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The gene Foxq1, controlled by Hoxc13, is crucial for hair follicle differentiation.

Researchers found 63 genes linked to male-pattern baldness, which could help in understanding its biology and developing new treatments.

Genetic screening is crucial for accurately diagnosing APS-1 due to its varied symptoms.

The peptide IMT-P8 can effectively deliver proteins into the skin and cells for potential skin treatments.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Products should be called 'sperm-safe' only after thorough, well-designed tests.

A49T gene variant linked to higher prostate cancer risk, lower hormone levels, and slightly reduced balding risk.

Vitamin D receptor is crucial for starting hair growth after birth.

Finasteride helps reduce heart issues and improves heart function.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

Finasteride for hair loss may cause persistent sexual symptoms, depression, anxiety, and lower quality of life.

The conclusion is that genetic changes in the glucocorticoid receptor can lead to conditions affecting stress response, immunity, and metabolism, requiring personalized treatment.

Polyamines help fix DNA damage accurately in cells.

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

FLRG and follistatin have different roles in wound healing.

Male genital development is driven by androgen signaling and understanding it could help address congenital anomalies.

Type 3 5α-reductase is more common and finasteride and dutasteride strongly inhibit it.

The gene KAP22-1 affects wool yield and fiber shape in sheep.

Genetic data can predict male-pattern baldness with moderate accuracy, especially for early-onset cases in some European men.

The study concludes that the EDA2R gene is activated by p53 during chemotherapy but is not necessary for chemotherapy-induced hair loss.

The review found no clear link between vitamin D receptor gene variations and polycystic ovary syndrome.

BMP6 and Wnt10b control whether hair follicles are resting or growing.

5α reductase inhibitors treat hair loss but may cause sexual side effects and risks.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

Hairless protein is crucial for healthy skin and hair, and its malfunction can cause hair loss.

Certain genetic variations are linked to increased androgen levels in PCOS, but more research is needed to understand these connections fully.

Loss of Fz6 disrupts hair follicle and associated structures' orientation.

Sp6 promotes tooth development by reducing follistatin levels.

The study concluded that three enzymes are important for plant development by affecting sugar composition and calcium binding in plants.

Oral contraceptives lower testosterone levels in women, especially those with certain genetic traits, and may be linked to increased breast cancer risk.