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A new genetic tool improves the study of hair growth and potential hair disorder treatments.

Defective nuclear transport may cause gene expression changes in Progeria.

Some prostate cancers have gene changes that may affect treatment with certain drugs.

Removing a specific gene in certain skin cells causes hair loss in mice by disrupting hair follicle development.

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

HuR is essential for Treg function and preventing autoimmunity.

AP-1 and TGFß work together to drive resistance in basal cell carcinoma, suggesting new treatment options.

CXXC5 is a protein that controls cell growth and healing processes, and changes in its activity can lead to diseases like cancer and hair loss.

BMP-2 activates the Dlx3 gene in mouse skin cells, important for hair and skin development.

Removing integrin α3β1 from hair stem cells lowers skin tumor growth by affecting CCN2 protein levels.

Hoxc13 gene expression and skin thickness change similarly during cashmere goat hair follicle development.

New treatments for hair growth and psoriasis may be possible, and gene differences could affect baldness and the severity of skin conditions.

Thymosin beta 4 may help hair growth and could be a treatment for hair issues.

The prolactin gene polymorphism doesn't affect cashmere quality in these goats.

A genetic variant in goats is linked to cashmere growth.

The glucocorticoid receptor helps protect skin from tumors and other issues.

Thymosin β4 helps with healing, inflammation, and organ protection.

Mutations in TBX3 cause horses to have more even hair color instead of Dun camouflage.

Mutations in the hairless gene cause hair loss and skin cysts in rhesus macaques.

The hairless gene mutation causes baldness by disrupting hair follicle structure.

The KAP13-3 gene in sheep affects wool quality by influencing keratin assembly.

Mutations in the FOXN1 gene cause severe immune issues but don't affect hair and nails.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

Human bone cells mainly produce a type 1 enzyme that may help regulate bone health.

Three new types of a skin blistering disease were found, caused by specific gene mutations.

Certain genetic variants in keratins increase the risk of tooth decay.

Increased PHGDH expression causes early melanin buildup in hair follicles.

Hair follicle cells resist turning into skin cells.