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Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

The hr gene is linked to hair loss in Valle del Belice sheep.

Mutation in hairless gene may increase hair loss risk.

Mutation in hairless gene may increase hair loss risk.

The gene GJA1 is important for regulating coarse hair density in goats.

Hairless protein and putrescine regulate each other, affecting hair growth and skin balance.

BMP signaling helps prevent skin tumors by blocking cancer-promoting pathways.

Rex rabbits' hair follicles develop dynamically in the first 8 weeks, with key genes and proteins changing over time.

Wnt-10b helps skin cells and hair grow.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

Different keratins have unique expression patterns in mouse skin cells.

Overexpression of the glucocorticoid receptor in mice causes developmental defects similar to ectodermal dysplasia.

Wnt-10b helps skin cells develop into hair-related structures.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

The Shh gene controls cell growth and death in cashmere goat hair follicles, affecting hair growth.

Naked-mouse hair lacks certain proteins and has less soluble fibril.

AGD1's PH domain is essential for its role in root hair growth and polarity.

Meis1 is crucial for skin health and tumor development.

IGN genes may regulate hair growth and could be targeted for hair-loss treatments.

Skin cells can naturally limit the growth of cancerous changes by balancing cell renewal and differentiation.

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

Blimp1 is crucial for hair follicle growth and skin health.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

The gene HDC is important for the development of hair follicles in newborn mice.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

CMG2 and TEM8 receptors have distinct roles in skin and growth disorders, affecting collagen breakdown and growth.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

Certain genes help dermal papillae cells in hair follicles grow and group together.

Activin A promotes ear hair cell development, while follistatin delays it.

Keratin gene expression helps understand different types of skin cells and their development, and should be used carefully as biological markers.