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LGR5 is a common marker of hair follicle stem cells in different animals and is important for hair growth and regeneration.

New mutations in the DSG4 gene cause a rare hair condition.

DKK4 can be used to improve wool quality in Zhexi Angora rabbits.

CD61 is important for mouse tooth cell growth and works through Lgr5.

A gene mutation in Lama3 is linked to a common type of hair loss.

Intu gene is crucial for hair follicle formation by helping keratinocytes differentiate through primary cilia.

GLABRA2 represses root hair formation by inhibiting a specific gene.

Skin cell types develop when specific genes are turned on by removing certain chemical tags from DNA.

Certain mice without specific receptors or mast cells don't lose hair from stress.

K42 and K124 keratins are only found in horse hoof lamellae.

ATR12-351 ointment safely delivers LEKTI protein to the skin, reducing enzyme activity in Netherton syndrome.

Long-lived proteins may predict age-related diseases.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

Rac1 is essential for proper hair structure and color.

Krox20 is important for maintaining stem cells in the skin and affects hair growth and color.

The POMP gene is active in various goat tissues and affects hair growth, with certain treatments influencing its expression.

CHI3L1 and CXCL5 proteins help promote hair growth.

New biological pathways and potential treatment targets for male pattern baldness were identified.

A defective gene causes hair loss and taste insensitivity in BTBR mice.

Laminin-511 may contribute to psoriasis by affecting skin cell growth and survival.

A gene in Arabidopsis thaliana, AtPRPL1, affects root hair length but not cell wall composition.

Matriptase is crucial for keeping epithelial tissues healthy and functioning properly.

SPT6 prevents excessive skin inflammation by blocking a feedback loop.

Epithelial-derived Pop-Up Keratinocytes (ePUKs) may enhance wound healing in regenerative medicine.

A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

Removing the Crif1 gene in mouse skin disrupts skin balance and hair growth.

A rare gene variant causes hair and nail issues in a family.