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

Forensic DNA Phenotyping accurately predicts physical traits and is used in investigations, but needs more diverse population data for confirmation.

Androgenetic alopecia is influenced by multiple genes and pathways, with genetic risk varying by population, and personalized treatments are being explored.

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

A specific gene variant is linked to a higher risk of hair loss from chemotherapy in breast cancer patients.

ASLAN004 was safe and well-tolerated, supporting further development for treating certain diseases.

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

A specific genetic variation affects wool quality in sheep.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

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

rwSALT provides precise hair regrowth measurement from scalp photos.

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

The protein RSL4 is crucial for making root hairs longer by controlling genes related to cell growth.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

The CTLA-4 gene polymorphism does not affect polycystic ovarian syndrome.

New genetic locations explain much of hair color variation in Europeans.

Drug repurposing offers promising strategies to improve tuberculosis treatment despite challenges.

AQB reduces harmful skin changes in systemic sclerosis.

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

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

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

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Seven new genetic risk areas for prostate cancer were found.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.