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IGF2BP3 and other m6A-related genes are linked to keloid formation and could be potential treatment targets.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

Keratinocytes can reverse the effects of the GNAQ oncogene, inhibiting melanoma cell growth.

Two new gene mutations cause a rare hair disorder.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

TBX5 gene influences feathered feet in Guangxi chickens by affecting cell growth and movement.

ATP6AP1‐CDG can cause hearing loss, hair loss, and protein issues, even in female carriers.

Removing SIX1 in fat cells reduces skin fibrosis.

Certain changes in the KAP6-1 gene affect the thickness and length of cashmere goat fibers.

Keratinocytes can reduce the survival of certain melanoma cells, suggesting new therapy paths.

A new gene, JMJD1C, may affect testosterone levels in men.

Integrin α6 helps identify different neural crest cell types in the skin.

A specific gene region can control targeted and responsive gene expression in mice, useful for skin disorder treatments.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

Keratin 75 might be important in oral cancer progression.

The protein DDX6 helps keep skin cells renewing properly by controlling the production of certain other proteins and breaking down those that cause cells to mature too quickly.

Inherited color dilution in Rex rabbits is linked to DNA methylation changes in hair follicles.

SQSTM1 is linked to increased risk of alopecia areata.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

S100A6 protein is linked to disease progression, especially in cancers.

CXXC5 can both suppress and promote cancer, making it a complex target for treatment.

The human keratin 6a gene's specific sequences trigger expression in skin layers after injury.

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

FGF13 gene changes cause excessive hair growth in a rare condition.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.