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Mutations in keratin genes cause skin disorders, but new treatments show promise.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

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

Hair keratin doesn't significantly affect rat organ function but may help detect early rejection through blood changes.

Mouse high-glycine/tyrosine proteins have distinct patterns in hair follicles, peaking at specific hair cycle days.

Alkylation of human hair keratin allows for adjustable drug release rates in hydrogels for medical use.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

HGF activator helps convert HGF to its active form, promoting hair growth.

Human-hair keratin artificial tendons are biocompatible and degrade well in rabbits.

Keratin 15 is not a reliable sole marker for identifying epidermal stem cells because it's found in various cell types.

Human hair proteins vary by individual, body site, and ethnicity, useful for forensics.

SETDB1 is essential for controlling DNA methylation, silencing retrotransposons, and maintaining skin cell health, with its absence leading to skin inflammation and hair loss.

New mutations in the hairless gene may cause hair loss and affect bone development.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

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

Interleukin-1 increases keratin K6 production in skin cells.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

HB-EGF boosts the hair growth ability of stem cells, making it a potential hair loss treatment.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

Hoxc13 and hair keratin are needed for forming rough skin on frog mating pads.

Hyper-keratinisation in Meibomian glands contributes to gland dysfunction.

Hair proteins have weak spots in their α-helical segments.

Keratinocytes contribute to hidradenitis suppurativa by causing inflammation and worsening the condition.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

Keratin hydrogels can be customized for better tissue healing.

Keratin-based scaffolds are safe and effective for tissue engineering.

Human hair proteins, especially keratins, can protect cells from oxidative stress in lab settings.

A new method effectively visualizes keratin in hair without harsh chemicals.

Disulfide bonds are crucial for hair structure during keratinization.

Keratin structure in hair is stable at pH 5-6 but disrupts between pH 6-7.