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Research 871–900 of 1000+
- Micropigmentation
- Polycystic ovary syndrome: Diagnosis and management
- Life Sciences Discovery and Technology Highlights
- Notch Signaling in Hair Follicle Development
- Acne Vulgaris
- Molecular Genetics of Human Hair Diseases
- TONGUE, RED
- Association of Acne Tarda with Endocrinological Disorders
- The Rotterdam Study: objectives and design update
- Metabolic Regulation of Hematopoietic Stem Cells in the Hypoxic Niche
- Solid Lipid Nanoparticles for Drug Delivery: Pharmacological and Biopharmaceutical Aspects
- Characterization and isolation of stem cell-enriched human hair follicle bulge cells
- Epithelial Stem Cells: Turning over New Leaves
- Proteasome Inhibitors: An Expanding Army Attacking a Unique Target
- Keratin 15 Promoter Targets Putative Epithelial Stem Cells in the Hair Follicle Bulge
- Spermidine/spermine-<i>N</i><sup>1</sup>-acetyltransferase: a key metabolic regulator
- Chitin and Chitosans: Characteristics, Eco-Friendly Processes, and Applications in Cosmetic Science
- Understanding variation in prevalence estimates of polycystic ovary syndrome: a systematic review and meta-analysis
- Keratin 15 Expression in Stratified Epithelia: Downregulation in Activated Keratinocytes
- Flavonoids as Potential Wound-Healing Molecules: Emphasis on Pathways Perspective
- Food Bioactive Compounds and Emerging Techniques for Their Extraction: Polyphenols as a Case Study
- UK guidelines on the management of iron deficiency in pregnancy
- European Society of Endocrinology Clinical Practice Guideline: Endocrine work-up in obesity
- Wound Healing and the Use of Medicinal Plants
- Dlx3 is a crucial regulator of hair follicle differentiation and cycling
- Intracrine androgen biosynthesis, metabolism and action revisited
- Microfluidic Technology for the Generation of Cell Spheroids and Their Applications
- Inflammatory priming enhances mesenchymal stromal cell secretome potential as a clinical product for regenerative medicine approaches through secreted factors and EV-miRNAs: the example of joint disease
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- Ultrasound-assisted extraction and analysis of maidenhairtree polysaccharides