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Scientists found a new type of skin cell that could help with skin repair and these cells work better with a certain protein.

A specific gene mutation causes a severe skin disorder in a family.

NKIRAS2 can suppress certain skin tumors but its effect on cancer varies with context and expression level.

Deleting the CD271 gene in mouse skin cells leads to disorganized skin and increased hair growth, suggesting CD271 is important for skin health.

GPRC5D is linked to the formation of hair, nails, and certain tongue areas.

The KRT84 gene is linked to better wool quality in Gansu Alpine Fine-wool sheep.

A chimeric keratin partially improved skin structure in mice lacking keratin 5, but didn't fully restore normal skin.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

Four specific keratins in hair follicles help understand hair structure and function.

The frizzy mouse and hairless rat mutations are due to changes in the Prss8 gene.

Trps1 is essential for proper hair follicle development.

A specific mutation in Kras causes abnormal tissue changes by making a cell signal continuously active, which disrupts normal cell coordination.

A new sheep gene, KRTAP36-1, may help breed sheep with better wool by reducing prickle factor.

Lack of TrkC receptor delays hair follicle development.

NCSTN gene mutation causes abnormal skin cell differentiation and more inflammation, contributing to Hidradenitis Suppurativa.

Only a few hair-specific keratins are linked to inherited hair disorders.

BKN-1 antibody targets specific keratin in basal cell epithelioma and normal skin basal cells.

Keratin-associated proteins have ancient origins and were used for different purposes before being adapted for hair in mammals.

An allele of the KRTAP13-2 gene may improve wool quality in sheep.

The study found nine new hair protein genes in human hair follicles.

A mutation in the KRT74 gene causes woolly hair by affecting hair texture.

Twist1 is crucial for UVB-induced skin cancer development.

The Itpr3 gene causes a specific hair pattern in mice.

Variant G of the KRTAP20-1 gene improves wool curliness in Chinese Tan sheep.

Researchers made a mouse model with curly hair and hair loss by editing a gene.

Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

Mutations in the KLHL24 gene cause a skin disorder in some Russian families.

Rapamycin reduces skin cell growth and tumor development by affecting cell signaling in mice.