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The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

Toothpaste containing α-tocopherol acetate, l-menthol, and stevioside can promote hair growth in mice.

Monilethrix causes fragile, patchy hair loss.

Oral minoxidil and growth factors improved hair density and thickness in a girl with hereditary hair loss.

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

KRTAP10 proteins help form the hair shaft's tough outer layer by interacting with specific hair keratins.

KRT17 may be a new target for endometrial cancer treatment because it helps cancer cells move and form new blood vessels.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

BK and Kv4.2 channels help Merkel cells in rat whiskers sense touch.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Keratin K6irs is a marker for the inner root sheath of hair follicles in mice and humans.

BRG1 is essential for skin cells to move and heal wounds properly.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

A mutation in the KRTHB5 gene causes hair and nail issues.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

Keratin structure changes during keratinization, but the exact model remains uncertain.

The study concluded that specific proteins are necessary to maintain the structure that holds epithelial cells tightly together.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

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.

PKM2 is a promising target for heart repair and regeneration.

The TRPV3 channel structure changes linked to severe itch and hyperkeratosis were identified using cryo-EM.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

The gene therapy showed significant wound healing and was safe for treating severe RDEB.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.