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Research 361–390 of 1000+
- Polycystic ovary syndrome: etiology, pathogenesis and diagnosis
- Polycystic ovary syndrome
- Deletion of the Developmentally Essential Gene ATR in Adult Mice Leads to Age-Related Phenotypes and Stem Cell Loss
- Erasing the methyl mark: histone demethylases at the center of cellular differentiation and disease
- Molecular Dissection of Mesenchymal–Epithelial Interactions in the Hair Follicle
- Treatment of Hair Loss
- The Rotterdam Study: 2018 update on objectives, design and main results
- Evidence-Based and Potential Benefits of Metformin in the Polycystic Ovary Syndrome: A Comprehensive Review
- The Rotterdam Study: 2016 objectives and design update
- Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
- Fibroblast heterogeneity: implications for human disease
- Leucine-Rich Repeat-Containing G-Protein-Coupled Receptors as Markers of Adult Stem Cells
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- Severe cutaneous adverse reactions to drugs
- Teriflunomide and Its Mechanism of Action in Multiple Sclerosis
- Wnt1/βcatenin injury response activates the epicardium and cardiac fibroblasts to promote cardiac repair
- Melanocyte stem cells: a melanocyte reservoir in hair follicles for hair and skin pigmentation
- Tracing the cellular origin of cancer
- Screening for 21-hydroxylase–deficient nonclassic adrenal hyperplasia among hyperandrogenic women: a prospective study
- The British Society for Rheumatology guideline for the management of systemic lupus erythematosus in adults
- Dermal papilla cell number specifies hair size, shape and cycling and its reduction causes follicular decline
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- COVID-19 and Sex Differences
- Roles of <i>jumonji</i> and <i>jumonji</i> family genes in chromatin regulation and development
- Why Some Women Look Young for Their Age
- In vivo transcriptional governance of hair follicle stem cells by canonical Wnt regulators
- Decreased Serum Ferritin is Associated With Alopecia in Women
- <i>AXR3</i>and<i>SHY2</i>interact to regulate root hair development