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A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

Scientists identified and cloned specific keratin proteins in mouse hair.

A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

Rac1 is essential for proper hair structure and color.

A virus protein can activate a pathway that may lead to abnormal hair follicle development.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

Hoxc genes control hair growth through Wnt signaling.

Keratin 15 expression in skin cells is regulated by two mechanisms involving PKC/AP-1 and FOXM1.

RIPK1 inhibitors may help prevent alopecia areata by reducing immune cell activity.

Whn is essential for hair growth, and its malfunction causes hair loss.

Mouse keratin 6 genes evolved independently from human ones and are regulated differently.

A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

Dlx3 is essential for hair growth and regeneration.

The K15 promoter effectively targets stem cells in the hair follicle bulge.

KLF4 is important for keeping hair follicle stem cells inactive.

A specific gene segment can make mouse skin cells glow, helping study hair growth and gene effects.

Certain mutations in the hairless protein disrupt its ability to regulate the hair cycle.

Mice genetically modified to produce more Del1 protein had faster hair regrowth.

Merkel cells develop independently of nerves and are linked to specific hair follicles in mice.

Too much IKZF1 and Ikaros protein may cause alopecia areata.

Glypican-1 is important for blood vessel growth in hair follicles and could help treat hair loss.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

Changing CDK4 levels affects the number of stem cells in mouse hair follicles.

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

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

Engineered skin can grow chimeric hair follicles only with mouse dermal papilla cells.

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

KIF18B is important for correctly positioning cell division machinery in skin cells, affecting hair follicle development.