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Research 781–810 of 1000+
- Genetically predicted levels of circulating cytokines and the risk of six immune skin diseases: a two-sample Mendelian randomization study
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- Engineered Dutasteride-Lipid Based Nanoparticle (DST-LNP) System Using Oleic and Stearic Acid for Topical Delivery
- Biological and Functional Properties of Wedelolactone in Human Chronic Diseases
- Case Report of Wound Treatment with Hyiodine Gel in an Occasional KID Syndrome Patient
- Understanding Polycystic Ovary Syndrome: A Comprehensive Guide
- Biotinidase Deficiency: Prevalence, Impact And Management Strategies.
- Overexpression of Sonic Hedgehog suppresses embryonic hair follicle morphogenesis
- Polycystic Ovary Syndrome and NC-CAH: Distinct Characteristics and Common Findings. A Systematic Review
- A systematic summary of survival and death signalling during the life of hair follicle stem cells
- Scientific opinion on the tolerable upper intake level for selenium
- Anti-Müllerian Hormone and Polycystic Ovary Syndrome in Women and Its Male Equivalent
- Gene network analysis reveals candidate genes related with the hair follicle development in sheep
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Dicer- and Bulge Stem Cell-Dependent MicroRNAs During Induced Anagen Hair Follicle Development
- Two siblings with a novel nonsense mutation, p.R50X, in the vitamin D receptor gene
- An update of polycystic ovary syndrome: causes and therapeutics options
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Keratinocyte Stem Cells: Role in Aging
- Vogt-Koyanagi-Harada Disease with Oral Manifestations: A Rare Case Report
- Application of big data analytics in minoxidil drug development: a data-driven model for predicting efficacy and side effect risks
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association
- Recent Approaches in the Treatment of Polycystic Ovary Syndrome: An Update
- Oral Presentations
- Highlights from the 68th Annual Meeting of the Society of Investigative Dermatology
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- The influence of interferon on healthy and diseased skin
- Immunopathology and Immunotherapy of Inflammatory Skin Diseases
- Rosmarinus officinalis and Skin: Antioxidant Activity and Possible Therapeutical Role in Cutaneous Diseases