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Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

Id2 gene helps keep hair follicle stem cells inactive.

Certain gene variations in AKT2 are more common in women with PCOS and are linked to higher levels of specific hormones and symptoms.

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

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Certain gene variations might increase the risk of a hair loss condition in Koreans.

Certain gene variants may raise the risk of prostate enlargement, but taking NSAIDs could reduce this risk.

Melatonin shortens the hair growth cycle by increasing PDGFA gene expression.

Certain gene variations and irregular X chromosome activity may contribute to hair loss in women who can have children.

Constant-release melatonin reduces SOX21 gene expression in goats during the hair follicle resting phase.

Methylated gene parts may cause finasteride-resistance in some enlarged prostate patients.

Mutations in the AR gene cause hair thinning and loss.

The number of CAG repeats in the androgen receptor gene doesn't significantly affect female pattern hair loss in the Han Chinese population.

Certain gene variations are significantly linked to hair loss, especially in white people.

The androgen receptor gene doesn't help identify women likely to have female pattern hair loss.

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

A genetic test can identify people at risk of male pattern baldness early, allowing for quicker treatment.

TGFα gene mutation in mice causes abnormal skin, wavy hair, curly whiskers, and sometimes eye inflammation.

The ZIP7 gene helps control zinc levels in cells by moving zinc from the Golgi apparatus to the cytoplasm.

Five new mutations in the androgen receptor gene were found, helping to understand androgen insensitivity syndrome better.

New treatments targeting specific genes show promise for treating keratin disorders.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

The FOXN1 gene is crucial for developing immune cells and preventing immune disorders.

HOXC13 is essential for hair and nail development by regulating Foxn1.

Obese women with PCOS show a male-like pattern in certain fat tissue gene expressions.

There's no significant link between the D19S884 marker at the insulin receptor gene and polycystic ovary syndrome.

Deleting part of a gene in mice causes wavy hair and high pup loss.

Mutations in the KRT85 gene cause hair and nail problems.

G allele of AR Stul polymorphism linked to higher hair loss risk, especially in white people.

Finger length ratios are not linked to the number of specific gene repeats affecting testosterone sensitivity.