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Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

The gene Tfap2b is essential for creating a type of stem cell in zebrafish that can become different pigment cells.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

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

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

Different types of skin fibroblasts have unique roles in skin health and disease.

Dermal papillae cells, important for hair growth, come from multiple cell lines and can be formed by skin cells, regardless of their origin or hair cycle phase. These cells rarely divide, but their ability to shape tissue may contribute to their efficiency in inducing hair growth.

Different types of skin cells have unique genetic markers that affect how likely they are to spread cancer.

Tumor suppressors help control inflammation in cancer and restoring their function could lead to new treatments.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

MFN2 mutations cause mitochondrial problems, leading to more upper body fat and lower leptin levels.

Pregnant women with PCOS have higher levels of Neurokinin B in the placenta, especially with female babies.

A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

Men are more likely to have severe COVID-19 cases and fatalities than women due to factors like lifestyle, aging, and biological differences.

Hair follicle stem cells are a promising source for tissue repair and treating skin or hair diseases.

Epidermal stem cells could lead to new treatments for skin and hair disorders.

The review suggests thorough evaluation and genetic testing for proper diagnosis and treatment of Chrousos syndrome.

Epidermal stem cells have various roles in skin beyond just maintenance, including forming specialized structures and aiding in skin repair and regeneration.

Skin cells show flexibility in healing wounds and forming tumors, with potential for treating hair disorders and chronic ulcers.

Different cell types work together to repair skin, and targeting them may improve healing and reduce scarring.

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

The circadian clock in skin cells controls their growth and rest cycles.

Certain changes in the VEGF gene can increase or decrease the risk of polycystic ovary syndrome.

Cyproterone acetate may cause liver cancer at high doses, but is considered safe at recommended doses for approved uses.

Helminth protein helps wounds heal better by reducing scarring and promoting tissue growth.