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The study suggests that a specific gene variation and higher gene activity are linked to increased baldness in Egyptian men.

Polycystic Ovary Syndrome should be seen mainly as a condition of excess male hormones, with a focus on this in its definition.

The report concludes that PCOS is mainly a condition of excess male hormones and its definition may change as new information is discovered.

The vitamin D receptor is crucial for bone health and affects various body systems, with mutations potentially leading to disease.

Male hormones may play a role in the development of heart disease, and more research is needed to understand their effects.

VEGF helps hair grow and determines follicle size by increasing blood vessel growth.

Alopecia Areata is an autoimmune condition causing hair loss with no cure and treatments that often don't work well.

Prostate cancer cells can make their own androgens to activate the androgen receptor, and treatments like abiraterone may increase this ability, suggesting new therapies should target the entire steroid-making pathway.

β-catenin is essential for stem cell activation and proliferation in hair follicles.

Human skin can make serotonin and melatonin, which help protect and maintain it.

Increasing mir-302 turns human hair cells into stem cells by changing gene regulation and demethylation.

Certain proteins, Lgr5 and Lgr6, are important markers of adult stem cells and are involved in tissue repair and cancer development.

Removing part of the vitamin D receptor stops vitamin D from working properly.

The research shows that a gene called Wnt3 affects hair growth and structure, causing short hair and balding when overactive.

Wnt signaling is crucial for pigmented hair regeneration by controlling stem cell activation and differentiation.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Exposure to too much androgen before birth might cause polycystic ovary syndrome later in life.

The immune system plays a key role in tissue repair, affecting both healing quality and regenerative ability.

Ectodin integrates BMP, SHH, and FGF signals in developing ectodermal organs.

Testing basal 17-HP levels is a good way to screen for nonclassic adrenal hyperplasia in women with high androgen levels.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Most women with excess hair growth have an underlying hormonal issue, often treated with medication and hair removal methods.

Hair follicle stem cells use specific chromatin changes to control their growth and differentiation.

Researchers found 19 genes important for root hair growth in a plant called Arabidopsis.

Shorter CAG repeats may cause hair and skin issues, while longer ones may link to acne.

Skin cells produce and activate vitamin D, which regulates skin functions and supports hair growth.

The PDGF/PDGFR pathway is a potential drug target with mixed success in treating various diseases, including some cancers and fibrosis.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Hair loss needs more research for better treatments.

Oestrogens are key for bone growth during puberty in both boys and girls.