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

A genetic change in the FGF5 gene affects hair growth in cashmere goats.

The IRF2BP2 gene affects sheep fleece quality by influencing fiber traits.

Mutating the gmds gene in zebrafish increases hair cell numbers and regeneration.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

Researchers found a genetic region that influences the number of coat layers in dogs.

The mouse hairy ears mutation causes longer ear hair due to changes in gene expression.

The agouti gene may help understand and treat obesity.

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

Mutations in the P2RY5 gene cause hereditary woolly hair.

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

High wool density in Rex rabbits is linked to specific gene activity affecting hair follicle development.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Folliculin helps regulate energy and nutrient sensing, impacting Birt–Hogg–Dubé syndrome.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

Certain genes and proteins may influence wool growth in Aohan fine wool sheep.

A specific gene variation in goats is linked to better growth traits.

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

FGF20 is essential for hair follicle stem cell growth and development in fine-wool sheep.

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

Fz3 and Fz6 can partially replace each other in tissue polarity and axon guidance.

A mutation in mice causes hair loss and immune problems.

A mutation in the MAP2 gene causes reduced hair follicle density, leading to hairlessness.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

A specific DNA region is crucial for Foxn1 gene expression in thymus cells but not in hair follicles.

The scraggly mutation causes hair loss and skin defects in mice.