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Twist1 helps maintain important features of cells crucial for hair growth by working with Tcf4 and β-catenin.

The treatment was ineffective in humans.

The gene Ascl4 is not necessary for the development of hair, teeth, or mammary glands.

Turkish Van cats' genotypes don't affect traits like eye color or hair length.

Keratin 18 helps diagnose and predict cancer progression and affects cancer growth and spread.

KFSD is a genetic disorder causing hair loss and skin issues, with no effective treatment.

A new goat gene affects cashmere fiber thickness; certain variations can make the fibers coarser.

CTP-543 is generally safe for treating alopecia areata.

Hair and nail cells share similar proteins, indicating a common differentiation pathway.

Activating cannabinoid receptor 1 reduces certain keratin levels, potentially aiding psoriasis treatment.

CCCA may involve the PD1/PDL1 pathway and increased caspase 3, leading to permanent hair loss.

BBS7 is crucial for maintaining healthy periodontal ligaments by supporting Shh signaling.

DEC cells show promise as a safe and effective treatment for Duchenne muscular dystrophy.

Activated LEF/TCF complexes are crucial for hair development and cycling.

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

Newly found stem cells in horse hooves show promise for treating a hoof disease called laminitis.

There is no standard treatment for the rare Cronkhite–Canada syndrome, which can be fatal and lead to cancer.

GATA6 is important for maintaining and differentiating cells in a key area of human skin.

SELP::KP improves hair strength, elasticity, and health, making it a promising hair cosmetic.

Trichothiodystrophy hair is structurally abnormal with protein and organization issues.

Most 46XX CAH patients have female identity, but a few identify as male and may need treatment and surgery.

Scientists found a new type of skin cell that could help with skin repair and these cells work better with a certain protein.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Four new genes related to sheep wool were discovered, showing genetic diversity.

RXRα is crucial for proper immune response and links diet to immune function.

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

Understanding wool keratin-associated proteins in sheep can help improve wool quality through selective breeding.