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ALRN-6924 may prevent hair loss caused by chemotherapy.

SNP rs2479106 in the DENND1A gene may increase PCOS risk in Saudi Arabian females.

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

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

The 1298CC genotype in RA patients leads to higher methotrexate toxicity, while the 1298AA genotype results in better treatment response.

miR-129-5p affects hair growth by targeting the HOXC13 gene.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

CP-690,550 significantly reduced itching in patients with moderate-to-severe plaque psoriasis.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.