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

Hairless protein can both repress and activate vitamin D receptor functions, affecting gene regulation.

Genetic testing can diagnose hair loss linked to DSG4 gene variants.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

CD8+ T cells expand significantly in alopecia areata, suggesting new treatment targets.

Hirsute women have lower type 2 17β-HSD enzyme levels, which improve with treatment.

Tandem repeats significantly influence hair color, especially darker shades, across different ancestries.

Certain gene variations in EGF and EGFR may increase the risk of alopecia areata in Koreans.

Recent selection on immune response genes was identified across seven ethnicities.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

A child with a rare vitamin D-resistant condition improved with treatment.

The 2012 criteria are better for diagnosing atypical lupus cases.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Targeting IL-15 may help treat Alopecia Areata.

A specific genetic trait in tumor cells is linked to longer survival without disease in certain lymphoma patients.

CD2 might be a new treatment target for patchy alopecia areata.

Somatic BHD mutations are rare in Japanese renal tumors.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

SRD5A2 gene variations affect PTSD symptoms differently in males and females.

BTNL2 helps protect hair follicles from immune attacks.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Low Vitamin D receptor levels in breast cancer are linked to worse outcomes and more bone metastases, and could be a marker for prognosis.

Mutations in the DSG4 gene cause a severe form of brittle hair and skin issues.

A specific gene mutation causes varying hair loss severity in a Pakistani family.

Most Recessive Dystrophic Epidermolysis Bullosa patients with a specific mutation likely have Sephardic ancestry from about 500 years ago.

A gene mutation in mice causes permanent hair loss and skin issues.

No significant link between CAG repeat numbers and female pattern hair loss in Han Chinese population.

Hairless protein can block vitamin D activation in skin cells.

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