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

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

A rare genetic mutation causes Woodhouse-Sakati syndrome symptoms.

Certain gene variations increase the risk of alopecia areata in Koreans.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

Some human genetic markers work for genetic studies in pig-tailed and stump-tailed macaques, which can help in their conservation.

Genetic differences within ethnic groups may affect prostate cancer treatment effectiveness.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

A new gene mutation is linked to monilethrix in the studied family.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Longer TA repeats in the SRD5A2 gene may increase acne risk in Chinese people.

Certain gene mutations are linked to wool quality in sheep and could help in breeding for better wool.

Mutations at Val-889 and Arg-752 disrupt key interactions in androgen receptor dimerization.

Raman spectroscopy can identify finasteride polymorphs in tablets.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

Longer CAG repeats in gene linked to more severe hair loss in females.

AR gene variations don't affect aging markers in men.

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

The SNP rs6457452 is linked to a higher risk of alopecia areata in Koreans.

A mutation in the KRT74 gene causes woolly hair by affecting hair texture.

Genetic variants can affect valproic acid's effectiveness, side effects, and levels in epilepsy treatment.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

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

Metformin works better for adolescent girls with PCOS who have certain genetic variations.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

The MTHFR C677T mutation may increase the risk of alopecia areata in the Turkish population.