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The ABCG2 gene variant increases the risk of high uric acid and cholesterol, especially in overweight or obese young Mexican males.

Increased EGFR gene variations may predict chemotherapy outcomes in small cell lung cancer patients.

VILLIN4 helps root hair growth by organizing actin with calcium.

A genetic variant linked to hair thinning in Japanese women was found.

Two new mutations in the AR gene linked to severe androgen insensitivity were found.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

HT-scCAT-seq helps understand gene regulation in embryonic skin development.

PADI4 enzyme slows down cell growth in developing hair follicles.

The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.

Certain genes may help Bulgarians live longer.

The B2 genes are crucial for hair growth in rats.

mrp/plf-mRNA can indicate tumor-promoting effects in skin.

Two specific genes are more active during hair growth in mice.

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

Mice without the Sp6 gene have problems developing several body parts, including hair, teeth, limbs, and lungs.

Certain genes affect udder shape in Holstein cows, important for health and milk production.

A genetic hair protein variant is more common in Japanese people and is inherited.

LEF1 is essential for the development of airway glands and is regulated by the Wnt/ß-catenin pathway.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Two new gene mutations cause a rare hair disorder.

The type of tumor suppressor gene lost affects the behavior of skin cancer.

A new genetic mutation in the CAST gene may link PLACK syndrome to alopecia areata.

Mutations in the ACTB gene cause Becker’s nevi and may lead to muscle issues in Becker’s nevus syndrome.

S100A4 promotes aggressive ovarian cancer and is a potential treatment target.

Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.

A faulty KLHL24 gene leads to hair loss by damaging hair follicle stem cells.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

The protein's size was reduced, but more work is needed to confirm its function.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.