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Research 301–330 of 319
- Saponins of Paris polyphylla for the Improvement of Acne: Anti-Inflammatory, Antibacterial, Antioxidant and Immunomodulatory Effects
- Protective Effects of <i>BCC</i> Against Oxidative Stress in Cardiomyocyte Cells
- Risk factors for prostate cancer: An umbrella review of prospective observational studies and mendelian randomization analyses
- Cinnamic acid promotes elongation of hair peg-like sprouting in hair follicle organoids via oxytocin receptor activation
- E-Poster
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- A population pharmacokinetic model for individualized regimens of finasteride according to CYP3A5 genotype and liver function
- Effects of oxytocin on the hair growth ability of dermal papilla cells
- Metabolic Engineering of Microorganisms to Produce L-Aspartate and Its Derivatives
- Role of the ABCA4 Gene Expression in the Clearance of Toxic Vitamin A Derivatives in Human Hair Follicle Stem Cells and Keratinocytes
- Recent Advances in Understanding of the Etiopathogenesis, Diagnosis, and Management of Hair Loss Diseases
- Oral Combination Treatment of Gefitinib (IressaTM) and Sasam-Kyeongokgo: Synergistic Effects on the NCI-H520 Tumor Cell Line
- COVID-19: How Effective Are the Repurposed Drugs and Novel Agents in Treating the Infection?
- Recent advances in neuropeptide-related omics and gene editing: Spotlight on NPY and somatostatin and their roles in growth and food intake of fish
- CAQ Corner: Basic concepts of transplant immunology
- Menstrual Irregularities in Adolescent Girls and Correlation with the Extent of Exposure to Plastics: A Case-Control Study
- Hair & Cutaneous Development
- Acanthosis nigricans, insulin resistance and cutaneous virilism
- Male-pattern hair loss: Comprehensive identification of the associated genes as a basis for understanding pathophysiology
- Cantú Syndrome Is Caused by Mutations in ABCC9
- ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Updated mutational spectrum and genotype-phenotype correlations in ichthyosis patients with ABCA12 pathogenic variants
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- Differential expression and functionality of ATP-binding cassette transporters in the human hair follicle
- Decay of Skin-Specific Gene Modules in Pangolins
- Convergent Decay of Skin-specific Gene Modules in Pangolins
- Pseudoxanthoma Elasticum: Progress in Research Toward Treatment: Summary of the 2012 PXE International Research Meeting
- Cantú syndrome with coexisting familial pituitary adenoma