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Fewer GGC sequences in the androgen receptor gene improve finasteride treatment for hair loss.

Indian Hedgehog helps control skin cell growth and protects against aggressive skin cancer.

A specific genetic deletion in goats affects cashmere yield and thickness.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

Scientists found a gene in mice that causes early hearing loss.

Changes in testosterone and estrogen receptor genes can affect how men age, influencing body fat, hair patterns, and possibly leading to skin disorders.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

A new genetic model may improve treatment and diagnosis for certain inherited skin diseases.

Researchers identified a new variant of the FGF5 gene in sheep that affects hair length.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

miR-182 may help treat hallux valgus by targeting FGF9.

Gamma-ray exposure improves genome editing efficiency in mice using the i-GONAD method.

The Agouti gene influences pigmentation and may have a developmental role in deer mice.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

Two gene areas linked to male pattern baldness found, more research needed.

The near-naked hairless mutation causes hair loss but is not due to a mutation in the hairless gene itself.

The TG5 gene affects beef cattle weight, and the CC genotype leads to higher weights.

A mutation in the KRT75 gene causes frizzle feathers in chickens.

Skin RAGE levels are linked to inflammation and cell death.

A specific gene mutation causes vitamin D resistance, but certain vitamin D analogs might help.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

Noggin gene inactivation causes skeletal defects in mice, varying by genetic background.

The Tru9I variant in the VDR gene may influence alopecia areata risk and vitamin D levels.

Researchers found a non-functional sheep keratin gene due to mutations.

HB-EGF boosts the hair growth ability of stem cells, making it a potential hair loss treatment.

Only one of the two K16 genes on chromosome 17 makes a functional protein for keratin filaments.

A variant in the ADAM17 gene causes hair loss by increasing protein degradation through TRIM47.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.