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Research 961–990 of 1000+
- MENSTRUAL DISORDERS IN ADOLESCENTS
- The genetics of alopecia areata: New approaches, new findings, new treatments
- Genetic Tools for Cell Lineage Tracing and Profiling Developmental Trajectories in the Skin
- Hair Graying: Mechanisms, Prevention, and Innovative Treatment Strategies – literature review
- Scarring Alopecia in Localized Dystrophic Epidermolysis Bullosa: A Case Report and a Scoping Review
- Dietary and Genetic Aspects of Polycystic Ovary Syndrome (PCOS) in Polish Women-Part II: Association of
- Moniletrix. Observación de esta infrecuente displasia pilosa en dos hermanos. Reporte clínico y dermatoscópico
- Risk factors for prostate cancer: a case-control study investigating selected key exposures and their interactions with predisposition genes
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Genetics of Wool and Cashmere Fibre: Progress, Challenges, and Future Research
- Genetic Control/Involvement in Hair Fiber Traits
- Genetic Variant of the Canine FGF5 Gene for the Hair Length Trait in the Akita: Utility for Hair Coat Variations and Welfare in Conservation Breeding
- The Rotterdam Study: 2016 objectives and design update
- Stem Cells and the Niche: A Dynamic Duo
- Polycystic Ovary Syndrome, Insulin Resistance, and Obesity: Navigating the Pathophysiologic Labyrinth
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- Keratin gene mutations in disorders of human skin and its appendages
- Biology of the wool follicle: an excursion into a unique tissue interaction system waiting to be re‐discovered
- Integument pattern formation involves genetic and epigenetic controls: feather arrays simulated by digital hormone models.
- Alopecia Areata: a Comprehensive Review of Pathogenesis and Management
- Genetic Ablation of the <i>CDP/Cux</i> Protein C Terminus Results in Hair Cycle Defects and Reduced Male Fertility
- A new mutation Rim3 resembling Re den is mapped close to retinoic acid receptor alpha (Rara) gene on mouse Chromosome 11
- Trichoscopy in genetic hair shaft abnormalities
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- Angora Mouse Mutation: Altered Hair Cycle, Follicular Dystrophy, Phenotypic Maintenance of Skin Grafts, and Changes in Keratin Expression
- Genetic interplays between Msx2 and Foxn1 are required for Notch1 expression and hair shaft differentiation
- Management of congenital ichthyoses: European guidelines of care, part two
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- Gsdma3 Mutation Causes Bulge Stem Cell Depletion and Alopecia Mediated by Skin Inflammation
- An Overview of Alopecias