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

A gene mutation in mice causes permanent hair loss and skin issues.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

Certain genetic markers may increase or decrease prostate cancer risk.

Mutant Cx43 causes slower wound healing and hair growth issues in ODDD.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

Two mutations in KRT74 and EDAR genes cause sheep to have finer wool.

The KRTAP36-2 gene in sheep affects wool yield.

OsPHR2 gene causes excessive phosphate in rice shoots, affecting plant growth and root development.

The research identified a gene in sheep important for wool quality, which could help improve wool traits.

Olmsted syndrome can be inherited as an autosomal recessive trait due to a rare TRPV3 gene mutation.

A gene variant causes a skin and hair disorder by disrupting protein balance.

61 functional keratin genes were identified in dogs and horses, leading to updated gene annotations.

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

Certain gene variants are linked to a higher risk of polycystic ovary syndrome, hair loss, and obesity in women from western Saudi Arabia.

RORA may help regulate hair growth by affecting hair follicle stem cells.

Certain SPINK5 gene mutations are common in Israeli families with Comèl-Netherton syndrome.

The fragrance cyclohexyl salicylate helps promote hair growth and increase hair stem cell numbers.

The B2C promoter works in sheep cells but not in mouse embryos.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

The KRTAP7-1 gene is very similar across different cattle and yak breeds and likely plays a role in hair strength and shape.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

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

The study found potential new DNA patterns in fertility genes, but further testing is needed.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

The ND1 gene of the Asian black bear Sichuan subspecies is similar to other bear species.