrhythmogenic cardiomyopathy, increased trabeculation, curly hair, and palmoplantar keratoderma
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- FGF5 is a crucial regulator of hair length in humans
- New developments in the molecular treatment of ichthyosis: review of the literature
- A Comprehensive Review of Acne Vulgaris
- Impact of Combined Baricitinib and FTI Treatment on Adipogenesis in Hutchinson–Gilford Progeria Syndrome and Other Lipodystrophic Laminopathies
- Recent Updates of the CRISPR/Cas9 Genome Editing System: Novel Approaches to Regulate Its Spatiotemporal Control by Genetic and Physicochemical Strategies
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- Phospholipase A2 in skin biology: new insights from gene-manipulated mice and lipidomics
- The Associations of Androgen-Related Genes CYP21A2 and CYP19A1 with Severe Acne Vulgaris in Patients from Southwest China
- Metabolic pathways of eicosanoids—derivatives of arachidonic acid and their significance in skin
- Hair shaft disorders in children – An update
- 2022 Update on Prostate Cancer Epidemiology and Risk Factors—A Systematic Review
- Wnt/β-catenin signalling: function, biological mechanisms, and therapeutic opportunities
- Unraveling the ECM-Immune Cell Crosstalk in Skin Diseases
- Advances in Chitosan-Based Nanoparticles for Drug Delivery
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- Ichthyosis with confetti: clinics, molecular genetics and management
- Stem Cell Therapies for Epidermolysis Bullosa Treatment
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- Loss of Msx2 Function Down-Regulates the FoxE3 Expression and Results in Anterior Segment Dysgenesis Resembling Peters Anomaly
- The Search for the Causes of Common Hyperandrogenism, 1965 to Circa 2015
- Eavesdropping on the conversation between immune cells and the skin epithelium