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Research 841–870 of 1000+
- The Genetic Architecture of Alopecia Areata
- Interventions for androgenic alopecia in women
- Interventions for androgenic alopecia in women
- Metabolic pathways of eicosanoids—derivatives of arachidonic acid and their significance in skin
- Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults
- Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults
- Evaluation of Olive Oil-Based Formulations Loaded with Baricitinib for Topical Treatment of Alopecia Areata
- Characterization of Hydrogels of Gelatin/O-Carboxymethyl Chitosan in Ovule Form with Curcumin and Retinyl Palmitate as a Treatment for Cervical Cancer
- The Genetics of Human Skin Disease
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- Dermatologic manifestations of thyroid disease: a literature review
- Wnt/β-catenin signalling: function, biological mechanisms, and therapeutic opportunities
- Scoping Review on the Use of Drugs Targeting JAK/STAT Pathway in Atopic Dermatitis, Vitiligo, and Alopecia Areata
- Role of β-Catenin Activation Levels and Fluctuations in Controlling Cell Fate
- An N-Ethyl-N-Nitrosourea Induced Corticotropin-Releasing Hormone Promoter Mutation Provides a Mouse Model for Endogenous Glucocorticoid Excess
- Elevated Dehydroepiandrosterone Sulfate Levels as the Reproductive Phenotype in the Brothers of Women with Polycystic Ovary Syndrome
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Loss of Msx2 Function Down-Regulates the FoxE3 Expression and Results in Anterior Segment Dysgenesis Resembling Peters Anomaly
- Monilethrix in pattern distribution in siblings: Diagnosis by trichoscopy
- Proof-of-Principle Study of Inflammasome Signaling Proteins as Diagnostic Biomarkers of the Inflammatory Response in Parkinson’s Disease
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
- Essential Role of STAT3 Signaling in Hair Follicle Homeostasis
- Hyperandrogenism in PCOS
- A rare cutis verticis gyrata secondary to cerebriform intradermal nevus: case report and literature review
- Roux-en-Y gastric bypass in the treatment of non-classic congenital adrenal hyperplasia due to 11-hydroxylase deficiency
- Prostaglandins: Key players in immunomodulation of the nervous system
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Beard Alopecia: An Updated and Comprehensive Review of Etiologies, Presentation and Treatment
- A Holistic Approach to Unravel Keloid Pathogenesis and Optimize Therapeutic Outcomes