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Research 421–450 of 1000+
- Polycystic ovary syndrome
- Erasing the methyl mark: histone demethylases at the center of cellular differentiation and disease
- Developmental origin of polycystic ovary syndrome - a hypothesis
- Health Care-Related Economic Burden of the Polycystic Ovary Syndrome during the Reproductive Life Span
- Treatment of Hair Loss
- Stem Cells and the Niche: A Dynamic Duo
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- Polycystic Ovary Syndrome
- Follow-up of Nutritional and Metabolic Problems After Bariatric Surgery
- Polycystic Ovary Syndrome, Insulin Resistance, and Obesity: Navigating the Pathophysiologic Labyrinth
- Screening for 21-hydroxylase–deficient nonclassic adrenal hyperplasia among hyperandrogenic women: a prospective study
- Dermatoses of pregnancy
- Fully functional hair follicle regeneration through the rearrangement of stem cells and their niches
- An Update of Congenital Adrenal Hyperplasia
- Smad7-Induced β-Catenin Degradation Alters Epidermal Appendage Development
- Telogen effluvium
- Linking diet to acne metabolomics, inflammation, and comedogenesis: an update
- Obesity and Polycystic Ovary Syndrome: Implications for Pathogenesis and Novel Management Strategies
- dsRNA Released by Tissue Damage Activates TLR3 to Drive Skin Regeneration
- Adult polycystic ovary syndrome begins in childhood
- Clinical Management of Youth with Gender Dysphoria in Vancouver
- Androgens and androgen receptor action in skin and hair follicles
- Obesity and polycystic ovary syndrome
- Health and fertility in World Health Organization group 2 anovulatory women
- TGF-β Family Signaling in Epithelial Differentiation and Epithelial–Mesenchymal Transition
- Polycystic ovary syndrome and impact on health
- The role of nuclear hormone receptors in cutaneous wound repair
- Telogen effluvium
- The Modulatable Stem Cell Niche: Tissue Interactions during Hair and Feather Follicle Regeneration
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice