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Repetin is a protein involved in skin and hair development, binding calcium and compensating for other proteins when needed.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

Targeting the p63 gene could help treat skin diseases.

ErbB2 signaling is crucial for skin cell growth and cancer development in mice.

Overexpression of PTHrP in chondrocytes causes short-limbed dwarfism and delayed bone formation in mice.

The PCR technique can identify genetic differences in a wool-related gene among different sheep breeds, which may help improve wool and pelt quality.

PPARγ is essential for maintaining healthy skin, controlling inflammation, and ensuring proper skin barrier function.

Loss of Msx2 function causes eye development issues similar to Peters anomaly.

New genes linked to male pattern baldness were found on chromosome 20p11.

Overexpression of ALK2 in hair follicles disrupts skin development and slows wound healing.

Blocking mTORC1 reduces skin tumor growth in mice.

CD133+ cells are crucial for hair growth.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

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

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

Runx1 helps control the KAP5 gene in human hair follicles.

The mutation causing Hutchinson-Gilford progeria syndrome leads to severe skin problems and early death in mice.

Hair shaft changes may be linked to CCCA, but their role is unclear.

Three genes linked to the development of trichilemmal cysts were found.

Different species use the same genes for tooth regeneration.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Mus pahari mice have fragile skin due to abnormal collagen and elastin.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

The PIRL laser cuts tissue with less damage and scarring than traditional methods.

A gene variation is linked to hair thickness in Asians.

PRMT5 inhibitors effectively fight adenoid cystic carcinoma in salivary glands.

Deleting TNFα gene reduces skin cancer risk in certain mice.