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Keratin-based hydrogels with calcium are effective for delivering anti-fibrotic drugs.

Pashmina goats produce long hair-fiber due to specific gene expressions related to hair growth.

Collagen peptides may boost skin and hair-related gene expression.

Collagen peptides may boost skin and hair-related gene expression.

The Bsk mutation doesn't involve keratin gene recombination and its cause is unknown.

KRT72 gene helps form hair.

Mutations in the KRT16 gene can cause skin and nail disorders.

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

The hair keratin gene KRT81 is found in both normal and breast cancer cells and helps them invade surrounding tissues.

A gene mutation causes curly hair and hair loss in rats.

K6 gene expression can be controlled and manipulated in mice for studying skin disorders.

Hoxc13 regulates specific hair protein genes on mouse chromosome 16.

A specific gene region can control targeted and responsive gene expression in mice, useful for skin disorder treatments.

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

Only one K16 gene on chromosome 17 makes a functional keratin protein.

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

A KRT32 gene variant causes loose anagen hair syndrome.

The document concludes that the human keratin gene cluster is complex, with a need for updated naming to reflect over 50 functional genes important for hair and skin biology.

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

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

Using special RNA to target a mutant gene fixed hair problems in mice.

Only one of the two K16 genes on chromosome 17 makes a functional protein for keratin filaments.

Too much keratin 16 in mice skin causes abnormal skin thickening and structure.

Mutations in the KRT85 gene cause hair and nail problems.

The human keratin 6a gene's specific sequences trigger expression in skin layers after injury.

A rare genetic deletion in the KRT1 gene causes unique skin symptoms in a family.

A unique gene mutation was found in a family with monilethrix.

A new keratin gene was found in mice, explaining hair growth.