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Certain inhibitors can potentially treat prostate cancer and other hormone-dependent conditions by controlling sex hormone levels in cells.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

A higher genetic risk score increases the chance of getting benign prostatic hyperplasia and affects treatment outcomes in Han Chinese men.

Polygenic risk scores can predict the risk and outcomes of benign prostatic hyperplasia.

Aromatase gene variation may increase female hair loss risk.

DNA analysis can help tailor alopecia treatment.

Fewer GGC sequences in the androgen receptor gene improve finasteride treatment for hair loss.

The study found genetic diversity in coat color dilution among Czech pointers in Slovakia.

Male-to-female skin grafts in mice are rejected due to sex-linked antigens.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Certain gene variations are linked to a higher risk of severe acne, suggesting a genetic influence on the condition.

Tanning ability is linked to specific DNA changes in skin genes.

TBX3 gene affects horse coat color, with higher expression in darker areas.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

Gender-affirming hormone therapy affects metabolism differently based on treatment type.

Certain gene variations may increase the risk of hair loss in Egyptians.

Eyebrow follicles are best for accurate genetic testing after stem cell transplants.

Increased PHGDH expression causes early melanin buildup in hair follicles.

People with androgenetic alopecia have different lipid levels in their blood, which vary between men and women, and may be linked to a higher risk of metabolic syndrome.

Finasteride side effects in young men may be linked to specific gene variations.

Sebocytes play a key role in controlling androgen levels in human skin.

Hair loss patterns differ between males and females due to 5 master regulators and JAK-STAT signaling affects hair growth.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

Common baldness is likely inherited through multiple genes, not just one.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

High levels of 3 alpha-diol glucuronide in the blood are a marker of increased androgen action in women with excessive hair growth of unknown cause.