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Keratin 75 is important for fast wound healing and works with SOX2 and the LINC complex to help skin cells move and repair damage.

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

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

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

Hirosaki hairless rats lack hair due to missing DNA with key keratin genes.

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

KSR1 is crucial for certain skin tumor formation and could be a cancer therapy target.

Genetic differences between young and old Tan sheep explain why their fleece changes from curly to straight as they age.

Sebaceous glands can regenerate after injury using stem cells from hair follicles.

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

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

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

Exosomes from dermal papilla cells help hair follicle stem cells grow and survive.

The hairy ear mutation in mice is linked to changes in gene expression affecting hair growth.

S100a4 is key for hair growth in cashmere goats.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

Removing UBE2N from skin cells causes inflammation and immune response, which can be lessened with specific inhibitors.

Melatonin affects when and how certain genes work during the different stages of goat hair growth.

Scientists found new and known long non-coding RNAs in mouse hair follicle stem cells that may be important for stem cell function and could be targets for cancer treatment.

Lrig1 and Lgr6 stem cells help maintain hair follicles and influence skin cancer development.

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

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

A KRT32 gene variant causes loose anagen hair syndrome.

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

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

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

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