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A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

A new protein linked to hair strength was identified, aiding in understanding brittle hair conditions.

Surfactants can protect or harm hair, skin, and nails, depending on their type and use.

A genetic mutation in the hHa1 gene creates a smaller, but still functional, hair protein without causing hair problems.

Scaffoldin helps form hard skin structures in chicken embryos.

Feather diversity is due to different keratin gene combinations, and chickens can help study human keratin diseases.

KAP-depleted hair causes less immune response and is more biocompatible for implants.

Human hair follicles can be used to create skin-like tissue for wound healing and drug testing.

Chemical treatments on bleached black hair change its internal structure by breaking and reforming bonds, and treatments with hydrolyzed eggwhite protein help repair it.

Abnormal gene expression related to keratin causes hair loss in certain mice.

The research found that people's hair proteins vary by individual and body part, with some differences between ethnic groups, which could help in forensics.

Keratin hydrogel from human hair helps rats recover better from spinal cord injuries.

The lipid in human hair follicles acts as a barrier, similar to the skin's lipid layer.

Keratin 10 end domains may increase skin cancer risk by reducing cell death.

Activated β-catenin affects hair growth and skin thickness, and changes are reversible.

Only two of the four keratin genes are expressed in wool fibers.

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

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

Hair is complex, varies in type, and plays a big role in attractiveness and culture.

SKH1 hairless mice have identifiable epidermal stem cells with specific markers.

Scientists created a long-lasting stem cell line from human hair that can turn into different skin and hair cell types.

Runx1 helps control the KAP5 gene in human hair follicles.

Most people have similar hair protein patterns, but a rare variant was found in two women.

The document introduced a new naming system for keratin-associated proteins to improve clarity and communication across species.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

Kerion is a rare but serious scalp infection that needs proper treatment.

Human tissue kallikreins help regulate skin barrier functions and affect skin health.