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Men with baldness due to androgenetic alopecia still have hair stem cells, but lack specific cells needed for hair growth.

Keratin 79 is linked to liver damage and may help diagnose liver diseases.

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

New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

KRT80 may worsen cancer by increasing growth and spread, but its full effects on treatment and outcomes need more research.

Mutations in the KLHL24 gene cause skin blistering in epidermolysis bullosa simplex.

KRT81 gene variations in sheep affect wool weight but not fiber length or thickness.

Inward rectifier potassium channels are important in many body functions and diseases, and could be potential drug targets.

KRT85 gene variations can help improve wool traits in sheep through selective breeding.

A KRT32 gene variant causes loose anagen hair syndrome.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

Krtap11-1 is important for hair strength and structure.

Certain genetic changes in the KRT82 gene may cause patchy skin in New Zealand rabbits.

RK81 can help promote hair growth.

K31 can identify clear secretory cells in human sweat glands.

The research cloned keratin 7 genes from humans, mice, and marsupials, found similarities between human and mouse genes, and discovered new areas of K7 expression in mice.

Mutations in specific llama genes may affect fiber quality for textiles.

KRT2.13 gene is similar to KRT2.9 but not expressed in hair follicles.

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

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

Lack of KSR1 stops certain skin tumors in mice.

TRIV-509 quickly improves skin barrier and cell health in atopic dermatitis.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Exosomes from dermal papilla cells help hair stem cells grow through a specific signaling pathway.

Krt6a-Cre transgenic mice help study gene effects on hair follicle development and tumor suppression.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.