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A protein called ectodysplasin-A2 increases a hair growth inhibitor in balding cells, which could be a target for hair loss treatment.

CD2 might be a new treatment target for patchy alopecia areata.

The review concludes that more research is needed to better improve the health outcomes for people with Polycystic Ovarian Syndrome.

Men who start balding at age 20 may have a higher chance of getting aggressive prostate cancer.

ESR2 gene linked to female-pattern hair loss.

A patient with total hair loss developed vitiligo after using a treatment called DCP.

Chronic inflammatory skin diseases are caused by disrupted interactions between skin cells and immune cells.

Oxidative stress may contribute to hair loss in alopecia areata and antioxidants could potentially help as a treatment.

Faulty inflammasome activation may lead to autoimmune skin diseases and could be a target for new treatments.

Researchers found four genes that could help diagnose severe alopecia areata early.

Certain genetic changes in the KAP22-1 gene are linked to better wool quality in Egyptian sheep.

Dupilumab can improve both atopic dermatitis and alopecia universalis.

Early diagnosis and combination therapy, especially with finasteride and dutasteride, are key to managing Frontal Fibrosing Alopecia effectively.

Men with hair loss may lack zinc, copper, and vitamin D; supplements could help.

Animal models, especially mice, are essential for advancing hair loss research and treatment.

Traditional Chinese Medicine and acupuncture may improve Polycystic Ovarian Syndrome symptoms and reduce costs, but more research is needed.

The document concludes that more research is needed to create suitable diagnostic criteria and understand PCOS in Korean women, and genetics may allow for personalized treatment.

The health of the gut may be important in developing new ways to prevent, diagnose, and treat alopecia areata.

Elastic Net DNA methylation clocks are inaccurate for predicting age and health status; a "noise barometer" may better indicate aging and disease.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

Keloid skin disorder involves abnormal fibroblast activation and immune response, linked to a group of genes including FGF11.

Higher social status is linked to earlier diagnosis and better treatment results for Frontal Fibrosing Alopecia in women.

The KRTAP7-1 gene is very similar across different cattle and yak breeds and likely plays a role in hair strength and shape.

Genetics, stress, and health issues can cause early hair greying, which affects self-esteem, and there's no cure, only hair dye.

Oral tofacitinib can treat both psoriasis and alopecia universalis by normalizing inflammatory pathways.

Alopecia Areata is an autoimmune condition causing hair loss, influenced by genetics, environment, and possibly improved by anti-MIF therapy, with many patients experiencing regrowth within a year.

The document explains the genetic causes and characteristics of inherited hair disorders.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

Quantifying hair shape is better than using racial categories for understanding hair characteristics.

Forensic medicine is crucial for justice and needs continuous innovation and technology integration.