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Misbehaving hair follicle stem cells can cause hair loss and offer new treatment options.

PCOS symptoms change with age; younger women have higher androgen levels and less metabolic issues, while older women face more metabolic challenges despite milder PCOS symptoms.

The research suggests that the global distribution of PCOS is likely due to historical human migration and that genes affecting PCOS may have different impacts on males and females.

Disrupted sleep patterns can harm skin and hair cell renewal, but melatonin might help.

Mothers have more hair proteins than their children, with age-related differences in protein patterns, and some proteins in hair could indicate early childhood development.

Fibroblasts are important in healing diabetic wounds, but high sugar levels can harm their function and slow down the healing process.

Certain immune cells are linked to non-scarring hair loss, suggesting potential for immune-targeted treatments.

Staphylococcus epidermidis A/C strains are more antibiotic-resistant and infection-adapted, while B strains thrive in hair follicles.

Sons of mothers with polycystic ovary syndrome (PCOS) have a higher risk of obesity and insulin resistance, possibly due to certain genes and factors passed down from their mothers.

Experts agree that PCOS affects women's health in complex ways, but more research is needed to understand and treat it effectively.

TTD hair brittleness is caused by multiple structural abnormalities.

Certain genes are more active during wound healing in axolotl and Acomys, which could help develop materials that improve human wound healing and regeneration.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

PDGFA/AKT signaling is important for the growth and maintenance of certain skin fat cells.

Mouse skin glands need healthy nerves to grow properly during hair growth phases.

Mesenchymal stem cells show promise for effective skin repair and regeneration.

Certain zinc transporters are essential for healthy skin and managing zinc in the body could help treat skin problems.

New materials that better mimic natural skin structure could improve healing, especially for chronic wounds.

Hair proteins in preschool children and their mothers could indicate developmental changes and health status.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

Certain metabolites can either protect against or increase the risk of hair loss.

Men are more likely to get infectious skin diseases, while women are more prone to autoimmune and pigment-related skin conditions, influenced by biological and environmental factors.

Fzd2 is important for skin and hair development through various signaling ways.

Vav2 changes how hair follicle stem cells' genes work as they age, which might improve regeneration but also raise cancer risk.

Using three different drugs together may better treat eye diseases like glaucoma and macular degeneration.

Applying the anti-cancer drug Bortezomib to skin can promote hair growth and increase hair proteins through the GATA-3 factor.

Hairlessness in mammals is due to complex genetic changes in both genes and regulatory regions.

The document concludes that hormonal biomarkers are key for diagnosing hyperandrogenemia in women and hypogonadism in men.

Male and female bodies respond differently to stress, influenced by hormones and development stages, with implications for stress-related diseases.

Nanog gene boosts stem cells, helps hair growth, and may treat hair loss.