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A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

A new mouse mutation causes skin and hair defects due to a gene change.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

hsa_circ_0002980 can help stop liver cancer cells from growing and spreading.

BMP4 gene is crucial for hair follicle development in Liaoning cashmere goats.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

HB24 helps convert IBA to IAA, promoting root hair growth.

Lnc056 helps hair follicle stem cells grow by increasing TRIP6 expression.

A new genetic mutation linked to Hutchinson-Gilford progeria syndrome was found in China.

Somatic BHD mutations are rare in Japanese renal tumors.

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

A single amino acid change in the vitamin D receptor can disrupt its function and lead to hair loss.

EPHA4 and Ephrin A3 are found in the skin of Aohan fine-wool sheep.

Hairless protein and putrescine regulate each other, affecting hair growth and skin balance.

RORA affects hair follicle stem cells' structure and movement, potentially helping treat hair loss.

Altering SSAT affects fat metabolism and body fat in mice.

rRSPO1 protein boosts hair growth by activating a key signaling pathway.

p2y5, now called LPA6, is a receptor important for human hair growth.

A genetic mutation in the hHa1 gene creates a smaller, but still functional, hair protein without causing hair problems.

Dab2 protein is crucial for hair follicle stem cell renewal and preventing early aging.

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

A new sheep gene, KRTAP36-1, may help breed sheep with better wool by reducing prickle factor.

A specific gene mutation causes congenital hair loss.

LONRF1 is important for oxidative damage response and tissue remodeling during wound healing.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

Esrp1 is important for skin health by helping form and maintain the skin barrier.

Mutations in the KLHL24 gene cause skin blistering in epidermolysis bullosa simplex.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

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