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

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

PTHrP is higher in certain dog tumors and may act as a local growth factor.

Artemis phosphorylation at Ser516 may help regulate skin and hair structures.

ARHGEF3 is essential for proper hair follicle development.

Mettl3 is essential for normal tissue development and self-renewal by regulating gene expression.

PAD3 plays a key role in hair and skin protein structure and may be linked to skin diseases.

MOF controls skin development by regulating genes for mitochondria and cilia.

Enzymatic phosphorylation of hair keratin improves the effectiveness of hair products with cationic ingredients.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

Alkaline phosphatase activity in Beagle dog hair follicles is weakest in anagen and strongest in telogen.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

Human hair contains diverse proteins, including keratins and histones, which could help assess hair health and aging.

Trichohyalin and peptidylarginine deiminase type III are found together in rat hair follicles, with trichohyalin being modified after expression.

ARHGEF3 is essential for proper hair follicle development in mice.

PHGDH promotes cancer growth by aiding cell proliferation and tumor progression.

Whn is crucial for hair growth in certain areas by controlling a specific gene.

S100A3 protein is crucial for hair shaft formation in mice.

A new compound, HTPI, promotes hair growth by protecting cells from damage and regulating energy use.

PTHrP regulates various normal body functions, including bone development, skin, and muscle function.

Parathyroid hormone-related protein helps control hair growth phases in mice.

THH and PAD type III appear together early in hair growth, but deiminated THH appears later, suggesting another factor is involved.

Mutations in the hairless protein gene cause hair loss.

The type 3 IP3 receptor is important for controlling hair loss and growth.

Increased 14-3-3 proteins may block hair cycle regression, causing hair loss.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

Not having the gene PLAAT3 leads to fat loss, high insulin resistance, and abnormal fat levels in the blood due to a disruption in fat cell development and function.

Histone demethylases play a key role in the development of many diseases and may be targets for treatment.

HOXC13 is crucial for regulating hair keratin genes in hair follicles.