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Genes play a significant role in male-pattern baldness, and understanding them could lead to new treatments and insights into related health issues.

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

Androgenetic alopecia is mainly caused by genetic factors and increased androgen activity, leading to hair follicle miniaturization.

Longer GGN repeats in the androgen receptor gene are linked to polycystic ovary syndrome.

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

Men may be more vulnerable to severe COVID-19 due to genetic and hormonal factors, but more research is needed.

A person with Turner Syndrome showed severe schizophrenia that didn't respond to treatment and had brain shrinkage.

A 6-year-old girl with Turner syndrome also had psoriasis, alopecia areata, and trachyonychia.

Men have worse COVID-19 outcomes than women due to genetic and hormonal differences.

The research found that genetic factors for male pattern baldness in African men differ significantly from those in Europeans.

Conditions affecting sex development show that sexual diversity is a natural part of human variation.

Dermatologists give better information on pathology forms, hypersensitivity vasculitis is a common skin issue, misdiagnoses can occur, and various skin conditions are linked to loss of elastin or genetic factors.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

Society's pressure to have children later in life favors genes that increase the risk of early baldness in male offspring.

AGA is caused by genetics and androgens, treatable with finasteride and minoxidil.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

Birt–Hogg–Dubé Syndrome requires genetic testing for accurate diagnosis due to its similarities with tuberous sclerosis.

DNA profiling in forensics has improved, but predicting physical traits and ancestry from DNA has limitations and requires ethical consideration.

S100A3 protein is crucial for hair shaft formation in mice.

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.

Researchers found genes linked to feather growth speed in Shouguang chickens, highlighting two genes that might explain differences in feathering.

Pallister-Killian Syndrome is a complex genetic disorder requiring coordinated care and genetic counseling.

Mutations in the AR gene cause hair thinning and loss.

Cancer cells often have more copies of TERT and TERC genes, which helps them grow and could affect patient outcomes.

Androgen receptors are key for development and health, affecting conditions like prostate cancer and male pattern baldness.

Hair growth is controlled by specific gene clusters and proteins, and cysteine affects hair gene expression in sheep.

Understanding how EDC genes are regulated can help develop better drugs for skin diseases.

The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.