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Research 391–420 of 1000+
- Genetic and hormonal influence on SARS-CoV-2-infection susceptibility
- Stem Cells Sheltered from Air-Raids Repair Airways
- Cómo hacer que dos más dos sumen cinco
- P447: Late onset biotinidase deficiency misdiagnosed as neuromyelitis optica: A case report and review of diagnostic challenges
- Genome-wide association study identifies a new locus JMJD1C at 10q21 that may influence serum androgen levels in men
- Genetic Variants Associated with Hyperandrogenemia in PCOS Pathophysiology
- Testing the impact of trait prevalence priors in Bayesian-based genetic prediction modeling of human appearance traits
- The Polycystic Ovary Syndrome - Challenges and Opportunities in Adolescent Medicine
- Human Pigmentation: A Review of Molecular Mechanisms, Genetic Architecture, Evolution, Forensic DNA Phenotyping and Health Implications
- Androgenetic Alopecia in Men: An Update On Genetics
- A genetic electrophoretic variant of high-sulfur hair proteins for forensic hair comparisons. I. Characterization of variant high-sulfur proteins of human hair.
- Dedifferentiation of committed epithelial cells into stem cells in vivo
- Stem Cells and the Niche: A Dynamic Duo
- Alopecia areata
- Biomaterials Functionalized with MSC Secreted Extracellular Vesicles and Soluble Factors for Tissue Regeneration
- Genetic Basis of Male Pattern Baldness
- Genetic architecture of mouse skin inflammation and tumour susceptibility
- Biology of the wool follicle: an excursion into a unique tissue interaction system waiting to be re‐discovered
- Phospholipase A2 Is Required for PIN-FORMED Protein Trafficking to the Plasma Membrane in the<i>Arabidopsis</i>Root
- Lichen Planopilaris and Frontal Fibrosing Alopecia as Model Epithelial Stem Cell Diseases
- MENSTRUAL DISORDERS IN ADOLESCENTS
- Hair Follicle: A Novel Source of Multipotent Stem Cells for Tissue Engineering and Regenerative Medicine
- The genetics of alopecia areata: New approaches, new findings, new treatments
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Molecular pathology of skin adnexal tumours
- Identifying molecular targets for reverse aging using integrated network analysis of transcriptomic and epigenomic changes during aging
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Characterization of DNA Methylation and Screening of Epigenetic Markers in Polycystic Ovary Syndrome
- Genetic Tools for Cell Lineage Tracing and Profiling Developmental Trajectories in the Skin
- Sebaceous carcinoma arising at a chronic candidiasis skin lesion of a patient with keratitis-ichthyosis-deafness (KID) syndrome