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Prostaglandin D2, found in higher levels in bald scalps, stops hair growth and could be a target for treating hair loss.

Certain genes and pathways are crucial for high-quality brush hair in Yangtze River Delta White Goats.

The document concludes that careful design of genetic fate mapping experiments is crucial for accurate cell lineage tracing in mice.

These gene variations are not linked to alopecia areata in Egyptians.

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

The method safely and efficiently delivers genes to the skin but may not work for conditions needing high levels of gene products.

OR2AT4 helps reduce aging and cell damage in human skin cells.

Certain genetic variants increase the risk of resistance to hormone therapy in prostate cancer patients.

A new gene mutation is linked to monilethrix in the studied family.

A 90-year-old man was diagnosed with heart failure due to wild-type transthyretin cardiac amyloidosis.

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

The G(S) alpha subunit gene may help start hair follicle growth in newborn mice.

Ganoderma lucidum extract and its component, ganoderic acid A, may effectively prevent hair loss.

AR polyglycine repeat doesn't cause baldness.

Certain proteins are essential for the growth of root hairs in barley.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

3,4,5-tri-O-caffeoylquinic acid promotes hair growth by activating the β-catenin pathway.

TG5 helps maintain hair follicle health, while TG3 aids in hair shaft development.

PRDX5 enzyme may contribute to alopecia areata by affecting oxidative stress and autoimmunity.

A gene called Taqpep affects cat coat patterns like stripes and blotches.

Mutations in specific genes cause certain congenital defects in dogs, aiding in understanding similar human diseases.

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

Compound 6 is a promising candidate for better wound healing.

Cystatin M/E strongly inhibits cathepsin V and cathepsin L, important for skin formation.

Prostaglandin D2 blocks new hair growth after skin injury through the Gpr44 receptor.

Nelfb is crucial for forming skin fat tissue by regulating genes needed for fat cell development.

Alloxan diabetes, methylthiouracil, cortisone, and adrenaline affect how white mice hair follicles use glucose and cystine and their cell division.

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

Loss of Dnmt3a and Dnmt3b leads to more aggressive skin tumors, but blocking PPAR-γ can reduce this effect.

Overexpressing Dsg3 in mice skin causes excessive cell growth and abnormal skin development.