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Triptolide effectively and safely reduces actinic keratosis lesions in mice.

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

Two siblings with tinea capitis improved after treatment with ketoconazole.

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

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

KAP genes are crucial for hair development and show both shared and unique traits in humans, chimpanzees, and baboons.

Normal cells outcompete and remove mutant cells in the pancreas with the help of the EphA2 receptor.

Akt2 protein is essential for normal cell division in early mouse embryos.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

PKM2 is a promising target for heart repair and regeneration.

Certain genetic variations in camels affect hair coarseness.

Keratins K6 and K16 are expressed more freely in regenerating mouse skin than K1 and K10.

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

Different keratins have unique expression patterns in mouse skin cells.

DS-2325a is safe and well-tolerated, supporting further development for Netherton Syndrome treatment.

A PKP1 gene mutation causes skin fragility and hair loss in Chesapeake Bay retriever puppies.

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

The P133R mutation in AKR1D1 enzyme causes harmful bile acid buildup, explaining related health issues.

The 3D structure of a key hair protein was modeled, revealing specific helical structures and stabilization features.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

KAP genes show significant genetic variability, but its impact on hair traits is unclear.