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The protein EZH2 blocks microRNA-22, increasing STK40 protein, which helps hair follicle stem cells change and grow hair.

The human keratin 6a gene's specific sequences trigger expression in skin layers after injury.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

c-Myc, Max, and Bin1 help hair follicle cells mature and die.

Inherited color dilution in rabbits is linked to DNA methylation changes.

Key genes linked to hair growth and cancer were identified in hairless mice.

Polycomb Repressive Complex 1 is crucial for keeping stem cells stable and maintaining healthy adult tissues.

Nuclear shape and chromatin changes affect gene expression in skin cell differentiation.

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

Keratin 17 is modified by RSK1 in response to growth and stress, affecting skin growth and stress response.

Par3 protein is essential for skin cell balance and stability.

CREB, a protein that can promote cancer traits, is controlled by β-catenin in skin cancer cells.

The protein p53 directly reduces the production of Keratin 17, a skin and hair protein, in rats with radiation dermatitis.

A new genetic region, 17q21.31, is linked to higher ovarian cancer risk.

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

Mutations in the Sgk3 gene cause fuzzy hair in mice.

Specific keratin gene mutations can cause monilethrix.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

hHb1, hHb3, and hHb6 mRNAs start expressing at the same time in hair follicles.

Keratin K80 is an ancient protein found in various tissues, important for cell structure and tissue differentiation.

New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.

A new keratin, hK6irs1, is found in all layers of the hair follicle's inner root sheath.

ALKBH5 helps wounds heal faster by stabilizing PELI2 mRNA.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

PTCH gene mutations contribute to basal cell carcinoma development.