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Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

Certain variations in the vitamin D receptor gene are linked to an increased risk of polycystic ovary syndrome.

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

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

CTIP2 may help in skin development and maintenance.

Mutations in the Whn gene affect hair keratin gene expression differently.

Activins and follistatins, part of the TGFβ family, are crucial for hair follicle development and skin health, affecting growth, repair, and the hair cycle.

FoxN1 overexpression in young mice harms immune cell and skin development.

Certain genetic variants may increase the risk of developing PCOS.

PRC2 is not essential for hair follicle stem cell maintenance or hair growth.

A new technology showed that the SOX9 gene might control heart scar formation after injury, suggesting new treatment possibilities.

ETS2 is crucial in squamous cell carcinoma development and could be a therapeutic target.

WWOX deficiency in mice causes skin and fat tissue problems due to disrupted cell survival signals.

ePUKs could be valuable for regenerative medicine due to their wound healing abilities.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

H19 may help cause PCOS by affecting CTGF levels, suggesting a new treatment target.

RORA boosts autophagy in hair follicle stem cells, potentially aiding hair growth.

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

AtZP1 protein stops root hair growth in plants by blocking certain genes.

People with alopecia areata have higher levels of osteopontin, which might be important in the disease's development, but this doesn't relate to how severe the disease is.

Scoparone may help stimulate hair growth by increasing stem cell-related proteins in skin cells.

Keratin gene regulation was emerging, with a key transcription factor found to influence hair growth and gene expression.

Endoglin is crucial for proper hair growth cycles and stem cell activation in mice.

Hairless protein reduces Msx2 gene activity, affecting hair follicle development.

Hair follicle stem cells use specific chromatin changes to control their growth and differentiation.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

The improved genome of the African spiny mouse helps study its tissue regeneration.